Item | Value |
---|---|
geneid | 222967 |
ensemblid | ENSG00000155026.17 |
hgncid | 27362 |
symbol | RSPH10B |
name | radial spoke head 10 homolog B |
refseq_nuc | NM_173565.5 |
refseq_prot | NP_775836.4 |
ensembl_nuc | ENST00000404406.6 |
ensembl_prot | ENSP00000384097.1 |
mane_status | MANE Select |
chr | chr7 |
start | 5926136 |
end | 5970689 |
strand | - |
ver | v1.2 |
region | chr7:5926136-5970689 |
region5000 | chr7:5921136-5975689 |
regionname0 | RSPH10B_chr7_5926136_5970689 |
regionname5000 | RSPH10B_chr7_5921136_5975689 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 0/0 | 870 | 20 | 5 | 5 | 10 | 0 | 0 | 2 | RSPH10B_chr7_5921136_5975689 | RSPH10B | copy fasta | chr7 | 5921136 | 5975689 |
a0002 | 0/0 | 870 | 11 | 3 | 2 | 1 | 4 | 1 | 0 | RSPH10B_chr7_5921136_5975689 | RSPH10B | copy fasta | chr7 | 5921136 | 5975689 |
a0003 | 0/0 | 870 | 9 | 1 | 5 | 1 | 2 | 0 | 0 | RSPH10B_chr7_5921136_5975689 | RSPH10B | copy fasta | chr7 | 5921136 | 5975689 |
a0004 | 0/0 | 870 | 9 | 5 | 1 | 1 | 1 | 1 | 0 | RSPH10B_chr7_5921136_5975689 | RSPH10B | copy fasta | chr7 | 5921136 | 5975689 |
a0005 | 0/0 | 870 | 9 | 3 | 2 | 2 | 2 | 0 | 0 | RSPH10B_chr7_5921136_5975689 | RSPH10B | copy fasta | chr7 | 5921136 | 5975689 |
a0006 | 0/0 | 870 | 5 | 1 | 4 | 0 | 0 | 0 | 0 | RSPH10B_chr7_5921136_5975689 | RSPH10B | copy fasta | chr7 | 5921136 | 5975689 |
a0007 | 0/0 | 870 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | RSPH10B_chr7_5921136_5975689 | RSPH10B | copy fasta | chr7 | 5921136 | 5975689 |
a0008 | 0/0 | 870 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | RSPH10B_chr7_5921136_5975689 | RSPH10B | copy fasta | chr7 | 5921136 | 5975689 |
a0009 | 0/0 | 870 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | RSPH10B_chr7_5921136_5975689 | RSPH10B | copy fasta | chr7 | 5921136 | 5975689 |
a0010 | 0/0 | 870 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | RSPH10B_chr7_5921136_5975689 | RSPH10B | copy fasta | chr7 | 5921136 | 5975689 |
a0011 | 0/0 | 870 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | RSPH10B_chr7_5921136_5975689 | RSPH10B | copy fasta | chr7 | 5921136 | 5975689 |
a0012 | 0/0 | 542 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | RSPH10B_chr7_5921136_5975689 | RSPH10B | copy fasta | chr7 | 5921136 | 5975689 |
chapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 0/0 | 2613 | 12 | 0 | 3 | 9 | 0 | 0 | RSPH10B_chr7_5921136_5975689 | RSPH10B | copy fasta | chr7 | 5921136 | 5975689 | |
c0002 | 0/0 | 2613 | 11 | 3 | 2 | 1 | 4 | 1 | RSPH10B_chr7_5921136_5975689 | RSPH10B | copy fasta | chr7 | 5921136 | 5975689 | |
c0003 | 0/0 | 2613 | 9 | 3 | 2 | 2 | 2 | 0 | RSPH10B_chr7_5921136_5975689 | RSPH10B | copy fasta | chr7 | 5921136 | 5975689 | |
c0004 | 0/0 | 2613 | 9 | 1 | 5 | 1 | 2 | 0 | RSPH10B_chr7_5921136_5975689 | RSPH10B | copy fasta | chr7 | 5921136 | 5975689 | |
c0005 | 0/0 | 2613 | 6 | 3 | 0 | 1 | 1 | 1 | RSPH10B_chr7_5921136_5975689 | RSPH10B | copy fasta | chr7 | 5921136 | 5975689 | |
c0006 | 0/0 | 2613 | 5 | 1 | 4 | 0 | 0 | 0 | RSPH10B_chr7_5921136_5975689 | RSPH10B | copy fasta | chr7 | 5921136 | 5975689 | |
c0007 | 0/0 | 2613 | 2 | 2 | 0 | 0 | 0 | 0 | RSPH10B_chr7_5921136_5975689 | RSPH10B | copy fasta | chr7 | 5921136 | 5975689 | |
c0008 | 0/0 | 2613 | 2 | 2 | 0 | 0 | 0 | 0 | RSPH10B_chr7_5921136_5975689 | RSPH10B | copy fasta | chr7 | 5921136 | 5975689 | |
c0009 | 0/0 | 2613 | 2 | 2 | 0 | 0 | 0 | 0 | RSPH10B_chr7_5921136_5975689 | RSPH10B | copy fasta | chr7 | 5921136 | 5975689 | |
c0010 | 0/0 | 2613 | 2 | 0 | 2 | 0 | 0 | 0 | RSPH10B_chr7_5921136_5975689 | RSPH10B | copy fasta | chr7 | 5921136 | 5975689 | |
c0011 | 0/0 | 2613 | 2 | 1 | 1 | 0 | 0 | 0 | RSPH10B_chr7_5921136_5975689 | RSPH10B | copy fasta | chr7 | 5921136 | 5975689 | |
c0012 | 0/0 | 2613 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH10B_chr7_5921136_5975689 | RSPH10B | copy fasta | chr7 | 5921136 | 5975689 | |
c0013 | 0/0 | 2613 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH10B_chr7_5921136_5975689 | RSPH10B | copy fasta | chr7 | 5921136 | 5975689 | |
c0014 | 0/0 | 2613 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH10B_chr7_5921136_5975689 | RSPH10B | copy fasta | chr7 | 5921136 | 5975689 | |
c0015 | 0/0 | 2613 | 1 | 0 | 1 | 0 | 0 | 0 | RSPH10B_chr7_5921136_5975689 | RSPH10B | copy fasta | chr7 | 5921136 | 5975689 | |
c0016 | 0/0 | 2613 | 1 | 0 | 0 | 0 | 1 | 0 | RSPH10B_chr7_5921136_5975689 | RSPH10B | copy fasta | chr7 | 5921136 | 5975689 | |
c0017 | 0/0 | 2613 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH10B_chr7_5921136_5975689 | RSPH10B | copy fasta | chr7 | 5921136 | 5975689 | |
c0018 | 0/0 | 2613 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH10B_chr7_5921136_5975689 | RSPH10B | copy fasta | chr7 | 5921136 | 5975689 | |
c0019 | 0/0 | 2613 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH10B_chr7_5921136_5975689 | RSPH10B | copy fasta | chr7 | 5921136 | 5975689 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 0/0 | 508 | 35 | 9 | 9 | 13 | 3 | 1 | RSPH10B_chr7_5921136_5975689 | RSPH10B | copy fasta | chr7 | 5921136 | 5975689 |
t0002 | 0/0 | 510 | 18 | 9 | 3 | 2 | 4 | 0 | RSPH10B_chr7_5921136_5975689 | RSPH10B | copy fasta | chr7 | 5921136 | 5975689 |
t0003 | 0/0 | 510 | 12 | 2 | 5 | 1 | 3 | 1 | RSPH10B_chr7_5921136_5975689 | RSPH10B | copy fasta | chr7 | 5921136 | 5975689 |
t0004 | 0/0 | 508 | 3 | 1 | 2 | 0 | 0 | 0 | RSPH10B_chr7_5921136_5975689 | RSPH10B | copy fasta | chr7 | 5921136 | 5975689 |
t0005 | 0/0 | 508 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH10B_chr7_5921136_5975689 | RSPH10B | copy fasta | chr7 | 5921136 | 5975689 |
t0006 | 0/0 | 508 | 1 | 0 | 1 | 0 | 0 | 0 | RSPH10B_chr7_5921136_5975689 | RSPH10B | copy fasta | chr7 | 5921136 | 5975689 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSPH10B_chr7_5921136_5975689 | RSPH10B | chr7 | 5921136 | 5975689 |
g0002 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSPH10B_chr7_5921136_5975689 | RSPH10B | chr7 | 5921136 | 5975689 |
g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH10B_chr7_5921136_5975689 | RSPH10B | chr7 | 5921136 | 5975689 |
g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH10B_chr7_5921136_5975689 | RSPH10B | chr7 | 5921136 | 5975689 |
g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH10B_chr7_5921136_5975689 | RSPH10B | chr7 | 5921136 | 5975689 |
g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH10B_chr7_5921136_5975689 | RSPH10B | chr7 | 5921136 | 5975689 |
g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH10B_chr7_5921136_5975689 | RSPH10B | chr7 | 5921136 | 5975689 |
g0008 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSPH10B_chr7_5921136_5975689 | RSPH10B | chr7 | 5921136 | 5975689 |
g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH10B_chr7_5921136_5975689 | RSPH10B | chr7 | 5921136 | 5975689 |
g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH10B_chr7_5921136_5975689 | RSPH10B | chr7 | 5921136 | 5975689 |
g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH10B_chr7_5921136_5975689 | RSPH10B | chr7 | 5921136 | 5975689 |
g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH10B_chr7_5921136_5975689 | RSPH10B | chr7 | 5921136 | 5975689 |
g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSPH10B_chr7_5921136_5975689 | RSPH10B | chr7 | 5921136 | 5975689 |
g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH10B_chr7_5921136_5975689 | RSPH10B | chr7 | 5921136 | 5975689 |
g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH10B_chr7_5921136_5975689 | RSPH10B | chr7 | 5921136 | 5975689 |
g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH10B_chr7_5921136_5975689 | RSPH10B | chr7 | 5921136 | 5975689 |
g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSPH10B_chr7_5921136_5975689 | RSPH10B | chr7 | 5921136 | 5975689 |
g0018 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RSPH10B_chr7_5921136_5975689 | RSPH10B | chr7 | 5921136 | 5975689 |
g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH10B_chr7_5921136_5975689 | RSPH10B | chr7 | 5921136 | 5975689 |
g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH10B_chr7_5921136_5975689 | RSPH10B | chr7 | 5921136 | 5975689 |
g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSPH10B_chr7_5921136_5975689 | RSPH10B | chr7 | 5921136 | 5975689 |
g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH10B_chr7_5921136_5975689 | RSPH10B | chr7 | 5921136 | 5975689 |
g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSPH10B_chr7_5921136_5975689 | RSPH10B | chr7 | 5921136 | 5975689 |
g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH10B_chr7_5921136_5975689 | RSPH10B | chr7 | 5921136 | 5975689 |
g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH10B_chr7_5921136_5975689 | RSPH10B | chr7 | 5921136 | 5975689 |
g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH10B_chr7_5921136_5975689 | RSPH10B | chr7 | 5921136 | 5975689 |
g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSPH10B_chr7_5921136_5975689 | RSPH10B | chr7 | 5921136 | 5975689 |
g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSPH10B_chr7_5921136_5975689 | RSPH10B | chr7 | 5921136 | 5975689 |
g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSPH10B_chr7_5921136_5975689 | RSPH10B | chr7 | 5921136 | 5975689 |
g0030 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RSPH10B_chr7_5921136_5975689 | RSPH10B | chr7 | 5921136 | 5975689 |
g0031 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RSPH10B_chr7_5921136_5975689 | RSPH10B | chr7 | 5921136 | 5975689 |
g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH10B_chr7_5921136_5975689 | RSPH10B | chr7 | 5921136 | 5975689 |
g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH10B_chr7_5921136_5975689 | RSPH10B | chr7 | 5921136 | 5975689 |
g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH10B_chr7_5921136_5975689 | RSPH10B | chr7 | 5921136 | 5975689 |
g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH10B_chr7_5921136_5975689 | RSPH10B | chr7 | 5921136 | 5975689 |
g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH10B_chr7_5921136_5975689 | RSPH10B | chr7 | 5921136 | 5975689 |
g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH10B_chr7_5921136_5975689 | RSPH10B | chr7 | 5921136 | 5975689 |
g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSPH10B_chr7_5921136_5975689 | RSPH10B | chr7 | 5921136 | 5975689 |
g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH10B_chr7_5921136_5975689 | RSPH10B | chr7 | 5921136 | 5975689 |
g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSPH10B_chr7_5921136_5975689 | RSPH10B | chr7 | 5921136 | 5975689 |
g0041 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RSPH10B_chr7_5921136_5975689 | RSPH10B | chr7 | 5921136 | 5975689 |
g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSPH10B_chr7_5921136_5975689 | RSPH10B | chr7 | 5921136 | 5975689 |
g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH10B_chr7_5921136_5975689 | RSPH10B | chr7 | 5921136 | 5975689 |
g0044 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RSPH10B_chr7_5921136_5975689 | RSPH10B | chr7 | 5921136 | 5975689 |
g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH10B_chr7_5921136_5975689 | RSPH10B | chr7 | 5921136 | 5975689 |
g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSPH10B_chr7_5921136_5975689 | RSPH10B | chr7 | 5921136 | 5975689 |
g0047 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RSPH10B_chr7_5921136_5975689 | RSPH10B | chr7 | 5921136 | 5975689 |
g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH10B_chr7_5921136_5975689 | RSPH10B | chr7 | 5921136 | 5975689 |
g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH10B_chr7_5921136_5975689 | RSPH10B | chr7 | 5921136 | 5975689 |
g0050 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RSPH10B_chr7_5921136_5975689 | RSPH10B | chr7 | 5921136 | 5975689 |
g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH10B_chr7_5921136_5975689 | RSPH10B | chr7 | 5921136 | 5975689 |
g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH10B_chr7_5921136_5975689 | RSPH10B | chr7 | 5921136 | 5975689 |
g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH10B_chr7_5921136_5975689 | RSPH10B | chr7 | 5921136 | 5975689 |
g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH10B_chr7_5921136_5975689 | RSPH10B | chr7 | 5921136 | 5975689 |
g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH10B_chr7_5921136_5975689 | RSPH10B | chr7 | 5921136 | 5975689 |
g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSPH10B_chr7_5921136_5975689 | RSPH10B | chr7 | 5921136 | 5975689 |
g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSPH10B_chr7_5921136_5975689 | RSPH10B | chr7 | 5921136 | 5975689 |
g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSPH10B_chr7_5921136_5975689 | RSPH10B | chr7 | 5921136 | 5975689 |
g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSPH10B_chr7_5921136_5975689 | RSPH10B | chr7 | 5921136 | 5975689 |
g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSPH10B_chr7_5921136_5975689 | RSPH10B | chr7 | 5921136 | 5975689 |
g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH10B_chr7_5921136_5975689 | RSPH10B | chr7 | 5921136 | 5975689 |
g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSPH10B_chr7_5921136_5975689 | RSPH10B | chr7 | 5921136 | 5975689 |
g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSPH10B_chr7_5921136_5975689 | RSPH10B | chr7 | 5921136 | 5975689 |
g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH10B_chr7_5921136_5975689 | RSPH10B | chr7 | 5921136 | 5975689 |
g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH10B_chr7_5921136_5975689 | RSPH10B | chr7 | 5921136 | 5975689 |
g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSPH10B_chr7_5921136_5975689 | RSPH10B | chr7 | 5921136 | 5975689 |
g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH10B_chr7_5921136_5975689 | RSPH10B | chr7 | 5921136 | 5975689 |
g0068 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RSPH10B_chr7_5921136_5975689 | RSPH10B | chr7 | 5921136 | 5975689 |
g0069 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RSPH10B_chr7_5921136_5975689 | RSPH10B | chr7 | 5921136 | 5975689 |
g0070 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RSPH10B_chr7_5921136_5975689 | RSPH10B | chr7 | 5921136 | 5975689 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 0/0 | 2613 | 12 | 0 | 3 | 9 | 0 | 0 | RSPH10B_chr7_5921136_5975689 | RSPH10B | copy fasta | chr7 | 5921136 | 5975689 | |
a0001c0008 | 0/0 | 2613 | 2 | 2 | 0 | 0 | 0 | 0 | RSPH10B_chr7_5921136_5975689 | RSPH10B | copy fasta | chr7 | 5921136 | 5975689 | |
a0001c0009 | 0/0 | 2613 | 2 | 2 | 0 | 0 | 0 | 0 | RSPH10B_chr7_5921136_5975689 | RSPH10B | copy fasta | chr7 | 5921136 | 5975689 | |
a0001c0010 | 0/0 | 2613 | 2 | 0 | 2 | 0 | 0 | 0 | RSPH10B_chr7_5921136_5975689 | RSPH10B | copy fasta | chr7 | 5921136 | 5975689 | |
a0001c0013 | 0/0 | 2613 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH10B_chr7_5921136_5975689 | RSPH10B | copy fasta | chr7 | 5921136 | 5975689 | |
a0001c0014 | 0/0 | 2613 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH10B_chr7_5921136_5975689 | RSPH10B | copy fasta | chr7 | 5921136 | 5975689 | |
a0002c0002 | 0/0 | 2613 | 11 | 3 | 2 | 1 | 4 | 1 | RSPH10B_chr7_5921136_5975689 | RSPH10B | copy fasta | chr7 | 5921136 | 5975689 | |
a0003c0004 | 0/0 | 2613 | 9 | 1 | 5 | 1 | 2 | 0 | RSPH10B_chr7_5921136_5975689 | RSPH10B | copy fasta | chr7 | 5921136 | 5975689 | |
a0004c0005 | 0/0 | 2613 | 6 | 3 | 0 | 1 | 1 | 1 | RSPH10B_chr7_5921136_5975689 | RSPH10B | copy fasta | chr7 | 5921136 | 5975689 | |
a0004c0011 | 0/0 | 2613 | 2 | 1 | 1 | 0 | 0 | 0 | RSPH10B_chr7_5921136_5975689 | RSPH10B | copy fasta | chr7 | 5921136 | 5975689 | |
a0004c0018 | 0/0 | 2613 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH10B_chr7_5921136_5975689 | RSPH10B | copy fasta | chr7 | 5921136 | 5975689 | |
a0005c0003 | 0/0 | 2613 | 9 | 3 | 2 | 2 | 2 | 0 | RSPH10B_chr7_5921136_5975689 | RSPH10B | copy fasta | chr7 | 5921136 | 5975689 | |
a0006c0006 | 0/0 | 2613 | 5 | 1 | 4 | 0 | 0 | 0 | RSPH10B_chr7_5921136_5975689 | RSPH10B | copy fasta | chr7 | 5921136 | 5975689 | |
a0007c0007 | 0/0 | 2613 | 2 | 2 | 0 | 0 | 0 | 0 | RSPH10B_chr7_5921136_5975689 | RSPH10B | copy fasta | chr7 | 5921136 | 5975689 | |
a0008c0017 | 0/0 | 2613 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH10B_chr7_5921136_5975689 | RSPH10B | copy fasta | chr7 | 5921136 | 5975689 | |
a0009c0016 | 0/0 | 2613 | 1 | 0 | 0 | 0 | 1 | 0 | RSPH10B_chr7_5921136_5975689 | RSPH10B | copy fasta | chr7 | 5921136 | 5975689 | |
a0010c0019 | 0/0 | 2613 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH10B_chr7_5921136_5975689 | RSPH10B | copy fasta | chr7 | 5921136 | 5975689 | |
a0011c0015 | 0/0 | 2613 | 1 | 0 | 1 | 0 | 0 | 0 | RSPH10B_chr7_5921136_5975689 | RSPH10B | copy fasta | chr7 | 5921136 | 5975689 | |
a0012c0012 | 0/0 | 2613 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH10B_chr7_5921136_5975689 | RSPH10B | copy fasta | chr7 | 5921136 | 5975689 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 3120 | 10 | 0 | 2 | 8 | 0 | 0 | RSPH10B_chr7_5921136_5975689 | RSPH10B | copy fasta | chr7 | 5921136 | 5975689 |
a0001c0001t0002 | 0/0 | 3122 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH10B_chr7_5921136_5975689 | RSPH10B | copy fasta | chr7 | 5921136 | 5975689 |
a0001c0001t0006 | 0/0 | 3120 | 1 | 0 | 1 | 0 | 0 | 0 | RSPH10B_chr7_5921136_5975689 | RSPH10B | copy fasta | chr7 | 5921136 | 5975689 |
a0001c0008t0002 | 0/0 | 3122 | 2 | 2 | 0 | 0 | 0 | 0 | RSPH10B_chr7_5921136_5975689 | RSPH10B | copy fasta | chr7 | 5921136 | 5975689 |
a0001c0009t0001 | 0/0 | 3120 | 2 | 2 | 0 | 0 | 0 | 0 | RSPH10B_chr7_5921136_5975689 | RSPH10B | copy fasta | chr7 | 5921136 | 5975689 |
a0001c0010t0004 | 0/0 | 3120 | 2 | 0 | 2 | 0 | 0 | 0 | RSPH10B_chr7_5921136_5975689 | RSPH10B | copy fasta | chr7 | 5921136 | 5975689 |
a0001c0013t0001 | 0/0 | 3120 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH10B_chr7_5921136_5975689 | RSPH10B | copy fasta | chr7 | 5921136 | 5975689 |
a0001c0014t0001 | 0/0 | 3120 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH10B_chr7_5921136_5975689 | RSPH10B | copy fasta | chr7 | 5921136 | 5975689 |
a0002c0002t0001 | 0/0 | 3120 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH10B_chr7_5921136_5975689 | RSPH10B | copy fasta | chr7 | 5921136 | 5975689 |
a0002c0002t0002 | 0/0 | 3122 | 9 | 2 | 2 | 1 | 4 | 0 | RSPH10B_chr7_5921136_5975689 | RSPH10B | copy fasta | chr7 | 5921136 | 5975689 |
a0002c0002t0003 | 0/0 | 3122 | 1 | 0 | 0 | 0 | 0 | 1 | RSPH10B_chr7_5921136_5975689 | RSPH10B | copy fasta | chr7 | 5921136 | 5975689 |
a0003c0004t0003 | 0/0 | 3122 | 9 | 1 | 5 | 1 | 2 | 0 | RSPH10B_chr7_5921136_5975689 | RSPH10B | copy fasta | chr7 | 5921136 | 5975689 |
a0004c0005t0001 | 0/0 | 3120 | 5 | 2 | 0 | 1 | 1 | 1 | RSPH10B_chr7_5921136_5975689 | RSPH10B | copy fasta | chr7 | 5921136 | 5975689 |
a0004c0005t0005 | 0/0 | 3120 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH10B_chr7_5921136_5975689 | RSPH10B | copy fasta | chr7 | 5921136 | 5975689 |
a0004c0011t0002 | 0/0 | 3122 | 2 | 1 | 1 | 0 | 0 | 0 | RSPH10B_chr7_5921136_5975689 | RSPH10B | copy fasta | chr7 | 5921136 | 5975689 |
a0004c0018t0001 | 0/0 | 3120 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH10B_chr7_5921136_5975689 | RSPH10B | copy fasta | chr7 | 5921136 | 5975689 |
a0005c0003t0001 | 0/0 | 3120 | 6 | 0 | 2 | 2 | 2 | 0 | RSPH10B_chr7_5921136_5975689 | RSPH10B | copy fasta | chr7 | 5921136 | 5975689 |
a0005c0003t0002 | 0/0 | 3122 | 2 | 2 | 0 | 0 | 0 | 0 | RSPH10B_chr7_5921136_5975689 | RSPH10B | copy fasta | chr7 | 5921136 | 5975689 |
a0005c0003t0004 | 0/0 | 3120 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH10B_chr7_5921136_5975689 | RSPH10B | copy fasta | chr7 | 5921136 | 5975689 |
a0006c0006t0001 | 0/0 | 3120 | 5 | 1 | 4 | 0 | 0 | 0 | RSPH10B_chr7_5921136_5975689 | RSPH10B | copy fasta | chr7 | 5921136 | 5975689 |
a0007c0007t0002 | 0/0 | 3122 | 2 | 2 | 0 | 0 | 0 | 0 | RSPH10B_chr7_5921136_5975689 | RSPH10B | copy fasta | chr7 | 5921136 | 5975689 |
a0008c0017t0003 | 0/0 | 3122 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH10B_chr7_5921136_5975689 | RSPH10B | copy fasta | chr7 | 5921136 | 5975689 |
a0009c0016t0003 | 0/0 | 3122 | 1 | 0 | 0 | 0 | 1 | 0 | RSPH10B_chr7_5921136_5975689 | RSPH10B | copy fasta | chr7 | 5921136 | 5975689 |
a0010c0019t0001 | 0/0 | 3120 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH10B_chr7_5921136_5975689 | RSPH10B | copy fasta | chr7 | 5921136 | 5975689 |
a0011c0015t0001 | 0/0 | 3120 | 1 | 0 | 1 | 0 | 0 | 0 | RSPH10B_chr7_5921136_5975689 | RSPH10B | copy fasta | chr7 | 5921136 | 5975689 |
a0012c0012t0001 | 0/0 | 3120 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH10B_chr7_5921136_5975689 | RSPH10B | copy fasta | chr7 | 5921136 | 5975689 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSPH10B_chr7_5921136_5975689 | RSPH10B | chr7 | 5921136 | 5975689 |
a0001c0001t0001g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH10B_chr7_5921136_5975689 | RSPH10B | chr7 | 5921136 | 5975689 |
a0001c0001t0001g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH10B_chr7_5921136_5975689 | RSPH10B | chr7 | 5921136 | 5975689 |
a0001c0001t0001g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH10B_chr7_5921136_5975689 | RSPH10B | chr7 | 5921136 | 5975689 |
a0001c0001t0001g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH10B_chr7_5921136_5975689 | RSPH10B | chr7 | 5921136 | 5975689 |
a0001c0001t0001g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH10B_chr7_5921136_5975689 | RSPH10B | chr7 | 5921136 | 5975689 |
a0001c0001t0001g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSPH10B_chr7_5921136_5975689 | RSPH10B | chr7 | 5921136 | 5975689 |
a0001c0001t0001g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH10B_chr7_5921136_5975689 | RSPH10B | chr7 | 5921136 | 5975689 |
a0001c0001t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH10B_chr7_5921136_5975689 | RSPH10B | chr7 | 5921136 | 5975689 |
a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH10B_chr7_5921136_5975689 | RSPH10B | chr7 | 5921136 | 5975689 |
a0001c0001t0002g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH10B_chr7_5921136_5975689 | RSPH10B | chr7 | 5921136 | 5975689 |
a0001c0001t0006g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSPH10B_chr7_5921136_5975689 | RSPH10B | chr7 | 5921136 | 5975689 |
a0001c0008t0002g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH10B_chr7_5921136_5975689 | RSPH10B | chr7 | 5921136 | 5975689 |
a0001c0008t0002g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH10B_chr7_5921136_5975689 | RSPH10B | chr7 | 5921136 | 5975689 |
a0001c0009t0001g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH10B_chr7_5921136_5975689 | RSPH10B | chr7 | 5921136 | 5975689 |
a0001c0009t0001g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH10B_chr7_5921136_5975689 | RSPH10B | chr7 | 5921136 | 5975689 |
a0001c0010t0004g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSPH10B_chr7_5921136_5975689 | RSPH10B | chr7 | 5921136 | 5975689 |
a0001c0010t0004g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSPH10B_chr7_5921136_5975689 | RSPH10B | chr7 | 5921136 | 5975689 |
a0001c0013t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH10B_chr7_5921136_5975689 | RSPH10B | chr7 | 5921136 | 5975689 |
a0001c0014t0001g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH10B_chr7_5921136_5975689 | RSPH10B | chr7 | 5921136 | 5975689 |
a0002c0002t0001g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH10B_chr7_5921136_5975689 | RSPH10B | chr7 | 5921136 | 5975689 |
a0002c0002t0002g0018 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RSPH10B_chr7_5921136_5975689 | RSPH10B | chr7 | 5921136 | 5975689 |
a0002c0002t0002g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSPH10B_chr7_5921136_5975689 | RSPH10B | chr7 | 5921136 | 5975689 |
a0002c0002t0002g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSPH10B_chr7_5921136_5975689 | RSPH10B | chr7 | 5921136 | 5975689 |
a0002c0002t0002g0044 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RSPH10B_chr7_5921136_5975689 | RSPH10B | chr7 | 5921136 | 5975689 |
a0002c0002t0002g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH10B_chr7_5921136_5975689 | RSPH10B | chr7 | 5921136 | 5975689 |
a0002c0002t0002g0047 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RSPH10B_chr7_5921136_5975689 | RSPH10B | chr7 | 5921136 | 5975689 |
a0002c0002t0002g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH10B_chr7_5921136_5975689 | RSPH10B | chr7 | 5921136 | 5975689 |
a0002c0002t0002g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH10B_chr7_5921136_5975689 | RSPH10B | chr7 | 5921136 | 5975689 |
a0002c0002t0002g0050 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RSPH10B_chr7_5921136_5975689 | RSPH10B | chr7 | 5921136 | 5975689 |
a0002c0002t0003g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSPH10B_chr7_5921136_5975689 | RSPH10B | chr7 | 5921136 | 5975689 |
a0003c0004t0003g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSPH10B_chr7_5921136_5975689 | RSPH10B | chr7 | 5921136 | 5975689 |
a0003c0004t0003g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSPH10B_chr7_5921136_5975689 | RSPH10B | chr7 | 5921136 | 5975689 |
a0003c0004t0003g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSPH10B_chr7_5921136_5975689 | RSPH10B | chr7 | 5921136 | 5975689 |
a0003c0004t0003g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSPH10B_chr7_5921136_5975689 | RSPH10B | chr7 | 5921136 | 5975689 |
a0003c0004t0003g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH10B_chr7_5921136_5975689 | RSPH10B | chr7 | 5921136 | 5975689 |
a0003c0004t0003g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSPH10B_chr7_5921136_5975689 | RSPH10B | chr7 | 5921136 | 5975689 |
a0003c0004t0003g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH10B_chr7_5921136_5975689 | RSPH10B | chr7 | 5921136 | 5975689 |
a0003c0004t0003g0069 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RSPH10B_chr7_5921136_5975689 | RSPH10B | chr7 | 5921136 | 5975689 |
a0003c0004t0003g0070 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RSPH10B_chr7_5921136_5975689 | RSPH10B | chr7 | 5921136 | 5975689 |
a0004c0005t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH10B_chr7_5921136_5975689 | RSPH10B | chr7 | 5921136 | 5975689 |
a0004c0005t0001g0041 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RSPH10B_chr7_5921136_5975689 | RSPH10B | chr7 | 5921136 | 5975689 |
a0004c0005t0001g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSPH10B_chr7_5921136_5975689 | RSPH10B | chr7 | 5921136 | 5975689 |
a0004c0005t0001g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH10B_chr7_5921136_5975689 | RSPH10B | chr7 | 5921136 | 5975689 |
a0004c0005t0001g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH10B_chr7_5921136_5975689 | RSPH10B | chr7 | 5921136 | 5975689 |
a0004c0005t0005g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH10B_chr7_5921136_5975689 | RSPH10B | chr7 | 5921136 | 5975689 |
a0004c0011t0002g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH10B_chr7_5921136_5975689 | RSPH10B | chr7 | 5921136 | 5975689 |
a0004c0011t0002g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSPH10B_chr7_5921136_5975689 | RSPH10B | chr7 | 5921136 | 5975689 |
a0004c0018t0001g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH10B_chr7_5921136_5975689 | RSPH10B | chr7 | 5921136 | 5975689 |
a0005c0003t0001g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH10B_chr7_5921136_5975689 | RSPH10B | chr7 | 5921136 | 5975689 |
a0005c0003t0001g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH10B_chr7_5921136_5975689 | RSPH10B | chr7 | 5921136 | 5975689 |
a0005c0003t0001g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSPH10B_chr7_5921136_5975689 | RSPH10B | chr7 | 5921136 | 5975689 |
a0005c0003t0001g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSPH10B_chr7_5921136_5975689 | RSPH10B | chr7 | 5921136 | 5975689 |
a0005c0003t0001g0030 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RSPH10B_chr7_5921136_5975689 | RSPH10B | chr7 | 5921136 | 5975689 |
a0005c0003t0001g0031 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RSPH10B_chr7_5921136_5975689 | RSPH10B | chr7 | 5921136 | 5975689 |
a0005c0003t0002g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH10B_chr7_5921136_5975689 | RSPH10B | chr7 | 5921136 | 5975689 |
a0005c0003t0002g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH10B_chr7_5921136_5975689 | RSPH10B | chr7 | 5921136 | 5975689 |
a0005c0003t0004g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH10B_chr7_5921136_5975689 | RSPH10B | chr7 | 5921136 | 5975689 |
a0006c0006t0001g0002 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSPH10B_chr7_5921136_5975689 | RSPH10B | chr7 | 5921136 | 5975689 |
a0006c0006t0001g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH10B_chr7_5921136_5975689 | RSPH10B | chr7 | 5921136 | 5975689 |
a0006c0006t0001g0008 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSPH10B_chr7_5921136_5975689 | RSPH10B | chr7 | 5921136 | 5975689 |
a0006c0006t0001g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSPH10B_chr7_5921136_5975689 | RSPH10B | chr7 | 5921136 | 5975689 |
a0006c0006t0001g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSPH10B_chr7_5921136_5975689 | RSPH10B | chr7 | 5921136 | 5975689 |
a0007c0007t0002g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH10B_chr7_5921136_5975689 | RSPH10B | chr7 | 5921136 | 5975689 |
a0007c0007t0002g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH10B_chr7_5921136_5975689 | RSPH10B | chr7 | 5921136 | 5975689 |
a0008c0017t0003g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH10B_chr7_5921136_5975689 | RSPH10B | chr7 | 5921136 | 5975689 |
a0009c0016t0003g0068 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RSPH10B_chr7_5921136_5975689 | RSPH10B | chr7 | 5921136 | 5975689 |
a0010c0019t0001g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH10B_chr7_5921136_5975689 | RSPH10B | chr7 | 5921136 | 5975689 |
a0011c0015t0001g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSPH10B_chr7_5921136_5975689 | RSPH10B | chr7 | 5921136 | 5975689 |
a0012c0012t0001g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH10B_chr7_5921136_5975689 | RSPH10B | chr7 | 5921136 | 5975689 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0004 | c0005 | t0001 | g0041 | EUR | GBR | RSPH10B_chr7_5921136_5975689 | RSPH10B | chr7 | 5921136 | 5975689 |
HG00099 | hp2 | a0005 | c0003 | t0001 | g0030 | EUR | GBR | RSPH10B_chr7_5921136_5975689 | RSPH10B | chr7 | 5921136 | 5975689 |
HG00280 | hp1 | a0002 | c0002 | t0002 | g0047 | EUR | FIN | RSPH10B_chr7_5921136_5975689 | RSPH10B | chr7 | 5921136 | 5975689 |
HG00280 | hp2 | a0009 | c0016 | t0003 | g0068 | EUR | FIN | RSPH10B_chr7_5921136_5975689 | RSPH10B | chr7 | 5921136 | 5975689 |
HG00621 | hp1 | a0005 | c0003 | t0001 | g0025 | EAS | CHS | RSPH10B_chr7_5921136_5975689 | RSPH10B | chr7 | 5921136 | 5975689 |
HG00621 | hp2 | a0001 | c0001 | t0001 | g0053 | EAS | CHS | RSPH10B_chr7_5921136_5975689 | RSPH10B | chr7 | 5921136 | 5975689 |
HG00639 | hp1 | a0001 | c0001 | t0001 | g0023 | AMR | PUR | RSPH10B_chr7_5921136_5975689 | RSPH10B | chr7 | 5921136 | 5975689 |
HG00639 | hp2 | a0006 | c0006 | t0001 | g0017 | AMR | PUR | RSPH10B_chr7_5921136_5975689 | RSPH10B | chr7 | 5921136 | 5975689 |
HG00735 | hp1 | a0006 | c0006 | t0001 | g0021 | AMR | PUR | RSPH10B_chr7_5921136_5975689 | RSPH10B | chr7 | 5921136 | 5975689 |
HG00735 | hp2 | a0001 | c0010 | t0004 | g0057 | AMR | PUR | RSPH10B_chr7_5921136_5975689 | RSPH10B | chr7 | 5921136 | 5975689 |
HG00741 | hp1 | a0006 | c0006 | t0001 | g0008 | AMR | PUR | RSPH10B_chr7_5921136_5975689 | RSPH10B | chr7 | 5921136 | 5975689 |
HG00741 | hp2 | a0003 | c0004 | t0003 | g0058 | AMR | PUR | RSPH10B_chr7_5921136_5975689 | RSPH10B | chr7 | 5921136 | 5975689 |
HG01069 | hp1 | a0005 | c0003 | t0001 | g0028 | AMR | PUR | RSPH10B_chr7_5921136_5975689 | RSPH10B | chr7 | 5921136 | 5975689 |
HG01069 | hp2 | a0001 | c0010 | t0004 | g0056 | AMR | PUR | RSPH10B_chr7_5921136_5975689 | RSPH10B | chr7 | 5921136 | 5975689 |
HG01071 | hp1 | a0005 | c0003 | t0001 | g0027 | AMR | PUR | RSPH10B_chr7_5921136_5975689 | RSPH10B | chr7 | 5921136 | 5975689 |
HG01071 | hp2 | a0001 | c0001 | t0006 | g0013 | AMR | PUR | RSPH10B_chr7_5921136_5975689 | RSPH10B | chr7 | 5921136 | 5975689 |
HG01175 | hp1 | a0004 | c0011 | t0002 | g0046 | AMR | PUR | RSPH10B_chr7_5921136_5975689 | RSPH10B | chr7 | 5921136 | 5975689 |
HG01175 | hp2 | a0002 | c0002 | t0002 | g0040 | AMR | PUR | RSPH10B_chr7_5921136_5975689 | RSPH10B | chr7 | 5921136 | 5975689 |
HG01261 | hp1 | a0011 | c0015 | t0001 | g0029 | AMR | CLM | RSPH10B_chr7_5921136_5975689 | RSPH10B | chr7 | 5921136 | 5975689 |
HG01261 | hp2 | a0003 | c0004 | t0003 | g0063 | AMR | CLM | RSPH10B_chr7_5921136_5975689 | RSPH10B | chr7 | 5921136 | 5975689 |
HG01515 | hp1 | a0003 | c0004 | t0003 | g0069 | EUR | IBS | RSPH10B_chr7_5921136_5975689 | RSPH10B | chr7 | 5921136 | 5975689 |
HG01515 | hp2 | a0005 | c0003 | t0001 | g0031 | EUR | IBS | RSPH10B_chr7_5921136_5975689 | RSPH10B | chr7 | 5921136 | 5975689 |
HG01517 | hp1 | a0003 | c0004 | t0003 | g0070 | EUR | IBS | RSPH10B_chr7_5921136_5975689 | RSPH10B | chr7 | 5921136 | 5975689 |
HG01517 | hp2 | a0002 | c0002 | t0002 | g0044 | EUR | IBS | RSPH10B_chr7_5921136_5975689 | RSPH10B | chr7 | 5921136 | 5975689 |
HG01934 | hp1 | a0002 | c0002 | t0002 | g0038 | AMR | PEL | RSPH10B_chr7_5921136_5975689 | RSPH10B | chr7 | 5921136 | 5975689 |
HG01934 | hp2 | a0003 | c0004 | t0003 | g0066 | AMR | PEL | RSPH10B_chr7_5921136_5975689 | RSPH10B | chr7 | 5921136 | 5975689 |
HG01978 | hp1 | a0003 | c0004 | t0003 | g0062 | AMR | PEL | RSPH10B_chr7_5921136_5975689 | RSPH10B | chr7 | 5921136 | 5975689 |
HG01978 | hp2 | a0006 | c0006 | t0001 | g0002 | AMR | PEL | RSPH10B_chr7_5921136_5975689 | RSPH10B | chr7 | 5921136 | 5975689 |
HG01981 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | RSPH10B_chr7_5921136_5975689 | RSPH10B | chr7 | 5921136 | 5975689 |
HG01981 | hp2 | a0003 | c0004 | t0003 | g0059 | AMR | PEL | RSPH10B_chr7_5921136_5975689 | RSPH10B | chr7 | 5921136 | 5975689 |
HG02056 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | KHV | RSPH10B_chr7_5921136_5975689 | RSPH10B | chr7 | 5921136 | 5975689 |
HG02056 | hp2 | a0004 | c0005 | t0001 | g0035 | EAS | KHV | RSPH10B_chr7_5921136_5975689 | RSPH10B | chr7 | 5921136 | 5975689 |
HG02071 | hp1 | a0010 | c0019 | t0001 | g0009 | EAS | KHV | RSPH10B_chr7_5921136_5975689 | RSPH10B | chr7 | 5921136 | 5975689 |
HG02071 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | KHV | RSPH10B_chr7_5921136_5975689 | RSPH10B | chr7 | 5921136 | 5975689 |
HG02074 | hp1 | a0001 | c0013 | t0001 | g0054 | EAS | KHV | RSPH10B_chr7_5921136_5975689 | RSPH10B | chr7 | 5921136 | 5975689 |
HG02074 | hp2 | a0001 | c0001 | t0001 | g0034 | EAS | KHV | RSPH10B_chr7_5921136_5975689 | RSPH10B | chr7 | 5921136 | 5975689 |
HG02145 | hp1 | a0003 | c0004 | t0003 | g0064 | AFR | ACB | RSPH10B_chr7_5921136_5975689 | RSPH10B | chr7 | 5921136 | 5975689 |
HG02145 | hp2 | a0001 | c0014 | t0001 | g0015 | AFR | ACB | RSPH10B_chr7_5921136_5975689 | RSPH10B | chr7 | 5921136 | 5975689 |
HG02165 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | CDX | RSPH10B_chr7_5921136_5975689 | RSPH10B | chr7 | 5921136 | 5975689 |
HG02165 | hp2 | a0001 | c0001 | t0002 | g0026 | EAS | CDX | RSPH10B_chr7_5921136_5975689 | RSPH10B | chr7 | 5921136 | 5975689 |
HG02258 | hp1 | a0007 | c0007 | t0002 | g0020 | AFR | ACB | RSPH10B_chr7_5921136_5975689 | RSPH10B | chr7 | 5921136 | 5975689 |
HG02258 | hp2 | a0005 | c0003 | t0002 | g0010 | AFR | ACB | RSPH10B_chr7_5921136_5975689 | RSPH10B | chr7 | 5921136 | 5975689 |
HG02523 | hp1 | a0003 | c0004 | t0003 | g0067 | EAS | KHV | RSPH10B_chr7_5921136_5975689 | RSPH10B | chr7 | 5921136 | 5975689 |
HG02523 | hp2 | a0005 | c0003 | t0001 | g0024 | EAS | KHV | RSPH10B_chr7_5921136_5975689 | RSPH10B | chr7 | 5921136 | 5975689 |
HG02615 | hp1 | a0006 | c0006 | t0001 | g0004 | AFR | GWD | RSPH10B_chr7_5921136_5975689 | RSPH10B | chr7 | 5921136 | 5975689 |
HG02615 | hp2 | a0002 | c0002 | t0002 | g0045 | AFR | GWD | RSPH10B_chr7_5921136_5975689 | RSPH10B | chr7 | 5921136 | 5975689 |
HG02622 | hp1 | a0004 | c0005 | t0001 | g0043 | AFR | GWD | RSPH10B_chr7_5921136_5975689 | RSPH10B | chr7 | 5921136 | 5975689 |
HG02622 | hp2 | a0002 | c0002 | t0001 | g0037 | AFR | GWD | RSPH10B_chr7_5921136_5975689 | RSPH10B | chr7 | 5921136 | 5975689 |
HG02717 | hp1 | a0004 | c0011 | t0002 | g0039 | AFR | GWD | RSPH10B_chr7_5921136_5975689 | RSPH10B | chr7 | 5921136 | 5975689 |
HG02717 | hp2 | a0001 | c0008 | t0002 | g0052 | AFR | GWD | RSPH10B_chr7_5921136_5975689 | RSPH10B | chr7 | 5921136 | 5975689 |
HG02976 | hp1 | a0004 | c0005 | t0001 | g0055 | AFR | ESN | RSPH10B_chr7_5921136_5975689 | RSPH10B | chr7 | 5921136 | 5975689 |
HG02976 | hp2 | a0004 | c0005 | t0005 | g0033 | AFR | ESN | RSPH10B_chr7_5921136_5975689 | RSPH10B | chr7 | 5921136 | 5975689 |
HG03453 | hp1 | a0007 | c0007 | t0002 | g0003 | AFR | MSL | RSPH10B_chr7_5921136_5975689 | RSPH10B | chr7 | 5921136 | 5975689 |
HG03453 | hp2 | a0004 | c0018 | t0001 | g0014 | AFR | MSL | RSPH10B_chr7_5921136_5975689 | RSPH10B | chr7 | 5921136 | 5975689 |
HG03834 | hp1 | a0004 | c0005 | t0001 | g0042 | SAS | BEB | RSPH10B_chr7_5921136_5975689 | RSPH10B | chr7 | 5921136 | 5975689 |
HG03834 | hp2 | a0002 | c0002 | t0003 | g0060 | SAS | BEB | RSPH10B_chr7_5921136_5975689 | RSPH10B | chr7 | 5921136 | 5975689 |
NA18747 | hp1 | a0002 | c0002 | t0002 | g0049 | EAS | CHB | RSPH10B_chr7_5921136_5975689 | RSPH10B | chr7 | 5921136 | 5975689 |
NA18747 | hp2 | a0001 | c0001 | t0001 | g0022 | EAS | CHB | RSPH10B_chr7_5921136_5975689 | RSPH10B | chr7 | 5921136 | 5975689 |
NA18906 | hp1 | a0012 | c0012 | t0001 | g0036 | AFR | YRI | RSPH10B_chr7_5921136_5975689 | RSPH10B | chr7 | 5921136 | 5975689 |
NA18906 | hp2 | a0001 | c0009 | t0001 | g0012 | AFR | YRI | RSPH10B_chr7_5921136_5975689 | RSPH10B | chr7 | 5921136 | 5975689 |
NA18971 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | RSPH10B_chr7_5921136_5975689 | RSPH10B | chr7 | 5921136 | 5975689 |
NA18971 | hp2 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | RSPH10B_chr7_5921136_5975689 | RSPH10B | chr7 | 5921136 | 5975689 |
NA20805 | hp1 | a0002 | c0002 | t0002 | g0050 | EUR | TSI | RSPH10B_chr7_5921136_5975689 | RSPH10B | chr7 | 5921136 | 5975689 |
NA20805 | hp2 | a0002 | c0002 | t0002 | g0018 | EUR | TSI | RSPH10B_chr7_5921136_5975689 | RSPH10B | chr7 | 5921136 | 5975689 |
HG02109 | hp1 | a0005 | c0003 | t0004 | g0061 | AFR | ACB | RSPH10B_chr7_5921136_5975689 | RSPH10B | chr7 | 5921136 | 5975689 |
HG02109 | hp2 | a0001 | c0009 | t0001 | g0007 | AFR | ACB | RSPH10B_chr7_5921136_5975689 | RSPH10B | chr7 | 5921136 | 5975689 |
HG03471 | hp1 | a0001 | c0008 | t0002 | g0051 | AFR | MSL | RSPH10B_chr7_5921136_5975689 | RSPH10B | chr7 | 5921136 | 5975689 |
HG03471 | hp2 | a0002 | c0002 | t0002 | g0048 | AFR | MSL | RSPH10B_chr7_5921136_5975689 | RSPH10B | chr7 | 5921136 | 5975689 |
HG06807 | hp1 | a0008 | c0017 | t0003 | g0065 | AFR | USA | RSPH10B_chr7_5921136_5975689 | RSPH10B | chr7 | 5921136 | 5975689 |
HG06807 | hp2 | a0005 | c0003 | t0002 | g0011 | AFR | USA | RSPH10B_chr7_5921136_5975689 | RSPH10B | chr7 | 5921136 | 5975689 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr7:5928329 | C | T | 1 | a0008 | 1 | HG06807.hp1 | missense_variant | MODERATE | c.2299G>A | p.Val767Ile | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 20/21 | 2576/3122 | 2299/2613 | 767/870 | chr7 | 5928329 | ||
chr7:5935124 | C | T | 1 | a0006 | 5 | HG00639.hp2 HG00735.hp1 HG00741.hp1 others(2): Show |
missense_variant | MODERATE | c.2035G>A | p.Ala679Thr | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 18/21 | 2312/3122 | 2035/2613 | 679/870 | chr7 | 5935124 | ||
chr7:5943432 | C | T | 1 | a0002 | 11 | HG00280.hp1 HG01175.hp2 HG01517.hp2 others(8): Show |
missense_variant | MODERATE | c.1650G>A | p.Met550Ile | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 15/21 | 1927/3122 | 1650/2613 | 550/870 | chr7 | 5943432 | ||
chr7:5943439 | T | C | 1 | a0006 | 5 | HG00639.hp2 HG00735.hp1 HG00741.hp1 others(2): Show |
missense_variant | MODERATE | c.1643A>G | p.Tyr548Cys | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 15/21 | 1920/3122 | 1643/2613 | 548/870 | chr7 | 5943439 | ||
chr7:5943455 | G | A | 1 | a0012 | 1 | NA18906.hp1 | stop_gained | HIGH | c.1627C>T | p.Gln543* | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 15/21 | 1904/3122 | 1627/2613 | 543/870 | chr7 | 5943455 | ||
chr7:5943922 | A | C | 9 | a0001a0002a0004others(6): Show | 59 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(56): Show |
missense_variant | MODERATE | c.1598T>G | p.Phe533Cys | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 14/21 | 1875/3122 | 1598/2613 | 533/870 | chr7 | 5943922 | ||
chr7:5943937 | A | C | 1 | a0009 | 1 | HG00280.hp2 | missense_variant | MODERATE | c.1583T>G | p.Ile528Ser | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 14/21 | 1860/3122 | 1583/2613 | 528/870 | chr7 | 5943937 | ||
chr7:5943944 | C | T | 1 | a0007 | 2 | HG02258.hp1 HG03453.hp1 |
missense_variant | MODERATE | c.1576G>A | p.Glu526Lys | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 14/21 | 1853/3122 | 1576/2613 | 526/870 | chr7 | 5943944 | ||
chr7:5958010 | A | G | 3 | a0005a0011a0012 | 11 | HG00099.hp2 HG00621.hp1 HG01069.hp1 others(8): Show |
missense_variant | MODERATE | c.677T>C | p.Ile226Thr | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 8/21 | 954/3122 | 677/2613 | 226/870 | chr7 | 5958010 | ||
chr7:5960821 | G | A | 2 | a0010a0011 | 2 | HG01261.hp1 HG02071.hp1 |
missense_variant | MODERATE | c.443C>T | p.Thr148Met | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 6/21 | 720/3122 | 443/2613 | 148/870 | chr7 | 5960821 | ||
chr7:5965692 | C | T | 3 | a0003a0008a0009 | 11 | HG00280.hp2 HG00741.hp2 HG01261.hp2 others(8): Show |
missense_variant | MODERATE | c.275G>A | p.Arg92His | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 4/21 | 552/3122 | 275/2613 | 92/870 | chr7 | 5965692 | ||
chr7:5966905 | G | C | 6 | a0002a0003a0004others(3): Show | 32 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(29): Show |
missense_variant | MODERATE | c.212C>G | p.Thr71Ser | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 3/21 | 489/3122 | 212/2613 | 71/870 | chr7 | 5966905 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr7:5943381 | A | G | 14 | a0001c0001a0001c0009a0001c0010others(11): Show | 52 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(49): Show |
synonymous_variant | LOW | c.1701T>C | p.Ser567Ser | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 15/21 | 1978/3122 | 1701/2613 | 567/870 | chr7 | 5943381 | ||
chr7:5945090 | C | T | 2 | a0001c0010a0001c0013 | 3 | HG00735.hp2 HG01069.hp2 HG02074.hp1 |
synonymous_variant | LOW | c.1503G>A | p.Ala501Ala | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 13/21 | 1780/3122 | 1503/2613 | 501/870 | chr7 | 5945090 | ||
chr7:5948365 | A | G | 12 | a0001c0001a0001c0008a0001c0010others(9): Show | 45 | HG00099.hp2 HG00280.hp1 HG00621.hp1 others(42): Show |
synonymous_variant | LOW | c.1269T>C | p.Ile423Ile | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 12/21 | 1546/3122 | 1269/2613 | 423/870 | chr7 | 5948365 | ||
chr7:5957931 | G | A | 1 | a0001c0010 | 2 | HG00735.hp2 HG01069.hp2 |
synonymous_variant | LOW | c.756C>T | p.Thr252Thr | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 8/21 | 1033/3122 | 756/2613 | 252/870 | chr7 | 5957931 | ||
chr7:5957976 | G | A | 1 | a0004c0018 | 1 | HG03453.hp2 | synonymous_variant | LOW | c.711C>T | p.His237His | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 8/21 | 988/3122 | 711/2613 | 237/870 | chr7 | 5957976 | ||
chr7:5960763 | G | A | 1 | a0001c0014 | 1 | HG02145.hp2 | synonymous_variant | LOW | c.501C>T | p.Phe167Phe | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 6/21 | 778/3122 | 501/2613 | 167/870 | chr7 | 5960763 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr7:5926178 | TGG | T | 16 | a0001c0001t0001a0001c0001t0006a0001c0009t0001others(13): Show | 40 | HG00099.hp1 HG00099.hp2 HG00621.hp1 others(37): Show |
3_prime_UTR_variant | MODIFIER | c.*188_*189delCC | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 21/21 | 188 | chr7 | 5926178 | |||||
chr7:5926284 | C | T | 1 | a0001c0001t0006 | 1 | HG01071.hp2 | 3_prime_UTR_variant | MODIFIER | c.*84G>A | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 21/21 | 84 | chr7 | 5926284 | |||||
chr7:5926329 | C | T | 1 | a0004c0005t0005 | 1 | HG02976.hp2 | 3_prime_UTR_variant | MODIFIER | c.*39G>A | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 21/21 | 39 | chr7 | 5926329 | |||||
chr7:5970651 | C | A | 6 | a0001c0010t0004a0002c0002t0003a0003c0004t0003others(3): Show | 15 | HG00280.hp2 HG00735.hp2 HG00741.hp2 others(12): Show |
5_prime_UTR_variant | MODIFIER | c.-239G>T | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 1/21 | 3535 | chr7 | 5970651 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr7:5926689 | C | T | 3 | a0001c0009t0001g0007a0002c0002t0001g0037a0004c0018t0001g0014 | 3 | HG02109.hp2 HG02622.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.2433-141G>A | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 20/20 | chr7 | 5926689 | ||||||
chr7:5926714 | C | T | 6 | a0001c0001t0006g0013a0006c0006t0001g0002a0006c0006t0001g0004others(3): Show | 6 | HG00639.hp2 HG00735.hp1 HG00741.hp1 others(3): Show |
intron_variant | MODIFIER | c.2433-166G>A | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 20/20 | chr7 | 5926714 | ||||||
chr7:5926726 | A | G | 1 | a0004c0018t0001g0014 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.2433-178T>C | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 20/20 | chr7 | 5926726 | ||||||
chr7:5926736 | C | T | 5 | a0001c0009t0001g0007a0001c0010t0004g0056a0001c0010t0004g0057others(2): Show | 5 | HG00735.hp2 HG01069.hp2 HG02109.hp2 others(2): Show |
intron_variant | MODIFIER | c.2433-188G>A | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 20/20 | chr7 | 5926736 | ||||||
chr7:5926748 | T | C | 5 | a0001c0009t0001g0007a0001c0010t0004g0056a0001c0010t0004g0057others(2): Show | 5 | HG00735.hp2 HG01069.hp2 HG02109.hp2 others(2): Show |
intron_variant | MODIFIER | c.2433-200A>G | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 20/20 | chr7 | 5926748 | ||||||
chr7:5926768 | GAGAC | G | 2 | a0005c0003t0002g0010a0005c0003t0002g0011 | 2 | HG02258.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.2433-224_2433-221d others(6): Show |
RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 20/20 | chr7 | 5926768 | ||||||
chr7:5926776 | C | CA | 5 | a0001c0009t0001g0007a0001c0010t0004g0056a0001c0010t0004g0057others(2): Show | 5 | HG00735.hp2 HG01069.hp2 HG02109.hp2 others(2): Show |
intron_variant | MODIFIER | c.2433-229dupT | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 20/20 | chr7 | 5926776 | ||||||
chr7:5926930 | A | AT | 13 | a0001c0001t0001g0022a0001c0001t0001g0034a0001c0001t0002g0026others(10): Show | 13 | HG00099.hp2 HG00621.hp1 HG01069.hp1 others(10): Show |
intron_variant | MODIFIER | c.2433-383dupA | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 20/20 | chr7 | 5926930 | ||||||
chr7:5926936 | A | T | 1 | a0001c0001t0002g0026 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.2433-388T>A | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 20/20 | chr7 | 5926936 | ||||||
chr7:5926946 | G | A | 1 | a0008c0017t0003g0065 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.2433-398C>T | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 20/20 | chr7 | 5926946 | ||||||
chr7:5927022 | CGTGTGTG others(5): Show |
C | 1 | a0004c0018t0001g0014 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.2433-486_2433-475d others(14): Show |
RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 20/20 | chr7 | 5927022 | ||||||
chr7:5927022 | CGTGTGTG others(22): Show |
C | 6 | a0001c0001t0006g0013a0006c0006t0001g0002a0006c0006t0001g0004others(3): Show | 6 | HG00639.hp2 HG00735.hp1 HG00741.hp1 others(3): Show |
intron_variant | MODIFIER | c.2433-503_2433-475d others(31): Show |
RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 20/20 | chr7 | 5927022 | ||||||
chr7:5927026 | T | TGTGTGTG others(4): Show |
1 | a0001c0001t0002g0026 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.2433-489_2433-479d others(13): Show |
RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 20/20 | chr7 | 5927026 | ||||||
chr7:5927035 | GTGTGTGT others(28): Show |
G | 2 | a0001c0009t0001g0007a0002c0002t0001g0037 | 2 | HG02109.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.2433-522_2433-488d others(37): Show |
RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 20/20 | chr7 | 5927035 | ||||||
chr7:5927039 | GTGTGTGT others(22): Show |
G | 10 | a0004c0005t0005g0033a0005c0003t0001g0024a0005c0003t0001g0025others(7): Show | 10 | HG00099.hp2 HG00621.hp1 HG01069.hp1 others(7): Show |
intron_variant | MODIFIER | c.2433-520_2433-492d others(31): Show |
RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 20/20 | chr7 | 5927039 | ||||||
chr7:5927045 | G | GTGTA | 27 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(24): Show | 27 | HG00099.hp1 HG00280.hp1 HG00621.hp2 others(24): Show |
intron_variant | MODIFIER | c.2433-498_2433-497i others(6): Show |
RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 20/20 | chr7 | 5927045 | ||||||
chr7:5927045 | G | GTGTGTA | 2 | a0001c0014t0001g0015a0004c0005t0001g0055 | 2 | HG02145.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.2433-498_2433-497i others(8): Show |
RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 20/20 | chr7 | 5927045 | ||||||
chr7:5927045 | G | GTGTGTGT others(1): Show |
2 | a0002c0002t0002g0049a0004c0011t0002g0039 | 2 | HG02717.hp1 NA18747.hp1 |
intron_variant | MODIFIER | c.2433-498_2433-497i others(10): Show |
RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 20/20 | chr7 | 5927045 | ||||||
chr7:5927045 | G | GTGTGTGT others(3): Show |
2 | a0005c0003t0002g0010a0005c0003t0002g0011 | 2 | HG02258.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.2433-498_2433-497i others(12): Show |
RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 20/20 | chr7 | 5927045 | ||||||
chr7:5927047 | A | ATAT | 2 | a0001c0010t0004g0056a0001c0010t0004g0057 | 2 | HG00735.hp2 HG01069.hp2 |
intron_variant | MODIFIER | c.2433-500_2433-499i others(5): Show |
RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 20/20 | chr7 | 5927047 | ||||||
chr7:5927047 | A | G | 3 | a0001c0001t0001g0022a0001c0001t0001g0034a0010c0019t0001g0009 | 3 | HG02071.hp1 HG02074.hp2 NA18747.hp2 |
intron_variant | MODIFIER | c.2433-499T>C | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 20/20 | chr7 | 5927047 | ||||||
chr7:5927050 | A | G | 2 | a0001c0010t0004g0056a0001c0010t0004g0057 | 2 | HG00735.hp2 HG01069.hp2 |
intron_variant | MODIFIER | c.2433-502T>C | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 20/20 | chr7 | 5927050 | ||||||
chr7:5927050 | A | T | 1 | a0001c0001t0002g0026 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.2433-502T>A | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 20/20 | chr7 | 5927050 | ||||||
chr7:5927052 | G | T | 3 | a0001c0001t0001g0022a0001c0001t0001g0034a0010c0019t0001g0009 | 3 | HG02071.hp1 HG02074.hp2 NA18747.hp2 |
intron_variant | MODIFIER | c.2433-504C>A | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 20/20 | chr7 | 5927052 | ||||||
chr7:5927060 | G | GTATATAT others(3): Show |
2 | a0001c0010t0004g0056a0001c0010t0004g0057 | 2 | HG00735.hp2 HG01069.hp2 |
intron_variant | MODIFIER | c.2433-513_2433-512i others(12): Show |
RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 20/20 | chr7 | 5927060 | ||||||
chr7:5927060 | G | GTTGTATA others(6): Show |
1 | a0001c0001t0002g0026 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.2433-513_2433-512i others(15): Show |
RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 20/20 | chr7 | 5927060 | ||||||
chr7:5927064 | G | GTATA | 3 | a0001c0001t0001g0022a0001c0001t0001g0034a0010c0019t0001g0009 | 3 | HG02071.hp1 HG02074.hp2 NA18747.hp2 |
intron_variant | MODIFIER | c.2433-517_2433-516i others(6): Show |
RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 20/20 | chr7 | 5927064 | ||||||
chr7:5927066 | G | A | 4 | a0001c0001t0001g0001a0001c0001t0001g0022a0001c0001t0001g0034others(1): Show | 4 | HG01981.hp1 HG02071.hp1 HG02074.hp2 others(1): Show |
intron_variant | MODIFIER | c.2433-518C>T | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 20/20 | chr7 | 5927066 | ||||||
chr7:5927066 | G | GTGTA | 6 | a0001c0009t0001g0012a0004c0005t0001g0035a0004c0005t0001g0041others(3): Show | 6 | HG00099.hp1 HG02056.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.2433-519_2433-518i others(6): Show |
RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 20/20 | chr7 | 5927066 | ||||||
chr7:5927066 | G | GTGTATAT others(17): Show |
1 | a0004c0018t0001g0014 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.2433-519_2433-518i others(26): Show |
RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 20/20 | chr7 | 5927066 | ||||||
chr7:5927068 | A | G | 2 | a0001c0008t0002g0051a0001c0014t0001g0015 | 2 | HG02145.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.2433-520T>C | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 20/20 | chr7 | 5927068 | ||||||
chr7:5927070 | A | ATG | 3 | a0003c0004t0003g0067a0005c0003t0002g0010a0005c0003t0002g0011 | 3 | HG02258.hp2 HG02523.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.2433-524_2433-523d others(4): Show |
RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 20/20 | chr7 | 5927070 | ||||||
chr7:5927070 | A | ATGTG | 14 | a0001c0008t0002g0052a0002c0002t0002g0018a0002c0002t0002g0038others(11): Show | 14 | HG00280.hp1 HG01175.hp1 HG01517.hp2 others(11): Show |
intron_variant | MODIFIER | c.2433-526_2433-523d others(6): Show |
RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 20/20 | chr7 | 5927070 | ||||||
chr7:5927070 | A | G | 6 | a0001c0009t0001g0012a0004c0005t0001g0035a0004c0005t0001g0041others(3): Show | 6 | HG00099.hp1 HG02056.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.2433-522T>C | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 20/20 | chr7 | 5927070 | ||||||
chr7:5927072 | G | A | 23 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(20): Show | 23 | HG00099.hp2 HG00621.hp1 HG00621.hp2 others(20): Show |
intron_variant | MODIFIER | c.2433-524C>T | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 20/20 | chr7 | 5927072 | ||||||
chr7:5927072 | G | T | 6 | a0001c0001t0006g0013a0006c0006t0001g0002a0006c0006t0001g0004others(3): Show | 6 | HG00639.hp2 HG00735.hp1 HG00741.hp1 others(3): Show |
intron_variant | MODIFIER | c.2433-524C>A | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 20/20 | chr7 | 5927072 | ||||||
chr7:5927074 | G | A | 10 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0016others(7): Show | 10 | HG00621.hp2 HG00735.hp2 HG01069.hp2 others(7): Show |
intron_variant | MODIFIER | c.2433-526C>T | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 20/20 | chr7 | 5927074 | ||||||
chr7:5927076 | G | A | 3 | a0001c0001t0002g0026a0001c0010t0004g0056a0001c0010t0004g0057 | 3 | HG00735.hp2 HG01069.hp2 HG02165.hp2 |
intron_variant | MODIFIER | c.2433-528C>T | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 20/20 | chr7 | 5927076 | ||||||
chr7:5927076 | G | GTATATAT others(3): Show |
3 | a0001c0001t0001g0022a0001c0001t0001g0034a0010c0019t0001g0009 | 3 | HG02071.hp1 HG02074.hp2 NA18747.hp2 |
intron_variant | MODIFIER | c.2433-529_2433-528i others(12): Show |
RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 20/20 | chr7 | 5927076 | ||||||
chr7:5927078 | G | GTATATAT others(5): Show |
1 | a0001c0001t0001g0001 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.2433-531_2433-530i others(14): Show |
RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 20/20 | chr7 | 5927078 | ||||||
chr7:5927078 | G | GTGTATAT others(7): Show |
7 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0016others(4): Show | 7 | HG00621.hp2 HG02056.hp1 HG02071.hp2 others(4): Show |
intron_variant | MODIFIER | c.2433-531_2433-530i others(16): Show |
RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 20/20 | chr7 | 5927078 | ||||||
chr7:5927117 | G | T | 6 | a0001c0001t0001g0022a0001c0001t0001g0034a0001c0001t0002g0026others(3): Show | 6 | HG00735.hp2 HG01069.hp2 HG02071.hp1 others(3): Show |
intron_variant | MODIFIER | c.2433-569C>A | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 20/20 | chr7 | 5927117 | ||||||
chr7:5927192 | C | T | 1 | a0004c0011t0002g0039 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.2433-644G>A | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 20/20 | chr7 | 5927192 | ||||||
chr7:5927339 | A | C | 59 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(56): Show | 59 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(56): Show |
intron_variant | MODIFIER | c.2433-791T>G | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 20/20 | chr7 | 5927339 | ||||||
chr7:5927347 | G | A | 52 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(49): Show | 52 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(49): Show |
intron_variant | MODIFIER | c.2433-799C>T | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 20/20 | chr7 | 5927347 | ||||||
chr7:5927519 | T | C | 59 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(56): Show | 59 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(56): Show |
intron_variant | MODIFIER | c.2432+677A>G | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 20/20 | chr7 | 5927519 | ||||||
chr7:5927542 | G | A | 1 | a0010c0019t0001g0009 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.2432+654C>T | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 20/20 | chr7 | 5927542 | ||||||
chr7:5927560 | C | G | 1 | a0004c0018t0001g0014 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.2432+636G>C | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 20/20 | chr7 | 5927560 | ||||||
chr7:5927594 | T | C | 7 | a0001c0001t0001g0022a0001c0001t0001g0034a0001c0001t0002g0026others(4): Show | 7 | HG00735.hp2 HG01069.hp2 HG02071.hp1 others(4): Show |
intron_variant | MODIFIER | c.2432+602A>G | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 20/20 | chr7 | 5927594 | ||||||
chr7:5927646 | T | C | 7 | a0001c0001t0001g0022a0001c0001t0001g0034a0001c0001t0002g0026others(4): Show | 7 | HG00735.hp2 HG01069.hp2 HG02071.hp1 others(4): Show |
intron_variant | MODIFIER | c.2432+550A>G | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 20/20 | chr7 | 5927646 | ||||||
chr7:5927653 | T | C | 1 | a0003c0004t0003g0062 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.2432+543A>G | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 20/20 | chr7 | 5927653 | ||||||
chr7:5927666 | T | C | 7 | a0001c0001t0001g0022a0001c0001t0001g0034a0001c0001t0002g0026others(4): Show | 7 | HG00735.hp2 HG01069.hp2 HG02071.hp1 others(4): Show |
intron_variant | MODIFIER | c.2432+530A>G | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 20/20 | chr7 | 5927666 | ||||||
chr7:5927702 | A | G | 7 | a0001c0001t0001g0022a0001c0001t0001g0034a0001c0001t0002g0026others(4): Show | 7 | HG00735.hp2 HG01069.hp2 HG02071.hp1 others(4): Show |
intron_variant | MODIFIER | c.2432+494T>C | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 20/20 | chr7 | 5927702 | ||||||
chr7:5927704 | A | G | 7 | a0001c0001t0001g0022a0001c0001t0001g0034a0001c0001t0002g0026others(4): Show | 7 | HG00735.hp2 HG01069.hp2 HG02071.hp1 others(4): Show |
intron_variant | MODIFIER | c.2432+492T>C | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 20/20 | chr7 | 5927704 | ||||||
chr7:5927733 | CGAGACCA others(5): Show |
C | 1 | a0005c0003t0001g0028 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.2432+451_2432+462d others(14): Show |
RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 20/20 | chr7 | 5927733 | ||||||
chr7:5927765 | G | T | 8 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(5): Show | 8 | HG00621.hp2 HG01981.hp1 HG02056.hp1 others(5): Show |
intron_variant | MODIFIER | c.2432+431C>A | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 20/20 | chr7 | 5927765 | ||||||
chr7:5927786 | A | T | 1 | a0001c0001t0002g0026 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.2432+410T>A | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 20/20 | chr7 | 5927786 | ||||||
chr7:5927813 | C | G | 7 | a0001c0001t0001g0022a0001c0001t0001g0034a0001c0001t0002g0026others(4): Show | 7 | HG00735.hp2 HG01069.hp2 HG02071.hp1 others(4): Show |
intron_variant | MODIFIER | c.2432+383G>C | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 20/20 | chr7 | 5927813 | ||||||
chr7:5927825 | G | A | 7 | a0001c0001t0001g0022a0001c0001t0001g0034a0001c0001t0002g0026others(4): Show | 7 | HG00735.hp2 HG01069.hp2 HG02071.hp1 others(4): Show |
intron_variant | MODIFIER | c.2432+371C>T | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 20/20 | chr7 | 5927825 | ||||||
chr7:5927898 | C | T | 45 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0034others(42): Show | 45 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(42): Show |
intron_variant | MODIFIER | c.2432+298G>A | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 20/20 | chr7 | 5927898 | ||||||
chr7:5927938 | C | A | 1 | a0004c0005t0001g0043 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.2432+258G>T | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 20/20 | chr7 | 5927938 | ||||||
chr7:5927944 | A | G | 2 | a0001c0009t0001g0007a0002c0002t0001g0037 | 2 | HG02109.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.2432+252T>C | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 20/20 | chr7 | 5927944 | ||||||
chr7:5927964 | C | T | 1 | a0004c0005t0001g0035 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.2432+232G>A | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 20/20 | chr7 | 5927964 | ||||||
chr7:5928156 | A | C | 5 | a0001c0001t0001g0001a0001c0013t0001g0054a0003c0004t0003g0058others(2): Show | 5 | HG00741.hp2 HG01981.hp1 HG02074.hp1 others(2): Show |
intron_variant | MODIFIER | c.2432+40T>G | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 20/20 | chr7 | 5928156 | ||||||
chr7:5928422 | A | G | 2 | a0004c0005t0001g0042a0004c0011t0002g0046 | 2 | HG01175.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.2234-28T>C | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 19/20 | chr7 | 5928422 | ||||||
chr7:5928455 | C | T | 9 | a0005c0003t0001g0024a0005c0003t0001g0025a0005c0003t0001g0027others(6): Show | 9 | HG00099.hp2 HG00621.hp1 HG01069.hp1 others(6): Show |
intron_variant | MODIFIER | c.2234-61G>A | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 19/20 | chr7 | 5928455 | ||||||
chr7:5928513 | G | A | 8 | a0001c0001t0001g0022a0001c0001t0001g0034a0001c0001t0002g0026others(5): Show | 8 | HG00735.hp2 HG01069.hp2 HG02071.hp1 others(5): Show |
intron_variant | MODIFIER | c.2234-119C>T | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 19/20 | chr7 | 5928513 | ||||||
chr7:5928634 | G | GT | 12 | a0001c0014t0001g0015a0004c0005t0001g0035a0004c0005t0001g0055others(9): Show | 12 | HG00099.hp2 HG00621.hp1 HG01069.hp1 others(9): Show |
intron_variant | MODIFIER | c.2234-241dupA | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 19/20 | chr7 | 5928634 | ||||||
chr7:5928634 | GT | G | 19 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0016others(16): Show | 19 | HG00621.hp2 HG00639.hp2 HG00735.hp1 others(16): Show |
intron_variant | MODIFIER | c.2234-241delA | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 19/20 | chr7 | 5928634 | ||||||
chr7:5928635 | T | G | 1 | a0001c0001t0001g0006 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.2234-241A>C | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 19/20 | chr7 | 5928635 | ||||||
chr7:5928658 | A | G | 15 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(12): Show | 15 | HG00621.hp2 HG00735.hp2 HG01069.hp2 others(12): Show |
intron_variant | MODIFIER | c.2234-264T>C | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 19/20 | chr7 | 5928658 | ||||||
chr7:5928766 | C | T | 1 | a0004c0018t0001g0014 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.2234-372G>A | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 19/20 | chr7 | 5928766 | ||||||
chr7:5928793 | T | A | 1 | a0001c0010t0004g0057 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.2234-399A>T | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 19/20 | chr7 | 5928793 | ||||||
chr7:5928846 | G | A | 2 | a0005c0003t0002g0010a0005c0003t0002g0011 | 2 | HG02258.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.2234-452C>T | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 19/20 | chr7 | 5928846 | ||||||
chr7:5928874 | CCTCGGCC others(535): Show |
C | 1 | a0004c0011t0002g0039 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.2234-1022_2234-481 others(3): Show |
RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 19/20 | chr7 | 5928874 | ||||||
chr7:5928922 | A | G | 17 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(14): Show | 17 | HG00621.hp2 HG00735.hp2 HG01069.hp2 others(14): Show |
intron_variant | MODIFIER | c.2234-528T>C | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 19/20 | chr7 | 5928922 | ||||||
chr7:5928925 | C | T | 1 | a0004c0018t0001g0014 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.2234-531G>A | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 19/20 | chr7 | 5928925 | ||||||
chr7:5928967 | C | T | 7 | a0001c0001t0001g0022a0001c0001t0001g0034a0001c0001t0002g0026others(4): Show | 7 | HG00735.hp2 HG01069.hp2 HG02071.hp1 others(4): Show |
intron_variant | MODIFIER | c.2234-573G>A | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 19/20 | chr7 | 5928967 | ||||||
chr7:5928992 | A | T | 1 | a0001c0009t0001g0007 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.2234-598T>A | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 19/20 | chr7 | 5928992 | ||||||
chr7:5929019 | C | CT | 4 | a0001c0001t0001g0022a0004c0005t0001g0041a0004c0005t0001g0042others(1): Show | 4 | HG00099.hp1 HG00741.hp1 HG03834.hp1 others(1): Show |
intron_variant | MODIFIER | c.2234-626dupA | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 19/20 | chr7 | 5929019 | ||||||
chr7:5929019 | CT | C | 5 | a0001c0001t0001g0006a0001c0001t0001g0034a0001c0001t0002g0026others(2): Show | 5 | HG01261.hp1 HG02074.hp2 HG02165.hp2 others(2): Show |
intron_variant | MODIFIER | c.2234-626delA | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 19/20 | chr7 | 5929019 | ||||||
chr7:5929040 | T | TCTCA | 7 | a0001c0001t0001g0022a0001c0001t0001g0034a0001c0001t0002g0026others(4): Show | 7 | HG00735.hp2 HG01069.hp2 HG02071.hp1 others(4): Show |
intron_variant | MODIFIER | c.2234-647_2234-646i others(6): Show |
RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 19/20 | chr7 | 5929040 | ||||||
chr7:5929123 | T | C | 7 | a0001c0001t0001g0022a0001c0001t0001g0034a0001c0001t0002g0026others(4): Show | 7 | HG00735.hp2 HG02071.hp1 HG02074.hp2 others(4): Show |
intron_variant | MODIFIER | c.2234-729A>G | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 19/20 | chr7 | 5929123 | ||||||
chr7:5929160 | T | C | 16 | a0001c0001t0001g0022a0001c0001t0001g0034a0001c0001t0002g0026others(13): Show | 16 | HG00099.hp2 HG00621.hp1 HG00735.hp2 others(13): Show |
intron_variant | MODIFIER | c.2234-766A>G | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 19/20 | chr7 | 5929160 | ||||||
chr7:5929201 | G | A | 8 | a0001c0001t0001g0022a0001c0001t0001g0034a0001c0001t0002g0026others(5): Show | 8 | HG00735.hp2 HG01069.hp2 HG02071.hp1 others(5): Show |
intron_variant | MODIFIER | c.2234-807C>T | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 19/20 | chr7 | 5929201 | ||||||
chr7:5929206 | A | G | 8 | a0001c0001t0001g0022a0001c0001t0001g0034a0001c0001t0002g0026others(5): Show | 8 | HG00735.hp2 HG01069.hp2 HG02071.hp1 others(5): Show |
intron_variant | MODIFIER | c.2234-812T>C | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 19/20 | chr7 | 5929206 | ||||||
chr7:5929209 | T | A | 8 | a0001c0001t0001g0022a0001c0001t0001g0034a0001c0001t0002g0026others(5): Show | 8 | HG00735.hp2 HG01069.hp2 HG02071.hp1 others(5): Show |
intron_variant | MODIFIER | c.2234-815A>T | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 19/20 | chr7 | 5929209 | ||||||
chr7:5929220 | T | C | 7 | a0001c0001t0001g0022a0001c0001t0001g0034a0001c0001t0002g0026others(4): Show | 7 | HG00735.hp2 HG01069.hp2 HG02071.hp1 others(4): Show |
intron_variant | MODIFIER | c.2234-826A>G | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 19/20 | chr7 | 5929220 | ||||||
chr7:5929325 | G | A | 1 | a0001c0001t0001g0023 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.2234-931C>T | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 19/20 | chr7 | 5929325 | ||||||
chr7:5929361 | A | G | 1 | a0004c0005t0001g0043 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.2234-967T>C | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 19/20 | chr7 | 5929361 | ||||||
chr7:5929367 | C | T | 1 | a0001c0009t0001g0007 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.2234-973G>A | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 19/20 | chr7 | 5929367 | ||||||
chr7:5929461 | C | T | 2 | a0002c0002t0002g0038a0002c0002t0003g0060 | 2 | HG01934.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.2234-1067G>A | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 19/20 | chr7 | 5929461 | ||||||
chr7:5929584 | C | T | 1 | a0004c0011t0002g0039 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.2234-1190G>A | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 19/20 | chr7 | 5929584 | ||||||
chr7:5929631 | C | T | 1 | a0001c0009t0001g0007 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.2234-1237G>A | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 19/20 | chr7 | 5929631 | ||||||
chr7:5929738 | AT | A | 2 | a0001c0001t0002g0026a0002c0002t0001g0037 | 2 | HG02165.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.2234-1345delA | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 19/20 | chr7 | 5929738 | ||||||
chr7:5929905 | A | AGCAGTCA others(4): Show |
6 | a0001c0001t0001g0032a0001c0001t0006g0013a0004c0018t0001g0014others(3): Show | 6 | HG00735.hp1 HG01071.hp2 HG01978.hp2 others(3): Show |
intron_variant | MODIFIER | c.2234-1522_2234-151 others(15): Show |
RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 19/20 | chr7 | 5929905 | ||||||
chr7:5930019 | G | A | 1 | a0001c0009t0001g0007 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.2234-1625C>T | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 19/20 | chr7 | 5930019 | ||||||
chr7:5930039 | A | C | 1 | a0010c0019t0001g0009 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.2234-1645T>G | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 19/20 | chr7 | 5930039 | ||||||
chr7:5930104 | T | A | 1 | a0002c0002t0001g0037 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.2234-1710A>T | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 19/20 | chr7 | 5930104 | ||||||
chr7:5930188 | G | A | 12 | a0001c0001t0001g0022a0001c0001t0001g0034a0001c0001t0002g0026others(9): Show | 12 | HG00735.hp2 HG01069.hp2 HG02071.hp1 others(9): Show |
intron_variant | MODIFIER | c.2234-1794C>T | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 19/20 | chr7 | 5930188 | ||||||
chr7:5930414 | C | T | 1 | a0005c0003t0004g0061 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.2234-2020G>A | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 19/20 | chr7 | 5930414 | ||||||
chr7:5930459 | CCT | C | 31 | a0001c0001t0001g0022a0001c0001t0001g0034a0001c0001t0006g0013others(28): Show | 31 | HG00099.hp2 HG00621.hp1 HG00639.hp2 others(28): Show |
intron_variant | MODIFIER | c.2234-2067_2234-206 others(6): Show |
RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 19/20 | chr7 | 5930459 | ||||||
chr7:5930487 | C | T | 2 | a0004c0005t0005g0033a0004c0011t0002g0046 | 2 | HG01175.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.2234-2093G>A | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 19/20 | chr7 | 5930487 | ||||||
chr7:5930593 | G | C | 12 | a0001c0001t0001g0006a0001c0001t0001g0016a0001c0001t0001g0022others(9): Show | 12 | HG00621.hp2 HG00735.hp2 HG00741.hp1 others(9): Show |
intron_variant | MODIFIER | c.2233+2189C>G | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 19/20 | chr7 | 5930593 | ||||||
chr7:5930617 | A | C | 1 | a0010c0019t0001g0009 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.2233+2165T>G | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 19/20 | chr7 | 5930617 | ||||||
chr7:5930629 | G | C | 1 | a0005c0003t0002g0010 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.2233+2153C>G | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 19/20 | chr7 | 5930629 | ||||||
chr7:5930632 | A | G | 59 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(56): Show | 59 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(56): Show |
intron_variant | MODIFIER | c.2233+2150T>C | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 19/20 | chr7 | 5930632 | ||||||
chr7:5930647 | G | A | 1 | a0001c0013t0001g0054 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.2233+2135C>T | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 19/20 | chr7 | 5930647 | ||||||
chr7:5930649 | T | G | 1 | a0001c0013t0001g0054 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.2233+2133A>C | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 19/20 | chr7 | 5930649 | ||||||
chr7:5930682 | C | T | 13 | a0002c0002t0001g0037a0002c0002t0002g0018a0002c0002t0002g0038others(10): Show | 13 | HG00280.hp1 HG01175.hp1 HG01175.hp2 others(10): Show |
intron_variant | MODIFIER | c.2233+2100G>A | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 19/20 | chr7 | 5930682 | ||||||
chr7:5930695 | G | A | 1 | a0006c0006t0001g0002 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.2233+2087C>T | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 19/20 | chr7 | 5930695 | ||||||
chr7:5930712 | A | G | 48 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(45): Show | 48 | HG00099.hp2 HG00280.hp1 HG00621.hp1 others(45): Show |
intron_variant | MODIFIER | c.2233+2070T>C | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 19/20 | chr7 | 5930712 | ||||||
chr7:5930763 | C | CGTACACA others(115): Show |
1 | a0001c0010t0004g0056 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.2233+2018_2233+201 others(126): Show |
RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 19/20 | chr7 | 5930763 | ||||||
chr7:5930763 | C | CGTACACA others(75): Show |
1 | a0012c0012t0001g0036 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.2233+2018_2233+201 others(86): Show |
RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 19/20 | chr7 | 5930763 | ||||||
chr7:5930763 | C | CGTACACA others(443): Show |
1 | a0006c0006t0001g0004 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.2233+2018_2233+201 others(454): Show |
RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 19/20 | chr7 | 5930763 | ||||||
chr7:5930763 | C | CGTACACA others(116): Show |
32 | a0001c0001t0001g0023a0001c0008t0002g0051a0001c0008t0002g0052others(29): Show | 32 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(29): Show |
intron_variant | MODIFIER | c.2233+2018_2233+201 others(127): Show |
RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 19/20 | chr7 | 5930763 | ||||||
chr7:5930763 | C | CGTACACA others(239): Show |
1 | a0001c0001t0001g0034 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.2233+2018_2233+201 others(250): Show |
RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 19/20 | chr7 | 5930763 | ||||||
chr7:5930763 | C | CGTACACA others(116): Show |
5 | a0001c0001t0001g0032a0001c0010t0004g0057a0001c0014t0001g0015others(2): Show | 5 | HG00735.hp2 HG02145.hp2 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.2233+2018_2233+201 others(127): Show |
RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 19/20 | chr7 | 5930763 | ||||||
chr7:5930763 | C | CGTACACA others(197): Show |
1 | a0001c0001t0001g0006 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.2233+2018_2233+201 others(208): Show |
RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 19/20 | chr7 | 5930763 | ||||||
chr7:5930763 | C | CGTACACA others(157): Show |
1 | a0001c0001t0001g0022 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.2233+2018_2233+201 others(168): Show |
RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 19/20 | chr7 | 5930763 | ||||||
chr7:5930763 | C | CGTACACA others(198): Show |
5 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0019others(2): Show | 5 | HG00621.hp2 HG01981.hp1 HG02056.hp1 others(2): Show |
intron_variant | MODIFIER | c.2233+2018_2233+201 others(209): Show |
RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 19/20 | chr7 | 5930763 | ||||||
chr7:5930763 | C | CGTACACA others(321): Show |
1 | a0006c0006t0001g0002 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.2233+2018_2233+201 others(332): Show |
RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 19/20 | chr7 | 5930763 | ||||||
chr7:5930763 | C | CGTACACA others(444): Show |
3 | a0001c0001t0006g0013a0006c0006t0001g0008a0006c0006t0001g0017 | 3 | HG00639.hp2 HG00741.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.2233+2018_2233+201 others(455): Show |
RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 19/20 | chr7 | 5930763 | ||||||
chr7:5930763 | C | CGTACACA others(320): Show |
1 | a0006c0006t0001g0021 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.2233+2018_2233+201 others(331): Show |
RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 19/20 | chr7 | 5930763 | ||||||
chr7:5930763 | C | CGTACACA others(158): Show |
1 | a0011c0015t0001g0029 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.2233+2018_2233+201 others(169): Show |
RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 19/20 | chr7 | 5930763 | ||||||
chr7:5930763 | C | CGTACACA others(199): Show |
1 | a0001c0001t0001g0016 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.2233+2018_2233+201 others(210): Show |
RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 19/20 | chr7 | 5930763 | ||||||
chr7:5930763 | C | CGTACACA others(158): Show |
1 | a0001c0001t0002g0026 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.2233+2018_2233+201 others(169): Show |
RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 19/20 | chr7 | 5930763 | ||||||
chr7:5930763 | C | CGTACACA others(158): Show |
1 | a0010c0019t0001g0009 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.2233+2018_2233+201 others(169): Show |
RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 19/20 | chr7 | 5930763 | ||||||
chr7:5930775 | C | A | 1 | a0004c0018t0001g0014 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.2233+2007G>T | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 19/20 | chr7 | 5930775 | ||||||
chr7:5930783 | A | ACCTAGCA others(198): Show |
1 | a0003c0004t0003g0067 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.2233+1998_2233+199 others(209): Show |
RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 19/20 | chr7 | 5930783 | ||||||
chr7:5930783 | A | ACCTAGCA others(34): Show |
1 | a0001c0009t0001g0007 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.2233+1958_2233+199 others(45): Show |
RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 19/20 | chr7 | 5930783 | ||||||
chr7:5930783 | A | G | 57 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(54): Show | 57 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(54): Show |
intron_variant | MODIFIER | c.2233+1999T>C | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 19/20 | chr7 | 5930783 | ||||||
chr7:5930783 | ACCTAGCA others(34): Show |
A | 1 | a0009c0016t0003g0068 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.2233+1958_2233+199 others(45): Show |
RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 19/20 | chr7 | 5930783 | ||||||
chr7:5930785 | C | CTAGCAGC others(76): Show |
1 | a0004c0018t0001g0014 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.2233+1996_2233+199 others(87): Show |
RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 19/20 | chr7 | 5930785 | ||||||
chr7:5930818 | C | G | 5 | a0001c0001t0001g0023a0004c0005t0001g0035a0004c0005t0001g0041others(2): Show | 5 | HG00099.hp1 HG00639.hp1 HG02056.hp2 others(2): Show |
intron_variant | MODIFIER | c.2233+1964G>C | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 19/20 | chr7 | 5930818 | ||||||
chr7:5930901 | C | T | 1 | a0011c0015t0001g0029 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.2233+1881G>A | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 19/20 | chr7 | 5930901 | ||||||
chr7:5930909 | G | A | 6 | a0001c0001t0006g0013a0006c0006t0001g0002a0006c0006t0001g0004others(3): Show | 6 | HG00639.hp2 HG00735.hp1 HG00741.hp1 others(3): Show |
intron_variant | MODIFIER | c.2233+1873C>T | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 19/20 | chr7 | 5930909 | ||||||
chr7:5930918 | A | G | 1 | a0010c0019t0001g0009 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.2233+1864T>C | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 19/20 | chr7 | 5930918 | ||||||
chr7:5930919 | G | A | 1 | a0010c0019t0001g0009 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.2233+1863C>T | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 19/20 | chr7 | 5930919 | ||||||
chr7:5930920 | A | G | 1 | a0010c0019t0001g0009 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.2233+1862T>C | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 19/20 | chr7 | 5930920 | ||||||
chr7:5930939 | CT | C | 24 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0016others(21): Show | 24 | HG00280.hp1 HG00621.hp2 HG00735.hp2 others(21): Show |
intron_variant | MODIFIER | c.2233+1842delA | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 19/20 | chr7 | 5930939 | ||||||
chr7:5930940 | T | C | 1 | a0005c0003t0001g0031 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.2233+1842A>G | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 19/20 | chr7 | 5930940 | ||||||
chr7:5930946 | T | G | 13 | a0002c0002t0001g0037a0002c0002t0002g0018a0002c0002t0002g0038others(10): Show | 13 | HG00280.hp1 HG01175.hp1 HG01175.hp2 others(10): Show |
intron_variant | MODIFIER | c.2233+1836A>C | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 19/20 | chr7 | 5930946 | ||||||
chr7:5931078 | C | CG | 2 | a0002c0002t0001g0037a0006c0006t0001g0002 | 2 | HG01978.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.2233+1703dupC | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 19/20 | chr7 | 5931078 | ||||||
chr7:5931291 | C | G | 8 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(5): Show | 8 | HG00621.hp2 HG01981.hp1 HG02056.hp1 others(5): Show |
intron_variant | MODIFIER | c.2233+1491G>C | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 19/20 | chr7 | 5931291 | ||||||
chr7:5931427 | C | A | 7 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(4): Show | 7 | HG00621.hp2 HG01981.hp1 HG02056.hp1 others(4): Show |
intron_variant | MODIFIER | c.2233+1355G>T | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 19/20 | chr7 | 5931427 | ||||||
chr7:5931453 | C | T | 1 | a0010c0019t0001g0009 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.2233+1329G>A | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 19/20 | chr7 | 5931453 | ||||||
chr7:5931513 | C | G | 13 | a0002c0002t0001g0037a0002c0002t0002g0018a0002c0002t0002g0038others(10): Show | 13 | HG00280.hp1 HG01175.hp1 HG01175.hp2 others(10): Show |
intron_variant | MODIFIER | c.2233+1269G>C | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 19/20 | chr7 | 5931513 | ||||||
chr7:5931698 | TA | T | 47 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0016others(44): Show | 47 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(44): Show |
intron_variant | MODIFIER | c.2233+1083delT | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 19/20 | chr7 | 5931698 | ||||||
chr7:5931727 | G | A | 1 | a0001c0009t0001g0007 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.2233+1055C>T | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 19/20 | chr7 | 5931727 | ||||||
chr7:5931766 | T | C | 48 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(45): Show | 48 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(45): Show |
intron_variant | MODIFIER | c.2233+1016A>G | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 19/20 | chr7 | 5931766 | ||||||
chr7:5932092 | G | A | 45 | a0001c0001t0001g0023a0001c0008t0002g0051a0001c0008t0002g0052others(42): Show | 45 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(42): Show |
intron_variant | MODIFIER | c.2233+690C>T | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 19/20 | chr7 | 5932092 | ||||||
chr7:5932145 | T | C | 46 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(43): Show | 46 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(43): Show |
intron_variant | MODIFIER | c.2233+637A>G | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 19/20 | chr7 | 5932145 | ||||||
chr7:5932183 | G | A | 13 | a0002c0002t0001g0037a0002c0002t0002g0018a0002c0002t0002g0038others(10): Show | 13 | HG00280.hp1 HG01175.hp1 HG01175.hp2 others(10): Show |
intron_variant | MODIFIER | c.2233+599C>T | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 19/20 | chr7 | 5932183 | ||||||
chr7:5932230 | G | C | 2 | a0005c0003t0001g0024a0005c0003t0001g0025 | 2 | HG00621.hp1 HG02523.hp2 |
intron_variant | MODIFIER | c.2233+552C>G | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 19/20 | chr7 | 5932230 | ||||||
chr7:5932293 | G | A | 32 | a0001c0008t0002g0051a0001c0008t0002g0052a0002c0002t0001g0037others(29): Show | 32 | HG00099.hp2 HG00280.hp1 HG00621.hp1 others(29): Show |
intron_variant | MODIFIER | c.2233+489C>T | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 19/20 | chr7 | 5932293 | ||||||
chr7:5932293 | G | T | 1 | a0004c0005t0001g0043 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.2233+489C>A | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 19/20 | chr7 | 5932293 | ||||||
chr7:5932326 | C | T | 40 | a0001c0001t0001g0023a0001c0008t0002g0051a0001c0008t0002g0052others(37): Show | 40 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(37): Show |
intron_variant | MODIFIER | c.2233+456G>A | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 19/20 | chr7 | 5932326 | ||||||
chr7:5932456 | C | T | 1 | a0010c0019t0001g0009 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.2233+326G>A | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 19/20 | chr7 | 5932456 | ||||||
chr7:5932580 | G | A | 13 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(10): Show | 13 | HG00621.hp2 HG00639.hp2 HG00735.hp1 others(10): Show |
intron_variant | MODIFIER | c.2233+202C>T | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 19/20 | chr7 | 5932580 | ||||||
chr7:5933015 | C | CT | 23 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0008t0002g0051others(20): Show | 23 | HG00099.hp1 HG00621.hp1 HG00741.hp1 others(20): Show |
intron_variant | MODIFIER | c.2140-141dupA | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 18/20 | chr7 | 5933015 | ||||||
chr7:5933015 | C | CTT | 6 | a0001c0001t0001g0022a0001c0001t0001g0034a0001c0001t0002g0026others(3): Show | 6 | HG00735.hp2 HG01071.hp2 HG02071.hp1 others(3): Show |
intron_variant | MODIFIER | c.2140-142_2140-141d others(4): Show |
RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 18/20 | chr7 | 5933015 | ||||||
chr7:5933060 | C | T | 2 | a0007c0007t0002g0003a0007c0007t0002g0020 | 2 | HG02258.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.2140-185G>A | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 18/20 | chr7 | 5933060 | ||||||
chr7:5933079 | G | A | 1 | a0002c0002t0002g0048 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.2140-204C>T | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 18/20 | chr7 | 5933079 | ||||||
chr7:5933085 | T | C | 5 | a0006c0006t0001g0002a0006c0006t0001g0004a0006c0006t0001g0008others(2): Show | 5 | HG00639.hp2 HG00735.hp1 HG00741.hp1 others(2): Show |
intron_variant | MODIFIER | c.2140-210A>G | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 18/20 | chr7 | 5933085 | ||||||
chr7:5933153 | G | C | 40 | a0001c0001t0001g0023a0001c0008t0002g0051a0001c0008t0002g0052others(37): Show | 40 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(37): Show |
intron_variant | MODIFIER | c.2140-278C>G | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 18/20 | chr7 | 5933153 | ||||||
chr7:5933269 | T | C | 5 | a0006c0006t0001g0002a0006c0006t0001g0004a0006c0006t0001g0008others(2): Show | 5 | HG00639.hp2 HG00735.hp1 HG00741.hp1 others(2): Show |
intron_variant | MODIFIER | c.2140-394A>G | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 18/20 | chr7 | 5933269 | ||||||
chr7:5933350 | A | G | 9 | a0005c0003t0001g0024a0005c0003t0001g0025a0005c0003t0001g0027others(6): Show | 9 | HG00099.hp2 HG00621.hp1 HG01069.hp1 others(6): Show |
intron_variant | MODIFIER | c.2140-475T>C | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 18/20 | chr7 | 5933350 | ||||||
chr7:5933369 | C | T | 59 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(56): Show | 59 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(56): Show |
intron_variant | MODIFIER | c.2140-494G>A | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 18/20 | chr7 | 5933369 | ||||||
chr7:5933401 | C | CA | 15 | a0001c0001t0001g0023a0001c0008t0002g0051a0001c0008t0002g0052others(12): Show | 15 | HG00099.hp1 HG00639.hp1 HG00735.hp2 others(12): Show |
intron_variant | MODIFIER | c.2140-527dupT | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 18/20 | chr7 | 5933401 | ||||||
chr7:5933410 | A | C | 16 | a0001c0009t0001g0007a0002c0002t0001g0037a0002c0002t0002g0018others(13): Show | 16 | HG00280.hp1 HG01175.hp1 HG01175.hp2 others(13): Show |
intron_variant | MODIFIER | c.2140-535T>G | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 18/20 | chr7 | 5933410 | ||||||
chr7:5933471 | C | T | 16 | a0001c0009t0001g0007a0002c0002t0001g0037a0002c0002t0002g0018others(13): Show | 16 | HG00280.hp1 HG01175.hp1 HG01175.hp2 others(13): Show |
intron_variant | MODIFIER | c.2140-596G>A | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 18/20 | chr7 | 5933471 | ||||||
chr7:5933472 | G | A | 43 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(40): Show | 43 | HG00099.hp1 HG00099.hp2 HG00621.hp1 others(40): Show |
intron_variant | MODIFIER | c.2140-597C>T | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 18/20 | chr7 | 5933472 | ||||||
chr7:5933532 | G | T | 30 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0034others(27): Show | 30 | HG00099.hp1 HG00099.hp2 HG00621.hp1 others(27): Show |
intron_variant | MODIFIER | c.2140-657C>A | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 18/20 | chr7 | 5933532 | ||||||
chr7:5933620 | C | T | 13 | a0002c0002t0001g0037a0002c0002t0002g0018a0002c0002t0002g0038others(10): Show | 13 | HG00280.hp1 HG01175.hp1 HG01175.hp2 others(10): Show |
intron_variant | MODIFIER | c.2140-745G>A | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 18/20 | chr7 | 5933620 | ||||||
chr7:5933700 | C | G | 6 | a0001c0001t0001g0022a0001c0001t0001g0034a0001c0001t0002g0026others(3): Show | 6 | HG00735.hp2 HG01069.hp2 HG01071.hp2 others(3): Show |
intron_variant | MODIFIER | c.2140-825G>C | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 18/20 | chr7 | 5933700 | ||||||
chr7:5933701 | A | G | 9 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(6): Show | 9 | HG00621.hp2 HG01981.hp1 HG02056.hp1 others(6): Show |
intron_variant | MODIFIER | c.2140-826T>C | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 18/20 | chr7 | 5933701 | ||||||
chr7:5933708 | C | G | 30 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0034others(27): Show | 30 | HG00099.hp1 HG00099.hp2 HG00621.hp1 others(27): Show |
intron_variant | MODIFIER | c.2140-833G>C | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 18/20 | chr7 | 5933708 | ||||||
chr7:5933737 | A | G | 13 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(10): Show | 13 | HG00621.hp2 HG00639.hp2 HG00735.hp1 others(10): Show |
intron_variant | MODIFIER | c.2140-862T>C | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 18/20 | chr7 | 5933737 | ||||||
chr7:5933746 | G | A | 5 | a0001c0001t0001g0022a0001c0001t0001g0034a0001c0001t0002g0026others(2): Show | 5 | HG00735.hp2 HG01069.hp2 HG02074.hp2 others(2): Show |
intron_variant | MODIFIER | c.2140-871C>T | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 18/20 | chr7 | 5933746 | ||||||
chr7:5933766 | CAA | C | 35 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0034others(32): Show | 35 | HG00099.hp1 HG00099.hp2 HG00621.hp1 others(32): Show |
intron_variant | MODIFIER | c.2140-893_2140-892d others(4): Show |
RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 18/20 | chr7 | 5933766 | ||||||
chr7:5933804 | C | T | 43 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(40): Show | 43 | HG00099.hp1 HG00099.hp2 HG00621.hp1 others(40): Show |
intron_variant | MODIFIER | c.2140-929G>A | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 18/20 | chr7 | 5933804 | ||||||
chr7:5933835 | G | A | 45 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(42): Show | 45 | HG00099.hp1 HG00099.hp2 HG00621.hp1 others(42): Show |
intron_variant | MODIFIER | c.2140-960C>T | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 18/20 | chr7 | 5933835 | ||||||
chr7:5933918 | G | C | 1 | a0010c0019t0001g0009 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.2140-1043C>G | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 18/20 | chr7 | 5933918 | ||||||
chr7:5933933 | C | T | 35 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0034others(32): Show | 35 | HG00099.hp1 HG00099.hp2 HG00621.hp1 others(32): Show |
intron_variant | MODIFIER | c.2140-1058G>A | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 18/20 | chr7 | 5933933 | ||||||
chr7:5933963 | C | T | 35 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0034others(32): Show | 35 | HG00099.hp1 HG00099.hp2 HG00621.hp1 others(32): Show |
intron_variant | MODIFIER | c.2139+1057G>A | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 18/20 | chr7 | 5933963 | ||||||
chr7:5933980 | G | T | 2 | a0002c0002t0002g0038a0002c0002t0003g0060 | 2 | HG01934.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.2139+1040C>A | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 18/20 | chr7 | 5933980 | ||||||
chr7:5933997 | A | AT | 43 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(40): Show | 43 | HG00099.hp1 HG00099.hp2 HG00621.hp1 others(40): Show |
intron_variant | MODIFIER | c.2139+1022dupA | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 18/20 | chr7 | 5933997 | ||||||
chr7:5933999 | A | T | 46 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(43): Show | 46 | HG00099.hp1 HG00099.hp2 HG00621.hp1 others(43): Show |
intron_variant | MODIFIER | c.2139+1021T>A | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 18/20 | chr7 | 5933999 | ||||||
chr7:5934042 | T | C | 43 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(40): Show | 43 | HG00099.hp1 HG00099.hp2 HG00621.hp1 others(40): Show |
intron_variant | MODIFIER | c.2139+978A>G | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 18/20 | chr7 | 5934042 | ||||||
chr7:5934114 | T | G | 16 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(13): Show | 16 | HG00735.hp2 HG01069.hp2 HG01071.hp2 others(13): Show |
intron_variant | MODIFIER | c.2139+906A>C | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 18/20 | chr7 | 5934114 | ||||||
chr7:5934143 | A | G | 4 | a0001c0009t0001g0007a0003c0004t0003g0067a0004c0018t0001g0014others(1): Show | 4 | HG02071.hp1 HG02109.hp2 HG02523.hp1 others(1): Show |
intron_variant | MODIFIER | c.2139+877T>C | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 18/20 | chr7 | 5934143 | ||||||
chr7:5934178 | C | T | 45 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(42): Show | 45 | HG00099.hp1 HG00099.hp2 HG00621.hp1 others(42): Show |
intron_variant | MODIFIER | c.2139+842G>A | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 18/20 | chr7 | 5934178 | ||||||
chr7:5934239 | C | T | 12 | a0002c0002t0001g0037a0002c0002t0002g0018a0002c0002t0002g0038others(9): Show | 12 | HG00280.hp1 HG01175.hp2 HG01517.hp2 others(9): Show |
intron_variant | MODIFIER | c.2139+781G>A | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 18/20 | chr7 | 5934239 | ||||||
chr7:5934502 | G | A | 20 | a0001c0008t0002g0051a0001c0008t0002g0052a0002c0002t0001g0037others(17): Show | 20 | HG00280.hp1 HG00639.hp2 HG00735.hp1 others(17): Show |
intron_variant | MODIFIER | c.2139+518C>T | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 18/20 | chr7 | 5934502 | ||||||
chr7:5934538 | A | G | 1 | a0004c0011t0002g0039 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.2139+482T>C | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 18/20 | chr7 | 5934538 | ||||||
chr7:5934592 | C | T | 1 | a0004c0018t0001g0014 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.2139+428G>A | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 18/20 | chr7 | 5934592 | ||||||
chr7:5934649 | G | A | 11 | a0001c0009t0001g0007a0004c0005t0005g0033a0005c0003t0001g0024others(8): Show | 11 | HG00099.hp2 HG00621.hp1 HG01069.hp1 others(8): Show |
intron_variant | MODIFIER | c.2139+371C>T | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 18/20 | chr7 | 5934649 | ||||||
chr7:5934746 | T | C | 11 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(8): Show | 11 | HG00621.hp2 HG01981.hp1 HG02056.hp1 others(8): Show |
intron_variant | MODIFIER | c.2139+274A>G | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 18/20 | chr7 | 5934746 | ||||||
chr7:5934858 | C | T | 16 | a0001c0001t0006g0013a0002c0002t0001g0037a0002c0002t0002g0018others(13): Show | 16 | HG00280.hp1 HG01071.hp2 HG01175.hp1 others(13): Show |
intron_variant | MODIFIER | c.2139+162G>A | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 18/20 | chr7 | 5934858 | ||||||
chr7:5934927 | T | C | 1 | a0010c0019t0001g0009 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.2139+93A>G | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 18/20 | chr7 | 5934927 | ||||||
chr7:5934949 | T | C | 1 | a0001c0009t0001g0007 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.2139+71A>G | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 18/20 | chr7 | 5934949 | ||||||
chr7:5935168 | C | T | 1 | a0003c0004t0003g0062 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.2011-20G>A | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 17/20 | chr7 | 5935168 | ||||||
chr7:5935462 | T | TA | 16 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(13): Show | 16 | HG00621.hp2 HG00639.hp2 HG00735.hp1 others(13): Show |
intron_variant | MODIFIER | c.2011-315dupT | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 17/20 | chr7 | 5935462 | ||||||
chr7:5935523 | G | A | 28 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0034others(25): Show | 28 | HG00099.hp1 HG00099.hp2 HG00621.hp1 others(25): Show |
intron_variant | MODIFIER | c.2011-375C>T | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 17/20 | chr7 | 5935523 | ||||||
chr7:5935634 | A | C | 13 | a0002c0002t0001g0037a0002c0002t0002g0018a0002c0002t0002g0038others(10): Show | 13 | HG00280.hp1 HG01175.hp1 HG01175.hp2 others(10): Show |
intron_variant | MODIFIER | c.2011-486T>G | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 17/20 | chr7 | 5935634 | ||||||
chr7:5935759 | C | CA | 13 | a0002c0002t0001g0037a0002c0002t0002g0018a0002c0002t0002g0038others(10): Show | 13 | HG00280.hp1 HG01175.hp1 HG01175.hp2 others(10): Show |
intron_variant | MODIFIER | c.2011-612dupT | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 17/20 | chr7 | 5935759 | ||||||
chr7:5935778 | A | AACAC | 21 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(18): Show | 21 | HG00621.hp2 HG00639.hp2 HG00735.hp1 others(18): Show |
intron_variant | MODIFIER | c.2011-634_2011-631d others(6): Show |
RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 17/20 | chr7 | 5935778 | ||||||
chr7:5935778 | A | AACACACA others(1): Show |
25 | a0001c0001t0001g0023a0001c0008t0002g0051a0001c0008t0002g0052others(22): Show | 25 | HG00099.hp1 HG00099.hp2 HG00621.hp1 others(22): Show |
intron_variant | MODIFIER | c.2011-638_2011-631d others(10): Show |
RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 17/20 | chr7 | 5935778 | ||||||
chr7:5935887 | C | T | 27 | a0001c0001t0001g0023a0001c0008t0002g0051a0001c0008t0002g0052others(24): Show | 27 | HG00099.hp1 HG00099.hp2 HG00621.hp1 others(24): Show |
intron_variant | MODIFIER | c.2011-739G>A | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 17/20 | chr7 | 5935887 | ||||||
chr7:5935926 | C | T | 4 | a0001c0008t0002g0051a0001c0008t0002g0052a0007c0007t0002g0003others(1): Show | 4 | HG02258.hp1 HG02717.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.2011-778G>A | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 17/20 | chr7 | 5935926 | ||||||
chr7:5935940 | T | TC | 16 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(13): Show | 16 | HG00621.hp2 HG00639.hp2 HG00735.hp1 others(13): Show |
intron_variant | MODIFIER | c.2011-793dupG | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 17/20 | chr7 | 5935940 | ||||||
chr7:5936003 | G | C | 46 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(43): Show | 46 | HG00099.hp1 HG00099.hp2 HG00621.hp1 others(43): Show |
intron_variant | MODIFIER | c.2011-855C>G | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 17/20 | chr7 | 5936003 | ||||||
chr7:5936086 | G | A | 5 | a0006c0006t0001g0002a0006c0006t0001g0004a0006c0006t0001g0008others(2): Show | 5 | HG00639.hp2 HG00735.hp1 HG00741.hp1 others(2): Show |
intron_variant | MODIFIER | c.2011-938C>T | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 17/20 | chr7 | 5936086 | ||||||
chr7:5936205 | C | T | 2 | a0001c0010t0004g0056a0001c0010t0004g0057 | 2 | HG00735.hp2 HG01069.hp2 |
intron_variant | MODIFIER | c.2011-1057G>A | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 17/20 | chr7 | 5936205 | ||||||
chr7:5936253 | G | A | 4 | a0006c0006t0001g0002a0006c0006t0001g0008a0006c0006t0001g0017others(1): Show | 4 | HG00639.hp2 HG00735.hp1 HG00741.hp1 others(1): Show |
intron_variant | MODIFIER | c.2011-1105C>T | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 17/20 | chr7 | 5936253 | ||||||
chr7:5936255 | G | C | 11 | a0001c0001t0001g0023a0001c0008t0002g0051a0001c0008t0002g0052others(8): Show | 11 | HG00639.hp1 HG02056.hp2 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.2011-1107C>G | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 17/20 | chr7 | 5936255 | ||||||
chr7:5936329 | G | C | 5 | a0006c0006t0001g0002a0006c0006t0001g0004a0006c0006t0001g0008others(2): Show | 5 | HG00639.hp2 HG00735.hp1 HG00741.hp1 others(2): Show |
intron_variant | MODIFIER | c.2011-1181C>G | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 17/20 | chr7 | 5936329 | ||||||
chr7:5936340 | C | T | 1 | a0004c0018t0001g0014 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.2011-1192G>A | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 17/20 | chr7 | 5936340 | ||||||
chr7:5936417 | C | T | 3 | a0001c0001t0006g0013a0001c0010t0004g0056a0001c0010t0004g0057 | 3 | HG00735.hp2 HG01069.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.2011-1269G>A | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 17/20 | chr7 | 5936417 | ||||||
chr7:5936419 | A | G | 2 | a0001c0010t0004g0056a0001c0010t0004g0057 | 2 | HG00735.hp2 HG01069.hp2 |
intron_variant | MODIFIER | c.2011-1271T>C | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 17/20 | chr7 | 5936419 | ||||||
chr7:5936467 | A | G | 59 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(56): Show | 59 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(56): Show |
intron_variant | MODIFIER | c.2010+1291T>C | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 17/20 | chr7 | 5936467 | ||||||
chr7:5936802 | C | T | 5 | a0006c0006t0001g0002a0006c0006t0001g0004a0006c0006t0001g0008others(2): Show | 5 | HG00639.hp2 HG00735.hp1 HG00741.hp1 others(2): Show |
intron_variant | MODIFIER | c.2010+956G>A | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 17/20 | chr7 | 5936802 | ||||||
chr7:5936863 | G | C | 1 | a0001c0009t0001g0012 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.2010+895C>G | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 17/20 | chr7 | 5936863 | ||||||
chr7:5936890 | C | A | 1 | a0006c0006t0001g0002 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.2010+868G>T | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 17/20 | chr7 | 5936890 | ||||||
chr7:5936916 | C | T | 1 | a0001c0014t0001g0015 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.2010+842G>A | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 17/20 | chr7 | 5936916 | ||||||
chr7:5937001 | C | T | 1 | a0002c0002t0001g0037 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.2010+757G>A | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 17/20 | chr7 | 5937001 | ||||||
chr7:5937050 | G | A | 3 | a0001c0001t0006g0013a0001c0010t0004g0056a0001c0010t0004g0057 | 3 | HG00735.hp2 HG01069.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.2010+708C>T | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 17/20 | chr7 | 5937050 | ||||||
chr7:5937077 | GCT | G | 4 | a0006c0006t0001g0002a0006c0006t0001g0004a0006c0006t0001g0017others(1): Show | 4 | HG00639.hp2 HG00735.hp1 HG01978.hp2 others(1): Show |
intron_variant | MODIFIER | c.2010+679_2010+680d others(4): Show |
RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 17/20 | chr7 | 5937077 | ||||||
chr7:5937080 | C | G | 38 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(35): Show | 38 | HG00099.hp1 HG00099.hp2 HG00621.hp1 others(35): Show |
intron_variant | MODIFIER | c.2010+678G>C | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 17/20 | chr7 | 5937080 | ||||||
chr7:5937082 | G | C | 2 | a0004c0005t0005g0033a0006c0006t0001g0008 | 2 | HG00741.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.2010+676C>G | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 17/20 | chr7 | 5937082 | ||||||
chr7:5937085 | T | A | 1 | a0006c0006t0001g0008 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.2010+673A>T | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 17/20 | chr7 | 5937085 | ||||||
chr7:5937086 | C | A | 1 | a0006c0006t0001g0008 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.2010+672G>T | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 17/20 | chr7 | 5937086 | ||||||
chr7:5937086 | C | CA | 11 | a0001c0008t0002g0051a0001c0008t0002g0052a0002c0002t0002g0038others(8): Show | 11 | HG00639.hp2 HG00735.hp1 HG01934.hp1 others(8): Show |
intron_variant | MODIFIER | c.2010+671dupT | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 17/20 | chr7 | 5937086 | ||||||
chr7:5937086 | C | CAA | 10 | a0004c0005t0005g0033a0005c0003t0001g0024a0005c0003t0001g0025others(7): Show | 10 | HG00099.hp2 HG00621.hp1 HG01071.hp1 others(7): Show |
intron_variant | MODIFIER | c.2010+670_2010+671d others(4): Show |
RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 17/20 | chr7 | 5937086 | ||||||
chr7:5937086 | C | CAAA | 6 | a0001c0001t0006g0013a0001c0010t0004g0056a0001c0010t0004g0057others(3): Show | 6 | HG00735.hp2 HG01069.hp1 HG01069.hp2 others(3): Show |
intron_variant | MODIFIER | c.2010+669_2010+671d others(5): Show |
RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 17/20 | chr7 | 5937086 | ||||||
chr7:5937104 | A | AAT | 18 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(15): Show | 18 | HG00099.hp1 HG00621.hp2 HG00639.hp1 others(15): Show |
intron_variant | MODIFIER | c.2010+653_2010+654i others(4): Show |
RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 17/20 | chr7 | 5937104 | ||||||
chr7:5937269 | A | G | 11 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(8): Show | 11 | HG00621.hp2 HG01981.hp1 HG02056.hp1 others(8): Show |
intron_variant | MODIFIER | c.2010+489T>C | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 17/20 | chr7 | 5937269 | ||||||
chr7:5937290 | T | C | 13 | a0002c0002t0001g0037a0002c0002t0002g0018a0002c0002t0002g0038others(10): Show | 13 | HG00280.hp1 HG01175.hp1 HG01175.hp2 others(10): Show |
intron_variant | MODIFIER | c.2010+468A>G | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 17/20 | chr7 | 5937290 | ||||||
chr7:5937372 | A | T | 1 | a0010c0019t0001g0009 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.2010+386T>A | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 17/20 | chr7 | 5937372 | ||||||
chr7:5937409 | G | T | 4 | a0004c0005t0001g0055a0004c0005t0005g0033a0005c0003t0002g0010others(1): Show | 4 | HG02258.hp2 HG02976.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.2010+349C>A | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 17/20 | chr7 | 5937409 | ||||||
chr7:5937412 | T | G | 1 | a0004c0005t0005g0033 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.2010+346A>C | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 17/20 | chr7 | 5937412 | ||||||
chr7:5937445 | G | A | 20 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(17): Show | 20 | HG00099.hp1 HG00621.hp2 HG00639.hp1 others(17): Show |
intron_variant | MODIFIER | c.2010+313C>T | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 17/20 | chr7 | 5937445 | ||||||
chr7:5937494 | C | T | 33 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(30): Show | 33 | HG00099.hp1 HG00099.hp2 HG00621.hp1 others(30): Show |
intron_variant | MODIFIER | c.2010+264G>A | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 17/20 | chr7 | 5937494 | ||||||
chr7:5937511 | T | C | 15 | a0003c0004t0003g0067a0004c0005t0001g0055a0004c0005t0005g0033others(12): Show | 15 | HG00099.hp2 HG00621.hp1 HG01069.hp1 others(12): Show |
intron_variant | MODIFIER | c.2010+247A>G | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 17/20 | chr7 | 5937511 | ||||||
chr7:5937564 | C | T | 14 | a0001c0009t0001g0007a0004c0005t0001g0055a0004c0005t0005g0033others(11): Show | 14 | HG00099.hp2 HG00621.hp1 HG01069.hp1 others(11): Show |
intron_variant | MODIFIER | c.2010+194G>A | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 17/20 | chr7 | 5937564 | ||||||
chr7:5937650 | C | T | 20 | a0001c0008t0002g0051a0001c0008t0002g0052a0002c0002t0001g0037others(17): Show | 20 | HG00280.hp1 HG00639.hp2 HG00735.hp1 others(17): Show |
intron_variant | MODIFIER | c.2010+108G>A | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 17/20 | chr7 | 5937650 | ||||||
chr7:5937739 | C | G | 2 | a0001c0008t0002g0051a0001c0008t0002g0052 | 2 | HG02717.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.2010+19G>C | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 17/20 | chr7 | 5937739 | ||||||
chr7:5937751 | G | A | 2 | a0001c0008t0002g0051a0001c0008t0002g0052 | 2 | HG02717.hp2 HG03471.hp1 |
splice_region_variant&intron_variant | LOW | c.2010+7C>T | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 17/20 | chr7 | 5937751 | ||||||
chr7:5938011 | C | CCA | 5 | a0001c0001t0006g0013a0001c0010t0004g0056a0001c0010t0004g0057others(2): Show | 5 | HG00735.hp2 HG01069.hp2 HG01071.hp2 others(2): Show |
intron_variant | MODIFIER | c.1867-112_1867-111d others(4): Show |
RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 16/20 | chr7 | 5938011 | ||||||
chr7:5938036 | C | T | 21 | a0001c0008t0002g0051a0001c0008t0002g0052a0002c0002t0001g0037others(18): Show | 21 | HG00280.hp1 HG00639.hp2 HG00735.hp1 others(18): Show |
intron_variant | MODIFIER | c.1867-135G>A | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 16/20 | chr7 | 5938036 | ||||||
chr7:5938246 | C | G | 19 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(16): Show | 19 | HG00099.hp1 HG00621.hp2 HG00639.hp1 others(16): Show |
intron_variant | MODIFIER | c.1867-345G>C | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 16/20 | chr7 | 5938246 | ||||||
chr7:5938289 | T | C | 1 | a0010c0019t0001g0009 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.1867-388A>G | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 16/20 | chr7 | 5938289 | ||||||
chr7:5938305 | T | C | 3 | a0001c0001t0006g0013a0001c0010t0004g0056a0001c0010t0004g0057 | 3 | HG00735.hp2 HG01069.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.1867-404A>G | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 16/20 | chr7 | 5938305 | ||||||
chr7:5938335 | A | G | 4 | a0001c0008t0002g0051a0001c0008t0002g0052a0007c0007t0002g0003others(1): Show | 4 | HG02258.hp1 HG02717.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.1866+387T>C | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 16/20 | chr7 | 5938335 | ||||||
chr7:5938399 | C | G | 1 | a0010c0019t0001g0009 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.1866+323G>C | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 16/20 | chr7 | 5938399 | ||||||
chr7:5938403 | T | TA | 16 | a0001c0008t0002g0051a0001c0008t0002g0052a0002c0002t0001g0037others(13): Show | 16 | HG00280.hp1 HG01175.hp1 HG01175.hp2 others(13): Show |
intron_variant | MODIFIER | c.1866+318dupT | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 16/20 | chr7 | 5938403 | ||||||
chr7:5938414 | C | CA | 5 | a0001c0001t0006g0013a0001c0010t0004g0057a0001c0014t0001g0015others(2): Show | 5 | HG00735.hp2 HG01071.hp2 HG01515.hp2 others(2): Show |
intron_variant | MODIFIER | c.1866+307dupT | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 16/20 | chr7 | 5938414 | ||||||
chr7:5938574 | C | T | 1 | a0011c0015t0001g0029 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.1866+148G>A | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 16/20 | chr7 | 5938574 | ||||||
chr7:5938575 | G | A | 1 | a0010c0019t0001g0009 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.1866+147C>T | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 16/20 | chr7 | 5938575 | ||||||
chr7:5938580 | C | CA | 18 | a0001c0008t0002g0051a0001c0008t0002g0052a0003c0004t0003g0064others(15): Show | 18 | HG00099.hp2 HG01069.hp1 HG01071.hp1 others(15): Show |
intron_variant | MODIFIER | c.1866+141dupT | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 16/20 | chr7 | 5938580 | ||||||
chr7:5938580 | C | CAA | 5 | a0002c0002t0001g0037a0002c0002t0002g0050a0005c0003t0001g0025others(2): Show | 5 | HG00621.hp1 HG00639.hp2 HG01515.hp2 others(2): Show |
intron_variant | MODIFIER | c.1866+140_1866+141d others(4): Show |
RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 16/20 | chr7 | 5938580 | ||||||
chr7:5938580 | C | CAAA | 14 | a0002c0002t0002g0018a0002c0002t0002g0038a0002c0002t0002g0040others(11): Show | 14 | HG00280.hp1 HG00735.hp1 HG00741.hp1 others(11): Show |
intron_variant | MODIFIER | c.1866+139_1866+141d others(5): Show |
RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 16/20 | chr7 | 5938580 | ||||||
chr7:5938841 | A | C | 2 | a0001c0001t0001g0005a0001c0013t0001g0054 | 2 | HG02056.hp1 HG02074.hp1 |
intron_variant | MODIFIER | c.1759-12T>G | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 15/20 | chr7 | 5938841 | ||||||
chr7:5938919 | G | A | 44 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(41): Show | 44 | HG00099.hp1 HG00280.hp1 HG00621.hp2 others(41): Show |
intron_variant | MODIFIER | c.1759-90C>T | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 15/20 | chr7 | 5938919 | ||||||
chr7:5938959 | G | A | 1 | a0010c0019t0001g0009 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.1759-130C>T | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 15/20 | chr7 | 5938959 | ||||||
chr7:5938975 | G | A | 5 | a0006c0006t0001g0002a0006c0006t0001g0004a0006c0006t0001g0008others(2): Show | 5 | HG00639.hp2 HG00735.hp1 HG00741.hp1 others(2): Show |
intron_variant | MODIFIER | c.1759-146C>T | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 15/20 | chr7 | 5938975 | ||||||
chr7:5939014 | C | T | 11 | a0005c0003t0001g0024a0005c0003t0001g0025a0005c0003t0001g0027others(8): Show | 11 | HG00099.hp2 HG00621.hp1 HG01069.hp1 others(8): Show |
intron_variant | MODIFIER | c.1759-185G>A | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 15/20 | chr7 | 5939014 | ||||||
chr7:5939018 | G | C | 39 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(36): Show | 39 | HG00099.hp1 HG00280.hp1 HG00621.hp2 others(36): Show |
intron_variant | MODIFIER | c.1759-189C>G | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 15/20 | chr7 | 5939018 | ||||||
chr7:5939216 | G | T | 38 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(35): Show | 38 | HG00099.hp1 HG00280.hp1 HG00621.hp2 others(35): Show |
intron_variant | MODIFIER | c.1759-387C>A | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 15/20 | chr7 | 5939216 | ||||||
chr7:5939376 | T | C | 59 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(56): Show | 59 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(56): Show |
intron_variant | MODIFIER | c.1759-547A>G | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 15/20 | chr7 | 5939376 | ||||||
chr7:5939383 | G | A | 1 | a0010c0019t0001g0009 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.1759-554C>T | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 15/20 | chr7 | 5939383 | ||||||
chr7:5939527 | T | G | 2 | a0005c0003t0001g0027a0005c0003t0001g0028 | 2 | HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.1759-698A>C | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 15/20 | chr7 | 5939527 | ||||||
chr7:5939585 | A | AAC | 10 | a0001c0001t0001g0022a0002c0002t0002g0018a0002c0002t0002g0040others(7): Show | 10 | HG01175.hp2 HG01978.hp1 HG01981.hp2 others(7): Show |
intron_variant | MODIFIER | c.1759-758_1759-757d others(4): Show |
RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 15/20 | chr7 | 5939585 | ||||||
chr7:5939585 | A | AACAC | 5 | a0003c0004t0003g0058a0003c0004t0003g0069a0003c0004t0003g0070others(2): Show | 5 | HG00280.hp2 HG00741.hp2 HG01175.hp1 others(2): Show |
intron_variant | MODIFIER | c.1759-760_1759-757d others(6): Show |
RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 15/20 | chr7 | 5939585 | ||||||
chr7:5939585 | AAC | A | 16 | a0001c0008t0002g0051a0001c0009t0001g0007a0001c0009t0001g0012others(13): Show | 16 | HG00280.hp1 HG00621.hp1 HG00639.hp2 others(13): Show |
intron_variant | MODIFIER | c.1759-758_1759-757d others(4): Show |
RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 15/20 | chr7 | 5939585 | ||||||
chr7:5939585 | AACAC | A | 12 | a0001c0001t0001g0019a0001c0001t0001g0034a0001c0001t0002g0026others(9): Show | 12 | HG00099.hp1 HG00099.hp2 HG01261.hp1 others(9): Show |
intron_variant | MODIFIER | c.1759-760_1759-757d others(6): Show |
RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 15/20 | chr7 | 5939585 | ||||||
chr7:5939585 | AACACACA others(3): Show |
A | 4 | a0001c0001t0006g0013a0005c0003t0001g0027a0005c0003t0001g0028others(1): Show | 4 | HG01069.hp1 HG01071.hp1 HG01071.hp2 others(1): Show |
intron_variant | MODIFIER | c.1759-766_1759-757d others(12): Show |
RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 15/20 | chr7 | 5939585 | ||||||
chr7:5939585 | AACACACA others(7): Show |
A | 2 | a0004c0005t0001g0055a0004c0011t0002g0039 | 2 | HG02717.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.1759-770_1759-757d others(16): Show |
RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 15/20 | chr7 | 5939585 | ||||||
chr7:5939696 | G | C | 1 | a0001c0001t0006g0013 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.1759-867C>G | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 15/20 | chr7 | 5939696 | ||||||
chr7:5939734 | C | T | 1 | a0004c0005t0001g0055 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1759-905G>A | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 15/20 | chr7 | 5939734 | ||||||
chr7:5939758 | C | T | 21 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(18): Show | 21 | HG00099.hp1 HG00621.hp2 HG00639.hp1 others(18): Show |
intron_variant | MODIFIER | c.1759-929G>A | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 15/20 | chr7 | 5939758 | ||||||
chr7:5939759 | G | A | 3 | a0001c0001t0006g0013a0001c0010t0004g0056a0001c0010t0004g0057 | 3 | HG00735.hp2 HG01069.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.1759-930C>T | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 15/20 | chr7 | 5939759 | ||||||
chr7:5939814 | T | G | 1 | a0002c0002t0002g0048 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1759-985A>C | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 15/20 | chr7 | 5939814 | ||||||
chr7:5940055 | C | G | 18 | a0002c0002t0001g0037a0002c0002t0002g0018a0002c0002t0002g0038others(15): Show | 18 | HG00280.hp1 HG00639.hp2 HG00735.hp1 others(15): Show |
intron_variant | MODIFIER | c.1759-1226G>C | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 15/20 | chr7 | 5940055 | ||||||
chr7:5940066 | G | A | 13 | a0002c0002t0001g0037a0002c0002t0002g0018a0002c0002t0002g0038others(10): Show | 13 | HG00280.hp1 HG01175.hp1 HG01175.hp2 others(10): Show |
intron_variant | MODIFIER | c.1759-1237C>T | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 15/20 | chr7 | 5940066 | ||||||
chr7:5940069 | T | C | 20 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(17): Show | 20 | HG00099.hp1 HG00621.hp2 HG00639.hp1 others(17): Show |
intron_variant | MODIFIER | c.1759-1240A>G | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 15/20 | chr7 | 5940069 | ||||||
chr7:5940090 | G | A | 2 | a0001c0008t0002g0051a0001c0008t0002g0052 | 2 | HG02717.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.1759-1261C>T | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 15/20 | chr7 | 5940090 | ||||||
chr7:5940116 | G | C | 1 | a0006c0006t0001g0017 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.1759-1287C>G | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 15/20 | chr7 | 5940116 | ||||||
chr7:5940155 | C | T | 1 | a0004c0018t0001g0014 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1759-1326G>A | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 15/20 | chr7 | 5940155 | ||||||
chr7:5940160 | G | A | 1 | a0010c0019t0001g0009 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.1759-1331C>T | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 15/20 | chr7 | 5940160 | ||||||
chr7:5940196 | A | AAAT | 3 | a0001c0001t0006g0013a0001c0010t0004g0056a0001c0010t0004g0057 | 3 | HG00735.hp2 HG01069.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.1759-1370_1759-136 others(7): Show |
RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 15/20 | chr7 | 5940196 | ||||||
chr7:5940375 | C | T | 2 | a0001c0008t0002g0051a0001c0008t0002g0052 | 2 | HG02717.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.1759-1546G>A | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 15/20 | chr7 | 5940375 | ||||||
chr7:5940464 | T | G | 13 | a0002c0002t0001g0037a0002c0002t0002g0018a0002c0002t0002g0038others(10): Show | 13 | HG00280.hp1 HG01175.hp1 HG01175.hp2 others(10): Show |
intron_variant | MODIFIER | c.1759-1635A>C | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 15/20 | chr7 | 5940464 | ||||||
chr7:5940505 | AAC | A | 5 | a0006c0006t0001g0002a0006c0006t0001g0004a0006c0006t0001g0008others(2): Show | 5 | HG00639.hp2 HG00735.hp1 HG00741.hp1 others(2): Show |
intron_variant | MODIFIER | c.1759-1678_1759-167 others(6): Show |
RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 15/20 | chr7 | 5940505 | ||||||
chr7:5940509 | C | A | 5 | a0006c0006t0001g0002a0006c0006t0001g0004a0006c0006t0001g0008others(2): Show | 5 | HG00639.hp2 HG00735.hp1 HG00741.hp1 others(2): Show |
intron_variant | MODIFIER | c.1759-1680G>T | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 15/20 | chr7 | 5940509 | ||||||
chr7:5940512 | C | A | 5 | a0006c0006t0001g0002a0006c0006t0001g0004a0006c0006t0001g0008others(2): Show | 5 | HG00639.hp2 HG00735.hp1 HG00741.hp1 others(2): Show |
intron_variant | MODIFIER | c.1759-1683G>T | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 15/20 | chr7 | 5940512 | ||||||
chr7:5940515 | C | A | 5 | a0006c0006t0001g0002a0006c0006t0001g0004a0006c0006t0001g0008others(2): Show | 5 | HG00639.hp2 HG00735.hp1 HG00741.hp1 others(2): Show |
intron_variant | MODIFIER | c.1759-1686G>T | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 15/20 | chr7 | 5940515 | ||||||
chr7:5940617 | C | T | 3 | a0001c0001t0006g0013a0001c0010t0004g0056a0001c0010t0004g0057 | 3 | HG00735.hp2 HG01069.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.1759-1788G>A | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 15/20 | chr7 | 5940617 | ||||||
chr7:5940643 | A | T | 21 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(18): Show | 21 | HG00099.hp1 HG00621.hp2 HG00639.hp1 others(18): Show |
intron_variant | MODIFIER | c.1759-1814T>A | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 15/20 | chr7 | 5940643 | ||||||
chr7:5940730 | C | G | 13 | a0002c0002t0001g0037a0002c0002t0002g0018a0002c0002t0002g0038others(10): Show | 13 | HG00280.hp1 HG01175.hp1 HG01175.hp2 others(10): Show |
intron_variant | MODIFIER | c.1759-1901G>C | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 15/20 | chr7 | 5940730 | ||||||
chr7:5940783 | G | A | 2 | a0001c0008t0002g0051a0001c0008t0002g0052 | 2 | HG02717.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.1759-1954C>T | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 15/20 | chr7 | 5940783 | ||||||
chr7:5940923 | AAAT | A | 10 | a0001c0008t0002g0051a0005c0003t0001g0024a0005c0003t0001g0025others(7): Show | 10 | HG00099.hp2 HG00621.hp1 HG01069.hp1 others(7): Show |
intron_variant | MODIFIER | c.1759-2097_1759-209 others(7): Show |
RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 15/20 | chr7 | 5940923 | ||||||
chr7:5940939 | A | T | 1 | a0005c0003t0001g0031 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.1759-2110T>A | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 15/20 | chr7 | 5940939 | ||||||
chr7:5940939 | AATAATT | A | 11 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(8): Show | 11 | HG00099.hp1 HG00621.hp2 HG01981.hp1 others(8): Show |
intron_variant | MODIFIER | c.1759-2116_1759-211 others(10): Show |
RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 15/20 | chr7 | 5940939 | ||||||
chr7:5940939 | AATAATTA others(2): Show |
A | 6 | a0001c0009t0001g0007a0002c0002t0001g0037a0002c0002t0002g0049others(3): Show | 6 | HG00735.hp1 HG01175.hp1 HG01978.hp2 others(3): Show |
intron_variant | MODIFIER | c.1759-2119_1759-211 others(13): Show |
RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 15/20 | chr7 | 5940939 | ||||||
chr7:5940939 | AATAATTA others(5): Show |
A | 3 | a0001c0001t0006g0013a0001c0010t0004g0056a0001c0010t0004g0057 | 3 | HG00735.hp2 HG01069.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.1759-2122_1759-211 others(16): Show |
RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 15/20 | chr7 | 5940939 | ||||||
chr7:5940942 | A | T | 9 | a0004c0005t0001g0043a0005c0003t0001g0024a0005c0003t0001g0025others(6): Show | 9 | HG00099.hp2 HG00621.hp1 HG01515.hp2 others(6): Show |
intron_variant | MODIFIER | c.1759-2113T>A | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 15/20 | chr7 | 5940942 | ||||||
chr7:5940942 | AATT | A | 3 | a0001c0008t0002g0052a0004c0005t0001g0055a0011c0015t0001g0029 | 3 | HG01261.hp1 HG02717.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.1759-2116_1759-211 others(7): Show |
RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 15/20 | chr7 | 5940942 | ||||||
chr7:5940942 | AATTATT | A | 5 | a0001c0001t0001g0023a0001c0001t0001g0032a0001c0009t0001g0012others(2): Show | 5 | HG00639.hp1 HG02056.hp2 HG03834.hp1 others(2): Show |
intron_variant | MODIFIER | c.1759-2119_1759-211 others(10): Show |
RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 15/20 | chr7 | 5940942 | ||||||
chr7:5940942 | AATTATTA others(2): Show |
A | 13 | a0002c0002t0002g0018a0002c0002t0002g0038a0002c0002t0002g0040others(10): Show | 13 | HG00280.hp1 HG00639.hp2 HG00741.hp1 others(10): Show |
intron_variant | MODIFIER | c.1759-2122_1759-211 others(13): Show |
RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 15/20 | chr7 | 5940942 | ||||||
chr7:5940945 | T | A | 2 | a0004c0005t0005g0033a0004c0018t0001g0014 | 2 | HG02976.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.1759-2116A>T | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 15/20 | chr7 | 5940945 | ||||||
chr7:5940948 | T | A | 1 | a0004c0018t0001g0014 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1759-2119A>T | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 15/20 | chr7 | 5940948 | ||||||
chr7:5941075 | A | G | 43 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(40): Show | 43 | HG00099.hp1 HG00280.hp1 HG00621.hp2 others(40): Show |
intron_variant | MODIFIER | c.1759-2246T>C | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 15/20 | chr7 | 5941075 | ||||||
chr7:5941226 | C | T | 1 | a0004c0011t0002g0039 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1758+2098G>A | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 15/20 | chr7 | 5941226 | ||||||
chr7:5941608 | G | A | 1 | a0010c0019t0001g0009 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.1758+1716C>T | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 15/20 | chr7 | 5941608 | ||||||
chr7:5941668 | C | T | 19 | a0001c0009t0001g0007a0002c0002t0001g0037a0002c0002t0002g0018others(16): Show | 19 | HG00280.hp1 HG00639.hp2 HG00735.hp1 others(16): Show |
intron_variant | MODIFIER | c.1758+1656G>A | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 15/20 | chr7 | 5941668 | ||||||
chr7:5941729 | C | T | 6 | a0001c0009t0001g0007a0006c0006t0001g0002a0006c0006t0001g0004others(3): Show | 6 | HG00639.hp2 HG00735.hp1 HG00741.hp1 others(3): Show |
intron_variant | MODIFIER | c.1758+1595G>A | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 15/20 | chr7 | 5941729 | ||||||
chr7:5941730 | G | A | 13 | a0002c0002t0001g0037a0002c0002t0002g0018a0002c0002t0002g0038others(10): Show | 13 | HG00280.hp1 HG01175.hp1 HG01175.hp2 others(10): Show |
intron_variant | MODIFIER | c.1758+1594C>T | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 15/20 | chr7 | 5941730 | ||||||
chr7:5941795 | T | C | 13 | a0002c0002t0001g0037a0002c0002t0002g0018a0002c0002t0002g0038others(10): Show | 13 | HG00280.hp1 HG01175.hp1 HG01175.hp2 others(10): Show |
intron_variant | MODIFIER | c.1758+1529A>G | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 15/20 | chr7 | 5941795 | ||||||
chr7:5941802 | A | G | 19 | a0001c0009t0001g0007a0002c0002t0001g0037a0002c0002t0002g0018others(16): Show | 19 | HG00280.hp1 HG00639.hp2 HG00735.hp1 others(16): Show |
intron_variant | MODIFIER | c.1758+1522T>C | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 15/20 | chr7 | 5941802 | ||||||
chr7:5941955 | C | T | 13 | a0002c0002t0001g0037a0002c0002t0002g0018a0002c0002t0002g0038others(10): Show | 13 | HG00280.hp1 HG01175.hp1 HG01175.hp2 others(10): Show |
intron_variant | MODIFIER | c.1758+1369G>A | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 15/20 | chr7 | 5941955 | ||||||
chr7:5941960 | C | T | 3 | a0001c0001t0006g0013a0001c0010t0004g0056a0001c0010t0004g0057 | 3 | HG00735.hp2 HG01069.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.1758+1364G>A | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 15/20 | chr7 | 5941960 | ||||||
chr7:5941978 | G | A | 6 | a0001c0009t0001g0007a0006c0006t0001g0002a0006c0006t0001g0004others(3): Show | 6 | HG00639.hp2 HG00735.hp1 HG00741.hp1 others(3): Show |
intron_variant | MODIFIER | c.1758+1346C>T | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 15/20 | chr7 | 5941978 | ||||||
chr7:5942013 | C | T | 1 | a0005c0003t0001g0024 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.1758+1311G>A | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 15/20 | chr7 | 5942013 | ||||||
chr7:5942061 | T | G | 1 | a0002c0002t0002g0018 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.1758+1263A>C | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 15/20 | chr7 | 5942061 | ||||||
chr7:5942129 | G | A | 19 | a0001c0009t0001g0007a0002c0002t0001g0037a0002c0002t0002g0018others(16): Show | 19 | HG00280.hp1 HG00639.hp2 HG00735.hp1 others(16): Show |
intron_variant | MODIFIER | c.1758+1195C>T | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 15/20 | chr7 | 5942129 | ||||||
chr7:5942560 | A | G | 23 | a0001c0001t0006g0013a0001c0009t0001g0007a0001c0010t0004g0056others(20): Show | 23 | HG00280.hp1 HG00639.hp2 HG00735.hp1 others(20): Show |
intron_variant | MODIFIER | c.1758+764T>C | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 15/20 | chr7 | 5942560 | ||||||
chr7:5942730 | C | T | 1 | a0001c0009t0001g0007 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1758+594G>A | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 15/20 | chr7 | 5942730 | ||||||
chr7:5942824 | T | C | 3 | a0001c0001t0006g0013a0001c0010t0004g0056a0001c0010t0004g0057 | 3 | HG00735.hp2 HG01069.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.1758+500A>G | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 15/20 | chr7 | 5942824 | ||||||
chr7:5942896 | T | TTATATAT others(15): Show |
1 | a0005c0003t0002g0010 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1758+427_1758+428i others(24): Show |
RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 15/20 | chr7 | 5942896 | ||||||
chr7:5942896 | T | TTATATAT others(17): Show |
1 | a0005c0003t0002g0011 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1758+427_1758+428i others(26): Show |
RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 15/20 | chr7 | 5942896 | ||||||
chr7:5942905 | T | C | 6 | a0001c0009t0001g0007a0006c0006t0001g0002a0006c0006t0001g0004others(3): Show | 6 | HG00639.hp2 HG00735.hp1 HG00741.hp1 others(3): Show |
intron_variant | MODIFIER | c.1758+419A>G | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 15/20 | chr7 | 5942905 | ||||||
chr7:5942910 | ATT | A | 6 | a0001c0009t0001g0007a0006c0006t0001g0002a0006c0006t0001g0004others(3): Show | 6 | HG00639.hp2 HG00735.hp1 HG00741.hp1 others(3): Show |
intron_variant | MODIFIER | c.1758+412_1758+413d others(4): Show |
RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 15/20 | chr7 | 5942910 | ||||||
chr7:5942912 | T | A | 12 | a0004c0005t0005g0033a0005c0003t0001g0024a0005c0003t0001g0025others(9): Show | 12 | HG00099.hp2 HG00621.hp1 HG01069.hp1 others(9): Show |
intron_variant | MODIFIER | c.1758+412A>T | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 15/20 | chr7 | 5942912 | ||||||
chr7:5942912 | TTA | T | 2 | a0001c0001t0001g0032a0004c0018t0001g0014 | 2 | HG03453.hp2 NA18971.hp2 |
intron_variant | MODIFIER | c.1758+410_1758+411d others(4): Show |
RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 15/20 | chr7 | 5942912 | ||||||
chr7:5942926 | A | T | 2 | a0005c0003t0001g0024a0005c0003t0001g0025 | 2 | HG00621.hp1 HG02523.hp2 |
intron_variant | MODIFIER | c.1758+398T>A | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 15/20 | chr7 | 5942926 | ||||||
chr7:5942926 | ATT | A | 27 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(24): Show | 27 | HG00280.hp1 HG00621.hp2 HG00639.hp1 others(24): Show |
intron_variant | MODIFIER | c.1758+396_1758+397d others(4): Show |
RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 15/20 | chr7 | 5942926 | ||||||
chr7:5942928 | T | A | 19 | a0001c0001t0001g0019a0001c0009t0001g0007a0001c0009t0001g0012others(16): Show | 19 | HG00099.hp1 HG00639.hp2 HG00735.hp1 others(16): Show |
intron_variant | MODIFIER | c.1758+396A>T | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 15/20 | chr7 | 5942928 | ||||||
chr7:5942929 | T | A | 1 | a0010c0019t0001g0009 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.1758+395A>T | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 15/20 | chr7 | 5942929 | ||||||
chr7:5942930 | T | A | 6 | a0001c0009t0001g0007a0006c0006t0001g0002a0006c0006t0001g0004others(3): Show | 6 | HG00639.hp2 HG00735.hp1 HG00741.hp1 others(3): Show |
intron_variant | MODIFIER | c.1758+394A>T | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 15/20 | chr7 | 5942930 | ||||||
chr7:5943013 | A | G | 23 | a0001c0001t0006g0013a0001c0009t0001g0007a0001c0010t0004g0056others(20): Show | 23 | HG00280.hp1 HG00639.hp2 HG00735.hp1 others(20): Show |
intron_variant | MODIFIER | c.1758+311T>C | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 15/20 | chr7 | 5943013 | ||||||
chr7:5943018 | G | A | 1 | a0004c0005t0005g0033 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1758+306C>T | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 15/20 | chr7 | 5943018 | ||||||
chr7:5943131 | G | A | 1 | a0001c0001t0001g0001 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.1758+193C>T | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 15/20 | chr7 | 5943131 | ||||||
chr7:5943208 | T | C | 1 | a0001c0001t0001g0034 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.1758+116A>G | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 15/20 | chr7 | 5943208 | ||||||
chr7:5943231 | T | A | 1 | a0001c0001t0001g0034 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.1758+93A>T | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 15/20 | chr7 | 5943231 | ||||||
chr7:5943554 | G | A | 2 | a0005c0003t0001g0024a0005c0003t0001g0025 | 2 | HG00621.hp1 HG02523.hp2 |
intron_variant | MODIFIER | c.1610-82C>T | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 14/20 | chr7 | 5943554 | ||||||
chr7:5943564 | C | A | 70 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(67): Show | 70 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(67): Show |
intron_variant | MODIFIER | c.1610-92G>T | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 14/20 | chr7 | 5943564 | ||||||
chr7:5943839 | G | A | 7 | a0001c0009t0001g0012a0001c0014t0001g0015a0004c0005t0001g0035others(4): Show | 7 | HG00099.hp1 HG02056.hp2 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.1609+72C>T | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 14/20 | chr7 | 5943839 | ||||||
chr7:5944035 | A | G | 6 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0016others(3): Show | 6 | HG00621.hp2 HG01981.hp1 HG02056.hp1 others(3): Show |
intron_variant | MODIFIER | c.1530-45T>C | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 13/20 | chr7 | 5944035 | ||||||
chr7:5944098 | T | C | 2 | a0005c0003t0001g0030a0005c0003t0001g0031 | 2 | HG00099.hp2 HG01515.hp2 |
intron_variant | MODIFIER | c.1530-108A>G | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 13/20 | chr7 | 5944098 | ||||||
chr7:5944355 | G | A | 1 | a0012c0012t0001g0036 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1530-365C>T | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 13/20 | chr7 | 5944355 | ||||||
chr7:5944480 | C | T | 7 | a0001c0009t0001g0012a0001c0014t0001g0015a0004c0005t0001g0035others(4): Show | 7 | HG00099.hp1 HG02056.hp2 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.1530-490G>A | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 13/20 | chr7 | 5944480 | ||||||
chr7:5944481 | A | G | 7 | a0001c0009t0001g0012a0001c0014t0001g0015a0004c0005t0001g0035others(4): Show | 7 | HG00099.hp1 HG02056.hp2 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.1530-491T>C | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 13/20 | chr7 | 5944481 | ||||||
chr7:5944527 | C | A | 5 | a0006c0006t0001g0002a0006c0006t0001g0004a0006c0006t0001g0008others(2): Show | 5 | HG00639.hp2 HG00735.hp1 HG00741.hp1 others(2): Show |
intron_variant | MODIFIER | c.1529+537G>T | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 13/20 | chr7 | 5944527 | ||||||
chr7:5944530 | C | T | 1 | a0006c0006t0001g0004 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1529+534G>A | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 13/20 | chr7 | 5944530 | ||||||
chr7:5944696 | C | T | 6 | a0001c0009t0001g0007a0006c0006t0001g0002a0006c0006t0001g0004others(3): Show | 6 | HG00639.hp2 HG00735.hp1 HG00741.hp1 others(3): Show |
intron_variant | MODIFIER | c.1529+368G>A | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 13/20 | chr7 | 5944696 | ||||||
chr7:5944804 | C | CAAAAAAA others(3): Show |
10 | a0001c0008t0002g0051a0001c0008t0002g0052a0001c0009t0001g0012others(7): Show | 10 | HG00099.hp1 HG02056.hp2 HG02145.hp2 others(7): Show |
intron_variant | MODIFIER | c.1529+259_1529+260i others(12): Show |
RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 13/20 | chr7 | 5944804 | ||||||
chr7:5944804 | C | CAAAAAAA others(4): Show |
1 | a0010c0019t0001g0009 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.1529+259_1529+260i others(13): Show |
RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 13/20 | chr7 | 5944804 | ||||||
chr7:5944835 | T | C | 24 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(21): Show | 24 | HG00099.hp1 HG00621.hp2 HG00639.hp1 others(21): Show |
intron_variant | MODIFIER | c.1529+229A>G | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 13/20 | chr7 | 5944835 | ||||||
chr7:5944863 | T | C | 24 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(21): Show | 24 | HG00099.hp1 HG00621.hp2 HG00639.hp1 others(21): Show |
intron_variant | MODIFIER | c.1529+201A>G | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 13/20 | chr7 | 5944863 | ||||||
chr7:5944949 | C | T | 8 | a0001c0009t0001g0012a0001c0014t0001g0015a0004c0005t0001g0035others(5): Show | 8 | HG00099.hp1 HG02056.hp2 HG02071.hp1 others(5): Show |
intron_variant | MODIFIER | c.1529+115G>A | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 13/20 | chr7 | 5944949 | ||||||
chr7:5945205 | C | G | 2 | a0001c0010t0004g0056a0001c0010t0004g0057 | 2 | HG00735.hp2 HG01069.hp2 |
intron_variant | MODIFIER | c.1415-27G>C | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 12/20 | chr7 | 5945205 | ||||||
chr7:5945235 | T | G | 1 | a0010c0019t0001g0009 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.1415-57A>C | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 12/20 | chr7 | 5945235 | ||||||
chr7:5945307 | C | T | 8 | a0001c0009t0001g0012a0001c0014t0001g0015a0004c0005t0001g0035others(5): Show | 8 | HG00099.hp1 HG02056.hp2 HG02071.hp1 others(5): Show |
intron_variant | MODIFIER | c.1415-129G>A | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 12/20 | chr7 | 5945307 | ||||||
chr7:5945369 | AG | A | 13 | a0002c0002t0001g0037a0002c0002t0002g0018a0002c0002t0002g0038others(10): Show | 13 | HG00280.hp1 HG01175.hp1 HG01175.hp2 others(10): Show |
intron_variant | MODIFIER | c.1415-192delC | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 12/20 | chr7 | 5945369 | ||||||
chr7:5945430 | C | A | 12 | a0002c0002t0001g0037a0002c0002t0002g0018a0002c0002t0002g0038others(9): Show | 12 | HG00280.hp1 HG01175.hp1 HG01175.hp2 others(9): Show |
intron_variant | MODIFIER | c.1415-252G>T | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 12/20 | chr7 | 5945430 | ||||||
chr7:5945486 | G | C | 1 | a0001c0009t0001g0012 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1415-308C>G | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 12/20 | chr7 | 5945486 | ||||||
chr7:5945567 | C | T | 12 | a0001c0008t0002g0051a0001c0008t0002g0052a0001c0009t0001g0012others(9): Show | 12 | HG00099.hp1 HG02056.hp2 HG02071.hp1 others(9): Show |
intron_variant | MODIFIER | c.1415-389G>A | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 12/20 | chr7 | 5945567 | ||||||
chr7:5945618 | C | CA | 12 | a0002c0002t0001g0037a0002c0002t0002g0018a0002c0002t0002g0038others(9): Show | 12 | HG00280.hp1 HG01175.hp2 HG01517.hp2 others(9): Show |
intron_variant | MODIFIER | c.1415-441dupT | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 12/20 | chr7 | 5945618 | ||||||
chr7:5945705 | T | C | 1 | a0003c0004t0003g0067 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.1415-527A>G | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 12/20 | chr7 | 5945705 | ||||||
chr7:5945828 | G | C | 23 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(20): Show | 23 | HG00099.hp1 HG00621.hp2 HG00639.hp1 others(20): Show |
intron_variant | MODIFIER | c.1415-650C>G | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 12/20 | chr7 | 5945828 | ||||||
chr7:5945843 | TTG | T | 3 | a0001c0001t0006g0013a0001c0010t0004g0056a0001c0010t0004g0057 | 3 | HG00735.hp2 HG01069.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.1415-667_1415-666d others(4): Show |
RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 12/20 | chr7 | 5945843 | ||||||
chr7:5945849 | A | ACTTCCT | 3 | a0001c0001t0006g0013a0001c0010t0004g0056a0001c0010t0004g0057 | 3 | HG00735.hp2 HG01069.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.1415-672_1415-671i others(8): Show |
RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 12/20 | chr7 | 5945849 | ||||||
chr7:5945851 | T | A | 3 | a0001c0001t0006g0013a0001c0010t0004g0056a0001c0010t0004g0057 | 3 | HG00735.hp2 HG01069.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.1415-673A>T | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 12/20 | chr7 | 5945851 | ||||||
chr7:5945853 | G | T | 3 | a0001c0001t0006g0013a0001c0010t0004g0056a0001c0010t0004g0057 | 3 | HG00735.hp2 HG01069.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.1415-675C>A | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 12/20 | chr7 | 5945853 | ||||||
chr7:5945855 | T | G | 3 | a0001c0001t0006g0013a0001c0010t0004g0056a0001c0010t0004g0057 | 3 | HG00735.hp2 HG01069.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.1415-677A>C | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 12/20 | chr7 | 5945855 | ||||||
chr7:5945951 | G | GT | 8 | a0001c0001t0001g0053a0001c0008t0002g0051a0001c0008t0002g0052others(5): Show | 8 | HG00621.hp2 HG01175.hp2 HG01934.hp1 others(5): Show |
intron_variant | MODIFIER | c.1415-774dupA | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 12/20 | chr7 | 5945951 | ||||||
chr7:5945956 | T | G | 7 | a0001c0009t0001g0012a0001c0014t0001g0015a0004c0005t0001g0035others(4): Show | 7 | HG00099.hp1 HG02056.hp2 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.1415-778A>C | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 12/20 | chr7 | 5945956 | ||||||
chr7:5945957 | T | G | 6 | a0001c0009t0001g0007a0006c0006t0001g0002a0006c0006t0001g0004others(3): Show | 6 | HG00639.hp2 HG00735.hp1 HG00741.hp1 others(3): Show |
intron_variant | MODIFIER | c.1415-779A>C | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 12/20 | chr7 | 5945957 | ||||||
chr7:5946037 | C | T | 1 | a0004c0011t0002g0039 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1415-859G>A | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 12/20 | chr7 | 5946037 | ||||||
chr7:5946043 | G | A | 5 | a0006c0006t0001g0002a0006c0006t0001g0004a0006c0006t0001g0008others(2): Show | 5 | HG00639.hp2 HG00735.hp1 HG00741.hp1 others(2): Show |
intron_variant | MODIFIER | c.1415-865C>T | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 12/20 | chr7 | 5946043 | ||||||
chr7:5946101 | A | G | 4 | a0001c0008t0002g0051a0001c0008t0002g0052a0007c0007t0002g0003others(1): Show | 4 | HG02258.hp1 HG02717.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.1415-923T>C | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 12/20 | chr7 | 5946101 | ||||||
chr7:5946129 | T | C | 1 | a0004c0005t0005g0033 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1415-951A>G | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 12/20 | chr7 | 5946129 | ||||||
chr7:5946141 | C | T | 3 | a0001c0001t0006g0013a0001c0010t0004g0056a0001c0010t0004g0057 | 3 | HG00735.hp2 HG01069.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.1415-963G>A | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 12/20 | chr7 | 5946141 | ||||||
chr7:5946203 | G | T | 4 | a0001c0008t0002g0051a0001c0008t0002g0052a0007c0007t0002g0003others(1): Show | 4 | HG02258.hp1 HG02717.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.1415-1025C>A | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 12/20 | chr7 | 5946203 | ||||||
chr7:5946439 | C | A | 8 | a0001c0009t0001g0012a0001c0014t0001g0015a0004c0005t0001g0035others(5): Show | 8 | HG00099.hp1 HG02056.hp2 HG02071.hp1 others(5): Show |
intron_variant | MODIFIER | c.1415-1261G>T | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 12/20 | chr7 | 5946439 | ||||||
chr7:5946837 | T | C | 47 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(44): Show | 47 | HG00099.hp1 HG00280.hp1 HG00621.hp2 others(44): Show |
intron_variant | MODIFIER | c.1414+1383A>G | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 12/20 | chr7 | 5946837 | ||||||
chr7:5947067 | G | A | 1 | a0001c0001t0006g0013 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.1414+1153C>T | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 12/20 | chr7 | 5947067 | ||||||
chr7:5947101 | A | G | 4 | a0001c0001t0006g0013a0001c0010t0004g0056a0001c0010t0004g0057others(1): Show | 4 | HG00735.hp2 HG01069.hp2 HG01071.hp2 others(1): Show |
intron_variant | MODIFIER | c.1414+1119T>C | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 12/20 | chr7 | 5947101 | ||||||
chr7:5947155 | T | C | 12 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(9): Show | 12 | HG00621.hp2 HG00639.hp1 HG01981.hp1 others(9): Show |
intron_variant | MODIFIER | c.1414+1065A>G | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 12/20 | chr7 | 5947155 | ||||||
chr7:5947516 | C | T | 13 | a0002c0002t0001g0037a0002c0002t0002g0018a0002c0002t0002g0038others(10): Show | 13 | HG00280.hp1 HG01175.hp1 HG01175.hp2 others(10): Show |
intron_variant | MODIFIER | c.1414+704G>A | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 12/20 | chr7 | 5947516 | ||||||
chr7:5947525 | C | A | 1 | a0001c0009t0001g0007 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1414+695G>T | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 12/20 | chr7 | 5947525 | ||||||
chr7:5947599 | T | C | 40 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(37): Show | 40 | HG00280.hp1 HG00621.hp2 HG00639.hp1 others(37): Show |
intron_variant | MODIFIER | c.1414+621A>G | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 12/20 | chr7 | 5947599 | ||||||
chr7:5947646 | C | G | 28 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(25): Show | 28 | HG00099.hp2 HG00621.hp1 HG00621.hp2 others(25): Show |
intron_variant | MODIFIER | c.1414+574G>C | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 12/20 | chr7 | 5947646 | ||||||
chr7:5947667 | A | T | 5 | a0006c0006t0001g0002a0006c0006t0001g0004a0006c0006t0001g0008others(2): Show | 5 | HG00639.hp2 HG00735.hp1 HG00741.hp1 others(2): Show |
intron_variant | MODIFIER | c.1414+553T>A | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 12/20 | chr7 | 5947667 | ||||||
chr7:5947729 | C | T | 1 | a0010c0019t0001g0009 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.1414+491G>A | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 12/20 | chr7 | 5947729 | ||||||
chr7:5947860 | T | TTGTGTGT others(9): Show |
1 | a0002c0002t0002g0045 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1414+344_1414+359d others(18): Show |
RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 12/20 | chr7 | 5947860 | ||||||
chr7:5947860 | T | TTGTGTGT others(13): Show |
5 | a0002c0002t0002g0044a0002c0002t0002g0047a0002c0002t0002g0049others(2): Show | 5 | HG00280.hp1 HG01175.hp1 HG01517.hp2 others(2): Show |
intron_variant | MODIFIER | c.1414+340_1414+359d others(22): Show |
RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 12/20 | chr7 | 5947860 | ||||||
chr7:5947860 | T | TTGTGTGT others(15): Show |
5 | a0002c0002t0001g0037a0002c0002t0002g0018a0002c0002t0002g0038others(2): Show | 5 | HG01934.hp1 HG02622.hp2 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.1414+338_1414+359d others(24): Show |
RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 12/20 | chr7 | 5947860 | ||||||
chr7:5947860 | T | TTGTGTGT others(17): Show |
2 | a0002c0002t0002g0040a0004c0011t0002g0039 | 2 | HG01175.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.1414+336_1414+359d others(26): Show |
RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 12/20 | chr7 | 5947860 | ||||||
chr7:5947860 | TTG | T | 9 | a0001c0001t0006g0013a0001c0010t0004g0056a0001c0010t0004g0057others(6): Show | 9 | HG00099.hp1 HG00735.hp2 HG01069.hp2 others(6): Show |
intron_variant | MODIFIER | c.1414+358_1414+359d others(4): Show |
RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 12/20 | chr7 | 5947860 | ||||||
chr7:5947860 | TTGTG | T | 2 | a0001c0009t0001g0012a0004c0018t0001g0014 | 2 | HG03453.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.1414+356_1414+359d others(6): Show |
RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 12/20 | chr7 | 5947860 | ||||||
chr7:5947860 | TTGTGTGT others(7): Show |
T | 5 | a0006c0006t0001g0002a0006c0006t0001g0004a0006c0006t0001g0008others(2): Show | 5 | HG00639.hp2 HG00735.hp1 HG00741.hp1 others(2): Show |
intron_variant | MODIFIER | c.1414+346_1414+359d others(16): Show |
RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 12/20 | chr7 | 5947860 | ||||||
chr7:5947888 | G | C | 2 | a0001c0001t0001g0006a0001c0001t0001g0023 | 2 | HG00639.hp1 NA18971.hp1 |
intron_variant | MODIFIER | c.1414+332C>G | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 12/20 | chr7 | 5947888 | ||||||
chr7:5947891 | T | TGTGTGTG others(5): Show |
2 | a0007c0007t0002g0003a0007c0007t0002g0020 | 2 | HG02258.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1414+328_1414+329i others(14): Show |
RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 12/20 | chr7 | 5947891 | ||||||
chr7:5947891 | T | TGTGTGTG others(7): Show |
3 | a0001c0008t0002g0051a0001c0008t0002g0052a0010c0019t0001g0009 | 3 | HG02071.hp1 HG02717.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.1414+328_1414+329i others(16): Show |
RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 12/20 | chr7 | 5947891 | ||||||
chr7:5947891 | T | TGTGTGTG others(9): Show |
9 | a0005c0003t0001g0024a0005c0003t0001g0025a0005c0003t0001g0027others(6): Show | 9 | HG00099.hp2 HG00621.hp1 HG01069.hp1 others(6): Show |
intron_variant | MODIFIER | c.1414+328_1414+329i others(18): Show |
RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 12/20 | chr7 | 5947891 | ||||||
chr7:5947891 | T | TGTGTGTG others(13): Show |
2 | a0005c0003t0002g0010a0005c0003t0002g0011 | 2 | HG02258.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.1414+328_1414+329i others(22): Show |
RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 12/20 | chr7 | 5947891 | ||||||
chr7:5948019 | G | A | 4 | a0001c0001t0006g0013a0001c0010t0004g0056a0001c0010t0004g0057others(1): Show | 4 | HG00735.hp2 HG01069.hp2 HG01071.hp2 others(1): Show |
intron_variant | MODIFIER | c.1414+201C>T | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 12/20 | chr7 | 5948019 | ||||||
chr7:5948039 | T | C | 13 | a0002c0002t0001g0037a0002c0002t0002g0018a0002c0002t0002g0038others(10): Show | 13 | HG00280.hp1 HG01175.hp1 HG01175.hp2 others(10): Show |
intron_variant | MODIFIER | c.1414+181A>G | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 12/20 | chr7 | 5948039 | ||||||
chr7:5948068 | T | A | 4 | a0001c0008t0002g0051a0001c0008t0002g0052a0007c0007t0002g0003others(1): Show | 4 | HG02258.hp1 HG02717.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.1414+152A>T | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 12/20 | chr7 | 5948068 | ||||||
chr7:5948115 | G | A | 1 | a0001c0009t0001g0007 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1414+105C>T | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 12/20 | chr7 | 5948115 | ||||||
chr7:5948451 | A | G | 33 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(30): Show | 33 | HG00099.hp2 HG00621.hp1 HG00621.hp2 others(30): Show |
intron_variant | MODIFIER | c.1225-42T>C | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 11/20 | chr7 | 5948451 | ||||||
chr7:5948540 | C | T | 11 | a0005c0003t0001g0024a0005c0003t0001g0025a0005c0003t0001g0027others(8): Show | 11 | HG00099.hp2 HG00621.hp1 HG01069.hp1 others(8): Show |
intron_variant | MODIFIER | c.1225-131G>A | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 11/20 | chr7 | 5948540 | ||||||
chr7:5948674 | C | T | 45 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(42): Show | 45 | HG00099.hp2 HG00280.hp1 HG00621.hp1 others(42): Show |
intron_variant | MODIFIER | c.1225-265G>A | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 11/20 | chr7 | 5948674 | ||||||
chr7:5948775 | A | G | 28 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(25): Show | 28 | HG00099.hp2 HG00621.hp1 HG00621.hp2 others(25): Show |
intron_variant | MODIFIER | c.1225-366T>C | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 11/20 | chr7 | 5948775 | ||||||
chr7:5948877 | A | T | 1 | a0004c0005t0005g0033 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1225-468T>A | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 11/20 | chr7 | 5948877 | ||||||
chr7:5948886 | T | C | 32 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(29): Show | 32 | HG00099.hp2 HG00621.hp1 HG00621.hp2 others(29): Show |
intron_variant | MODIFIER | c.1225-477A>G | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 11/20 | chr7 | 5948886 | ||||||
chr7:5949126 | G | A | 6 | a0001c0009t0001g0007a0006c0006t0001g0002a0006c0006t0001g0004others(3): Show | 6 | HG00639.hp2 HG00735.hp1 HG00741.hp1 others(3): Show |
intron_variant | MODIFIER | c.1225-717C>T | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 11/20 | chr7 | 5949126 | ||||||
chr7:5949129 | G | T | 19 | a0001c0009t0001g0007a0002c0002t0001g0037a0002c0002t0002g0018others(16): Show | 19 | HG00280.hp1 HG00639.hp2 HG00735.hp1 others(16): Show |
intron_variant | MODIFIER | c.1225-720C>A | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 11/20 | chr7 | 5949129 | ||||||
chr7:5949136 | G | A | 3 | a0001c0001t0006g0013a0001c0010t0004g0056a0001c0010t0004g0057 | 3 | HG00735.hp2 HG01069.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.1225-727C>T | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 11/20 | chr7 | 5949136 | ||||||
chr7:5949256 | C | A | 1 | a0004c0018t0001g0014 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1225-847G>T | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 11/20 | chr7 | 5949256 | ||||||
chr7:5949605 | C | A | 1 | a0004c0018t0001g0014 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1225-1196G>T | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 11/20 | chr7 | 5949605 | ||||||
chr7:5949777 | C | T | 11 | a0005c0003t0001g0024a0005c0003t0001g0025a0005c0003t0001g0027others(8): Show | 11 | HG00099.hp2 HG00621.hp1 HG01069.hp1 others(8): Show |
intron_variant | MODIFIER | c.1225-1368G>A | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 11/20 | chr7 | 5949777 | ||||||
chr7:5949862 | T | C | 4 | a0001c0008t0002g0051a0001c0008t0002g0052a0007c0007t0002g0003others(1): Show | 4 | HG02258.hp1 HG02717.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.1224+1433A>G | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 11/20 | chr7 | 5949862 | ||||||
chr7:5949921 | C | T | 19 | a0001c0009t0001g0007a0002c0002t0001g0037a0002c0002t0002g0018others(16): Show | 19 | HG00280.hp1 HG00639.hp2 HG00735.hp1 others(16): Show |
intron_variant | MODIFIER | c.1224+1374G>A | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 11/20 | chr7 | 5949921 | ||||||
chr7:5949923 | T | G | 59 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(56): Show | 59 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(56): Show |
intron_variant | MODIFIER | c.1224+1372A>C | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 11/20 | chr7 | 5949923 | ||||||
chr7:5949994 | C | A | 51 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(48): Show | 51 | HG00099.hp2 HG00280.hp1 HG00621.hp1 others(48): Show |
intron_variant | MODIFIER | c.1224+1301G>T | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 11/20 | chr7 | 5949994 | ||||||
chr7:5949997 | G | GA | 17 | a0001c0009t0001g0007a0002c0002t0001g0037a0002c0002t0002g0018others(14): Show | 17 | HG00280.hp1 HG00639.hp2 HG00741.hp1 others(14): Show |
intron_variant | MODIFIER | c.1224+1297dupT | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 11/20 | chr7 | 5949997 | ||||||
chr7:5949997 | GA | G | 8 | a0001c0001t0006g0013a0001c0008t0002g0051a0001c0008t0002g0052others(5): Show | 8 | HG00735.hp2 HG01069.hp2 HG01071.hp2 others(5): Show |
intron_variant | MODIFIER | c.1224+1297delT | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 11/20 | chr7 | 5949997 | ||||||
chr7:5950010 | AC | A | 21 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(18): Show | 21 | HG00099.hp2 HG00621.hp1 HG00621.hp2 others(18): Show |
intron_variant | MODIFIER | c.1224+1284delG | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 11/20 | chr7 | 5950010 | ||||||
chr7:5950011 | C | A | 1 | a0005c0003t0004g0061 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1224+1284G>T | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 11/20 | chr7 | 5950011 | ||||||
chr7:5950330 | G | T | 11 | a0005c0003t0001g0024a0005c0003t0001g0025a0005c0003t0001g0027others(8): Show | 11 | HG00099.hp2 HG00621.hp1 HG01069.hp1 others(8): Show |
intron_variant | MODIFIER | c.1224+965C>A | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 11/20 | chr7 | 5950330 | ||||||
chr7:5950425 | G | C | 1 | a0002c0002t0001g0037 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1224+870C>G | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 11/20 | chr7 | 5950425 | ||||||
chr7:5950496 | G | A | 1 | a0004c0011t0002g0046 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1224+799C>T | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 11/20 | chr7 | 5950496 | ||||||
chr7:5950526 | G | A | 1 | a0004c0005t0005g0033 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1224+769C>T | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 11/20 | chr7 | 5950526 | ||||||
chr7:5950555 | A | G | 16 | a0001c0008t0002g0051a0001c0008t0002g0052a0005c0003t0001g0024others(13): Show | 16 | HG00099.hp2 HG00621.hp1 HG01069.hp1 others(13): Show |
intron_variant | MODIFIER | c.1224+740T>C | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 11/20 | chr7 | 5950555 | ||||||
chr7:5950569 | C | CA | 33 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(30): Show | 33 | HG00280.hp1 HG00621.hp2 HG00639.hp1 others(30): Show |
intron_variant | MODIFIER | c.1224+725dupT | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 11/20 | chr7 | 5950569 | ||||||
chr7:5950734 | C | A | 4 | a0001c0001t0006g0013a0001c0010t0004g0056a0001c0010t0004g0057others(1): Show | 4 | HG00735.hp2 HG01069.hp2 HG01071.hp2 others(1): Show |
intron_variant | MODIFIER | c.1224+561G>T | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 11/20 | chr7 | 5950734 | ||||||
chr7:5950878 | A | C | 2 | a0001c0010t0004g0056a0001c0010t0004g0057 | 2 | HG00735.hp2 HG01069.hp2 |
intron_variant | MODIFIER | c.1224+417T>G | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 11/20 | chr7 | 5950878 | ||||||
chr7:5950896 | A | G | 4 | a0001c0001t0006g0013a0001c0010t0004g0056a0001c0010t0004g0057others(1): Show | 4 | HG00735.hp2 HG01069.hp2 HG01071.hp2 others(1): Show |
intron_variant | MODIFIER | c.1224+399T>C | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 11/20 | chr7 | 5950896 | ||||||
chr7:5950899 | C | T | 4 | a0001c0001t0006g0013a0001c0010t0004g0056a0001c0010t0004g0057others(1): Show | 4 | HG00735.hp2 HG01069.hp2 HG01071.hp2 others(1): Show |
intron_variant | MODIFIER | c.1224+396G>A | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 11/20 | chr7 | 5950899 | ||||||
chr7:5950900 | A | C | 4 | a0001c0001t0006g0013a0001c0010t0004g0056a0001c0010t0004g0057others(1): Show | 4 | HG00735.hp2 HG01069.hp2 HG01071.hp2 others(1): Show |
intron_variant | MODIFIER | c.1224+395T>G | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 11/20 | chr7 | 5950900 | ||||||
chr7:5951153 | T | G | 1 | a0002c0002t0003g0060 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.1224+142A>C | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 11/20 | chr7 | 5951153 | ||||||
chr7:5951257 | T | C | 50 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(47): Show | 50 | HG00099.hp2 HG00280.hp1 HG00621.hp1 others(47): Show |
intron_variant | MODIFIER | c.1224+38A>G | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 11/20 | chr7 | 5951257 | ||||||
chr7:5951470 | GT | G | 8 | a0001c0009t0001g0007a0004c0018t0001g0014a0006c0006t0001g0002others(5): Show | 8 | HG00639.hp2 HG00735.hp1 HG00741.hp1 others(5): Show |
intron_variant | MODIFIER | c.1103-55delA | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 10/20 | chr7 | 5951470 | ||||||
chr7:5951470 | GTT | G | 12 | a0002c0002t0001g0037a0002c0002t0002g0018a0002c0002t0002g0038others(9): Show | 12 | HG00280.hp1 HG01175.hp2 HG01517.hp2 others(9): Show |
intron_variant | MODIFIER | c.1103-56_1103-55del others(2): Show |
RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 10/20 | chr7 | 5951470 | ||||||
chr7:5951474 | T | G | 1 | a0004c0018t0001g0014 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1103-58A>C | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 10/20 | chr7 | 5951474 | ||||||
chr7:5951633 | T | G | 14 | a0001c0001t0001g0019a0002c0002t0001g0037a0002c0002t0002g0018others(11): Show | 14 | HG00280.hp1 HG01175.hp1 HG01175.hp2 others(11): Show |
intron_variant | MODIFIER | c.1103-217A>C | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 10/20 | chr7 | 5951633 | ||||||
chr7:5951740 | G | A | 2 | a0001c0010t0004g0056a0001c0010t0004g0057 | 2 | HG00735.hp2 HG01069.hp2 |
intron_variant | MODIFIER | c.1103-324C>T | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 10/20 | chr7 | 5951740 | ||||||
chr7:5952001 | T | C | 4 | a0001c0008t0002g0051a0001c0008t0002g0052a0007c0007t0002g0003others(1): Show | 4 | HG02258.hp1 HG02717.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.1103-585A>G | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 10/20 | chr7 | 5952001 | ||||||
chr7:5952235 | T | C | 48 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(45): Show | 48 | HG00099.hp2 HG00280.hp1 HG00621.hp1 others(45): Show |
intron_variant | MODIFIER | c.1103-819A>G | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 10/20 | chr7 | 5952235 | ||||||
chr7:5952244 | A | G | 39 | a0001c0009t0001g0007a0001c0009t0001g0012a0001c0014t0001g0015others(36): Show | 39 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(36): Show |
intron_variant | MODIFIER | c.1103-828T>C | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 10/20 | chr7 | 5952244 | ||||||
chr7:5952352 | A | C | 29 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(26): Show | 29 | HG00280.hp1 HG00621.hp2 HG00639.hp1 others(26): Show |
intron_variant | MODIFIER | c.1102+723T>G | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 10/20 | chr7 | 5952352 | ||||||
chr7:5952356 | G | A | 13 | a0002c0002t0001g0037a0002c0002t0002g0018a0002c0002t0002g0038others(10): Show | 13 | HG00280.hp1 HG01175.hp1 HG01175.hp2 others(10): Show |
intron_variant | MODIFIER | c.1102+719C>T | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 10/20 | chr7 | 5952356 | ||||||
chr7:5952384 | G | A | 1 | a0002c0002t0002g0018 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.1102+691C>T | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 10/20 | chr7 | 5952384 | ||||||
chr7:5952493 | G | A | 1 | a0003c0004t0003g0067 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.1102+582C>T | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 10/20 | chr7 | 5952493 | ||||||
chr7:5952511 | C | A | 6 | a0001c0009t0001g0007a0006c0006t0001g0002a0006c0006t0001g0004others(3): Show | 6 | HG00639.hp2 HG00735.hp1 HG00741.hp1 others(3): Show |
intron_variant | MODIFIER | c.1102+564G>T | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 10/20 | chr7 | 5952511 | ||||||
chr7:5952608 | G | A | 6 | a0001c0009t0001g0007a0006c0006t0001g0002a0006c0006t0001g0004others(3): Show | 6 | HG00639.hp2 HG00735.hp1 HG00741.hp1 others(3): Show |
intron_variant | MODIFIER | c.1102+467C>T | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 10/20 | chr7 | 5952608 | ||||||
chr7:5952729 | C | CT | 19 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(16): Show | 19 | HG00621.hp2 HG00639.hp1 HG00639.hp2 others(16): Show |
intron_variant | MODIFIER | c.1102+345dupA | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 10/20 | chr7 | 5952729 | ||||||
chr7:5952758 | C | G | 51 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(48): Show | 51 | HG00099.hp2 HG00280.hp1 HG00621.hp1 others(48): Show |
intron_variant | MODIFIER | c.1102+317G>C | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 10/20 | chr7 | 5952758 | ||||||
chr7:5952778 | T | G | 38 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(35): Show | 38 | HG00099.hp2 HG00621.hp1 HG00621.hp2 others(35): Show |
intron_variant | MODIFIER | c.1102+297A>C | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 10/20 | chr7 | 5952778 | ||||||
chr7:5952862 | C | T | 2 | a0002c0002t0002g0044a0002c0002t0002g0047 | 2 | HG00280.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.1102+213G>A | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 10/20 | chr7 | 5952862 | ||||||
chr7:5952864 | T | C | 13 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(10): Show | 13 | HG00621.hp2 HG00639.hp1 HG01981.hp1 others(10): Show |
intron_variant | MODIFIER | c.1102+211A>G | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 10/20 | chr7 | 5952864 | ||||||
chr7:5952884 | C | T | 2 | a0001c0010t0004g0056a0001c0010t0004g0057 | 2 | HG00735.hp2 HG01069.hp2 |
intron_variant | MODIFIER | c.1102+191G>A | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 10/20 | chr7 | 5952884 | ||||||
chr7:5952888 | T | C | 31 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(28): Show | 31 | HG00099.hp2 HG00621.hp1 HG00621.hp2 others(28): Show |
intron_variant | MODIFIER | c.1102+187A>G | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 10/20 | chr7 | 5952888 | ||||||
chr7:5952935 | T | A | 15 | a0001c0001t0006g0013a0001c0010t0004g0056a0001c0010t0004g0057others(12): Show | 15 | HG00099.hp2 HG00621.hp1 HG00735.hp2 others(12): Show |
intron_variant | MODIFIER | c.1102+140A>T | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 10/20 | chr7 | 5952935 | ||||||
chr7:5953041 | A | G | 20 | a0001c0009t0001g0007a0002c0002t0001g0037a0002c0002t0002g0018others(17): Show | 20 | HG00280.hp1 HG00639.hp2 HG00735.hp1 others(17): Show |
intron_variant | MODIFIER | c.1102+34T>C | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 10/20 | chr7 | 5953041 | ||||||
chr7:5953276 | T | G | 12 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(9): Show | 12 | HG00621.hp2 HG00639.hp1 HG01981.hp1 others(9): Show |
intron_variant | MODIFIER | c.958-57A>C | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 9/20 | chr7 | 5953276 | ||||||
chr7:5953286 | G | T | 19 | a0001c0001t0006g0013a0001c0008t0002g0051a0001c0008t0002g0052others(16): Show | 19 | HG00099.hp2 HG00621.hp1 HG00735.hp2 others(16): Show |
intron_variant | MODIFIER | c.958-67C>A | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 9/20 | chr7 | 5953286 | ||||||
chr7:5953293 | A | G | 31 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(28): Show | 31 | HG00099.hp2 HG00621.hp1 HG00621.hp2 others(28): Show |
intron_variant | MODIFIER | c.958-74T>C | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 9/20 | chr7 | 5953293 | ||||||
chr7:5953395 | C | T | 4 | a0001c0008t0002g0051a0001c0008t0002g0052a0007c0007t0002g0003others(1): Show | 4 | HG02258.hp1 HG02717.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.958-176G>A | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 9/20 | chr7 | 5953395 | ||||||
chr7:5953558 | C | CA | 8 | a0001c0009t0001g0007a0001c0010t0004g0057a0004c0018t0001g0014others(5): Show | 8 | HG00639.hp2 HG00735.hp1 HG00735.hp2 others(5): Show |
intron_variant | MODIFIER | c.958-340dupT | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 9/20 | chr7 | 5953558 | ||||||
chr7:5953560 | A | G | 1 | a0002c0002t0002g0038 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.958-341T>C | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 9/20 | chr7 | 5953560 | ||||||
chr7:5953600 | A | G | 31 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(28): Show | 31 | HG00099.hp2 HG00621.hp1 HG00621.hp2 others(28): Show |
intron_variant | MODIFIER | c.958-381T>C | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 9/20 | chr7 | 5953600 | ||||||
chr7:5953651 | T | A | 2 | a0001c0010t0004g0056a0001c0010t0004g0057 | 2 | HG00735.hp2 HG01069.hp2 |
intron_variant | MODIFIER | c.958-432A>T | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 9/20 | chr7 | 5953651 | ||||||
chr7:5953912 | C | T | 1 | a0012c0012t0001g0036 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.958-693G>A | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 9/20 | chr7 | 5953912 | ||||||
chr7:5953968 | T | C | 31 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(28): Show | 31 | HG00099.hp2 HG00621.hp1 HG00621.hp2 others(28): Show |
intron_variant | MODIFIER | c.958-749A>G | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 9/20 | chr7 | 5953968 | ||||||
chr7:5954003 | A | C | 59 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(56): Show | 59 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(56): Show |
intron_variant | MODIFIER | c.958-784T>G | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 9/20 | chr7 | 5954003 | ||||||
chr7:5954034 | A | G | 8 | a0001c0009t0001g0007a0004c0018t0001g0014a0005c0003t0004g0061others(5): Show | 8 | HG00639.hp2 HG00735.hp1 HG00741.hp1 others(5): Show |
intron_variant | MODIFIER | c.958-815T>C | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 9/20 | chr7 | 5954034 | ||||||
chr7:5954143 | AT | A | 36 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(33): Show | 36 | HG00099.hp2 HG00621.hp1 HG00621.hp2 others(33): Show |
intron_variant | MODIFIER | c.958-925delA | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 9/20 | chr7 | 5954143 | ||||||
chr7:5954168 | C | A | 13 | a0002c0002t0001g0037a0002c0002t0002g0018a0002c0002t0002g0038others(10): Show | 13 | HG00280.hp1 HG01175.hp1 HG01175.hp2 others(10): Show |
intron_variant | MODIFIER | c.958-949G>T | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 9/20 | chr7 | 5954168 | ||||||
chr7:5954323 | G | C | 19 | a0001c0009t0001g0007a0002c0002t0001g0037a0002c0002t0002g0018others(16): Show | 19 | HG00280.hp1 HG00639.hp2 HG00735.hp1 others(16): Show |
intron_variant | MODIFIER | c.958-1104C>G | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 9/20 | chr7 | 5954323 | ||||||
chr7:5954873 | G | T | 1 | a0001c0001t0001g0005 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.957+1132C>A | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 9/20 | chr7 | 5954873 | ||||||
chr7:5954988 | T | TA | 8 | a0003c0004t0003g0058a0003c0004t0003g0062a0003c0004t0003g0063others(5): Show | 8 | HG00741.hp2 HG01261.hp2 HG01515.hp1 others(5): Show |
intron_variant | MODIFIER | c.957+1016dupT | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 9/20 | chr7 | 5954988 | ||||||
chr7:5954988 | T | TAAAAAAA others(3): Show |
2 | a0006c0006t0001g0002a0006c0006t0001g0017 | 2 | HG00639.hp2 HG01978.hp2 |
intron_variant | MODIFIER | c.957+1007_957+1016d others(12): Show |
RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 9/20 | chr7 | 5954988 | ||||||
chr7:5954988 | T | TAAAAAAA others(4): Show |
2 | a0001c0009t0001g0007a0006c0006t0001g0008 | 2 | HG00741.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.957+1006_957+1016d others(13): Show |
RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 9/20 | chr7 | 5954988 | ||||||
chr7:5954988 | T | TAAAAAAA others(5): Show |
1 | a0006c0006t0001g0004 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.957+1005_957+1016d others(14): Show |
RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 9/20 | chr7 | 5954988 | ||||||
chr7:5954988 | TA | T | 13 | a0002c0002t0001g0037a0002c0002t0002g0038a0002c0002t0002g0040others(10): Show | 13 | HG00280.hp1 HG01175.hp1 HG01175.hp2 others(10): Show |
intron_variant | MODIFIER | c.957+1016delT | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 9/20 | chr7 | 5954988 | ||||||
chr7:5954988 | TAAA | T | 6 | a0001c0001t0001g0005a0001c0001t0001g0016a0001c0010t0004g0057others(3): Show | 6 | HG00735.hp2 HG01515.hp2 HG02056.hp1 others(3): Show |
intron_variant | MODIFIER | c.957+1014_957+1016d others(5): Show |
RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 9/20 | chr7 | 5954988 | ||||||
chr7:5954988 | TAAAA | T | 18 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0019others(15): Show | 18 | HG00099.hp2 HG00621.hp2 HG00639.hp1 others(15): Show |
intron_variant | MODIFIER | c.957+1013_957+1016d others(6): Show |
RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 9/20 | chr7 | 5954988 | ||||||
chr7:5954988 | TAAAAA | T | 7 | a0001c0008t0002g0051a0001c0008t0002g0052a0005c0003t0001g0024others(4): Show | 7 | HG00621.hp1 HG02071.hp1 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.957+1012_957+1016d others(7): Show |
RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 9/20 | chr7 | 5954988 | ||||||
chr7:5955025 | C | T | 1 | a0001c0001t0001g0006 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.957+980G>A | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 9/20 | chr7 | 5955025 | ||||||
chr7:5955041 | T | C | 1 | a0001c0001t0001g0034 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.957+964A>G | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 9/20 | chr7 | 5955041 | ||||||
chr7:5955085 | C | T | 31 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(28): Show | 31 | HG00099.hp2 HG00621.hp1 HG00621.hp2 others(28): Show |
intron_variant | MODIFIER | c.957+920G>A | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 9/20 | chr7 | 5955085 | ||||||
chr7:5955113 | C | T | 24 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(21): Show | 24 | HG00099.hp2 HG00621.hp1 HG00621.hp2 others(21): Show |
intron_variant | MODIFIER | c.957+892G>A | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 9/20 | chr7 | 5955113 | ||||||
chr7:5955386 | A | G | 11 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(8): Show | 11 | HG00621.hp2 HG00639.hp1 HG01981.hp1 others(8): Show |
intron_variant | MODIFIER | c.957+619T>C | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 9/20 | chr7 | 5955386 | ||||||
chr7:5955474 | C | T | 23 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(20): Show | 23 | HG00099.hp2 HG00621.hp1 HG00621.hp2 others(20): Show |
intron_variant | MODIFIER | c.957+531G>A | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 9/20 | chr7 | 5955474 | ||||||
chr7:5955747 | TC | T | 13 | a0002c0002t0001g0037a0002c0002t0002g0018a0002c0002t0002g0038others(10): Show | 13 | HG00280.hp1 HG01175.hp1 HG01175.hp2 others(10): Show |
intron_variant | MODIFIER | c.957+257delG | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 9/20 | chr7 | 5955747 | ||||||
chr7:5955748 | CA | C | 6 | a0001c0008t0002g0051a0001c0008t0002g0052a0001c0010t0004g0056others(3): Show | 6 | HG00735.hp2 HG01069.hp2 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.957+256delT | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 9/20 | chr7 | 5955748 | ||||||
chr7:5955748 | CAA | C | 22 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(19): Show | 22 | HG00099.hp2 HG00621.hp1 HG00621.hp2 others(19): Show |
intron_variant | MODIFIER | c.957+255_957+256del others(2): Show |
RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 9/20 | chr7 | 5955748 | ||||||
chr7:5955749 | A | T | 13 | a0002c0002t0001g0037a0002c0002t0002g0018a0002c0002t0002g0038others(10): Show | 13 | HG00280.hp1 HG01175.hp1 HG01175.hp2 others(10): Show |
intron_variant | MODIFIER | c.957+256T>A | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 9/20 | chr7 | 5955749 | ||||||
chr7:5955964 | C | T | 11 | a0005c0003t0001g0024a0005c0003t0001g0025a0005c0003t0001g0027others(8): Show | 11 | HG00099.hp2 HG00621.hp1 HG01069.hp1 others(8): Show |
intron_variant | MODIFIER | c.957+41G>A | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 9/20 | chr7 | 5955964 | ||||||
chr7:5956466 | G | T | 70 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(67): Show | 70 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(67): Show |
intron_variant | MODIFIER | c.781-285C>A | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 8/20 | chr7 | 5956466 | ||||||
chr7:5956467 | A | T | 70 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(67): Show | 70 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(67): Show |
intron_variant | MODIFIER | c.781-286T>A | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 8/20 | chr7 | 5956467 | ||||||
chr7:5956473 | T | C | 70 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(67): Show | 70 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(67): Show |
intron_variant | MODIFIER | c.781-292A>G | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 8/20 | chr7 | 5956473 | ||||||
chr7:5956515 | C | T | 7 | a0001c0001t0006g0013a0001c0009t0001g0007a0006c0006t0001g0002others(4): Show | 7 | HG00639.hp2 HG00735.hp1 HG00741.hp1 others(4): Show |
intron_variant | MODIFIER | c.781-334G>A | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 8/20 | chr7 | 5956515 | ||||||
chr7:5956690 | T | C | 1 | a0004c0005t0001g0035 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.781-509A>G | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 8/20 | chr7 | 5956690 | ||||||
chr7:5956719 | C | A | 50 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(47): Show | 50 | HG00099.hp2 HG00280.hp1 HG00621.hp1 others(47): Show |
intron_variant | MODIFIER | c.781-538G>T | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 8/20 | chr7 | 5956719 | ||||||
chr7:5956720 | A | G | 50 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(47): Show | 50 | HG00099.hp2 HG00280.hp1 HG00621.hp1 others(47): Show |
intron_variant | MODIFIER | c.781-539T>C | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 8/20 | chr7 | 5956720 | ||||||
chr7:5956732 | C | G | 1 | a0004c0005t0001g0055 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.781-551G>C | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 8/20 | chr7 | 5956732 | ||||||
chr7:5956802 | C | T | 13 | a0002c0002t0001g0037a0002c0002t0002g0018a0002c0002t0002g0038others(10): Show | 13 | HG00280.hp1 HG01175.hp1 HG01175.hp2 others(10): Show |
intron_variant | MODIFIER | c.781-621G>A | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 8/20 | chr7 | 5956802 | ||||||
chr7:5956804 | A | G | 1 | a0004c0011t0002g0046 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.781-623T>C | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 8/20 | chr7 | 5956804 | ||||||
chr7:5957008 | T | TA | 27 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(24): Show | 27 | HG00099.hp2 HG00621.hp1 HG00621.hp2 others(24): Show |
intron_variant | MODIFIER | c.781-828dupT | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 8/20 | chr7 | 5957008 | ||||||
chr7:5957196 | G | A | 1 | a0001c0001t0001g0023 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.780+711C>T | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 8/20 | chr7 | 5957196 | ||||||
chr7:5957499 | A | C | 1 | a0010c0019t0001g0009 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.780+408T>G | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 8/20 | chr7 | 5957499 | ||||||
chr7:5957583 | C | G | 7 | a0001c0001t0006g0013a0001c0009t0001g0007a0006c0006t0001g0002others(4): Show | 7 | HG00639.hp2 HG00735.hp1 HG00741.hp1 others(4): Show |
intron_variant | MODIFIER | c.780+324G>C | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 8/20 | chr7 | 5957583 | ||||||
chr7:5957614 | C | T | 4 | a0001c0008t0002g0051a0001c0008t0002g0052a0007c0007t0002g0003others(1): Show | 4 | HG02258.hp1 HG02717.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.780+293G>A | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 8/20 | chr7 | 5957614 | ||||||
chr7:5957657 | G | A | 1 | a0004c0018t0001g0014 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.780+250C>T | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 8/20 | chr7 | 5957657 | ||||||
chr7:5957764 | C | T | 1 | a0004c0018t0001g0014 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.780+143G>A | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 8/20 | chr7 | 5957764 | ||||||
chr7:5957799 | CAAAACA | C | 21 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0016others(18): Show | 21 | HG00099.hp1 HG00621.hp2 HG00639.hp1 others(18): Show |
intron_variant | MODIFIER | c.780+102_780+107del others(6): Show |
RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 8/20 | chr7 | 5957799 | ||||||
chr7:5957810 | C | T | 7 | a0001c0009t0001g0012a0001c0014t0001g0015a0004c0005t0001g0035others(4): Show | 7 | HG00099.hp1 HG02056.hp2 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.780+97G>A | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 8/20 | chr7 | 5957810 | ||||||
chr7:5958344 | G | GAA | 5 | a0001c0008t0002g0051a0001c0008t0002g0052a0004c0005t0005g0033others(2): Show | 5 | HG02258.hp1 HG02717.hp2 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.660-319_660-318dup others(2): Show |
RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 7/20 | chr7 | 5958344 | ||||||
chr7:5958344 | GA | G | 12 | a0004c0018t0001g0014a0005c0003t0001g0024a0005c0003t0001g0025others(9): Show | 12 | HG00099.hp2 HG00621.hp1 HG01069.hp1 others(9): Show |
intron_variant | MODIFIER | c.660-318delT | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 7/20 | chr7 | 5958344 | ||||||
chr7:5958506 | G | A | 6 | a0001c0009t0001g0007a0006c0006t0001g0002a0006c0006t0001g0004others(3): Show | 6 | HG00639.hp2 HG00735.hp1 HG00741.hp1 others(3): Show |
intron_variant | MODIFIER | c.660-479C>T | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 7/20 | chr7 | 5958506 | ||||||
chr7:5958633 | G | A | 11 | a0005c0003t0001g0024a0005c0003t0001g0025a0005c0003t0001g0027others(8): Show | 11 | HG00099.hp2 HG00621.hp1 HG01069.hp1 others(8): Show |
intron_variant | MODIFIER | c.659+360C>T | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 7/20 | chr7 | 5958633 | ||||||
chr7:5958840 | C | T | 1 | a0004c0005t0005g0033 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.659+153G>A | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 7/20 | chr7 | 5958840 | ||||||
chr7:5958878 | G | C | 9 | a0005c0003t0001g0024a0005c0003t0001g0025a0005c0003t0001g0027others(6): Show | 9 | HG00099.hp2 HG00621.hp1 HG01069.hp1 others(6): Show |
intron_variant | MODIFIER | c.659+115C>G | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 7/20 | chr7 | 5958878 | ||||||
chr7:5958891 | G | A | 7 | a0001c0009t0001g0012a0001c0014t0001g0015a0004c0005t0001g0035others(4): Show | 7 | HG00099.hp1 HG02056.hp2 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.659+102C>T | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 7/20 | chr7 | 5958891 | ||||||
chr7:5958978 | G | A | 20 | a0001c0009t0001g0012a0001c0014t0001g0015a0002c0002t0001g0037others(17): Show | 20 | HG00099.hp1 HG00280.hp1 HG01175.hp1 others(17): Show |
intron_variant | MODIFIER | c.659+15C>T | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 7/20 | chr7 | 5958978 | ||||||
chr7:5959785 | C | T | 48 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(45): Show | 48 | HG00099.hp2 HG00280.hp1 HG00621.hp1 others(45): Show |
intron_variant | MODIFIER | c.574-707G>A | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 6/20 | chr7 | 5959785 | ||||||
chr7:5959796 | C | G | 2 | a0004c0005t0001g0041a0004c0005t0001g0042 | 2 | HG00099.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.574-718G>C | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 6/20 | chr7 | 5959796 | ||||||
chr7:5960044 | A | AAC | 5 | a0003c0004t0003g0058a0003c0004t0003g0059a0003c0004t0003g0062others(2): Show | 5 | HG00741.hp2 HG01261.hp2 HG01517.hp1 others(2): Show |
intron_variant | MODIFIER | c.573+645_573+646dup others(2): Show |
RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 6/20 | chr7 | 5960044 | ||||||
chr7:5960044 | AACACACA others(3): Show |
A | 1 | a0004c0018t0001g0014 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.573+637_573+646del others(10): Show |
RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 6/20 | chr7 | 5960044 | ||||||
chr7:5960064 | CACACACA others(8): Show |
C | 2 | a0006c0006t0001g0002a0006c0006t0001g0021 | 2 | HG00735.hp1 HG01978.hp2 |
intron_variant | MODIFIER | c.573+612_573+626del others(15): Show |
RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 6/20 | chr7 | 5960064 | ||||||
chr7:5960068 | CACACACA others(4): Show |
C | 16 | a0001c0008t0002g0051a0001c0008t0002g0052a0002c0002t0001g0037others(13): Show | 16 | HG00280.hp1 HG01175.hp1 HG01175.hp2 others(13): Show |
intron_variant | MODIFIER | c.573+612_573+622del others(11): Show |
RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 6/20 | chr7 | 5960068 | ||||||
chr7:5960070 | CACACACA others(2): Show |
C | 27 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(24): Show | 27 | HG00099.hp1 HG00099.hp2 HG00621.hp1 others(24): Show |
intron_variant | MODIFIER | c.573+612_573+620del others(9): Show |
RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 6/20 | chr7 | 5960070 | ||||||
chr7:5960072 | CACACACA | C | 6 | a0001c0009t0001g0007a0001c0009t0001g0012a0004c0005t0001g0055others(3): Show | 6 | HG00639.hp2 HG00741.hp1 HG02109.hp2 others(3): Show |
intron_variant | MODIFIER | c.573+612_573+618del others(7): Show |
RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 6/20 | chr7 | 5960072 | ||||||
chr7:5960074 | CACACA | C | 3 | a0001c0001t0001g0016a0001c0001t0006g0013a0007c0007t0002g0020 | 3 | HG01071.hp2 HG02071.hp2 HG02258.hp1 |
intron_variant | MODIFIER | c.573+612_573+616del others(5): Show |
RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 6/20 | chr7 | 5960074 | ||||||
chr7:5960076 | CACAACA | C | 2 | a0001c0010t0004g0056a0001c0010t0004g0057 | 2 | HG00735.hp2 HG01069.hp2 |
intron_variant | MODIFIER | c.573+609_573+614del others(6): Show |
RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 6/20 | chr7 | 5960076 | ||||||
chr7:5960383 | C | A | 22 | a0001c0009t0001g0007a0002c0002t0001g0037a0002c0002t0002g0018others(19): Show | 22 | HG00099.hp2 HG00621.hp1 HG01069.hp1 others(19): Show |
intron_variant | MODIFIER | c.573+308G>T | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 6/20 | chr7 | 5960383 | ||||||
chr7:5960392 | G | A | 1 | a0002c0002t0003g0060 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.573+299C>T | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 6/20 | chr7 | 5960392 | ||||||
chr7:5960412 | CA | C | 35 | a0001c0001t0006g0013a0001c0008t0002g0051a0001c0008t0002g0052others(32): Show | 35 | HG00099.hp1 HG00280.hp1 HG00639.hp2 others(32): Show |
intron_variant | MODIFIER | c.573+278delT | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 6/20 | chr7 | 5960412 | ||||||
chr7:5960434 | A | G | 25 | a0002c0002t0001g0037a0002c0002t0002g0018a0002c0002t0002g0038others(22): Show | 25 | HG00099.hp2 HG00280.hp1 HG00621.hp1 others(22): Show |
intron_variant | MODIFIER | c.573+257T>C | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 6/20 | chr7 | 5960434 | ||||||
chr7:5960442 | A | C | 4 | a0001c0009t0001g0007a0006c0006t0001g0002a0006c0006t0001g0017others(1): Show | 4 | HG00639.hp2 HG00735.hp1 HG01978.hp2 others(1): Show |
intron_variant | MODIFIER | c.573+249T>G | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 6/20 | chr7 | 5960442 | ||||||
chr7:5960489 | C | G | 16 | a0001c0001t0001g0001a0001c0001t0001g0016a0001c0001t0001g0019others(13): Show | 16 | HG00621.hp2 HG00735.hp1 HG00741.hp1 others(13): Show |
intron_variant | MODIFIER | c.573+202G>C | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 6/20 | chr7 | 5960489 | ||||||
chr7:5960590 | C | T | 2 | a0001c0001t0001g0019a0001c0001t0006g0013 | 2 | HG01071.hp2 HG02165.hp1 |
intron_variant | MODIFIER | c.573+101G>A | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 6/20 | chr7 | 5960590 | ||||||
chr7:5960597 | T | C | 60 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(57): Show | 60 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(57): Show |
intron_variant | MODIFIER | c.573+94A>G | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 6/20 | chr7 | 5960597 | ||||||
chr7:5960637 | G | A | 3 | a0001c0001t0001g0019a0001c0001t0006g0013a0004c0018t0001g0014 | 3 | HG01071.hp2 HG02165.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.573+54C>T | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 6/20 | chr7 | 5960637 | ||||||
chr7:5960900 | T | C | 44 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(41): Show | 44 | HG00099.hp1 HG00099.hp2 HG00621.hp1 others(41): Show |
intron_variant | MODIFIER | c.400-36A>G | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 5/20 | chr7 | 5960900 | ||||||
chr7:5960934 | C | T | 1 | a0004c0018t0001g0014 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.400-70G>A | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 5/20 | chr7 | 5960934 | ||||||
chr7:5961119 | T | C | 59 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(56): Show | 59 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(56): Show |
intron_variant | MODIFIER | c.400-255A>G | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 5/20 | chr7 | 5961119 | ||||||
chr7:5961122 | G | C | 14 | a0001c0009t0001g0012a0002c0002t0001g0037a0002c0002t0002g0018others(11): Show | 14 | HG00280.hp1 HG01175.hp1 HG01175.hp2 others(11): Show |
intron_variant | MODIFIER | c.400-258C>G | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 5/20 | chr7 | 5961122 | ||||||
chr7:5961144 | C | T | 8 | a0004c0005t0001g0035a0004c0005t0001g0041a0004c0005t0001g0042others(5): Show | 8 | HG00099.hp1 HG00639.hp2 HG00741.hp1 others(5): Show |
intron_variant | MODIFIER | c.400-280G>A | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 5/20 | chr7 | 5961144 | ||||||
chr7:5961145 | G | A | 1 | a0011c0015t0001g0029 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.400-281C>T | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 5/20 | chr7 | 5961145 | ||||||
chr7:5961336 | ATTTG | A | 10 | a0004c0005t0001g0035a0004c0005t0001g0041a0004c0005t0001g0042others(7): Show | 10 | HG00099.hp1 HG00639.hp2 HG00741.hp1 others(7): Show |
intron_variant | MODIFIER | c.400-476_400-473del others(4): Show |
RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 5/20 | chr7 | 5961336 | ||||||
chr7:5961522 | T | C | 15 | a0001c0001t0006g0013a0002c0002t0001g0037a0002c0002t0002g0018others(12): Show | 15 | HG00280.hp1 HG01071.hp2 HG01175.hp1 others(12): Show |
intron_variant | MODIFIER | c.400-658A>G | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 5/20 | chr7 | 5961522 | ||||||
chr7:5961675 | G | GT | 13 | a0002c0002t0001g0037a0002c0002t0002g0018a0002c0002t0002g0038others(10): Show | 13 | HG00280.hp1 HG01175.hp1 HG01175.hp2 others(10): Show |
intron_variant | MODIFIER | c.400-812dupA | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 5/20 | chr7 | 5961675 | ||||||
chr7:5961683 | GT | G | 11 | a0004c0005t0005g0033a0005c0003t0001g0024a0005c0003t0001g0025others(8): Show | 11 | HG00099.hp2 HG00621.hp1 HG01069.hp1 others(8): Show |
intron_variant | MODIFIER | c.400-820delA | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 5/20 | chr7 | 5961683 | ||||||
chr7:5961986 | C | T | 1 | a0012c0012t0001g0036 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.400-1122G>A | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 5/20 | chr7 | 5961986 | ||||||
chr7:5962018 | C | T | 13 | a0002c0002t0001g0037a0002c0002t0002g0018a0002c0002t0002g0038others(10): Show | 13 | HG00280.hp1 HG01175.hp1 HG01175.hp2 others(10): Show |
intron_variant | MODIFIER | c.400-1154G>A | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 5/20 | chr7 | 5962018 | ||||||
chr7:5962089 | G | A | 2 | a0001c0001t0006g0013a0004c0005t0005g0033 | 2 | HG01071.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.400-1225C>T | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 5/20 | chr7 | 5962089 | ||||||
chr7:5962101 | T | A | 1 | a0001c0014t0001g0015 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.400-1237A>T | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 5/20 | chr7 | 5962101 | ||||||
chr7:5962161 | CA | C | 25 | a0001c0001t0006g0013a0002c0002t0001g0037a0002c0002t0002g0018others(22): Show | 25 | HG00099.hp2 HG00280.hp1 HG00621.hp1 others(22): Show |
intron_variant | MODIFIER | c.400-1298delT | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 5/20 | chr7 | 5962161 | ||||||
chr7:5962202 | C | CT | 13 | a0002c0002t0001g0037a0002c0002t0002g0018a0002c0002t0002g0038others(10): Show | 13 | HG00280.hp1 HG01175.hp1 HG01175.hp2 others(10): Show |
intron_variant | MODIFIER | c.400-1339dupA | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 5/20 | chr7 | 5962202 | ||||||
chr7:5962202 | CT | C | 6 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0009t0001g0007others(3): Show | 6 | HG00735.hp1 HG01978.hp2 HG02056.hp1 others(3): Show |
intron_variant | MODIFIER | c.400-1339delA | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 5/20 | chr7 | 5962202 | ||||||
chr7:5962382 | G | A | 1 | a0004c0005t0005g0033 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.400-1518C>T | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 5/20 | chr7 | 5962382 | ||||||
chr7:5962456 | A | C | 7 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0006g0013others(4): Show | 7 | HG00735.hp1 HG01071.hp2 HG01978.hp2 others(4): Show |
intron_variant | MODIFIER | c.400-1592T>G | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 5/20 | chr7 | 5962456 | ||||||
chr7:5962554 | GCCTGCCC others(8): Show |
G | 13 | a0002c0002t0001g0037a0002c0002t0002g0018a0002c0002t0002g0038others(10): Show | 13 | HG00280.hp1 HG01175.hp1 HG01175.hp2 others(10): Show |
intron_variant | MODIFIER | c.400-1705_400-1691d others(17): Show |
RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 5/20 | chr7 | 5962554 | ||||||
chr7:5962851 | C | A | 1 | a0007c0007t0002g0020 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.399+1651G>T | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 5/20 | chr7 | 5962851 | ||||||
chr7:5962874 | A | G | 1 | a0001c0014t0001g0015 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.399+1628T>C | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 5/20 | chr7 | 5962874 | ||||||
chr7:5963163 | C | G | 59 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(56): Show | 59 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(56): Show |
intron_variant | MODIFIER | c.399+1339G>C | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 5/20 | chr7 | 5963163 | ||||||
chr7:5963311 | C | T | 7 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0008t0002g0051others(4): Show | 7 | HG00735.hp1 HG01978.hp2 HG02056.hp1 others(4): Show |
intron_variant | MODIFIER | c.399+1191G>A | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 5/20 | chr7 | 5963311 | ||||||
chr7:5963348 | C | T | 10 | a0001c0001t0006g0013a0004c0005t0001g0035a0004c0005t0001g0041others(7): Show | 10 | HG00099.hp1 HG00639.hp2 HG00741.hp1 others(7): Show |
intron_variant | MODIFIER | c.399+1154G>A | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 5/20 | chr7 | 5963348 | ||||||
chr7:5963365 | T | A | 1 | a0004c0018t0001g0014 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.399+1137A>T | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 5/20 | chr7 | 5963365 | ||||||
chr7:5963370 | C | T | 1 | a0010c0019t0001g0009 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.399+1132G>A | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 5/20 | chr7 | 5963370 | ||||||
chr7:5963410 | A | G | 5 | a0001c0001t0001g0005a0001c0001t0001g0006a0006c0006t0001g0002others(2): Show | 5 | HG00735.hp1 HG01978.hp2 HG02056.hp1 others(2): Show |
intron_variant | MODIFIER | c.399+1092T>C | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 5/20 | chr7 | 5963410 | ||||||
chr7:5963493 | T | C | 2 | a0007c0007t0002g0003a0007c0007t0002g0020 | 2 | HG02258.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.399+1009A>G | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 5/20 | chr7 | 5963493 | ||||||
chr7:5963505 | T | C | 13 | a0002c0002t0001g0037a0002c0002t0002g0018a0002c0002t0002g0038others(10): Show | 13 | HG00280.hp1 HG01175.hp1 HG01175.hp2 others(10): Show |
intron_variant | MODIFIER | c.399+997A>G | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 5/20 | chr7 | 5963505 | ||||||
chr7:5963732 | A | G | 13 | a0002c0002t0001g0037a0002c0002t0002g0018a0002c0002t0002g0038others(10): Show | 13 | HG00280.hp1 HG01175.hp1 HG01175.hp2 others(10): Show |
intron_variant | MODIFIER | c.399+770T>C | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 5/20 | chr7 | 5963732 | ||||||
chr7:5963831 | C | A | 1 | a0004c0005t0005g0033 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.399+671G>T | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 5/20 | chr7 | 5963831 | ||||||
chr7:5963902 | C | CA | 16 | a0001c0014t0001g0015a0002c0002t0001g0037a0002c0002t0002g0018others(13): Show | 16 | HG00280.hp1 HG01175.hp1 HG01175.hp2 others(13): Show |
intron_variant | MODIFIER | c.399+599dupT | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 5/20 | chr7 | 5963902 | ||||||
chr7:5963902 | CA | C | 7 | a0001c0008t0002g0051a0001c0008t0002g0052a0004c0005t0001g0035others(4): Show | 7 | HG00099.hp1 HG02056.hp2 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.399+599delT | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 5/20 | chr7 | 5963902 | ||||||
chr7:5963981 | G | A | 8 | a0004c0005t0001g0035a0004c0005t0001g0041a0004c0005t0001g0042others(5): Show | 8 | HG00099.hp1 HG00639.hp2 HG00741.hp1 others(5): Show |
intron_variant | MODIFIER | c.399+521C>T | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 5/20 | chr7 | 5963981 | ||||||
chr7:5963995 | G | A | 1 | a0001c0001t0006g0013 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.399+507C>T | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 5/20 | chr7 | 5963995 | ||||||
chr7:5964268 | C | T | 8 | a0004c0005t0001g0035a0004c0005t0001g0041a0004c0005t0001g0042others(5): Show | 8 | HG00099.hp1 HG00639.hp2 HG00741.hp1 others(5): Show |
intron_variant | MODIFIER | c.399+234G>A | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 5/20 | chr7 | 5964268 | ||||||
chr7:5964271 | G | A | 1 | a0010c0019t0001g0009 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.399+231C>T | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 5/20 | chr7 | 5964271 | ||||||
chr7:5964492 | T | C | 13 | a0002c0002t0001g0037a0002c0002t0002g0018a0002c0002t0002g0038others(10): Show | 13 | HG00280.hp1 HG01175.hp1 HG01175.hp2 others(10): Show |
intron_variant | MODIFIER | c.399+10A>G | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 5/20 | chr7 | 5964492 | ||||||
chr7:5964815 | T | C | 6 | a0004c0005t0001g0035a0004c0005t0001g0042a0004c0005t0001g0043others(3): Show | 6 | HG02056.hp2 HG02622.hp1 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.331-245A>G | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 4/20 | chr7 | 5964815 | ||||||
chr7:5964950 | C | T | 11 | a0003c0004t0003g0058a0003c0004t0003g0059a0003c0004t0003g0062others(8): Show | 11 | HG00280.hp2 HG00741.hp2 HG01261.hp2 others(8): Show |
intron_variant | MODIFIER | c.331-380G>A | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 4/20 | chr7 | 5964950 | ||||||
chr7:5964981 | A | G | 13 | a0002c0002t0001g0037a0002c0002t0002g0018a0002c0002t0002g0038others(10): Show | 13 | HG00280.hp1 HG01175.hp1 HG01175.hp2 others(10): Show |
intron_variant | MODIFIER | c.331-411T>C | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 4/20 | chr7 | 5964981 | ||||||
chr7:5965217 | G | A | 1 | a0001c0001t0006g0013 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.330+420C>T | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 4/20 | chr7 | 5965217 | ||||||
chr7:5965238 | C | CA | 23 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0008t0002g0051others(20): Show | 23 | HG00280.hp2 HG00639.hp2 HG00735.hp1 others(20): Show |
intron_variant | MODIFIER | c.330+398dupT | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 4/20 | chr7 | 5965238 | ||||||
chr7:5965253 | A | AT | 3 | a0001c0010t0004g0056a0001c0010t0004g0057a0012c0012t0001g0036 | 3 | HG00735.hp2 HG01069.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.330+383_330+384ins others(1): Show |
RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 4/20 | chr7 | 5965253 | ||||||
chr7:5965253 | A | T | 1 | a0001c0001t0006g0013 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.330+384T>A | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 4/20 | chr7 | 5965253 | ||||||
chr7:5965254 | A | T | 4 | a0001c0001t0006g0013a0001c0010t0004g0056a0001c0010t0004g0057others(1): Show | 4 | HG00735.hp2 HG01069.hp2 HG01071.hp2 others(1): Show |
intron_variant | MODIFIER | c.330+383T>A | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 4/20 | chr7 | 5965254 | ||||||
chr7:5965814 | G | GA | 8 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0019others(5): Show | 8 | HG00639.hp2 HG00735.hp1 HG00741.hp1 others(5): Show |
intron_variant | MODIFIER | c.255-103dupT | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 3/20 | chr7 | 5965814 | ||||||
chr7:5965814 | G | GAA | 11 | a0001c0001t0001g0001a0001c0001t0001g0016a0001c0001t0001g0022others(8): Show | 11 | HG00621.hp2 HG01175.hp1 HG01981.hp1 others(8): Show |
intron_variant | MODIFIER | c.255-104_255-103dup others(2): Show |
RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 3/20 | chr7 | 5965814 | ||||||
chr7:5965814 | G | GAAA | 6 | a0002c0002t0002g0018a0002c0002t0002g0038a0002c0002t0002g0040others(3): Show | 6 | HG00280.hp1 HG01175.hp2 HG01517.hp2 others(3): Show |
intron_variant | MODIFIER | c.255-105_255-103dup others(3): Show |
RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 3/20 | chr7 | 5965814 | ||||||
chr7:5965824 | A | AAAT | 10 | a0002c0002t0001g0037a0002c0002t0002g0048a0002c0002t0002g0049others(7): Show | 10 | HG00099.hp2 HG01069.hp1 HG01071.hp1 others(7): Show |
intron_variant | MODIFIER | c.255-113_255-112ins others(3): Show |
RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 3/20 | chr7 | 5965824 | ||||||
chr7:5965824 | A | ATAT | 6 | a0001c0014t0001g0015a0005c0003t0001g0024a0005c0003t0001g0025others(3): Show | 6 | HG00621.hp1 HG01261.hp1 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.255-113_255-112ins others(3): Show |
RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 3/20 | chr7 | 5965824 | ||||||
chr7:5965826 | T | A | 1 | a0001c0001t0001g0016 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.255-114A>T | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 3/20 | chr7 | 5965826 | ||||||
chr7:5965830 | T | A | 2 | a0001c0010t0004g0056a0001c0010t0004g0057 | 2 | HG00735.hp2 HG01069.hp2 |
intron_variant | MODIFIER | c.255-118A>T | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 3/20 | chr7 | 5965830 | ||||||
chr7:5965884 | A | G | 9 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0009t0001g0007others(6): Show | 9 | HG00639.hp2 HG00735.hp1 HG00741.hp1 others(6): Show |
intron_variant | MODIFIER | c.255-172T>C | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 3/20 | chr7 | 5965884 | ||||||
chr7:5965905 | G | A | 41 | a0001c0001t0001g0001a0001c0001t0001g0016a0001c0001t0001g0019others(38): Show | 41 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(38): Show |
intron_variant | MODIFIER | c.255-193C>T | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 3/20 | chr7 | 5965905 | ||||||
chr7:5966403 | CT | C | 40 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0008t0002g0051others(37): Show | 40 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(37): Show |
intron_variant | MODIFIER | c.254+459delA | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 3/20 | chr7 | 5966403 | ||||||
chr7:5966535 | G | A | 10 | a0005c0003t0001g0024a0005c0003t0001g0025a0005c0003t0001g0027others(7): Show | 10 | HG00099.hp2 HG00621.hp1 HG01069.hp1 others(7): Show |
intron_variant | MODIFIER | c.254+328C>T | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 3/20 | chr7 | 5966535 | ||||||
chr7:5966800 | G | A | 67 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(64): Show | 67 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(64): Show |
intron_variant | MODIFIER | c.254+63C>T | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 3/20 | chr7 | 5966800 | ||||||
chr7:5967244 | T | C | 1 | a0010c0019t0001g0009 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.-85-43A>G | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 2/20 | chr7 | 5967244 | ||||||
chr7:5967580 | T | A | 11 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0008t0002g0051others(8): Show | 11 | HG00639.hp2 HG00735.hp1 HG00741.hp1 others(8): Show |
intron_variant | MODIFIER | c.-205-143A>T | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 1/20 | chr7 | 5967580 | ||||||
chr7:5967883 | C | A | 14 | a0001c0010t0004g0056a0001c0010t0004g0057a0001c0014t0001g0015others(11): Show | 14 | HG00099.hp2 HG00621.hp1 HG00735.hp2 others(11): Show |
intron_variant | MODIFIER | c.-205-446G>T | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 1/20 | chr7 | 5967883 | ||||||
chr7:5968084 | A | G | 24 | a0001c0001t0001g0001a0001c0001t0001g0016a0001c0001t0001g0019others(21): Show | 24 | HG00099.hp2 HG00621.hp1 HG00621.hp2 others(21): Show |
intron_variant | MODIFIER | c.-205-647T>C | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 1/20 | chr7 | 5968084 | ||||||
chr7:5968086 | T | A | 1 | a0001c0001t0002g0026 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.-205-649A>T | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 1/20 | chr7 | 5968086 | ||||||
chr7:5968173 | G | A | 10 | a0001c0001t0001g0005a0001c0008t0002g0051a0001c0008t0002g0052others(7): Show | 10 | HG00639.hp2 HG00735.hp1 HG00735.hp2 others(7): Show |
intron_variant | MODIFIER | c.-205-736C>T | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 1/20 | chr7 | 5968173 | ||||||
chr7:5968304 | C | G | 2 | a0001c0008t0002g0051a0001c0008t0002g0052 | 2 | HG02717.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.-205-867G>C | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 1/20 | chr7 | 5968304 | ||||||
chr7:5968362 | C | T | 6 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0009t0001g0007others(3): Show | 6 | HG00735.hp1 HG01978.hp2 HG02056.hp1 others(3): Show |
intron_variant | MODIFIER | c.-205-925G>A | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 1/20 | chr7 | 5968362 | ||||||
chr7:5968393 | A | C | 3 | a0004c0018t0001g0014a0006c0006t0001g0021a0007c0007t0002g0003 | 3 | HG00735.hp1 HG03453.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.-205-956T>G | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 1/20 | chr7 | 5968393 | ||||||
chr7:5968499 | G | GTTTA | 17 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0016others(14): Show | 17 | HG00621.hp2 HG00639.hp1 HG00639.hp2 others(14): Show |
intron_variant | MODIFIER | c.-205-1066_-205-106 others(8): Show |
RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 1/20 | chr7 | 5968499 | ||||||
chr7:5968499 | G | GTTTATTT others(9): Show |
5 | a0001c0010t0004g0056a0001c0010t0004g0057a0005c0003t0001g0027others(2): Show | 5 | HG00735.hp2 HG01069.hp1 HG01069.hp2 others(2): Show |
intron_variant | MODIFIER | c.-205-1078_-205-106 others(20): Show |
RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 1/20 | chr7 | 5968499 | ||||||
chr7:5968631 | T | C | 1 | a0001c0001t0001g0006 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.-205-1194A>G | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 1/20 | chr7 | 5968631 | ||||||
chr7:5968640 | A | G | 29 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0006g0013others(26): Show | 29 | HG00099.hp1 HG00099.hp2 HG00621.hp1 others(26): Show |
intron_variant | MODIFIER | c.-205-1203T>C | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 1/20 | chr7 | 5968640 | ||||||
chr7:5968651 | C | T | 1 | a0001c0001t0002g0026 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.-205-1214G>A | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 1/20 | chr7 | 5968651 | ||||||
chr7:5968652 | G | A | 66 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(63): Show | 66 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(63): Show |
intron_variant | MODIFIER | c.-205-1215C>T | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 1/20 | chr7 | 5968652 | ||||||
chr7:5968656 | A | G | 24 | a0001c0001t0001g0019a0001c0008t0002g0051a0001c0010t0004g0056others(21): Show | 24 | HG00099.hp2 HG00280.hp2 HG00621.hp1 others(21): Show |
intron_variant | MODIFIER | c.-205-1219T>C | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 1/20 | chr7 | 5968656 | ||||||
chr7:5968706 | C | T | 1 | a0004c0018t0001g0014 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-205-1269G>A | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 1/20 | chr7 | 5968706 | ||||||
chr7:5968707 | A | C | 1 | a0004c0018t0001g0014 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-205-1270T>G | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 1/20 | chr7 | 5968707 | ||||||
chr7:5968708 | C | A | 1 | a0004c0018t0001g0014 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-205-1271G>T | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 1/20 | chr7 | 5968708 | ||||||
chr7:5968730 | A | G | 60 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(57): Show | 60 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(57): Show |
intron_variant | MODIFIER | c.-205-1293T>C | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 1/20 | chr7 | 5968730 | ||||||
chr7:5968792 | T | C | 5 | a0001c0001t0001g0001a0001c0001t0001g0023a0001c0001t0002g0026others(2): Show | 5 | HG00639.hp1 HG01981.hp1 HG02074.hp1 others(2): Show |
intron_variant | MODIFIER | c.-205-1355A>G | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 1/20 | chr7 | 5968792 | ||||||
chr7:5968824 | G | A | 3 | a0004c0005t0005g0033a0007c0007t0002g0003a0010c0019t0001g0009 | 3 | HG02071.hp1 HG02976.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.-205-1387C>T | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 1/20 | chr7 | 5968824 | ||||||
chr7:5968837 | G | GT | 16 | a0001c0001t0001g0001a0001c0001t0001g0022a0001c0001t0001g0023others(13): Show | 16 | HG00099.hp1 HG00639.hp1 HG01069.hp1 others(13): Show |
intron_variant | MODIFIER | c.-205-1401dupA | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 1/20 | chr7 | 5968837 | ||||||
chr7:5968837 | G | GTT | 20 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0053others(17): Show | 20 | HG00280.hp2 HG00621.hp1 HG00621.hp2 others(17): Show |
intron_variant | MODIFIER | c.-205-1402_-205-140 others(6): Show |
RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 1/20 | chr7 | 5968837 | ||||||
chr7:5968837 | G | GTTT | 4 | a0001c0001t0001g0032a0004c0005t0005g0033a0007c0007t0002g0003others(1): Show | 4 | HG02071.hp1 HG02976.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.-205-1403_-205-140 others(7): Show |
RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 1/20 | chr7 | 5968837 | ||||||
chr7:5968837 | G | T | 1 | a0001c0014t0001g0015 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.-205-1400C>A | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 1/20 | chr7 | 5968837 | ||||||
chr7:5968837 | GT | G | 4 | a0001c0010t0004g0056a0001c0010t0004g0057a0006c0006t0001g0002others(1): Show | 4 | HG00735.hp2 HG01069.hp2 HG01978.hp2 others(1): Show |
intron_variant | MODIFIER | c.-205-1401delA | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 1/20 | chr7 | 5968837 | ||||||
chr7:5968840 | T | TG | 2 | a0001c0009t0001g0007a0004c0011t0002g0039 | 2 | HG02109.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.-205-1404_-205-140 others(5): Show |
RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 1/20 | chr7 | 5968840 | ||||||
chr7:5968879 | G | T | 3 | a0001c0001t0001g0032a0006c0006t0001g0002a0010c0019t0001g0009 | 3 | HG01978.hp2 HG02071.hp1 NA18971.hp2 |
intron_variant | MODIFIER | c.-205-1442C>A | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 1/20 | chr7 | 5968879 | ||||||
chr7:5968905 | TTGGCTCA others(1): Show |
T | 4 | a0001c0010t0004g0056a0001c0010t0004g0057a0005c0003t0001g0024others(1): Show | 4 | HG00735.hp2 HG01069.hp2 HG02523.hp2 others(1): Show |
intron_variant | MODIFIER | c.-205-1476_-205-146 others(12): Show |
RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 1/20 | chr7 | 5968905 | ||||||
chr7:5969074 | C | A | 1 | a0004c0005t0001g0055 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.-206+1544G>T | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 1/20 | chr7 | 5969074 | ||||||
chr7:5969114 | A | T | 18 | a0001c0010t0004g0056a0001c0010t0004g0057a0002c0002t0001g0037others(15): Show | 18 | HG00099.hp1 HG00280.hp1 HG00639.hp2 others(15): Show |
intron_variant | MODIFIER | c.-206+1504T>A | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 1/20 | chr7 | 5969114 | ||||||
chr7:5969147 | C | CT | 21 | a0001c0001t0001g0016a0001c0001t0006g0013a0001c0008t0002g0051others(18): Show | 21 | HG00099.hp2 HG00280.hp2 HG01069.hp1 others(18): Show |
intron_variant | MODIFIER | c.-206+1470dupA | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 1/20 | chr7 | 5969147 | ||||||
chr7:5969147 | C | CTT | 9 | a0002c0002t0001g0037a0002c0002t0002g0038a0003c0004t0003g0058others(6): Show | 9 | HG00621.hp1 HG00741.hp2 HG01934.hp1 others(6): Show |
intron_variant | MODIFIER | c.-206+1469_-206+147 others(6): Show |
RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 1/20 | chr7 | 5969147 | ||||||
chr7:5969147 | C | CTTTTTT | 4 | a0001c0001t0001g0001a0001c0001t0001g0022a0001c0001t0001g0023others(1): Show | 4 | HG00621.hp2 HG00639.hp1 HG01981.hp1 others(1): Show |
intron_variant | MODIFIER | c.-206+1465_-206+147 others(10): Show |
RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 1/20 | chr7 | 5969147 | ||||||
chr7:5969147 | C | T | 1 | a0001c0001t0002g0026 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.-206+1471G>A | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 1/20 | chr7 | 5969147 | ||||||
chr7:5969147 | CTTTTTTT others(3): Show |
C | 7 | a0001c0001t0001g0005a0001c0001t0001g0006a0004c0005t0001g0035others(4): Show | 7 | HG00741.hp1 HG01978.hp2 HG02056.hp1 others(4): Show |
intron_variant | MODIFIER | c.-206+1461_-206+147 others(14): Show |
RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 1/20 | chr7 | 5969147 | ||||||
chr7:5969147 | CTTTTTTT others(6): Show |
C | 2 | a0006c0006t0001g0021a0010c0019t0001g0009 | 2 | HG00735.hp1 HG02071.hp1 |
intron_variant | MODIFIER | c.-206+1458_-206+147 others(17): Show |
RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 1/20 | chr7 | 5969147 | ||||||
chr7:5969271 | G | A | 2 | a0001c0009t0001g0007a0004c0005t0001g0035 | 2 | HG02056.hp2 HG02109.hp2 |
intron_variant | MODIFIER | c.-206+1347C>T | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 1/20 | chr7 | 5969271 | ||||||
chr7:5969373 | T | C | 1 | a0006c0006t0001g0008 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.-206+1245A>G | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 1/20 | chr7 | 5969373 | ||||||
chr7:5969574 | G | A | 1 | a0010c0019t0001g0009 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.-206+1044C>T | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 1/20 | chr7 | 5969574 | ||||||
chr7:5969967 | C | T | 4 | a0001c0009t0001g0012a0005c0003t0002g0010a0005c0003t0002g0011others(1): Show | 4 | HG02071.hp1 HG02258.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.-206+651G>A | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 1/20 | chr7 | 5969967 | ||||||
chr7:5970070 | C | A | 8 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(5): Show | 8 | HG00741.hp1 HG01978.hp2 HG01981.hp1 others(5): Show |
intron_variant | MODIFIER | c.-206+548G>T | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 1/20 | chr7 | 5970070 | ||||||
chr7:5970102 | C | CA | 3 | a0001c0008t0002g0051a0001c0008t0002g0052a0012c0012t0001g0036 | 3 | HG02717.hp2 HG03471.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.-206+515dupT | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 1/20 | chr7 | 5970102 | ||||||
chr7:5970173 | C | G | 1 | a0005c0003t0002g0010 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.-206+445G>C | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 1/20 | chr7 | 5970173 | ||||||
chr7:5970187 | C | G | 1 | a0005c0003t0002g0010 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.-206+431G>C | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 1/20 | chr7 | 5970187 | ||||||
chr7:5970194 | G | T | 43 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(40): Show | 43 | HG00099.hp2 HG00280.hp2 HG00621.hp1 others(40): Show |
intron_variant | MODIFIER | c.-206+424C>A | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 1/20 | chr7 | 5970194 | ||||||
chr7:5970271 | A | G | 2 | a0001c0010t0004g0056a0001c0010t0004g0057 | 2 | HG00735.hp2 HG01069.hp2 |
intron_variant | MODIFIER | c.-206+347T>C | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 1/20 | chr7 | 5970271 | ||||||
chr7:5970382 | C | T | 1 | a0010c0019t0001g0009 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.-206+236G>A | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 1/20 | chr7 | 5970382 | ||||||
chr7:5970437 | T | G | 2 | a0001c0008t0002g0051a0001c0008t0002g0052 | 2 | HG02717.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.-206+181A>C | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 1/20 | chr7 | 5970437 | ||||||
chr7:5970455 | G | A | 41 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0032others(38): Show | 41 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(38): Show |
intron_variant | MODIFIER | c.-206+163C>T | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 1/20 | chr7 | 5970455 | ||||||
chr7:5970487 | G | A | 2 | a0001c0001t0001g0053a0001c0013t0001g0054 | 2 | HG00621.hp2 HG02074.hp1 |
intron_variant | MODIFIER | c.-206+131C>T | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 1/20 | chr7 | 5970487 | ||||||
chr7:5970575 | T | C | 1 | a0004c0005t0001g0055 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.-206+43A>G | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 1/20 | chr7 | 5970575 | ||||||
chr7:5970591 | C | G | 15 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(12): Show | 15 | HG00741.hp1 HG01071.hp2 HG01978.hp2 others(12): Show |
intron_variant | MODIFIER | c.-206+27G>C | RSPH10B | ENSG00000155026.17 | transcript | ENST00000404406.6 | protein_coding | 1/20 | chr7 | 5970591 |