geneid | 27156 |
---|---|
ensemblid | ENSG00000100218.12 |
hgncid | 13437 |
symbol | RSPH14 |
name | radial spoke head 14 homolog |
refseq_nuc | NM_014433.3 |
refseq_prot | NP_055248.1 |
ensembl_nuc | ENST00000216036.9 |
ensembl_prot | ENSP00000216036.4 |
mane_status | MANE Select |
chr | chr22 |
start | 23059415 |
end | 23141990 |
strand | - |
ver | v1.2 |
region | chr22:23059415-23141990 |
region5000 | chr22:23054415-23146990 |
regionname0 | RSPH14_chr22_23059415_23141990 |
regionname5000 | RSPH14_chr22_23054415_23146990 |
ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 348 | 282 | 73 | 54 | 111 | 13 | 29 | 81 | RSPH14_chr22_23054415_23146990 | RSPH14 | copy fasta | chr22 | 23054415 | 23146990 |
a0002 | 0/0 | 348 | 14 | 3 | 2 | 2 | 1 | 6 | 2 | RSPH14_chr22_23054415_23146990 | RSPH14 | copy fasta | chr22 | 23054415 | 23146990 |
a0003 | 0/0 | 348 | 7 | 7 | 0 | 0 | 0 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | copy fasta | chr22 | 23054415 | 23146990 |
a0004 | 0/0 | 348 | 4 | 3 | 1 | 0 | 0 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | copy fasta | chr22 | 23054415 | 23146990 |
a0005 | 0/0 | 348 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | copy fasta | chr22 | 23054415 | 23146990 |
a0006 | 0/0 | 348 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | copy fasta | chr22 | 23054415 | 23146990 |
a0007 | 0/0 | 348 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | copy fasta | chr22 | 23054415 | 23146990 |
a0008 | 0/0 | 348 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | RSPH14_chr22_23054415_23146990 | RSPH14 | copy fasta | chr22 | 23054415 | 23146990 |
a0009 | 0/0 | 348 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | copy fasta | chr22 | 23054415 | 23146990 |
chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 0/0 | 1047 | 161 | 49 | 31 | 54 | 11 | 16 | RSPH14_chr22_23054415_23146990 | RSPH14 | copy fasta | chr22 | 23054415 | 23146990 |
c0002 | 1/1 | 1047 | 119 | 23 | 23 | 56 | 2 | 13 | RSPH14_chr22_23054415_23146990 | RSPH14 | copy fasta | chr22 | 23054415 | 23146990 |
c0003 | 0/0 | 1047 | 14 | 3 | 2 | 2 | 1 | 6 | RSPH14_chr22_23054415_23146990 | RSPH14 | copy fasta | chr22 | 23054415 | 23146990 |
c0004 | 0/0 | 1047 | 7 | 7 | 0 | 0 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | copy fasta | chr22 | 23054415 | 23146990 |
c0005 | 0/0 | 1047 | 2 | 2 | 0 | 0 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | copy fasta | chr22 | 23054415 | 23146990 |
c0006 | 0/0 | 1047 | 2 | 2 | 0 | 0 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | copy fasta | chr22 | 23054415 | 23146990 |
c0007 | 0/0 | 1047 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | copy fasta | chr22 | 23054415 | 23146990 |
c0008 | 0/0 | 1047 | 1 | 0 | 0 | 0 | 0 | 1 | RSPH14_chr22_23054415_23146990 | RSPH14 | copy fasta | chr22 | 23054415 | 23146990 |
c0009 | 0/0 | 1047 | 1 | 0 | 1 | 0 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | copy fasta | chr22 | 23054415 | 23146990 |
c0010 | 0/0 | 1047 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | copy fasta | chr22 | 23054415 | 23146990 |
c0011 | 0/0 | 1047 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | copy fasta | chr22 | 23054415 | 23146990 |
c0012 | 0/0 | 1047 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | copy fasta | chr22 | 23054415 | 23146990 |
c0013 | 0/0 | 1047 | 1 | 0 | 1 | 0 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | copy fasta | chr22 | 23054415 | 23146990 |
c0014 | 0/0 | 1047 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | copy fasta | chr22 | 23054415 | 23146990 |
c0015 | 0/0 | 1047 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | copy fasta | chr22 | 23054415 | 23146990 |
thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 1/1 | 142 | 300 | 77 | 57 | 114 | 14 | 36 | RSPH14_chr22_23054415_23146990 | RSPH14 | copy fasta | chr22 | 23054415 | 23146990 |
t0002 | 0/0 | 142 | 12 | 11 | 1 | 0 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | copy fasta | chr22 | 23054415 | 23146990 |
t0003 | 0/0 | 142 | 2 | 2 | 0 | 0 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | copy fasta | chr22 | 23054415 | 23146990 |
ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
g0002 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
g0007 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
g0008 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
g0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
g0018 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
g0027 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
g0033 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
g0036 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
g0037 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
g0113 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
g0149 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
g0150 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
g0213 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
g0221 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
g0236 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
g0248 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
g0249 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
g0250 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
g0256 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
g0261 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
g0262 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
g0263 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
g0264 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
g0265 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
g0267 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
g0268 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
g0279 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
g0284 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
g0285 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
g0295 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
g0300 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
g0309 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
g0311 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 0/0 | 1047 | 161 | 49 | 31 | 54 | 11 | 16 | RSPH14_chr22_23054415_23146990 | RSPH14 | copy fasta | chr22 | 23054415 | 23146990 |
a0001c0002 | 1/1 | 1047 | 119 | 23 | 23 | 56 | 2 | 13 | RSPH14_chr22_23054415_23146990 | RSPH14 | copy fasta | chr22 | 23054415 | 23146990 |
a0001c0010 | 0/0 | 1047 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | copy fasta | chr22 | 23054415 | 23146990 |
a0001c0011 | 0/0 | 1047 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | copy fasta | chr22 | 23054415 | 23146990 |
a0002c0003 | 0/0 | 1047 | 14 | 3 | 2 | 2 | 1 | 6 | RSPH14_chr22_23054415_23146990 | RSPH14 | copy fasta | chr22 | 23054415 | 23146990 |
a0003c0004 | 0/0 | 1047 | 7 | 7 | 0 | 0 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | copy fasta | chr22 | 23054415 | 23146990 |
a0004c0006 | 0/0 | 1047 | 2 | 2 | 0 | 0 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | copy fasta | chr22 | 23054415 | 23146990 |
a0004c0009 | 0/0 | 1047 | 1 | 0 | 1 | 0 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | copy fasta | chr22 | 23054415 | 23146990 |
a0004c0014 | 0/0 | 1047 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | copy fasta | chr22 | 23054415 | 23146990 |
a0005c0005 | 0/0 | 1047 | 2 | 2 | 0 | 0 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | copy fasta | chr22 | 23054415 | 23146990 |
a0005c0015 | 0/0 | 1047 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | copy fasta | chr22 | 23054415 | 23146990 |
a0006c0008 | 0/0 | 1047 | 1 | 0 | 0 | 0 | 0 | 1 | RSPH14_chr22_23054415_23146990 | RSPH14 | copy fasta | chr22 | 23054415 | 23146990 |
a0007c0013 | 0/0 | 1047 | 1 | 0 | 1 | 0 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | copy fasta | chr22 | 23054415 | 23146990 |
a0008c0007 | 0/0 | 1047 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | copy fasta | chr22 | 23054415 | 23146990 |
a0009c0012 | 0/0 | 1047 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | copy fasta | chr22 | 23054415 | 23146990 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 1188 | 159 | 47 | 31 | 54 | 11 | 16 | RSPH14_chr22_23054415_23146990 | RSPH14 | copy fasta | chr22 | 23054415 | 23146990 |
a0001c0001t0003 | 0/0 | 1188 | 2 | 2 | 0 | 0 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | copy fasta | chr22 | 23054415 | 23146990 |
a0001c0002t0001 | 1/1 | 1188 | 110 | 15 | 22 | 56 | 2 | 13 | RSPH14_chr22_23054415_23146990 | RSPH14 | copy fasta | chr22 | 23054415 | 23146990 |
a0001c0002t0002 | 0/0 | 1188 | 9 | 8 | 1 | 0 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | copy fasta | chr22 | 23054415 | 23146990 |
a0001c0010t0001 | 0/0 | 1188 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | copy fasta | chr22 | 23054415 | 23146990 |
a0001c0011t0001 | 0/0 | 1188 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | copy fasta | chr22 | 23054415 | 23146990 |
a0002c0003t0001 | 0/0 | 1188 | 14 | 3 | 2 | 2 | 1 | 6 | RSPH14_chr22_23054415_23146990 | RSPH14 | copy fasta | chr22 | 23054415 | 23146990 |
a0003c0004t0001 | 0/0 | 1188 | 7 | 7 | 0 | 0 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | copy fasta | chr22 | 23054415 | 23146990 |
a0004c0006t0002 | 0/0 | 1188 | 2 | 2 | 0 | 0 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | copy fasta | chr22 | 23054415 | 23146990 |
a0004c0009t0001 | 0/0 | 1188 | 1 | 0 | 1 | 0 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | copy fasta | chr22 | 23054415 | 23146990 |
a0004c0014t0001 | 0/0 | 1188 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | copy fasta | chr22 | 23054415 | 23146990 |
a0005c0005t0001 | 0/0 | 1188 | 2 | 2 | 0 | 0 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | copy fasta | chr22 | 23054415 | 23146990 |
a0005c0015t0002 | 0/0 | 1188 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | copy fasta | chr22 | 23054415 | 23146990 |
a0006c0008t0001 | 0/0 | 1188 | 1 | 0 | 0 | 0 | 0 | 1 | RSPH14_chr22_23054415_23146990 | RSPH14 | copy fasta | chr22 | 23054415 | 23146990 |
a0007c0013t0001 | 0/0 | 1188 | 1 | 0 | 1 | 0 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | copy fasta | chr22 | 23054415 | 23146990 |
a0008c0007t0001 | 0/0 | 1188 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | copy fasta | chr22 | 23054415 | 23146990 |
a0009c0012t0001 | 0/0 | 1188 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | copy fasta | chr22 | 23054415 | 23146990 |
actghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
a0001c0001t0001g0002 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
a0001c0001t0001g0008 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
a0001c0001t0001g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
a0001c0001t0001g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
a0001c0001t0001g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
a0001c0001t0001g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
a0001c0001t0001g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
a0001c0001t0001g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
a0001c0001t0001g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
a0001c0001t0001g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
a0001c0001t0001g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
a0001c0001t0001g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
a0001c0001t0001g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
a0001c0001t0001g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
a0001c0001t0001g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
a0001c0001t0001g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
a0001c0001t0001g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
a0001c0001t0001g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
a0001c0001t0001g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
a0001c0001t0001g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
a0001c0001t0001g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
a0001c0001t0001g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
a0001c0001t0001g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
a0001c0001t0001g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
a0001c0001t0001g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
a0001c0001t0001g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
a0001c0001t0001g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
a0001c0001t0001g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
a0001c0001t0001g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
a0001c0001t0001g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
a0001c0001t0001g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
a0001c0001t0001g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
a0001c0001t0001g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
a0001c0001t0001g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
a0001c0001t0001g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
a0001c0001t0001g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
a0001c0001t0001g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
a0001c0001t0001g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
a0001c0001t0001g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
a0001c0001t0001g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
a0001c0001t0001g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
a0001c0001t0001g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
a0001c0001t0001g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
a0001c0001t0001g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
a0001c0001t0001g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
a0001c0001t0001g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
a0001c0001t0001g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
a0001c0001t0001g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
a0001c0001t0001g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
a0001c0001t0001g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
a0001c0001t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
a0001c0001t0001g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
a0001c0001t0001g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
a0001c0001t0001g0262 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
a0001c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
a0001c0001t0001g0264 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
a0001c0001t0001g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
a0001c0001t0001g0267 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
a0001c0001t0001g0268 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
a0001c0001t0001g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
a0001c0001t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
a0001c0001t0001g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
a0001c0001t0001g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
a0001c0001t0001g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
a0001c0001t0001g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
a0001c0001t0001g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
a0001c0001t0001g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
a0001c0001t0001g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
a0001c0001t0001g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
a0001c0001t0001g0279 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
a0001c0001t0001g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
a0001c0001t0001g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
a0001c0001t0001g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
a0001c0001t0001g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
a0001c0001t0001g0284 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
a0001c0001t0001g0285 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
a0001c0001t0001g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
a0001c0001t0001g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
a0001c0001t0001g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
a0001c0001t0001g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
a0001c0001t0001g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
a0001c0001t0001g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
a0001c0001t0001g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
a0001c0001t0001g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
a0001c0001t0001g0295 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
a0001c0001t0001g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
a0001c0001t0001g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
a0001c0001t0001g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
a0001c0001t0001g0300 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
a0001c0001t0001g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
a0001c0001t0001g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
a0001c0001t0001g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
a0001c0001t0001g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
a0001c0001t0001g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
a0001c0001t0001g0309 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
a0001c0001t0001g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
a0001c0001t0001g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
a0001c0001t0003g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
a0001c0001t0003g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
a0001c0002t0001g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
a0001c0002t0001g0007 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
a0001c0002t0001g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
a0001c0002t0001g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
a0001c0002t0001g0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
a0001c0002t0001g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
a0001c0002t0001g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
a0001c0002t0001g0018 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
a0001c0002t0001g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
a0001c0002t0001g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
a0001c0002t0001g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
a0001c0002t0001g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
a0001c0002t0001g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
a0001c0002t0001g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
a0001c0002t0001g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
a0001c0002t0001g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
a0001c0002t0001g0027 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
a0001c0002t0001g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
a0001c0002t0001g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
a0001c0002t0001g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
a0001c0002t0001g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
a0001c0002t0001g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
a0001c0002t0001g0033 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
a0001c0002t0001g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
a0001c0002t0001g0036 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
a0001c0002t0001g0037 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
a0001c0002t0001g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
a0001c0002t0001g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
a0001c0002t0001g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
a0001c0002t0001g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
a0001c0002t0001g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
a0001c0002t0001g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
a0001c0002t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
a0001c0002t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
a0001c0002t0001g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
a0001c0002t0001g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
a0001c0002t0001g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
a0001c0002t0001g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
a0001c0002t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
a0001c0002t0001g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
a0001c0002t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
a0001c0002t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
a0001c0002t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
a0001c0002t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
a0001c0002t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
a0001c0002t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
a0001c0002t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
a0001c0002t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
a0001c0002t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
a0001c0002t0001g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
a0001c0002t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
a0001c0002t0001g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
a0001c0002t0001g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
a0001c0002t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
a0001c0002t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
a0001c0002t0001g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
a0001c0002t0001g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
a0001c0002t0001g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
a0001c0002t0001g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
a0001c0002t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
a0001c0002t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
a0001c0002t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
a0001c0002t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
a0001c0002t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
a0001c0002t0001g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
a0001c0002t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
a0001c0002t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
a0001c0002t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
a0001c0002t0001g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
a0001c0002t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
a0001c0002t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
a0001c0002t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
a0001c0002t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
a0001c0002t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
a0001c0002t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
a0001c0002t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
a0001c0002t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
a0001c0002t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
a0001c0002t0001g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
a0001c0002t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
a0001c0002t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
a0001c0002t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
a0001c0002t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
a0001c0002t0001g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
a0001c0002t0001g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
a0001c0002t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
a0001c0002t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
a0001c0002t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
a0001c0002t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
a0001c0002t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
a0001c0002t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
a0001c0002t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
a0001c0002t0001g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
a0001c0002t0001g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
a0001c0002t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
a0001c0002t0001g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
a0001c0002t0001g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
a0001c0002t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
a0001c0002t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
a0001c0002t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
a0001c0002t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
a0001c0002t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
a0001c0002t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
a0001c0002t0001g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
a0001c0002t0001g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
a0001c0002t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
a0001c0002t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
a0001c0002t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
a0001c0002t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
a0001c0002t0001g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
a0001c0002t0002g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
a0001c0002t0002g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
a0001c0002t0002g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
a0001c0002t0002g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
a0001c0002t0002g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
a0001c0002t0002g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
a0001c0002t0002g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
a0001c0002t0002g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
a0001c0002t0002g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
a0001c0010t0001g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
a0001c0011t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
a0002c0003t0001g0113 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
a0002c0003t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
a0002c0003t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
a0002c0003t0001g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
a0002c0003t0001g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
a0002c0003t0001g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
a0002c0003t0001g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
a0002c0003t0001g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
a0002c0003t0001g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
a0002c0003t0001g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
a0002c0003t0001g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
a0002c0003t0001g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
a0002c0003t0001g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
a0002c0003t0001g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
a0003c0004t0001g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
a0003c0004t0001g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
a0003c0004t0001g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
a0003c0004t0001g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
a0003c0004t0001g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
a0003c0004t0001g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
a0003c0004t0001g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
a0004c0006t0002g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
a0004c0006t0002g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
a0004c0009t0001g0311 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
a0004c0014t0001g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
a0005c0005t0001g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
a0005c0005t0001g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
a0005c0015t0002g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
a0006c0008t0001g0265 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
a0007c0013t0001g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
a0008c0007t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
a0009c0012t0001g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0001 | g0249 | EUR | GBR | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
HG00099 | hp2 | a0001 | c0001 | t0001 | g0256 | EUR | GBR | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
HG00280 | hp1 | a0001 | c0001 | t0001 | g0263 | EUR | FIN | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
HG00280 | hp2 | a0001 | c0001 | t0001 | g0221 | EUR | FIN | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
HG00544 | hp1 | a0001 | c0002 | t0001 | g0142 | EAS | CHS | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
HG00544 | hp2 | a0001 | c0002 | t0001 | g0129 | EAS | CHS | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
HG00558 | hp1 | a0001 | c0001 | t0001 | g0205 | EAS | CHS | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
HG00558 | hp2 | a0001 | c0002 | t0001 | g0060 | EAS | CHS | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
HG00597 | hp1 | a0001 | c0002 | t0001 | g0144 | EAS | CHS | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
HG00597 | hp2 | a0001 | c0001 | t0001 | g0220 | EAS | CHS | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
HG00609 | hp1 | a0001 | c0001 | t0001 | g0203 | EAS | CHS | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
HG00609 | hp2 | a0001 | c0001 | t0001 | g0185 | EAS | CHS | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
HG00639 | hp1 | a0001 | c0001 | t0001 | g0216 | AMR | PUR | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
HG00639 | hp2 | a0001 | c0002 | t0001 | g0026 | AMR | PUR | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
HG00642 | hp1 | a0001 | c0001 | t0001 | g0266 | AMR | PUR | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
HG00642 | hp2 | a0001 | c0001 | t0001 | g0126 | AMR | PUR | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
HG00673 | hp1 | a0001 | c0001 | t0001 | g0289 | EAS | CHS | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
HG00673 | hp2 | a0001 | c0002 | t0001 | g0099 | EAS | CHS | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
HG00735 | hp1 | a0001 | c0002 | t0001 | g0048 | AMR | PUR | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
HG00735 | hp2 | a0001 | c0001 | t0001 | g0214 | AMR | PUR | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
HG00738 | hp1 | a0001 | c0001 | t0001 | g0269 | AMR | PUR | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
HG00738 | hp2 | a0002 | c0003 | t0001 | g0118 | AMR | PUR | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
HG00741 | hp1 | a0001 | c0002 | t0001 | g0038 | AMR | PUR | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
HG00741 | hp2 | a0001 | c0001 | t0001 | g0300 | AMR | PUR | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
HG01070 | hp1 | a0001 | c0002 | t0001 | g0007 | AMR | PUR | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
HG01070 | hp2 | a0001 | c0001 | t0001 | g0274 | AMR | PUR | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
HG01071 | hp1 | a0001 | c0002 | t0001 | g0049 | AMR | PUR | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
HG01071 | hp2 | a0001 | c0001 | t0001 | g0284 | AMR | PUR | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
HG01081 | hp1 | a0001 | c0001 | t0001 | g0247 | AMR | PUR | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
HG01081 | hp2 | a0001 | c0002 | t0001 | g0139 | AMR | PUR | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
HG01106 | hp1 | a0001 | c0001 | t0001 | g0309 | AMR | PUR | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
HG01106 | hp2 | a0001 | c0002 | t0001 | g0030 | AMR | PUR | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
HG01109 | hp1 | a0004 | c0009 | t0001 | g0311 | AMR | PUR | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
HG01109 | hp2 | a0001 | c0002 | t0001 | g0015 | AMR | PUR | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
HG01169 | hp1 | a0001 | c0002 | t0001 | g0021 | AMR | PUR | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
HG01169 | hp2 | a0001 | c0001 | t0001 | g0260 | AMR | PUR | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
HG01175 | hp1 | a0002 | c0003 | t0001 | g0119 | AMR | PUR | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
HG01175 | hp2 | a0001 | c0001 | t0001 | g0288 | AMR | PUR | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
HG01192 | hp1 | a0001 | c0002 | t0001 | g0031 | AMR | PUR | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
HG01192 | hp2 | a0001 | c0001 | t0001 | g0008 | AMR | PUR | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
HG01243 | hp1 | a0001 | c0002 | t0002 | g0132 | AMR | PUR | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
HG01243 | hp2 | a0001 | c0001 | t0001 | g0242 | AMR | PUR | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
HG01255 | hp1 | a0007 | c0013 | t0001 | g0035 | AMR | CLM | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
HG01255 | hp2 | a0001 | c0001 | t0001 | g0282 | AMR | CLM | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
HG01257 | hp1 | a0001 | c0002 | t0001 | g0097 | AMR | CLM | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
HG01257 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
HG01258 | hp1 | a0001 | c0002 | t0001 | g0028 | AMR | CLM | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
HG01258 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
HG01261 | hp1 | a0001 | c0002 | t0001 | g0040 | AMR | CLM | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
HG01261 | hp2 | a0001 | c0001 | t0001 | g0244 | AMR | CLM | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
HG01346 | hp1 | a0001 | c0001 | t0001 | g0212 | AMR | CLM | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
HG01346 | hp2 | a0001 | c0001 | t0001 | g0287 | AMR | CLM | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
HG01358 | hp1 | a0001 | c0001 | t0001 | g0252 | AMR | CLM | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
HG01358 | hp2 | a0001 | c0001 | t0001 | g0271 | AMR | CLM | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
HG01361 | hp1 | a0001 | c0001 | t0001 | g0283 | AMR | CLM | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
HG01361 | hp2 | a0001 | c0002 | t0001 | g0032 | AMR | CLM | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
HG01433 | hp1 | a0001 | c0001 | t0001 | g0259 | AMR | CLM | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
HG01433 | hp2 | a0001 | c0002 | t0001 | g0140 | AMR | CLM | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
HG01515 | hp1 | a0001 | c0001 | t0001 | g0149 | EUR | IBS | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
HG01515 | hp2 | a0001 | c0001 | t0001 | g0262 | EUR | IBS | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
HG01516 | hp1 | a0001 | c0002 | t0001 | g0027 | EUR | IBS | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
HG01516 | hp2 | a0001 | c0001 | t0001 | g0150 | EUR | IBS | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
HG01517 | hp1 | a0001 | c0001 | t0001 | g0261 | EUR | IBS | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
HG01517 | hp2 | a0001 | c0001 | t0001 | g0236 | EUR | IBS | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
HG01884 | hp1 | a0005 | c0005 | t0001 | g0299 | AFR | ACB | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
HG01884 | hp2 | a0001 | c0001 | t0001 | g0235 | AFR | ACB | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
HG01891 | hp1 | a0001 | c0001 | t0001 | g0198 | AFR | ACB | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
HG01891 | hp2 | a0004 | c0006 | t0002 | g0009 | AFR | ACB | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
HG01928 | hp1 | a0001 | c0001 | t0001 | g0254 | AMR | PEL | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
HG01928 | hp2 | a0001 | c0002 | t0001 | g0105 | AMR | PEL | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
HG01934 | hp1 | a0001 | c0001 | t0001 | g0285 | AMR | PEL | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
HG01934 | hp2 | a0001 | c0002 | t0001 | g0034 | AMR | PEL | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
HG01943 | hp1 | a0001 | c0002 | t0001 | g0090 | AMR | PEL | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
HG01943 | hp2 | a0001 | c0001 | t0001 | g0253 | AMR | PEL | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
HG01975 | hp1 | a0001 | c0002 | t0001 | g0076 | AMR | PEL | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
HG01975 | hp2 | a0001 | c0001 | t0001 | g0217 | AMR | PEL | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
HG01981 | hp1 | a0001 | c0002 | t0001 | g0029 | AMR | PEL | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
HG01981 | hp2 | a0001 | c0001 | t0001 | g0182 | AMR | PEL | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
HG02004 | hp1 | a0001 | c0001 | t0001 | g0251 | AMR | PEL | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
HG02004 | hp2 | a0001 | c0002 | t0001 | g0061 | AMR | PEL | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
HG02015 | hp1 | a0001 | c0001 | t0001 | g0218 | EAS | KHV | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
HG02015 | hp2 | a0001 | c0001 | t0001 | g0281 | EAS | KHV | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
HG02027 | hp1 | a0001 | c0001 | t0001 | g0291 | EAS | KHV | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
HG02027 | hp2 | a0001 | c0002 | t0001 | g0050 | EAS | KHV | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
HG02055 | hp1 | a0001 | c0002 | t0002 | g0012 | AFR | ACB | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
HG02055 | hp2 | a0001 | c0001 | t0001 | g0148 | AFR | ACB | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
HG02056 | hp1 | a0001 | c0001 | t0001 | g0184 | EAS | KHV | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
HG02056 | hp2 | a0001 | c0002 | t0001 | g0102 | EAS | KHV | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
HG02080 | hp1 | a0001 | c0001 | t0001 | g0229 | EAS | KHV | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
HG02080 | hp2 | a0001 | c0002 | t0001 | g0082 | EAS | KHV | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
HG02083 | hp1 | a0001 | c0002 | t0001 | g0111 | EAS | KHV | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
HG02083 | hp2 | a0001 | c0001 | t0001 | g0270 | EAS | KHV | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
HG02129 | hp1 | a0001 | c0002 | t0001 | g0083 | EAS | KHV | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
HG02129 | hp2 | a0001 | c0001 | t0001 | g0224 | EAS | KHV | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
HG02135 | hp1 | a0001 | c0002 | t0001 | g0110 | EAS | KHV | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
HG02135 | hp2 | a0001 | c0001 | t0001 | g0215 | EAS | KHV | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
HG02145 | hp1 | a0001 | c0002 | t0001 | g0039 | AFR | ACB | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
HG02145 | hp2 | a0001 | c0001 | t0001 | g0179 | AFR | ACB | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
HG02155 | hp1 | a0001 | c0001 | t0001 | g0204 | EAS | CDX | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
HG02155 | hp2 | a0001 | c0002 | t0001 | g0103 | EAS | CDX | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
HG02257 | hp1 | a0005 | c0015 | t0002 | g0010 | AFR | ACB | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
HG02257 | hp2 | a0001 | c0001 | t0001 | g0152 | AFR | ACB | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
HG02258 | hp1 | a0001 | c0001 | t0001 | g0177 | AFR | ACB | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
HG02258 | hp2 | a0001 | c0001 | t0001 | g0164 | AFR | ACB | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
HG02280 | hp1 | a0001 | c0002 | t0001 | g0020 | AFR | ACB | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
HG02280 | hp2 | a0001 | c0001 | t0001 | g0305 | AFR | ACB | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
HG02293 | hp1 | a0001 | c0001 | t0001 | g0237 | AMR | PEL | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
HG02293 | hp2 | a0001 | c0002 | t0001 | g0080 | AMR | PEL | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
HG02523 | hp1 | a0001 | c0002 | t0001 | g0071 | EAS | KHV | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
HG02523 | hp2 | a0001 | c0002 | t0001 | g0087 | EAS | KHV | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
HG02602 | hp1 | a0001 | c0002 | t0001 | g0096 | SAS | PJL | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
HG02602 | hp2 | a0001 | c0001 | t0001 | g0268 | SAS | PJL | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
HG02615 | hp1 | a0001 | c0002 | t0002 | g0137 | AFR | GWD | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
HG02615 | hp2 | a0001 | c0010 | t0001 | g0290 | AFR | GWD | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
HG02630 | hp1 | a0001 | c0001 | t0001 | g0155 | AFR | GWD | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
HG02630 | hp2 | a0001 | c0001 | t0001 | g0163 | AFR | GWD | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
HG02647 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
HG02647 | hp2 | a0001 | c0001 | t0001 | g0167 | AFR | GWD | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
HG02698 | hp1 | a0002 | c0003 | t0001 | g0124 | SAS | PJL | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
HG02698 | hp2 | a0001 | c0001 | t0001 | g0210 | SAS | PJL | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
HG02723 | hp1 | a0003 | c0004 | t0001 | g0303 | AFR | GWD | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
HG02723 | hp2 | a0001 | c0001 | t0001 | g0156 | AFR | GWD | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
HG02735 | hp1 | a0001 | c0002 | t0001 | g0070 | SAS | PJL | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
HG02735 | hp2 | a0001 | c0001 | t0001 | g0209 | SAS | PJL | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
HG02738 | hp1 | a0002 | c0003 | t0001 | g0122 | SAS | PJL | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
HG02738 | hp2 | a0001 | c0002 | t0001 | g0047 | SAS | PJL | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
HG02809 | hp1 | a0001 | c0002 | t0001 | g0043 | AFR | GWD | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
HG02809 | hp2 | a0001 | c0002 | t0001 | g0014 | AFR | GWD | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
HG02818 | hp1 | a0001 | c0002 | t0001 | g0145 | AFR | GWD | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
HG02818 | hp2 | a0001 | c0002 | t0001 | g0019 | AFR | GWD | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
HG02886 | hp1 | a0001 | c0001 | t0001 | g0277 | AFR | GWD | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
HG02886 | hp2 | a0001 | c0002 | t0002 | g0131 | AFR | GWD | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
HG02895 | hp1 | a0001 | c0001 | t0001 | g0169 | AFR | GWD | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
HG02895 | hp2 | a0002 | c0003 | t0001 | g0121 | AFR | GWD | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
HG02896 | hp1 | a0004 | c0006 | t0002 | g0134 | AFR | GWD | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
HG02896 | hp2 | a0001 | c0001 | t0001 | g0151 | AFR | GWD | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
HG02897 | hp1 | a0001 | c0001 | t0001 | g0286 | AFR | GWD | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
HG02897 | hp2 | a0001 | c0001 | t0001 | g0170 | AFR | GWD | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
HG02922 | hp1 | a0001 | c0001 | t0001 | g0160 | AFR | ESN | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
HG02922 | hp2 | a0001 | c0001 | t0001 | g0171 | AFR | ESN | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
HG02965 | hp1 | a0001 | c0001 | t0001 | g0296 | AFR | ESN | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
HG02965 | hp2 | a0001 | c0001 | t0001 | g0173 | AFR | ESN | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
HG02970 | hp1 | a0001 | c0001 | t0001 | g0304 | AFR | ESN | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
HG02970 | hp2 | a0001 | c0001 | t0003 | g0003 | AFR | ESN | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
HG02976 | hp1 | a0001 | c0001 | t0001 | g0234 | AFR | ESN | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
HG02976 | hp2 | a0001 | c0001 | t0001 | g0157 | AFR | ESN | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
HG03017 | hp1 | a0001 | c0001 | t0001 | g0264 | SAS | PJL | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
HG03017 | hp2 | a0001 | c0001 | t0001 | g0267 | SAS | PJL | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
HG03041 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
HG03041 | hp2 | a0001 | c0001 | t0001 | g0154 | AFR | GWD | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
HG03098 | hp1 | a0001 | c0001 | t0001 | g0158 | AFR | MSL | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
HG03098 | hp2 | a0003 | c0004 | t0001 | g0178 | AFR | MSL | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
HG03139 | hp1 | a0003 | c0004 | t0001 | g0176 | AFR | ESN | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
HG03139 | hp2 | a0001 | c0001 | t0001 | g0172 | AFR | ESN | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
HG03195 | hp1 | a0001 | c0002 | t0002 | g0138 | AFR | ESN | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
HG03195 | hp2 | a0001 | c0001 | t0001 | g0297 | AFR | ESN | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
HG03209 | hp1 | a0003 | c0004 | t0001 | g0005 | AFR | MSL | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
HG03209 | hp2 | a0005 | c0005 | t0001 | g0243 | AFR | MSL | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
HG03225 | hp1 | a0001 | c0001 | t0001 | g0162 | AFR | MSL | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
HG03225 | hp2 | a0001 | c0001 | t0001 | g0298 | AFR | MSL | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
HG03239 | hp1 | a0001 | c0002 | t0001 | g0108 | SAS | PJL | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
HG03239 | hp2 | a0001 | c0001 | t0001 | g0250 | SAS | PJL | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
HG03453 | hp1 | a0001 | c0002 | t0001 | g0109 | AFR | MSL | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
HG03453 | hp2 | a0001 | c0001 | t0001 | g0191 | AFR | MSL | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
HG03486 | hp1 | a0001 | c0002 | t0001 | g0023 | AFR | MSL | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
HG03486 | hp2 | a0001 | c0001 | t0001 | g0165 | AFR | MSL | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
HG03490 | hp1 | a0001 | c0001 | t0001 | g0226 | SAS | PJL | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
HG03490 | hp2 | a0001 | c0002 | t0001 | g0063 | SAS | PJL | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
HG03491 | hp1 | a0001 | c0001 | t0001 | g0231 | SAS | PJL | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
HG03491 | hp2 | a0002 | c0003 | t0001 | g0116 | SAS | PJL | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
HG03492 | hp1 | a0001 | c0001 | t0001 | g0232 | SAS | PJL | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
HG03492 | hp2 | a0001 | c0002 | t0001 | g0064 | SAS | PJL | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
HG03516 | hp1 | a0001 | c0002 | t0001 | g0016 | AFR | ESN | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
HG03516 | hp2 | a0001 | c0001 | t0003 | g0004 | AFR | ESN | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
HG03540 | hp1 | a0001 | c0002 | t0001 | g0017 | AFR | GWD | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
HG03540 | hp2 | a0001 | c0001 | t0001 | g0159 | AFR | GWD | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
HG03579 | hp1 | a0003 | c0004 | t0001 | g0175 | AFR | MSL | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
HG03579 | hp2 | a0001 | c0002 | t0002 | g0133 | AFR | MSL | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
HG03654 | hp1 | a0002 | c0003 | t0001 | g0117 | SAS | PJL | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
HG03654 | hp2 | a0006 | c0008 | t0001 | g0265 | SAS | PJL | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
HG03688 | hp1 | a0002 | c0003 | t0001 | g0123 | SAS | STU | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
HG03688 | hp2 | a0001 | c0001 | t0001 | g0246 | SAS | STU | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
HG03704 | hp1 | a0001 | c0001 | t0001 | g0127 | SAS | PJL | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
HG03704 | hp2 | a0001 | c0001 | t0001 | g0230 | SAS | PJL | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
HG03834 | hp1 | a0002 | c0003 | t0001 | g0146 | SAS | BEB | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
HG03834 | hp2 | a0001 | c0002 | t0001 | g0046 | SAS | BEB | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
HG03942 | hp1 | a0001 | c0002 | t0001 | g0067 | SAS | BEB | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
HG03942 | hp2 | a0001 | c0001 | t0001 | g0295 | SAS | BEB | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
HG04199 | hp1 | a0001 | c0002 | t0001 | g0106 | SAS | STU | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
HG04199 | hp2 | a0001 | c0001 | t0001 | g0228 | SAS | STU | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
HG04204 | hp1 | a0001 | c0002 | t0001 | g0018 | SAS | STU | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
HG04204 | hp2 | a0001 | c0002 | t0001 | g0051 | SAS | STU | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
HG04228 | hp1 | a0001 | c0001 | t0001 | g0279 | SAS | STU | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
HG04228 | hp2 | a0001 | c0002 | t0001 | g0068 | SAS | STU | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
NA18522 | hp1 | a0001 | c0001 | t0001 | g0161 | AFR | YRI | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
NA18522 | hp2 | a0001 | c0001 | t0001 | g0153 | AFR | YRI | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
NA18747 | hp1 | a0001 | c0002 | t0001 | g0078 | EAS | CHB | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
NA18747 | hp2 | a0001 | c0001 | t0001 | g0219 | EAS | CHB | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
NA18906 | hp1 | a0003 | c0004 | t0001 | g0301 | AFR | YRI | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
NA18906 | hp2 | a0004 | c0014 | t0001 | g0095 | AFR | YRI | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
NA18942 | hp1 | a0001 | c0011 | t0001 | g0211 | EAS | JPT | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
NA18942 | hp2 | a0001 | c0002 | t0001 | g0065 | EAS | JPT | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
NA18944 | hp1 | a0001 | c0001 | t0001 | g0227 | EAS | JPT | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
NA18944 | hp2 | a0001 | c0002 | t0001 | g0141 | EAS | JPT | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
NA18946 | hp1 | a0001 | c0002 | t0001 | g0066 | EAS | JPT | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
NA18946 | hp2 | a0001 | c0001 | t0001 | g0292 | EAS | JPT | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
NA18947 | hp1 | a0001 | c0001 | t0001 | g0273 | EAS | JPT | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
NA18947 | hp2 | a0001 | c0002 | t0001 | g0130 | EAS | JPT | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
NA18950 | hp1 | a0001 | c0002 | t0001 | g0055 | EAS | JPT | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
NA18950 | hp2 | a0001 | c0001 | t0001 | g0200 | EAS | JPT | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
NA18952 | hp1 | a0001 | c0001 | t0001 | g0187 | EAS | JPT | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
NA18952 | hp2 | a0001 | c0002 | t0001 | g0084 | EAS | JPT | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
NA18957 | hp1 | a0001 | c0001 | t0001 | g0196 | EAS | JPT | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
NA18957 | hp2 | a0001 | c0002 | t0001 | g0079 | EAS | JPT | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
NA18959 | hp1 | a0001 | c0001 | t0001 | g0240 | EAS | JPT | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
NA18959 | hp2 | a0001 | c0002 | t0001 | g0085 | EAS | JPT | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
NA18960 | hp1 | a0001 | c0001 | t0001 | g0194 | EAS | JPT | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
NA18960 | hp2 | a0001 | c0002 | t0001 | g0075 | EAS | JPT | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
NA18965 | hp1 | a0001 | c0002 | t0001 | g0086 | EAS | JPT | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
NA18965 | hp2 | a0001 | c0002 | t0001 | g0112 | EAS | JPT | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
NA18967 | hp1 | a0001 | c0002 | t0001 | g0143 | EAS | JPT | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
NA18967 | hp2 | a0001 | c0001 | t0001 | g0239 | EAS | JPT | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
NA18968 | hp1 | a0001 | c0001 | t0001 | g0183 | EAS | JPT | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
NA18968 | hp2 | a0001 | c0002 | t0001 | g0101 | EAS | JPT | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
NA18970 | hp1 | a0001 | c0001 | t0001 | g0241 | EAS | JPT | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
NA18970 | hp2 | a0001 | c0002 | t0001 | g0077 | EAS | JPT | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
NA18971 | hp1 | a0001 | c0002 | t0001 | g0128 | EAS | JPT | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
NA18971 | hp2 | a0001 | c0002 | t0001 | g0092 | EAS | JPT | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
NA18973 | hp1 | a0001 | c0001 | t0001 | g0195 | EAS | JPT | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
NA18973 | hp2 | a0001 | c0002 | t0001 | g0044 | EAS | JPT | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
NA18978 | hp1 | a0001 | c0002 | t0001 | g0056 | EAS | JPT | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
NA18978 | hp2 | a0001 | c0001 | t0001 | g0306 | EAS | JPT | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
NA18981 | hp1 | a0001 | c0001 | t0001 | g0206 | EAS | JPT | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
NA18981 | hp2 | a0001 | c0002 | t0001 | g0088 | EAS | JPT | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
NA18982 | hp1 | a0001 | c0001 | t0001 | g0294 | EAS | JPT | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
NA18982 | hp2 | a0001 | c0002 | t0001 | g0100 | EAS | JPT | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
NA18983 | hp1 | a0001 | c0002 | t0001 | g0072 | EAS | JPT | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
NA18983 | hp2 | a0001 | c0001 | t0001 | g0275 | EAS | JPT | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
NA18984 | hp1 | a0001 | c0001 | t0001 | g0222 | EAS | JPT | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
NA18984 | hp2 | a0001 | c0001 | t0001 | g0280 | EAS | JPT | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
NA18986 | hp1 | a0001 | c0002 | t0001 | g0006 | EAS | JPT | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
NA18986 | hp2 | a0001 | c0001 | t0001 | g0258 | EAS | JPT | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
NA18989 | hp1 | a0001 | c0002 | t0001 | g0013 | EAS | JPT | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
NA18989 | hp2 | a0001 | c0001 | t0001 | g0225 | EAS | JPT | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
NA19002 | hp1 | a0001 | c0002 | t0001 | g0053 | EAS | JPT | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
NA19002 | hp2 | a0001 | c0001 | t0001 | g0293 | EAS | JPT | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
NA19004 | hp1 | a0001 | c0001 | t0001 | g0245 | EAS | JPT | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
NA19004 | hp2 | a0001 | c0002 | t0001 | g0058 | EAS | JPT | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
NA19007 | hp1 | a0001 | c0001 | t0001 | g0188 | EAS | JPT | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
NA19007 | hp2 | a0001 | c0002 | t0001 | g0107 | EAS | JPT | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
NA19009 | hp1 | a0001 | c0001 | t0001 | g0202 | EAS | JPT | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
NA19009 | hp2 | a0001 | c0001 | t0001 | g0208 | EAS | JPT | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
NA19010 | hp1 | a0001 | c0001 | t0001 | g0190 | EAS | JPT | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
NA19010 | hp2 | a0002 | c0003 | t0001 | g0115 | EAS | JPT | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
NA19012 | hp1 | a0001 | c0001 | t0001 | g0201 | EAS | JPT | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
NA19012 | hp2 | a0001 | c0002 | t0001 | g0062 | EAS | JPT | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
NA19030 | hp1 | a0001 | c0002 | t0002 | g0136 | AFR | LWK | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
NA19030 | hp2 | a0001 | c0002 | t0001 | g0041 | AFR | LWK | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
NA19043 | hp1 | a0001 | c0002 | t0002 | g0135 | AFR | LWK | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
NA19043 | hp2 | a0001 | c0001 | t0001 | g0180 | AFR | LWK | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
NA19056 | hp1 | a0001 | c0001 | t0001 | g0193 | EAS | JPT | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
NA19056 | hp2 | a0001 | c0002 | t0001 | g0081 | EAS | JPT | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
NA19057 | hp1 | a0001 | c0001 | t0001 | g0189 | EAS | JPT | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
NA19057 | hp2 | a0001 | c0002 | t0001 | g0045 | EAS | JPT | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
NA19058 | hp1 | a0001 | c0001 | t0001 | g0255 | EAS | JPT | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
NA19058 | hp2 | a0001 | c0002 | t0001 | g0059 | EAS | JPT | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
NA19060 | hp1 | a0001 | c0001 | t0001 | g0307 | EAS | JPT | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
NA19060 | hp2 | a0001 | c0002 | t0001 | g0094 | EAS | JPT | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
NA19068 | hp1 | a0001 | c0001 | t0001 | g0238 | EAS | JPT | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
NA19068 | hp2 | a0002 | c0003 | t0001 | g0114 | EAS | JPT | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
NA19070 | hp1 | a0001 | c0001 | t0001 | g0223 | EAS | JPT | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
NA19070 | hp2 | a0001 | c0002 | t0001 | g0052 | EAS | JPT | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
NA19074 | hp1 | a0001 | c0002 | t0001 | g0104 | EAS | JPT | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
NA19074 | hp2 | a0001 | c0001 | t0001 | g0199 | EAS | JPT | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
NA19079 | hp1 | a0001 | c0002 | t0001 | g0098 | EAS | JPT | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
NA19079 | hp2 | a0001 | c0001 | t0001 | g0186 | EAS | JPT | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
NA19081 | hp1 | a0001 | c0002 | t0001 | g0091 | EAS | JPT | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
NA19081 | hp2 | a0008 | c0007 | t0001 | g0192 | EAS | JPT | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
NA19085 | hp1 | a0001 | c0001 | t0001 | g0207 | EAS | JPT | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
NA19085 | hp2 | a0001 | c0002 | t0001 | g0073 | EAS | JPT | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
NA19086 | hp1 | a0001 | c0001 | t0001 | g0197 | EAS | JPT | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
NA19086 | hp2 | a0001 | c0002 | t0001 | g0057 | EAS | JPT | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
NA19088 | hp1 | a0001 | c0002 | t0001 | g0089 | EAS | JPT | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
NA19088 | hp2 | a0001 | c0002 | t0001 | g0093 | EAS | JPT | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
NA19090 | hp1 | a0001 | c0002 | t0001 | g0074 | EAS | JPT | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
NA19090 | hp2 | a0001 | c0001 | t0001 | g0310 | EAS | JPT | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
NA19091 | hp1 | a0001 | c0002 | t0001 | g0054 | EAS | JPT | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
NA19091 | hp2 | a0001 | c0001 | t0001 | g0308 | EAS | JPT | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
NA19240 | hp1 | a0001 | c0002 | t0001 | g0024 | AFR | YRI | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
NA19240 | hp2 | a0001 | c0002 | t0001 | g0042 | AFR | YRI | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
NA20129 | hp1 | a0009 | c0012 | t0001 | g0181 | AFR | ASW | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
NA20129 | hp2 | a0001 | c0002 | t0001 | g0022 | AFR | ASW | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
NA20752 | hp1 | a0002 | c0003 | t0001 | g0113 | EUR | TSI | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
NA20752 | hp2 | a0001 | c0001 | t0001 | g0248 | EUR | TSI | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
NA20805 | hp1 | a0001 | c0001 | t0001 | g0213 | EUR | TSI | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
NA20805 | hp2 | a0001 | c0002 | t0001 | g0037 | EUR | TSI | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
NA20905 | hp1 | a0001 | c0001 | t0001 | g0233 | SAS | GIH | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
NA20905 | hp2 | a0001 | c0002 | t0001 | g0069 | SAS | GIH | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
HG02109 | hp1 | a0001 | c0001 | t0001 | g0312 | AFR | ACB | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
HG02109 | hp2 | a0001 | c0001 | t0001 | g0278 | AFR | ACB | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
HG02486 | hp1 | a0002 | c0003 | t0001 | g0120 | AFR | ACB | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
HG02486 | hp2 | a0001 | c0001 | t0001 | g0168 | AFR | ACB | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
HG02559 | hp1 | a0001 | c0001 | t0001 | g0276 | AFR | ACB | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
HG02559 | hp2 | a0001 | c0001 | t0001 | g0147 | AFR | ACB | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
HG03471 | hp1 | a0001 | c0001 | t0001 | g0257 | AFR | MSL | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
HG03471 | hp2 | a0001 | c0002 | t0002 | g0011 | AFR | MSL | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
HG06807 | hp1 | a0003 | c0004 | t0001 | g0302 | AFR | USA | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
HG06807 | hp2 | a0001 | c0001 | t0001 | g0272 | AFR | USA | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
NA20300 | hp1 | a0001 | c0001 | t0001 | g0166 | AFR | USA | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
NA20300 | hp2 | a0002 | c0003 | t0001 | g0125 | AFR | USA | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
NA21309 | hp1 | a0001 | c0002 | t0001 | g0025 | AFR | LWK | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
NA21309 | hp2 | a0001 | c0001 | t0001 | g0174 | AFR | LWK | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
homoSapiens_chm13v2 | hp1 | a0001 | c0002 | t0001 | g0033 | REF | REF | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
homoSapiens_grch38 | hp1 | a0001 | c0002 | t0001 | g0036 | REF | REF | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr22:23059518
|
C | T | 1 | a0005 | 3 | HG01884.hp1 HG02257.hp1 HG03209.hp2 |
missense_variant | MODERATE | c.991G>A | p.Glu331Lys | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 7/7 | 1085/1188 | 991/1047 | 331/348 | chr22 | 23059518 | ||
chr22:23059592
|
C | T | 1 | a0004 | 4 | HG01109.hp1 HG01891.hp2 HG02896.hp1 others(1): Show |
missense_variant | MODERATE | c.917G>A | p.Arg306His | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 7/7 | 1011/1188 | 917/1047 | 306/348 | chr22 | 23059592 | ||
chr22:23061860
|
C | T | 1 | a0007 | 1 | HG01255.hp1 | missense_variant | MODERATE | c.739G>A | p.Val247Met | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 6/7 | 833/1188 | 739/1047 | 247/348 | chr22 | 23061860 | ||
chr22:23061868
|
A | G | 1 | a0006 | 1 | HG03654.hp2 | missense_variant | MODERATE | c.731T>C | p.Val244Ala | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 6/7 | 825/1188 | 731/1047 | 244/348 | chr22 | 23061868 | ||
chr22:23064002
|
C | G | 1 | a0008 | 1 | NA19081.hp2 | missense_variant | MODERATE | c.553G>C | p.Glu185Gln | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 5/7 | 647/1188 | 553/1047 | 185/348 | chr22 | 23064002 | ||
chr22:23064004
|
G | A | 2 | a0003a0009 | 8 | HG02723.hp1 HG03098.hp2 HG03139.hp1 others(5): Show |
missense_variant | MODERATE | c.551C>T | p.Thr184Ile | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 5/7 | 645/1188 | 551/1047 | 184/348 | chr22 | 23064004 | ||
chr22:23140258
|
G | A | 1 | a0009 | 1 | NA20129.hp1 | missense_variant | MODERATE | c.163C>T | p.His55Tyr | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 2/7 | 257/1188 | 163/1047 | 55/348 | chr22 | 23140258 | ||
chr22:23140296
|
G | A | 1 | a0002 | 14 | HG00738.hp2 HG01175.hp1 HG02486.hp1 others(11): Show |
missense_variant | MODERATE | c.125C>T | p.Thr42Met | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 2/7 | 219/1188 | 125/1047 | 42/348 | chr22 | 23140296 | ||
chr22:23140471
|
C | T | 3 | a0001a0004a0005 | 12 | HG01243.hp1 HG01891.hp2 HG02055.hp1 others(9): Show |
splice_region_variant | LOW | c.-51G>A | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 2/7 | chr22 | 23140471 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr22:23059506
|
G | T | 1 | a0004c0014 | 1 | NA18906.hp2 | synonymous_variant | LOW | c.1003C>A | p.Arg335Arg | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 7/7 | 1097/1188 | 1003/1047 | 335/348 | chr22 | 23059506 | ||
chr22:23063925
|
G | A | 1 | a0001c0010 | 1 | HG02615.hp2 | synonymous_variant | LOW | c.630C>T | p.Ala210Ala | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 5/7 | 724/1188 | 630/1047 | 210/348 | chr22 | 23063925 | ||
chr22:23063952
|
G | A | 1 | a0001c0011 | 1 | NA18942.hp1 | synonymous_variant | LOW | c.603C>T | p.Ser201Ser | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 5/7 | 697/1188 | 603/1047 | 201/348 | chr22 | 23063952 | ||
chr22:23140273
|
A | G | 9 | a0001c0001a0001c0010a0001c0011others(6): Show | 176 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(173): Show |
synonymous_variant | LOW | c.148T>C | p.Leu50Leu | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 2/7 | 242/1188 | 148/1047 | 50/348 | chr22 | 23140273 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr22:23141955
|
C | G | 1 | a0001c0001t0003 | 2 | HG02970.hp2 HG03516.hp2 |
5_prime_UTR_variant | MODIFIER | c.-59G>C | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 1/7 | 1535 | chr22 | 23141955 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr22:23059825
|
G | T | 1 | a0001c0001t0001g0157 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.791-107C>A | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 6/6 | chr22 | 23059825 | ||||||
chr22:23060241
|
G | T | 16 | a0001c0001t0001g0166a0001c0001t0001g0167a0001c0001t0001g0168others(13): Show | 16 | HG01070.hp2 HG02109.hp2 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.791-523C>A | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 6/6 | chr22 | 23060241 | ||||||
chr22:23060272
|
C | T | 1 | a0001c0002t0001g0145 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.791-554G>A | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 6/6 | chr22 | 23060272 | ||||||
chr22:23060289
|
G | A | 4 | a0001c0001t0001g0312a0004c0006t0002g0009a0004c0006t0002g0134others(1): Show | 4 | HG01109.hp1 HG01891.hp2 HG02109.hp1 others(1): Show |
intron_variant | MODIFIER | c.791-571C>T | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 6/6 | chr22 | 23060289 | ||||||
chr22:23060325
|
G | T | 1 | a0001c0001t0001g0312 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.791-607C>A | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 6/6 | chr22 | 23060325 | ||||||
chr22:23060340
|
G | A | 222 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(219): Show | 224 | HG00099.hp1 HG00280.hp2 HG00544.hp1 others(221): Show |
intron_variant | MODIFIER | c.791-622C>T | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 6/6 | chr22 | 23060340 | ||||||
chr22:23060457
|
G | A | 1 | a0001c0002t0001g0051 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.791-739C>T | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 6/6 | chr22 | 23060457 | ||||||
chr22:23060469
|
C | CA | 11 | a0001c0001t0001g0179a0001c0002t0001g0037a0001c0002t0002g0011others(8): Show | 11 | HG01243.hp1 HG02055.hp1 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.791-752dupT | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 6/6 | chr22 | 23060469 | ||||||
chr22:23060571
|
C | T | 11 | a0001c0001t0001g0001a0001c0001t0001g0158a0001c0001t0001g0159others(8): Show | 12 | HG02630.hp2 HG02647.hp1 HG02922.hp1 others(9): Show |
intron_variant | MODIFIER | c.791-853G>A | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 6/6 | chr22 | 23060571 | ||||||
chr22:23060586
|
C | A | 1 | a0001c0001t0001g0280 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.791-868G>T | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 6/6 | chr22 | 23060586 | ||||||
chr22:23060697
|
A | G | 3 | a0001c0001t0001g0164a0001c0001t0001g0304a0001c0002t0001g0038 | 3 | HG00741.hp1 HG02258.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.791-979T>C | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 6/6 | chr22 | 23060697 | ||||||
chr22:23060893
|
C | G | 16 | a0001c0001t0001g0166a0001c0001t0001g0167a0001c0001t0001g0168others(13): Show | 16 | HG01070.hp2 HG02109.hp2 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.790+916G>C | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 6/6 | chr22 | 23060893 | ||||||
chr22:23061212
|
G | A | 1 | a0002c0003t0001g0122 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.790+597C>T | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 6/6 | chr22 | 23061212 | ||||||
chr22:23061536
|
G | A | 1 | a0001c0001t0001g0257 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.790+273C>T | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 6/6 | chr22 | 23061536 | ||||||
chr22:23061567
|
C | T | 1 | a0001c0001t0001g0157 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.790+242G>A | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 6/6 | chr22 | 23061567 | ||||||
chr22:23061568
|
G | A | 2 | a0001c0002t0001g0128a0001c0002t0001g0142 | 2 | HG00544.hp1 NA18971.hp1 |
intron_variant | MODIFIER | c.790+241C>T | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 6/6 | chr22 | 23061568 | ||||||
chr22:23061685
|
G | GT | 21 | a0001c0001t0001g0001a0001c0001t0001g0153a0001c0001t0001g0154others(18): Show | 22 | HG00738.hp1 HG00738.hp2 HG00741.hp1 others(19): Show |
intron_variant | MODIFIER | c.790+123dupA | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 6/6 | chr22 | 23061685 | ||||||
chr22:23061708
|
T | G | 3 | a0001c0001t0001g0164a0001c0001t0001g0304a0001c0002t0001g0038 | 3 | HG00741.hp1 HG02258.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.790+101A>C | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 6/6 | chr22 | 23061708 | ||||||
chr22:23061710
|
G | A | 2 | a0001c0002t0001g0073a0001c0002t0001g0101 | 2 | NA18968.hp2 NA19085.hp2 |
intron_variant | MODIFIER | c.790+99C>T | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 6/6 | chr22 | 23061710 | ||||||
chr22:23061734
|
CCT | C | 3 | a0005c0005t0001g0243a0005c0005t0001g0299a0005c0015t0002g0010 | 3 | HG01884.hp1 HG02257.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.790+73_790+74delAG | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 6/6 | chr22 | 23061734 | ||||||
chr22:23061769
|
G | A | 1 | a0001c0001t0001g0247 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.790+40C>T | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 6/6 | chr22 | 23061769 | ||||||
chr22:23061789
|
G | A | 12 | a0001c0001t0001g0153a0001c0001t0001g0154a0001c0001t0001g0155others(9): Show | 12 | HG00741.hp1 HG01891.hp1 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.790+20C>T | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 6/6 | chr22 | 23061789 | ||||||
chr22:23061798
|
C | T | 4 | a0001c0001t0001g0289a0001c0001t0001g0300a0001c0002t0001g0085others(1): Show | 4 | HG00673.hp1 HG00741.hp2 HG03491.hp2 others(1): Show |
intron_variant | MODIFIER | c.790+11G>A | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 6/6 | chr22 | 23061798 | ||||||
chr22:23062136
|
C | T | 12 | a0001c0001t0001g0001a0001c0001t0001g0158a0001c0001t0001g0159others(9): Show | 13 | HG02630.hp2 HG02647.hp1 HG02922.hp1 others(10): Show |
intron_variant | MODIFIER | c.654-191G>A | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 5/6 | chr22 | 23062136 | ||||||
chr22:23062728
|
C | T | 1 | a0002c0003t0001g0119 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.654-783G>A | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 5/6 | chr22 | 23062728 | ||||||
chr22:23062790
|
G | A | 4 | a0001c0002t0001g0071a0001c0002t0001g0086a0001c0002t0001g0100others(1): Show | 4 | HG00544.hp2 HG02523.hp1 NA18965.hp1 others(1): Show |
intron_variant | MODIFIER | c.654-845C>T | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 5/6 | chr22 | 23062790 | ||||||
chr22:23062819
|
C | T | 1 | a0001c0001t0001g0195 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.654-874G>A | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 5/6 | chr22 | 23062819 | ||||||
chr22:23062910
|
C | T | 24 | a0001c0001t0001g0166a0001c0001t0001g0167a0001c0001t0001g0169others(21): Show | 24 | HG01070.hp2 HG02109.hp2 HG02258.hp1 others(21): Show |
intron_variant | MODIFIER | c.654-965G>A | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 5/6 | chr22 | 23062910 | ||||||
chr22:23063115
|
C | T | 1 | a0001c0001t0001g0184 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.653+787G>A | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 5/6 | chr22 | 23063115 | ||||||
chr22:23063252
|
G | A | 1 | a0001c0001t0001g0264 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.653+650C>T | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 5/6 | chr22 | 23063252 | ||||||
chr22:23063296
|
T | C | 1 | a0005c0005t0001g0243 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.653+606A>G | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 5/6 | chr22 | 23063296 | ||||||
chr22:23063363
|
G | A | 1 | a0001c0001t0001g0152 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.653+539C>T | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 5/6 | chr22 | 23063363 | ||||||
chr22:23063395
|
G | A | 1 | a0001c0002t0001g0098 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.653+507C>T | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 5/6 | chr22 | 23063395 | ||||||
chr22:23063459
|
G | A | 1 | a0001c0001t0001g0174 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.653+443C>T | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 5/6 | chr22 | 23063459 | ||||||
chr22:23063693
|
G | A | 2 | a0001c0001t0001g0206a0001c0002t0001g0088 | 2 | NA18981.hp1 NA18981.hp2 |
intron_variant | MODIFIER | c.653+209C>T | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 5/6 | chr22 | 23063693 | ||||||
chr22:23063704
|
T | C | 1 | a0001c0001t0001g0281 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.653+198A>G | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 5/6 | chr22 | 23063704 | ||||||
chr22:23063728
|
G | C | 2 | a0001c0001t0001g0284a0001c0001t0001g0288 | 2 | HG01071.hp2 HG01175.hp2 |
intron_variant | MODIFIER | c.653+174C>G | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 5/6 | chr22 | 23063728 | ||||||
chr22:23063779
|
A | G | 275 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0147others(272): Show | 276 | HG00099.hp1 HG00280.hp2 HG00544.hp1 others(273): Show |
intron_variant | MODIFIER | c.653+123T>C | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 5/6 | chr22 | 23063779 | ||||||
chr22:23064375
|
C | G | 1 | a0001c0001t0001g0158 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.422-242G>C | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23064375 | ||||||
chr22:23064441
|
A | G | 275 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0147others(272): Show | 276 | HG00099.hp1 HG00280.hp2 HG00544.hp1 others(273): Show |
intron_variant | MODIFIER | c.422-308T>C | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23064441 | ||||||
chr22:23064480
|
G | A | 1 | a0001c0002t0001g0145 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.422-347C>T | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23064480 | ||||||
chr22:23064506
|
A | G | 2 | a0001c0001t0001g0177a0001c0001t0001g0257 | 2 | HG02258.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.422-373T>C | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23064506 | ||||||
chr22:23064571
|
T | C | 1 | a0001c0002t0001g0052 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.422-438A>G | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23064571 | ||||||
chr22:23064875
|
T | C | 1 | a0001c0002t0001g0046 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.422-742A>G | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23064875 | ||||||
chr22:23064885
|
A | G | 275 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0147others(272): Show | 276 | HG00099.hp1 HG00280.hp2 HG00544.hp1 others(273): Show |
intron_variant | MODIFIER | c.422-752T>C | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23064885 | ||||||
chr22:23064999
|
C | T | 1 | a0001c0002t0001g0145 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.422-866G>A | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23064999 | ||||||
chr22:23065005
|
G | A | 3 | a0003c0004t0001g0301a0003c0004t0001g0302a0003c0004t0001g0303 | 3 | HG02723.hp1 HG06807.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.422-872C>T | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23065005 | ||||||
chr22:23065017
|
G | A | 11 | a0001c0001t0001g0157a0001c0002t0002g0011a0001c0002t0002g0012others(8): Show | 11 | HG01243.hp1 HG01884.hp1 HG02055.hp1 others(8): Show |
intron_variant | MODIFIER | c.422-884C>T | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23065017 | ||||||
chr22:23065063
|
C | T | 4 | a0001c0001t0001g0153a0001c0001t0001g0154a0001c0001t0001g0155others(1): Show | 4 | HG02630.hp1 HG02723.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.422-930G>A | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23065063 | ||||||
chr22:23065083
|
A | C | 276 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0147others(273): Show | 277 | HG00099.hp1 HG00280.hp2 HG00544.hp1 others(274): Show |
intron_variant | MODIFIER | c.422-950T>G | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23065083 | ||||||
chr22:23065123
|
A | C | 97 | a0001c0001t0001g0008a0001c0001t0001g0149a0001c0001t0001g0153others(94): Show | 97 | HG00099.hp1 HG00544.hp2 HG00558.hp1 others(94): Show |
intron_variant | MODIFIER | c.422-990T>G | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23065123 | ||||||
chr22:23065334
|
G | A | 2 | a0001c0001t0001g0209a0001c0001t0001g0242 | 2 | HG01243.hp2 HG02735.hp2 |
intron_variant | MODIFIER | c.422-1201C>T | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23065334 | ||||||
chr22:23065357
|
T | C | 3 | a0001c0001t0001g0289a0001c0002t0001g0085a0002c0003t0001g0116 | 3 | HG00673.hp1 HG03491.hp2 NA18959.hp2 |
intron_variant | MODIFIER | c.422-1224A>G | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23065357 | ||||||
chr22:23065502
|
G | A | 1 | a0005c0005t0001g0243 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.422-1369C>T | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23065502 | ||||||
chr22:23065534
|
C | CA | 112 | a0001c0001t0001g0150a0001c0001t0001g0153a0001c0001t0001g0155others(109): Show | 112 | HG00280.hp2 HG00544.hp1 HG00558.hp2 others(109): Show |
intron_variant | MODIFIER | c.422-1402dupT | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23065534 | ||||||
chr22:23065534
|
C | CAA | 55 | a0001c0001t0001g0147a0001c0001t0001g0148a0001c0001t0001g0152others(52): Show | 55 | HG00741.hp1 HG01081.hp2 HG01175.hp1 others(52): Show |
intron_variant | MODIFIER | c.422-1403_422-1402d others(4): Show |
RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23065534 | ||||||
chr22:23065534
|
C | CAAA | 10 | a0001c0001t0001g0166a0001c0001t0001g0167a0001c0001t0001g0171others(7): Show | 10 | HG00673.hp2 HG01109.hp1 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.422-1404_422-1402d others(5): Show |
RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23065534 | ||||||
chr22:23065534
|
CA | C | 8 | a0001c0001t0001g0164a0001c0001t0001g0281a0001c0002t0001g0014others(5): Show | 8 | HG01243.hp1 HG02015.hp2 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.422-1402delT | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23065534 | ||||||
chr22:23065534
|
CAAAAAAA others(2): Show |
C | 63 | a0001c0001t0001g0008a0001c0001t0001g0149a0001c0001t0001g0183others(60): Show | 63 | HG00099.hp1 HG00544.hp2 HG00558.hp1 others(60): Show |
intron_variant | MODIFIER | c.422-1410_422-1402d others(11): Show |
RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23065534 | ||||||
chr22:23065534
|
CAAAAAAA others(3): Show |
C | 4 | a0001c0001t0001g0199a0001c0001t0001g0231a0001c0001t0001g0239others(1): Show | 4 | HG00673.hp1 HG03491.hp1 NA18967.hp2 others(1): Show |
intron_variant | MODIFIER | c.422-1411_422-1402d others(12): Show |
RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23065534 | ||||||
chr22:23065534
|
CAAAAAAA others(4): Show |
C | 13 | a0001c0001t0001g0001a0001c0001t0001g0158a0001c0001t0001g0159others(10): Show | 14 | HG02630.hp2 HG02647.hp1 HG02922.hp1 others(11): Show |
intron_variant | MODIFIER | c.422-1412_422-1402d others(13): Show |
RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23065534 | ||||||
chr22:23065821
|
G | A | 1 | a0001c0002t0001g0052 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.422-1688C>T | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23065821 | ||||||
chr22:23065939
|
T | G | 276 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0147others(273): Show | 277 | HG00099.hp1 HG00280.hp2 HG00544.hp1 others(274): Show |
intron_variant | MODIFIER | c.422-1806A>C | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23065939 | ||||||
chr22:23066032
|
C | T | 1 | a0001c0001t0001g0152 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.422-1899G>A | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23066032 | ||||||
chr22:23066040
|
A | T | 1 | a0005c0005t0001g0243 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.422-1907T>A | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23066040 | ||||||
chr22:23066281
|
A | T | 1 | a0001c0002t0001g0145 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.422-2148T>A | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23066281 | ||||||
chr22:23066568
|
G | A | 1 | a0001c0002t0001g0068 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.422-2435C>T | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23066568 | ||||||
chr22:23066661
|
G | A | 5 | a0001c0001t0001g0153a0001c0001t0001g0154a0001c0001t0001g0155others(2): Show | 5 | HG02145.hp2 HG02630.hp1 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.422-2528C>T | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23066661 | ||||||
chr22:23067001
|
G | C | 1 | a0001c0002t0001g0046 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.422-2868C>G | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23067001 | ||||||
chr22:23067065
|
T | C | 2 | a0001c0001t0001g0219a0001c0001t0001g0224 | 2 | HG02129.hp2 NA18747.hp2 |
intron_variant | MODIFIER | c.422-2932A>G | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23067065 | ||||||
chr22:23067205
|
T | G | 4 | a0001c0001t0001g0289a0001c0001t0001g0300a0001c0002t0001g0085others(1): Show | 4 | HG00673.hp1 HG00741.hp2 HG03491.hp2 others(1): Show |
intron_variant | MODIFIER | c.422-3072A>C | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23067205 | ||||||
chr22:23067223
|
T | C | 3 | a0001c0001t0001g0289a0001c0002t0001g0085a0002c0003t0001g0116 | 3 | HG00673.hp1 HG03491.hp2 NA18959.hp2 |
intron_variant | MODIFIER | c.422-3090A>G | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23067223 | ||||||
chr22:23067493
|
C | A | 11 | a0001c0002t0002g0011a0001c0002t0002g0012a0001c0002t0002g0131others(8): Show | 11 | HG01243.hp1 HG01884.hp1 HG02055.hp1 others(8): Show |
intron_variant | MODIFIER | c.422-3360G>T | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23067493 | ||||||
chr22:23067854
|
A | G | 2 | a0001c0001t0001g0152a0001c0002t0001g0145 | 2 | HG02257.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.422-3721T>C | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23067854 | ||||||
chr22:23068108
|
C | G | 4 | a0001c0001t0001g0258a0001c0001t0001g0273a0001c0001t0001g0275others(1): Show | 4 | NA18946.hp2 NA18947.hp1 NA18983.hp2 others(1): Show |
intron_variant | MODIFIER | c.422-3975G>C | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23068108 | ||||||
chr22:23068154
|
G | A | 2 | a0001c0001t0001g0152a0001c0002t0001g0145 | 2 | HG02257.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.422-4021C>T | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23068154 | ||||||
chr22:23068171
|
T | C | 9 | a0001c0001t0001g0166a0001c0001t0001g0167a0001c0001t0001g0168others(6): Show | 9 | HG02486.hp2 HG02647.hp2 HG02895.hp1 others(6): Show |
intron_variant | MODIFIER | c.422-4038A>G | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23068171 | ||||||
chr22:23068180
|
C | A | 1 | a0001c0001t0001g0276 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.422-4047G>T | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23068180 | ||||||
chr22:23068182
|
G | A | 1 | a0001c0002t0001g0032 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.422-4049C>T | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23068182 | ||||||
chr22:23068211
|
A | G | 11 | a0001c0001t0001g0001a0001c0001t0001g0158a0001c0001t0001g0159others(8): Show | 12 | HG02630.hp2 HG02647.hp1 HG02922.hp1 others(9): Show |
intron_variant | MODIFIER | c.422-4078T>C | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23068211 | ||||||
chr22:23068345
|
C | T | 11 | a0001c0001t0001g0001a0001c0001t0001g0158a0001c0001t0001g0159others(8): Show | 12 | HG02630.hp2 HG02647.hp1 HG02922.hp1 others(9): Show |
intron_variant | MODIFIER | c.422-4212G>A | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23068345 | ||||||
chr22:23068688
|
G | A | 3 | a0001c0001t0001g0229a0001c0002t0001g0103a0008c0007t0001g0192 | 3 | HG02080.hp1 HG02155.hp2 NA19081.hp2 |
intron_variant | MODIFIER | c.422-4555C>T | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23068688 | ||||||
chr22:23068739
|
A | T | 277 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0147others(274): Show | 278 | HG00099.hp1 HG00280.hp2 HG00544.hp1 others(275): Show |
intron_variant | MODIFIER | c.422-4606T>A | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23068739 | ||||||
chr22:23068878
|
C | G | 1 | a0001c0001t0001g0294 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.422-4745G>C | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23068878 | ||||||
chr22:23068904
|
A | C | 2 | a0001c0001t0001g0164a0004c0014t0001g0095 | 2 | HG02258.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.422-4771T>G | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23068904 | ||||||
chr22:23069235
|
C | T | 1 | a0001c0001t0001g0206 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.422-5102G>A | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23069235 | ||||||
chr22:23069237
|
G | T | 1 | a0001c0001t0001g0206 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.422-5104C>A | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23069237 | ||||||
chr22:23069240
|
C | A | 1 | a0001c0001t0001g0206 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.422-5107G>T | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23069240 | ||||||
chr22:23069269
|
C | A | 1 | a0001c0001t0001g0206 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.422-5136G>T | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23069269 | ||||||
chr22:23069460
|
C | T | 3 | a0001c0001t0001g0289a0001c0002t0001g0085a0002c0003t0001g0116 | 3 | HG00673.hp1 HG03491.hp2 NA18959.hp2 |
intron_variant | MODIFIER | c.422-5327G>A | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23069460 | ||||||
chr22:23069491
|
T | C | 1 | a0001c0002t0001g0024 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.422-5358A>G | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23069491 | ||||||
chr22:23069623
|
C | T | 1 | a0001c0002t0001g0047 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.422-5490G>A | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23069623 | ||||||
chr22:23069654
|
C | T | 1 | a0001c0001t0001g0287 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.422-5521G>A | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23069654 | ||||||
chr22:23069817
|
G | T | 1 | a0005c0015t0002g0010 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.422-5684C>A | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23069817 | ||||||
chr22:23069838
|
A | G | 150 | a0001c0001t0001g0147a0001c0001t0001g0148a0001c0001t0001g0150others(147): Show | 150 | HG00280.hp2 HG00544.hp1 HG00558.hp2 others(147): Show |
intron_variant | MODIFIER | c.422-5705T>C | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23069838 | ||||||
chr22:23069879
|
A | G | 263 | a0001c0001t0001g0008a0001c0001t0001g0147a0001c0001t0001g0148others(260): Show | 263 | HG00099.hp1 HG00280.hp2 HG00544.hp1 others(260): Show |
intron_variant | MODIFIER | c.422-5746T>C | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23069879 | ||||||
chr22:23069921
|
G | C | 1 | a0001c0001t0001g0312 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.422-5788C>G | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23069921 | ||||||
chr22:23070011
|
G | A | 2 | a0001c0001t0001g0259a0001c0001t0001g0260 | 2 | HG01169.hp2 HG01433.hp1 |
intron_variant | MODIFIER | c.422-5878C>T | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23070011 | ||||||
chr22:23070041
|
G | C | 1 | a0005c0005t0001g0243 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.422-5908C>G | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23070041 | ||||||
chr22:23070099
|
C | T | 3 | a0003c0004t0001g0301a0003c0004t0001g0302a0003c0004t0001g0303 | 3 | HG02723.hp1 HG06807.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.422-5966G>A | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23070099 | ||||||
chr22:23070130
|
A | AC | 5 | a0001c0001t0001g0170a0001c0002t0001g0038a0001c0002t0001g0047others(2): Show | 5 | HG00741.hp1 HG02056.hp2 HG02738.hp2 others(2): Show |
intron_variant | MODIFIER | c.422-5998dupG | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23070130 | ||||||
chr22:23070157
|
C | A | 3 | a0001c0002t0001g0007a0001c0002t0001g0048a0001c0002t0001g0049 | 3 | HG00735.hp1 HG01070.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.422-6024G>T | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23070157 | ||||||
chr22:23070210
|
G | A | 1 | a0001c0001t0001g0126 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.422-6077C>T | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23070210 | ||||||
chr22:23070214
|
C | A | 1 | a0001c0001t0001g0218 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.422-6081G>T | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23070214 | ||||||
chr22:23070222
|
A | AGGTGCCC others(7): Show |
1 | a0001c0001t0001g0152 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.422-6103_422-6090d others(16): Show |
RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23070222 | ||||||
chr22:23070249
|
G | A | 1 | a0001c0001t0001g0202 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.422-6116C>T | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23070249 | ||||||
chr22:23070321
|
C | T | 1 | a0001c0001t0001g0259 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.422-6188G>A | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23070321 | ||||||
chr22:23070353
|
T | TGGCGGCG | 126 | a0001c0001t0001g0147a0001c0001t0001g0148a0001c0001t0001g0150others(123): Show | 126 | HG00280.hp2 HG00544.hp1 HG00558.hp2 others(123): Show |
intron_variant | MODIFIER | c.422-6227_422-6221d others(9): Show |
RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23070353 | ||||||
chr22:23070353
|
T | TGGCGGCG others(7): Show |
20 | a0001c0001t0001g0208a0001c0001t0001g0229a0001c0001t0001g0254others(17): Show | 20 | HG00741.hp1 HG01106.hp2 HG01928.hp1 others(17): Show |
intron_variant | MODIFIER | c.422-6234_422-6221d others(16): Show |
RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23070353 | ||||||
chr22:23070353
|
T | TGGCGGCG others(14): Show |
2 | a0001c0001t0001g0247a0001c0002t0001g0069 | 2 | HG01081.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.422-6241_422-6221d others(23): Show |
RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23070353 | ||||||
chr22:23070353
|
TGGCGGCG | T | 5 | a0001c0001t0001g0220a0001c0002t0001g0007a0001c0002t0001g0048others(2): Show | 5 | HG00597.hp2 HG00735.hp1 HG01070.hp1 others(2): Show |
intron_variant | MODIFIER | c.422-6227_422-6221d others(9): Show |
RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23070353 | ||||||
chr22:23070353
|
TGGCGGCG others(7): Show |
T | 1 | a0001c0001t0001g0276 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.422-6234_422-6221d others(16): Show |
RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23070353 | ||||||
chr22:23070449
|
C | A | 1 | a0001c0001t0001g0189 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.422-6316G>T | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23070449 | ||||||
chr22:23070483
|
G | T | 4 | a0001c0001t0001g0153a0001c0001t0001g0154a0001c0001t0001g0155others(1): Show | 4 | HG02630.hp1 HG02723.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.422-6350C>A | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23070483 | ||||||
chr22:23070518
|
C | CGCCCCGC others(3): Show |
1 | a0001c0002t0001g0062 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.422-6395_422-6386d others(12): Show |
RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23070518 | ||||||
chr22:23070600
|
C | CGCCGCTG others(1): Show |
19 | a0001c0001t0001g0247a0001c0001t0001g0267a0001c0001t0001g0285others(16): Show | 19 | HG00738.hp2 HG00741.hp1 HG01081.hp1 others(16): Show |
intron_variant | MODIFIER | c.422-6475_422-6468d others(10): Show |
RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23070600 | ||||||
chr22:23070628
|
C | T | 1 | a0001c0001t0001g0152 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.422-6495G>A | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23070628 | ||||||
chr22:23070682
|
C | T | 1 | a0005c0005t0001g0243 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.422-6549G>A | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23070682 | ||||||
chr22:23070713
|
C | T | 3 | a0001c0001t0001g0289a0001c0002t0001g0085a0002c0003t0001g0116 | 3 | HG00673.hp1 HG03491.hp2 NA18959.hp2 |
intron_variant | MODIFIER | c.422-6580G>A | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23070713 | ||||||
chr22:23070836
|
G | C | 1 | a0001c0001t0001g0312 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.422-6703C>G | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23070836 | ||||||
chr22:23070929
|
G | C | 1 | a0001c0002t0001g0018 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.422-6796C>G | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23070929 | ||||||
chr22:23070951
|
G | A | 5 | a0003c0004t0001g0005a0003c0004t0001g0175a0003c0004t0001g0176others(2): Show | 5 | HG03098.hp2 HG03139.hp1 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.422-6818C>T | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23070951 | ||||||
chr22:23071156
|
C | T | 1 | a0002c0003t0001g0116 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.422-7023G>A | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23071156 | ||||||
chr22:23071280
|
G | C | 2 | a0001c0001t0001g0248a0001c0001t0001g0249 | 2 | HG00099.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.422-7147C>G | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23071280 | ||||||
chr22:23071470
|
A | G | 1 | a0001c0001t0001g0306 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.422-7337T>C | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23071470 | ||||||
chr22:23071578
|
G | T | 1 | a0001c0001t0001g0157 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.422-7445C>A | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23071578 | ||||||
chr22:23071837
|
G | C | 1 | a0001c0001t0001g0312 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.422-7704C>G | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23071837 | ||||||
chr22:23071942
|
G | A | 1 | a0001c0002t0001g0067 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.422-7809C>T | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23071942 | ||||||
chr22:23072009
|
G | A | 1 | a0001c0001t0001g0152 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.422-7876C>T | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23072009 | ||||||
chr22:23072141
|
G | C | 1 | a0001c0002t0001g0104 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.422-8008C>G | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23072141 | ||||||
chr22:23072325
|
G | A | 1 | a0001c0002t0001g0091 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.422-8192C>T | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23072325 | ||||||
chr22:23072562
|
T | A | 1 | a0001c0002t0001g0143 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.422-8429A>T | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23072562 | ||||||
chr22:23072566
|
C | A | 1 | a0001c0002t0001g0143 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.422-8433G>T | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23072566 | ||||||
chr22:23072567
|
T | G | 1 | a0001c0002t0001g0143 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.422-8434A>C | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23072567 | ||||||
chr22:23072568
|
T | A | 1 | a0001c0002t0001g0143 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.422-8435A>T | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23072568 | ||||||
chr22:23072570
|
G | C | 1 | a0001c0002t0001g0143 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.422-8437C>G | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23072570 | ||||||
chr22:23072571
|
T | G | 1 | a0001c0002t0001g0143 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.422-8438A>C | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23072571 | ||||||
chr22:23072572
|
A | C | 1 | a0001c0002t0001g0143 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.422-8439T>G | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23072572 | ||||||
chr22:23072635
|
G | A | 1 | a0002c0003t0001g0120 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.422-8502C>T | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23072635 | ||||||
chr22:23072656
|
G | C | 1 | a0001c0001t0001g0291 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.422-8523C>G | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23072656 | ||||||
chr22:23072897
|
C | T | 1 | a0001c0001t0001g0177 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.422-8764G>A | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23072897 | ||||||
chr22:23072960
|
C | T | 72 | a0001c0001t0001g0182a0001c0001t0001g0208a0001c0001t0001g0214others(69): Show | 72 | HG00280.hp2 HG00544.hp1 HG00558.hp2 others(69): Show |
intron_variant | MODIFIER | c.422-8827G>A | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23072960 | ||||||
chr22:23073055
|
T | G | 1 | a0001c0001t0001g0215 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.422-8922A>C | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23073055 | ||||||
chr22:23073060
|
C | A | 1 | a0001c0001t0001g0283 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.422-8927G>T | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23073060 | ||||||
chr22:23073194
|
G | A | 1 | a0001c0001t0001g0189 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.422-9061C>T | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23073194 | ||||||
chr22:23073400
|
C | T | 1 | a0004c0009t0001g0311 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.422-9267G>A | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23073400 | ||||||
chr22:23073434
|
G | A | 1 | a0001c0002t0001g0144 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.422-9301C>T | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23073434 | ||||||
chr22:23073475
|
G | A | 2 | a0001c0001t0001g0289a0001c0002t0001g0085 | 2 | HG00673.hp1 NA18959.hp2 |
intron_variant | MODIFIER | c.422-9342C>T | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23073475 | ||||||
chr22:23073504
|
C | T | 1 | a0001c0001t0001g0268 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.422-9371G>A | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23073504 | ||||||
chr22:23073597
|
T | G | 1 | a0004c0006t0002g0009 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.422-9464A>C | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23073597 | ||||||
chr22:23073630
|
G | A | 10 | a0001c0001t0001g0001a0001c0001t0001g0158a0001c0001t0001g0159others(7): Show | 11 | HG02630.hp2 HG02647.hp1 HG02922.hp1 others(8): Show |
intron_variant | MODIFIER | c.422-9497C>T | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23073630 | ||||||
chr22:23073819
|
G | A | 135 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0149others(132): Show | 136 | HG00099.hp1 HG00544.hp2 HG00558.hp1 others(133): Show |
intron_variant | MODIFIER | c.422-9686C>T | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23073819 | ||||||
chr22:23073840
|
C | G | 1 | a0005c0005t0001g0299 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.422-9707G>C | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23073840 | ||||||
chr22:23074100
|
G | A | 1 | a0001c0001t0001g0247 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.422-9967C>T | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23074100 | ||||||
chr22:23074201
|
A | C | 1 | a0001c0002t0001g0094 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.422-10068T>G | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23074201 | ||||||
chr22:23074296
|
G | A | 9 | a0001c0001t0001g0166a0001c0001t0001g0167a0001c0001t0001g0168others(6): Show | 9 | HG02486.hp2 HG02647.hp2 HG02895.hp1 others(6): Show |
intron_variant | MODIFIER | c.422-10163C>T | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23074296 | ||||||
chr22:23074396
|
G | A | 1 | a0001c0002t0001g0142 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.422-10263C>T | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23074396 | ||||||
chr22:23074653
|
C | T | 5 | a0001c0001t0001g0152a0001c0001t0001g0153a0001c0001t0001g0154others(2): Show | 5 | HG02257.hp2 HG02630.hp1 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.422-10520G>A | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23074653 | ||||||
chr22:23074666
|
T | C | 1 | a0001c0002t0001g0024 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.422-10533A>G | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23074666 | ||||||
chr22:23074693
|
G | A | 3 | a0001c0001t0001g0289a0001c0001t0001g0300a0001c0002t0001g0085 | 3 | HG00673.hp1 HG00741.hp2 NA18959.hp2 |
intron_variant | MODIFIER | c.422-10560C>T | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23074693 | ||||||
chr22:23074755
|
G | A | 65 | a0001c0001t0001g0008a0001c0001t0001g0149a0001c0001t0001g0183others(62): Show | 65 | HG00099.hp1 HG00544.hp2 HG00558.hp1 others(62): Show |
intron_variant | MODIFIER | c.422-10622C>T | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23074755 | ||||||
chr22:23074823
|
G | A | 2 | a0001c0001t0001g0289a0001c0002t0001g0085 | 2 | HG00673.hp1 NA18959.hp2 |
intron_variant | MODIFIER | c.422-10690C>T | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23074823 | ||||||
chr22:23074944
|
G | A | 1 | a0001c0001t0001g0260 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.422-10811C>T | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23074944 | ||||||
chr22:23075007
|
A | T | 1 | a0001c0001t0001g0127 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.422-10874T>A | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23075007 | ||||||
chr22:23075131
|
G | A | 1 | a0003c0004t0001g0005 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.422-10998C>T | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23075131 | ||||||
chr22:23075275
|
C | G | 1 | a0001c0001t0001g0157 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.422-11142G>C | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23075275 | ||||||
chr22:23075298
|
A | G | 1 | a0002c0003t0001g0146 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.422-11165T>C | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23075298 | ||||||
chr22:23075361
|
A | C | 20 | a0001c0001t0001g0157a0001c0001t0001g0247a0001c0002t0001g0013others(17): Show | 20 | HG00738.hp2 HG00741.hp1 HG01081.hp1 others(17): Show |
intron_variant | MODIFIER | c.422-11228T>G | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23075361 | ||||||
chr22:23075398
|
G | T | 5 | a0001c0002t0001g0018a0001c0002t0001g0037a0001c0002t0001g0047others(2): Show | 5 | HG02735.hp1 HG02738.hp2 HG03942.hp1 others(2): Show |
intron_variant | MODIFIER | c.422-11265C>A | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23075398 | ||||||
chr22:23075486
|
C | T | 1 | a0001c0001t0001g0126 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.422-11353G>A | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23075486 | ||||||
chr22:23075491
|
A | G | 107 | a0001c0001t0001g0008a0001c0001t0001g0149a0001c0001t0001g0152others(104): Show | 107 | HG00099.hp1 HG00544.hp2 HG00558.hp1 others(104): Show |
intron_variant | MODIFIER | c.422-11358T>C | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23075491 | ||||||
chr22:23075526
|
G | C | 138 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0149others(135): Show | 139 | HG00099.hp1 HG00544.hp2 HG00558.hp1 others(136): Show |
intron_variant | MODIFIER | c.422-11393C>G | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23075526 | ||||||
chr22:23075572
|
A | G | 134 | a0001c0001t0001g0147a0001c0001t0001g0148a0001c0001t0001g0150others(131): Show | 134 | HG00280.hp2 HG00544.hp1 HG00558.hp2 others(131): Show |
intron_variant | MODIFIER | c.422-11439T>C | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23075572 | ||||||
chr22:23075694
|
T | G | 3 | a0001c0002t0001g0028a0001c0002t0001g0029a0001c0002t0001g0030 | 3 | HG01106.hp2 HG01258.hp1 HG01981.hp1 |
intron_variant | MODIFIER | c.422-11561A>C | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23075694 | ||||||
chr22:23075717
|
A | G | 1 | a0001c0001t0001g0213 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.422-11584T>C | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23075717 | ||||||
chr22:23076012
|
G | A | 1 | a0001c0001t0001g0149 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.422-11879C>T | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23076012 | ||||||
chr22:23076023
|
G | A | 1 | a0001c0001t0001g0218 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.422-11890C>T | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23076023 | ||||||
chr22:23076266
|
C | T | 2 | a0001c0001t0001g0264a0001c0001t0001g0268 | 2 | HG02602.hp2 HG03017.hp1 |
intron_variant | MODIFIER | c.422-12133G>A | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23076266 | ||||||
chr22:23076267
|
G | C | 2 | a0001c0001t0001g0157a0001c0002t0001g0145 | 2 | HG02818.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.422-12134C>G | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23076267 | ||||||
chr22:23076306
|
C | T | 3 | a0001c0001t0001g0210a0001c0001t0001g0212a0001c0001t0001g0213 | 3 | HG01346.hp1 HG02698.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.422-12173G>A | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23076306 | ||||||
chr22:23076347
|
G | A | 1 | a0001c0001t0001g0300 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.422-12214C>T | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23076347 | ||||||
chr22:23076640
|
C | T | 1 | a0001c0001t0001g0312 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.422-12507G>A | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23076640 | ||||||
chr22:23076652
|
A | G | 68 | a0001c0001t0001g0008a0001c0001t0001g0149a0001c0001t0001g0183others(65): Show | 68 | HG00099.hp1 HG00544.hp2 HG00558.hp1 others(65): Show |
intron_variant | MODIFIER | c.422-12519T>C | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23076652 | ||||||
chr22:23076767
|
G | A | 1 | a0001c0001t0001g0153 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.422-12634C>T | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23076767 | ||||||
chr22:23077170
|
C | G | 3 | a0001c0001t0001g0296a0001c0001t0001g0297a0001c0001t0001g0298 | 3 | HG02965.hp1 HG03195.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.422-13037G>C | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23077170 | ||||||
chr22:23077323
|
C | T | 2 | a0001c0001t0001g0169a0001c0001t0001g0170 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.422-13190G>A | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23077323 | ||||||
chr22:23077470
|
G | A | 1 | a0001c0001t0001g0156 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.422-13337C>T | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23077470 | ||||||
chr22:23077855
|
C | T | 1 | a0001c0001t0001g0274 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.422-13722G>A | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23077855 | ||||||
chr22:23078113
|
G | A | 1 | a0001c0002t0001g0017 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.422-13980C>T | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23078113 | ||||||
chr22:23078155
|
C | A | 1 | a0001c0002t0001g0093 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.422-14022G>T | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23078155 | ||||||
chr22:23078259
|
G | A | 1 | a0001c0002t0001g0078 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.422-14126C>T | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23078259 | ||||||
chr22:23078322
|
G | A | 1 | a0001c0002t0001g0076 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.422-14189C>T | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23078322 | ||||||
chr22:23078380
|
G | C | 1 | a0001c0001t0001g0204 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.422-14247C>G | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23078380 | ||||||
chr22:23078438
|
C | T | 2 | a0001c0002t0001g0016a0005c0005t0001g0243 | 2 | HG03209.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.422-14305G>A | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23078438 | ||||||
chr22:23078445
|
T | A | 1 | a0001c0001t0001g0199 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.422-14312A>T | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23078445 | ||||||
chr22:23078476
|
C | T | 10 | a0001c0001t0001g0166a0001c0001t0001g0167a0001c0001t0001g0168others(7): Show | 10 | HG01109.hp1 HG01884.hp1 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.422-14343G>A | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23078476 | ||||||
chr22:23078488
|
CA | C | 78 | a0001c0001t0001g0008a0001c0001t0001g0149a0001c0001t0001g0179others(75): Show | 78 | HG00099.hp1 HG00544.hp2 HG00558.hp1 others(75): Show |
intron_variant | MODIFIER | c.422-14356delT | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23078488 | ||||||
chr22:23078499
|
T | C | 10 | a0001c0001t0001g0001a0001c0001t0001g0158a0001c0001t0001g0159others(7): Show | 11 | HG02630.hp2 HG02647.hp1 HG02922.hp1 others(8): Show |
intron_variant | MODIFIER | c.422-14366A>G | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23078499 | ||||||
chr22:23078548
|
G | T | 9 | a0001c0002t0001g0059a0001c0002t0001g0061a0001c0002t0001g0065others(6): Show | 9 | HG02004.hp2 HG02083.hp1 NA18942.hp2 others(6): Show |
intron_variant | MODIFIER | c.422-14415C>A | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23078548 | ||||||
chr22:23078558
|
C | T | 1 | a0001c0001t0001g0177 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.422-14425G>A | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23078558 | ||||||
chr22:23078727
|
T | G | 281 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0147others(278): Show | 282 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(279): Show |
intron_variant | MODIFIER | c.422-14594A>C | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23078727 | ||||||
chr22:23078791
|
G | T | 2 | a0001c0002t0001g0019a0001c0002t0001g0020 | 2 | HG02280.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.422-14658C>A | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23078791 | ||||||
chr22:23078855
|
G | A | 1 | a0001c0001t0001g0268 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.422-14722C>T | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23078855 | ||||||
chr22:23078872
|
C | A | 200 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0148others(197): Show | 201 | HG00099.hp1 HG00544.hp1 HG00544.hp2 others(198): Show |
intron_variant | MODIFIER | c.422-14739G>T | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23078872 | ||||||
chr22:23078915
|
C | A | 3 | a0001c0001t0001g0148a0001c0001t0001g0171a0001c0002t0001g0023 | 3 | HG02055.hp2 HG02922.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.422-14782G>T | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23078915 | ||||||
chr22:23078928
|
C | T | 1 | a0002c0003t0001g0122 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.422-14795G>A | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23078928 | ||||||
chr22:23078995
|
C | T | 1 | a0001c0002t0001g0108 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.422-14862G>A | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23078995 | ||||||
chr22:23078996
|
G | A | 1 | a0001c0001t0001g0164 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.422-14863C>T | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23078996 | ||||||
chr22:23079031
|
A | G | 5 | a0001c0001t0001g0228a0001c0001t0001g0230a0001c0001t0001g0231others(2): Show | 5 | HG03491.hp1 HG03492.hp1 HG03688.hp1 others(2): Show |
intron_variant | MODIFIER | c.422-14898T>C | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23079031 | ||||||
chr22:23079078
|
A | T | 254 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0126others(251): Show | 256 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(253): Show |
intron_variant | MODIFIER | c.422-14945T>A | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23079078 | ||||||
chr22:23079092
|
G | A | 1 | a0001c0001t0001g0272 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.422-14959C>T | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23079092 | ||||||
chr22:23079197
|
A | G | 1 | a0001c0001t0001g0127 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.422-15064T>C | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23079197 | ||||||
chr22:23079377
|
G | C | 1 | a0001c0001t0001g0246 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.422-15244C>G | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23079377 | ||||||
chr22:23079550
|
T | C | 41 | a0001c0001t0001g0166a0001c0001t0001g0167a0001c0001t0001g0168others(38): Show | 41 | HG00609.hp1 HG01169.hp1 HG01891.hp1 others(38): Show |
intron_variant | MODIFIER | c.422-15417A>G | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23079550 | ||||||
chr22:23079565
|
G | A | 5 | a0001c0001t0001g0008a0001c0001t0001g0251a0001c0001t0001g0252others(2): Show | 5 | HG01192.hp2 HG01358.hp1 HG01928.hp1 others(2): Show |
intron_variant | MODIFIER | c.422-15432C>T | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23079565 | ||||||
chr22:23079662
|
G | A | 3 | a0001c0001t0001g0151a0001c0001t0001g0286a0001c0001t0001g0287 | 3 | HG01346.hp2 HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.422-15529C>T | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23079662 | ||||||
chr22:23079731
|
G | A | 1 | a0001c0002t0001g0084 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.422-15598C>T | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23079731 | ||||||
chr22:23079866
|
G | A | 94 | a0001c0001t0001g0008a0001c0001t0001g0147a0001c0001t0001g0148others(91): Show | 94 | HG00099.hp1 HG00280.hp2 HG00558.hp1 others(91): Show |
intron_variant | MODIFIER | c.422-15733C>T | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23079866 | ||||||
chr22:23079953
|
G | A | 1 | a0005c0005t0001g0243 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.422-15820C>T | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23079953 | ||||||
chr22:23079999
|
A | G | 96 | a0001c0001t0001g0008a0001c0001t0001g0147a0001c0001t0001g0148others(93): Show | 96 | HG00099.hp1 HG00280.hp2 HG00558.hp1 others(93): Show |
intron_variant | MODIFIER | c.422-15866T>C | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23079999 | ||||||
chr22:23080064
|
G | A | 1 | a0001c0001t0001g0177 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.422-15931C>T | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23080064 | ||||||
chr22:23080346
|
A | G | 1 | a0001c0001t0001g0157 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.422-16213T>C | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23080346 | ||||||
chr22:23080400
|
CAGA | C | 35 | a0001c0001t0001g0001a0001c0001t0001g0157a0001c0001t0001g0158others(32): Show | 36 | HG00673.hp1 HG00741.hp2 HG02258.hp1 others(33): Show |
intron_variant | MODIFIER | c.422-16270_422-1626 others(7): Show |
RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23080400 | ||||||
chr22:23080438
|
G | C | 1 | a0001c0002t0001g0139 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.422-16305C>G | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23080438 | ||||||
chr22:23080570
|
C | A | 2 | a0001c0001t0001g0219a0001c0001t0001g0224 | 2 | HG02129.hp2 NA18747.hp2 |
intron_variant | MODIFIER | c.422-16437G>T | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23080570 | ||||||
chr22:23080573
|
G | A | 1 | a0001c0001t0001g0157 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.422-16440C>T | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23080573 | ||||||
chr22:23080578
|
G | A | 19 | a0001c0001t0001g0166a0001c0001t0001g0167a0001c0001t0001g0168others(16): Show | 19 | HG02258.hp1 HG02280.hp2 HG02486.hp2 others(16): Show |
intron_variant | MODIFIER | c.422-16445C>T | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23080578 | ||||||
chr22:23080619
|
A | G | 1 | a0001c0001t0001g0160 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.422-16486T>C | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23080619 | ||||||
chr22:23080704
|
T | C | 150 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0147others(147): Show | 151 | HG00099.hp1 HG00280.hp2 HG00558.hp1 others(148): Show |
intron_variant | MODIFIER | c.422-16571A>G | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23080704 | ||||||
chr22:23080824
|
G | A | 1 | a0001c0001t0001g0157 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.422-16691C>T | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23080824 | ||||||
chr22:23080915
|
C | G | 1 | a0001c0001t0001g0263 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.422-16782G>C | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23080915 | ||||||
chr22:23080921
|
T | G | 150 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0147others(147): Show | 151 | HG00099.hp1 HG00280.hp2 HG00558.hp1 others(148): Show |
intron_variant | MODIFIER | c.422-16788A>C | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23080921 | ||||||
chr22:23080937
|
C | T | 11 | a0001c0001t0001g0166a0001c0001t0001g0167a0001c0001t0001g0168others(8): Show | 11 | HG02280.hp2 HG02486.hp2 HG02647.hp2 others(8): Show |
intron_variant | MODIFIER | c.422-16804G>A | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23080937 | ||||||
chr22:23081056
|
A | G | 1 | a0001c0002t0001g0021 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.422-16923T>C | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23081056 | ||||||
chr22:23081061
|
G | A | 131 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0147others(128): Show | 132 | HG00099.hp1 HG00280.hp2 HG00558.hp1 others(129): Show |
intron_variant | MODIFIER | c.422-16928C>T | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23081061 | ||||||
chr22:23081257
|
G | C | 1 | a0001c0001t0001g0283 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.422-17124C>G | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23081257 | ||||||
chr22:23081261
|
G | A | 1 | a0005c0005t0001g0243 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.422-17128C>T | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23081261 | ||||||
chr22:23081395
|
G | A | 1 | a0001c0001t0001g0157 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.422-17262C>T | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23081395 | ||||||
chr22:23081500
|
A | T | 2 | a0001c0001t0001g0289a0001c0001t0001g0300 | 2 | HG00673.hp1 HG00741.hp2 |
intron_variant | MODIFIER | c.422-17367T>A | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23081500 | ||||||
chr22:23081506
|
TGTTATAG others(9): Show |
T | 20 | a0001c0001t0001g0166a0001c0001t0001g0167a0001c0001t0001g0168others(17): Show | 20 | HG02258.hp1 HG02280.hp2 HG02486.hp2 others(17): Show |
intron_variant | MODIFIER | c.422-17389_422-1737 others(20): Show |
RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23081506 | ||||||
chr22:23081572
|
AG | A | 15 | a0001c0001t0001g0164a0001c0001t0001g0312a0001c0002t0002g0011others(12): Show | 15 | HG01109.hp1 HG01243.hp1 HG01891.hp2 others(12): Show |
intron_variant | MODIFIER | c.422-17440delC | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23081572 | ||||||
chr22:23081617
|
T | A | 1 | a0001c0001t0001g0189 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.422-17484A>T | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23081617 | ||||||
chr22:23081648
|
C | G | 2 | a0001c0001t0001g0289a0001c0001t0001g0300 | 2 | HG00673.hp1 HG00741.hp2 |
intron_variant | MODIFIER | c.422-17515G>C | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23081648 | ||||||
chr22:23081691
|
G | C | 1 | a0001c0002t0001g0037 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.422-17558C>G | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23081691 | ||||||
chr22:23081777
|
G | A | 130 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0147others(127): Show | 131 | HG00099.hp1 HG00280.hp2 HG00558.hp1 others(128): Show |
intron_variant | MODIFIER | c.422-17644C>T | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23081777 | ||||||
chr22:23081786
|
C | T | 3 | a0003c0004t0001g0005a0003c0004t0001g0176a0003c0004t0001g0178 | 3 | HG03098.hp2 HG03139.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.422-17653G>A | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23081786 | ||||||
chr22:23081808
|
T | C | 1 | a0001c0001t0001g0194 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.422-17675A>G | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23081808 | ||||||
chr22:23081821
|
C | CA | 42 | a0001c0001t0001g0225a0001c0001t0001g0259a0001c0001t0001g0268others(39): Show | 42 | HG00597.hp1 HG00639.hp2 HG00741.hp1 others(39): Show |
intron_variant | MODIFIER | c.422-17689dupT | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23081821 | ||||||
chr22:23081821
|
C | CAA | 8 | a0001c0001t0001g0164a0001c0001t0001g0312a0001c0002t0001g0030others(5): Show | 8 | HG01106.hp2 HG01192.hp1 HG01243.hp1 others(5): Show |
intron_variant | MODIFIER | c.422-17690_422-1768 others(6): Show |
RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23081821 | ||||||
chr22:23081821
|
CA | C | 105 | a0001c0001t0001g0001a0001c0001t0001g0149a0001c0001t0001g0150others(102): Show | 106 | HG00099.hp1 HG00280.hp2 HG00558.hp1 others(103): Show |
intron_variant | MODIFIER | c.422-17689delT | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23081821 | ||||||
chr22:23081851
|
C | T | 1 | a0001c0002t0001g0080 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.422-17718G>A | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23081851 | ||||||
chr22:23081854
|
A | G | 1 | a0002c0003t0001g0114 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.422-17721T>C | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23081854 | ||||||
chr22:23081891
|
C | T | 20 | a0001c0001t0001g0166a0001c0001t0001g0167a0001c0001t0001g0168others(17): Show | 20 | HG02258.hp1 HG02280.hp2 HG02486.hp2 others(17): Show |
intron_variant | MODIFIER | c.422-17758G>A | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23081891 | ||||||
chr22:23081922
|
G | C | 33 | a0001c0001t0001g0001a0001c0001t0001g0158a0001c0001t0001g0159others(30): Show | 34 | HG02258.hp1 HG02280.hp2 HG02486.hp2 others(31): Show |
intron_variant | MODIFIER | c.422-17789C>G | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23081922 | ||||||
chr22:23082056
|
C | T | 33 | a0001c0001t0001g0001a0001c0001t0001g0158a0001c0001t0001g0159others(30): Show | 34 | HG02258.hp1 HG02280.hp2 HG02486.hp2 others(31): Show |
intron_variant | MODIFIER | c.422-17923G>A | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23082056 | ||||||
chr22:23082084
|
C | T | 86 | a0001c0001t0001g0008a0001c0001t0001g0148a0001c0001t0001g0149others(83): Show | 86 | HG00099.hp1 HG00280.hp2 HG00558.hp1 others(83): Show |
intron_variant | MODIFIER | c.422-17951G>A | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23082084 | ||||||
chr22:23082104
|
G | A | 4 | a0001c0001t0001g0222a0001c0001t0001g0223a0001c0001t0001g0307others(1): Show | 4 | NA18984.hp1 NA19060.hp1 NA19070.hp1 others(1): Show |
intron_variant | MODIFIER | c.422-17971C>T | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23082104 | ||||||
chr22:23082135
|
C | A | 1 | a0001c0002t0001g0097 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.422-18002G>T | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23082135 | ||||||
chr22:23082135
|
C | CA | 11 | a0001c0001t0001g0126a0001c0001t0001g0127a0001c0001t0001g0258others(8): Show | 11 | HG00642.hp2 HG01192.hp1 HG02015.hp2 others(8): Show |
intron_variant | MODIFIER | c.422-18003dupT | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23082135 | ||||||
chr22:23082135
|
CA | C | 19 | a0001c0001t0001g0157a0001c0001t0001g0164a0001c0001t0001g0183others(16): Show | 19 | HG01109.hp1 HG01243.hp1 HG01891.hp2 others(16): Show |
intron_variant | MODIFIER | c.422-18003delT | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23082135 | ||||||
chr22:23082135
|
CAA | C | 129 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0147others(126): Show | 130 | HG00099.hp1 HG00280.hp2 HG00558.hp1 others(127): Show |
intron_variant | MODIFIER | c.422-18004_422-1800 others(6): Show |
RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23082135 | ||||||
chr22:23082137
|
A | C | 1 | a0001c0001t0001g0295 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.422-18004T>G | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23082137 | ||||||
chr22:23082138
|
A | C | 1 | a0001c0002t0001g0032 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.422-18005T>G | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23082138 | ||||||
chr22:23082139
|
A | C | 2 | a0001c0001t0001g0277a0001c0002t0001g0139 | 2 | HG01081.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.422-18006T>G | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23082139 | ||||||
chr22:23082140
|
A | C | 1 | a0001c0002t0001g0037 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.422-18007T>G | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23082140 | ||||||
chr22:23082251
|
C | T | 1 | a0001c0001t0001g0157 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.422-18118G>A | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23082251 | ||||||
chr22:23082285
|
C | T | 12 | a0001c0001t0001g0001a0001c0001t0001g0158a0001c0001t0001g0159others(9): Show | 13 | HG02615.hp2 HG02630.hp2 HG02647.hp1 others(10): Show |
intron_variant | MODIFIER | c.422-18152G>A | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23082285 | ||||||
chr22:23082375
|
C | T | 1 | a0005c0015t0002g0010 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.422-18242G>A | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23082375 | ||||||
chr22:23082377
|
A | AT | 13 | a0001c0001t0001g0174a0001c0001t0001g0215a0001c0001t0001g0273others(10): Show | 13 | HG00673.hp1 HG00673.hp2 HG00741.hp2 others(10): Show |
intron_variant | MODIFIER | c.422-18245dupA | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23082377 | ||||||
chr22:23082377
|
A | T | 1 | a0005c0005t0001g0243 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.422-18244T>A | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23082377 | ||||||
chr22:23082377
|
AT | A | 100 | a0001c0001t0001g0008a0001c0001t0001g0147a0001c0001t0001g0148others(97): Show | 100 | HG00099.hp1 HG00280.hp2 HG00558.hp1 others(97): Show |
intron_variant | MODIFIER | c.422-18245delA | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23082377 | ||||||
chr22:23082466
|
G | A | 7 | a0001c0001t0001g0147a0001c0001t0001g0152a0001c0001t0001g0153others(4): Show | 7 | HG02145.hp2 HG02257.hp2 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.422-18333C>T | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23082466 | ||||||
chr22:23082938
|
A | G | 2 | a0001c0001t0001g0289a0001c0001t0001g0300 | 2 | HG00673.hp1 HG00741.hp2 |
intron_variant | MODIFIER | c.422-18805T>C | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23082938 | ||||||
chr22:23082982
|
C | T | 1 | a0007c0013t0001g0035 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.422-18849G>A | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23082982 | ||||||
chr22:23083199
|
T | C | 2 | a0001c0002t0001g0096a0001c0002t0001g0097 | 2 | HG01257.hp1 HG02602.hp1 |
intron_variant | MODIFIER | c.422-19066A>G | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23083199 | ||||||
chr22:23083341
|
G | C | 149 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0147others(146): Show | 150 | HG00099.hp1 HG00280.hp2 HG00558.hp1 others(147): Show |
intron_variant | MODIFIER | c.422-19208C>G | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23083341 | ||||||
chr22:23083430
|
G | A | 1 | a0001c0002t0001g0087 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.422-19297C>T | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23083430 | ||||||
chr22:23083736
|
A | G | 133 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0147others(130): Show | 134 | HG00099.hp1 HG00280.hp2 HG00558.hp1 others(131): Show |
intron_variant | MODIFIER | c.422-19603T>C | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23083736 | ||||||
chr22:23083744
|
G | C | 133 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0147others(130): Show | 134 | HG00099.hp1 HG00280.hp2 HG00558.hp1 others(131): Show |
intron_variant | MODIFIER | c.422-19611C>G | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23083744 | ||||||
chr22:23083798
|
C | T | 1 | a0001c0002t0001g0079 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.422-19665G>A | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23083798 | ||||||
chr22:23083891
|
A | G | 5 | a0001c0001t0001g0185a0001c0001t0001g0199a0001c0001t0001g0237others(2): Show | 5 | HG00609.hp2 HG01261.hp2 HG02293.hp1 others(2): Show |
intron_variant | MODIFIER | c.422-19758T>C | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23083891 | ||||||
chr22:23084188
|
A | G | 2 | a0001c0002t0001g0057a0001c0002t0001g0058 | 2 | NA19004.hp2 NA19086.hp2 |
intron_variant | MODIFIER | c.422-20055T>C | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23084188 | ||||||
chr22:23084298
|
C | G | 1 | a0001c0001t0001g0200 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.422-20165G>C | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23084298 | ||||||
chr22:23084468
|
G | T | 1 | a0001c0001t0001g0152 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.422-20335C>A | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23084468 | ||||||
chr22:23084691
|
T | C | 5 | a0001c0001t0001g0274a0001c0001t0001g0276a0001c0001t0001g0277others(2): Show | 5 | HG01070.hp2 HG02109.hp2 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.422-20558A>G | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23084691 | ||||||
chr22:23084746
|
A | G | 133 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0147others(130): Show | 134 | HG00099.hp1 HG00280.hp2 HG00558.hp1 others(131): Show |
intron_variant | MODIFIER | c.422-20613T>C | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23084746 | ||||||
chr22:23084780
|
G | A | 2 | a0001c0002t0001g0084a0001c0002t0001g0098 | 2 | NA18952.hp2 NA19079.hp1 |
intron_variant | MODIFIER | c.422-20647C>T | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23084780 | ||||||
chr22:23084832
|
G | A | 1 | a0001c0002t0001g0081 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.422-20699C>T | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23084832 | ||||||
chr22:23084917
|
C | T | 1 | a0001c0001t0001g0157 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.422-20784G>A | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23084917 | ||||||
chr22:23084918
|
G | A | 2 | a0001c0001t0001g0289a0001c0001t0001g0300 | 2 | HG00673.hp1 HG00741.hp2 |
intron_variant | MODIFIER | c.422-20785C>T | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23084918 | ||||||
chr22:23085486
|
G | A | 1 | a0005c0005t0001g0243 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.422-21353C>T | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23085486 | ||||||
chr22:23085805
|
G | A | 1 | a0001c0001t0001g0157 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.422-21672C>T | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23085805 | ||||||
chr22:23085982
|
G | A | 10 | a0001c0001t0001g0001a0001c0001t0001g0158a0001c0001t0001g0159others(7): Show | 11 | HG02630.hp2 HG02647.hp1 HG02922.hp1 others(8): Show |
intron_variant | MODIFIER | c.422-21849C>T | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23085982 | ||||||
chr22:23086247
|
T | C | 133 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0147others(130): Show | 134 | HG00099.hp1 HG00280.hp2 HG00558.hp1 others(131): Show |
intron_variant | MODIFIER | c.422-22114A>G | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23086247 | ||||||
chr22:23086384
|
G | A | 2 | a0001c0002t0001g0084a0001c0002t0001g0098 | 2 | NA18952.hp2 NA19079.hp1 |
intron_variant | MODIFIER | c.422-22251C>T | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23086384 | ||||||
chr22:23086437
|
G | A | 1 | a0001c0001t0001g0157 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.422-22304C>T | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23086437 | ||||||
chr22:23086509
|
C | T | 1 | a0005c0005t0001g0243 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.422-22376G>A | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23086509 | ||||||
chr22:23086511
|
C | T | 2 | a0001c0001t0001g0264a0001c0001t0001g0268 | 2 | HG02602.hp2 HG03017.hp1 |
intron_variant | MODIFIER | c.422-22378G>A | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23086511 | ||||||
chr22:23086623
|
A | C | 134 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0147others(131): Show | 135 | HG00099.hp1 HG00280.hp2 HG00558.hp1 others(132): Show |
intron_variant | MODIFIER | c.422-22490T>G | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23086623 | ||||||
chr22:23086883
|
C | T | 1 | a0005c0005t0001g0243 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.422-22750G>A | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23086883 | ||||||
chr22:23086897
|
C | A | 32 | a0001c0001t0001g0001a0001c0001t0001g0158a0001c0001t0001g0159others(29): Show | 33 | HG02258.hp1 HG02280.hp2 HG02486.hp2 others(30): Show |
intron_variant | MODIFIER | c.422-22764G>T | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23086897 | ||||||
chr22:23086994
|
G | A | 2 | a0001c0002t0001g0066a0001c0002t0001g0100 | 2 | NA18946.hp1 NA18982.hp2 |
intron_variant | MODIFIER | c.422-22861C>T | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23086994 | ||||||
chr22:23087037
|
C | T | 91 | a0001c0001t0001g0008a0001c0001t0001g0148a0001c0001t0001g0149others(88): Show | 91 | HG00099.hp1 HG00280.hp2 HG00558.hp1 others(88): Show |
intron_variant | MODIFIER | c.422-22904G>A | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23087037 | ||||||
chr22:23087343
|
G | A | 1 | a0005c0005t0001g0299 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.422-23210C>T | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23087343 | ||||||
chr22:23087358
|
C | T | 1 | a0002c0003t0001g0117 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.422-23225G>A | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23087358 | ||||||
chr22:23087365
|
C | G | 99 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0147others(96): Show | 100 | HG00099.hp1 HG00280.hp2 HG00558.hp1 others(97): Show |
intron_variant | MODIFIER | c.422-23232G>C | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23087365 | ||||||
chr22:23087377
|
T | C | 8 | a0001c0001t0001g0147a0001c0001t0001g0152a0001c0001t0001g0153others(5): Show | 8 | HG02145.hp2 HG02257.hp2 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.422-23244A>G | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23087377 | ||||||
chr22:23087395
|
T | C | 11 | a0001c0001t0001g0001a0001c0001t0001g0158a0001c0001t0001g0159others(8): Show | 12 | HG02258.hp2 HG02630.hp2 HG02647.hp1 others(9): Show |
intron_variant | MODIFIER | c.422-23262A>G | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23087395 | ||||||
chr22:23087501
|
C | T | 1 | a0002c0003t0001g0119 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.422-23368G>A | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23087501 | ||||||
chr22:23087569
|
T | C | 132 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0147others(129): Show | 133 | HG00099.hp1 HG00280.hp2 HG00558.hp1 others(130): Show |
intron_variant | MODIFIER | c.422-23436A>G | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23087569 | ||||||
chr22:23087601
|
C | T | 1 | a0001c0001t0001g0269 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.422-23468G>A | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23087601 | ||||||
chr22:23087966
|
A | G | 130 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0147others(127): Show | 131 | HG00099.hp1 HG00280.hp2 HG00558.hp1 others(128): Show |
intron_variant | MODIFIER | c.422-23833T>C | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23087966 | ||||||
chr22:23088223
|
A | G | 131 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0147others(128): Show | 132 | HG00099.hp1 HG00280.hp2 HG00558.hp1 others(129): Show |
intron_variant | MODIFIER | c.422-24090T>C | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23088223 | ||||||
chr22:23088506
|
A | G | 130 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0147others(127): Show | 131 | HG00099.hp1 HG00280.hp2 HG00558.hp1 others(128): Show |
intron_variant | MODIFIER | c.422-24373T>C | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23088506 | ||||||
chr22:23088540
|
C | T | 1 | a0001c0002t0002g0131 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.422-24407G>A | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23088540 | ||||||
chr22:23088681
|
T | C | 20 | a0001c0001t0001g0166a0001c0001t0001g0167a0001c0001t0001g0168others(17): Show | 20 | HG02258.hp1 HG02280.hp2 HG02486.hp2 others(17): Show |
intron_variant | MODIFIER | c.422-24548A>G | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23088681 | ||||||
chr22:23088695
|
C | T | 1 | a0001c0002t0001g0014 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.422-24562G>A | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23088695 | ||||||
chr22:23088702
|
A | G | 3 | a0001c0001t0001g0266a0001c0001t0001g0271a0001c0001t0001g0272 | 3 | HG00642.hp1 HG01358.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.422-24569T>C | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23088702 | ||||||
chr22:23088729
|
G | A | 1 | a0001c0002t0001g0110 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.422-24596C>T | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23088729 | ||||||
chr22:23088903
|
T | C | 129 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0147others(126): Show | 130 | HG00099.hp1 HG00280.hp2 HG00558.hp1 others(127): Show |
intron_variant | MODIFIER | c.422-24770A>G | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23088903 | ||||||
chr22:23088967
|
G | T | 1 | a0005c0005t0001g0299 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.422-24834C>A | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23088967 | ||||||
chr22:23089160
|
G | A | 86 | a0001c0001t0001g0008a0001c0001t0001g0148a0001c0001t0001g0149others(83): Show | 86 | HG00099.hp1 HG00280.hp2 HG00558.hp1 others(83): Show |
intron_variant | MODIFIER | c.422-25027C>T | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23089160 | ||||||
chr22:23089193
|
A | T | 5 | a0001c0001t0001g0152a0001c0001t0001g0153a0001c0001t0001g0154others(2): Show | 5 | HG02257.hp2 HG02630.hp1 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.422-25060T>A | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23089193 | ||||||
chr22:23089205
|
G | A | 1 | a0001c0001t0001g0185 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.422-25072C>T | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23089205 | ||||||
chr22:23089400
|
G | A | 1 | a0001c0001t0001g0002 | 2 | HG01257.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.422-25267C>T | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23089400 | ||||||
chr22:23089550
|
G | A | 20 | a0001c0001t0001g0166a0001c0001t0001g0167a0001c0001t0001g0168others(17): Show | 20 | HG02258.hp1 HG02280.hp2 HG02486.hp2 others(17): Show |
intron_variant | MODIFIER | c.422-25417C>T | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23089550 | ||||||
chr22:23089576
|
A | C | 129 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0147others(126): Show | 130 | HG00099.hp1 HG00280.hp2 HG00558.hp1 others(127): Show |
intron_variant | MODIFIER | c.422-25443T>G | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23089576 | ||||||
chr22:23089669
|
G | A | 31 | a0001c0001t0001g0001a0001c0001t0001g0158a0001c0001t0001g0159others(28): Show | 32 | HG02258.hp1 HG02258.hp2 HG02280.hp2 others(29): Show |
intron_variant | MODIFIER | c.422-25536C>T | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23089669 | ||||||
chr22:23089776
|
T | C | 1 | a0001c0001t0001g0164 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.422-25643A>G | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23089776 | ||||||
chr22:23090019
|
C | T | 1 | a0001c0002t0001g0145 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.422-25886G>A | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23090019 | ||||||
chr22:23090020
|
C | G | 1 | a0001c0002t0001g0078 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.422-25887G>C | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23090020 | ||||||
chr22:23090047
|
C | T | 127 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0147others(124): Show | 128 | HG00099.hp1 HG00280.hp2 HG00558.hp1 others(125): Show |
intron_variant | MODIFIER | c.422-25914G>A | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23090047 | ||||||
chr22:23090457
|
G | A | 85 | a0001c0001t0001g0008a0001c0001t0001g0148a0001c0001t0001g0149others(82): Show | 85 | HG00099.hp1 HG00280.hp2 HG00558.hp1 others(82): Show |
intron_variant | MODIFIER | c.422-26324C>T | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23090457 | ||||||
chr22:23090562
|
C | T | 2 | a0001c0001t0001g0191a0001c0001t0001g0198 | 2 | HG01891.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.422-26429G>A | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23090562 | ||||||
chr22:23090850
|
C | G | 2 | a0001c0001t0001g0289a0001c0001t0001g0300 | 2 | HG00673.hp1 HG00741.hp2 |
intron_variant | MODIFIER | c.422-26717G>C | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23090850 | ||||||
chr22:23091056
|
C | G | 91 | a0001c0001t0001g0008a0001c0001t0001g0148a0001c0001t0001g0149others(88): Show | 91 | HG00099.hp1 HG00280.hp2 HG00558.hp1 others(88): Show |
intron_variant | MODIFIER | c.422-26923G>C | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23091056 | ||||||
chr22:23091069
|
C | T | 1 | a0005c0005t0001g0243 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.422-26936G>A | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23091069 | ||||||
chr22:23091079
|
C | G | 20 | a0001c0001t0001g0166a0001c0001t0001g0167a0001c0001t0001g0168others(17): Show | 20 | HG02258.hp1 HG02280.hp2 HG02486.hp2 others(17): Show |
intron_variant | MODIFIER | c.422-26946G>C | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23091079 | ||||||
chr22:23091208
|
G | A | 1 | a0001c0001t0001g0157 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.422-27075C>T | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23091208 | ||||||
chr22:23091229
|
C | T | 1 | a0001c0001t0001g0295 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.422-27096G>A | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23091229 | ||||||
chr22:23091461
|
C | T | 1 | a0001c0001t0001g0202 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.422-27328G>A | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23091461 | ||||||
chr22:23091476
|
A | G | 2 | a0001c0002t0001g0024a0001c0010t0001g0290 | 2 | HG02615.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.422-27343T>C | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23091476 | ||||||
chr22:23091561
|
T | C | 134 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0147others(131): Show | 135 | HG00099.hp1 HG00280.hp2 HG00558.hp1 others(132): Show |
intron_variant | MODIFIER | c.422-27428A>G | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23091561 | ||||||
chr22:23091567
|
C | T | 1 | a0001c0001t0001g0177 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.422-27434G>A | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23091567 | ||||||
chr22:23091611
|
C | T | 5 | a0001c0001t0001g0001a0001c0001t0001g0163a0001c0001t0001g0165others(2): Show | 6 | HG02630.hp2 HG02647.hp1 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.422-27478G>A | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23091611 | ||||||
chr22:23091612
|
G | A | 2 | a0002c0003t0001g0114a0002c0003t0001g0115 | 2 | NA19010.hp2 NA19068.hp2 |
intron_variant | MODIFIER | c.422-27479C>T | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23091612 | ||||||
chr22:23091617
|
T | C | 134 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0147others(131): Show | 135 | HG00099.hp1 HG00280.hp2 HG00558.hp1 others(132): Show |
intron_variant | MODIFIER | c.422-27484A>G | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23091617 | ||||||
chr22:23091636
|
A | G | 1 | a0004c0006t0002g0009 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.422-27503T>C | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23091636 | ||||||
chr22:23091642
|
A | T | 2 | a0001c0001t0001g0256a0001c0001t0001g0309 | 2 | HG00099.hp2 HG01106.hp1 |
intron_variant | MODIFIER | c.422-27509T>A | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23091642 | ||||||
chr22:23091676
|
G | A | 131 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0147others(128): Show | 132 | HG00099.hp1 HG00280.hp2 HG00558.hp1 others(129): Show |
intron_variant | MODIFIER | c.422-27543C>T | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23091676 | ||||||
chr22:23091703
|
G | A | 44 | a0001c0001t0001g0001a0001c0001t0001g0147a0001c0001t0001g0152others(41): Show | 45 | HG00673.hp1 HG00741.hp2 HG02145.hp2 others(42): Show |
intron_variant | MODIFIER | c.422-27570C>T | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23091703 | ||||||
chr22:23091910
|
T | G | 2 | a0001c0001t0001g0148a0001c0002t0001g0023 | 2 | HG02055.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.422-27777A>C | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23091910 | ||||||
chr22:23091959
|
C | T | 14 | a0001c0001t0001g0312a0001c0002t0002g0011a0001c0002t0002g0012others(11): Show | 14 | HG01109.hp1 HG01243.hp1 HG01891.hp2 others(11): Show |
intron_variant | MODIFIER | c.422-27826G>A | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23091959 | ||||||
chr22:23092124
|
T | TC | 134 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0147others(131): Show | 135 | HG00099.hp1 HG00280.hp2 HG00558.hp1 others(132): Show |
intron_variant | MODIFIER | c.422-27992dupG | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23092124 | ||||||
chr22:23092140
|
G | A | 74 | a0001c0001t0001g0225a0001c0001t0001g0291a0001c0002t0001g0006others(71): Show | 74 | HG00544.hp1 HG00544.hp2 HG00558.hp2 others(71): Show |
intron_variant | MODIFIER | c.422-28007C>T | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23092140 | ||||||
chr22:23092392
|
C | T | 1 | a0001c0002t0001g0145 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.422-28259G>A | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23092392 | ||||||
chr22:23092406
|
C | G | 151 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0147others(148): Show | 152 | HG00099.hp1 HG00280.hp2 HG00558.hp1 others(149): Show |
intron_variant | MODIFIER | c.422-28273G>C | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23092406 | ||||||
chr22:23092421
|
G | A | 1 | a0003c0004t0001g0175 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.422-28288C>T | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23092421 | ||||||
chr22:23092557
|
T | C | 1 | a0004c0006t0002g0009 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.422-28424A>G | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23092557 | ||||||
chr22:23092618
|
G | A | 1 | a0001c0001t0001g0157 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.422-28485C>T | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23092618 | ||||||
chr22:23092854
|
C | T | 1 | a0001c0002t0001g0143 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.422-28721G>A | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23092854 | ||||||
chr22:23092855
|
G | A | 5 | a0001c0001t0001g0152a0001c0001t0001g0153a0001c0001t0001g0154others(2): Show | 5 | HG02257.hp2 HG02630.hp1 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.422-28722C>T | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23092855 | ||||||
chr22:23092964
|
G | A | 43 | a0001c0001t0001g0001a0001c0001t0001g0147a0001c0001t0001g0152others(40): Show | 44 | HG00673.hp1 HG00741.hp2 HG02145.hp2 others(41): Show |
intron_variant | MODIFIER | c.422-28831C>T | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23092964 | ||||||
chr22:23093208
|
C | T | 1 | a0001c0002t0002g0138 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.422-29075G>A | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23093208 | ||||||
chr22:23093219
|
T | A | 1 | a0001c0002t0001g0110 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.422-29086A>T | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23093219 | ||||||
chr22:23093293
|
C | T | 1 | a0001c0001t0001g0242 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.422-29160G>A | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23093293 | ||||||
chr22:23093426
|
C | T | 20 | a0001c0001t0001g0166a0001c0001t0001g0167a0001c0001t0001g0168others(17): Show | 20 | HG02258.hp1 HG02280.hp2 HG02486.hp2 others(17): Show |
intron_variant | MODIFIER | c.422-29293G>A | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23093426 | ||||||
chr22:23093439
|
G | T | 1 | a0001c0002t0001g0041 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.422-29306C>A | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23093439 | ||||||
chr22:23093468
|
G | C | 21 | a0001c0001t0001g0001a0001c0001t0001g0147a0001c0001t0001g0152others(18): Show | 22 | HG02145.hp2 HG02257.hp2 HG02258.hp2 others(19): Show |
intron_variant | MODIFIER | c.422-29335C>G | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23093468 | ||||||
chr22:23094098
|
C | T | 43 | a0001c0001t0001g0001a0001c0001t0001g0147a0001c0001t0001g0152others(40): Show | 44 | HG00673.hp1 HG00741.hp2 HG02145.hp2 others(41): Show |
intron_variant | MODIFIER | c.422-29965G>A | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23094098 | ||||||
chr22:23094157
|
G | A | 14 | a0001c0001t0001g0312a0001c0002t0002g0011a0001c0002t0002g0012others(11): Show | 14 | HG01109.hp1 HG01243.hp1 HG01891.hp2 others(11): Show |
intron_variant | MODIFIER | c.422-30024C>T | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23094157 | ||||||
chr22:23094158
|
C | G | 14 | a0001c0001t0001g0312a0001c0002t0002g0011a0001c0002t0002g0012others(11): Show | 14 | HG01109.hp1 HG01243.hp1 HG01891.hp2 others(11): Show |
intron_variant | MODIFIER | c.422-30025G>C | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23094158 | ||||||
chr22:23094180
|
G | T | 1 | a0004c0009t0001g0311 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.422-30047C>A | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23094180 | ||||||
chr22:23094237
|
T | C | 150 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0147others(147): Show | 151 | HG00099.hp1 HG00280.hp2 HG00558.hp1 others(148): Show |
intron_variant | MODIFIER | c.422-30104A>G | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23094237 | ||||||
chr22:23094308
|
C | T | 1 | a0001c0002t0001g0145 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.422-30175G>A | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23094308 | ||||||
chr22:23094400
|
GC | G | 3 | a0001c0002t0001g0047a0002c0003t0001g0122a0002c0003t0001g0124 | 3 | HG02698.hp1 HG02738.hp1 HG02738.hp2 |
intron_variant | MODIFIER | c.422-30268delG | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23094400 | ||||||
chr22:23094437
|
G | A | 1 | a0007c0013t0001g0035 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.422-30304C>T | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23094437 | ||||||
chr22:23094708
|
C | T | 5 | a0001c0001t0001g0152a0001c0001t0001g0153a0001c0001t0001g0154others(2): Show | 5 | HG02257.hp2 HG02630.hp1 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.422-30575G>A | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23094708 | ||||||
chr22:23094819
|
C | T | 1 | a0001c0011t0001g0211 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.422-30686G>A | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23094819 | ||||||
chr22:23094854
|
C | T | 1 | a0001c0001t0001g0157 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.422-30721G>A | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23094854 | ||||||
chr22:23095065
|
G | A | 11 | a0001c0001t0001g0001a0001c0001t0001g0158a0001c0001t0001g0159others(8): Show | 12 | HG02258.hp2 HG02630.hp2 HG02647.hp1 others(9): Show |
intron_variant | MODIFIER | c.422-30932C>T | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23095065 | ||||||
chr22:23095075
|
A | G | 11 | a0001c0001t0001g0312a0001c0002t0002g0011a0001c0002t0002g0012others(8): Show | 11 | HG01243.hp1 HG02055.hp1 HG02109.hp1 others(8): Show |
intron_variant | MODIFIER | c.422-30942T>C | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23095075 | ||||||
chr22:23095084
|
G | A | 127 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0148others(124): Show | 128 | HG00099.hp1 HG00280.hp2 HG00558.hp1 others(125): Show |
intron_variant | MODIFIER | c.422-30951C>T | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23095084 | ||||||
chr22:23095109
|
G | A | 11 | a0001c0001t0001g0001a0001c0001t0001g0158a0001c0001t0001g0159others(8): Show | 12 | HG02258.hp2 HG02630.hp2 HG02647.hp1 others(9): Show |
intron_variant | MODIFIER | c.422-30976C>T | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23095109 | ||||||
chr22:23095170
|
A | G | 1 | a0001c0001t0001g0263 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.422-31037T>C | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23095170 | ||||||
chr22:23095197
|
T | G | 1 | a0001c0002t0001g0128 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.422-31064A>C | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23095197 | ||||||
chr22:23095280
|
C | T | 1 | a0001c0002t0002g0133 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.422-31147G>A | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23095280 | ||||||
chr22:23095289
|
G | A | 1 | a0001c0001t0001g0267 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.422-31156C>T | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23095289 | ||||||
chr22:23095312
|
C | T | 1 | a0001c0002t0001g0100 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.422-31179G>A | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23095312 | ||||||
chr22:23095611
|
G | A | 20 | a0001c0001t0001g0166a0001c0001t0001g0167a0001c0001t0001g0168others(17): Show | 20 | HG02258.hp1 HG02280.hp2 HG02486.hp2 others(17): Show |
intron_variant | MODIFIER | c.422-31478C>T | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23095611 | ||||||
chr22:23095705
|
C | A | 1 | a0001c0001t0001g0202 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.422-31572G>T | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23095705 | ||||||
chr22:23095929
|
C | T | 2 | a0001c0001t0001g0126a0001c0001t0001g0127 | 2 | HG00642.hp2 HG03704.hp1 |
intron_variant | MODIFIER | c.422-31796G>A | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23095929 | ||||||
chr22:23096004
|
C | T | 87 | a0001c0001t0001g0008a0001c0001t0001g0148a0001c0001t0001g0149others(84): Show | 87 | HG00099.hp1 HG00280.hp2 HG00558.hp1 others(84): Show |
intron_variant | MODIFIER | c.422-31871G>A | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23096004 | ||||||
chr22:23096010
|
G | A | 1 | a0001c0002t0001g0094 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.422-31877C>T | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23096010 | ||||||
chr22:23096094
|
C | T | 2 | a0001c0002t0001g0019a0001c0002t0001g0020 | 2 | HG02280.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.422-31961G>A | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23096094 | ||||||
chr22:23096154
|
G | A | 1 | a0001c0001t0001g0285 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.422-32021C>T | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23096154 | ||||||
chr22:23096244
|
G | T | 2 | a0001c0001t0001g0284a0001c0001t0001g0288 | 2 | HG01071.hp2 HG01175.hp2 |
intron_variant | MODIFIER | c.422-32111C>A | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23096244 | ||||||
chr22:23096319
|
G | A | 1 | a0001c0001t0001g0157 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.422-32186C>T | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23096319 | ||||||
chr22:23096382
|
C | T | 1 | a0001c0001t0001g0300 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.422-32249G>A | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23096382 | ||||||
chr22:23096549
|
G | A | 1 | a0005c0005t0001g0243 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.422-32416C>T | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23096549 | ||||||
chr22:23096600
|
G | A | 1 | a0001c0002t0001g0030 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.422-32467C>T | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23096600 | ||||||
chr22:23096675
|
G | A | 1 | a0001c0001t0001g0233 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.422-32542C>T | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23096675 | ||||||
chr22:23096841
|
A | G | 5 | a0001c0001t0001g0152a0001c0001t0001g0153a0001c0001t0001g0154others(2): Show | 5 | HG02257.hp2 HG02630.hp1 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.422-32708T>C | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23096841 | ||||||
chr22:23096909
|
C | T | 20 | a0001c0001t0001g0166a0001c0001t0001g0167a0001c0001t0001g0168others(17): Show | 20 | HG02258.hp1 HG02280.hp2 HG02486.hp2 others(17): Show |
intron_variant | MODIFIER | c.422-32776G>A | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23096909 | ||||||
chr22:23097198
|
G | T | 5 | a0001c0002t0001g0059a0001c0002t0001g0065a0001c0002t0001g0093others(2): Show | 5 | NA18942.hp2 NA18944.hp2 NA19007.hp2 others(2): Show |
intron_variant | MODIFIER | c.422-33065C>A | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23097198 | ||||||
chr22:23097343
|
C | T | 86 | a0001c0001t0001g0008a0001c0001t0001g0148a0001c0001t0001g0149others(83): Show | 86 | HG00099.hp1 HG00280.hp2 HG00558.hp1 others(83): Show |
intron_variant | MODIFIER | c.422-33210G>A | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23097343 | ||||||
chr22:23097408
|
C | T | 1 | a0001c0001t0001g0157 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.422-33275G>A | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23097408 | ||||||
chr22:23097569
|
C | T | 41 | a0001c0001t0001g0001a0001c0001t0001g0147a0001c0001t0001g0152others(38): Show | 42 | HG00673.hp1 HG00741.hp2 HG02145.hp2 others(39): Show |
intron_variant | MODIFIER | c.422-33436G>A | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23097569 | ||||||
chr22:23097573
|
C | T | 1 | a0001c0001t0001g0308 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.422-33440G>A | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23097573 | ||||||
chr22:23097580
|
G | A | 1 | a0001c0001t0001g0304 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.422-33447C>T | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23097580 | ||||||
chr22:23097749
|
C | T | 1 | a0001c0002t0002g0131 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.422-33616G>A | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23097749 | ||||||
chr22:23097782
|
G | T | 1 | a0001c0002t0001g0060 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.422-33649C>A | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23097782 | ||||||
chr22:23097834
|
T | C | 2 | a0001c0002t0001g0024a0001c0010t0001g0290 | 2 | HG02615.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.422-33701A>G | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23097834 | ||||||
chr22:23097850
|
A | G | 12 | a0001c0001t0001g0001a0001c0001t0001g0158a0001c0001t0001g0159others(9): Show | 13 | HG02258.hp2 HG02630.hp2 HG02647.hp1 others(10): Show |
intron_variant | MODIFIER | c.422-33717T>C | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23097850 | ||||||
chr22:23097851
|
C | T | 5 | a0001c0001t0001g0001a0001c0001t0001g0163a0001c0001t0001g0165others(2): Show | 6 | HG02630.hp2 HG02647.hp1 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.422-33718G>A | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23097851 | ||||||
chr22:23097912
|
A | G | 134 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0147others(131): Show | 135 | HG00099.hp1 HG00280.hp2 HG00558.hp1 others(132): Show |
intron_variant | MODIFIER | c.422-33779T>C | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23097912 | ||||||
chr22:23098146
|
G | A | 1 | a0001c0001t0001g0251 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.422-34013C>T | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23098146 | ||||||
chr22:23098191
|
T | G | 1 | a0001c0002t0001g0039 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.422-34058A>C | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23098191 | ||||||
chr22:23098339
|
C | G | 92 | a0001c0001t0001g0008a0001c0001t0001g0148a0001c0001t0001g0149others(89): Show | 92 | HG00099.hp1 HG00280.hp2 HG00558.hp1 others(89): Show |
intron_variant | MODIFIER | c.422-34206G>C | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23098339 | ||||||
chr22:23098545
|
C | A | 2 | a0001c0002t0001g0024a0001c0010t0001g0290 | 2 | HG02615.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.422-34412G>T | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23098545 | ||||||
chr22:23098571
|
C | T | 1 | a0001c0001t0001g0201 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.422-34438G>A | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23098571 | ||||||
chr22:23098775
|
G | A | 1 | a0001c0001t0001g0294 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.422-34642C>T | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23098775 | ||||||
chr22:23098800
|
G | A | 2 | a0001c0001t0001g0289a0001c0001t0001g0300 | 2 | HG00673.hp1 HG00741.hp2 |
intron_variant | MODIFIER | c.422-34667C>T | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23098800 | ||||||
chr22:23098860
|
C | T | 1 | a0001c0002t0001g0145 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.422-34727G>A | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23098860 | ||||||
chr22:23098888
|
C | T | 1 | a0001c0002t0001g0017 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.422-34755G>A | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23098888 | ||||||
chr22:23099045
|
G | A | 2 | a0001c0001t0001g0193a0001c0001t0001g0201 | 2 | NA19012.hp1 NA19056.hp1 |
intron_variant | MODIFIER | c.422-34912C>T | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23099045 | ||||||
chr22:23099151
|
C | T | 1 | a0001c0002t0001g0024 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.421+34875G>A | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23099151 | ||||||
chr22:23099261
|
G | A | 1 | a0001c0001t0001g0285 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.421+34765C>T | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23099261 | ||||||
chr22:23099328
|
G | C | 121 | a0001c0001t0001g0225a0001c0001t0001g0233a0001c0001t0001g0291others(118): Show | 121 | HG00544.hp1 HG00544.hp2 HG00558.hp2 others(118): Show |
intron_variant | MODIFIER | c.421+34698C>G | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23099328 | ||||||
chr22:23099371
|
C | T | 1 | a0001c0001t0001g0164 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.421+34655G>A | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23099371 | ||||||
chr22:23099503
|
G | A | 2 | a0001c0002t0001g0076a0001c0002t0001g0080 | 2 | HG01975.hp1 HG02293.hp2 |
intron_variant | MODIFIER | c.421+34523C>T | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23099503 | ||||||
chr22:23099693
|
A | C | 1 | a0001c0002t0001g0066 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.421+34333T>G | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23099693 | ||||||
chr22:23100015
|
T | C | 2 | a0001c0002t0001g0024a0001c0010t0001g0290 | 2 | HG02615.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.421+34011A>G | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23100015 | ||||||
chr22:23100076
|
C | G | 1 | a0006c0008t0001g0265 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.421+33950G>C | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23100076 | ||||||
chr22:23100097
|
C | CCTG | 4 | a0001c0001t0001g0296a0001c0001t0001g0297a0001c0001t0001g0298others(1): Show | 4 | HG01884.hp1 HG02965.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.421+33926_421+3392 others(7): Show |
RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23100097 | ||||||
chr22:23100145
|
T | C | 2 | a0001c0002t0001g0024a0001c0010t0001g0290 | 2 | HG02615.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.421+33881A>G | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23100145 | ||||||
chr22:23100301
|
A | G | 1 | a0001c0002t0001g0092 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.421+33725T>C | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23100301 | ||||||
chr22:23100482
|
T | C | 1 | a0001c0001t0001g0208 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.421+33544A>G | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23100482 | ||||||
chr22:23100504
|
G | T | 5 | a0001c0001t0001g0152a0001c0001t0001g0153a0001c0001t0001g0154others(2): Show | 5 | HG02257.hp2 HG02630.hp1 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.421+33522C>A | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23100504 | ||||||
chr22:23100565
|
C | T | 1 | a0001c0001t0001g0127 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.421+33461G>A | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23100565 | ||||||
chr22:23100729
|
G | T | 90 | a0001c0001t0001g0008a0001c0001t0001g0148a0001c0001t0001g0149others(87): Show | 90 | HG00099.hp1 HG00280.hp2 HG00558.hp1 others(87): Show |
intron_variant | MODIFIER | c.421+33297C>A | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23100729 | ||||||
chr22:23100799
|
A | G | 11 | a0001c0001t0001g0001a0001c0001t0001g0158a0001c0001t0001g0159others(8): Show | 12 | HG02258.hp2 HG02630.hp2 HG02647.hp1 others(9): Show |
intron_variant | MODIFIER | c.421+33227T>C | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23100799 | ||||||
chr22:23100835
|
C | G | 311 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(308): Show | 313 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(310): Show |
intron_variant | MODIFIER | c.421+33191G>C | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23100835 | ||||||
chr22:23100865
|
G | T | 7 | a0001c0001t0001g0147a0001c0001t0001g0152a0001c0001t0001g0153others(4): Show | 7 | HG02145.hp2 HG02257.hp2 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.421+33161C>A | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23100865 | ||||||
chr22:23100902
|
G | A | 13 | a0001c0001t0001g0147a0001c0001t0001g0152a0001c0001t0001g0153others(10): Show | 13 | HG01175.hp1 HG02145.hp2 HG02257.hp2 others(10): Show |
intron_variant | MODIFIER | c.421+33124C>T | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23100902 | ||||||
chr22:23101101
|
G | C | 1 | a0001c0001t0001g0188 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.421+32925C>G | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23101101 | ||||||
chr22:23101216
|
G | A | 1 | a0001c0002t0001g0052 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.421+32810C>T | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23101216 | ||||||
chr22:23101323
|
C | T | 1 | a0001c0001t0001g0227 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.421+32703G>A | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23101323 | ||||||
chr22:23101423
|
A | G | 1 | a0001c0002t0001g0111 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.421+32603T>C | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23101423 | ||||||
chr22:23101722
|
G | A | 6 | a0001c0002t0001g0025a0002c0003t0001g0113a0002c0003t0001g0117others(3): Show | 6 | HG01175.hp1 HG02486.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.421+32304C>T | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23101722 | ||||||
chr22:23101865
|
C | A | 3 | a0001c0002t0001g0006a0001c0002t0001g0044a0001c0002t0001g0045 | 3 | NA18973.hp2 NA18986.hp1 NA19057.hp2 |
intron_variant | MODIFIER | c.421+32161G>T | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23101865 | ||||||
chr22:23101880
|
G | C | 91 | a0001c0001t0001g0008a0001c0001t0001g0148a0001c0001t0001g0149others(88): Show | 91 | HG00099.hp1 HG00280.hp2 HG00558.hp1 others(88): Show |
intron_variant | MODIFIER | c.421+32146C>G | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23101880 | ||||||
chr22:23102003
|
C | T | 2 | a0001c0001t0001g0289a0001c0001t0001g0300 | 2 | HG00673.hp1 HG00741.hp2 |
intron_variant | MODIFIER | c.421+32023G>A | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23102003 | ||||||
chr22:23102029
|
G | T | 43 | a0001c0001t0001g0001a0001c0001t0001g0147a0001c0001t0001g0152others(40): Show | 44 | HG00673.hp1 HG00741.hp2 HG02145.hp2 others(41): Show |
intron_variant | MODIFIER | c.421+31997C>A | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23102029 | ||||||
chr22:23102063
|
G | C | 1 | a0001c0002t0001g0078 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.421+31963C>G | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23102063 | ||||||
chr22:23102120
|
C | T | 1 | a0001c0011t0001g0211 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.421+31906G>A | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23102120 | ||||||
chr22:23102149
|
G | C | 135 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0147others(132): Show | 136 | HG00099.hp1 HG00280.hp2 HG00558.hp1 others(133): Show |
intron_variant | MODIFIER | c.421+31877C>G | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23102149 | ||||||
chr22:23102214
|
G | A | 2 | a0001c0001t0001g0126a0001c0001t0001g0127 | 2 | HG00642.hp2 HG03704.hp1 |
intron_variant | MODIFIER | c.421+31812C>T | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23102214 | ||||||
chr22:23102392
|
T | C | 1 | a0001c0001t0001g0191 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.421+31634A>G | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23102392 | ||||||
chr22:23102567
|
G | A | 1 | a0001c0001t0001g0157 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.421+31459C>T | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23102567 | ||||||
chr22:23102605
|
C | T | 43 | a0001c0001t0001g0001a0001c0001t0001g0147a0001c0001t0001g0152others(40): Show | 44 | HG00673.hp1 HG00741.hp2 HG02145.hp2 others(41): Show |
intron_variant | MODIFIER | c.421+31421G>A | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23102605 | ||||||
chr22:23102609
|
A | C | 92 | a0001c0001t0001g0008a0001c0001t0001g0148a0001c0001t0001g0149others(89): Show | 92 | HG00099.hp1 HG00280.hp2 HG00558.hp1 others(89): Show |
intron_variant | MODIFIER | c.421+31417T>G | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23102609 | ||||||
chr22:23102896
|
T | C | 152 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0147others(149): Show | 153 | HG00099.hp1 HG00280.hp2 HG00558.hp1 others(150): Show |
intron_variant | MODIFIER | c.421+31130A>G | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23102896 | ||||||
chr22:23103296
|
G | A | 1 | a0001c0002t0001g0026 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.421+30730C>T | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23103296 | ||||||
chr22:23103472
|
C | T | 2 | a0002c0003t0001g0117a0002c0003t0001g0120 | 2 | HG02486.hp1 HG03654.hp1 |
intron_variant | MODIFIER | c.421+30554G>A | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23103472 | ||||||
chr22:23103505
|
C | T | 2 | a0001c0001t0001g0289a0001c0001t0001g0300 | 2 | HG00673.hp1 HG00741.hp2 |
intron_variant | MODIFIER | c.421+30521G>A | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23103505 | ||||||
chr22:23103639
|
A | AT | 11 | a0001c0001t0001g0001a0001c0001t0001g0158a0001c0001t0001g0159others(8): Show | 12 | HG02258.hp2 HG02630.hp2 HG02647.hp1 others(9): Show |
intron_variant | MODIFIER | c.421+30386dupA | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23103639 | ||||||
chr22:23103931
|
C | T | 1 | a0001c0001t0001g0177 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.421+30095G>A | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23103931 | ||||||
chr22:23104119
|
G | A | 7 | a0001c0001t0001g0147a0001c0001t0001g0152a0001c0001t0001g0153others(4): Show | 7 | HG02145.hp2 HG02257.hp2 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.421+29907C>T | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23104119 | ||||||
chr22:23104199
|
G | A | 146 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0147others(143): Show | 147 | HG00099.hp1 HG00280.hp2 HG00558.hp1 others(144): Show |
intron_variant | MODIFIER | c.421+29827C>T | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23104199 | ||||||
chr22:23104231
|
A | G | 3 | a0001c0002t0001g0006a0001c0002t0001g0044a0001c0002t0001g0045 | 3 | NA18973.hp2 NA18986.hp1 NA19057.hp2 |
intron_variant | MODIFIER | c.421+29795T>C | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23104231 | ||||||
chr22:23104369
|
T | C | 1 | a0005c0005t0001g0243 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.421+29657A>G | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23104369 | ||||||
chr22:23104858
|
G | A | 1 | a0001c0001t0001g0157 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.421+29168C>T | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23104858 | ||||||
chr22:23105160
|
C | G | 272 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0147others(269): Show | 273 | HG00099.hp1 HG00280.hp2 HG00544.hp1 others(270): Show |
intron_variant | MODIFIER | c.421+28866G>C | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23105160 | ||||||
chr22:23105224
|
T | C | 1 | a0001c0001t0001g0157 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.421+28802A>G | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23105224 | ||||||
chr22:23105282
|
G | A | 1 | a0001c0002t0001g0025 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.421+28744C>T | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23105282 | ||||||
chr22:23105327
|
C | T | 1 | a0001c0001t0001g0250 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.421+28699G>A | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23105327 | ||||||
chr22:23105726
|
A | G | 44 | a0001c0001t0001g0001a0001c0001t0001g0147a0001c0001t0001g0152others(41): Show | 45 | HG00673.hp1 HG00741.hp2 HG02145.hp2 others(42): Show |
intron_variant | MODIFIER | c.421+28300T>C | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23105726 | ||||||
chr22:23105782
|
G | A | 1 | a0001c0001t0001g0312 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.421+28244C>T | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23105782 | ||||||
chr22:23105904
|
T | A | 44 | a0001c0001t0001g0001a0001c0001t0001g0147a0001c0001t0001g0152others(41): Show | 45 | HG00673.hp1 HG00741.hp2 HG02145.hp2 others(42): Show |
intron_variant | MODIFIER | c.421+28122A>T | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23105904 | ||||||
chr22:23105983
|
G | A | 58 | a0001c0001t0001g0001a0001c0001t0001g0147a0001c0001t0001g0152others(55): Show | 59 | HG00673.hp1 HG00741.hp2 HG01109.hp1 others(56): Show |
intron_variant | MODIFIER | c.421+28043C>T | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23105983 | ||||||
chr22:23106037
|
A | G | 1 | a0001c0001t0001g0198 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.421+27989T>C | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23106037 | ||||||
chr22:23106044
|
A | T | 2 | a0001c0001t0001g0148a0001c0002t0001g0023 | 2 | HG02055.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.421+27982T>A | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23106044 | ||||||
chr22:23106109
|
C | CCCGCCAC others(35): Show |
1 | a0001c0002t0001g0056 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.421+27916_421+2791 others(46): Show |
RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23106109 | ||||||
chr22:23106280
|
C | T | 2 | a0001c0001t0001g0289a0001c0001t0001g0300 | 2 | HG00673.hp1 HG00741.hp2 |
intron_variant | MODIFIER | c.421+27746G>A | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23106280 | ||||||
chr22:23106402
|
G | A | 1 | a0001c0001t0001g0226 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.421+27624C>T | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23106402 | ||||||
chr22:23106460
|
A | ACTGTGGG others(13): Show |
3 | a0001c0002t0001g0076a0001c0002t0001g0080a0001c0002t0001g0102 | 3 | HG01975.hp1 HG02056.hp2 HG02293.hp2 |
intron_variant | MODIFIER | c.421+27546_421+2756 others(24): Show |
RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23106460 | ||||||
chr22:23106509
|
C | A | 1 | a0006c0008t0001g0265 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.421+27517G>T | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23106509 | ||||||
chr22:23106568
|
C | T | 1 | a0001c0001t0001g0227 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.421+27458G>A | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23106568 | ||||||
chr22:23106696
|
C | T | 19 | a0001c0001t0001g0001a0001c0001t0001g0147a0001c0001t0001g0152others(16): Show | 20 | HG02145.hp2 HG02257.hp2 HG02258.hp2 others(17): Show |
intron_variant | MODIFIER | c.421+27330G>A | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23106696 | ||||||
chr22:23106796
|
C | T | 1 | a0001c0001t0001g0165 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.421+27230G>A | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23106796 | ||||||
chr22:23106814
|
G | C | 1 | a0004c0009t0001g0311 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.421+27212C>G | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23106814 | ||||||
chr22:23106854
|
C | T | 4 | a0001c0001t0001g0228a0001c0001t0001g0230a0001c0001t0001g0231others(1): Show | 4 | HG03491.hp1 HG03492.hp1 HG03704.hp2 others(1): Show |
intron_variant | MODIFIER | c.421+27172G>A | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23106854 | ||||||
chr22:23107180
|
C | T | 2 | a0001c0001t0001g0264a0001c0001t0001g0268 | 2 | HG02602.hp2 HG03017.hp1 |
intron_variant | MODIFIER | c.421+26846G>A | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23107180 | ||||||
chr22:23107291
|
C | T | 2 | a0001c0002t0001g0024a0001c0010t0001g0290 | 2 | HG02615.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.421+26735G>A | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23107291 | ||||||
chr22:23107350
|
T | C | 43 | a0001c0001t0001g0001a0001c0001t0001g0147a0001c0001t0001g0152others(40): Show | 44 | HG00673.hp1 HG00741.hp2 HG02145.hp2 others(41): Show |
intron_variant | MODIFIER | c.421+26676A>G | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23107350 | ||||||
chr22:23107372
|
A | G | 1 | a0001c0001t0001g0157 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.421+26654T>C | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23107372 | ||||||
chr22:23107768
|
A | G | 152 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0147others(149): Show | 153 | HG00099.hp1 HG00280.hp2 HG00558.hp1 others(150): Show |
intron_variant | MODIFIER | c.421+26258T>C | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23107768 | ||||||
chr22:23107870
|
C | T | 1 | a0001c0001t0001g0312 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.421+26156G>A | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23107870 | ||||||
chr22:23107918
|
C | T | 1 | a0001c0001t0001g0235 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.421+26108G>A | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23107918 | ||||||
chr22:23108152
|
A | G | 1 | a0001c0002t0001g0050 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.421+25874T>C | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23108152 | ||||||
chr22:23108258
|
G | A | 2 | a0001c0001t0001g0157a0001c0002t0001g0029 | 2 | HG01981.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.421+25768C>T | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23108258 | ||||||
chr22:23108454
|
C | T | 2 | a0001c0002t0002g0132a0001c0002t0002g0133 | 2 | HG01243.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.421+25572G>A | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23108454 | ||||||
chr22:23108462
|
C | T | 2 | a0001c0002t0001g0024a0001c0010t0001g0290 | 2 | HG02615.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.421+25564G>A | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23108462 | ||||||
chr22:23108577
|
TGGATCCT others(6): Show |
T | 1 | a0001c0002t0001g0056 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.421+25436_421+2544 others(17): Show |
RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23108577 | ||||||
chr22:23108695
|
G | A | 43 | a0001c0001t0001g0001a0001c0001t0001g0147a0001c0001t0001g0152others(40): Show | 44 | HG00673.hp1 HG00741.hp2 HG02145.hp2 others(41): Show |
intron_variant | MODIFIER | c.421+25331C>T | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23108695 | ||||||
chr22:23108716
|
A | G | 43 | a0001c0001t0001g0001a0001c0001t0001g0147a0001c0001t0001g0152others(40): Show | 44 | HG00673.hp1 HG00741.hp2 HG02145.hp2 others(41): Show |
intron_variant | MODIFIER | c.421+25310T>C | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23108716 | ||||||
chr22:23108928
|
C | T | 20 | a0001c0001t0001g0166a0001c0001t0001g0167a0001c0001t0001g0168others(17): Show | 20 | HG02258.hp1 HG02280.hp2 HG02486.hp2 others(17): Show |
intron_variant | MODIFIER | c.421+25098G>A | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23108928 | ||||||
chr22:23109049
|
G | T | 41 | a0001c0001t0001g0001a0001c0001t0001g0152a0001c0001t0001g0153others(38): Show | 42 | HG00673.hp1 HG00741.hp2 HG02257.hp2 others(39): Show |
intron_variant | MODIFIER | c.421+24977C>A | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23109049 | ||||||
chr22:23109169
|
A | G | 20 | a0001c0001t0001g0166a0001c0001t0001g0167a0001c0001t0001g0168others(17): Show | 20 | HG02258.hp1 HG02280.hp2 HG02486.hp2 others(17): Show |
intron_variant | MODIFIER | c.421+24857T>C | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23109169 | ||||||
chr22:23109236
|
C | A | 1 | a0001c0001t0001g0295 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.421+24790G>T | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23109236 | ||||||
chr22:23109264
|
G | A | 2 | a0001c0002t0001g0024a0001c0010t0001g0290 | 2 | HG02615.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.421+24762C>T | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23109264 | ||||||
chr22:23109287
|
G | A | 1 | a0001c0002t0001g0014 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.421+24739C>T | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23109287 | ||||||
chr22:23109588
|
G | C | 96 | a0001c0001t0001g0008a0001c0001t0001g0148a0001c0001t0001g0149others(93): Show | 96 | HG00099.hp1 HG00280.hp2 HG00558.hp1 others(93): Show |
intron_variant | MODIFIER | c.421+24438C>G | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23109588 | ||||||
chr22:23109639
|
T | A | 1 | a0001c0002t0001g0056 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.421+24387A>T | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23109639 | ||||||
chr22:23109650
|
C | T | 3 | a0001c0002t0001g0016a0001c0002t0001g0042a0001c0002t0001g0043 | 3 | HG02809.hp1 HG03516.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.421+24376G>A | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23109650 | ||||||
chr22:23109655
|
G | A | 8 | a0003c0004t0001g0005a0003c0004t0001g0175a0003c0004t0001g0176others(5): Show | 8 | HG02723.hp1 HG03098.hp2 HG03139.hp1 others(5): Show |
intron_variant | MODIFIER | c.421+24371C>T | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23109655 | ||||||
chr22:23109876
|
C | A | 7 | a0001c0001t0001g0147a0001c0001t0001g0152a0001c0001t0001g0153others(4): Show | 7 | HG02145.hp2 HG02257.hp2 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.421+24150G>T | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23109876 | ||||||
chr22:23109878
|
C | T | 1 | a0001c0001t0001g0153 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.421+24148G>A | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23109878 | ||||||
chr22:23109901
|
G | A | 19 | a0001c0001t0001g0001a0001c0001t0001g0147a0001c0001t0001g0152others(16): Show | 20 | HG02145.hp2 HG02257.hp2 HG02258.hp2 others(17): Show |
intron_variant | MODIFIER | c.421+24125C>T | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23109901 | ||||||
chr22:23109929
|
C | T | 7 | a0001c0001t0001g0147a0001c0001t0001g0152a0001c0001t0001g0153others(4): Show | 7 | HG02145.hp2 HG02257.hp2 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.421+24097G>A | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23109929 | ||||||
chr22:23110244
|
C | G | 15 | a0001c0001t0001g0157a0001c0001t0001g0177a0001c0001t0001g0312others(12): Show | 15 | HG01243.hp1 HG01891.hp2 HG02055.hp1 others(12): Show |
intron_variant | MODIFIER | c.421+23782G>C | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23110244 | ||||||
chr22:23110579
|
G | A | 4 | a0001c0001t0001g0160a0001c0001t0001g0161a0001c0001t0001g0162others(1): Show | 4 | HG02258.hp2 HG02922.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.421+23447C>T | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23110579 | ||||||
chr22:23110656
|
A | T | 1 | a0001c0002t0001g0056 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.421+23370T>A | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23110656 | ||||||
chr22:23110868
|
C | A | 1 | a0001c0001t0001g0235 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.421+23158G>T | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23110868 | ||||||
chr22:23111027
|
G | GGGGGTAG others(3): Show |
1 | a0001c0002t0001g0056 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.421+22989_421+2299 others(14): Show |
RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23111027 | ||||||
chr22:23111101
|
G | A | 1 | a0001c0002t0001g0052 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.421+22925C>T | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23111101 | ||||||
chr22:23111153
|
C | T | 1 | a0001c0001t0001g0257 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.421+22873G>A | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23111153 | ||||||
chr22:23111206
|
C | G | 1 | a0001c0001t0001g0213 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.421+22820G>C | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23111206 | ||||||
chr22:23111321
|
C | T | 9 | a0001c0001t0001g0195a0001c0001t0001g0196a0001c0001t0001g0197others(6): Show | 9 | HG00558.hp1 NA18957.hp1 NA18973.hp1 others(6): Show |
intron_variant | MODIFIER | c.421+22705G>A | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23111321 | ||||||
chr22:23111380
|
C | T | 21 | a0001c0001t0001g0166a0001c0001t0001g0167a0001c0001t0001g0168others(18): Show | 21 | HG01243.hp1 HG02055.hp1 HG02109.hp1 others(18): Show |
intron_variant | MODIFIER | c.421+22646G>A | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23111380 | ||||||
chr22:23111389
|
G | A | 2 | a0001c0002t0001g0057a0001c0002t0001g0058 | 2 | NA19004.hp2 NA19086.hp2 |
intron_variant | MODIFIER | c.421+22637C>T | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23111389 | ||||||
chr22:23111610
|
A | C | 1 | a0001c0002t0001g0046 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.421+22416T>G | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23111610 | ||||||
chr22:23111768
|
G | A | 2 | a0001c0001t0001g0187a0001c0001t0001g0188 | 2 | NA18952.hp1 NA19007.hp1 |
intron_variant | MODIFIER | c.421+22258C>T | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23111768 | ||||||
chr22:23111844
|
C | A | 1 | a0001c0001t0001g0289 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.421+22182G>T | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23111844 | ||||||
chr22:23111857
|
G | C | 1 | a0001c0002t0001g0050 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.421+22169C>G | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23111857 | ||||||
chr22:23112260
|
C | A | 1 | a0001c0001t0001g0183 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.421+21766G>T | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23112260 | ||||||
chr22:23112298
|
C | T | 5 | a0001c0002t0001g0059a0001c0002t0001g0065a0001c0002t0001g0093others(2): Show | 5 | NA18942.hp2 NA18944.hp2 NA19007.hp2 others(2): Show |
intron_variant | MODIFIER | c.421+21728G>A | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23112298 | ||||||
chr22:23112302
|
C | T | 1 | a0001c0001t0001g0215 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.421+21724G>A | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23112302 | ||||||
chr22:23112387
|
A | G | 2 | a0001c0001t0001g0150a0001c0001t0001g0236 | 2 | HG01516.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.421+21639T>C | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23112387 | ||||||
chr22:23112535
|
C | T | 84 | a0001c0001t0001g0008a0001c0001t0001g0149a0001c0001t0001g0150others(81): Show | 84 | HG00099.hp1 HG00280.hp2 HG00558.hp1 others(81): Show |
intron_variant | MODIFIER | c.421+21491G>A | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23112535 | ||||||
chr22:23112694
|
A | G | 168 | a0001c0001t0001g0147a0001c0001t0001g0148a0001c0001t0001g0152others(165): Show | 168 | HG00544.hp1 HG00544.hp2 HG00558.hp2 others(165): Show |
intron_variant | MODIFIER | c.421+21332T>C | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23112694 | ||||||
chr22:23112699
|
C | T | 1 | a0003c0004t0001g0176 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.421+21327G>A | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23112699 | ||||||
chr22:23112741
|
G | A | 1 | a0001c0001t0001g0171 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.421+21285C>T | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23112741 | ||||||
chr22:23112932
|
C | T | 1 | a0001c0002t0001g0016 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.421+21094G>A | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23112932 | ||||||
chr22:23112950
|
G | A | 2 | a0001c0001t0001g0157a0004c0009t0001g0311 | 2 | HG01109.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.421+21076C>T | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23112950 | ||||||
chr22:23113095
|
G | A | 2 | a0001c0001t0003g0003a0001c0001t0003g0004 | 2 | HG02970.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.421+20931C>T | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23113095 | ||||||
chr22:23113179
|
C | T | 156 | a0001c0001t0001g0147a0001c0001t0001g0148a0001c0001t0001g0152others(153): Show | 156 | HG00544.hp1 HG00544.hp2 HG00558.hp2 others(153): Show |
intron_variant | MODIFIER | c.421+20847G>A | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23113179 | ||||||
chr22:23113680
|
C | T | 1 | a0001c0001t0001g0166 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.421+20346G>A | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23113680 | ||||||
chr22:23113696
|
C | T | 1 | a0001c0001t0001g0304 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.421+20330G>A | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23113696 | ||||||
chr22:23113793
|
C | T | 1 | a0001c0001t0001g0157 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.421+20233G>A | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23113793 | ||||||
chr22:23113974
|
C | A | 1 | a0001c0001t0001g0282 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.421+20052G>T | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23113974 | ||||||
chr22:23113988
|
A | T | 1 | a0001c0001t0001g0183 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.421+20038T>A | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23113988 | ||||||
chr22:23114017
|
G | A | 25 | a0001c0001t0001g0147a0001c0001t0001g0148a0001c0001t0001g0152others(22): Show | 25 | HG02055.hp2 HG02145.hp2 HG02257.hp2 others(22): Show |
intron_variant | MODIFIER | c.421+20009C>T | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23114017 | ||||||
chr22:23114206
|
G | A | 2 | a0001c0002t0001g0084a0001c0002t0001g0098 | 2 | NA18952.hp2 NA19079.hp1 |
intron_variant | MODIFIER | c.421+19820C>T | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23114206 | ||||||
chr22:23114266
|
C | T | 3 | a0001c0002t0001g0007a0001c0002t0001g0048a0001c0002t0001g0049 | 3 | HG00735.hp1 HG01070.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.421+19760G>A | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23114266 | ||||||
chr22:23114286
|
A | G | 1 | a0001c0002t0001g0145 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.421+19740T>C | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23114286 | ||||||
chr22:23114413
|
C | T | 6 | a0001c0001t0001g0177a0003c0004t0001g0005a0003c0004t0001g0175others(3): Show | 6 | HG02258.hp1 HG03098.hp2 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.421+19613G>A | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23114413 | ||||||
chr22:23114509
|
T | C | 177 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(174): Show | 179 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(176): Show |
intron_variant | MODIFIER | c.421+19517A>G | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23114509 | ||||||
chr22:23114515
|
T | C | 159 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(156): Show | 161 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(158): Show |
intron_variant | MODIFIER | c.421+19511A>G | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23114515 | ||||||
chr22:23114621
|
T | C | 1 | a0001c0001t0001g0164 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.421+19405A>G | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23114621 | ||||||
chr22:23114835
|
G | C | 1 | a0001c0002t0001g0017 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.421+19191C>G | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23114835 | ||||||
chr22:23114911
|
A | G | 177 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(174): Show | 179 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(176): Show |
intron_variant | MODIFIER | c.421+19115T>C | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23114911 | ||||||
chr22:23114991
|
G | A | 1 | a0001c0001t0001g0204 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.421+19035C>T | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23114991 | ||||||
chr22:23115002
|
G | T | 1 | a0001c0001t0001g0157 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.421+19024C>A | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23115002 | ||||||
chr22:23115233
|
T | C | 157 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(154): Show | 159 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(156): Show |
intron_variant | MODIFIER | c.421+18793A>G | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23115233 | ||||||
chr22:23115299
|
C | T | 142 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0126others(139): Show | 143 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(140): Show |
intron_variant | MODIFIER | c.421+18727G>A | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23115299 | ||||||
chr22:23115607
|
C | T | 1 | a0001c0002t0001g0145 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.421+18419G>A | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23115607 | ||||||
chr22:23115630
|
G | A | 1 | a0001c0001t0001g0177 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.421+18396C>T | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23115630 | ||||||
chr22:23115802
|
A | G | 3 | a0001c0001t0001g0289a0001c0001t0001g0291a0001c0001t0001g0300 | 3 | HG00673.hp1 HG00741.hp2 HG02027.hp1 |
intron_variant | MODIFIER | c.421+18224T>C | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23115802 | ||||||
chr22:23116104
|
C | T | 1 | a0001c0001t0001g0160 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.421+17922G>A | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23116104 | ||||||
chr22:23116301
|
G | A | 2 | a0001c0001t0001g0196a0001c0001t0001g0197 | 2 | NA18957.hp1 NA19086.hp1 |
intron_variant | MODIFIER | c.421+17725C>T | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23116301 | ||||||
chr22:23116382
|
G | A | 1 | a0001c0002t0001g0070 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.421+17644C>T | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23116382 | ||||||
chr22:23116390
|
G | A | 129 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0126others(126): Show | 130 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(127): Show |
intron_variant | MODIFIER | c.421+17636C>T | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23116390 | ||||||
chr22:23116548
|
C | T | 1 | a0001c0001t0001g0257 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.421+17478G>A | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23116548 | ||||||
chr22:23116597
|
A | G | 11 | a0001c0001t0001g0001a0001c0001t0001g0158a0001c0001t0001g0159others(8): Show | 12 | HG02258.hp2 HG02630.hp2 HG02647.hp1 others(9): Show |
intron_variant | MODIFIER | c.421+17429T>C | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23116597 | ||||||
chr22:23116611
|
G | T | 2 | a0001c0002t0001g0084a0001c0002t0001g0098 | 2 | NA18952.hp2 NA19079.hp1 |
intron_variant | MODIFIER | c.421+17415C>A | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23116611 | ||||||
chr22:23116766
|
G | A | 2 | a0001c0001t0001g0149a0001c0001t0001g0235 | 2 | HG01515.hp1 HG01884.hp2 |
intron_variant | MODIFIER | c.421+17260C>T | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23116766 | ||||||
chr22:23117003
|
G | A | 1 | a0001c0001t0001g0304 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.421+17023C>T | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23117003 | ||||||
chr22:23117228
|
T | C | 2 | a0002c0003t0001g0114a0002c0003t0001g0115 | 2 | NA19010.hp2 NA19068.hp2 |
intron_variant | MODIFIER | c.421+16798A>G | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23117228 | ||||||
chr22:23117243
|
T | TGA | 175 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(172): Show | 177 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(174): Show |
intron_variant | MODIFIER | c.421+16781_421+1678 others(6): Show |
RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23117243 | ||||||
chr22:23117257
|
C | T | 3 | a0001c0001t0001g0147a0001c0001t0001g0148a0001c0001t0001g0179 | 3 | HG02055.hp2 HG02145.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.421+16769G>A | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23117257 | ||||||
chr22:23117268
|
G | A | 1 | a0001c0002t0001g0145 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.421+16758C>T | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23117268 | ||||||
chr22:23117356
|
G | A | 1 | a0001c0002t0001g0129 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.421+16670C>T | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23117356 | ||||||
chr22:23117397
|
C | A | 1 | a0001c0001t0001g0219 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.421+16629G>T | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23117397 | ||||||
chr22:23117676
|
G | A | 173 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(170): Show | 175 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(172): Show |
intron_variant | MODIFIER | c.421+16350C>T | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23117676 | ||||||
chr22:23117771
|
G | C | 1 | a0001c0001t0001g0246 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.421+16255C>G | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23117771 | ||||||
chr22:23117850
|
C | G | 7 | a0001c0001t0001g0187a0001c0001t0001g0188a0001c0001t0001g0193others(4): Show | 7 | HG02080.hp1 NA18952.hp1 NA18967.hp2 others(4): Show |
intron_variant | MODIFIER | c.421+16176G>C | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23117850 | ||||||
chr22:23117887
|
C | G | 1 | a0001c0001t0001g0162 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.421+16139G>C | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23117887 | ||||||
chr22:23118022
|
C | T | 2 | a0001c0001t0001g0289a0001c0001t0001g0300 | 2 | HG00673.hp1 HG00741.hp2 |
intron_variant | MODIFIER | c.421+16004G>A | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23118022 | ||||||
chr22:23118256
|
G | A | 4 | a0001c0001t0001g0002a0001c0001t0001g0266a0001c0001t0001g0271others(1): Show | 5 | HG00642.hp1 HG01257.hp2 HG01258.hp2 others(2): Show |
intron_variant | MODIFIER | c.421+15770C>T | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23118256 | ||||||
chr22:23118413
|
G | A | 1 | a0001c0002t0002g0137 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.421+15613C>T | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23118413 | ||||||
chr22:23118467
|
T | TCCCCG | 3 | a0003c0004t0001g0301a0003c0004t0001g0302a0003c0004t0001g0303 | 3 | HG02723.hp1 HG06807.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.421+15554_421+1555 others(9): Show |
RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23118467 | ||||||
chr22:23118482
|
A | C | 1 | a0001c0001t0001g0206 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.421+15544T>G | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23118482 | ||||||
chr22:23118482
|
A | G | 138 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0126others(135): Show | 139 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(136): Show |
intron_variant | MODIFIER | c.421+15544T>C | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23118482 | ||||||
chr22:23118497
|
C | CT | 42 | a0001c0001t0001g0002a0001c0001t0001g0126a0001c0001t0001g0127others(39): Show | 43 | HG00099.hp2 HG00280.hp1 HG00642.hp1 others(40): Show |
intron_variant | MODIFIER | c.421+15528dupA | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23118497 | ||||||
chr22:23118539
|
G | C | 11 | a0001c0001t0001g0001a0001c0001t0001g0158a0001c0001t0001g0159others(8): Show | 12 | HG02258.hp2 HG02630.hp2 HG02647.hp1 others(9): Show |
intron_variant | MODIFIER | c.421+15487C>G | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23118539 | ||||||
chr22:23118575
|
C | G | 18 | a0001c0001t0001g0166a0001c0001t0001g0167a0001c0001t0001g0168others(15): Show | 18 | HG02258.hp1 HG02280.hp2 HG02486.hp2 others(15): Show |
intron_variant | MODIFIER | c.421+15451G>C | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23118575 | ||||||
chr22:23118589
|
G | A | 11 | a0001c0001t0001g0001a0001c0001t0001g0158a0001c0001t0001g0159others(8): Show | 12 | HG02258.hp2 HG02630.hp2 HG02647.hp1 others(9): Show |
intron_variant | MODIFIER | c.421+15437C>T | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23118589 | ||||||
chr22:23118730
|
A | G | 1 | a0001c0002t0001g0014 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.421+15296T>C | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23118730 | ||||||
chr22:23118752
|
G | T | 140 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0126others(137): Show | 141 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(138): Show |
intron_variant | MODIFIER | c.421+15274C>A | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23118752 | ||||||
chr22:23118816
|
G | C | 137 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0126others(134): Show | 138 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(135): Show |
intron_variant | MODIFIER | c.421+15210C>G | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23118816 | ||||||
chr22:23118907
|
A | G | 4 | a0001c0001t0001g0296a0001c0001t0001g0297a0001c0001t0001g0298others(1): Show | 4 | HG01884.hp1 HG02965.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.421+15119T>C | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23118907 | ||||||
chr22:23119000
|
G | A | 1 | a0001c0001t0001g0154 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.421+15026C>T | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23119000 | ||||||
chr22:23119011
|
A | G | 6 | a0001c0001t0001g0177a0003c0004t0001g0005a0003c0004t0001g0175others(3): Show | 6 | HG02258.hp1 HG03098.hp2 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.421+15015T>C | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23119011 | ||||||
chr22:23119113
|
G | A | 4 | a0001c0001t0001g0216a0001c0001t0001g0217a0001c0001t0001g0226others(1): Show | 4 | HG00639.hp1 HG01109.hp2 HG01975.hp2 others(1): Show |
intron_variant | MODIFIER | c.421+14913C>T | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23119113 | ||||||
chr22:23119174
|
C | A | 1 | a0004c0009t0001g0311 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.421+14852G>T | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23119174 | ||||||
chr22:23119209
|
C | T | 1 | a0001c0001t0001g0167 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.421+14817G>A | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23119209 | ||||||
chr22:23119238
|
A | G | 176 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(173): Show | 178 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(175): Show |
intron_variant | MODIFIER | c.421+14788T>C | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23119238 | ||||||
chr22:23119409
|
G | A | 1 | a0005c0005t0001g0299 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.421+14617C>T | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23119409 | ||||||
chr22:23119536
|
A | G | 133 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0126others(130): Show | 134 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(131): Show |
intron_variant | MODIFIER | c.421+14490T>C | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23119536 | ||||||
chr22:23119727
|
C | T | 1 | a0001c0002t0001g0018 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.421+14299G>A | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23119727 | ||||||
chr22:23120067
|
C | T | 1 | a0001c0002t0001g0066 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.421+13959G>A | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23120067 | ||||||
chr22:23120141
|
C | T | 1 | a0001c0001t0001g0267 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.421+13885G>A | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23120141 | ||||||
chr22:23120260
|
A | C | 1 | a0001c0002t0001g0013 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.421+13766T>G | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23120260 | ||||||
chr22:23120711
|
G | A | 1 | a0001c0001t0001g0279 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.421+13315C>T | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23120711 | ||||||
chr22:23120838
|
T | C | 1 | a0001c0002t0001g0139 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.421+13188A>G | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23120838 | ||||||
chr22:23120866
|
A | G | 8 | a0001c0002t0002g0012a0001c0002t0002g0132a0001c0002t0002g0133others(5): Show | 8 | HG01243.hp1 HG02055.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.421+13160T>C | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23120866 | ||||||
chr22:23120882
|
G | A | 1 | a0002c0003t0001g0124 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.421+13144C>T | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23120882 | ||||||
chr22:23120886
|
T | C | 1 | a0001c0001t0001g0157 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.421+13140A>G | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23120886 | ||||||
chr22:23120897
|
T | C | 25 | a0001c0001t0001g0147a0001c0001t0001g0148a0001c0001t0001g0152others(22): Show | 25 | HG02055.hp2 HG02145.hp2 HG02257.hp2 others(22): Show |
intron_variant | MODIFIER | c.421+13129A>G | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23120897 | ||||||
chr22:23120996
|
A | G | 141 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0126others(138): Show | 142 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(139): Show |
intron_variant | MODIFIER | c.421+13030T>C | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23120996 | ||||||
chr22:23121066
|
A | G | 1 | a0001c0001t0001g0157 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.421+12960T>C | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23121066 | ||||||
chr22:23121105
|
C | T | 6 | a0001c0001t0001g0177a0003c0004t0001g0005a0003c0004t0001g0175others(3): Show | 6 | HG02258.hp1 HG03098.hp2 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.421+12921G>A | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23121105 | ||||||
chr22:23121417
|
G | T | 11 | a0001c0001t0001g0166a0001c0001t0001g0167a0001c0001t0001g0168others(8): Show | 11 | HG02280.hp2 HG02486.hp2 HG02647.hp2 others(8): Show |
intron_variant | MODIFIER | c.421+12609C>A | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23121417 | ||||||
chr22:23121720
|
CT | C | 42 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0152others(39): Show | 43 | HG01192.hp2 HG01517.hp2 HG01891.hp2 others(40): Show |
intron_variant | MODIFIER | c.421+12305delA | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23121720 | ||||||
chr22:23121720
|
CTT | C | 128 | a0001c0001t0001g0002a0001c0001t0001g0126a0001c0001t0001g0127others(125): Show | 129 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(126): Show |
intron_variant | MODIFIER | c.421+12304_421+1230 others(6): Show |
RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23121720 | ||||||
chr22:23121720
|
CTTT | C | 8 | a0001c0001t0001g0226a0001c0001t0001g0235a0001c0001t0001g0259others(5): Show | 8 | HG01433.hp1 HG01515.hp2 HG01884.hp1 others(5): Show |
intron_variant | MODIFIER | c.421+12303_421+1230 others(7): Show |
RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23121720 | ||||||
chr22:23121783
|
A | G | 1 | a0001c0001t0001g0177 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.421+12243T>C | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23121783 | ||||||
chr22:23121890
|
TTTG | T | 13 | a0001c0001t0001g0312a0001c0002t0002g0011a0001c0002t0002g0012others(10): Show | 13 | HG01243.hp1 HG01891.hp2 HG02055.hp1 others(10): Show |
intron_variant | MODIFIER | c.421+12133_421+1213 others(7): Show |
RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23121890 | ||||||
chr22:23121933
|
G | A | 137 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0126others(134): Show | 138 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(135): Show |
intron_variant | MODIFIER | c.421+12093C>T | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23121933 | ||||||
chr22:23122270
|
A | G | 137 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0126others(134): Show | 138 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(135): Show |
intron_variant | MODIFIER | c.421+11756T>C | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23122270 | ||||||
chr22:23122277
|
G | T | 1 | a0001c0002t0001g0038 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.421+11749C>A | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23122277 | ||||||
chr22:23122422
|
C | T | 1 | a0002c0003t0001g0118 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.421+11604G>A | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23122422 | ||||||
chr22:23122567
|
G | A | 9 | a0001c0001t0001g0166a0001c0001t0001g0167a0001c0001t0001g0169others(6): Show | 9 | HG02647.hp2 HG02895.hp1 HG02897.hp2 others(6): Show |
intron_variant | MODIFIER | c.421+11459C>T | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23122567 | ||||||
chr22:23122578
|
A | G | 1 | a0001c0001t0001g0278 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.421+11448T>C | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23122578 | ||||||
chr22:23122620
|
T | C | 3 | a0001c0001t0001g0296a0001c0001t0001g0297a0001c0001t0001g0298 | 3 | HG02965.hp1 HG03195.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.421+11406A>G | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23122620 | ||||||
chr22:23122623
|
G | A | 124 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0126others(121): Show | 125 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(122): Show |
intron_variant | MODIFIER | c.421+11403C>T | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23122623 | ||||||
chr22:23122759
|
G | T | 1 | a0001c0002t0001g0060 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.421+11267C>A | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23122759 | ||||||
chr22:23122778
|
G | C | 5 | a0001c0001t0001g0168a0001c0001t0001g0234a0001c0001t0001g0297others(2): Show | 5 | HG02486.hp2 HG02976.hp1 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.421+11248C>G | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23122778 | ||||||
chr22:23122811
|
T | G | 2 | a0001c0002t0001g0069a0001c0002t0001g0070 | 2 | HG02735.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.421+11215A>C | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23122811 | ||||||
chr22:23122891
|
A | G | 89 | a0001c0001t0001g0008a0001c0001t0001g0149a0001c0001t0001g0150others(86): Show | 89 | HG00099.hp1 HG00280.hp2 HG00544.hp2 others(86): Show |
intron_variant | MODIFIER | c.421+11135T>C | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23122891 | ||||||
chr22:23123254
|
C | T | 1 | a0003c0004t0001g0301 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.421+10772G>A | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23123254 | ||||||
chr22:23123377
|
C | T | 1 | a0001c0002t0002g0137 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.421+10649G>A | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23123377 | ||||||
chr22:23123444
|
G | A | 4 | a0001c0001t0001g0289a0001c0001t0001g0291a0001c0001t0001g0300others(1): Show | 4 | HG00673.hp1 HG00741.hp2 HG02027.hp1 others(1): Show |
intron_variant | MODIFIER | c.421+10582C>T | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23123444 | ||||||
chr22:23123489
|
A | G | 1 | a0001c0002t0001g0019 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.421+10537T>C | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23123489 | ||||||
chr22:23123595
|
A | C | 1 | a0001c0002t0001g0074 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.421+10431T>G | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23123595 | ||||||
chr22:23123641
|
A | G | 4 | a0001c0001t0001g0296a0001c0001t0001g0297a0001c0001t0001g0298others(1): Show | 4 | HG01884.hp1 HG02965.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.421+10385T>C | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23123641 | ||||||
chr22:23123844
|
G | A | 136 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0126others(133): Show | 137 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(134): Show |
intron_variant | MODIFIER | c.421+10182C>T | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23123844 | ||||||
chr22:23123870
|
C | T | 2 | a0001c0002t0001g0084a0001c0002t0001g0098 | 2 | NA18952.hp2 NA19079.hp1 |
intron_variant | MODIFIER | c.421+10156G>A | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23123870 | ||||||
chr22:23124089
|
C | T | 1 | a0001c0002t0001g0103 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.421+9937G>A | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23124089 | ||||||
chr22:23124099
|
G | A | 1 | a0001c0002t0001g0024 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.421+9927C>T | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23124099 | ||||||
chr22:23124190
|
A | AT | 14 | a0001c0002t0001g0109a0001c0002t0001g0145a0001c0002t0002g0011others(11): Show | 14 | HG01243.hp1 HG01891.hp2 HG02055.hp1 others(11): Show |
intron_variant | MODIFIER | c.421+9835dupA | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23124190 | ||||||
chr22:23124199
|
T | G | 1 | a0001c0001t0001g0179 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.421+9827A>C | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23124199 | ||||||
chr22:23124199
|
T | TG | 173 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(170): Show | 175 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(172): Show |
intron_variant | MODIFIER | c.421+9826_421+9827i others(3): Show |
RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23124199 | ||||||
chr22:23124201
|
G | T | 174 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(171): Show | 176 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(173): Show |
intron_variant | MODIFIER | c.421+9825C>A | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23124201 | ||||||
chr22:23124214
|
G | GT | 35 | a0001c0001t0001g0001a0001c0001t0001g0158a0001c0001t0001g0159others(32): Show | 36 | HG00673.hp1 HG00735.hp1 HG00741.hp1 others(33): Show |
intron_variant | MODIFIER | c.421+9811dupA | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23124214 | ||||||
chr22:23124214
|
GT | G | 10 | a0001c0001t0001g0177a0001c0001t0001g0304a0001c0002t0001g0054others(7): Show | 10 | HG02258.hp1 HG02970.hp1 HG03098.hp2 others(7): Show |
intron_variant | MODIFIER | c.421+9811delA | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23124214 | ||||||
chr22:23124314
|
A | G | 1 | a0001c0002t0001g0094 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.421+9712T>C | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23124314 | ||||||
chr22:23124442
|
G | A | 1 | a0001c0002t0001g0046 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.421+9584C>T | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23124442 | ||||||
chr22:23124722
|
G | A | 1 | a0002c0003t0001g0121 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.421+9304C>T | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23124722 | ||||||
chr22:23124782
|
A | G | 1 | a0001c0002t0001g0037 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.421+9244T>C | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23124782 | ||||||
chr22:23124880
|
C | G | 1 | a0001c0001t0001g0263 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.421+9146G>C | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23124880 | ||||||
chr22:23124893
|
C | T | 141 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0126others(138): Show | 142 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(139): Show |
intron_variant | MODIFIER | c.421+9133G>A | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23124893 | ||||||
chr22:23125302
|
G | A | 1 | a0004c0009t0001g0311 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.421+8724C>T | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23125302 | ||||||
chr22:23125302
|
G | C | 2 | a0001c0002t0001g0042a0001c0002t0001g0043 | 2 | HG02809.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.421+8724C>G | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23125302 | ||||||
chr22:23125559
|
G | A | 3 | a0003c0004t0001g0301a0003c0004t0001g0302a0003c0004t0001g0303 | 3 | HG02723.hp1 HG06807.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.421+8467C>T | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23125559 | ||||||
chr22:23125617
|
G | A | 138 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0126others(135): Show | 139 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(136): Show |
intron_variant | MODIFIER | c.421+8409C>T | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23125617 | ||||||
chr22:23125759
|
G | C | 142 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0126others(139): Show | 143 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(140): Show |
intron_variant | MODIFIER | c.421+8267C>G | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23125759 | ||||||
chr22:23125763
|
A | G | 142 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0126others(139): Show | 143 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(140): Show |
intron_variant | MODIFIER | c.421+8263T>C | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23125763 | ||||||
chr22:23125837
|
G | C | 19 | a0001c0001t0001g0166a0001c0001t0001g0167a0001c0001t0001g0168others(16): Show | 19 | HG02258.hp1 HG02280.hp2 HG02486.hp2 others(16): Show |
intron_variant | MODIFIER | c.421+8189C>G | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23125837 | ||||||
chr22:23125902
|
G | A | 1 | a0001c0001t0001g0246 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.421+8124C>T | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23125902 | ||||||
chr22:23125913
|
A | G | 1 | a0001c0002t0001g0038 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.421+8113T>C | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23125913 | ||||||
chr22:23125937
|
A | G | 3 | a0001c0001t0001g0147a0001c0001t0001g0148a0001c0001t0001g0179 | 3 | HG02055.hp2 HG02145.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.421+8089T>C | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23125937 | ||||||
chr22:23125955
|
A | G | 1 | a0001c0002t0001g0109 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.421+8071T>C | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23125955 | ||||||
chr22:23126005
|
C | T | 1 | a0004c0009t0001g0311 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.421+8021G>A | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23126005 | ||||||
chr22:23126069
|
T | G | 1 | a0004c0014t0001g0095 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.421+7957A>C | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23126069 | ||||||
chr22:23126153
|
C | CTGTGAGC others(45): Show |
1 | a0001c0002t0001g0056 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.421+7872_421+7873i others(54): Show |
RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23126153 | ||||||
chr22:23126281
|
C | T | 172 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(169): Show | 174 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(171): Show |
intron_variant | MODIFIER | c.421+7745G>A | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23126281 | ||||||
chr22:23126345
|
C | T | 21 | a0001c0001t0001g0147a0001c0001t0001g0148a0001c0001t0001g0166others(18): Show | 21 | HG02055.hp2 HG02145.hp2 HG02258.hp1 others(18): Show |
intron_variant | MODIFIER | c.421+7681G>A | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23126345 | ||||||
chr22:23126351
|
T | C | 138 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0126others(135): Show | 139 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(136): Show |
intron_variant | MODIFIER | c.421+7675A>G | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23126351 | ||||||
chr22:23126434
|
G | A | 3 | a0001c0001t0001g0296a0001c0001t0001g0297a0001c0001t0001g0298 | 3 | HG02965.hp1 HG03195.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.421+7592C>T | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23126434 | ||||||
chr22:23126573
|
G | A | 7 | a0001c0001t0001g0177a0001c0001t0001g0304a0003c0004t0001g0005others(4): Show | 7 | HG02258.hp1 HG02970.hp1 HG03098.hp2 others(4): Show |
intron_variant | MODIFIER | c.421+7453C>T | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23126573 | ||||||
chr22:23126603
|
T | C | 2 | a0002c0003t0001g0117a0002c0003t0001g0120 | 2 | HG02486.hp1 HG03654.hp1 |
intron_variant | MODIFIER | c.421+7423A>G | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23126603 | ||||||
chr22:23126637
|
G | T | 3 | a0001c0001t0001g0186a0001c0001t0001g0190a0001c0001t0001g0207 | 3 | NA19010.hp1 NA19079.hp2 NA19085.hp1 |
intron_variant | MODIFIER | c.421+7389C>A | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23126637 | ||||||
chr22:23126772
|
G | T | 2 | a0001c0001t0001g0289a0001c0001t0001g0291 | 2 | HG00673.hp1 HG02027.hp1 |
intron_variant | MODIFIER | c.421+7254C>A | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23126772 | ||||||
chr22:23126981
|
T | C | 1 | a0001c0002t0001g0038 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.421+7045A>G | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23126981 | ||||||
chr22:23126994
|
T | C | 138 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0126others(135): Show | 139 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(136): Show |
intron_variant | MODIFIER | c.421+7032A>G | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23126994 | ||||||
chr22:23127071
|
C | T | 1 | a0001c0001t0001g0305 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.421+6955G>A | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23127071 | ||||||
chr22:23127080
|
C | T | 154 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(151): Show | 156 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(153): Show |
intron_variant | MODIFIER | c.421+6946G>A | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23127080 | ||||||
chr22:23127152
|
C | G | 11 | a0001c0001t0001g0001a0001c0001t0001g0158a0001c0001t0001g0159others(8): Show | 12 | HG02258.hp2 HG02630.hp2 HG02647.hp1 others(9): Show |
intron_variant | MODIFIER | c.421+6874G>C | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23127152 | ||||||
chr22:23127228
|
A | C | 1 | a0001c0002t0001g0085 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.421+6798T>G | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23127228 | ||||||
chr22:23127246
|
A | G | 154 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(151): Show | 156 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(153): Show |
intron_variant | MODIFIER | c.421+6780T>C | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23127246 | ||||||
chr22:23127251
|
G | A | 142 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0126others(139): Show | 143 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(140): Show |
intron_variant | MODIFIER | c.421+6775C>T | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23127251 | ||||||
chr22:23127523
|
A | G | 11 | a0001c0001t0001g0001a0001c0001t0001g0158a0001c0001t0001g0159others(8): Show | 12 | HG02258.hp2 HG02630.hp2 HG02647.hp1 others(9): Show |
intron_variant | MODIFIER | c.421+6503T>C | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23127523 | ||||||
chr22:23127593
|
G | C | 1 | a0001c0001t0001g0287 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.421+6433C>G | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23127593 | ||||||
chr22:23127731
|
C | T | 17 | a0001c0002t0001g0024a0001c0002t0001g0025a0001c0002t0001g0038others(14): Show | 17 | HG00738.hp2 HG00741.hp1 HG01175.hp1 others(14): Show |
intron_variant | MODIFIER | c.421+6295G>A | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23127731 | ||||||
chr22:23127903
|
G | A | 142 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0126others(139): Show | 143 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(140): Show |
intron_variant | MODIFIER | c.421+6123C>T | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23127903 | ||||||
chr22:23127978
|
C | T | 1 | a0001c0001t0001g0157 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.421+6048G>A | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23127978 | ||||||
chr22:23128172
|
C | T | 1 | a0001c0001t0001g0291 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.421+5854G>A | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23128172 | ||||||
chr22:23128220
|
T | G | 11 | a0001c0001t0001g0001a0001c0001t0001g0158a0001c0001t0001g0159others(8): Show | 12 | HG02258.hp2 HG02630.hp2 HG02647.hp1 others(9): Show |
intron_variant | MODIFIER | c.421+5806A>C | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23128220 | ||||||
chr22:23128301
|
T | A | 1 | a0001c0002t0001g0079 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.421+5725A>T | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23128301 | ||||||
chr22:23128473
|
G | A | 141 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0126others(138): Show | 142 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(139): Show |
intron_variant | MODIFIER | c.421+5553C>T | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23128473 | ||||||
chr22:23128524
|
C | T | 14 | a0001c0002t0001g0109a0001c0002t0001g0145a0001c0002t0002g0011others(11): Show | 14 | HG01243.hp1 HG01891.hp2 HG02055.hp1 others(11): Show |
intron_variant | MODIFIER | c.421+5502G>A | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23128524 | ||||||
chr22:23128599
|
G | T | 1 | a0001c0002t0002g0131 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.421+5427C>A | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23128599 | ||||||
chr22:23128712
|
C | T | 4 | a0001c0001t0001g0274a0001c0001t0001g0276a0001c0001t0001g0277others(1): Show | 4 | HG01070.hp2 HG02109.hp2 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.421+5314G>A | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23128712 | ||||||
chr22:23129067
|
C | T | 10 | a0001c0001t0001g0195a0001c0001t0001g0196a0001c0001t0001g0197others(7): Show | 10 | HG00558.hp1 NA18957.hp1 NA18970.hp1 others(7): Show |
intron_variant | MODIFIER | c.421+4959G>A | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23129067 | ||||||
chr22:23129104
|
G | C | 1 | a0001c0002t0001g0047 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.421+4922C>G | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23129104 | ||||||
chr22:23129233
|
G | C | 3 | a0003c0004t0001g0301a0003c0004t0001g0302a0003c0004t0001g0303 | 3 | HG02723.hp1 HG06807.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.421+4793C>G | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23129233 | ||||||
chr22:23129346
|
C | T | 138 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0126others(135): Show | 139 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(136): Show |
intron_variant | MODIFIER | c.421+4680G>A | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23129346 | ||||||
chr22:23129437
|
G | A | 142 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0126others(139): Show | 143 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(140): Show |
intron_variant | MODIFIER | c.421+4589C>T | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23129437 | ||||||
chr22:23129706
|
G | A | 3 | a0001c0001t0001g0289a0001c0001t0001g0291a0001c0001t0001g0300 | 3 | HG00673.hp1 HG00741.hp2 HG02027.hp1 |
intron_variant | MODIFIER | c.421+4320C>T | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23129706 | ||||||
chr22:23129813
|
G | A | 11 | a0001c0001t0001g0166a0001c0001t0001g0167a0001c0001t0001g0168others(8): Show | 11 | HG02280.hp2 HG02486.hp2 HG02647.hp2 others(8): Show |
intron_variant | MODIFIER | c.421+4213C>T | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23129813 | ||||||
chr22:23129824
|
T | G | 174 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(171): Show | 176 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(173): Show |
intron_variant | MODIFIER | c.421+4202A>C | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23129824 | ||||||
chr22:23130053
|
GAAAGAAA others(18): Show |
G | 1 | a0001c0001t0001g0264 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.421+3948_421+3972d others(27): Show |
RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23130053 | ||||||
chr22:23130059
|
A | AAAAG | 10 | a0001c0002t0001g0007a0001c0002t0001g0048a0001c0002t0001g0049others(7): Show | 10 | HG00735.hp1 HG01070.hp1 HG01071.hp1 others(7): Show |
intron_variant | MODIFIER | c.421+3963_421+3966d others(6): Show |
RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23130059 | ||||||
chr22:23130059
|
AAAAGAAA others(21): Show |
A | 18 | a0001c0001t0001g0001a0001c0001t0001g0156a0001c0001t0001g0161others(15): Show | 19 | HG00099.hp2 HG00738.hp1 HG01070.hp2 others(16): Show |
intron_variant | MODIFIER | c.421+3939_421+3966d others(30): Show |
RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23130059 | ||||||
chr22:23130059
|
AAAAGAAA others(25): Show |
A | 17 | a0001c0001t0001g0002a0001c0001t0001g0148a0001c0001t0001g0158others(14): Show | 18 | HG00280.hp1 HG00673.hp1 HG01257.hp2 others(15): Show |
intron_variant | MODIFIER | c.421+3935_421+3966d others(34): Show |
RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23130059 | ||||||
chr22:23130059
|
AAAAGAAA others(29): Show |
A | 7 | a0001c0001t0001g0166a0001c0001t0001g0168a0001c0001t0001g0173others(4): Show | 7 | HG00639.hp1 HG01169.hp2 HG01255.hp2 others(4): Show |
intron_variant | MODIFIER | c.421+3931_421+3966d others(38): Show |
RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23130059 | ||||||
chr22:23130059
|
AAAAGAAA others(33): Show |
A | 8 | a0001c0001t0001g0151a0001c0001t0001g0171a0001c0001t0001g0226others(5): Show | 8 | HG01071.hp2 HG01109.hp2 HG01884.hp1 others(5): Show |
intron_variant | MODIFIER | c.421+3927_421+3966d others(42): Show |
RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23130059 | ||||||
chr22:23130059
|
AAAAGAAA others(37): Show |
A | 11 | a0001c0001t0001g0150a0001c0001t0001g0167a0001c0001t0001g0206others(8): Show | 11 | HG01081.hp1 HG01175.hp2 HG01516.hp2 others(8): Show |
intron_variant | MODIFIER | c.421+3923_421+3966d others(46): Show |
RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23130059 | ||||||
chr22:23130059
|
AAAAGAAA others(41): Show |
A | 5 | a0001c0001t0001g0200a0001c0001t0001g0209a0001c0001t0001g0217others(2): Show | 5 | HG01975.hp2 HG02080.hp1 HG02735.hp2 others(2): Show |
intron_variant | MODIFIER | c.421+3919_421+3966d others(50): Show |
RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23130059 | ||||||
chr22:23130059
|
AAAAGAAA others(45): Show |
A | 15 | a0001c0001t0001g0149a0001c0001t0001g0182a0001c0001t0001g0184others(12): Show | 15 | HG00099.hp1 HG00597.hp2 HG00609.hp2 others(12): Show |
intron_variant | MODIFIER | c.421+3915_421+3966d others(54): Show |
RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23130059 | ||||||
chr22:23130059
|
AAAAGAAA others(49): Show |
A | 22 | a0001c0001t0001g0183a0001c0001t0001g0190a0001c0001t0001g0191others(19): Show | 22 | HG00280.hp2 HG00735.hp2 HG01346.hp1 others(19): Show |
intron_variant | MODIFIER | c.421+3911_421+3966d others(58): Show |
RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23130059 | ||||||
chr22:23130059
|
AAAAGAAA others(53): Show |
A | 24 | a0001c0001t0001g0195a0001c0001t0001g0196a0001c0001t0001g0197others(21): Show | 24 | HG00609.hp1 HG01261.hp2 HG01358.hp1 others(21): Show |
intron_variant | MODIFIER | c.421+3907_421+3966d others(62): Show |
RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23130059 | ||||||
chr22:23130059
|
AAAAGAAA others(57): Show |
A | 14 | a0001c0001t0001g0008a0001c0001t0001g0205a0001c0001t0001g0218others(11): Show | 14 | HG00558.hp1 HG01192.hp2 HG02004.hp1 others(11): Show |
intron_variant | MODIFIER | c.421+3903_421+3966d others(66): Show |
RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23130059 | ||||||
chr22:23130059
|
AAAAGAAA others(61): Show |
A | 2 | a0001c0001t0001g0225a0001c0001t0001g0227 | 2 | NA18944.hp1 NA18989.hp2 |
intron_variant | MODIFIER | c.421+3899_421+3966d others(70): Show |
RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23130059 | ||||||
chr22:23130060
|
AAAGAAAG others(17): Show |
A | 12 | a0001c0001t0001g0127a0001c0001t0001g0159a0001c0001t0001g0160others(9): Show | 12 | HG00741.hp2 HG01515.hp2 HG01517.hp1 others(9): Show |
intron_variant | MODIFIER | c.421+3942_421+3965d others(26): Show |
RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23130060 | ||||||
chr22:23130064
|
AAAGAAAG others(13): Show |
A | 12 | a0001c0001t0001g0126a0001c0001t0001g0155a0001c0001t0001g0163others(9): Show | 12 | HG00642.hp1 HG00642.hp2 HG01934.hp1 others(9): Show |
intron_variant | MODIFIER | c.421+3942_421+3961d others(22): Show |
RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23130064 | ||||||
chr22:23130068
|
AAAGAAAG others(9): Show |
A | 6 | a0001c0001t0001g0152a0001c0002t0001g0064a0001c0002t0001g0099others(3): Show | 6 | HG00673.hp2 HG01109.hp1 HG02257.hp2 others(3): Show |
intron_variant | MODIFIER | c.421+3942_421+3957d others(18): Show |
RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23130068 | ||||||
chr22:23130072
|
AAAGAAAG others(5): Show |
A | 1 | a0009c0012t0001g0181 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.421+3942_421+3953d others(14): Show |
RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23130072 | ||||||
chr22:23130084
|
G | A | 5 | a0001c0001t0001g0147a0001c0001t0001g0157a0001c0001t0001g0287others(2): Show | 5 | HG01346.hp2 HG02027.hp1 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.421+3942C>T | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23130084 | ||||||
chr22:23130084
|
G | GAAGA | 5 | a0001c0002t0001g0025a0001c0002t0001g0046a0001c0002t0001g0083others(2): Show | 5 | HG01175.hp1 HG02129.hp1 HG02155.hp2 others(2): Show |
intron_variant | MODIFIER | c.421+3938_421+3941d others(6): Show |
RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23130084 | ||||||
chr22:23130084
|
GAAGA | G | 32 | a0001c0002t0001g0006a0001c0002t0001g0017a0001c0002t0001g0018others(29): Show | 32 | HG00558.hp2 HG01081.hp2 HG01106.hp2 others(29): Show |
intron_variant | MODIFIER | c.421+3938_421+3941d others(6): Show |
RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23130084 | ||||||
chr22:23130084
|
GAAGAAAG others(1): Show |
G | 33 | a0001c0002t0001g0013a0001c0002t0001g0014a0001c0002t0001g0029others(30): Show | 33 | HG00544.hp1 HG00597.hp1 HG01255.hp1 others(30): Show |
intron_variant | MODIFIER | c.421+3934_421+3941d others(10): Show |
RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23130084 | ||||||
chr22:23130084
|
GAAGAAAG others(5): Show |
G | 13 | a0001c0002t0001g0007a0001c0002t0001g0022a0001c0002t0001g0028others(10): Show | 13 | HG00735.hp1 HG01070.hp1 HG01071.hp1 others(10): Show |
intron_variant | MODIFIER | c.421+3930_421+3941d others(14): Show |
RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23130084 | ||||||
chr22:23130084
|
GAAGAAAG others(9): Show |
G | 11 | a0001c0002t0001g0020a0001c0002t0001g0032a0001c0002t0001g0090others(8): Show | 11 | HG01243.hp1 HG01361.hp2 HG01943.hp1 others(8): Show |
intron_variant | MODIFIER | c.421+3926_421+3941d others(18): Show |
RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23130084 | ||||||
chr22:23130084
|
GAAGAAAG others(13): Show |
G | 5 | a0001c0001t0001g0153a0001c0002t0001g0019a0001c0002t0001g0024others(2): Show | 5 | HG00741.hp1 HG02818.hp2 HG04204.hp2 others(2): Show |
intron_variant | MODIFIER | c.421+3922_421+3941d others(22): Show |
RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23130084 | ||||||
chr22:23130084
|
GAAGAAAG others(17): Show |
G | 3 | a0001c0002t0001g0023a0001c0002t0001g0129a0001c0002t0001g0145 | 3 | HG00544.hp2 HG02818.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.421+3918_421+3941d others(26): Show |
RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23130084 | ||||||
chr22:23130084
|
GAAGAAAG others(21): Show |
G | 1 | a0001c0002t0001g0104 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.421+3914_421+3941d others(30): Show |
RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23130084 | ||||||
chr22:23130096
|
A | G | 3 | a0001c0002t0001g0064a0001c0002t0001g0099a0001c0002t0001g0109 | 3 | HG00673.hp2 HG03453.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.421+3930T>C | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23130096 | ||||||
chr22:23130096
|
AAAGAAAG others(24): Show |
A | 1 | a0001c0001t0001g0147 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.421+3899_421+3929d others(33): Show |
RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23130096 | ||||||
chr22:23130100
|
A | G | 2 | a0001c0002t0001g0063a0001c0002t0001g0106 | 2 | HG03490.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.421+3926T>C | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23130100 | ||||||
chr22:23130115
|
GAAAGAAA others(39): Show |
G | 1 | a0001c0001t0001g0287 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.421+3865_421+3910d others(48): Show |
RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23130115 | ||||||
chr22:23130138
|
A | G | 1 | a0001c0001t0001g0304 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.421+3888T>C | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23130138 | ||||||
chr22:23130139
|
GAAAGAAA others(15): Show |
G | 1 | a0001c0001t0001g0291 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.421+3865_421+3886d others(24): Show |
RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23130139 | ||||||
chr22:23130161
|
A | G | 1 | a0001c0002t0001g0017 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.421+3865T>C | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23130161 | ||||||
chr22:23130197
|
T | G | 35 | a0001c0001t0001g0002a0001c0001t0001g0126a0001c0001t0001g0127others(32): Show | 36 | HG00099.hp2 HG00280.hp1 HG00642.hp1 others(33): Show |
intron_variant | MODIFIER | c.421+3829A>C | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23130197 | ||||||
chr22:23130222
|
G | A | 2 | a0001c0001t0001g0150a0001c0001t0001g0236 | 2 | HG01516.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.421+3804C>T | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23130222 | ||||||
chr22:23130393
|
T | C | 1 | a0001c0002t0001g0109 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.421+3633A>G | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23130393 | ||||||
chr22:23130412
|
A | G | 185 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(182): Show | 187 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(184): Show |
intron_variant | MODIFIER | c.421+3614T>C | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23130412 | ||||||
chr22:23130476
|
G | C | 1 | a0001c0001t0001g0285 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.421+3550C>G | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23130476 | ||||||
chr22:23130485
|
A | G | 1 | a0004c0009t0001g0311 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.421+3541T>C | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23130485 | ||||||
chr22:23130489
|
G | A | 1 | a0004c0009t0001g0311 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.421+3537C>T | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23130489 | ||||||
chr22:23130489
|
G | GAAGAAAG others(23): Show |
1 | a0009c0012t0001g0181 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.421+3536_421+3537i others(32): Show |
RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23130489 | ||||||
chr22:23130489
|
G | GGAGAAAG others(15): Show |
1 | a0001c0002t0001g0067 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.421+3536_421+3537i others(24): Show |
RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23130489 | ||||||
chr22:23130489
|
GGAAAGAA others(7): Show |
G | 1 | a0001c0002t0001g0017 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.421+3523_421+3536d others(16): Show |
RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23130489 | ||||||
chr22:23130490
|
GAAAGAA | G | 5 | a0001c0001t0001g0001a0001c0001t0001g0163a0001c0001t0001g0165others(2): Show | 6 | HG02630.hp2 HG02647.hp1 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.421+3530_421+3535d others(8): Show |
RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23130490 | ||||||
chr22:23130493
|
A | G | 1 | a0001c0002t0001g0062 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.421+3533T>C | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23130493 | ||||||
chr22:23130494
|
GAA | G | 3 | a0001c0001t0001g0158a0001c0002t0001g0025a0001c0002t0001g0027 | 3 | HG01516.hp1 HG03098.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.421+3530_421+3531d others(4): Show |
RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23130494 | ||||||
chr22:23130496
|
A | AAG | 8 | a0001c0001t0001g0153a0001c0001t0001g0159a0001c0002t0001g0018others(5): Show | 8 | HG01258.hp1 HG01981.hp1 HG03540.hp2 others(5): Show |
intron_variant | MODIFIER | c.421+3529_421+3530i others(4): Show |
RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23130496 | ||||||
chr22:23130496
|
A | AAGAAAG | 29 | a0001c0001t0001g0160a0001c0001t0001g0161a0001c0001t0001g0184others(26): Show | 29 | HG00609.hp2 HG01081.hp1 HG01106.hp2 others(26): Show |
intron_variant | MODIFIER | c.421+3529_421+3530i others(8): Show |
RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23130496 | ||||||
chr22:23130496
|
A | AAGAAAGA others(3): Show |
28 | a0001c0001t0001g0149a0001c0001t0001g0200a0001c0001t0001g0201others(25): Show | 28 | HG00558.hp1 HG00609.hp1 HG00741.hp2 others(25): Show |
intron_variant | MODIFIER | c.421+3529_421+3530i others(12): Show |
RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23130496 | ||||||
chr22:23130496
|
A | AAGAAAGA others(7): Show |
25 | a0001c0001t0001g0162a0001c0001t0001g0182a0001c0001t0001g0206others(22): Show | 25 | HG00099.hp1 HG01070.hp2 HG01109.hp1 others(22): Show |
intron_variant | MODIFIER | c.421+3529_421+3530i others(16): Show |
RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23130496 | ||||||
chr22:23130496
|
A | AAGAAAGA others(11): Show |
36 | a0001c0001t0001g0008a0001c0001t0001g0150a0001c0001t0001g0151others(33): Show | 36 | HG00558.hp2 HG01071.hp2 HG01192.hp2 others(33): Show |
intron_variant | MODIFIER | c.421+3529_421+3530i others(20): Show |
RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23130496 | ||||||
chr22:23130496
|
A | AAGAAAGA others(15): Show |
38 | a0001c0001t0001g0154a0001c0001t0001g0155a0001c0001t0001g0156others(35): Show | 38 | HG00639.hp1 HG00735.hp2 HG01175.hp2 others(35): Show |
intron_variant | MODIFIER | c.421+3529_421+3530i others(24): Show |
RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23130496 | ||||||
chr22:23130496
|
A | AAGAAAGA others(19): Show |
43 | a0001c0001t0001g0147a0001c0001t0001g0166a0001c0001t0001g0167others(40): Show | 43 | HG00280.hp1 HG00280.hp2 HG00597.hp2 others(40): Show |
intron_variant | MODIFIER | c.421+3529_421+3530i others(28): Show |
RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23130496 | ||||||
chr22:23130496
|
A | AAGAAAGA others(23): Show |
32 | a0001c0001t0001g0126a0001c0001t0001g0148a0001c0001t0001g0168others(29): Show | 32 | HG00099.hp2 HG00642.hp1 HG00642.hp2 others(29): Show |
intron_variant | MODIFIER | c.421+3529_421+3530i others(32): Show |
RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23130496 | ||||||
chr22:23130496
|
A | AAGAAAGA others(27): Show |
20 | a0001c0001t0001g0002a0001c0001t0001g0127a0001c0001t0001g0174others(17): Show | 21 | HG00544.hp2 HG00597.hp1 HG00673.hp2 others(18): Show |
intron_variant | MODIFIER | c.421+3529_421+3530i others(36): Show |
RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23130496 | ||||||
chr22:23130496
|
A | AAGAAAGA others(31): Show |
15 | a0001c0001t0001g0269a0001c0001t0001g0270a0001c0001t0001g0289others(12): Show | 15 | HG00544.hp1 HG00673.hp1 HG00738.hp1 others(12): Show |
intron_variant | MODIFIER | c.421+3529_421+3530i others(40): Show |
RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23130496 | ||||||
chr22:23130496
|
A | AAGAAAGA others(35): Show |
8 | a0001c0001t0001g0250a0001c0001t0001g0271a0001c0001t0001g0280others(5): Show | 8 | HG01255.hp2 HG01358.hp2 HG02155.hp2 others(5): Show |
intron_variant | MODIFIER | c.421+3529_421+3530i others(44): Show |
RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23130496 | ||||||
chr22:23130496
|
A | AAGAAAGA others(39): Show |
6 | a0001c0001t0001g0226a0001c0002t0001g0007a0001c0002t0001g0048others(3): Show | 6 | HG00735.hp1 HG01070.hp1 HG01071.hp1 others(3): Show |
intron_variant | MODIFIER | c.421+3529_421+3530i others(48): Show |
RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23130496 | ||||||
chr22:23130496
|
A | AAGAAAGA others(43): Show |
2 | a0001c0001t0001g0272a0001c0002t0001g0083 | 2 | HG02129.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.421+3529_421+3530i others(52): Show |
RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23130496 | ||||||
chr22:23130496
|
A | AAGAAAGA others(47): Show |
2 | a0001c0002t0001g0098a0001c0002t0001g0104 | 2 | NA19074.hp1 NA19079.hp1 |
intron_variant | MODIFIER | c.421+3529_421+3530i others(56): Show |
RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23130496 | ||||||
chr22:23130496
|
A | AAGAAAGA others(51): Show |
1 | a0001c0002t0001g0084 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.421+3529_421+3530i others(60): Show |
RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23130496 | ||||||
chr22:23130496
|
A | AAGAAAGA others(59): Show |
1 | a0001c0001t0001g0292 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.421+3529_421+3530i others(68): Show |
RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23130496 | ||||||
chr22:23130496
|
A | AAGAAAGA others(63): Show |
1 | a0001c0001t0001g0227 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.421+3529_421+3530i others(72): Show |
RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23130496 | ||||||
chr22:23130496
|
A | AAGAAAGA others(67): Show |
1 | a0001c0002t0001g0085 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.421+3529_421+3530i others(76): Show |
RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23130496 | ||||||
chr22:23130496
|
A | AAGAAAGA others(46): Show |
1 | a0001c0002t0001g0056 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.421+3529_421+3530i others(55): Show |
RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23130496 | ||||||
chr22:23130529
|
A | AAAGAAAG others(24): Show |
1 | a0001c0002t0001g0055 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.421+3496_421+3497i others(33): Show |
RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23130529 | ||||||
chr22:23130534
|
G | A | 4 | a0001c0001t0001g0152a0001c0001t0001g0154a0001c0001t0001g0155others(1): Show | 4 | HG02257.hp2 HG02630.hp1 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.421+3492C>T | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23130534 | ||||||
chr22:23130627
|
T | C | 1 | a0001c0001t0001g0293 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.421+3399A>G | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23130627 | ||||||
chr22:23130767
|
T | C | 153 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(150): Show | 155 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(152): Show |
intron_variant | MODIFIER | c.421+3259A>G | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23130767 | ||||||
chr22:23130812
|
G | A | 3 | a0001c0002t0001g0086a0001c0002t0001g0087a0001c0002t0001g0142 | 3 | HG00544.hp1 HG02523.hp2 NA18965.hp1 |
intron_variant | MODIFIER | c.421+3214C>T | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23130812 | ||||||
chr22:23130873
|
G | A | 3 | a0001c0001t0001g0147a0001c0001t0001g0148a0001c0001t0001g0179 | 3 | HG02055.hp2 HG02145.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.421+3153C>T | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23130873 | ||||||
chr22:23130936
|
A | G | 11 | a0001c0001t0001g0001a0001c0001t0001g0158a0001c0001t0001g0159others(8): Show | 12 | HG02258.hp2 HG02630.hp2 HG02647.hp1 others(9): Show |
intron_variant | MODIFIER | c.421+3090T>C | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23130936 | ||||||
chr22:23130958
|
G | A | 11 | a0001c0001t0001g0001a0001c0001t0001g0158a0001c0001t0001g0159others(8): Show | 12 | HG02258.hp2 HG02630.hp2 HG02647.hp1 others(9): Show |
intron_variant | MODIFIER | c.421+3068C>T | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23130958 | ||||||
chr22:23131044
|
T | C | 153 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(150): Show | 155 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(152): Show |
intron_variant | MODIFIER | c.421+2982A>G | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23131044 | ||||||
chr22:23131063
|
A | C | 3 | a0001c0002t0001g0016a0001c0002t0001g0042a0001c0002t0001g0043 | 3 | HG02809.hp1 HG03516.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.421+2963T>G | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23131063 | ||||||
chr22:23131072
|
A | G | 11 | a0001c0001t0001g0001a0001c0001t0001g0158a0001c0001t0001g0159others(8): Show | 12 | HG02258.hp2 HG02630.hp2 HG02647.hp1 others(9): Show |
intron_variant | MODIFIER | c.421+2954T>C | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23131072 | ||||||
chr22:23131389
|
AG | A | 18 | a0001c0001t0001g0166a0001c0001t0001g0167a0001c0001t0001g0168others(15): Show | 18 | HG02258.hp1 HG02280.hp2 HG02486.hp2 others(15): Show |
intron_variant | MODIFIER | c.421+2636delC | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23131389 | ||||||
chr22:23131611
|
G | A | 1 | a0001c0002t0001g0046 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.421+2415C>T | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23131611 | ||||||
chr22:23131646
|
G | A | 1 | a0001c0001t0001g0272 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.421+2380C>T | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23131646 | ||||||
chr22:23131652
|
T | A | 11 | a0001c0001t0001g0001a0001c0001t0001g0158a0001c0001t0001g0159others(8): Show | 12 | HG02258.hp2 HG02630.hp2 HG02647.hp1 others(9): Show |
intron_variant | MODIFIER | c.421+2374A>T | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23131652 | ||||||
chr22:23131675
|
T | A | 3 | a0003c0004t0001g0301a0003c0004t0001g0302a0003c0004t0001g0303 | 3 | HG02723.hp1 HG06807.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.421+2351A>T | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23131675 | ||||||
chr22:23131687
|
G | A | 1 | a0001c0001t0001g0235 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.421+2339C>T | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23131687 | ||||||
chr22:23131898
|
G | A | 41 | a0001c0001t0001g0002a0001c0001t0001g0126a0001c0001t0001g0127others(38): Show | 42 | HG00099.hp2 HG00280.hp1 HG00642.hp1 others(39): Show |
intron_variant | MODIFIER | c.421+2128C>T | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23131898 | ||||||
chr22:23132243
|
G | A | 5 | a0001c0001t0001g0001a0001c0001t0001g0163a0001c0001t0001g0165others(2): Show | 6 | HG02630.hp2 HG02647.hp1 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.421+1783C>T | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23132243 | ||||||
chr22:23132281
|
C | T | 1 | a0001c0002t0001g0026 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.421+1745G>A | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23132281 | ||||||
chr22:23132392
|
C | T | 1 | a0001c0001t0001g0242 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.421+1634G>A | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23132392 | ||||||
chr22:23132565
|
A | AAT | 153 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(150): Show | 155 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(152): Show |
intron_variant | MODIFIER | c.421+1459_421+1460d others(4): Show |
RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23132565 | ||||||
chr22:23132569
|
T | C | 15 | a0001c0002t0001g0025a0002c0003t0001g0113a0002c0003t0001g0114others(12): Show | 15 | HG00738.hp2 HG01175.hp1 HG02486.hp1 others(12): Show |
intron_variant | MODIFIER | c.421+1457A>G | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23132569 | ||||||
chr22:23132608
|
A | G | 142 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0126others(139): Show | 143 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(140): Show |
intron_variant | MODIFIER | c.421+1418T>C | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23132608 | ||||||
chr22:23132637
|
A | ACCC | 138 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0126others(135): Show | 139 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(136): Show |
intron_variant | MODIFIER | c.421+1388_421+1389i others(5): Show |
RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23132637 | ||||||
chr22:23132638
|
A | T | 138 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0126others(135): Show | 139 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(136): Show |
intron_variant | MODIFIER | c.421+1388T>A | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23132638 | ||||||
chr22:23132721
|
A | C | 11 | a0001c0001t0001g0001a0001c0001t0001g0158a0001c0001t0001g0159others(8): Show | 12 | HG02258.hp2 HG02630.hp2 HG02647.hp1 others(9): Show |
intron_variant | MODIFIER | c.421+1305T>G | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23132721 | ||||||
chr22:23132785
|
A | G | 153 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(150): Show | 155 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(152): Show |
intron_variant | MODIFIER | c.421+1241T>C | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23132785 | ||||||
chr22:23132880
|
T | A | 21 | a0001c0001t0001g0150a0001c0001t0001g0182a0001c0001t0001g0215others(18): Show | 21 | HG00280.hp2 HG00597.hp2 HG00639.hp1 others(18): Show |
intron_variant | MODIFIER | c.421+1146A>T | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23132880 | ||||||
chr22:23132915
|
G | A | 8 | a0001c0002t0001g0050a0001c0002t0001g0054a0001c0002t0001g0088others(5): Show | 8 | HG01928.hp2 HG01943.hp1 HG02027.hp2 others(5): Show |
intron_variant | MODIFIER | c.421+1111C>T | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23132915 | ||||||
chr22:23132930
|
G | A | 20 | a0001c0001t0001g0166a0001c0001t0001g0167a0001c0001t0001g0168others(17): Show | 20 | HG01243.hp1 HG02258.hp1 HG02280.hp2 others(17): Show |
intron_variant | MODIFIER | c.421+1096C>T | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23132930 | ||||||
chr22:23133140
|
T | C | 1 | a0001c0001t0001g0295 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.421+886A>G | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23133140 | ||||||
chr22:23133451
|
C | T | 1 | a0001c0002t0001g0047 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.421+575G>A | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23133451 | ||||||
chr22:23133563
|
G | A | 142 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0126others(139): Show | 143 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(140): Show |
intron_variant | MODIFIER | c.421+463C>T | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23133563 | ||||||
chr22:23133575
|
C | T | 141 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0126others(138): Show | 142 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(139): Show |
intron_variant | MODIFIER | c.421+451G>A | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23133575 | ||||||
chr22:23133576
|
G | A | 1 | a0001c0002t0001g0109 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.421+450C>T | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23133576 | ||||||
chr22:23133675
|
C | T | 3 | a0003c0004t0001g0301a0003c0004t0001g0302a0003c0004t0001g0303 | 3 | HG02723.hp1 HG06807.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.421+351G>A | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23133675 | ||||||
chr22:23133781
|
G | C | 1 | a0001c0002t0001g0143 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.421+245C>G | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23133781 | ||||||
chr22:23133878
|
A | T | 4 | a0001c0001t0001g0157a0003c0004t0001g0301a0003c0004t0001g0302others(1): Show | 4 | HG02723.hp1 HG02976.hp2 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.421+148T>A | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23133878 | ||||||
chr22:23134015
|
C | T | 1 | a0001c0002t0002g0131 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.421+11G>A | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23134015 | ||||||
chr22:23134237
|
A | G | 3 | a0001c0001t0001g0184a0001c0001t0001g0185a0001c0001t0001g0255 | 3 | HG00609.hp2 HG02056.hp1 NA19058.hp1 |
intron_variant | MODIFIER | c.303-93T>C | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 3/6 | chr22 | 23134237 | ||||||
chr22:23134548
|
CA | C | 191 | a0001c0001t0001g0008a0001c0001t0001g0149a0001c0001t0001g0151others(188): Show | 191 | HG00099.hp1 HG00280.hp2 HG00544.hp1 others(188): Show |
intron_variant | MODIFIER | c.303-405delT | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 3/6 | chr22 | 23134548 | ||||||
chr22:23134548
|
CAA | C | 46 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0126others(43): Show | 48 | HG00099.hp2 HG00280.hp1 HG00642.hp1 others(45): Show |
intron_variant | MODIFIER | c.303-406_303-405del others(2): Show |
RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 3/6 | chr22 | 23134548 | ||||||
chr22:23134548
|
CAAAAAAA others(7): Show |
C | 3 | a0001c0001t0001g0147a0001c0001t0001g0148a0001c0001t0001g0179 | 3 | HG02055.hp2 HG02145.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.303-418_303-405del others(14): Show |
RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 3/6 | chr22 | 23134548 | ||||||
chr22:23134808
|
T | G | 1 | a0001c0001t0001g0244 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.303-664A>C | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 3/6 | chr22 | 23134808 | ||||||
chr22:23134852
|
G | A | 4 | a0001c0001t0001g0157a0003c0004t0001g0301a0003c0004t0001g0302others(1): Show | 4 | HG02723.hp1 HG02976.hp2 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.303-708C>T | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 3/6 | chr22 | 23134852 | ||||||
chr22:23135007
|
C | T | 1 | a0001c0002t0001g0051 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.303-863G>A | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 3/6 | chr22 | 23135007 | ||||||
chr22:23135182
|
A | G | 5 | a0001c0001t0001g0152a0001c0001t0001g0153a0001c0001t0001g0154others(2): Show | 5 | HG02257.hp2 HG02630.hp1 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.303-1038T>C | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 3/6 | chr22 | 23135182 | ||||||
chr22:23135212
|
G | A | 1 | a0001c0001t0001g0152 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.303-1068C>T | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 3/6 | chr22 | 23135212 | ||||||
chr22:23135287
|
C | G | 85 | a0001c0001t0001g0008a0001c0001t0001g0149a0001c0001t0001g0150others(82): Show | 85 | HG00099.hp1 HG00280.hp2 HG00558.hp1 others(82): Show |
intron_variant | MODIFIER | c.303-1143G>C | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 3/6 | chr22 | 23135287 | ||||||
chr22:23135290
|
A | G | 1 | a0002c0003t0001g0113 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.303-1146T>C | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 3/6 | chr22 | 23135290 | ||||||
chr22:23135315
|
T | C | 39 | a0001c0001t0001g0002a0001c0001t0001g0126a0001c0001t0001g0127others(36): Show | 40 | HG00099.hp2 HG00280.hp1 HG00642.hp1 others(37): Show |
intron_variant | MODIFIER | c.303-1171A>G | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 3/6 | chr22 | 23135315 | ||||||
chr22:23135317
|
C | CA | 34 | a0001c0001t0001g0169a0001c0001t0001g0170a0001c0001t0001g0171others(31): Show | 34 | HG00544.hp2 HG00741.hp1 HG01261.hp1 others(31): Show |
intron_variant | MODIFIER | c.303-1174dupT | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 3/6 | chr22 | 23135317 | ||||||
chr22:23135317
|
CA | C | 36 | a0001c0001t0001g0002a0001c0001t0001g0126a0001c0001t0001g0127others(33): Show | 37 | HG00099.hp2 HG00280.hp1 HG00642.hp1 others(34): Show |
intron_variant | MODIFIER | c.303-1174delT | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 3/6 | chr22 | 23135317 | ||||||
chr22:23135317
|
CAA | C | 16 | a0001c0001t0001g0152a0001c0001t0001g0157a0001c0001t0001g0165others(13): Show | 16 | HG01243.hp2 HG01261.hp2 HG01928.hp1 others(13): Show |
intron_variant | MODIFIER | c.303-1175_303-1174d others(4): Show |
RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 3/6 | chr22 | 23135317 | ||||||
chr22:23135317
|
CAAA | C | 85 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0149others(82): Show | 86 | HG00099.hp1 HG00280.hp2 HG00558.hp1 others(83): Show |
intron_variant | MODIFIER | c.303-1176_303-1174d others(5): Show |
RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 3/6 | chr22 | 23135317 | ||||||
chr22:23135319
|
A | C | 2 | a0001c0001t0001g0257a0001c0001t0001g0258 | 2 | HG03471.hp1 NA18986.hp2 |
intron_variant | MODIFIER | c.303-1175T>G | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 3/6 | chr22 | 23135319 | ||||||
chr22:23135364
|
C | T | 1 | a0001c0002t0001g0050 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.303-1220G>A | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 3/6 | chr22 | 23135364 | ||||||
chr22:23135422
|
G | A | 1 | a0001c0001t0001g0157 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.303-1278C>T | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 3/6 | chr22 | 23135422 | ||||||
chr22:23135446
|
C | T | 3 | a0001c0001t0001g0147a0001c0001t0001g0148a0001c0001t0001g0179 | 3 | HG02055.hp2 HG02145.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.303-1302G>A | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 3/6 | chr22 | 23135446 | ||||||
chr22:23135457
|
G | A | 142 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0126others(139): Show | 143 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(140): Show |
intron_variant | MODIFIER | c.303-1313C>T | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 3/6 | chr22 | 23135457 | ||||||
chr22:23135498
|
G | GTAAATAA others(5): Show |
130 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0126others(127): Show | 131 | HG00280.hp1 HG00280.hp2 HG00558.hp1 others(128): Show |
intron_variant | MODIFIER | c.303-1366_303-1355d others(14): Show |
RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 3/6 | chr22 | 23135498 | ||||||
chr22:23135498
|
G | GTAAATAA others(9): Show |
10 | a0001c0001t0001g0151a0001c0001t0001g0247a0001c0001t0001g0248others(7): Show | 10 | HG00099.hp1 HG01071.hp2 HG01081.hp1 others(7): Show |
intron_variant | MODIFIER | c.303-1370_303-1355d others(18): Show |
RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 3/6 | chr22 | 23135498 | ||||||
chr22:23135516
|
A | G | 3 | a0001c0002t0001g0007a0001c0002t0001g0048a0001c0002t0001g0049 | 3 | HG00735.hp1 HG01070.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.303-1372T>C | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 3/6 | chr22 | 23135516 | ||||||
chr22:23135623
|
C | T | 2 | a0001c0002t0001g0046a0001c0002t0001g0047 | 2 | HG02738.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.303-1479G>A | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 3/6 | chr22 | 23135623 | ||||||
chr22:23135711
|
A | G | 1 | a0001c0002t0002g0131 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.303-1567T>C | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 3/6 | chr22 | 23135711 | ||||||
chr22:23135783
|
A | G | 175 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(172): Show | 177 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(174): Show |
intron_variant | MODIFIER | c.303-1639T>C | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 3/6 | chr22 | 23135783 | ||||||
chr22:23135840
|
G | A | 1 | a0001c0002t0001g0042 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.303-1696C>T | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 3/6 | chr22 | 23135840 | ||||||
chr22:23135952
|
T | C | 5 | a0001c0001t0001g0152a0001c0001t0001g0153a0001c0001t0001g0154others(2): Show | 5 | HG02257.hp2 HG02630.hp1 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.303-1808A>G | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 3/6 | chr22 | 23135952 | ||||||
chr22:23135963
|
G | A | 6 | a0001c0002t0002g0012a0001c0002t0002g0135a0001c0002t0002g0136others(3): Show | 6 | HG02055.hp1 HG02615.hp1 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.303-1819C>T | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 3/6 | chr22 | 23135963 | ||||||
chr22:23135996
|
A | AT | 3 | a0001c0001t0001g0147a0001c0001t0001g0148a0001c0001t0001g0179 | 3 | HG02055.hp2 HG02145.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.303-1853dupA | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 3/6 | chr22 | 23135996 | ||||||
chr22:23136081
|
G | A | 6 | a0001c0001t0001g0177a0003c0004t0001g0005a0003c0004t0001g0175others(3): Show | 6 | HG02258.hp1 HG03098.hp2 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.303-1937C>T | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 3/6 | chr22 | 23136081 | ||||||
chr22:23136241
|
ATGTCATG others(1124): Show |
A | 92 | a0001c0001t0001g0008a0001c0001t0001g0149a0001c0001t0001g0150others(89): Show | 92 | HG00099.hp1 HG00280.hp2 HG00558.hp1 others(89): Show |
intron_variant | MODIFIER | c.302+1468_303-2098d others(2): Show |
RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 3/6 | chr22 | 23136241 | ||||||
chr22:23136508
|
C | T | 50 | a0001c0001t0001g0002a0001c0001t0001g0126a0001c0001t0001g0127others(47): Show | 51 | HG00099.hp2 HG00280.hp1 HG00642.hp1 others(48): Show |
intron_variant | MODIFIER | c.302+2332G>A | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 3/6 | chr22 | 23136508 | ||||||
chr22:23136630
|
G | A | 1 | a0001c0002t0001g0107 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.302+2210C>T | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 3/6 | chr22 | 23136630 | ||||||
chr22:23136650
|
C | T | 50 | a0001c0001t0001g0002a0001c0001t0001g0126a0001c0001t0001g0127others(47): Show | 51 | HG00099.hp2 HG00280.hp1 HG00642.hp1 others(48): Show |
intron_variant | MODIFIER | c.302+2190G>A | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 3/6 | chr22 | 23136650 | ||||||
chr22:23136893
|
G | A | 1 | a0001c0002t0001g0108 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.302+1947C>T | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 3/6 | chr22 | 23136893 | ||||||
chr22:23137372
|
G | A | 50 | a0001c0001t0001g0002a0001c0001t0001g0126a0001c0001t0001g0127others(47): Show | 51 | HG00099.hp2 HG00280.hp1 HG00642.hp1 others(48): Show |
intron_variant | MODIFIER | c.302+1468C>T | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 3/6 | chr22 | 23137372 | ||||||
chr22:23137431
|
A | G | 1 | a0001c0001t0001g0251 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.302+1409T>C | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 3/6 | chr22 | 23137431 | ||||||
chr22:23137476
|
A | G | 11 | a0001c0001t0001g0001a0001c0001t0001g0158a0001c0001t0001g0159others(8): Show | 12 | HG02258.hp2 HG02630.hp2 HG02647.hp1 others(9): Show |
intron_variant | MODIFIER | c.302+1364T>C | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 3/6 | chr22 | 23137476 | ||||||
chr22:23137503
|
C | T | 1 | a0001c0002t0001g0014 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.302+1337G>A | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 3/6 | chr22 | 23137503 | ||||||
chr22:23137569
|
C | T | 1 | a0001c0001t0001g0296 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.302+1271G>A | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 3/6 | chr22 | 23137569 | ||||||
chr22:23137571
|
G | GT | 41 | a0001c0001t0001g0002a0001c0001t0001g0126a0001c0001t0001g0127others(38): Show | 42 | HG00099.hp2 HG00280.hp1 HG00642.hp1 others(39): Show |
intron_variant | MODIFIER | c.302+1268dupA | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 3/6 | chr22 | 23137571 | ||||||
chr22:23137578
|
T | A | 1 | a0001c0001t0001g0250 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.302+1262A>T | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 3/6 | chr22 | 23137578 | ||||||
chr22:23137696
|
G | A | 11 | a0001c0001t0001g0001a0001c0001t0001g0158a0001c0001t0001g0159others(8): Show | 12 | HG02258.hp2 HG02630.hp2 HG02647.hp1 others(9): Show |
intron_variant | MODIFIER | c.302+1144C>T | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 3/6 | chr22 | 23137696 | ||||||
chr22:23137928
|
T | C | 5 | a0001c0001t0001g0008a0001c0001t0001g0251a0001c0001t0001g0252others(2): Show | 5 | HG01192.hp2 HG01358.hp1 HG01928.hp1 others(2): Show |
intron_variant | MODIFIER | c.302+912A>G | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 3/6 | chr22 | 23137928 | ||||||
chr22:23138327
|
C | T | 3 | a0001c0002t0001g0006a0001c0002t0001g0044a0001c0002t0001g0045 | 3 | NA18973.hp2 NA18986.hp1 NA19057.hp2 |
intron_variant | MODIFIER | c.302+513G>A | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 3/6 | chr22 | 23138327 | ||||||
chr22:23138454
|
A | G | 6 | a0001c0001t0001g0177a0003c0004t0001g0005a0003c0004t0001g0175others(3): Show | 6 | HG02258.hp1 HG03098.hp2 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.302+386T>C | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 3/6 | chr22 | 23138454 | ||||||
chr22:23138473
|
A | T | 6 | a0001c0001t0001g0177a0003c0004t0001g0005a0003c0004t0001g0175others(3): Show | 6 | HG02258.hp1 HG03098.hp2 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.302+367T>A | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 3/6 | chr22 | 23138473 | ||||||
chr22:23138561
|
C | CA | 6 | a0001c0001t0001g0177a0003c0004t0001g0005a0003c0004t0001g0175others(3): Show | 6 | HG02258.hp1 HG03098.hp2 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.302+278dupT | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 3/6 | chr22 | 23138561 | ||||||
chr22:23138597
|
G | A | 1 | a0001c0002t0001g0043 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.302+243C>T | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 3/6 | chr22 | 23138597 | ||||||
chr22:23138651
|
C | T | 1 | a0001c0002t0001g0145 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.302+189G>A | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 3/6 | chr22 | 23138651 | ||||||
chr22:23138738
|
G | A | 78 | a0001c0002t0001g0006a0001c0002t0001g0007a0001c0002t0001g0013others(75): Show | 78 | HG00544.hp1 HG00544.hp2 HG00558.hp2 others(75): Show |
intron_variant | MODIFIER | c.302+102C>T | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 3/6 | chr22 | 23138738 | ||||||
chr22:23138775
|
T | G | 188 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(185): Show | 190 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(187): Show |
intron_variant | MODIFIER | c.302+65A>C | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 3/6 | chr22 | 23138775 | ||||||
chr22:23138946
|
G | GA | 6 | a0001c0001t0001g0147a0001c0001t0001g0148a0001c0001t0001g0179others(3): Show | 6 | HG02055.hp2 HG02135.hp1 HG02145.hp2 others(3): Show |
splice_region_variant&intron_variant | LOW | c.200-5dupT | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 2/6 | chr22 | 23138946 | ||||||
chr22:23138946
|
GA | G | 74 | a0001c0001t0001g0002a0001c0001t0001g0126a0001c0001t0001g0127others(71): Show | 75 | HG00099.hp2 HG00280.hp1 HG00642.hp1 others(72): Show |
splice_region_variant&intron_variant | LOW | c.200-5delT | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 2/6 | chr22 | 23138946 | ||||||
chr22:23138946
|
GAA | G | 79 | a0001c0001t0001g0008a0001c0001t0001g0149a0001c0001t0001g0150others(76): Show | 79 | HG00099.hp1 HG00280.hp2 HG00558.hp1 others(76): Show |
splice_region_variant&intron_variant | LOW | c.200-6_200-5delTT | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 2/6 | chr22 | 23138946 | ||||||
chr22:23139085
|
T | A | 2 | a0001c0002t0001g0111a0001c0002t0001g0112 | 2 | HG02083.hp1 NA18965.hp2 |
intron_variant | MODIFIER | c.200-143A>T | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 2/6 | chr22 | 23139085 | ||||||
chr22:23139396
|
G | A | 3 | a0003c0004t0001g0301a0003c0004t0001g0302a0003c0004t0001g0303 | 3 | HG02723.hp1 HG06807.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.200-454C>T | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 2/6 | chr22 | 23139396 | ||||||
chr22:23139623
|
AAAAT | A | 142 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0126others(139): Show | 143 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(140): Show |
intron_variant | MODIFIER | c.199+595_199+598del others(4): Show |
RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 2/6 | chr22 | 23139623 | ||||||
chr22:23139684
|
G | A | 4 | a0001c0001t0001g0296a0001c0001t0001g0297a0001c0001t0001g0298others(1): Show | 4 | HG01884.hp1 HG02965.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.199+538C>T | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 2/6 | chr22 | 23139684 | ||||||
chr22:23139903
|
T | A | 1 | a0001c0001t0001g0180 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.199+319A>T | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 2/6 | chr22 | 23139903 | ||||||
chr22:23139909
|
T | G | 1 | a0001c0001t0001g0300 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.199+313A>C | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 2/6 | chr22 | 23139909 | ||||||
chr22:23140531
|
C | T | 142 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0126others(139): Show | 143 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(140): Show |
intron_variant | MODIFIER | c.-52-59G>A | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 1/6 | chr22 | 23140531 | ||||||
chr22:23140557
|
C | A | 142 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0126others(139): Show | 143 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(140): Show |
intron_variant | MODIFIER | c.-52-85G>T | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 1/6 | chr22 | 23140557 | ||||||
chr22:23140775
|
A | C | 11 | a0001c0001t0001g0001a0001c0001t0001g0158a0001c0001t0001g0159others(8): Show | 12 | HG02258.hp2 HG02630.hp2 HG02647.hp1 others(9): Show |
intron_variant | MODIFIER | c.-52-303T>G | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 1/6 | chr22 | 23140775 | ||||||
chr22:23141068
|
G | A | 140 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0149others(137): Show | 141 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(138): Show |
intron_variant | MODIFIER | c.-52-596C>T | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 1/6 | chr22 | 23141068 | ||||||
chr22:23141081
|
G | A | 2 | a0001c0002t0001g0128a0001c0002t0001g0129 | 2 | HG00544.hp2 NA18971.hp1 |
intron_variant | MODIFIER | c.-52-609C>T | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 1/6 | chr22 | 23141081 | ||||||
chr22:23141242
|
T | C | 3 | a0003c0004t0001g0301a0003c0004t0001g0302a0003c0004t0001g0303 | 3 | HG02723.hp1 HG06807.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.-53+707A>G | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 1/6 | chr22 | 23141242 | ||||||
chr22:23141244
|
G | A | 4 | a0001c0001t0001g0157a0003c0004t0001g0301a0003c0004t0001g0302others(1): Show | 4 | HG02723.hp1 HG02976.hp2 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.-53+705C>T | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 1/6 | chr22 | 23141244 | ||||||
chr22:23141324
|
T | C | 1 | a0001c0002t0001g0130 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.-53+625A>G | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 1/6 | chr22 | 23141324 | ||||||
chr22:23141327
|
C | CA | 16 | a0001c0002t0001g0139a0001c0002t0001g0140a0001c0002t0001g0141others(13): Show | 16 | HG00544.hp1 HG00597.hp1 HG01081.hp2 others(13): Show |
intron_variant | MODIFIER | c.-53+621dupT | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 1/6 | chr22 | 23141327 | ||||||
chr22:23141327
|
CA | C | 155 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(152): Show | 157 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(154): Show |
intron_variant | MODIFIER | c.-53+621delT | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 1/6 | chr22 | 23141327 | ||||||
chr22:23141327
|
CAA | C | 11 | a0001c0001t0001g0147a0001c0001t0001g0148a0001c0001t0001g0149others(8): Show | 11 | HG01515.hp1 HG01516.hp2 HG02055.hp2 others(8): Show |
intron_variant | MODIFIER | c.-53+620_-53+621del others(2): Show |
RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 1/6 | chr22 | 23141327 | ||||||
chr22:23141582
|
C | A | 171 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0147others(168): Show | 173 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(170): Show |
intron_variant | MODIFIER | c.-53+367G>T | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 1/6 | chr22 | 23141582 | ||||||
chr22:23141846
|
G | A | 2 | a0001c0001t0001g0312a0004c0009t0001g0311 | 2 | HG01109.hp1 HG02109.hp1 |
intron_variant | MODIFIER | c.-53+103C>T | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 1/6 | chr22 | 23141846 | ||||||
chr22:23141883
|
A | C | 1 | a0003c0004t0001g0005 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.-53+66T>G | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 1/6 | chr22 | 23141883 |