geneid | 10083 |
---|---|
ensemblid | ENSG00000006611.17 |
hgncid | 12597 |
symbol | USH1C |
name | USH1 protein network component harmonin |
refseq_nuc | NM_153676.4 |
refseq_prot | NP_710142.1 |
ensembl_nuc | ENST00000005226.12 |
ensembl_prot | ENSP00000005226.7 |
mane_status | MANE Select |
chr | chr11 |
start | 17493900 |
end | 17544416 |
strand | - |
ver | v1.2 |
region | chr11:17493900-17544416 |
region5000 | chr11:17488900-17549416 |
regionname0 | USH1C_chr11_17493900_17544416 |
regionname5000 | USH1C_chr11_17488900_17549416 |
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 | 0/0 | 899 | 211 | 44 | 39 | 107 | 4 | 17 | 82 | USH1C_chr11_17488900_17549416 | USH1C | copy fasta | chr11 | 17488900 | 17549416 |
a0002 | 0/0 | 899 | 128 | 30 | 22 | 50 | 8 | 18 | 37 | USH1C_chr11_17488900_17549416 | USH1C | copy fasta | chr11 | 17488900 | 17549416 |
a0003 | 0/0 | 899 | 5 | 4 | 1 | 0 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | copy fasta | chr11 | 17488900 | 17549416 |
a0004 | 0/0 | 899 | 3 | 2 | 1 | 0 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | copy fasta | chr11 | 17488900 | 17549416 |
a0005 | 0/0 | 899 | 2 | 1 | 1 | 0 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | copy fasta | chr11 | 17488900 | 17549416 |
a0006 | 0/0 | 899 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | copy fasta | chr11 | 17488900 | 17549416 |
a0007 | 0/0 | 899 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | USH1C_chr11_17488900_17549416 | USH1C | copy fasta | chr11 | 17488900 | 17549416 |
a0008 | 0/0 | 899 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | copy fasta | chr11 | 17488900 | 17549416 |
a0009 | 0/0 | 899 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | copy fasta | chr11 | 17488900 | 17549416 |
a0010 | 0/0 | 899 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | copy fasta | chr11 | 17488900 | 17549416 |
a0011 | 0/0 | 899 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | copy fasta | chr11 | 17488900 | 17549416 |
a0012 | 0/0 | 899 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | copy fasta | chr11 | 17488900 | 17549416 |
a0013 | 0/0 | 899 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | copy fasta | chr11 | 17488900 | 17549416 |
a0014 | 0/0 | 899 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | USH1C_chr11_17488900_17549416 | USH1C | copy fasta | chr11 | 17488900 | 17549416 |
a0015 | 0/0 | 899 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | copy fasta | chr11 | 17488900 | 17549416 |
a0016 | 0/0 | 899 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | copy fasta | chr11 | 17488900 | 17549416 |
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 | 2700 | 102 | 18 | 23 | 52 | 3 | 6 | USH1C_chr11_17488900_17549416 | USH1C | copy fasta | chr11 | 17488900 | 17549416 |
c0002 | 0/0 | 2700 | 46 | 2 | 11 | 21 | 4 | 8 | USH1C_chr11_17488900_17549416 | USH1C | copy fasta | chr11 | 17488900 | 17549416 |
c0003 | 0/0 | 2700 | 39 | 19 | 7 | 10 | 0 | 3 | USH1C_chr11_17488900_17549416 | USH1C | copy fasta | chr11 | 17488900 | 17549416 |
c0004 | 0/0 | 2700 | 26 | 0 | 4 | 20 | 1 | 1 | USH1C_chr11_17488900_17549416 | USH1C | copy fasta | chr11 | 17488900 | 17549416 |
c0005 | 0/0 | 2700 | 25 | 18 | 3 | 2 | 0 | 2 | USH1C_chr11_17488900_17549416 | USH1C | copy fasta | chr11 | 17488900 | 17549416 |
c0006 | 0/0 | 2700 | 22 | 0 | 6 | 10 | 1 | 5 | USH1C_chr11_17488900_17549416 | USH1C | copy fasta | chr11 | 17488900 | 17549416 |
c0007 | 0/0 | 2700 | 12 | 0 | 2 | 7 | 0 | 3 | USH1C_chr11_17488900_17549416 | USH1C | copy fasta | chr11 | 17488900 | 17549416 |
c0008 | 0/0 | 2700 | 11 | 1 | 2 | 6 | 0 | 2 | USH1C_chr11_17488900_17549416 | USH1C | copy fasta | chr11 | 17488900 | 17549416 |
c0009 | 0/0 | 2700 | 9 | 0 | 0 | 9 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | copy fasta | chr11 | 17488900 | 17549416 |
c0010 | 0/0 | 2700 | 9 | 0 | 2 | 5 | 2 | 0 | USH1C_chr11_17488900_17549416 | USH1C | copy fasta | chr11 | 17488900 | 17549416 |
c0011 | 0/0 | 2700 | 5 | 4 | 1 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | copy fasta | chr11 | 17488900 | 17549416 |
c0012 | 0/0 | 2700 | 5 | 1 | 0 | 0 | 1 | 3 | USH1C_chr11_17488900_17549416 | USH1C | copy fasta | chr11 | 17488900 | 17549416 |
c0013 | 0/0 | 2700 | 4 | 0 | 0 | 4 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | copy fasta | chr11 | 17488900 | 17549416 |
c0014 | 0/0 | 2700 | 3 | 2 | 1 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | copy fasta | chr11 | 17488900 | 17549416 |
c0015 | 0/0 | 2700 | 3 | 3 | 0 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | copy fasta | chr11 | 17488900 | 17549416 |
c0016 | 0/0 | 2700 | 2 | 0 | 0 | 2 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | copy fasta | chr11 | 17488900 | 17549416 |
c0017 | 0/0 | 2700 | 2 | 2 | 0 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | copy fasta | chr11 | 17488900 | 17549416 |
c0018 | 0/0 | 2700 | 2 | 0 | 0 | 1 | 0 | 1 | USH1C_chr11_17488900_17549416 | USH1C | copy fasta | chr11 | 17488900 | 17549416 |
c0019 | 0/0 | 2700 | 2 | 2 | 0 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | copy fasta | chr11 | 17488900 | 17549416 |
c0020 | 0/0 | 2700 | 2 | 2 | 0 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | copy fasta | chr11 | 17488900 | 17549416 |
c0021 | 0/0 | 2700 | 2 | 2 | 0 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | copy fasta | chr11 | 17488900 | 17549416 |
c0022 | 0/0 | 2700 | 1 | 1 | 0 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | copy fasta | chr11 | 17488900 | 17549416 |
c0023 | 0/0 | 2700 | 1 | 0 | 0 | 1 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | copy fasta | chr11 | 17488900 | 17549416 |
c0024 | 0/0 | 2700 | 1 | 0 | 0 | 0 | 0 | 1 | USH1C_chr11_17488900_17549416 | USH1C | copy fasta | chr11 | 17488900 | 17549416 |
c0025 | 0/0 | 2700 | 1 | 1 | 0 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | copy fasta | chr11 | 17488900 | 17549416 |
c0026 | 0/0 | 2700 | 1 | 0 | 0 | 1 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | copy fasta | chr11 | 17488900 | 17549416 |
c0027 | 0/0 | 2700 | 1 | 0 | 0 | 1 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | copy fasta | chr11 | 17488900 | 17549416 |
c0028 | 0/0 | 2700 | 1 | 0 | 0 | 1 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | copy fasta | chr11 | 17488900 | 17549416 |
c0029 | 0/0 | 2700 | 1 | 1 | 0 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | copy fasta | chr11 | 17488900 | 17549416 |
c0030 | 0/0 | 2700 | 1 | 0 | 1 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | copy fasta | chr11 | 17488900 | 17549416 |
c0031 | 0/0 | 2700 | 1 | 0 | 0 | 1 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | copy fasta | chr11 | 17488900 | 17549416 |
c0032 | 0/0 | 2700 | 1 | 1 | 0 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | copy fasta | chr11 | 17488900 | 17549416 |
c0033 | 0/0 | 2700 | 1 | 1 | 0 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | copy fasta | chr11 | 17488900 | 17549416 |
c0034 | 0/0 | 2700 | 1 | 0 | 1 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | copy fasta | chr11 | 17488900 | 17549416 |
c0035 | 0/0 | 2700 | 1 | 1 | 0 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | copy fasta | chr11 | 17488900 | 17549416 |
c0036 | 0/0 | 2700 | 1 | 0 | 0 | 1 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | copy fasta | chr11 | 17488900 | 17549416 |
c0037 | 0/0 | 2700 | 1 | 0 | 0 | 1 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | copy fasta | chr11 | 17488900 | 17549416 |
c0038 | 0/0 | 2700 | 1 | 0 | 1 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | copy fasta | chr11 | 17488900 | 17549416 |
c0039 | 0/0 | 2700 | 1 | 0 | 0 | 1 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | copy fasta | chr11 | 17488900 | 17549416 |
c0040 | 0/0 | 2700 | 1 | 0 | 0 | 1 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | copy fasta | chr11 | 17488900 | 17549416 |
c0041 | 0/0 | 2700 | 1 | 0 | 0 | 0 | 0 | 1 | USH1C_chr11_17488900_17549416 | USH1C | copy fasta | chr11 | 17488900 | 17549416 |
c0042 | 0/0 | 2700 | 1 | 0 | 1 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | copy fasta | chr11 | 17488900 | 17549416 |
c0043 | 0/0 | 2700 | 1 | 1 | 0 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | copy fasta | chr11 | 17488900 | 17549416 |
c0044 | 0/0 | 2700 | 1 | 1 | 0 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | copy fasta | chr11 | 17488900 | 17549416 |
c0045 | 0/0 | 2700 | 1 | 1 | 0 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | copy fasta | chr11 | 17488900 | 17549416 |
c0046 | 0/0 | 2700 | 1 | 1 | 0 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | copy fasta | chr11 | 17488900 | 17549416 |
c0047 | 0/0 | 2700 | 1 | 1 | 0 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | copy fasta | chr11 | 17488900 | 17549416 |
c0048 | 0/0 | 2700 | 1 | 1 | 0 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | copy fasta | chr11 | 17488900 | 17549416 |
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 | 0/0 | 546 | 218 | 52 | 43 | 96 | 7 | 20 | USH1C_chr11_17488900_17549416 | USH1C | copy fasta | chr11 | 17488900 | 17549416 |
t0002 | 0/0 | 546 | 106 | 22 | 18 | 47 | 5 | 14 | USH1C_chr11_17488900_17549416 | USH1C | copy fasta | chr11 | 17488900 | 17549416 |
t0003 | 0/0 | 542 | 14 | 1 | 3 | 9 | 0 | 1 | USH1C_chr11_17488900_17549416 | USH1C | copy fasta | chr11 | 17488900 | 17549416 |
t0004 | 0/0 | 546 | 3 | 3 | 0 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | copy fasta | chr11 | 17488900 | 17549416 |
t0005 | 0/0 | 546 | 3 | 2 | 1 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | copy fasta | chr11 | 17488900 | 17549416 |
t0006 | 0/0 | 546 | 2 | 2 | 0 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | copy fasta | chr11 | 17488900 | 17549416 |
t0007 | 0/0 | 546 | 2 | 0 | 0 | 2 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | copy fasta | chr11 | 17488900 | 17549416 |
t0008 | 0/0 | 546 | 2 | 2 | 0 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | copy fasta | chr11 | 17488900 | 17549416 |
t0009 | 0/0 | 542 | 2 | 2 | 0 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | copy fasta | chr11 | 17488900 | 17549416 |
t0010 | 0/0 | 546 | 1 | 0 | 0 | 1 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | copy fasta | chr11 | 17488900 | 17549416 |
t0011 | 0/0 | 546 | 1 | 1 | 0 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | copy fasta | chr11 | 17488900 | 17549416 |
t0012 | 0/0 | 546 | 1 | 0 | 0 | 0 | 0 | 1 | USH1C_chr11_17488900_17549416 | USH1C | copy fasta | chr11 | 17488900 | 17549416 |
t0013 | 0/0 | 546 | 1 | 0 | 1 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | copy fasta | chr11 | 17488900 | 17549416 |
t0014 | 0/0 | 546 | 1 | 0 | 0 | 1 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | copy fasta | chr11 | 17488900 | 17549416 |
t0015 | 0/0 | 546 | 1 | 0 | 0 | 1 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | copy fasta | chr11 | 17488900 | 17549416 |
t0016 | 0/0 | 542 | 1 | 1 | 0 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | copy fasta | chr11 | 17488900 | 17549416 |
t0017 | 0/0 | 546 | 1 | 0 | 0 | 1 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | copy fasta | chr11 | 17488900 | 17549416 |
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 | 5 | 0 | 1 | 2 | 1 | 1 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
g0002 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
g0003 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
g0004 | 0/0 | 3 | 0 | 0 | 0 | 0 | 3 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
g0005 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
g0006 | 0/0 | 3 | 0 | 2 | 1 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
g0007 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
g0010 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
g0011 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
g0012 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
g0013 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
g0014 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
g0017 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
g0020 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
g0021 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
g0022 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
g0024 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
g0025 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
g0037 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
g0053 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
g0077 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
g0098 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
g0155 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
g0178 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
g0185 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
g0208 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
g0212 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
g0216 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
g0247 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
g0274 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
g0275 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
g0285 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
g0296 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
g0312 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
g0321 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
g0322 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
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 | 2700 | 102 | 18 | 23 | 52 | 3 | 6 | USH1C_chr11_17488900_17549416 | USH1C | copy fasta | chr11 | 17488900 | 17549416 |
a0001c0003 | 0/0 | 2700 | 39 | 19 | 7 | 10 | 0 | 3 | USH1C_chr11_17488900_17549416 | USH1C | copy fasta | chr11 | 17488900 | 17549416 |
a0001c0004 | 0/0 | 2700 | 26 | 0 | 4 | 20 | 1 | 1 | USH1C_chr11_17488900_17549416 | USH1C | copy fasta | chr11 | 17488900 | 17549416 |
a0001c0007 | 0/0 | 2700 | 12 | 0 | 2 | 7 | 0 | 3 | USH1C_chr11_17488900_17549416 | USH1C | copy fasta | chr11 | 17488900 | 17549416 |
a0001c0008 | 0/0 | 2700 | 11 | 1 | 2 | 6 | 0 | 2 | USH1C_chr11_17488900_17549416 | USH1C | copy fasta | chr11 | 17488900 | 17549416 |
a0001c0013 | 0/0 | 2700 | 4 | 0 | 0 | 4 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | copy fasta | chr11 | 17488900 | 17549416 |
a0001c0016 | 0/0 | 2700 | 2 | 0 | 0 | 2 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | copy fasta | chr11 | 17488900 | 17549416 |
a0001c0017 | 0/0 | 2700 | 2 | 2 | 0 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | copy fasta | chr11 | 17488900 | 17549416 |
a0001c0018 | 0/0 | 2700 | 2 | 0 | 0 | 1 | 0 | 1 | USH1C_chr11_17488900_17549416 | USH1C | copy fasta | chr11 | 17488900 | 17549416 |
a0001c0021 | 0/0 | 2700 | 2 | 2 | 0 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | copy fasta | chr11 | 17488900 | 17549416 |
a0001c0023 | 0/0 | 2700 | 1 | 0 | 0 | 1 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | copy fasta | chr11 | 17488900 | 17549416 |
a0001c0024 | 0/0 | 2700 | 1 | 0 | 0 | 0 | 0 | 1 | USH1C_chr11_17488900_17549416 | USH1C | copy fasta | chr11 | 17488900 | 17549416 |
a0001c0028 | 0/0 | 2700 | 1 | 0 | 0 | 1 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | copy fasta | chr11 | 17488900 | 17549416 |
a0001c0037 | 0/0 | 2700 | 1 | 0 | 0 | 1 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | copy fasta | chr11 | 17488900 | 17549416 |
a0001c0039 | 0/0 | 2700 | 1 | 0 | 0 | 1 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | copy fasta | chr11 | 17488900 | 17549416 |
a0001c0040 | 0/0 | 2700 | 1 | 0 | 0 | 1 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | copy fasta | chr11 | 17488900 | 17549416 |
a0001c0042 | 0/0 | 2700 | 1 | 0 | 1 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | copy fasta | chr11 | 17488900 | 17549416 |
a0001c0043 | 0/0 | 2700 | 1 | 1 | 0 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | copy fasta | chr11 | 17488900 | 17549416 |
a0001c0047 | 0/0 | 2700 | 1 | 1 | 0 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | copy fasta | chr11 | 17488900 | 17549416 |
a0002c0002 | 0/0 | 2700 | 46 | 2 | 11 | 21 | 4 | 8 | USH1C_chr11_17488900_17549416 | USH1C | copy fasta | chr11 | 17488900 | 17549416 |
a0002c0005 | 0/0 | 2700 | 25 | 18 | 3 | 2 | 0 | 2 | USH1C_chr11_17488900_17549416 | USH1C | copy fasta | chr11 | 17488900 | 17549416 |
a0002c0006 | 0/0 | 2700 | 22 | 0 | 6 | 10 | 1 | 5 | USH1C_chr11_17488900_17549416 | USH1C | copy fasta | chr11 | 17488900 | 17549416 |
a0002c0009 | 0/0 | 2700 | 9 | 0 | 0 | 9 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | copy fasta | chr11 | 17488900 | 17549416 |
a0002c0010 | 0/0 | 2700 | 9 | 0 | 2 | 5 | 2 | 0 | USH1C_chr11_17488900_17549416 | USH1C | copy fasta | chr11 | 17488900 | 17549416 |
a0002c0012 | 0/0 | 2700 | 5 | 1 | 0 | 0 | 1 | 3 | USH1C_chr11_17488900_17549416 | USH1C | copy fasta | chr11 | 17488900 | 17549416 |
a0002c0015 | 0/0 | 2700 | 3 | 3 | 0 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | copy fasta | chr11 | 17488900 | 17549416 |
a0002c0019 | 0/0 | 2700 | 2 | 2 | 0 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | copy fasta | chr11 | 17488900 | 17549416 |
a0002c0020 | 0/0 | 2700 | 2 | 2 | 0 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | copy fasta | chr11 | 17488900 | 17549416 |
a0002c0027 | 0/0 | 2700 | 1 | 0 | 0 | 1 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | copy fasta | chr11 | 17488900 | 17549416 |
a0002c0031 | 0/0 | 2700 | 1 | 0 | 0 | 1 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | copy fasta | chr11 | 17488900 | 17549416 |
a0002c0036 | 0/0 | 2700 | 1 | 0 | 0 | 1 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | copy fasta | chr11 | 17488900 | 17549416 |
a0002c0044 | 0/0 | 2700 | 1 | 1 | 0 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | copy fasta | chr11 | 17488900 | 17549416 |
a0002c0046 | 0/0 | 2700 | 1 | 1 | 0 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | copy fasta | chr11 | 17488900 | 17549416 |
a0003c0011 | 0/0 | 2700 | 5 | 4 | 1 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | copy fasta | chr11 | 17488900 | 17549416 |
a0004c0014 | 0/0 | 2700 | 3 | 2 | 1 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | copy fasta | chr11 | 17488900 | 17549416 |
a0005c0035 | 0/0 | 2700 | 1 | 1 | 0 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | copy fasta | chr11 | 17488900 | 17549416 |
a0005c0038 | 0/0 | 2700 | 1 | 0 | 1 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | copy fasta | chr11 | 17488900 | 17549416 |
a0006c0025 | 0/0 | 2700 | 1 | 1 | 0 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | copy fasta | chr11 | 17488900 | 17549416 |
a0007c0026 | 0/0 | 2700 | 1 | 0 | 0 | 1 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | copy fasta | chr11 | 17488900 | 17549416 |
a0008c0030 | 0/0 | 2700 | 1 | 0 | 1 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | copy fasta | chr11 | 17488900 | 17549416 |
a0009c0045 | 0/0 | 2700 | 1 | 1 | 0 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | copy fasta | chr11 | 17488900 | 17549416 |
a0010c0034 | 0/0 | 2700 | 1 | 0 | 1 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | copy fasta | chr11 | 17488900 | 17549416 |
a0011c0048 | 0/0 | 2700 | 1 | 1 | 0 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | copy fasta | chr11 | 17488900 | 17549416 |
a0012c0032 | 0/0 | 2700 | 1 | 1 | 0 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | copy fasta | chr11 | 17488900 | 17549416 |
a0013c0033 | 0/0 | 2700 | 1 | 1 | 0 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | copy fasta | chr11 | 17488900 | 17549416 |
a0014c0041 | 0/0 | 2700 | 1 | 0 | 0 | 0 | 0 | 1 | USH1C_chr11_17488900_17549416 | USH1C | copy fasta | chr11 | 17488900 | 17549416 |
a0015c0029 | 0/0 | 2700 | 1 | 1 | 0 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | copy fasta | chr11 | 17488900 | 17549416 |
a0016c0022 | 0/0 | 2700 | 1 | 1 | 0 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | copy fasta | chr11 | 17488900 | 17549416 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 3245 | 91 | 13 | 20 | 49 | 3 | 6 | USH1C_chr11_17488900_17549416 | USH1C | copy fasta | chr11 | 17488900 | 17549416 |
a0001c0001t0002 | 0/0 | 3245 | 2 | 0 | 2 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | copy fasta | chr11 | 17488900 | 17549416 |
a0001c0001t0003 | 0/0 | 3241 | 4 | 1 | 1 | 2 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | copy fasta | chr11 | 17488900 | 17549416 |
a0001c0001t0008 | 0/0 | 3245 | 1 | 1 | 0 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | copy fasta | chr11 | 17488900 | 17549416 |
a0001c0001t0009 | 0/0 | 3241 | 2 | 2 | 0 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | copy fasta | chr11 | 17488900 | 17549416 |
a0001c0001t0011 | 0/0 | 3245 | 1 | 1 | 0 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | copy fasta | chr11 | 17488900 | 17549416 |
a0001c0001t0014 | 0/0 | 3245 | 1 | 0 | 0 | 1 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | copy fasta | chr11 | 17488900 | 17549416 |
a0001c0003t0001 | 0/0 | 3245 | 30 | 13 | 5 | 10 | 0 | 2 | USH1C_chr11_17488900_17549416 | USH1C | copy fasta | chr11 | 17488900 | 17549416 |
a0001c0003t0002 | 0/0 | 3245 | 1 | 1 | 0 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | copy fasta | chr11 | 17488900 | 17549416 |
a0001c0003t0003 | 0/0 | 3241 | 3 | 0 | 2 | 0 | 0 | 1 | USH1C_chr11_17488900_17549416 | USH1C | copy fasta | chr11 | 17488900 | 17549416 |
a0001c0003t0004 | 0/0 | 3245 | 2 | 2 | 0 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | copy fasta | chr11 | 17488900 | 17549416 |
a0001c0003t0005 | 0/0 | 3245 | 1 | 1 | 0 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | copy fasta | chr11 | 17488900 | 17549416 |
a0001c0003t0006 | 0/0 | 3245 | 1 | 1 | 0 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | copy fasta | chr11 | 17488900 | 17549416 |
a0001c0003t0008 | 0/0 | 3245 | 1 | 1 | 0 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | copy fasta | chr11 | 17488900 | 17549416 |
a0001c0004t0001 | 0/0 | 3245 | 22 | 0 | 4 | 16 | 1 | 1 | USH1C_chr11_17488900_17549416 | USH1C | copy fasta | chr11 | 17488900 | 17549416 |
a0001c0004t0002 | 0/0 | 3245 | 1 | 0 | 0 | 1 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | copy fasta | chr11 | 17488900 | 17549416 |
a0001c0004t0003 | 0/0 | 3241 | 3 | 0 | 0 | 3 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | copy fasta | chr11 | 17488900 | 17549416 |
a0001c0007t0001 | 0/0 | 3245 | 10 | 0 | 2 | 5 | 0 | 3 | USH1C_chr11_17488900_17549416 | USH1C | copy fasta | chr11 | 17488900 | 17549416 |
a0001c0007t0003 | 0/0 | 3241 | 2 | 0 | 0 | 2 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | copy fasta | chr11 | 17488900 | 17549416 |
a0001c0008t0001 | 0/0 | 3245 | 11 | 1 | 2 | 6 | 0 | 2 | USH1C_chr11_17488900_17549416 | USH1C | copy fasta | chr11 | 17488900 | 17549416 |
a0001c0013t0001 | 0/0 | 3245 | 3 | 0 | 0 | 3 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | copy fasta | chr11 | 17488900 | 17549416 |
a0001c0013t0010 | 0/0 | 3245 | 1 | 0 | 0 | 1 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | copy fasta | chr11 | 17488900 | 17549416 |
a0001c0016t0001 | 0/0 | 3245 | 2 | 0 | 0 | 2 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | copy fasta | chr11 | 17488900 | 17549416 |
a0001c0017t0001 | 0/0 | 3245 | 2 | 2 | 0 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | copy fasta | chr11 | 17488900 | 17549416 |
a0001c0018t0001 | 0/0 | 3245 | 1 | 0 | 0 | 0 | 0 | 1 | USH1C_chr11_17488900_17549416 | USH1C | copy fasta | chr11 | 17488900 | 17549416 |
a0001c0018t0015 | 0/0 | 3245 | 1 | 0 | 0 | 1 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | copy fasta | chr11 | 17488900 | 17549416 |
a0001c0021t0001 | 0/0 | 3245 | 1 | 1 | 0 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | copy fasta | chr11 | 17488900 | 17549416 |
a0001c0021t0002 | 0/0 | 3245 | 1 | 1 | 0 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | copy fasta | chr11 | 17488900 | 17549416 |
a0001c0023t0017 | 0/0 | 3245 | 1 | 0 | 0 | 1 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | copy fasta | chr11 | 17488900 | 17549416 |
a0001c0024t0001 | 0/0 | 3245 | 1 | 0 | 0 | 0 | 0 | 1 | USH1C_chr11_17488900_17549416 | USH1C | copy fasta | chr11 | 17488900 | 17549416 |
a0001c0028t0003 | 0/0 | 3241 | 1 | 0 | 0 | 1 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | copy fasta | chr11 | 17488900 | 17549416 |
a0001c0037t0001 | 0/0 | 3245 | 1 | 0 | 0 | 1 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | copy fasta | chr11 | 17488900 | 17549416 |
a0001c0039t0001 | 0/0 | 3245 | 1 | 0 | 0 | 1 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | copy fasta | chr11 | 17488900 | 17549416 |
a0001c0040t0001 | 0/0 | 3245 | 1 | 0 | 0 | 1 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | copy fasta | chr11 | 17488900 | 17549416 |
a0001c0042t0001 | 0/0 | 3245 | 1 | 0 | 1 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | copy fasta | chr11 | 17488900 | 17549416 |
a0001c0043t0006 | 0/0 | 3245 | 1 | 1 | 0 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | copy fasta | chr11 | 17488900 | 17549416 |
a0001c0047t0001 | 0/0 | 3245 | 1 | 1 | 0 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | copy fasta | chr11 | 17488900 | 17549416 |
a0002c0002t0001 | 0/0 | 3245 | 4 | 1 | 1 | 0 | 2 | 0 | USH1C_chr11_17488900_17549416 | USH1C | copy fasta | chr11 | 17488900 | 17549416 |
a0002c0002t0002 | 0/0 | 3245 | 39 | 1 | 10 | 18 | 2 | 8 | USH1C_chr11_17488900_17549416 | USH1C | copy fasta | chr11 | 17488900 | 17549416 |
a0002c0002t0003 | 0/0 | 3241 | 1 | 0 | 0 | 1 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | copy fasta | chr11 | 17488900 | 17549416 |
a0002c0002t0007 | 0/0 | 3245 | 2 | 0 | 0 | 2 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | copy fasta | chr11 | 17488900 | 17549416 |
a0002c0005t0001 | 0/0 | 3245 | 8 | 8 | 0 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | copy fasta | chr11 | 17488900 | 17549416 |
a0002c0005t0002 | 0/0 | 3245 | 16 | 10 | 2 | 2 | 0 | 2 | USH1C_chr11_17488900_17549416 | USH1C | copy fasta | chr11 | 17488900 | 17549416 |
a0002c0005t0013 | 0/0 | 3245 | 1 | 0 | 1 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | copy fasta | chr11 | 17488900 | 17549416 |
a0002c0006t0001 | 0/0 | 3245 | 5 | 0 | 4 | 0 | 0 | 1 | USH1C_chr11_17488900_17549416 | USH1C | copy fasta | chr11 | 17488900 | 17549416 |
a0002c0006t0002 | 0/0 | 3245 | 17 | 0 | 2 | 10 | 1 | 4 | USH1C_chr11_17488900_17549416 | USH1C | copy fasta | chr11 | 17488900 | 17549416 |
a0002c0009t0001 | 0/0 | 3245 | 1 | 0 | 0 | 1 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | copy fasta | chr11 | 17488900 | 17549416 |
a0002c0009t0002 | 0/0 | 3245 | 8 | 0 | 0 | 8 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | copy fasta | chr11 | 17488900 | 17549416 |
a0002c0010t0001 | 0/0 | 3245 | 2 | 0 | 2 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | copy fasta | chr11 | 17488900 | 17549416 |
a0002c0010t0002 | 0/0 | 3245 | 7 | 0 | 0 | 5 | 2 | 0 | USH1C_chr11_17488900_17549416 | USH1C | copy fasta | chr11 | 17488900 | 17549416 |
a0002c0012t0001 | 0/0 | 3245 | 4 | 1 | 0 | 0 | 1 | 2 | USH1C_chr11_17488900_17549416 | USH1C | copy fasta | chr11 | 17488900 | 17549416 |
a0002c0012t0012 | 0/0 | 3245 | 1 | 0 | 0 | 0 | 0 | 1 | USH1C_chr11_17488900_17549416 | USH1C | copy fasta | chr11 | 17488900 | 17549416 |
a0002c0015t0001 | 0/0 | 3245 | 1 | 1 | 0 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | copy fasta | chr11 | 17488900 | 17549416 |
a0002c0015t0002 | 0/0 | 3245 | 2 | 2 | 0 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | copy fasta | chr11 | 17488900 | 17549416 |
a0002c0019t0002 | 0/0 | 3245 | 2 | 2 | 0 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | copy fasta | chr11 | 17488900 | 17549416 |
a0002c0020t0001 | 0/0 | 3245 | 1 | 1 | 0 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | copy fasta | chr11 | 17488900 | 17549416 |
a0002c0020t0002 | 0/0 | 3245 | 1 | 1 | 0 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | copy fasta | chr11 | 17488900 | 17549416 |
a0002c0027t0001 | 0/0 | 3245 | 1 | 0 | 0 | 1 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | copy fasta | chr11 | 17488900 | 17549416 |
a0002c0031t0002 | 0/0 | 3245 | 1 | 0 | 0 | 1 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | copy fasta | chr11 | 17488900 | 17549416 |
a0002c0036t0002 | 0/0 | 3245 | 1 | 0 | 0 | 1 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | copy fasta | chr11 | 17488900 | 17549416 |
a0002c0044t0001 | 0/0 | 3245 | 1 | 1 | 0 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | copy fasta | chr11 | 17488900 | 17549416 |
a0002c0046t0002 | 0/0 | 3245 | 1 | 1 | 0 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | copy fasta | chr11 | 17488900 | 17549416 |
a0003c0011t0001 | 0/0 | 3245 | 3 | 3 | 0 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | copy fasta | chr11 | 17488900 | 17549416 |
a0003c0011t0002 | 0/0 | 3245 | 2 | 1 | 1 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | copy fasta | chr11 | 17488900 | 17549416 |
a0004c0014t0001 | 0/0 | 3245 | 1 | 1 | 0 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | copy fasta | chr11 | 17488900 | 17549416 |
a0004c0014t0005 | 0/0 | 3245 | 2 | 1 | 1 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | copy fasta | chr11 | 17488900 | 17549416 |
a0005c0035t0004 | 0/0 | 3245 | 1 | 1 | 0 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | copy fasta | chr11 | 17488900 | 17549416 |
a0005c0038t0001 | 0/0 | 3245 | 1 | 0 | 1 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | copy fasta | chr11 | 17488900 | 17549416 |
a0006c0025t0001 | 0/0 | 3245 | 1 | 1 | 0 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | copy fasta | chr11 | 17488900 | 17549416 |
a0007c0026t0002 | 0/0 | 3245 | 1 | 0 | 0 | 1 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | copy fasta | chr11 | 17488900 | 17549416 |
a0008c0030t0001 | 0/0 | 3245 | 1 | 0 | 1 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | copy fasta | chr11 | 17488900 | 17549416 |
a0009c0045t0016 | 0/0 | 3241 | 1 | 1 | 0 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | copy fasta | chr11 | 17488900 | 17549416 |
a0010c0034t0002 | 0/0 | 3245 | 1 | 0 | 1 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | copy fasta | chr11 | 17488900 | 17549416 |
a0011c0048t0001 | 0/0 | 3245 | 1 | 1 | 0 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | copy fasta | chr11 | 17488900 | 17549416 |
a0012c0032t0002 | 0/0 | 3245 | 1 | 1 | 0 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | copy fasta | chr11 | 17488900 | 17549416 |
a0013c0033t0001 | 0/0 | 3245 | 1 | 1 | 0 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | copy fasta | chr11 | 17488900 | 17549416 |
a0014c0041t0001 | 0/0 | 3245 | 1 | 0 | 0 | 0 | 0 | 1 | USH1C_chr11_17488900_17549416 | USH1C | copy fasta | chr11 | 17488900 | 17549416 |
a0015c0029t0001 | 0/0 | 3245 | 1 | 1 | 0 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | copy fasta | chr11 | 17488900 | 17549416 |
a0016c0022t0002 | 0/0 | 3245 | 1 | 1 | 0 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | copy fasta | chr11 | 17488900 | 17549416 |
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 | 5 | 0 | 1 | 2 | 1 | 1 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
a0001c0001t0001g0005 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
a0001c0001t0001g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
a0001c0001t0001g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
a0001c0001t0001g0010 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
a0001c0001t0001g0011 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
a0001c0001t0001g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
a0001c0001t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
a0001c0001t0001g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
a0001c0001t0001g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
a0001c0001t0001g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
a0001c0001t0001g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
a0001c0001t0001g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
a0001c0001t0001g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
a0001c0001t0001g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
a0001c0001t0001g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
a0001c0001t0001g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
a0001c0001t0001g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
a0001c0001t0001g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
a0001c0001t0001g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
a0001c0001t0001g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
a0001c0001t0001g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
a0001c0001t0001g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
a0001c0001t0001g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
a0001c0001t0001g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
a0001c0001t0001g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
a0001c0001t0001g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
a0001c0001t0001g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
a0001c0001t0001g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
a0001c0001t0001g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
a0001c0001t0001g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
a0001c0001t0001g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
a0001c0001t0001g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
a0001c0001t0001g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
a0001c0001t0001g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
a0001c0001t0001g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
a0001c0001t0001g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
a0001c0001t0001g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
a0001c0001t0001g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
a0001c0001t0001g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
a0001c0001t0001g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
a0001c0001t0001g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
a0001c0001t0001g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
a0001c0001t0002g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
a0001c0001t0002g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
a0001c0001t0003g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
a0001c0001t0003g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
a0001c0001t0003g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
a0001c0001t0003g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
a0001c0001t0008g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
a0001c0001t0009g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
a0001c0001t0009g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
a0001c0001t0011g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
a0001c0001t0014g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
a0001c0003t0001g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
a0001c0003t0001g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
a0001c0003t0001g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
a0001c0003t0001g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
a0001c0003t0001g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
a0001c0003t0001g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
a0001c0003t0001g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
a0001c0003t0001g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
a0001c0003t0001g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
a0001c0003t0001g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
a0001c0003t0001g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
a0001c0003t0001g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
a0001c0003t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
a0001c0003t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
a0001c0003t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
a0001c0003t0001g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
a0001c0003t0001g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
a0001c0003t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
a0001c0003t0001g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
a0001c0003t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
a0001c0003t0001g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
a0001c0003t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
a0001c0003t0001g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
a0001c0003t0001g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
a0001c0003t0001g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
a0001c0003t0001g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
a0001c0003t0001g0296 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
a0001c0003t0001g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
a0001c0003t0001g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
a0001c0003t0001g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
a0001c0003t0002g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
a0001c0003t0003g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
a0001c0003t0003g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
a0001c0003t0003g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
a0001c0003t0004g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
a0001c0003t0004g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
a0001c0003t0005g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
a0001c0003t0006g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
a0001c0003t0008g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
a0001c0004t0001g0003 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
a0001c0004t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
a0001c0004t0001g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
a0001c0004t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
a0001c0004t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
a0001c0004t0001g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
a0001c0004t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
a0001c0004t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
a0001c0004t0001g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
a0001c0004t0001g0208 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
a0001c0004t0001g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
a0001c0004t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
a0001c0004t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
a0001c0004t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
a0001c0004t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
a0001c0004t0001g0247 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
a0001c0004t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
a0001c0004t0001g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
a0001c0004t0001g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
a0001c0004t0002g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
a0001c0004t0003g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
a0001c0004t0003g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
a0001c0004t0003g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
a0001c0007t0001g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
a0001c0007t0001g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
a0001c0007t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
a0001c0007t0001g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
a0001c0007t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
a0001c0007t0001g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
a0001c0007t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
a0001c0007t0001g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
a0001c0007t0001g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
a0001c0007t0001g0321 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
a0001c0007t0003g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
a0001c0007t0003g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
a0001c0008t0001g0006 | 0/0 | 3 | 0 | 2 | 1 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
a0001c0008t0001g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
a0001c0008t0001g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
a0001c0008t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
a0001c0008t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
a0001c0008t0001g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
a0001c0008t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
a0001c0008t0001g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
a0001c0008t0001g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
a0001c0013t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
a0001c0013t0001g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
a0001c0013t0001g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
a0001c0013t0010g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
a0001c0016t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
a0001c0016t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
a0001c0017t0001g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
a0001c0017t0001g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
a0001c0018t0001g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
a0001c0018t0015g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
a0001c0021t0001g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
a0001c0021t0002g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
a0001c0023t0017g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
a0001c0024t0001g0312 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
a0001c0028t0003g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
a0001c0037t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
a0001c0039t0001g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
a0001c0040t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
a0001c0042t0001g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
a0001c0043t0006g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
a0001c0047t0001g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
a0002c0002t0001g0098 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
a0002c0002t0001g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
a0002c0002t0001g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
a0002c0002t0001g0216 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
a0002c0002t0002g0004 | 0/0 | 3 | 0 | 0 | 0 | 0 | 3 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
a0002c0002t0002g0012 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
a0002c0002t0002g0013 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
a0002c0002t0002g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
a0002c0002t0002g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
a0002c0002t0002g0037 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
a0002c0002t0002g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
a0002c0002t0002g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
a0002c0002t0002g0053 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
a0002c0002t0002g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
a0002c0002t0002g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
a0002c0002t0002g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
a0002c0002t0002g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
a0002c0002t0002g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
a0002c0002t0002g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
a0002c0002t0002g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
a0002c0002t0002g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
a0002c0002t0002g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
a0002c0002t0002g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
a0002c0002t0002g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
a0002c0002t0002g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
a0002c0002t0002g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
a0002c0002t0002g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
a0002c0002t0002g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
a0002c0002t0002g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
a0002c0002t0002g0185 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
a0002c0002t0002g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
a0002c0002t0002g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
a0002c0002t0002g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
a0002c0002t0002g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
a0002c0002t0002g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
a0002c0002t0002g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
a0002c0002t0002g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
a0002c0002t0003g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
a0002c0002t0007g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
a0002c0002t0007g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
a0002c0005t0001g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
a0002c0005t0001g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
a0002c0005t0001g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
a0002c0005t0001g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
a0002c0005t0001g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
a0002c0005t0001g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
a0002c0005t0001g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
a0002c0005t0001g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
a0002c0005t0002g0020 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
a0002c0005t0002g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
a0002c0005t0002g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
a0002c0005t0002g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
a0002c0005t0002g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
a0002c0005t0002g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
a0002c0005t0002g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
a0002c0005t0002g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
a0002c0005t0002g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
a0002c0005t0002g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
a0002c0005t0002g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
a0002c0005t0002g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
a0002c0005t0002g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
a0002c0005t0002g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
a0002c0005t0002g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
a0002c0005t0013g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
a0002c0006t0001g0021 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
a0002c0006t0001g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
a0002c0006t0001g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
a0002c0006t0001g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
a0002c0006t0002g0002 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
a0002c0006t0002g0017 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
a0002c0006t0002g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
a0002c0006t0002g0022 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
a0002c0006t0002g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
a0002c0006t0002g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
a0002c0006t0002g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
a0002c0006t0002g0274 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
a0002c0006t0002g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
a0002c0006t0002g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
a0002c0006t0002g0322 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
a0002c0009t0001g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
a0002c0009t0002g0007 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
a0002c0009t0002g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
a0002c0009t0002g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
a0002c0009t0002g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
a0002c0009t0002g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
a0002c0010t0001g0014 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
a0002c0010t0002g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
a0002c0010t0002g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
a0002c0010t0002g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
a0002c0010t0002g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
a0002c0010t0002g0155 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
a0002c0010t0002g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
a0002c0010t0002g0275 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
a0002c0012t0001g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
a0002c0012t0001g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
a0002c0012t0001g0178 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
a0002c0012t0001g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
a0002c0012t0012g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
a0002c0015t0001g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
a0002c0015t0002g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
a0002c0015t0002g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
a0002c0019t0002g0025 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
a0002c0020t0001g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
a0002c0020t0002g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
a0002c0027t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
a0002c0031t0002g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
a0002c0036t0002g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
a0002c0044t0001g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
a0002c0046t0002g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
a0003c0011t0001g0024 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
a0003c0011t0001g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
a0003c0011t0002g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
a0003c0011t0002g0285 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
a0004c0014t0001g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
a0004c0014t0005g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
a0004c0014t0005g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
a0005c0035t0004g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
a0005c0038t0001g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
a0006c0025t0001g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
a0007c0026t0002g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
a0008c0030t0001g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
a0009c0045t0016g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
a0010c0034t0002g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
a0011c0048t0001g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
a0012c0032t0002g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
a0013c0033t0001g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
a0014c0041t0001g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
a0015c0029t0001g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
a0016c0022t0002g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0004 | t0001 | g0208 | EUR | GBR | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
HG00099 | hp2 | a0002 | c0012 | t0001 | g0178 | EUR | GBR | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
HG00280 | hp1 | a0001 | c0001 | t0001 | g0212 | EUR | FIN | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
HG00280 | hp2 | a0002 | c0002 | t0001 | g0216 | EUR | FIN | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
HG00323 | hp1 | a0001 | c0001 | t0001 | g0077 | EUR | FIN | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
HG00323 | hp2 | a0002 | c0010 | t0002 | g0155 | EUR | FIN | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
HG00438 | hp1 | a0001 | c0008 | t0001 | g0264 | EAS | CHS | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
HG00438 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
HG00544 | hp1 | a0002 | c0006 | t0002 | g0092 | EAS | CHS | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
HG00544 | hp2 | a0001 | c0001 | t0001 | g0076 | EAS | CHS | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
HG00558 | hp1 | a0001 | c0001 | t0001 | g0303 | EAS | CHS | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
HG00558 | hp2 | a0002 | c0002 | t0002 | g0019 | EAS | CHS | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
HG00597 | hp1 | a0001 | c0001 | t0001 | g0064 | EAS | CHS | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
HG00597 | hp2 | a0001 | c0001 | t0001 | g0307 | EAS | CHS | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
HG00621 | hp1 | a0001 | c0001 | t0001 | g0039 | EAS | CHS | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
HG00621 | hp2 | a0002 | c0010 | t0002 | g0049 | EAS | CHS | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
HG00639 | hp1 | a0001 | c0001 | t0003 | g0206 | AMR | PUR | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
HG00639 | hp2 | a0001 | c0003 | t0001 | g0043 | AMR | PUR | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
HG00642 | hp1 | a0002 | c0002 | t0002 | g0104 | AMR | PUR | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
HG00642 | hp2 | a0001 | c0001 | t0002 | g0218 | AMR | PUR | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
HG00673 | hp1 | a0002 | c0002 | t0002 | g0093 | EAS | CHS | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
HG00673 | hp2 | a0002 | c0031 | t0002 | g0258 | EAS | CHS | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
HG00733 | hp1 | a0002 | c0002 | t0002 | g0013 | AMR | PUR | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
HG00733 | hp2 | a0001 | c0008 | t0001 | g0006 | AMR | PUR | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
HG00735 | hp1 | a0004 | c0014 | t0005 | g0225 | AMR | PUR | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
HG00735 | hp2 | a0001 | c0001 | t0001 | g0105 | AMR | PUR | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
HG00738 | hp1 | a0001 | c0001 | t0001 | g0041 | AMR | PUR | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
HG00738 | hp2 | a0001 | c0003 | t0001 | g0150 | AMR | PUR | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
HG00741 | hp1 | a0001 | c0003 | t0001 | g0151 | AMR | PUR | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
HG00741 | hp2 | a0002 | c0006 | t0002 | g0288 | AMR | PUR | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
HG01069 | hp1 | a0002 | c0006 | t0002 | g0017 | AMR | PUR | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
HG01069 | hp2 | a0001 | c0001 | t0001 | g0010 | AMR | PUR | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
HG01070 | hp1 | a0001 | c0001 | t0001 | g0011 | AMR | PUR | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
HG01070 | hp2 | a0001 | c0007 | t0001 | g0177 | AMR | PUR | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
HG01071 | hp1 | a0001 | c0001 | t0001 | g0010 | AMR | PUR | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
HG01071 | hp2 | a0001 | c0001 | t0001 | g0011 | AMR | PUR | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
HG01074 | hp1 | a0002 | c0006 | t0001 | g0233 | AMR | PUR | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
HG01074 | hp2 | a0001 | c0001 | t0001 | g0147 | AMR | PUR | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
HG01081 | hp1 | a0002 | c0002 | t0002 | g0126 | AMR | PUR | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
HG01081 | hp2 | a0002 | c0006 | t0001 | g0266 | AMR | PUR | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
HG01099 | hp1 | a0001 | c0008 | t0001 | g0006 | AMR | PUR | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
HG01099 | hp2 | a0001 | c0001 | t0001 | g0131 | AMR | PUR | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
HG01106 | hp1 | a0001 | c0003 | t0003 | g0235 | AMR | PUR | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
HG01106 | hp2 | a0002 | c0005 | t0002 | g0254 | AMR | PUR | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
HG01109 | hp1 | a0010 | c0034 | t0002 | g0261 | AMR | PUR | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
HG01109 | hp2 | a0001 | c0001 | t0001 | g0278 | AMR | PUR | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
HG01167 | hp1 | a0008 | c0030 | t0001 | g0142 | AMR | PUR | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
HG01167 | hp2 | a0005 | c0038 | t0001 | g0273 | AMR | PUR | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
HG01168 | hp1 | a0001 | c0003 | t0001 | g0268 | AMR | PUR | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
HG01168 | hp2 | a0002 | c0002 | t0001 | g0153 | AMR | PUR | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
HG01175 | hp1 | a0001 | c0001 | t0001 | g0139 | AMR | PUR | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
HG01175 | hp2 | a0002 | c0005 | t0002 | g0259 | AMR | PUR | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
HG01243 | hp1 | a0001 | c0001 | t0001 | g0166 | AMR | PUR | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
HG01243 | hp2 | a0003 | c0011 | t0002 | g0285 | AMR | PUR | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
HG01255 | hp1 | a0001 | c0042 | t0001 | g0033 | AMR | CLM | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
HG01255 | hp2 | a0002 | c0002 | t0002 | g0012 | AMR | CLM | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
HG01256 | hp1 | a0001 | c0001 | t0001 | g0059 | AMR | CLM | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
HG01256 | hp2 | a0002 | c0010 | t0001 | g0014 | AMR | CLM | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
HG01257 | hp1 | a0001 | c0004 | t0001 | g0209 | AMR | CLM | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
HG01257 | hp2 | a0002 | c0002 | t0002 | g0190 | AMR | CLM | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
HG01258 | hp1 | a0001 | c0004 | t0001 | g0207 | AMR | CLM | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
HG01258 | hp2 | a0002 | c0010 | t0001 | g0014 | AMR | CLM | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
HG01261 | hp1 | a0001 | c0001 | t0001 | g0082 | AMR | CLM | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
HG01261 | hp2 | a0002 | c0002 | t0002 | g0168 | AMR | CLM | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
HG01346 | hp1 | a0001 | c0001 | t0001 | g0217 | AMR | CLM | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
HG01346 | hp2 | a0002 | c0002 | t0002 | g0013 | AMR | CLM | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
HG01358 | hp1 | a0002 | c0002 | t0002 | g0061 | AMR | CLM | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
HG01358 | hp2 | a0001 | c0001 | t0001 | g0128 | AMR | CLM | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
HG01433 | hp1 | a0002 | c0002 | t0002 | g0012 | AMR | CLM | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
HG01433 | hp2 | a0002 | c0002 | t0002 | g0127 | AMR | CLM | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
HG01496 | hp1 | a0001 | c0003 | t0003 | g0253 | AMR | CLM | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
HG01496 | hp2 | a0001 | c0007 | t0001 | g0321 | AMR | CLM | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
HG01515 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | IBS | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
HG01515 | hp2 | a0002 | c0006 | t0002 | g0322 | EUR | IBS | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
HG01884 | hp1 | a0011 | c0048 | t0001 | g0161 | AFR | ACB | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
HG01884 | hp2 | a0001 | c0003 | t0001 | g0072 | AFR | ACB | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
HG01891 | hp1 | a0001 | c0001 | t0008 | g0229 | AFR | ACB | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
HG01891 | hp2 | a0003 | c0011 | t0001 | g0024 | AFR | ACB | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
HG01943 | hp1 | a0001 | c0001 | t0001 | g0154 | AMR | PEL | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
HG01943 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
HG01975 | hp1 | a0001 | c0004 | t0001 | g0135 | AMR | PEL | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
HG01975 | hp2 | a0001 | c0003 | t0001 | g0249 | AMR | PEL | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
HG01978 | hp1 | a0001 | c0001 | t0001 | g0137 | AMR | PEL | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
HG01978 | hp2 | a0002 | c0005 | t0013 | g0220 | AMR | PEL | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
HG02004 | hp1 | a0001 | c0001 | t0001 | g0228 | AMR | PEL | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
HG02004 | hp2 | a0001 | c0004 | t0001 | g0084 | AMR | PEL | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
HG02015 | hp1 | a0002 | c0002 | t0003 | g0116 | EAS | KHV | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
HG02015 | hp2 | a0001 | c0003 | t0001 | g0260 | EAS | KHV | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
HG02027 | hp1 | a0001 | c0001 | t0001 | g0119 | EAS | KHV | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
HG02027 | hp2 | a0001 | c0001 | t0001 | g0056 | EAS | KHV | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
HG02040 | hp1 | a0001 | c0001 | t0001 | g0111 | EAS | KHV | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
HG02040 | hp2 | a0001 | c0013 | t0001 | g0214 | EAS | KHV | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
HG02055 | hp1 | a0002 | c0002 | t0001 | g0129 | AFR | ACB | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
HG02055 | hp2 | a0001 | c0003 | t0001 | g0223 | AFR | ACB | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
HG02056 | hp1 | a0002 | c0036 | t0002 | g0074 | EAS | KHV | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
HG02056 | hp2 | a0001 | c0016 | t0001 | g0227 | EAS | KHV | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
HG02071 | hp1 | a0001 | c0007 | t0001 | g0308 | EAS | KHV | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
HG02071 | hp2 | a0001 | c0001 | t0003 | g0132 | EAS | KHV | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
HG02074 | hp1 | a0002 | c0002 | t0002 | g0213 | EAS | KHV | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
HG02074 | hp2 | a0001 | c0001 | t0001 | g0085 | EAS | KHV | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
HG02080 | hp1 | a0001 | c0001 | t0001 | g0078 | EAS | KHV | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
HG02080 | hp2 | a0001 | c0001 | t0001 | g0048 | EAS | KHV | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
HG02083 | hp1 | a0001 | c0003 | t0001 | g0267 | EAS | KHV | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
HG02083 | hp2 | a0002 | c0002 | t0002 | g0115 | EAS | KHV | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
HG02129 | hp1 | a0002 | c0002 | t0002 | g0242 | EAS | KHV | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
HG02129 | hp2 | a0001 | c0001 | t0003 | g0102 | EAS | KHV | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
HG02135 | hp1 | a0002 | c0009 | t0002 | g0318 | EAS | KHV | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
HG02135 | hp2 | a0001 | c0013 | t0001 | g0279 | EAS | KHV | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
HG02145 | hp1 | a0002 | c0015 | t0002 | g0319 | AFR | ACB | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
HG02145 | hp2 | a0001 | c0003 | t0001 | g0144 | AFR | ACB | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
HG02148 | hp1 | a0001 | c0001 | t0001 | g0114 | AMR | PEL | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
HG02148 | hp2 | a0002 | c0006 | t0001 | g0263 | AMR | PEL | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
HG02155 | hp1 | a0001 | c0001 | t0001 | g0089 | EAS | CDX | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
HG02155 | hp2 | a0001 | c0003 | t0001 | g0324 | EAS | CDX | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
HG02165 | hp1 | a0001 | c0004 | t0003 | g0138 | EAS | CDX | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
HG02165 | hp2 | a0002 | c0009 | t0001 | g0317 | EAS | CDX | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
HG02257 | hp1 | a0003 | c0011 | t0001 | g0024 | AFR | ACB | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
HG02257 | hp2 | a0002 | c0005 | t0001 | g0070 | AFR | ACB | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
HG02258 | hp1 | a0001 | c0001 | t0001 | g0051 | AFR | ACB | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
HG02258 | hp2 | a0001 | c0003 | t0006 | g0031 | AFR | ACB | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
HG02280 | hp1 | a0002 | c0005 | t0002 | g0236 | AFR | ACB | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
HG02280 | hp2 | a0002 | c0020 | t0001 | g0158 | AFR | ACB | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
HG02451 | hp1 | a0009 | c0045 | t0016 | g0159 | AFR | ACB | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
HG02451 | hp2 | a0006 | c0025 | t0001 | g0205 | AFR | ACB | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
HG02523 | hp1 | a0001 | c0004 | t0001 | g0300 | EAS | KHV | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
HG02523 | hp2 | a0002 | c0002 | t0002 | g0106 | EAS | KHV | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
HG02572 | hp1 | a0001 | c0017 | t0001 | g0314 | AFR | GWD | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
HG02572 | hp2 | a0001 | c0001 | t0001 | g0046 | AFR | GWD | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
HG02602 | hp1 | a0001 | c0008 | t0001 | g0171 | SAS | PJL | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
HG02602 | hp2 | a0001 | c0001 | t0001 | g0123 | SAS | PJL | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
HG02615 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | GWD | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
HG02615 | hp2 | a0002 | c0005 | t0001 | g0036 | AFR | GWD | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
HG02647 | hp1 | a0002 | c0019 | t0002 | g0025 | AFR | GWD | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
HG02647 | hp2 | a0002 | c0005 | t0001 | g0252 | AFR | GWD | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
HG02717 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | GWD | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
HG02717 | hp2 | a0001 | c0003 | t0001 | g0295 | AFR | GWD | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
HG02723 | hp1 | a0002 | c0046 | t0002 | g0160 | AFR | GWD | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
HG02723 | hp2 | a0001 | c0017 | t0001 | g0315 | AFR | GWD | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
HG02735 | hp1 | a0002 | c0002 | t0002 | g0040 | SAS | PJL | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
HG02735 | hp2 | a0001 | c0024 | t0001 | g0312 | SAS | PJL | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
HG02738 | hp1 | a0014 | c0041 | t0001 | g0183 | SAS | PJL | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
HG02738 | hp2 | a0001 | c0001 | t0001 | g0112 | SAS | PJL | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
HG02809 | hp1 | a0016 | c0022 | t0002 | g0222 | AFR | GWD | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
HG02809 | hp2 | a0001 | c0001 | t0009 | g0071 | AFR | GWD | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
HG02818 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | GWD | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
HG02818 | hp2 | a0002 | c0005 | t0001 | g0124 | AFR | GWD | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
HG02895 | hp1 | a0001 | c0003 | t0001 | g0170 | AFR | GWD | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
HG02895 | hp2 | a0001 | c0001 | t0001 | g0167 | AFR | GWD | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
HG02896 | hp1 | a0001 | c0001 | t0001 | g0231 | AFR | GWD | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
HG02896 | hp2 | a0002 | c0005 | t0002 | g0020 | AFR | GWD | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
HG02897 | hp1 | a0001 | c0001 | t0001 | g0230 | AFR | GWD | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
HG02897 | hp2 | a0001 | c0003 | t0001 | g0169 | AFR | GWD | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
HG02922 | hp1 | a0002 | c0005 | t0001 | g0141 | AFR | ESN | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
HG02922 | hp2 | a0001 | c0003 | t0001 | g0256 | AFR | ESN | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
HG02965 | hp1 | a0012 | c0032 | t0002 | g0250 | AFR | ESN | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
HG02965 | hp2 | a0003 | c0011 | t0001 | g0283 | AFR | ESN | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
HG02970 | hp1 | a0002 | c0015 | t0001 | g0035 | AFR | ESN | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
HG02970 | hp2 | a0004 | c0014 | t0001 | g0269 | AFR | ESN | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
HG02976 | hp1 | a0001 | c0001 | t0001 | g0184 | AFR | ESN | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
HG02976 | hp2 | a0001 | c0043 | t0006 | g0029 | AFR | ESN | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
HG03017 | hp1 | a0001 | c0001 | t0001 | g0052 | SAS | PJL | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
HG03017 | hp2 | a0002 | c0012 | t0001 | g0175 | SAS | PJL | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
HG03041 | hp1 | a0001 | c0003 | t0001 | g0191 | AFR | GWD | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
HG03041 | hp2 | a0002 | c0005 | t0001 | g0237 | AFR | GWD | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
HG03098 | hp1 | a0001 | c0003 | t0001 | g0226 | AFR | MSL | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
HG03098 | hp2 | a0002 | c0005 | t0001 | g0224 | AFR | MSL | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
HG03130 | hp1 | a0002 | c0005 | t0002 | g0290 | AFR | ESN | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
HG03130 | hp2 | a0001 | c0001 | t0001 | g0118 | AFR | ESN | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
HG03139 | hp1 | a0002 | c0005 | t0002 | g0067 | AFR | ESN | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
HG03139 | hp2 | a0001 | c0001 | t0001 | g0276 | AFR | ESN | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
HG03209 | hp1 | a0001 | c0003 | t0008 | g0272 | AFR | MSL | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
HG03209 | hp2 | a0001 | c0003 | t0002 | g0068 | AFR | MSL | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
HG03225 | hp1 | a0002 | c0005 | t0002 | g0251 | AFR | MSL | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
HG03225 | hp2 | a0001 | c0021 | t0001 | g0163 | AFR | MSL | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
HG03453 | hp1 | a0001 | c0001 | t0009 | g0122 | AFR | MSL | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
HG03453 | hp2 | a0002 | c0005 | t0002 | g0020 | AFR | MSL | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
HG03486 | hp1 | a0001 | c0003 | t0004 | g0030 | AFR | MSL | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
HG03486 | hp2 | a0001 | c0001 | t0003 | g0055 | AFR | MSL | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
HG03490 | hp1 | a0001 | c0007 | t0001 | g0193 | SAS | PJL | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
HG03490 | hp2 | a0002 | c0006 | t0002 | g0022 | SAS | PJL | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
HG03491 | hp1 | a0002 | c0002 | t0002 | g0004 | SAS | PJL | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
HG03491 | hp2 | a0002 | c0005 | t0002 | g0186 | SAS | PJL | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
HG03492 | hp1 | a0002 | c0006 | t0002 | g0022 | SAS | PJL | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
HG03492 | hp2 | a0002 | c0002 | t0002 | g0004 | SAS | PJL | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
HG03516 | hp1 | a0004 | c0014 | t0005 | g0062 | AFR | ESN | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
HG03516 | hp2 | a0013 | c0033 | t0001 | g0232 | AFR | ESN | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
HG03540 | hp1 | a0001 | c0003 | t0001 | g0121 | AFR | GWD | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
HG03540 | hp2 | a0002 | c0012 | t0001 | g0143 | AFR | GWD | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
HG03579 | hp1 | a0001 | c0021 | t0002 | g0162 | AFR | MSL | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
HG03579 | hp2 | a0002 | c0005 | t0002 | g0045 | AFR | MSL | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
HG03654 | hp1 | a0002 | c0002 | t0002 | g0037 | SAS | PJL | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
HG03654 | hp2 | a0001 | c0018 | t0001 | g0149 | SAS | PJL | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
HG03669 | hp1 | a0002 | c0012 | t0012 | g0180 | SAS | PJL | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
HG03669 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
HG03688 | hp1 | a0001 | c0003 | t0001 | g0296 | SAS | STU | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
HG03688 | hp2 | a0001 | c0001 | t0001 | g0125 | SAS | STU | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
HG03831 | hp1 | a0001 | c0007 | t0001 | g0189 | SAS | BEB | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
HG03831 | hp2 | a0001 | c0001 | t0001 | g0140 | SAS | BEB | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
HG03834 | hp1 | a0002 | c0006 | t0001 | g0021 | SAS | BEB | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
HG03834 | hp2 | a0001 | c0003 | t0003 | g0165 | SAS | BEB | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
HG04115 | hp1 | a0002 | c0002 | t0002 | g0004 | SAS | STU | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
HG04115 | hp2 | a0001 | c0004 | t0001 | g0247 | SAS | STU | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
HG04184 | hp1 | a0002 | c0002 | t0002 | g0164 | SAS | BEB | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
HG04184 | hp2 | a0002 | c0006 | t0002 | g0274 | SAS | BEB | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
HG04199 | hp1 | a0001 | c0007 | t0001 | g0176 | SAS | STU | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
HG04199 | hp2 | a0002 | c0006 | t0002 | g0188 | SAS | STU | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
HG04204 | hp1 | a0001 | c0003 | t0001 | g0156 | SAS | STU | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
HG04204 | hp2 | a0002 | c0005 | t0002 | g0172 | SAS | STU | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
HG04228 | hp1 | a0002 | c0012 | t0001 | g0182 | SAS | STU | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
HG04228 | hp2 | a0002 | c0002 | t0002 | g0081 | SAS | STU | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
NA18522 | hp1 | a0002 | c0005 | t0001 | g0270 | AFR | YRI | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
NA18522 | hp2 | a0002 | c0020 | t0002 | g0157 | AFR | YRI | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
NA18906 | hp1 | a0002 | c0002 | t0002 | g0057 | AFR | YRI | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
NA18906 | hp2 | a0002 | c0005 | t0002 | g0311 | AFR | YRI | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
NA18940 | hp1 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
NA18940 | hp2 | a0002 | c0006 | t0002 | g0017 | EAS | JPT | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
NA18941 | hp1 | a0002 | c0002 | t0002 | g0050 | EAS | JPT | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
NA18941 | hp2 | a0002 | c0002 | t0002 | g0015 | EAS | JPT | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
NA18942 | hp1 | a0007 | c0026 | t0002 | g0133 | EAS | JPT | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
NA18942 | hp2 | a0001 | c0037 | t0001 | g0195 | EAS | JPT | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
NA18943 | hp1 | a0002 | c0006 | t0002 | g0313 | EAS | JPT | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
NA18943 | hp2 | a0001 | c0007 | t0001 | g0298 | EAS | JPT | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
NA18947 | hp1 | a0001 | c0001 | t0001 | g0291 | EAS | JPT | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
NA18947 | hp2 | a0001 | c0001 | t0001 | g0305 | EAS | JPT | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
NA18948 | hp1 | a0001 | c0023 | t0017 | g0281 | EAS | JPT | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
NA18948 | hp2 | a0001 | c0004 | t0001 | g0211 | EAS | JPT | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
NA18950 | hp1 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
NA18950 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
NA18952 | hp1 | a0001 | c0001 | t0001 | g0248 | EAS | JPT | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
NA18952 | hp2 | a0002 | c0002 | t0002 | g0100 | EAS | JPT | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
NA18953 | hp1 | a0002 | c0010 | t0002 | g0090 | EAS | JPT | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
NA18953 | hp2 | a0001 | c0004 | t0001 | g0215 | EAS | JPT | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
NA18956 | hp1 | a0001 | c0004 | t0001 | g0003 | EAS | JPT | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
NA18956 | hp2 | a0002 | c0005 | t0002 | g0265 | EAS | JPT | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
NA18957 | hp1 | a0001 | c0039 | t0001 | g0309 | EAS | JPT | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
NA18957 | hp2 | a0001 | c0001 | t0001 | g0240 | EAS | JPT | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
NA18959 | hp1 | a0001 | c0007 | t0003 | g0179 | EAS | JPT | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
NA18959 | hp2 | a0002 | c0027 | t0001 | g0080 | EAS | JPT | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
NA18960 | hp1 | a0001 | c0007 | t0003 | g0181 | EAS | JPT | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
NA18960 | hp2 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
NA18963 | hp1 | a0001 | c0013 | t0010 | g0026 | EAS | JPT | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
NA18963 | hp2 | a0002 | c0010 | t0002 | g0091 | EAS | JPT | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
NA18964 | hp1 | a0002 | c0002 | t0002 | g0019 | EAS | JPT | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
NA18964 | hp2 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
NA18965 | hp1 | a0002 | c0009 | t0002 | g0007 | EAS | JPT | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
NA18965 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
NA18966 | hp1 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
NA18966 | hp2 | a0001 | c0003 | t0001 | g0204 | EAS | JPT | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
NA18968 | hp1 | a0001 | c0008 | t0001 | g0219 | EAS | JPT | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
NA18968 | hp2 | a0002 | c0010 | t0002 | g0099 | EAS | JPT | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
NA18969 | hp1 | a0001 | c0013 | t0001 | g0282 | EAS | JPT | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
NA18969 | hp2 | a0001 | c0001 | t0001 | g0246 | EAS | JPT | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
NA18970 | hp1 | a0001 | c0001 | t0001 | g0073 | EAS | JPT | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
NA18970 | hp2 | a0001 | c0003 | t0001 | g0255 | EAS | JPT | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
NA18971 | hp1 | a0001 | c0018 | t0015 | g0310 | EAS | JPT | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
NA18971 | hp2 | a0001 | c0003 | t0001 | g0320 | EAS | JPT | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
NA18973 | hp1 | a0001 | c0008 | t0001 | g0289 | EAS | JPT | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
NA18973 | hp2 | a0001 | c0001 | t0014 | g0047 | EAS | JPT | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
NA18977 | hp1 | a0002 | c0002 | t0002 | g0058 | EAS | JPT | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
NA18977 | hp2 | a0001 | c0004 | t0001 | g0003 | EAS | JPT | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
NA18979 | hp1 | a0001 | c0004 | t0001 | g0136 | EAS | JPT | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
NA18979 | hp2 | a0002 | c0002 | t0007 | g0095 | EAS | JPT | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
NA18980 | hp1 | a0001 | c0001 | t0001 | g0287 | EAS | JPT | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
NA18980 | hp2 | a0002 | c0009 | t0002 | g0201 | EAS | JPT | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
NA18982 | hp1 | a0001 | c0016 | t0001 | g0075 | EAS | JPT | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
NA18982 | hp2 | a0002 | c0002 | t0002 | g0243 | EAS | JPT | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
NA18983 | hp1 | a0001 | c0003 | t0001 | g0323 | EAS | JPT | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
NA18983 | hp2 | a0001 | c0001 | t0001 | g0245 | EAS | JPT | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
NA18984 | hp1 | a0001 | c0003 | t0001 | g0202 | EAS | JPT | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
NA18984 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
NA18987 | hp1 | a0001 | c0001 | t0001 | g0130 | EAS | JPT | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
NA18987 | hp2 | a0001 | c0007 | t0001 | g0187 | EAS | JPT | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
NA18988 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
NA18988 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
NA18992 | hp1 | a0001 | c0004 | t0003 | g0301 | EAS | JPT | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
NA18992 | hp2 | a0002 | c0009 | t0002 | g0023 | EAS | JPT | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
NA18993 | hp1 | a0001 | c0004 | t0001 | g0038 | EAS | JPT | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
NA18993 | hp2 | a0002 | c0002 | t0002 | g0200 | EAS | JPT | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
NA18994 | hp1 | a0001 | c0004 | t0001 | g0210 | EAS | JPT | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
NA18994 | hp2 | a0001 | c0003 | t0001 | g0198 | EAS | JPT | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
NA18997 | hp1 | a0001 | c0001 | t0001 | g0297 | EAS | JPT | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
NA18997 | hp2 | a0001 | c0001 | t0001 | g0113 | EAS | JPT | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
NA18998 | hp1 | a0002 | c0002 | t0002 | g0079 | EAS | JPT | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
NA18998 | hp2 | a0001 | c0004 | t0001 | g0234 | EAS | JPT | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
NA18999 | hp1 | a0001 | c0004 | t0001 | g0003 | EAS | JPT | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
NA18999 | hp2 | a0001 | c0001 | t0001 | g0304 | EAS | JPT | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
NA19000 | hp1 | a0001 | c0001 | t0001 | g0083 | EAS | JPT | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
NA19000 | hp2 | a0002 | c0002 | t0002 | g0244 | EAS | JPT | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
NA19002 | hp1 | a0001 | c0003 | t0001 | g0239 | EAS | JPT | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
NA19002 | hp2 | a0001 | c0008 | t0001 | g0221 | EAS | JPT | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
NA19005 | hp1 | a0001 | c0001 | t0001 | g0145 | EAS | JPT | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
NA19005 | hp2 | a0002 | c0002 | t0002 | g0015 | EAS | JPT | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
NA19007 | hp1 | a0002 | c0006 | t0002 | g0002 | EAS | JPT | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
NA19007 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
NA19009 | hp1 | a0002 | c0006 | t0002 | g0002 | EAS | JPT | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
NA19009 | hp2 | a0001 | c0001 | t0001 | g0097 | EAS | JPT | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
NA19010 | hp1 | a0001 | c0004 | t0001 | g0316 | EAS | JPT | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
NA19010 | hp2 | a0001 | c0001 | t0001 | g0086 | EAS | JPT | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
NA19011 | hp1 | a0001 | c0028 | t0003 | g0063 | EAS | JPT | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
NA19011 | hp2 | a0002 | c0002 | t0002 | g0286 | EAS | JPT | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
NA19012 | hp1 | a0001 | c0001 | t0001 | g0203 | EAS | JPT | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
NA19012 | hp2 | a0002 | c0006 | t0002 | g0002 | EAS | JPT | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
NA19030 | hp1 | a0015 | c0029 | t0001 | g0293 | AFR | LWK | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
NA19030 | hp2 | a0002 | c0005 | t0002 | g0069 | AFR | LWK | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
NA19043 | hp1 | a0001 | c0003 | t0001 | g0271 | AFR | LWK | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
NA19043 | hp2 | a0001 | c0047 | t0001 | g0196 | AFR | LWK | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
NA19057 | hp1 | a0002 | c0009 | t0002 | g0007 | EAS | JPT | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
NA19057 | hp2 | a0001 | c0007 | t0001 | g0194 | EAS | JPT | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
NA19060 | hp1 | a0001 | c0001 | t0001 | g0302 | EAS | JPT | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
NA19060 | hp2 | a0002 | c0010 | t0002 | g0238 | EAS | JPT | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
NA19063 | hp1 | a0002 | c0009 | t0002 | g0023 | EAS | JPT | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
NA19063 | hp2 | a0001 | c0001 | t0001 | g0292 | EAS | JPT | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
NA19065 | hp1 | a0001 | c0008 | t0001 | g0006 | EAS | JPT | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
NA19065 | hp2 | a0001 | c0004 | t0001 | g0277 | EAS | JPT | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
NA19066 | hp1 | a0002 | c0006 | t0002 | g0002 | EAS | JPT | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
NA19066 | hp2 | a0002 | c0002 | t0007 | g0103 | EAS | JPT | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
NA19067 | hp1 | a0001 | c0004 | t0001 | g0199 | EAS | JPT | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
NA19067 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
NA19070 | hp1 | a0002 | c0005 | t0002 | g0152 | EAS | JPT | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
NA19070 | hp2 | a0001 | c0007 | t0001 | g0192 | EAS | JPT | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
NA19074 | hp1 | a0001 | c0001 | t0001 | g0110 | EAS | JPT | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
NA19074 | hp2 | a0002 | c0006 | t0002 | g0018 | EAS | JPT | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
NA19076 | hp1 | a0002 | c0009 | t0002 | g0280 | EAS | JPT | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
NA19076 | hp2 | a0001 | c0001 | t0001 | g0066 | EAS | JPT | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
NA19079 | hp1 | a0001 | c0004 | t0001 | g0087 | EAS | JPT | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
NA19079 | hp2 | a0002 | c0009 | t0002 | g0007 | EAS | JPT | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
NA19081 | hp1 | a0001 | c0040 | t0001 | g0094 | EAS | JPT | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
NA19081 | hp2 | a0001 | c0004 | t0002 | g0241 | EAS | JPT | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
NA19084 | hp1 | a0001 | c0004 | t0001 | g0003 | EAS | JPT | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
NA19084 | hp2 | a0002 | c0006 | t0002 | g0257 | EAS | JPT | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
NA19085 | hp1 | a0001 | c0004 | t0003 | g0299 | EAS | JPT | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
NA19085 | hp2 | a0001 | c0008 | t0001 | g0294 | EAS | JPT | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
NA19088 | hp1 | a0002 | c0002 | t0002 | g0096 | EAS | JPT | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
NA19088 | hp2 | a0001 | c0001 | t0001 | g0306 | EAS | JPT | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
NA19090 | hp1 | a0001 | c0004 | t0001 | g0134 | EAS | JPT | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
NA19090 | hp2 | a0001 | c0001 | t0001 | g0065 | EAS | JPT | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
NA20129 | hp1 | a0002 | c0005 | t0002 | g0044 | AFR | ASW | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
NA20129 | hp2 | a0002 | c0019 | t0002 | g0025 | AFR | ASW | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
NA20752 | hp1 | a0002 | c0002 | t0001 | g0098 | EUR | TSI | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
NA20752 | hp2 | a0002 | c0010 | t0002 | g0275 | EUR | TSI | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
NA20805 | hp1 | a0002 | c0002 | t0002 | g0053 | EUR | TSI | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
NA20805 | hp2 | a0002 | c0002 | t0002 | g0185 | EUR | TSI | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
NA20905 | hp1 | a0001 | c0008 | t0001 | g0174 | SAS | GIH | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
NA20905 | hp2 | a0002 | c0002 | t0002 | g0117 | SAS | GIH | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
HG01123 | hp1 | a0001 | c0001 | t0002 | g0101 | AMR | CLM | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
HG01123 | hp2 | a0002 | c0006 | t0001 | g0021 | AMR | CLM | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
HG02109 | hp1 | a0001 | c0001 | t0011 | g0027 | AFR | ACB | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
HG02109 | hp2 | a0001 | c0003 | t0001 | g0173 | AFR | ACB | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
HG02486 | hp1 | a0001 | c0003 | t0001 | g0054 | AFR | ACB | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
HG02486 | hp2 | a0002 | c0015 | t0002 | g0034 | AFR | ACB | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
HG02559 | hp1 | a0001 | c0003 | t0005 | g0042 | AFR | ACB | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
HG02559 | hp2 | a0001 | c0001 | t0001 | g0060 | AFR | ACB | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
HG06807 | hp1 | a0001 | c0003 | t0004 | g0028 | AFR | USA | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
HG06807 | hp2 | a0003 | c0011 | t0002 | g0284 | AFR | USA | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
NA18955 | hp1 | a0002 | c0006 | t0002 | g0018 | EAS | JPT | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
NA18955 | hp2 | a0001 | c0001 | t0001 | g0146 | EAS | JPT | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
NA20300 | hp1 | a0002 | c0044 | t0001 | g0197 | AFR | USA | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
NA20300 | hp2 | a0001 | c0001 | t0001 | g0120 | AFR | USA | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
NA21309 | hp1 | a0001 | c0008 | t0001 | g0262 | AFR | LWK | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
NA21309 | hp2 | a0005 | c0035 | t0004 | g0032 | AFR | LWK | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr11:17495613
|
C | T | 1 | a0010 | 1 | HG01109.hp1 | missense_variant | MODERATE | c.2611G>A | p.Ala871Thr | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 26/27 | 2720/3241 | 2611/2700 | 871/899 | chr11 | 17495613 | ||
chr11:17498164
|
C | T | 1 | a0011 | 1 | HG01884.hp1 | missense_variant&splice_region_variant | MODERATE | c.2488G>A | p.Gly830Arg | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 24/27 | 2597/3241 | 2488/2700 | 830/899 | chr11 | 17498164 | ||
chr11:17498195
|
C | G | 7 | a0002a0003a0007others(4): Show | 138 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(135): Show |
missense_variant | MODERATE | c.2457G>C | p.Glu819Asp | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 24/27 | 2566/3241 | 2457/2700 | 819/899 | chr11 | 17498195 | ||
chr11:17501084
|
C | A | 3 | a0009a0012a0013 | 3 | HG02451.hp1 HG02965.hp1 HG03516.hp2 |
missense_variant | MODERATE | c.2347G>T | p.Ala783Ser | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 23/27 | 2456/3241 | 2347/2700 | 783/899 | chr11 | 17501084 | ||
chr11:17509463
|
G | A | 1 | a0005 | 2 | HG01167.hp2 NA21309.hp2 |
missense_variant | MODERATE | c.1906C>T | p.Arg636Cys | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 18/27 | 2015/3241 | 1906/2700 | 636/899 | chr11 | 17509463 | ||
chr11:17509510
|
C | A | 1 | a0004 | 3 | HG00735.hp1 HG02970.hp2 HG03516.hp1 |
missense_variant | MODERATE | c.1859G>T | p.Arg620Leu | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 18/27 | 1968/3241 | 1859/2700 | 620/899 | chr11 | 17509510 | ||
chr11:17509778
|
G | A | 1 | a0009 | 1 | HG02451.hp1 | missense_variant | MODERATE | c.1591C>T | p.Arg531Cys | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 18/27 | 1700/3241 | 1591/2700 | 531/899 | chr11 | 17509778 | ||
chr11:17520944
|
C | T | 1 | a0008 | 1 | HG01167.hp1 | missense_variant | MODERATE | c.1136G>A | p.Gly379Asp | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 14/27 | 1245/3241 | 1136/2700 | 379/899 | chr11 | 17520944 | ||
chr11:17521362
|
G | A | 1 | a0014 | 1 | HG02738.hp1 | missense_variant | MODERATE | c.1069C>T | p.Arg357Trp | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 13/27 | 1178/3241 | 1069/2700 | 357/899 | chr11 | 17521362 | ||
chr11:17522857
|
C | G | 1 | a0015 | 1 | NA19030.hp1 | missense_variant | MODERATE | c.946G>C | p.Glu316Gln | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 12/27 | 1055/3241 | 946/2700 | 316/899 | chr11 | 17522857 | ||
chr11:17527255
|
C | G | 1 | a0007 | 1 | NA18942.hp1 | missense_variant | MODERATE | c.464G>C | p.Arg155Pro | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 5/27 | 573/3241 | 464/2700 | 155/899 | chr11 | 17527255 | ||
chr11:17527331
|
C | T | 2 | a0003a0006 | 6 | HG01243.hp2 HG01891.hp2 HG02257.hp1 others(3): Show |
missense_variant&splice_region_variant | MODERATE | c.388G>A | p.Val130Ile | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 5/27 | 497/3241 | 388/2700 | 130/899 | chr11 | 17527331 | ||
chr11:17531537
|
A | G | 1 | a0016 | 1 | HG02809.hp1 | missense_variant | MODERATE | c.110T>C | p.Met37Thr | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 3/27 | 219/3241 | 110/2700 | 37/899 | chr11 | 17531537 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr11:17501091
|
G | A | 14 | a0001c0004a0001c0008a0001c0013others(11): Show | 89 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(86): Show |
synonymous_variant | LOW | c.2340C>T | p.Val780Val | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 23/27 | 2449/3241 | 2340/2700 | 780/899 | chr11 | 17501091 | ||
chr11:17509497
|
C | T | 4 | a0006c0025a0009c0045a0012c0032others(1): Show | 4 | HG02451.hp1 HG02451.hp2 HG02965.hp1 others(1): Show |
synonymous_variant | LOW | c.1872G>A | p.Ser624Ser | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 18/27 | 1981/3241 | 1872/2700 | 624/899 | chr11 | 17509497 | ||
chr11:17509545
|
C | T | 1 | a0001c0039 | 1 | NA18957.hp1 | synonymous_variant | LOW | c.1824G>A | p.Pro608Pro | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 18/27 | 1933/3241 | 1824/2700 | 608/899 | chr11 | 17509545 | ||
chr11:17509599
|
G | A | 7 | a0001c0007a0001c0018a0001c0037others(4): Show | 23 | HG00099.hp2 HG01070.hp2 HG01496.hp2 others(20): Show |
synonymous_variant | LOW | c.1770C>T | p.Ala590Ala | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 18/27 | 1879/3241 | 1770/2700 | 590/899 | chr11 | 17509599 | ||
chr11:17509629
|
A | G | 1 | a0002c0031 | 1 | HG00673.hp2 | synonymous_variant | LOW | c.1740T>C | p.Pro580Pro | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 18/27 | 1849/3241 | 1740/2700 | 580/899 | chr11 | 17509629 | ||
chr11:17509737
|
G | A | 1 | a0001c0017 | 2 | HG02572.hp1 HG02723.hp2 |
synonymous_variant | LOW | c.1632C>T | p.Asp544Asp | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 18/27 | 1741/3241 | 1632/2700 | 544/899 | chr11 | 17509737 | ||
chr11:17509767
|
G | A | 1 | a0001c0040 | 1 | NA19081.hp1 | synonymous_variant | LOW | c.1602C>T | p.Gly534Gly | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 18/27 | 1711/3241 | 1602/2700 | 534/899 | chr11 | 17509767 | ||
chr11:17510477
|
A | G | 1 | a0009c0045 | 1 | HG02451.hp1 | synonymous_variant | LOW | c.1458T>C | p.Ile486Ile | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 17/27 | 1567/3241 | 1458/2700 | 486/899 | chr11 | 17510477 | ||
chr11:17520892
|
T | C | 18 | a0001c0001a0001c0004a0001c0016others(15): Show | 202 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(199): Show |
synonymous_variant | LOW | c.1188A>G | p.Pro396Pro | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 14/27 | 1297/3241 | 1188/2700 | 396/899 | chr11 | 17520892 | ||
chr11:17526370
|
T | C | 4 | a0001c0042a0001c0043a0002c0015others(1): Show | 7 | HG01255.hp1 HG02145.hp1 HG02486.hp2 others(4): Show |
synonymous_variant | LOW | c.651A>G | p.Val217Val | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 8/27 | 760/3241 | 651/2700 | 217/899 | chr11 | 17526370 | ||
chr11:17526373
|
C | T | 2 | a0001c0016a0001c0028 | 3 | HG02056.hp2 NA18982.hp1 NA19011.hp1 |
synonymous_variant | LOW | c.648G>A | p.Leu216Leu | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 8/27 | 757/3241 | 648/2700 | 216/899 | chr11 | 17526373 | ||
chr11:17527239
|
C | T | 1 | a0002c0027 | 1 | NA18959.hp2 | synonymous_variant | LOW | c.480G>A | p.Val160Val | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 5/27 | 589/3241 | 480/2700 | 160/899 | chr11 | 17527239 | ||
chr11:17531181
|
G | A | 1 | a0002c0044 | 1 | NA20300.hp1 | synonymous_variant | LOW | c.360C>T | p.Gly120Gly | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 4/27 | 469/3241 | 360/2700 | 120/899 | chr11 | 17531181 | ||
chr11:17531217
|
A | G | 1 | a0001c0024 | 1 | HG02735.hp2 | synonymous_variant | LOW | c.324T>C | p.Phe108Phe | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 4/27 | 433/3241 | 324/2700 | 108/899 | chr11 | 17531217 | ||
chr11:17531247
|
G | A | 6 | a0001c0021a0001c0047a0002c0020others(3): Show | 8 | HG01884.hp1 HG02280.hp2 HG02451.hp1 others(5): Show |
synonymous_variant | LOW | c.294C>T | p.Leu98Leu | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 4/27 | 403/3241 | 294/2700 | 98/899 | chr11 | 17531247 | ||
chr11:17531422
|
A | G | 3 | a0001c0013a0001c0023a0002c0009 | 14 | HG02040.hp2 HG02135.hp1 HG02135.hp2 others(11): Show |
synonymous_variant | LOW | c.225T>C | p.Asp75Asp | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 3/27 | 334/3241 | 225/2700 | 75/899 | chr11 | 17531422 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr11:17493912
|
C | CTGTT | 71 | a0001c0001t0001a0001c0001t0002a0001c0001t0008others(68): Show | 343 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(340): Show |
3_prime_UTR_variant | MODIFIER | c.*419_*420insAACA | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 27/27 | 419 | chr11 | 17493912 | |||||
chr11:17493927
|
G | C | 2 | a0001c0001t0008a0001c0003t0008 | 2 | HG01891.hp1 HG03209.hp1 |
3_prime_UTR_variant | MODIFIER | c.*405C>G | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 27/27 | 405 | chr11 | 17493927 | |||||
chr11:17493975
|
G | A | 1 | a0001c0001t0014 | 1 | NA18973.hp2 | 3_prime_UTR_variant | MODIFIER | c.*357C>T | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 27/27 | 357 | chr11 | 17493975 | |||||
chr11:17494041
|
C | A | 1 | a0002c0005t0013 | 1 | HG01978.hp2 | 3_prime_UTR_variant | MODIFIER | c.*291G>T | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 27/27 | 291 | chr11 | 17494041 | |||||
chr11:17494091
|
G | C | 1 | a0001c0018t0015 | 1 | NA18971.hp1 | 3_prime_UTR_variant | MODIFIER | c.*241C>G | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 27/27 | 241 | chr11 | 17494091 | |||||
chr11:17494121
|
T | C | 30 | a0001c0001t0002a0001c0001t0008a0001c0003t0002others(27): Show | 118 | HG00323.hp2 HG00544.hp1 HG00558.hp2 others(115): Show |
3_prime_UTR_variant | MODIFIER | c.*211A>G | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 27/27 | 211 | chr11 | 17494121 | |||||
chr11:17494146
|
G | A | 26 | a0001c0001t0002a0001c0001t0008a0001c0003t0002others(23): Show | 112 | HG00323.hp2 HG00544.hp1 HG00558.hp2 others(109): Show |
3_prime_UTR_variant | MODIFIER | c.*186C>T | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 27/27 | 186 | chr11 | 17494146 | |||||
chr11:17494201
|
C | G | 1 | a0002c0012t0012 | 1 | HG03669.hp1 | 3_prime_UTR_variant | MODIFIER | c.*131G>C | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 27/27 | 131 | chr11 | 17494201 | |||||
chr11:17494222
|
G | C | 1 | a0001c0023t0017 | 1 | NA18948.hp1 | 3_prime_UTR_variant | MODIFIER | c.*110C>G | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 27/27 | 110 | chr11 | 17494222 | |||||
chr11:17494286
|
A | G | 27 | a0001c0001t0002a0001c0001t0008a0001c0003t0002others(24): Show | 114 | HG00323.hp2 HG00544.hp1 HG00558.hp2 others(111): Show |
3_prime_UTR_variant | MODIFIER | c.*46T>C | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 27/27 | 46 | chr11 | 17494286 | |||||
chr11:17494290
|
G | A | 1 | a0001c0001t0009 | 2 | HG02809.hp2 HG03453.hp1 |
3_prime_UTR_variant | MODIFIER | c.*42C>T | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 27/27 | 42 | chr11 | 17494290 | |||||
chr11:17544367
|
A | G | 4 | a0001c0003t0004a0001c0003t0006a0001c0043t0006others(1): Show | 5 | HG02258.hp2 HG02976.hp2 HG03486.hp1 others(2): Show |
5_prime_UTR_variant | MODIFIER | c.-60T>C | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 1/27 | 60 | chr11 | 17544367 | |||||
chr11:17544378
|
A | C | 1 | a0001c0001t0011 | 1 | HG02109.hp1 | 5_prime_UTR_variant | MODIFIER | c.-71T>G | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 1/27 | 71 | chr11 | 17544378 | |||||
chr11:17544401
|
A | T | 1 | a0001c0013t0010 | 1 | NA18963.hp1 | 5_prime_UTR_variant | MODIFIER | c.-94T>A | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 1/27 | 94 | chr11 | 17544401 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr11:17494423
|
G | A | 89 | a0001c0001t0002g0218a0001c0004t0002g0241a0002c0002t0002g0004others(86): Show | 106 | HG00323.hp2 HG00544.hp1 HG00558.hp2 others(103): Show |
intron_variant | MODIFIER | c.2656-47C>T | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 26/26 | chr11 | 17494423 | ||||||
chr11:17494482
|
A | G | 65 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0048others(62): Show | 72 | HG00280.hp1 HG00558.hp1 HG00597.hp1 others(69): Show |
intron_variant | MODIFIER | c.2656-106T>C | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 26/26 | chr11 | 17494482 | ||||||
chr11:17494491
|
C | T | 97 | a0001c0001t0002g0101a0001c0001t0002g0218a0001c0001t0008g0229others(94): Show | 114 | HG00323.hp2 HG00544.hp1 HG00558.hp2 others(111): Show |
intron_variant | MODIFIER | c.2656-115G>A | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 26/26 | chr11 | 17494491 | ||||||
chr11:17494534
|
CA | C | 5 | a0001c0001t0002g0101a0001c0003t0002g0068a0001c0021t0002g0162others(2): Show | 5 | HG01123.hp1 HG02976.hp2 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.2656-159delT | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 26/26 | chr11 | 17494534 | ||||||
chr11:17494636
|
T | C | 304 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0008others(301): Show | 340 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(337): Show |
intron_variant | MODIFIER | c.2656-260A>G | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 26/26 | chr11 | 17494636 | ||||||
chr11:17494702
|
G | A | 1 | a0001c0001t0011g0027 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.2656-326C>T | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 26/26 | chr11 | 17494702 | ||||||
chr11:17494775
|
G | C | 2 | a0004c0014t0005g0062a0004c0014t0005g0225 | 2 | HG00735.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.2656-399C>G | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 26/26 | chr11 | 17494775 | ||||||
chr11:17494820
|
C | A | 1 | a0001c0003t0001g0151 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.2656-444G>T | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 26/26 | chr11 | 17494820 | ||||||
chr11:17494842
|
CA | C | 65 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0048others(62): Show | 72 | HG00280.hp1 HG00558.hp1 HG00597.hp1 others(69): Show |
intron_variant | MODIFIER | c.2656-467delT | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 26/26 | chr11 | 17494842 | ||||||
chr11:17494891
|
A | G | 2 | a0001c0001t0008g0229a0001c0003t0008g0272 | 2 | HG01891.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.2656-515T>C | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 26/26 | chr11 | 17494891 | ||||||
chr11:17494975
|
C | T | 2 | a0001c0001t0002g0101a0002c0002t0002g0106 | 2 | HG01123.hp1 HG02523.hp2 |
intron_variant | MODIFIER | c.2655+594G>A | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 26/26 | chr11 | 17494975 | ||||||
chr11:17495024
|
C | T | 8 | a0001c0001t0001g0005a0001c0001t0001g0118a0001c0001t0001g0120others(5): Show | 10 | HG02109.hp1 HG02109.hp2 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.2655+545G>A | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 26/26 | chr11 | 17495024 | ||||||
chr11:17495101
|
A | G | 90 | a0001c0001t0002g0218a0001c0004t0002g0241a0002c0002t0002g0004others(87): Show | 107 | HG00323.hp2 HG00544.hp1 HG00558.hp2 others(104): Show |
intron_variant | MODIFIER | c.2655+468T>C | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 26/26 | chr11 | 17495101 | ||||||
chr11:17495305
|
A | G | 17 | a0001c0001t0001g0005a0001c0001t0001g0118a0001c0001t0001g0120others(14): Show | 19 | HG00735.hp1 HG01884.hp1 HG02109.hp1 others(16): Show |
intron_variant | MODIFIER | c.2655+264T>C | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 26/26 | chr11 | 17495305 | ||||||
chr11:17495389
|
G | T | 6 | a0001c0001t0001g0046a0001c0001t0001g0051a0001c0001t0001g0059others(3): Show | 6 | HG01256.hp1 HG02258.hp1 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.2655+180C>A | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 26/26 | chr11 | 17495389 | ||||||
chr11:17495501
|
G | A | 1 | a0001c0003t0006g0031 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.2655+68C>T | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 26/26 | chr11 | 17495501 | ||||||
chr11:17495536
|
A | T | 1 | a0001c0008t0001g0294 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.2655+33T>A | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 26/26 | chr11 | 17495536 | ||||||
chr11:17495685
|
T | C | 1 | a0001c0003t0005g0042 | 1 | HG02559.hp1 | splice_region_variant&intron_variant | LOW | c.2547-8A>G | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 25/26 | chr11 | 17495685 | ||||||
chr11:17495688
|
A | G | 120 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0011others(117): Show | 130 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(127): Show |
intron_variant | MODIFIER | c.2547-11T>C | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 25/26 | chr11 | 17495688 | ||||||
chr11:17495834
|
CAT | C | 189 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(186): Show | 206 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(203): Show |
intron_variant | MODIFIER | c.2547-159_2547-158d others(4): Show |
USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 25/26 | chr11 | 17495834 | ||||||
chr11:17495860
|
G | C | 300 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(297): Show | 334 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(331): Show |
intron_variant | MODIFIER | c.2547-183C>G | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 25/26 | chr11 | 17495860 | ||||||
chr11:17496149
|
G | A | 65 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0048others(62): Show | 72 | HG00280.hp1 HG00558.hp1 HG00597.hp1 others(69): Show |
intron_variant | MODIFIER | c.2547-472C>T | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 25/26 | chr11 | 17496149 | ||||||
chr11:17496332
|
C | A | 124 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0011others(121): Show | 134 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(131): Show |
intron_variant | MODIFIER | c.2546+426G>T | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 25/26 | chr11 | 17496332 | ||||||
chr11:17496485
|
A | G | 1 | a0001c0003t0001g0156 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.2546+273T>C | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 25/26 | chr11 | 17496485 | ||||||
chr11:17496560
|
G | A | 2 | a0002c0002t0002g0096a0002c0002t0002g0244 | 2 | NA19000.hp2 NA19088.hp1 |
intron_variant | MODIFIER | c.2546+198C>T | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 25/26 | chr11 | 17496560 | ||||||
chr11:17496569
|
C | T | 1 | a0001c0004t0001g0134 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.2546+189G>A | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 25/26 | chr11 | 17496569 | ||||||
chr11:17496633
|
T | C | 73 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0011others(70): Show | 80 | HG00323.hp1 HG00438.hp1 HG00438.hp2 others(77): Show |
intron_variant | MODIFIER | c.2546+125A>G | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 25/26 | chr11 | 17496633 | ||||||
chr11:17496829
|
G | A | 1 | a0001c0003t0006g0031 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.2491-16C>T | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 24/26 | chr11 | 17496829 | ||||||
chr11:17496869
|
C | T | 1 | a0001c0001t0001g0130 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.2491-56G>A | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 24/26 | chr11 | 17496869 | ||||||
chr11:17496978
|
G | T | 124 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0011others(121): Show | 134 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(131): Show |
intron_variant | MODIFIER | c.2491-165C>A | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 24/26 | chr11 | 17496978 | ||||||
chr11:17497124
|
G | A | 1 | a0012c0032t0002g0250 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.2491-311C>T | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 24/26 | chr11 | 17497124 | ||||||
chr11:17497173
|
TTAACAAC | T | 2 | a0002c0002t0002g0015a0002c0002t0002g0200 | 3 | NA18941.hp2 NA18993.hp2 NA19005.hp2 |
intron_variant | MODIFIER | c.2491-367_2491-361d others(9): Show |
USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 24/26 | chr11 | 17497173 | ||||||
chr11:17497191
|
A | C | 5 | a0001c0001t0008g0229a0001c0003t0001g0173a0001c0003t0004g0030others(2): Show | 5 | HG01891.hp1 HG02109.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.2491-378T>G | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 24/26 | chr11 | 17497191 | ||||||
chr11:17497362
|
A | G | 75 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0046others(72): Show | 82 | HG00280.hp1 HG00558.hp1 HG00597.hp1 others(79): Show |
intron_variant | MODIFIER | c.2491-549T>C | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 24/26 | chr11 | 17497362 | ||||||
chr11:17497747
|
G | A | 1 | a0001c0003t0006g0031 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.2490+415C>T | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 24/26 | chr11 | 17497747 | ||||||
chr11:17497988
|
C | T | 2 | a0001c0001t0008g0229a0001c0003t0008g0272 | 2 | HG01891.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.2490+174G>A | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 24/26 | chr11 | 17497988 | ||||||
chr11:17498106
|
C | G | 2 | a0001c0004t0001g0207a0001c0004t0001g0209 | 2 | HG01257.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.2490+56G>C | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 24/26 | chr11 | 17498106 | ||||||
chr11:17498110
|
G | A | 1 | a0001c0021t0001g0163 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.2490+52C>T | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 24/26 | chr11 | 17498110 | ||||||
chr11:17498150
|
C | G | 64 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0048others(61): Show | 71 | HG00280.hp1 HG00558.hp1 HG00597.hp1 others(68): Show |
intron_variant | MODIFIER | c.2490+12G>C | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 24/26 | chr11 | 17498150 | ||||||
chr11:17498317
|
C | T | 63 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0048others(60): Show | 68 | HG00280.hp1 HG00544.hp2 HG00558.hp1 others(65): Show |
intron_variant | MODIFIER | c.2381-46G>A | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 23/26 | chr11 | 17498317 | ||||||
chr11:17498702
|
C | T | 80 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0011others(77): Show | 87 | HG00323.hp1 HG00438.hp1 HG00438.hp2 others(84): Show |
intron_variant | MODIFIER | c.2381-431G>A | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 23/26 | chr11 | 17498702 | ||||||
chr11:17498792
|
A | G | 192 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(189): Show | 216 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(213): Show |
intron_variant | MODIFIER | c.2381-521T>C | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 23/26 | chr11 | 17498792 | ||||||
chr11:17498841
|
G | A | 1 | a0002c0031t0002g0258 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.2381-570C>T | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 23/26 | chr11 | 17498841 | ||||||
chr11:17499238
|
C | T | 2 | a0001c0003t0001g0191a0013c0033t0001g0232 | 2 | HG03041.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.2381-967G>A | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 23/26 | chr11 | 17499238 | ||||||
chr11:17499239
|
C | G | 13 | a0001c0001t0001g0060a0001c0001t0001g0125a0001c0003t0001g0226others(10): Show | 13 | HG00099.hp1 HG01109.hp1 HG01168.hp1 others(10): Show |
intron_variant | MODIFIER | c.2381-968G>C | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 23/26 | chr11 | 17499239 | ||||||
chr11:17499418
|
G | A | 23 | a0001c0001t0001g0008a0001c0001t0001g0016a0001c0001t0001g0082others(20): Show | 28 | HG01261.hp1 HG01261.hp2 HG01975.hp1 others(25): Show |
intron_variant | MODIFIER | c.2381-1147C>T | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 23/26 | chr11 | 17499418 | ||||||
chr11:17499522
|
T | G | 1 | a0001c0001t0001g0125 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.2381-1251A>C | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 23/26 | chr11 | 17499522 | ||||||
chr11:17499550
|
T | C | 3 | a0001c0003t0004g0030a0001c0017t0001g0314a0001c0017t0001g0315 | 3 | HG02572.hp1 HG02723.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.2381-1279A>G | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 23/26 | chr11 | 17499550 | ||||||
chr11:17499562
|
C | A | 1 | a0001c0003t0001g0054 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.2381-1291G>T | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 23/26 | chr11 | 17499562 | ||||||
chr11:17499744
|
T | C | 1 | a0001c0003t0005g0042 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.2380+1307A>G | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 23/26 | chr11 | 17499744 | ||||||
chr11:17499797
|
T | G | 1 | a0001c0001t0001g0120 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.2380+1254A>C | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 23/26 | chr11 | 17499797 | ||||||
chr11:17499868
|
C | T | 3 | a0001c0003t0003g0253a0002c0005t0001g0252a0002c0005t0001g0270 | 3 | HG01496.hp1 HG02647.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.2380+1183G>A | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 23/26 | chr11 | 17499868 | ||||||
chr11:17500043
|
A | G | 23 | a0001c0001t0011g0027a0001c0003t0001g0223a0001c0003t0002g0068others(20): Show | 23 | HG00735.hp1 HG01255.hp1 HG02055.hp2 others(20): Show |
intron_variant | MODIFIER | c.2380+1008T>C | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 23/26 | chr11 | 17500043 | ||||||
chr11:17500207
|
G | A | 1 | a0001c0001t0009g0071 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.2380+844C>T | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 23/26 | chr11 | 17500207 | ||||||
chr11:17500215
|
G | A | 83 | a0001c0003t0001g0121a0001c0003t0001g0150a0001c0003t0001g0151others(80): Show | 99 | HG00099.hp1 HG00323.hp2 HG00544.hp1 others(96): Show |
intron_variant | MODIFIER | c.2380+836C>T | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 23/26 | chr11 | 17500215 | ||||||
chr11:17500278
|
C | T | 19 | a0001c0001t0001g0052a0001c0001t0001g0154a0001c0001t0001g0230others(16): Show | 20 | HG01081.hp2 HG01167.hp1 HG01168.hp2 others(17): Show |
intron_variant | MODIFIER | c.2380+773G>A | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 23/26 | chr11 | 17500278 | ||||||
chr11:17500345
|
G | T | 1 | a0001c0042t0001g0033 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.2380+706C>A | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 23/26 | chr11 | 17500345 | ||||||
chr11:17500493
|
T | C | 1 | a0001c0001t0001g0125 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.2380+558A>G | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 23/26 | chr11 | 17500493 | ||||||
chr11:17500533
|
C | T | 1 | a0001c0003t0006g0031 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.2380+518G>A | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 23/26 | chr11 | 17500533 | ||||||
chr11:17500539
|
C | T | 82 | a0001c0001t0001g0052a0001c0001t0001g0154a0001c0001t0001g0230others(79): Show | 85 | HG00099.hp2 HG00735.hp1 HG01070.hp2 others(82): Show |
intron_variant | MODIFIER | c.2380+512G>A | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 23/26 | chr11 | 17500539 | ||||||
chr11:17500569
|
C | A | 2 | a0001c0003t0001g0072a0001c0003t0001g0144 | 2 | HG01884.hp2 HG02145.hp2 |
intron_variant | MODIFIER | c.2380+482G>T | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 23/26 | chr11 | 17500569 | ||||||
chr11:17500600
|
G | A | 2 | a0001c0003t0001g0072a0001c0003t0001g0144 | 2 | HG01884.hp2 HG02145.hp2 |
intron_variant | MODIFIER | c.2380+451C>T | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 23/26 | chr11 | 17500600 | ||||||
chr11:17500622
|
G | A | 2 | a0012c0032t0002g0250a0013c0033t0001g0232 | 2 | HG02965.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.2380+429C>T | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 23/26 | chr11 | 17500622 | ||||||
chr11:17500643
|
C | T | 1 | a0001c0001t0001g0112 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.2380+408G>A | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 23/26 | chr11 | 17500643 | ||||||
chr11:17500647
|
T | C | 8 | a0001c0003t0001g0156a0001c0003t0001g0202a0001c0003t0001g0204others(5): Show | 8 | HG01106.hp1 HG02055.hp2 HG03688.hp1 others(5): Show |
intron_variant | MODIFIER | c.2380+404A>G | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 23/26 | chr11 | 17500647 | ||||||
chr11:17500724
|
T | C | 6 | a0001c0003t0001g0191a0001c0003t0001g0295a0003c0011t0001g0024others(3): Show | 7 | HG01243.hp2 HG01891.hp2 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.2380+327A>G | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 23/26 | chr11 | 17500724 | ||||||
chr11:17500730
|
C | G | 1 | a0001c0043t0006g0029 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.2380+321G>C | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 23/26 | chr11 | 17500730 | ||||||
chr11:17500871
|
T | G | 1 | a0001c0001t0003g0102 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.2380+180A>C | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 23/26 | chr11 | 17500871 | ||||||
chr11:17500912
|
C | G | 1 | a0001c0003t0001g0173 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.2380+139G>C | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 23/26 | chr11 | 17500912 | ||||||
chr11:17501263
|
T | C | 182 | a0001c0001t0001g0052a0001c0001t0001g0056a0001c0001t0001g0154others(179): Show | 202 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(199): Show |
intron_variant | MODIFIER | c.2281-113A>G | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 22/26 | chr11 | 17501263 | ||||||
chr11:17501341
|
C | T | 1 | a0001c0007t0001g0298 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.2280+141G>A | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 22/26 | chr11 | 17501341 | ||||||
chr11:17501453
|
G | A | 5 | a0001c0003t0001g0072a0001c0003t0001g0144a0004c0014t0001g0269others(2): Show | 5 | HG00735.hp1 HG01884.hp2 HG02145.hp2 others(2): Show |
intron_variant | MODIFIER | c.2280+29C>T | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 22/26 | chr11 | 17501453 | ||||||
chr11:17501574
|
T | G | 1 | a0001c0001t0001g0010 | 2 | HG01069.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.2227-39A>C | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 21/26 | chr11 | 17501574 | ||||||
chr11:17501653
|
A | C | 3 | a0009c0045t0016g0159a0012c0032t0002g0250a0013c0033t0001g0232 | 3 | HG02451.hp1 HG02965.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.2227-118T>G | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 21/26 | chr11 | 17501653 | ||||||
chr11:17501671
|
C | T | 4 | a0001c0003t0001g0156a0001c0003t0001g0223a0001c0003t0001g0296others(1): Show | 4 | HG01106.hp1 HG02055.hp2 HG03688.hp1 others(1): Show |
intron_variant | MODIFIER | c.2227-136G>A | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 21/26 | chr11 | 17501671 | ||||||
chr11:17501742
|
C | T | 31 | a0001c0001t0001g0052a0001c0001t0001g0056a0001c0001t0001g0154others(28): Show | 33 | HG01167.hp1 HG01168.hp2 HG01255.hp1 others(30): Show |
intron_variant | MODIFIER | c.2226+197G>A | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 21/26 | chr11 | 17501742 | ||||||
chr11:17501927
|
G | A | 29 | a0001c0007t0001g0176a0001c0007t0001g0177a0001c0007t0001g0187others(26): Show | 30 | HG00099.hp2 HG01070.hp2 HG01496.hp2 others(27): Show |
intron_variant | MODIFIER | c.2226+12C>T | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 21/26 | chr11 | 17501927 | ||||||
chr11:17502246
|
C | T | 1 | a0001c0003t0003g0165 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.2185-266G>A | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 20/26 | chr11 | 17502246 | ||||||
chr11:17502252
|
C | T | 1 | a0008c0030t0001g0142 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.2185-272G>A | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 20/26 | chr11 | 17502252 | ||||||
chr11:17502470
|
C | T | 1 | a0001c0007t0003g0181 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.2185-490G>A | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 20/26 | chr11 | 17502470 | ||||||
chr11:17502471
|
A | G | 81 | a0001c0001t0001g0052a0001c0001t0001g0056a0001c0001t0001g0154others(78): Show | 85 | HG00099.hp2 HG01070.hp2 HG01106.hp1 others(82): Show |
intron_variant | MODIFIER | c.2185-491T>C | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 20/26 | chr11 | 17502471 | ||||||
chr11:17502641
|
G | C | 1 | a0001c0008t0001g0264 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.2185-661C>G | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 20/26 | chr11 | 17502641 | ||||||
chr11:17502962
|
C | G | 4 | a0001c0003t0001g0156a0001c0003t0001g0223a0001c0003t0001g0296others(1): Show | 4 | HG01106.hp1 HG02055.hp2 HG03688.hp1 others(1): Show |
intron_variant | MODIFIER | c.2185-982G>C | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 20/26 | chr11 | 17502962 | ||||||
chr11:17502984
|
G | T | 1 | a0001c0003t0008g0272 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.2185-1004C>A | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 20/26 | chr11 | 17502984 | ||||||
chr11:17503001
|
T | C | 70 | a0001c0001t0011g0027a0001c0003t0001g0072a0001c0003t0001g0144others(67): Show | 73 | HG00099.hp2 HG00735.hp1 HG01070.hp2 others(70): Show |
intron_variant | MODIFIER | c.2185-1021A>G | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 20/26 | chr11 | 17503001 | ||||||
chr11:17503145
|
G | A | 2 | a0001c0003t0001g0156a0001c0003t0001g0296 | 2 | HG03688.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.2185-1165C>T | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 20/26 | chr11 | 17503145 | ||||||
chr11:17503283
|
C | T | 1 | a0001c0003t0004g0028 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.2185-1303G>A | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 20/26 | chr11 | 17503283 | ||||||
chr11:17503505
|
G | A | 1 | a0002c0005t0001g0070 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.2184+1142C>T | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 20/26 | chr11 | 17503505 | ||||||
chr11:17503593
|
T | C | 1 | a0001c0003t0004g0028 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.2184+1054A>G | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 20/26 | chr11 | 17503593 | ||||||
chr11:17503709
|
C | G | 1 | a0001c0008t0001g0171 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.2184+938G>C | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 20/26 | chr11 | 17503709 | ||||||
chr11:17503787
|
A | G | 7 | a0001c0001t0001g0052a0001c0001t0001g0056a0001c0001t0001g0154others(4): Show | 7 | HG01167.hp1 HG01168.hp2 HG01943.hp1 others(4): Show |
intron_variant | MODIFIER | c.2184+860T>C | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 20/26 | chr11 | 17503787 | ||||||
chr11:17504393
|
G | C | 11 | a0001c0003t0001g0072a0001c0003t0001g0144a0001c0003t0001g0223others(8): Show | 12 | HG00735.hp1 HG01106.hp1 HG01243.hp2 others(9): Show |
intron_variant | MODIFIER | c.2184+254C>G | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 20/26 | chr11 | 17504393 | ||||||
chr11:17504418
|
G | A | 9 | a0001c0001t0001g0052a0001c0001t0001g0056a0001c0001t0001g0154others(6): Show | 10 | HG01167.hp1 HG01168.hp2 HG01943.hp1 others(7): Show |
intron_variant | MODIFIER | c.2184+229C>T | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 20/26 | chr11 | 17504418 | ||||||
chr11:17504547
|
T | C | 1 | a0002c0002t0002g0126 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.2184+100A>G | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 20/26 | chr11 | 17504547 | ||||||
chr11:17504586
|
C | T | 4 | a0001c0003t0004g0028a0003c0011t0001g0024a0003c0011t0001g0283others(1): Show | 5 | HG01243.hp2 HG01891.hp2 HG02257.hp1 others(2): Show |
intron_variant | MODIFIER | c.2184+61G>A | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 20/26 | chr11 | 17504586 | ||||||
chr11:17504600
|
C | T | 3 | a0001c0001t0001g0005a0001c0001t0001g0118a0001c0001t0001g0120 | 5 | HG02615.hp1 HG02717.hp1 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.2184+47G>A | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 20/26 | chr11 | 17504600 | ||||||
chr11:17504604
|
G | A | 4 | a0001c0003t0001g0156a0001c0003t0001g0223a0001c0003t0001g0296others(1): Show | 4 | HG01106.hp1 HG02055.hp2 HG03688.hp1 others(1): Show |
intron_variant | MODIFIER | c.2184+43C>T | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 20/26 | chr11 | 17504604 | ||||||
chr11:17504626
|
A | C | 6 | a0001c0042t0001g0033a0002c0005t0001g0124a0002c0005t0001g0141others(3): Show | 6 | HG01255.hp1 HG02486.hp2 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.2184+21T>G | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 20/26 | chr11 | 17504626 | ||||||
chr11:17504635
|
G | A | 2 | a0002c0020t0001g0158a0002c0020t0002g0157 | 2 | HG02280.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.2184+12C>T | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 20/26 | chr11 | 17504635 | ||||||
chr11:17504707
|
G | GA | 5 | a0001c0003t0004g0028a0001c0008t0001g0289a0003c0011t0001g0024others(2): Show | 6 | HG01243.hp2 HG01891.hp2 HG02257.hp1 others(3): Show |
intron_variant | MODIFIER | c.2134-11dupT | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 19/26 | chr11 | 17504707 | ||||||
chr11:17504708
|
A | G | 2 | a0001c0001t0001g0076a0001c0001t0001g0108 | 2 | HG00544.hp2 NA18966.hp1 |
intron_variant | MODIFIER | c.2134-11T>C | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 19/26 | chr11 | 17504708 | ||||||
chr11:17504709
|
A | G | 7 | a0001c0001t0001g0125a0001c0001t0001g0128a0001c0001t0001g0131others(4): Show | 8 | HG00280.hp1 HG00733.hp1 HG01099.hp2 others(5): Show |
intron_variant | MODIFIER | c.2134-12T>C | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 19/26 | chr11 | 17504709 | ||||||
chr11:17504974
|
G | T | 1 | a0001c0001t0001g0048 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.2134-277C>A | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 19/26 | chr11 | 17504974 | ||||||
chr11:17505036
|
C | T | 4 | a0001c0003t0001g0156a0001c0003t0001g0223a0001c0003t0001g0296others(1): Show | 4 | HG01106.hp1 HG02055.hp2 HG03688.hp1 others(1): Show |
intron_variant | MODIFIER | c.2134-339G>A | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 19/26 | chr11 | 17505036 | ||||||
chr11:17505575
|
G | A | 1 | a0001c0001t0001g0107 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.2133+255C>T | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 19/26 | chr11 | 17505575 | ||||||
chr11:17505579
|
C | T | 3 | a0003c0011t0001g0024a0003c0011t0001g0283a0003c0011t0002g0285 | 4 | HG01243.hp2 HG01891.hp2 HG02257.hp1 others(1): Show |
intron_variant | MODIFIER | c.2133+251G>A | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 19/26 | chr11 | 17505579 | ||||||
chr11:17506254
|
C | G | 4 | a0006c0025t0001g0205a0009c0045t0016g0159a0012c0032t0002g0250others(1): Show | 4 | HG02451.hp1 HG02451.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.2014-305G>C | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 18/26 | chr11 | 17506254 | ||||||
chr11:17506360
|
T | C | 13 | a0001c0003t0001g0072a0001c0003t0001g0144a0001c0017t0001g0314others(10): Show | 13 | HG00735.hp1 HG01255.hp1 HG01884.hp2 others(10): Show |
intron_variant | MODIFIER | c.2014-411A>G | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 18/26 | chr11 | 17506360 | ||||||
chr11:17506471
|
A | G | 1 | a0001c0013t0001g0282 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.2014-522T>C | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 18/26 | chr11 | 17506471 | ||||||
chr11:17506521
|
C | T | 1 | a0001c0001t0001g0051 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.2014-572G>A | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 18/26 | chr11 | 17506521 | ||||||
chr11:17506609
|
C | T | 1 | a0001c0004t0003g0299 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.2014-660G>A | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 18/26 | chr11 | 17506609 | ||||||
chr11:17506614
|
C | T | 1 | a0001c0001t0001g0064 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.2014-665G>A | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 18/26 | chr11 | 17506614 | ||||||
chr11:17506615
|
G | A | 3 | a0003c0011t0001g0024a0003c0011t0001g0283a0003c0011t0002g0285 | 4 | HG01243.hp2 HG01891.hp2 HG02257.hp1 others(1): Show |
intron_variant | MODIFIER | c.2014-666C>T | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 18/26 | chr11 | 17506615 | ||||||
chr11:17506629
|
C | T | 5 | a0001c0003t0001g0072a0001c0003t0001g0144a0004c0014t0001g0269others(2): Show | 5 | HG00735.hp1 HG01884.hp2 HG02145.hp2 others(2): Show |
intron_variant | MODIFIER | c.2014-680G>A | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 18/26 | chr11 | 17506629 | ||||||
chr11:17506684
|
C | T | 3 | a0003c0011t0001g0024a0003c0011t0001g0283a0003c0011t0002g0285 | 4 | HG01243.hp2 HG01891.hp2 HG02257.hp1 others(1): Show |
intron_variant | MODIFIER | c.2014-735G>A | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 18/26 | chr11 | 17506684 | ||||||
chr11:17506726
|
G | A | 81 | a0001c0001t0001g0052a0001c0001t0001g0056a0001c0001t0001g0154others(78): Show | 84 | HG00099.hp2 HG00735.hp1 HG01070.hp2 others(81): Show |
intron_variant | MODIFIER | c.2014-777C>T | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 18/26 | chr11 | 17506726 | ||||||
chr11:17506813
|
C | T | 1 | a0002c0002t0002g0079 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.2014-864G>A | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 18/26 | chr11 | 17506813 | ||||||
chr11:17506927
|
G | A | 1 | a0001c0003t0008g0272 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.2014-978C>T | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 18/26 | chr11 | 17506927 | ||||||
chr11:17507046
|
G | A | 4 | a0006c0025t0001g0205a0009c0045t0016g0159a0012c0032t0002g0250others(1): Show | 4 | HG02451.hp1 HG02451.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.2014-1097C>T | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 18/26 | chr11 | 17507046 | ||||||
chr11:17507049
|
G | A | 1 | a0001c0004t0001g0247 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.2014-1100C>T | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 18/26 | chr11 | 17507049 | ||||||
chr11:17507180
|
T | G | 1 | a0001c0024t0001g0312 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.2014-1231A>C | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 18/26 | chr11 | 17507180 | ||||||
chr11:17507231
|
G | A | 1 | a0001c0021t0002g0162 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.2014-1282C>T | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 18/26 | chr11 | 17507231 | ||||||
chr11:17507336
|
C | T | 2 | a0001c0003t0001g0072a0001c0003t0001g0144 | 2 | HG01884.hp2 HG02145.hp2 |
intron_variant | MODIFIER | c.2014-1387G>A | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 18/26 | chr11 | 17507336 | ||||||
chr11:17507399
|
G | A | 1 | a0001c0003t0001g0223 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.2014-1450C>T | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 18/26 | chr11 | 17507399 | ||||||
chr11:17507539
|
C | A | 1 | a0002c0019t0002g0025 | 2 | HG02647.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.2014-1590G>T | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 18/26 | chr11 | 17507539 | ||||||
chr11:17507671
|
G | A | 53 | a0001c0001t0001g0052a0001c0001t0001g0056a0001c0001t0001g0154others(50): Show | 55 | HG00099.hp2 HG01070.hp2 HG01167.hp1 others(52): Show |
intron_variant | MODIFIER | c.2013+1685C>T | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 18/26 | chr11 | 17507671 | ||||||
chr11:17507687
|
T | G | 1 | a0001c0003t0004g0028 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.2013+1669A>C | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 18/26 | chr11 | 17507687 | ||||||
chr11:17507827
|
A | C | 4 | a0006c0025t0001g0205a0009c0045t0016g0159a0012c0032t0002g0250others(1): Show | 4 | HG02451.hp1 HG02451.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.2013+1529T>G | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 18/26 | chr11 | 17507827 | ||||||
chr11:17507905
|
T | A | 2 | a0001c0003t0001g0256a0016c0022t0002g0222 | 2 | HG02809.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.2013+1451A>T | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 18/26 | chr11 | 17507905 | ||||||
chr11:17507961
|
C | A | 6 | a0001c0042t0001g0033a0002c0005t0001g0124a0002c0005t0001g0141others(3): Show | 6 | HG01255.hp1 HG02486.hp2 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.2013+1395G>T | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 18/26 | chr11 | 17507961 | ||||||
chr11:17508094
|
A | G | 9 | a0001c0003t0001g0072a0001c0003t0001g0144a0004c0014t0001g0269others(6): Show | 9 | HG00735.hp1 HG01884.hp2 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.2013+1262T>C | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 18/26 | chr11 | 17508094 | ||||||
chr11:17508108
|
A | T | 1 | a0001c0001t0003g0055 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.2013+1248T>A | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 18/26 | chr11 | 17508108 | ||||||
chr11:17508131
|
G | A | 1 | a0001c0001t0001g0130 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.2013+1225C>T | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 18/26 | chr11 | 17508131 | ||||||
chr11:17508198
|
C | G | 2 | a0001c0003t0001g0191a0001c0003t0001g0295 | 2 | HG02717.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.2013+1158G>C | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 18/26 | chr11 | 17508198 | ||||||
chr11:17508213
|
C | T | 1 | a0001c0001t0011g0027 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.2013+1143G>A | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 18/26 | chr11 | 17508213 | ||||||
chr11:17508217
|
G | A | 1 | a0002c0010t0002g0238 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.2013+1139C>T | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 18/26 | chr11 | 17508217 | ||||||
chr11:17508354
|
T | A | 2 | a0001c0001t0001g0139a0001c0001t0001g0147 | 2 | HG01074.hp2 HG01175.hp1 |
intron_variant | MODIFIER | c.2013+1002A>T | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 18/26 | chr11 | 17508354 | ||||||
chr11:17508519
|
C | T | 2 | a0001c0008t0001g0174a0002c0006t0002g0288 | 2 | HG00741.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.2013+837G>A | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 18/26 | chr11 | 17508519 | ||||||
chr11:17508624
|
C | A | 7 | a0001c0003t0001g0072a0001c0003t0001g0144a0001c0003t0002g0068others(4): Show | 7 | HG00735.hp1 HG01884.hp2 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.2013+732G>T | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 18/26 | chr11 | 17508624 | ||||||
chr11:17508635
|
G | A | 1 | a0001c0001t0003g0132 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.2013+721C>T | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 18/26 | chr11 | 17508635 | ||||||
chr11:17508849
|
C | T | 1 | a0001c0003t0001g0223 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.2013+507G>A | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 18/26 | chr11 | 17508849 | ||||||
chr11:17508896
|
C | T | 1 | a0001c0001t0001g0114 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.2013+460G>A | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 18/26 | chr11 | 17508896 | ||||||
chr11:17508916
|
C | A | 121 | a0001c0001t0001g0005a0001c0001t0001g0016a0001c0001t0001g0046others(118): Show | 129 | HG00099.hp2 HG00558.hp1 HG00558.hp2 others(126): Show |
intron_variant | MODIFIER | c.2013+440G>T | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 18/26 | chr11 | 17508916 | ||||||
chr11:17508937
|
G | A | 142 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0008others(139): Show | 158 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(155): Show |
intron_variant | MODIFIER | c.2013+419C>T | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 18/26 | chr11 | 17508937 | ||||||
chr11:17508945
|
A | T | 1 | a0001c0003t0006g0031 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.2013+411T>A | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 18/26 | chr11 | 17508945 | ||||||
chr11:17509147
|
A | G | 1 | a0002c0005t0002g0251 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.2013+209T>C | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 18/26 | chr11 | 17509147 | ||||||
chr11:17509257
|
T | C | 2 | a0001c0003t0001g0323a0001c0003t0001g0324 | 2 | HG02155.hp2 NA18983.hp1 |
intron_variant | MODIFIER | c.2013+99A>G | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 18/26 | chr11 | 17509257 | ||||||
chr11:17509902
|
G | T | 237 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0008others(234): Show | 256 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(253): Show |
intron_variant | MODIFIER | c.1531-64C>A | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 17/26 | chr11 | 17509902 | ||||||
chr11:17510132
|
G | C | 3 | a0006c0025t0001g0205a0012c0032t0002g0250a0013c0033t0001g0232 | 3 | HG02451.hp2 HG02965.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.1530+273C>G | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 17/26 | chr11 | 17510132 | ||||||
chr11:17510184
|
A | C | 1 | a0001c0004t0001g0277 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.1530+221T>G | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 17/26 | chr11 | 17510184 | ||||||
chr11:17510284
|
A | T | 149 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0008others(146): Show | 166 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(163): Show |
intron_variant | MODIFIER | c.1530+121T>A | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 17/26 | chr11 | 17510284 | ||||||
chr11:17510555
|
C | T | 76 | a0001c0001t0001g0052a0001c0001t0001g0056a0001c0001t0001g0137others(73): Show | 78 | HG00099.hp2 HG01070.hp2 HG01106.hp1 others(75): Show |
intron_variant | MODIFIER | c.1414-34G>A | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 16/26 | chr11 | 17510555 | ||||||
chr11:17510576
|
A | G | 1 | a0003c0011t0001g0283 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1414-55T>C | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 16/26 | chr11 | 17510576 | ||||||
chr11:17511050
|
G | A | 148 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0008others(145): Show | 165 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(162): Show |
intron_variant | MODIFIER | c.1414-529C>T | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 16/26 | chr11 | 17511050 | ||||||
chr11:17511228
|
G | C | 3 | a0001c0007t0001g0194a0001c0007t0001g0298a0001c0037t0001g0195 | 3 | NA18942.hp2 NA18943.hp2 NA19057.hp2 |
intron_variant | MODIFIER | c.1413+674C>G | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 16/26 | chr11 | 17511228 | ||||||
chr11:17511269
|
C | T | 7 | a0001c0003t0001g0072a0001c0003t0001g0144a0001c0003t0002g0068others(4): Show | 7 | HG00735.hp1 HG01884.hp2 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.1413+633G>A | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 16/26 | chr11 | 17511269 | ||||||
chr11:17511338
|
TG | T | 156 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0008others(153): Show | 173 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(170): Show |
intron_variant | MODIFIER | c.1413+563delC | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 16/26 | chr11 | 17511338 | ||||||
chr11:17511340
|
G | T | 6 | a0001c0001t0001g0230a0001c0001t0001g0231a0001c0001t0008g0229others(3): Show | 6 | HG01891.hp1 HG02280.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.1413+562C>A | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 16/26 | chr11 | 17511340 | ||||||
chr11:17511470
|
G | A | 1 | a0001c0003t0001g0043 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.1413+432C>T | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 16/26 | chr11 | 17511470 | ||||||
chr11:17511699
|
A | G | 1 | a0002c0044t0001g0197 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1413+203T>C | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 16/26 | chr11 | 17511699 | ||||||
chr11:17511850
|
G | A | 146 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0008others(143): Show | 162 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(159): Show |
intron_variant | MODIFIER | c.1413+52C>T | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 16/26 | chr11 | 17511850 | ||||||
chr11:17512088
|
G | A | 243 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0008others(240): Show | 262 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(259): Show |
intron_variant | MODIFIER | c.1261-34C>T | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 15/26 | chr11 | 17512088 | ||||||
chr11:17512255
|
C | T | 1 | a0001c0001t0001g0097 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.1261-201G>A | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 15/26 | chr11 | 17512255 | ||||||
chr11:17512569
|
T | C | 2 | a0001c0003t0001g0249a0002c0005t0013g0220 | 2 | HG01975.hp2 HG01978.hp2 |
intron_variant | MODIFIER | c.1261-515A>G | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 15/26 | chr11 | 17512569 | ||||||
chr11:17512619
|
C | T | 2 | a0001c0001t0001g0119a0001c0001t0001g0292 | 2 | HG02027.hp1 NA19063.hp2 |
intron_variant | MODIFIER | c.1261-565G>A | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 15/26 | chr11 | 17512619 | ||||||
chr11:17512853
|
T | G | 1 | a0001c0001t0001g0217 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.1261-799A>C | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 15/26 | chr11 | 17512853 | ||||||
chr11:17512866
|
A | G | 36 | a0001c0003t0001g0169a0001c0003t0001g0170a0001c0003t0001g0173others(33): Show | 37 | HG00099.hp2 HG01070.hp2 HG01496.hp2 others(34): Show |
intron_variant | MODIFIER | c.1261-812T>C | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 15/26 | chr11 | 17512866 | ||||||
chr11:17512914
|
C | T | 1 | a0001c0001t0001g0217 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.1261-860G>A | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 15/26 | chr11 | 17512914 | ||||||
chr11:17513068
|
C | T | 1 | a0001c0003t0006g0031 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1261-1014G>A | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 15/26 | chr11 | 17513068 | ||||||
chr11:17513110
|
T | A | 154 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0008others(151): Show | 174 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(171): Show |
intron_variant | MODIFIER | c.1261-1056A>T | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 15/26 | chr11 | 17513110 | ||||||
chr11:17513125
|
T | C | 36 | a0001c0003t0001g0169a0001c0003t0001g0170a0001c0003t0001g0173others(33): Show | 37 | HG00099.hp2 HG01070.hp2 HG01496.hp2 others(34): Show |
intron_variant | MODIFIER | c.1261-1071A>G | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 15/26 | chr11 | 17513125 | ||||||
chr11:17513131
|
G | C | 1 | a0001c0043t0006g0029 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1261-1077C>G | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 15/26 | chr11 | 17513131 | ||||||
chr11:17513201
|
C | T | 1 | a0001c0003t0001g0202 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.1261-1147G>A | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 15/26 | chr11 | 17513201 | ||||||
chr11:17513261
|
G | T | 9 | a0001c0017t0001g0314a0001c0017t0001g0315a0001c0042t0001g0033others(6): Show | 9 | HG01255.hp1 HG02257.hp2 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.1261-1207C>A | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 15/26 | chr11 | 17513261 | ||||||
chr11:17513304
|
G | C | 36 | a0001c0003t0001g0169a0001c0003t0001g0170a0001c0003t0001g0173others(33): Show | 37 | HG00099.hp2 HG01070.hp2 HG01496.hp2 others(34): Show |
intron_variant | MODIFIER | c.1261-1250C>G | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 15/26 | chr11 | 17513304 | ||||||
chr11:17513339
|
C | G | 6 | a0001c0001t0011g0027a0001c0003t0005g0042a0006c0025t0001g0205others(3): Show | 6 | HG02109.hp1 HG02451.hp1 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.1261-1285G>C | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 15/26 | chr11 | 17513339 | ||||||
chr11:17513341
|
C | A | 2 | a0001c0001t0001g0154a0002c0002t0002g0053 | 2 | HG01943.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.1261-1287G>T | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 15/26 | chr11 | 17513341 | ||||||
chr11:17513341
|
CG | C | 6 | a0001c0001t0001g0230a0001c0001t0001g0231a0001c0001t0008g0229others(3): Show | 6 | HG01891.hp1 HG02280.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.1261-1288delC | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 15/26 | chr11 | 17513341 | ||||||
chr11:17513342
|
G | A | 1 | a0002c0005t0002g0044 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1261-1288C>T | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 15/26 | chr11 | 17513342 | ||||||
chr11:17513342
|
G | C | 35 | a0001c0001t0001g0052a0001c0001t0001g0056a0001c0001t0001g0137others(32): Show | 36 | HG01106.hp1 HG01167.hp1 HG01168.hp2 others(33): Show |
intron_variant | MODIFIER | c.1261-1288C>G | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 15/26 | chr11 | 17513342 | ||||||
chr11:17513470
|
G | C | 2 | a0002c0005t0001g0070a0005c0035t0004g0032 | 2 | HG02257.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1261-1416C>G | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 15/26 | chr11 | 17513470 | ||||||
chr11:17513520
|
G | A | 2 | a0002c0005t0002g0044a0002c0005t0002g0045 | 2 | HG03579.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1261-1466C>T | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 15/26 | chr11 | 17513520 | ||||||
chr11:17513522
|
C | T | 1 | a0002c0005t0001g0036 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1261-1468G>A | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 15/26 | chr11 | 17513522 | ||||||
chr11:17513600
|
C | T | 1 | a0002c0002t0002g0126 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1261-1546G>A | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 15/26 | chr11 | 17513600 | ||||||
chr11:17513693
|
G | A | 1 | a0001c0003t0001g0239 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.1261-1639C>T | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 15/26 | chr11 | 17513693 | ||||||
chr11:17513726
|
G | A | 25 | a0001c0001t0001g0052a0001c0001t0001g0056a0001c0001t0001g0137others(22): Show | 26 | HG01167.hp1 HG01168.hp2 HG01891.hp1 others(23): Show |
intron_variant | MODIFIER | c.1261-1672C>T | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 15/26 | chr11 | 17513726 | ||||||
chr11:17513836
|
G | GA | 7 | a0001c0003t0001g0072a0001c0003t0001g0144a0001c0003t0002g0068others(4): Show | 7 | HG00735.hp1 HG01884.hp2 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.1261-1783dupT | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 15/26 | chr11 | 17513836 | ||||||
chr11:17513836
|
GA | G | 200 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0008others(197): Show | 220 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(217): Show |
intron_variant | MODIFIER | c.1261-1783delT | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 15/26 | chr11 | 17513836 | ||||||
chr11:17513841
|
A | G | 5 | a0001c0007t0001g0192a0001c0007t0001g0193a0001c0007t0001g0308others(2): Show | 5 | HG02071.hp1 HG03490.hp1 NA18957.hp1 others(2): Show |
intron_variant | MODIFIER | c.1261-1787T>C | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 15/26 | chr11 | 17513841 | ||||||
chr11:17513995
|
G | A | 155 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0008others(152): Show | 174 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(171): Show |
intron_variant | MODIFIER | c.1261-1941C>T | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 15/26 | chr11 | 17513995 | ||||||
chr11:17514034
|
G | A | 1 | a0002c0002t0002g0012 | 2 | HG01255.hp2 HG01433.hp1 |
intron_variant | MODIFIER | c.1261-1980C>T | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 15/26 | chr11 | 17514034 | ||||||
chr11:17514098
|
A | T | 1 | a0002c0012t0012g0180 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1261-2044T>A | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 15/26 | chr11 | 17514098 | ||||||
chr11:17514159
|
C | T | 8 | a0001c0001t0003g0132a0001c0003t0001g0202a0001c0003t0001g0204others(5): Show | 9 | HG01255.hp2 HG01433.hp1 HG01975.hp2 others(6): Show |
intron_variant | MODIFIER | c.1260+2082G>A | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 15/26 | chr11 | 17514159 | ||||||
chr11:17514204
|
A | G | 9 | a0001c0017t0001g0314a0001c0017t0001g0315a0001c0042t0001g0033others(6): Show | 9 | HG01255.hp1 HG02257.hp2 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.1260+2037T>C | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 15/26 | chr11 | 17514204 | ||||||
chr11:17514210
|
T | A | 155 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0008others(152): Show | 174 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(171): Show |
intron_variant | MODIFIER | c.1260+2031A>T | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 15/26 | chr11 | 17514210 | ||||||
chr11:17514288
|
G | A | 155 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0008others(152): Show | 174 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(171): Show |
intron_variant | MODIFIER | c.1260+1953C>T | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 15/26 | chr11 | 17514288 | ||||||
chr11:17514303
|
C | G | 5 | a0001c0003t0001g0202a0001c0003t0001g0204a0001c0003t0001g0249others(2): Show | 6 | HG01255.hp2 HG01433.hp1 HG01975.hp2 others(3): Show |
intron_variant | MODIFIER | c.1260+1938G>C | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 15/26 | chr11 | 17514303 | ||||||
chr11:17514454
|
C | T | 26 | a0001c0001t0001g0052a0001c0001t0001g0056a0001c0001t0001g0137others(23): Show | 27 | HG01167.hp1 HG01168.hp2 HG01891.hp1 others(24): Show |
intron_variant | MODIFIER | c.1260+1787G>A | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 15/26 | chr11 | 17514454 | ||||||
chr11:17514472
|
G | C | 2 | a0001c0003t0001g0072a0001c0003t0001g0144 | 2 | HG01884.hp2 HG02145.hp2 |
intron_variant | MODIFIER | c.1260+1769C>G | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 15/26 | chr11 | 17514472 | ||||||
chr11:17514728
|
C | T | 155 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0008others(152): Show | 174 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(171): Show |
intron_variant | MODIFIER | c.1260+1513G>A | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 15/26 | chr11 | 17514728 | ||||||
chr11:17514761
|
G | T | 1 | a0002c0044t0001g0197 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1260+1480C>A | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 15/26 | chr11 | 17514761 | ||||||
chr11:17514766
|
A | G | 1 | a0001c0001t0001g0248 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.1260+1475T>C | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 15/26 | chr11 | 17514766 | ||||||
chr11:17514797
|
C | CT | 7 | a0001c0003t0001g0144a0001c0003t0002g0068a0002c0005t0002g0067others(4): Show | 7 | HG00735.hp1 HG02145.hp2 HG02970.hp2 others(4): Show |
intron_variant | MODIFIER | c.1260+1443dupA | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 15/26 | chr11 | 17514797 | ||||||
chr11:17514797
|
CT | C | 33 | a0001c0001t0001g0231a0001c0003t0001g0170a0001c0004t0001g0209others(30): Show | 34 | HG00099.hp2 HG01070.hp2 HG01257.hp1 others(31): Show |
intron_variant | MODIFIER | c.1260+1443delA | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 15/26 | chr11 | 17514797 | ||||||
chr11:17514797
|
CTTT | C | 151 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0008others(148): Show | 170 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(167): Show |
intron_variant | MODIFIER | c.1260+1441_1260+144 others(7): Show |
USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 15/26 | chr11 | 17514797 | ||||||
chr11:17514797
|
CTTTTTTT others(4): Show |
C | 1 | a0001c0043t0006g0029 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1260+1433_1260+144 others(15): Show |
USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 15/26 | chr11 | 17514797 | ||||||
chr11:17514802
|
T | C | 3 | a0001c0003t0001g0054a0002c0005t0002g0044a0002c0005t0002g0045 | 3 | HG02486.hp1 HG03579.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1260+1439A>G | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 15/26 | chr11 | 17514802 | ||||||
chr11:17514803
|
T | C | 151 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0008others(148): Show | 170 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(167): Show |
intron_variant | MODIFIER | c.1260+1438A>G | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 15/26 | chr11 | 17514803 | ||||||
chr11:17514804
|
T | C | 1 | a0001c0001t0001g0130 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.1260+1437A>G | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 15/26 | chr11 | 17514804 | ||||||
chr11:17515016
|
TTTA | T | 4 | a0006c0025t0001g0205a0009c0045t0016g0159a0012c0032t0002g0250others(1): Show | 4 | HG02451.hp1 HG02451.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.1260+1222_1260+122 others(7): Show |
USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 15/26 | chr11 | 17515016 | ||||||
chr11:17515065
|
T | TTGTG | 156 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0008others(153): Show | 175 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(172): Show |
intron_variant | MODIFIER | c.1260+1172_1260+117 others(8): Show |
USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 15/26 | chr11 | 17515065 | ||||||
chr11:17515292
|
C | T | 252 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0008others(249): Show | 274 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(271): Show |
intron_variant | MODIFIER | c.1260+949G>A | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 15/26 | chr11 | 17515292 | ||||||
chr11:17515298
|
G | T | 252 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0008others(249): Show | 274 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(271): Show |
intron_variant | MODIFIER | c.1260+943C>A | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 15/26 | chr11 | 17515298 | ||||||
chr11:17515322
|
C | G | 156 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0008others(153): Show | 175 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(172): Show |
intron_variant | MODIFIER | c.1260+919G>C | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 15/26 | chr11 | 17515322 | ||||||
chr11:17515374
|
G | A | 2 | a0001c0017t0001g0314a0001c0017t0001g0315 | 2 | HG02572.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.1260+867C>T | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 15/26 | chr11 | 17515374 | ||||||
chr11:17515486
|
A | G | 81 | a0001c0001t0001g0052a0001c0001t0001g0056a0001c0001t0001g0137others(78): Show | 84 | HG00099.hp2 HG01070.hp2 HG01106.hp1 others(81): Show |
intron_variant | MODIFIER | c.1260+755T>C | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 15/26 | chr11 | 17515486 | ||||||
chr11:17515716
|
A | G | 254 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0008others(251): Show | 276 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(273): Show |
intron_variant | MODIFIER | c.1260+525T>C | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 15/26 | chr11 | 17515716 | ||||||
chr11:17515920
|
T | A | 9 | a0001c0017t0001g0314a0001c0017t0001g0315a0001c0042t0001g0033others(6): Show | 9 | HG01255.hp1 HG02257.hp2 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.1260+321A>T | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 15/26 | chr11 | 17515920 | ||||||
chr11:17515959
|
C | T | 5 | a0001c0001t0001g0046a0001c0001t0001g0166a0001c0001t0001g0167others(2): Show | 5 | HG01243.hp1 HG02572.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.1260+282G>A | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 15/26 | chr11 | 17515959 | ||||||
chr11:17516158
|
G | C | 69 | a0001c0001t0001g0005a0001c0001t0001g0016a0001c0001t0001g0046others(66): Show | 74 | HG00558.hp1 HG00558.hp2 HG00597.hp2 others(71): Show |
intron_variant | MODIFIER | c.1260+83C>G | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 15/26 | chr11 | 17516158 | ||||||
chr11:17516363
|
A | G | 1 | a0002c0002t0002g0096 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.1211-73T>C | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 14/26 | chr11 | 17516363 | ||||||
chr11:17516501
|
G | A | 56 | a0001c0001t0001g0005a0001c0001t0001g0016a0001c0001t0001g0046others(53): Show | 61 | HG00558.hp1 HG00558.hp2 HG00597.hp2 others(58): Show |
intron_variant | MODIFIER | c.1211-211C>T | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 14/26 | chr11 | 17516501 | ||||||
chr11:17516506
|
G | A | 1 | a0001c0001t0001g0110 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.1211-216C>T | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 14/26 | chr11 | 17516506 | ||||||
chr11:17516906
|
G | A | 250 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0008others(247): Show | 272 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(269): Show |
intron_variant | MODIFIER | c.1211-616C>T | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 14/26 | chr11 | 17516906 | ||||||
chr11:17516958
|
C | A | 1 | a0001c0003t0003g0235 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.1211-668G>T | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 14/26 | chr11 | 17516958 | ||||||
chr11:17516960
|
C | T | 1 | a0009c0045t0016g0159 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1211-670G>A | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 14/26 | chr11 | 17516960 | ||||||
chr11:17516992
|
T | C | 74 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0016others(71): Show | 80 | HG00558.hp1 HG00558.hp2 HG00597.hp2 others(77): Show |
intron_variant | MODIFIER | c.1211-702A>G | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 14/26 | chr11 | 17516992 | ||||||
chr11:17517225
|
C | T | 64 | a0001c0001t0001g0005a0001c0001t0001g0016a0001c0001t0001g0046others(61): Show | 68 | HG00558.hp1 HG00597.hp2 HG00639.hp2 others(65): Show |
intron_variant | MODIFIER | c.1211-935G>A | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 14/26 | chr11 | 17517225 | ||||||
chr11:17517226
|
G | A | 1 | a0002c0005t0001g0224 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1211-936C>T | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 14/26 | chr11 | 17517226 | ||||||
chr11:17517419
|
C | T | 1 | a0001c0003t0004g0028 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1211-1129G>A | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 14/26 | chr11 | 17517419 | ||||||
chr11:17517424
|
C | T | 7 | a0001c0017t0001g0314a0001c0017t0001g0315a0001c0042t0001g0033others(4): Show | 7 | HG01255.hp1 HG02486.hp2 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.1211-1134G>A | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 14/26 | chr11 | 17517424 | ||||||
chr11:17517442
|
C | T | 10 | a0001c0013t0001g0214a0001c0013t0001g0279a0001c0013t0001g0282others(7): Show | 13 | HG02040.hp2 HG02135.hp2 HG02165.hp2 others(10): Show |
intron_variant | MODIFIER | c.1211-1152G>A | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 14/26 | chr11 | 17517442 | ||||||
chr11:17517539
|
G | A | 8 | a0001c0017t0001g0314a0001c0017t0001g0315a0001c0042t0001g0033others(5): Show | 8 | HG01255.hp1 HG02486.hp2 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.1211-1249C>T | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 14/26 | chr11 | 17517539 | ||||||
chr11:17517546
|
C | G | 2 | a0002c0005t0002g0044a0002c0005t0002g0045 | 2 | HG03579.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1211-1256G>C | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 14/26 | chr11 | 17517546 | ||||||
chr11:17517665
|
T | C | 208 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0008others(205): Show | 229 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(226): Show |
intron_variant | MODIFIER | c.1211-1375A>G | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 14/26 | chr11 | 17517665 | ||||||
chr11:17517708
|
C | T | 15 | a0001c0001t0001g0052a0001c0001t0001g0056a0001c0001t0001g0137others(12): Show | 15 | HG01167.hp1 HG01168.hp2 HG01943.hp1 others(12): Show |
intron_variant | MODIFIER | c.1211-1418G>A | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 14/26 | chr11 | 17517708 | ||||||
chr11:17517799
|
G | T | 23 | a0001c0001t0001g0052a0001c0001t0001g0056a0001c0001t0001g0137others(20): Show | 24 | HG01167.hp1 HG01168.hp2 HG01891.hp1 others(21): Show |
intron_variant | MODIFIER | c.1211-1509C>A | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 14/26 | chr11 | 17517799 | ||||||
chr11:17517860
|
A | T | 257 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0008others(254): Show | 279 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(276): Show |
intron_variant | MODIFIER | c.1211-1570T>A | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 14/26 | chr11 | 17517860 | ||||||
chr11:17518011
|
G | C | 1 | a0001c0001t0001g0248 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.1211-1721C>G | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 14/26 | chr11 | 17518011 | ||||||
chr11:17518015
|
T | C | 45 | a0001c0003t0001g0156a0001c0003t0001g0169a0001c0003t0001g0170others(42): Show | 46 | HG00099.hp2 HG00544.hp1 HG01070.hp2 others(43): Show |
intron_variant | MODIFIER | c.1211-1725A>G | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 14/26 | chr11 | 17518015 | ||||||
chr11:17518103
|
T | C | 1 | a0001c0003t0001g0144 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1211-1813A>G | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 14/26 | chr11 | 17518103 | ||||||
chr11:17518106
|
C | T | 1 | a0001c0001t0001g0118 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1211-1816G>A | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 14/26 | chr11 | 17518106 | ||||||
chr11:17518107
|
C | T | 1 | a0001c0001t0001g0073 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.1211-1817G>A | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 14/26 | chr11 | 17518107 | ||||||
chr11:17518161
|
T | C | 10 | a0001c0003t0001g0072a0001c0003t0001g0144a0001c0003t0002g0068others(7): Show | 10 | HG00735.hp1 HG01884.hp2 HG02145.hp2 others(7): Show |
intron_variant | MODIFIER | c.1211-1871A>G | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 14/26 | chr11 | 17518161 | ||||||
chr11:17518210
|
A | C | 6 | a0001c0001t0011g0027a0001c0003t0005g0042a0006c0025t0001g0205others(3): Show | 6 | HG02109.hp1 HG02451.hp1 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.1211-1920T>G | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 14/26 | chr11 | 17518210 | ||||||
chr11:17518273
|
A | T | 1 | a0001c0003t0001g0121 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1211-1983T>A | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 14/26 | chr11 | 17518273 | ||||||
chr11:17518274
|
A | T | 1 | a0001c0003t0001g0121 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1211-1984T>A | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 14/26 | chr11 | 17518274 | ||||||
chr11:17518275
|
C | A | 1 | a0001c0003t0001g0121 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1211-1985G>T | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 14/26 | chr11 | 17518275 | ||||||
chr11:17518389
|
G | A | 8 | a0001c0017t0001g0314a0001c0017t0001g0315a0001c0042t0001g0033others(5): Show | 8 | HG01255.hp1 HG02486.hp2 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.1211-2099C>T | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 14/26 | chr11 | 17518389 | ||||||
chr11:17518532
|
T | C | 157 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(154): Show | 173 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(170): Show |
intron_variant | MODIFIER | c.1211-2242A>G | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 14/26 | chr11 | 17518532 | ||||||
chr11:17518556
|
G | C | 2 | a0002c0005t0001g0036a0011c0048t0001g0161 | 2 | HG01884.hp1 HG02615.hp2 |
intron_variant | MODIFIER | c.1211-2266C>G | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 14/26 | chr11 | 17518556 | ||||||
chr11:17518589
|
C | A | 37 | a0001c0003t0001g0169a0001c0003t0001g0170a0001c0003t0001g0173others(34): Show | 37 | HG00099.hp2 HG00544.hp1 HG01070.hp2 others(34): Show |
intron_variant | MODIFIER | c.1210+2281G>T | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 14/26 | chr11 | 17518589 | ||||||
chr11:17518592
|
C | T | 6 | a0001c0001t0011g0027a0001c0003t0005g0042a0006c0025t0001g0205others(3): Show | 6 | HG02109.hp1 HG02451.hp1 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.1210+2278G>A | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 14/26 | chr11 | 17518592 | ||||||
chr11:17518593
|
G | T | 1 | a0001c0003t0001g0223 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1210+2277C>A | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 14/26 | chr11 | 17518593 | ||||||
chr11:17518634
|
G | A | 1 | a0001c0003t0006g0031 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1210+2236C>T | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 14/26 | chr11 | 17518634 | ||||||
chr11:17518674
|
G | A | 35 | a0001c0001t0001g0052a0001c0001t0001g0056a0001c0001t0001g0137others(32): Show | 36 | HG00735.hp1 HG01167.hp1 HG01168.hp2 others(33): Show |
intron_variant | MODIFIER | c.1210+2196C>T | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 14/26 | chr11 | 17518674 | ||||||
chr11:17518695
|
G | A | 7 | a0001c0001t0011g0027a0001c0003t0005g0042a0001c0043t0006g0029others(4): Show | 7 | HG02109.hp1 HG02451.hp1 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.1210+2175C>T | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 14/26 | chr11 | 17518695 | ||||||
chr11:17518707
|
G | A | 1 | a0002c0002t0002g0057 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1210+2163C>T | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 14/26 | chr11 | 17518707 | ||||||
chr11:17518708
|
C | G | 1 | a0001c0001t0001g0240 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.1210+2162G>C | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 14/26 | chr11 | 17518708 | ||||||
chr11:17518740
|
C | T | 6 | a0001c0001t0011g0027a0001c0003t0005g0042a0006c0025t0001g0205others(3): Show | 6 | HG02109.hp1 HG02451.hp1 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.1210+2130G>A | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 14/26 | chr11 | 17518740 | ||||||
chr11:17518887
|
C | T | 37 | a0001c0003t0001g0169a0001c0003t0001g0170a0001c0003t0001g0173others(34): Show | 37 | HG00099.hp2 HG00544.hp1 HG01070.hp2 others(34): Show |
intron_variant | MODIFIER | c.1210+1983G>A | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 14/26 | chr11 | 17518887 | ||||||
chr11:17518891
|
T | C | 4 | a0001c0013t0001g0282a0001c0013t0010g0026a0002c0009t0001g0317others(1): Show | 4 | HG02165.hp2 NA18963.hp1 NA18969.hp1 others(1): Show |
intron_variant | MODIFIER | c.1210+1979A>G | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 14/26 | chr11 | 17518891 | ||||||
chr11:17518951
|
G | A | 1 | a0014c0041t0001g0183 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.1210+1919C>T | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 14/26 | chr11 | 17518951 | ||||||
chr11:17518953
|
G | A | 2 | a0001c0001t0011g0027a0001c0003t0005g0042 | 2 | HG02109.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.1210+1917C>T | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 14/26 | chr11 | 17518953 | ||||||
chr11:17519024
|
GA | G | 72 | a0001c0001t0001g0052a0001c0001t0001g0056a0001c0001t0001g0137others(69): Show | 73 | HG00099.hp2 HG00544.hp1 HG00735.hp1 others(70): Show |
intron_variant | MODIFIER | c.1210+1845delT | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 14/26 | chr11 | 17519024 | ||||||
chr11:17519098
|
T | TC | 86 | a0001c0001t0001g0052a0001c0001t0001g0056a0001c0001t0001g0137others(83): Show | 87 | HG00099.hp2 HG00544.hp1 HG00735.hp1 others(84): Show |
intron_variant | MODIFIER | c.1210+1771_1210+177 others(5): Show |
USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 14/26 | chr11 | 17519098 | ||||||
chr11:17519099
|
G | C | 86 | a0001c0001t0001g0052a0001c0001t0001g0056a0001c0001t0001g0137others(83): Show | 87 | HG00099.hp2 HG00544.hp1 HG00735.hp1 others(84): Show |
intron_variant | MODIFIER | c.1210+1771C>G | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 14/26 | chr11 | 17519099 | ||||||
chr11:17519176
|
A | C | 51 | a0001c0001t0011g0027a0001c0003t0001g0169a0001c0003t0001g0170others(48): Show | 51 | HG00099.hp2 HG00544.hp1 HG01070.hp2 others(48): Show |
intron_variant | MODIFIER | c.1210+1694T>G | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 14/26 | chr11 | 17519176 | ||||||
chr11:17519181
|
G | A | 10 | a0001c0003t0001g0072a0001c0003t0001g0144a0001c0003t0002g0068others(7): Show | 10 | HG00735.hp1 HG01884.hp2 HG02145.hp2 others(7): Show |
intron_variant | MODIFIER | c.1210+1689C>T | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 14/26 | chr11 | 17519181 | ||||||
chr11:17519313
|
G | T | 1 | a0006c0025t0001g0205 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1210+1557C>A | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 14/26 | chr11 | 17519313 | ||||||
chr11:17519330
|
C | A | 1 | a0001c0001t0001g0111 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.1210+1540G>T | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 14/26 | chr11 | 17519330 | ||||||
chr11:17519475
|
C | T | 89 | a0001c0001t0001g0052a0001c0001t0001g0056a0001c0001t0001g0137others(86): Show | 90 | HG00099.hp2 HG00544.hp1 HG00735.hp1 others(87): Show |
intron_variant | MODIFIER | c.1210+1395G>A | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 14/26 | chr11 | 17519475 | ||||||
chr11:17519885
|
A | G | 1 | a0001c0001t0001g0051 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1210+985T>C | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 14/26 | chr11 | 17519885 | ||||||
chr11:17520218
|
C | T | 1 | a0001c0047t0001g0196 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1210+652G>A | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 14/26 | chr11 | 17520218 | ||||||
chr11:17520251
|
G | A | 78 | a0001c0001t0001g0056a0001c0001t0001g0123a0001c0001t0001g0137others(75): Show | 81 | HG00544.hp1 HG00735.hp1 HG01167.hp1 others(78): Show |
intron_variant | MODIFIER | c.1210+619C>T | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 14/26 | chr11 | 17520251 | ||||||
chr11:17520255
|
G | A | 1 | a0001c0001t0001g0011 | 2 | HG01070.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.1210+615C>T | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 14/26 | chr11 | 17520255 | ||||||
chr11:17520307
|
C | G | 3 | a0006c0025t0001g0205a0009c0045t0016g0159a0012c0032t0002g0250 | 3 | HG02451.hp1 HG02451.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.1210+563G>C | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 14/26 | chr11 | 17520307 | ||||||
chr11:17520309
|
A | G | 1 | a0001c0004t0001g0038 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.1210+561T>C | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 14/26 | chr11 | 17520309 | ||||||
chr11:17520712
|
C | G | 7 | a0001c0003t0004g0030a0001c0003t0005g0042a0001c0043t0006g0029others(4): Show | 7 | HG02451.hp1 HG02451.hp2 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.1210+158G>C | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 14/26 | chr11 | 17520712 | ||||||
chr11:17520854
|
G | A | 1 | a0002c0006t0002g0322 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.1210+16C>T | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 14/26 | chr11 | 17520854 | ||||||
chr11:17521006
|
C | T | 36 | a0001c0001t0001g0052a0001c0001t0001g0056a0001c0001t0001g0137others(33): Show | 38 | HG00639.hp2 HG01167.hp1 HG01168.hp2 others(35): Show |
intron_variant | MODIFIER | c.1086-12G>A | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 13/26 | chr11 | 17521006 | ||||||
chr11:17521036
|
C | T | 219 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0008others(216): Show | 242 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(239): Show |
intron_variant | MODIFIER | c.1086-42G>A | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 13/26 | chr11 | 17521036 | ||||||
chr11:17521039
|
T | C | 219 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0008others(216): Show | 242 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(239): Show |
intron_variant | MODIFIER | c.1086-45A>G | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 13/26 | chr11 | 17521039 | ||||||
chr11:17521102
|
T | C | 212 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0008others(209): Show | 235 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(232): Show |
intron_variant | MODIFIER | c.1086-108A>G | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 13/26 | chr11 | 17521102 | ||||||
chr11:17521173
|
C | T | 3 | a0002c0005t0002g0020a0002c0005t0002g0251a0013c0033t0001g0232 | 4 | HG02896.hp2 HG03225.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.1085+173G>A | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 13/26 | chr11 | 17521173 | ||||||
chr11:17521325
|
G | C | 150 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0008others(147): Show | 170 | HG00280.hp1 HG00323.hp1 HG00438.hp2 others(167): Show |
intron_variant | MODIFIER | c.1085+21C>G | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 13/26 | chr11 | 17521325 | ||||||
chr11:17521621
|
G | T | 2 | a0002c0020t0001g0158a0002c0020t0002g0157 | 2 | HG02280.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.1020-210C>A | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 12/26 | chr11 | 17521621 | ||||||
chr11:17521656
|
G | C | 30 | a0001c0003t0001g0169a0001c0003t0001g0170a0001c0003t0001g0173others(27): Show | 30 | HG00099.hp2 HG01070.hp2 HG01496.hp2 others(27): Show |
intron_variant | MODIFIER | c.1020-245C>G | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 12/26 | chr11 | 17521656 | ||||||
chr11:17522024
|
A | G | 2 | a0001c0003t0001g0226a0012c0032t0002g0250 | 2 | HG02965.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.1020-613T>C | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 12/26 | chr11 | 17522024 | ||||||
chr11:17522063
|
C | T | 1 | a0015c0029t0001g0293 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1020-652G>A | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 12/26 | chr11 | 17522063 | ||||||
chr11:17522149
|
G | A | 2 | a0002c0005t0001g0070a0005c0035t0004g0032 | 2 | HG02257.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1019+635C>T | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 12/26 | chr11 | 17522149 | ||||||
chr11:17522462
|
C | T | 3 | a0001c0001t0001g0048a0002c0002t0002g0050a0002c0010t0002g0049 | 3 | HG00621.hp2 HG02080.hp2 NA18941.hp1 |
intron_variant | MODIFIER | c.1019+322G>A | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 12/26 | chr11 | 17522462 | ||||||
chr11:17522557
|
G | A | 2 | a0001c0001t0001g0105a0002c0002t0002g0104 | 2 | HG00642.hp1 HG00735.hp2 |
intron_variant | MODIFIER | c.1019+227C>T | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 12/26 | chr11 | 17522557 | ||||||
chr11:17522562
|
G | C | 31 | a0001c0003t0001g0169a0001c0003t0001g0170a0001c0003t0001g0173others(28): Show | 31 | HG00099.hp2 HG01070.hp2 HG01496.hp2 others(28): Show |
intron_variant | MODIFIER | c.1019+222C>G | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 12/26 | chr11 | 17522562 | ||||||
chr11:17522630
|
C | T | 5 | a0001c0003t0001g0202a0001c0003t0001g0204a0001c0003t0001g0249others(2): Show | 5 | HG00544.hp1 HG01975.hp2 HG01978.hp2 others(2): Show |
intron_variant | MODIFIER | c.1019+154G>A | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 12/26 | chr11 | 17522630 | ||||||
chr11:17522732
|
C | T | 1 | a0002c0002t0001g0216 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.1019+52G>A | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 12/26 | chr11 | 17522732 | ||||||
chr11:17522948
|
C | T | 1 | a0002c0002t0002g0106 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.877-22G>A | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 11/26 | chr11 | 17522948 | ||||||
chr11:17523178
|
C | T | 4 | a0001c0021t0002g0162a0002c0046t0002g0160a0009c0045t0016g0159others(1): Show | 4 | HG01884.hp1 HG02451.hp1 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.876+33G>A | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 11/26 | chr11 | 17523178 | ||||||
chr11:17523269
|
T | G | 1 | a0001c0008t0001g0294 | 1 | NA19085.hp2 | splice_acceptor_variant&intron_variant | HIGH | c.820-2A>C | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 10/26 | chr11 | 17523269 | ||||||
chr11:17523326
|
G | A | 1 | a0002c0002t0001g0153 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.820-59C>T | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 10/26 | chr11 | 17523326 | ||||||
chr11:17523544
|
A | G | 205 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0008others(202): Show | 225 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(222): Show |
intron_variant | MODIFIER | c.760-66T>C | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 9/26 | chr11 | 17523544 | ||||||
chr11:17523594
|
C | T | 27 | a0001c0001t0001g0052a0001c0001t0001g0056a0001c0001t0001g0137others(24): Show | 27 | HG00639.hp2 HG01167.hp1 HG01168.hp2 others(24): Show |
intron_variant | MODIFIER | c.760-116G>A | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 9/26 | chr11 | 17523594 | ||||||
chr11:17523711
|
A | G | 3 | a0001c0042t0001g0033a0002c0015t0001g0035a0002c0015t0002g0034 | 3 | HG01255.hp1 HG02486.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.760-233T>C | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 9/26 | chr11 | 17523711 | ||||||
chr11:17523717
|
T | A | 1 | a0002c0012t0001g0175 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.760-239A>T | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 9/26 | chr11 | 17523717 | ||||||
chr11:17523719
|
A | T | 1 | a0002c0012t0001g0175 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.760-241T>A | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 9/26 | chr11 | 17523719 | ||||||
chr11:17523721
|
A | G | 1 | a0001c0003t0001g0191 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.760-243T>C | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 9/26 | chr11 | 17523721 | ||||||
chr11:17523863
|
A | G | 1 | a0001c0013t0001g0279 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.760-385T>C | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 9/26 | chr11 | 17523863 | ||||||
chr11:17523867
|
G | T | 1 | a0001c0001t0001g0083 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.760-389C>A | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 9/26 | chr11 | 17523867 | ||||||
chr11:17524157
|
G | A | 28 | a0001c0001t0001g0052a0001c0001t0001g0056a0001c0001t0001g0137others(25): Show | 28 | HG00639.hp2 HG01167.hp1 HG01168.hp2 others(25): Show |
intron_variant | MODIFIER | c.759+294C>T | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 9/26 | chr11 | 17524157 | ||||||
chr11:17524179
|
T | C | 66 | a0001c0001t0001g0052a0001c0001t0001g0056a0001c0001t0001g0137others(63): Show | 66 | HG00099.hp2 HG00639.hp2 HG01070.hp2 others(63): Show |
intron_variant | MODIFIER | c.759+272A>G | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 9/26 | chr11 | 17524179 | ||||||
chr11:17524307
|
T | C | 5 | a0001c0003t0004g0030a0001c0021t0002g0162a0002c0046t0002g0160others(2): Show | 5 | HG01884.hp1 HG02451.hp1 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.759+144A>G | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 9/26 | chr11 | 17524307 | ||||||
chr11:17524335
|
C | T | 2 | a0001c0043t0006g0029a0005c0035t0004g0032 | 2 | HG02976.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.759+116G>A | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 9/26 | chr11 | 17524335 | ||||||
chr11:17524372
|
C | T | 1 | a0001c0043t0006g0029 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.759+79G>A | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 9/26 | chr11 | 17524372 | ||||||
chr11:17524387
|
G | A | 1 | a0001c0003t0001g0226 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.759+64C>T | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 9/26 | chr11 | 17524387 | ||||||
chr11:17524562
|
G | A | 1 | a0002c0002t0002g0106 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.675-27C>T | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 8/26 | chr11 | 17524562 | ||||||
chr11:17524631
|
G | A | 9 | a0001c0001t0001g0052a0001c0001t0001g0056a0001c0001t0003g0055others(6): Show | 9 | HG01167.hp1 HG01168.hp2 HG02027.hp2 others(6): Show |
intron_variant | MODIFIER | c.675-96C>T | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 8/26 | chr11 | 17524631 | ||||||
chr11:17524668
|
C | T | 4 | a0001c0021t0002g0162a0002c0046t0002g0160a0009c0045t0016g0159others(1): Show | 4 | HG01884.hp1 HG02451.hp1 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.675-133G>A | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 8/26 | chr11 | 17524668 | ||||||
chr11:17524726
|
A | C | 7 | a0001c0042t0001g0033a0001c0043t0006g0029a0002c0015t0001g0035others(4): Show | 8 | HG01255.hp1 HG02145.hp1 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.675-191T>G | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 8/26 | chr11 | 17524726 | ||||||
chr11:17524793
|
C | T | 6 | a0001c0042t0001g0033a0001c0043t0006g0029a0002c0015t0001g0035others(3): Show | 7 | HG01255.hp1 HG02145.hp1 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.675-258G>A | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 8/26 | chr11 | 17524793 | ||||||
chr11:17524795
|
A | C | 6 | a0001c0042t0001g0033a0001c0043t0006g0029a0002c0015t0001g0035others(3): Show | 7 | HG01255.hp1 HG02145.hp1 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.675-260T>G | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 8/26 | chr11 | 17524795 | ||||||
chr11:17524831
|
T | C | 237 | a0001c0001t0001g0005a0001c0001t0001g0016a0001c0001t0001g0046others(234): Show | 261 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(258): Show |
intron_variant | MODIFIER | c.675-296A>G | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 8/26 | chr11 | 17524831 | ||||||
chr11:17524842
|
C | CTTATTTT others(7): Show |
1 | a0002c0002t0002g0057 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.675-321_675-308dup others(14): Show |
USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 8/26 | chr11 | 17524842 | ||||||
chr11:17524844
|
T | TATTTTTT others(3): Show |
1 | a0001c0003t0004g0028 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.675-319_675-310dup others(10): Show |
USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 8/26 | chr11 | 17524844 | ||||||
chr11:17524956
|
T | C | 6 | a0001c0042t0001g0033a0001c0043t0006g0029a0002c0015t0001g0035others(3): Show | 7 | HG01255.hp1 HG02145.hp1 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.675-421A>G | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 8/26 | chr11 | 17524956 | ||||||
chr11:17524988
|
T | C | 6 | a0001c0042t0001g0033a0001c0043t0006g0029a0002c0015t0001g0035others(3): Show | 7 | HG01255.hp1 HG02145.hp1 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.675-453A>G | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 8/26 | chr11 | 17524988 | ||||||
chr11:17524997
|
A | G | 1 | a0001c0001t0001g0010 | 2 | HG01069.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.675-462T>C | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 8/26 | chr11 | 17524997 | ||||||
chr11:17525018
|
T | C | 4 | a0001c0001t0009g0071a0001c0003t0001g0144a0002c0005t0001g0070others(1): Show | 4 | HG02145.hp2 HG02257.hp2 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.675-483A>G | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 8/26 | chr11 | 17525018 | ||||||
chr11:17525067
|
AT | A | 12 | a0001c0001t0001g0065a0001c0001t0001g0073a0001c0001t0001g0107others(9): Show | 13 | HG00673.hp1 HG01255.hp2 HG01433.hp1 others(10): Show |
intron_variant | MODIFIER | c.675-533delA | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 8/26 | chr11 | 17525067 | ||||||
chr11:17525072
|
C | T | 6 | a0001c0042t0001g0033a0001c0043t0006g0029a0002c0015t0001g0035others(3): Show | 7 | HG01255.hp1 HG02145.hp1 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.675-537G>A | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 8/26 | chr11 | 17525072 | ||||||
chr11:17525089
|
G | A | 1 | a0001c0001t0001g0041 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.675-554C>T | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 8/26 | chr11 | 17525089 | ||||||
chr11:17525098
|
G | T | 6 | a0001c0042t0001g0033a0001c0043t0006g0029a0002c0015t0001g0035others(3): Show | 7 | HG01255.hp1 HG02145.hp1 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.675-563C>A | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 8/26 | chr11 | 17525098 | ||||||
chr11:17525104
|
C | T | 6 | a0001c0042t0001g0033a0001c0043t0006g0029a0002c0015t0001g0035others(3): Show | 7 | HG01255.hp1 HG02145.hp1 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.675-569G>A | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 8/26 | chr11 | 17525104 | ||||||
chr11:17525212
|
T | C | 2 | a0002c0005t0002g0044a0002c0005t0002g0045 | 2 | HG03579.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.675-677A>G | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 8/26 | chr11 | 17525212 | ||||||
chr11:17525213
|
C | A | 6 | a0001c0042t0001g0033a0001c0043t0006g0029a0002c0015t0001g0035others(3): Show | 7 | HG01255.hp1 HG02145.hp1 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.675-678G>T | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 8/26 | chr11 | 17525213 | ||||||
chr11:17525219
|
C | T | 6 | a0001c0042t0001g0033a0001c0043t0006g0029a0002c0015t0001g0035others(3): Show | 7 | HG01255.hp1 HG02145.hp1 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.675-684G>A | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 8/26 | chr11 | 17525219 | ||||||
chr11:17525249
|
C | A | 6 | a0001c0042t0001g0033a0001c0043t0006g0029a0002c0015t0001g0035others(3): Show | 7 | HG01255.hp1 HG02145.hp1 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.675-714G>T | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 8/26 | chr11 | 17525249 | ||||||
chr11:17525265
|
G | A | 6 | a0001c0042t0001g0033a0001c0043t0006g0029a0002c0015t0001g0035others(3): Show | 7 | HG01255.hp1 HG02145.hp1 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.675-730C>T | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 8/26 | chr11 | 17525265 | ||||||
chr11:17525268
|
C | T | 1 | a0001c0043t0006g0029 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.675-733G>A | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 8/26 | chr11 | 17525268 | ||||||
chr11:17525282
|
C | T | 3 | a0001c0042t0001g0033a0002c0015t0001g0035a0002c0015t0002g0034 | 3 | HG01255.hp1 HG02486.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.675-747G>A | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 8/26 | chr11 | 17525282 | ||||||
chr11:17525309
|
G | A | 37 | a0001c0001t0001g0016a0001c0001t0001g0166a0001c0001t0001g0167others(34): Show | 38 | HG00099.hp2 HG01070.hp2 HG01243.hp1 others(35): Show |
intron_variant | MODIFIER | c.675-774C>T | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 8/26 | chr11 | 17525309 | ||||||
chr11:17525342
|
T | C | 6 | a0001c0042t0001g0033a0001c0043t0006g0029a0002c0015t0001g0035others(3): Show | 7 | HG01255.hp1 HG02145.hp1 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.675-807A>G | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 8/26 | chr11 | 17525342 | ||||||
chr11:17525348
|
T | C | 2 | a0001c0003t0001g0043a0001c0003t0005g0042 | 2 | HG00639.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.675-813A>G | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 8/26 | chr11 | 17525348 | ||||||
chr11:17525355
|
C | T | 6 | a0001c0042t0001g0033a0001c0043t0006g0029a0002c0015t0001g0035others(3): Show | 7 | HG01255.hp1 HG02145.hp1 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.675-820G>A | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 8/26 | chr11 | 17525355 | ||||||
chr11:17525360
|
G | A | 6 | a0001c0042t0001g0033a0001c0043t0006g0029a0002c0015t0001g0035others(3): Show | 7 | HG01255.hp1 HG02145.hp1 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.675-825C>T | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 8/26 | chr11 | 17525360 | ||||||
chr11:17525460
|
G | A | 6 | a0001c0042t0001g0033a0001c0043t0006g0029a0002c0015t0001g0035others(3): Show | 7 | HG01255.hp1 HG02145.hp1 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.674+887C>T | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 8/26 | chr11 | 17525460 | ||||||
chr11:17525469
|
T | C | 6 | a0001c0042t0001g0033a0001c0043t0006g0029a0002c0015t0001g0035others(3): Show | 7 | HG01255.hp1 HG02145.hp1 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.674+878A>G | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 8/26 | chr11 | 17525469 | ||||||
chr11:17525490
|
C | T | 6 | a0001c0042t0001g0033a0001c0043t0006g0029a0002c0015t0001g0035others(3): Show | 7 | HG01255.hp1 HG02145.hp1 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.674+857G>A | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 8/26 | chr11 | 17525490 | ||||||
chr11:17525491
|
A | G | 6 | a0001c0042t0001g0033a0001c0043t0006g0029a0002c0015t0001g0035others(3): Show | 7 | HG01255.hp1 HG02145.hp1 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.674+856T>C | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 8/26 | chr11 | 17525491 | ||||||
chr11:17525492
|
A | C | 6 | a0001c0042t0001g0033a0001c0043t0006g0029a0002c0015t0001g0035others(3): Show | 7 | HG01255.hp1 HG02145.hp1 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.674+855T>G | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 8/26 | chr11 | 17525492 | ||||||
chr11:17525519
|
C | T | 12 | a0001c0003t0001g0043a0001c0003t0004g0028a0001c0003t0005g0042others(9): Show | 12 | HG00639.hp2 HG01884.hp1 HG02280.hp2 others(9): Show |
intron_variant | MODIFIER | c.674+828G>A | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 8/26 | chr11 | 17525519 | ||||||
chr11:17525610
|
A | G | 1 | a0001c0001t0001g0059 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.674+737T>C | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 8/26 | chr11 | 17525610 | ||||||
chr11:17525701
|
C | T | 6 | a0001c0042t0001g0033a0001c0043t0006g0029a0002c0015t0001g0035others(3): Show | 7 | HG01255.hp1 HG02145.hp1 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.674+646G>A | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 8/26 | chr11 | 17525701 | ||||||
chr11:17525702
|
A | G | 6 | a0001c0042t0001g0033a0001c0043t0006g0029a0002c0015t0001g0035others(3): Show | 7 | HG01255.hp1 HG02145.hp1 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.674+645T>C | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 8/26 | chr11 | 17525702 | ||||||
chr11:17525747
|
C | T | 6 | a0001c0042t0001g0033a0001c0043t0006g0029a0002c0015t0001g0035others(3): Show | 7 | HG01255.hp1 HG02145.hp1 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.674+600G>A | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 8/26 | chr11 | 17525747 | ||||||
chr11:17525748
|
A | G | 6 | a0001c0042t0001g0033a0001c0043t0006g0029a0002c0015t0001g0035others(3): Show | 7 | HG01255.hp1 HG02145.hp1 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.674+599T>C | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 8/26 | chr11 | 17525748 | ||||||
chr11:17525788
|
A | C | 2 | a0001c0004t0001g0199a0002c0010t0002g0238 | 2 | NA19060.hp2 NA19067.hp1 |
intron_variant | MODIFIER | c.674+559T>G | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 8/26 | chr11 | 17525788 | ||||||
chr11:17525912
|
A | T | 6 | a0001c0042t0001g0033a0001c0043t0006g0029a0002c0015t0001g0035others(3): Show | 7 | HG01255.hp1 HG02145.hp1 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.674+435T>A | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 8/26 | chr11 | 17525912 | ||||||
chr11:17526004
|
C | T | 6 | a0001c0042t0001g0033a0001c0043t0006g0029a0002c0015t0001g0035others(3): Show | 7 | HG01255.hp1 HG02145.hp1 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.674+343G>A | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 8/26 | chr11 | 17526004 | ||||||
chr11:17526157
|
T | C | 6 | a0001c0042t0001g0033a0001c0043t0006g0029a0002c0015t0001g0035others(3): Show | 7 | HG01255.hp1 HG02145.hp1 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.674+190A>G | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 8/26 | chr11 | 17526157 | ||||||
chr11:17526165
|
C | T | 1 | a0005c0035t0004g0032 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.674+182G>A | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 8/26 | chr11 | 17526165 | ||||||
chr11:17526192
|
C | A | 1 | a0001c0003t0004g0028 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.674+155G>T | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 8/26 | chr11 | 17526192 | ||||||
chr11:17526294
|
G | A | 1 | a0001c0003t0004g0030 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.674+53C>T | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 8/26 | chr11 | 17526294 | ||||||
chr11:17526343
|
C | T | 2 | a0001c0017t0001g0314a0001c0017t0001g0315 | 2 | HG02572.hp1 HG02723.hp2 |
splice_region_variant&intron_variant | LOW | c.674+4G>A | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 8/26 | chr11 | 17526343 | ||||||
chr11:17526468
|
C | T | 117 | a0001c0001t0001g0046a0001c0001t0001g0203a0001c0001t0001g0217others(114): Show | 134 | HG00280.hp2 HG00438.hp1 HG00558.hp1 others(131): Show |
intron_variant | MODIFIER | c.580-27G>A | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 7/26 | chr11 | 17526468 | ||||||
chr11:17526484
|
G | A | 1 | a0001c0003t0003g0165 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.580-43C>T | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 7/26 | chr11 | 17526484 | ||||||
chr11:17526521
|
C | T | 1 | a0005c0035t0004g0032 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.580-80G>A | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 7/26 | chr11 | 17526521 | ||||||
chr11:17526586
|
T | C | 6 | a0001c0042t0001g0033a0001c0043t0006g0029a0002c0015t0001g0035others(3): Show | 7 | HG01255.hp1 HG02145.hp1 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.580-145A>G | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 7/26 | chr11 | 17526586 | ||||||
chr11:17526589
|
G | A | 6 | a0001c0042t0001g0033a0001c0043t0006g0029a0002c0015t0001g0035others(3): Show | 7 | HG01255.hp1 HG02145.hp1 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.580-148C>T | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 7/26 | chr11 | 17526589 | ||||||
chr11:17526637
|
A | G | 6 | a0001c0042t0001g0033a0001c0043t0006g0029a0002c0015t0001g0035others(3): Show | 7 | HG01255.hp1 HG02145.hp1 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.579+116T>C | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 7/26 | chr11 | 17526637 | ||||||
chr11:17526639
|
C | T | 6 | a0001c0042t0001g0033a0001c0043t0006g0029a0002c0015t0001g0035others(3): Show | 7 | HG01255.hp1 HG02145.hp1 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.579+114G>A | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 7/26 | chr11 | 17526639 | ||||||
chr11:17526661
|
G | A | 6 | a0001c0042t0001g0033a0001c0043t0006g0029a0002c0015t0001g0035others(3): Show | 7 | HG01255.hp1 HG02145.hp1 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.579+92C>T | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 7/26 | chr11 | 17526661 | ||||||
chr11:17526692
|
C | T | 68 | a0001c0001t0001g0016a0001c0001t0001g0154a0001c0001t0001g0166others(65): Show | 72 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(69): Show |
intron_variant | MODIFIER | c.579+61G>A | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 7/26 | chr11 | 17526692 | ||||||
chr11:17526854
|
CG | C | 124 | a0001c0001t0001g0046a0001c0001t0001g0203a0001c0001t0001g0217others(121): Show | 142 | HG00280.hp2 HG00438.hp1 HG00558.hp1 others(139): Show |
intron_variant | MODIFIER | c.522-45delC | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 6/26 | chr11 | 17526854 | ||||||
chr11:17526960
|
T | C | 31 | a0001c0001t0001g0016a0001c0001t0001g0166a0001c0001t0001g0167others(28): Show | 32 | HG00099.hp2 HG01070.hp2 HG01243.hp1 others(29): Show |
intron_variant | MODIFIER | c.521+56A>G | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 6/26 | chr11 | 17526960 | ||||||
chr11:17527070
|
A | AGCTCCCC others(129): Show |
1 | a0001c0001t0001g0112 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.497-31_497-30insAG others(134): Show |
USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 5/26 | chr11 | 17527070 | ||||||
chr11:17527070
|
A | AGCTCCCC others(128): Show |
1 | a0001c0003t0006g0031 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.496+18_497-31dupAG others(133): Show |
USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 5/26 | chr11 | 17527070 | ||||||
chr11:17527070
|
A | AGCTCCCC others(38): Show |
1 | a0002c0002t0002g0115 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.497-31_497-30insAG others(43): Show |
USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 5/26 | chr11 | 17527070 | ||||||
chr11:17527070
|
A | AGCTCCCC others(83): Show |
3 | a0001c0001t0001g0066a0001c0001t0001g0113a0001c0001t0001g0148 | 3 | NA18940.hp1 NA18997.hp2 NA19076.hp2 |
intron_variant | MODIFIER | c.497-31_497-30insAG others(88): Show |
USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 5/26 | chr11 | 17527070 | ||||||
chr11:17527070
|
A | AGCTCCCC others(128): Show |
3 | a0001c0001t0014g0047a0001c0040t0001g0094a0002c0002t0007g0095 | 3 | NA18973.hp2 NA18979.hp2 NA19081.hp1 |
intron_variant | MODIFIER | c.497-31_497-30insAG others(133): Show |
USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 5/26 | chr11 | 17527070 | ||||||
chr11:17527070
|
A | AGCTCCCC others(173): Show |
15 | a0001c0001t0001g0009a0001c0001t0001g0083a0001c0001t0001g0085others(12): Show | 16 | HG00544.hp1 HG00673.hp1 HG01074.hp2 others(13): Show |
intron_variant | MODIFIER | c.497-31_497-30insAG others(178): Show |
USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 5/26 | chr11 | 17527070 | ||||||
chr11:17527070
|
AGCTCCCC others(38): Show |
A | 17 | a0001c0001t0001g0046a0001c0001t0001g0137a0001c0001t0001g0303others(14): Show | 18 | HG00558.hp1 HG01884.hp1 HG01978.hp1 others(15): Show |
intron_variant | MODIFIER | c.497-75_497-31delAG others(43): Show |
USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 5/26 | chr11 | 17527070 | ||||||
chr11:17527070
|
AGCTCCCC others(83): Show |
A | 1 | a0001c0023t0017g0281 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.496+63_497-31delAG others(88): Show |
USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 5/26 | chr11 | 17527070 | ||||||
chr11:17527078
|
C | T | 1 | a0001c0001t0001g0056 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.497-38G>A | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 5/26 | chr11 | 17527078 | ||||||
chr11:17527092
|
C | T | 1 | a0002c0006t0001g0233 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.497-52G>A | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 5/26 | chr11 | 17527092 | ||||||
chr11:17527111
|
G | C | 1 | a0002c0005t0002g0152 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.497-71C>G | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 5/26 | chr11 | 17527111 | ||||||
chr11:17527112
|
A | ACCTGCTC others(38): Show |
5 | a0002c0002t0002g0012a0002c0002t0002g0117a0002c0002t0003g0116others(2): Show | 6 | HG00621.hp2 HG01255.hp2 HG01433.hp1 others(3): Show |
intron_variant | MODIFIER | c.496+66_497-73dupGC others(43): Show |
USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 5/26 | chr11 | 17527112 | ||||||
chr11:17527112
|
A | ACCTGCTC others(83): Show |
4 | a0001c0001t0001g0041a0001c0001t0001g0048a0001c0001t0001g0114others(1): Show | 4 | HG00738.hp1 HG02080.hp2 HG02148.hp1 others(1): Show |
intron_variant | MODIFIER | c.496+21_497-73dupGC others(88): Show |
USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 5/26 | chr11 | 17527112 | ||||||
chr11:17527112
|
A | ACCTGCTC others(128): Show |
48 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0011others(45): Show | 57 | HG00280.hp1 HG00323.hp1 HG00438.hp2 others(54): Show |
intron_variant | MODIFIER | c.497-73_497-72insGC others(133): Show |
USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 5/26 | chr11 | 17527112 | ||||||
chr11:17527112
|
A | ACCTGCTC others(173): Show |
2 | a0001c0001t0001g0125a0001c0016t0001g0075 | 2 | HG03688.hp2 NA18982.hp1 |
intron_variant | MODIFIER | c.497-73_497-72insGC others(178): Show |
USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 5/26 | chr11 | 17527112 | ||||||
chr11:17527112
|
A | ACCTGCTC others(218): Show |
1 | a0001c0001t0001g0082 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.497-73_497-72insGC others(223): Show |
USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 5/26 | chr11 | 17527112 | ||||||
chr11:17527112
|
A | ACCTGCTC others(308): Show |
1 | a0001c0001t0001g0131 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.497-73_497-72insGC others(313): Show |
USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 5/26 | chr11 | 17527112 | ||||||
chr11:17527112
|
A | ACCTGCTC others(353): Show |
1 | a0001c0001t0001g0010 | 2 | HG01069.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.497-73_497-72insGC others(358): Show |
USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 5/26 | chr11 | 17527112 | ||||||
chr11:17527112
|
A | ACCTGCTC others(173): Show |
1 | a0002c0002t0002g0081 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.497-73_497-72insGC others(178): Show |
USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 5/26 | chr11 | 17527112 | ||||||
chr11:17527112
|
A | C | 33 | a0001c0001t0001g0009a0001c0001t0001g0066a0001c0001t0001g0083others(30): Show | 34 | HG00544.hp1 HG00639.hp2 HG00673.hp1 others(31): Show |
intron_variant | MODIFIER | c.497-72T>G | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 5/26 | chr11 | 17527112 | ||||||
chr11:17527112
|
ACCTGCTC others(38): Show |
A | 141 | a0001c0001t0001g0056a0001c0001t0001g0123a0001c0001t0001g0154others(138): Show | 161 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(158): Show |
intron_variant | MODIFIER | c.496+66_497-73delGC others(43): Show |
USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 5/26 | chr11 | 17527112 | ||||||
chr11:17527118
|
T | TCCCCCGC others(129): Show |
1 | a0001c0001t0001g0140 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.497-79_497-78insGA others(134): Show |
USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 5/26 | chr11 | 17527118 | ||||||
chr11:17527157
|
C | A | 1 | a0001c0001t0009g0122 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.496+66G>T | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 5/26 | chr11 | 17527157 | ||||||
chr11:17527168
|
C | T | 1 | a0001c0047t0001g0196 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.496+55G>A | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 5/26 | chr11 | 17527168 | ||||||
chr11:17527421
|
C | T | 1 | a0001c0003t0001g0156 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.388-90G>A | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 4/26 | chr11 | 17527421 | ||||||
chr11:17527492
|
G | C | 1 | a0001c0003t0001g0295 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.388-161C>G | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 4/26 | chr11 | 17527492 | ||||||
chr11:17527526
|
A | G | 1 | a0002c0006t0002g0018 | 2 | NA18955.hp1 NA19074.hp2 |
intron_variant | MODIFIER | c.388-195T>C | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 4/26 | chr11 | 17527526 | ||||||
chr11:17527528
|
C | G | 5 | a0001c0001t0001g0076a0001c0001t0001g0077a0001c0001t0001g0078others(2): Show | 5 | HG00323.hp1 HG00544.hp2 HG02080.hp1 others(2): Show |
intron_variant | MODIFIER | c.388-197G>C | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 4/26 | chr11 | 17527528 | ||||||
chr11:17527586
|
G | A | 2 | a0002c0015t0002g0319a0002c0019t0002g0025 | 3 | HG02145.hp1 HG02647.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.388-255C>T | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 4/26 | chr11 | 17527586 | ||||||
chr11:17527600
|
G | C | 1 | a0001c0001t0001g0278 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.388-269C>G | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 4/26 | chr11 | 17527600 | ||||||
chr11:17527643
|
C | A | 2 | a0002c0015t0002g0319a0002c0019t0002g0025 | 3 | HG02145.hp1 HG02647.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.388-312G>T | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 4/26 | chr11 | 17527643 | ||||||
chr11:17527860
|
T | C | 3 | a0001c0043t0006g0029a0002c0015t0002g0319a0002c0019t0002g0025 | 4 | HG02145.hp1 HG02647.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.388-529A>G | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 4/26 | chr11 | 17527860 | ||||||
chr11:17527862
|
T | C | 54 | a0001c0001t0001g0016a0001c0001t0001g0166a0001c0001t0001g0167others(51): Show | 56 | HG00099.hp2 HG00639.hp2 HG01070.hp2 others(53): Show |
intron_variant | MODIFIER | c.388-531A>G | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 4/26 | chr11 | 17527862 | ||||||
chr11:17527877
|
A | G | 1 | a0002c0002t0002g0057 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.388-546T>C | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 4/26 | chr11 | 17527877 | ||||||
chr11:17528104
|
G | A | 5 | a0001c0003t0001g0043a0001c0003t0004g0028a0001c0003t0005g0042others(2): Show | 6 | HG00639.hp2 HG02145.hp1 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.388-773C>T | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 4/26 | chr11 | 17528104 | ||||||
chr11:17528268
|
G | C | 1 | a0001c0001t0001g0228 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.388-937C>G | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 4/26 | chr11 | 17528268 | ||||||
chr11:17528277
|
A | G | 1 | a0001c0004t0001g0215 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.388-946T>C | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 4/26 | chr11 | 17528277 | ||||||
chr11:17528282
|
G | T | 37 | a0001c0001t0001g0016a0001c0001t0001g0166a0001c0001t0001g0167others(34): Show | 38 | HG00099.hp2 HG01070.hp2 HG01243.hp1 others(35): Show |
intron_variant | MODIFIER | c.388-951C>A | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 4/26 | chr11 | 17528282 | ||||||
chr11:17528347
|
C | T | 3 | a0001c0003t0001g0043a0001c0003t0004g0028a0001c0003t0005g0042 | 3 | HG00639.hp2 HG02559.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.388-1016G>A | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 4/26 | chr11 | 17528347 | ||||||
chr11:17528395
|
A | C | 1 | a0013c0033t0001g0232 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.388-1064T>G | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 4/26 | chr11 | 17528395 | ||||||
chr11:17528409
|
G | A | 37 | a0001c0001t0001g0016a0001c0001t0001g0166a0001c0001t0001g0167others(34): Show | 38 | HG00099.hp2 HG01070.hp2 HG01243.hp1 others(35): Show |
intron_variant | MODIFIER | c.388-1078C>T | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 4/26 | chr11 | 17528409 | ||||||
chr11:17528488
|
G | C | 3 | a0001c0021t0001g0163a0002c0020t0001g0158a0002c0020t0002g0157 | 3 | HG02280.hp2 HG03225.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.388-1157C>G | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 4/26 | chr11 | 17528488 | ||||||
chr11:17528552
|
G | A | 2 | a0001c0013t0001g0282a0001c0013t0010g0026 | 2 | NA18963.hp1 NA18969.hp1 |
intron_variant | MODIFIER | c.388-1221C>T | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 4/26 | chr11 | 17528552 | ||||||
chr11:17528553
|
T | G | 2 | a0001c0013t0001g0282a0001c0013t0010g0026 | 2 | NA18963.hp1 NA18969.hp1 |
intron_variant | MODIFIER | c.388-1222A>C | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 4/26 | chr11 | 17528553 | ||||||
chr11:17528591
|
T | C | 230 | a0001c0001t0001g0016a0001c0001t0001g0046a0001c0001t0001g0052others(227): Show | 252 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(249): Show |
intron_variant | MODIFIER | c.388-1260A>G | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 4/26 | chr11 | 17528591 | ||||||
chr11:17528760
|
T | C | 1 | a0001c0043t0006g0029 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.388-1429A>G | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 4/26 | chr11 | 17528760 | ||||||
chr11:17528873
|
C | T | 2 | a0001c0003t0004g0030a0001c0003t0006g0031 | 2 | HG02258.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.388-1542G>A | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 4/26 | chr11 | 17528873 | ||||||
chr11:17529030
|
C | T | 4 | a0001c0003t0004g0030a0001c0003t0006g0031a0001c0016t0001g0075others(1): Show | 4 | HG02258.hp2 HG03486.hp1 NA18982.hp1 others(1): Show |
intron_variant | MODIFIER | c.388-1699G>A | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 4/26 | chr11 | 17529030 | ||||||
chr11:17529133
|
TG | T | 152 | a0001c0001t0001g0154a0001c0001t0001g0203a0001c0001t0001g0217others(149): Show | 173 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(170): Show |
intron_variant | MODIFIER | c.388-1803delC | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 4/26 | chr11 | 17529133 | ||||||
chr11:17529145
|
C | G | 2 | a0001c0003t0004g0030a0001c0003t0006g0031 | 2 | HG02258.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.388-1814G>C | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 4/26 | chr11 | 17529145 | ||||||
chr11:17529273
|
A | C | 1 | a0001c0001t0001g0009 | 2 | NA18984.hp2 NA18988.hp2 |
intron_variant | MODIFIER | c.387+1881T>G | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 4/26 | chr11 | 17529273 | ||||||
chr11:17529356
|
C | A | 1 | a0002c0009t0002g0007 | 3 | NA18965.hp1 NA19057.hp1 NA19079.hp2 |
intron_variant | MODIFIER | c.387+1798G>T | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 4/26 | chr11 | 17529356 | ||||||
chr11:17529441
|
C | T | 1 | a0001c0043t0006g0029 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.387+1713G>A | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 4/26 | chr11 | 17529441 | ||||||
chr11:17529442
|
G | C | 2 | a0001c0003t0004g0030a0001c0003t0006g0031 | 2 | HG02258.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.387+1712C>G | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 4/26 | chr11 | 17529442 | ||||||
chr11:17529644
|
C | A | 145 | a0001c0001t0001g0154a0001c0001t0001g0203a0001c0001t0001g0217others(142): Show | 165 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(162): Show |
intron_variant | MODIFIER | c.387+1510G>T | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 4/26 | chr11 | 17529644 | ||||||
chr11:17529728
|
C | T | 6 | a0001c0001t0001g0166a0001c0001t0001g0167a0001c0001t0001g0184others(3): Show | 6 | HG01243.hp1 HG01891.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.387+1426G>A | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 4/26 | chr11 | 17529728 | ||||||
chr11:17529861
|
C | T | 3 | a0001c0001t0001g0016a0002c0002t0002g0190a0002c0002t0002g0213 | 4 | HG01257.hp2 HG02074.hp1 NA18965.hp2 others(1): Show |
intron_variant | MODIFIER | c.387+1293G>A | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 4/26 | chr11 | 17529861 | ||||||
chr11:17529939
|
A | C | 1 | a0001c0003t0005g0042 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.387+1215T>G | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 4/26 | chr11 | 17529939 | ||||||
chr11:17529940
|
C | T | 2 | a0001c0017t0001g0314a0001c0017t0001g0315 | 2 | HG02572.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.387+1214G>A | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 4/26 | chr11 | 17529940 | ||||||
chr11:17530020
|
G | A | 3 | a0001c0021t0002g0162a0002c0046t0002g0160a0011c0048t0001g0161 | 3 | HG01884.hp1 HG02723.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.387+1134C>T | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 4/26 | chr11 | 17530020 | ||||||
chr11:17530080
|
G | A | 4 | a0001c0001t0001g0052a0001c0001t0003g0055a0001c0008t0001g0294others(1): Show | 4 | HG01167.hp1 HG03017.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.387+1074C>T | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 4/26 | chr11 | 17530080 | ||||||
chr11:17530094
|
C | T | 37 | a0001c0001t0001g0016a0001c0001t0001g0166a0001c0001t0001g0167others(34): Show | 38 | HG00099.hp2 HG01070.hp2 HG01243.hp1 others(35): Show |
intron_variant | MODIFIER | c.387+1060G>A | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 4/26 | chr11 | 17530094 | ||||||
chr11:17530242
|
C | T | 1 | a0001c0001t0008g0229 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.387+912G>A | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 4/26 | chr11 | 17530242 | ||||||
chr11:17530270
|
T | G | 1 | a0001c0043t0006g0029 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.387+884A>C | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 4/26 | chr11 | 17530270 | ||||||
chr11:17530346
|
G | A | 11 | a0001c0001t0001g0125a0001c0001t0001g0128a0001c0001t0001g0131others(8): Show | 12 | HG00280.hp1 HG00639.hp2 HG00733.hp1 others(9): Show |
intron_variant | MODIFIER | c.387+808C>T | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 4/26 | chr11 | 17530346 | ||||||
chr11:17530387
|
CAGTT | C | 3 | a0001c0003t0004g0030a0001c0003t0006g0031a0005c0035t0004g0032 | 3 | HG02258.hp2 HG03486.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.387+763_387+766del others(4): Show |
USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 4/26 | chr11 | 17530387 | ||||||
chr11:17530455
|
C | G | 3 | a0001c0003t0004g0030a0001c0003t0006g0031a0005c0035t0004g0032 | 3 | HG02258.hp2 HG03486.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.387+699G>C | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 4/26 | chr11 | 17530455 | ||||||
chr11:17530519
|
G | A | 2 | a0001c0017t0001g0314a0001c0017t0001g0315 | 2 | HG02572.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.387+635C>T | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 4/26 | chr11 | 17530519 | ||||||
chr11:17530555
|
G | A | 3 | a0001c0003t0004g0030a0001c0003t0006g0031a0005c0035t0004g0032 | 3 | HG02258.hp2 HG03486.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.387+599C>T | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 4/26 | chr11 | 17530555 | ||||||
chr11:17530661
|
T | C | 1 | a0002c0005t0002g0311 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.387+493A>G | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 4/26 | chr11 | 17530661 | ||||||
chr11:17530773
|
C | T | 37 | a0001c0001t0001g0016a0001c0001t0001g0166a0001c0001t0001g0167others(34): Show | 38 | HG00099.hp2 HG01070.hp2 HG01243.hp1 others(35): Show |
intron_variant | MODIFIER | c.387+381G>A | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 4/26 | chr11 | 17530773 | ||||||
chr11:17530809
|
T | C | 1 | a0001c0003t0001g0173 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.387+345A>G | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 4/26 | chr11 | 17530809 | ||||||
chr11:17530816
|
A | T | 1 | a0002c0036t0002g0074 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.387+338T>A | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 4/26 | chr11 | 17530816 | ||||||
chr11:17530882
|
G | T | 3 | a0001c0003t0004g0030a0001c0003t0006g0031a0005c0035t0004g0032 | 3 | HG02258.hp2 HG03486.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.387+272C>A | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 4/26 | chr11 | 17530882 | ||||||
chr11:17530981
|
G | A | 3 | a0001c0003t0004g0030a0001c0003t0006g0031a0005c0035t0004g0032 | 3 | HG02258.hp2 HG03486.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.387+173C>T | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 4/26 | chr11 | 17530981 | ||||||
chr11:17531054
|
G | A | 1 | a0001c0003t0001g0072 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.387+100C>T | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 4/26 | chr11 | 17531054 | ||||||
chr11:17531118
|
C | T | 1 | a0001c0003t0001g0202 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.387+36G>A | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 4/26 | chr11 | 17531118 | ||||||
chr11:17531130
|
C | A | 1 | a0001c0001t0001g0130 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.387+24G>T | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 4/26 | chr11 | 17531130 | ||||||
chr11:17531137
|
G | A | 3 | a0001c0001t0001g0046a0002c0005t0002g0044a0002c0005t0002g0045 | 3 | HG02572.hp2 HG03579.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.387+17C>T | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 4/26 | chr11 | 17531137 | ||||||
chr11:17531558
|
G | A | 147 | a0001c0001t0001g0154a0001c0001t0001g0203a0001c0001t0001g0217others(144): Show | 167 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(164): Show |
intron_variant | MODIFIER | c.105-16C>T | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 2/26 | chr11 | 17531558 | ||||||
chr11:17531690
|
G | A | 2 | a0001c0001t0001g0056a0001c0003t0004g0028 | 2 | HG02027.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.105-148C>T | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 2/26 | chr11 | 17531690 | ||||||
chr11:17531814
|
C | G | 3 | a0001c0003t0004g0030a0001c0003t0006g0031a0005c0035t0004g0032 | 3 | HG02258.hp2 HG03486.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.105-272G>C | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 2/26 | chr11 | 17531814 | ||||||
chr11:17532021
|
T | C | 1 | a0001c0001t0001g0131 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.105-479A>G | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 2/26 | chr11 | 17532021 | ||||||
chr11:17532080
|
C | T | 155 | a0001c0001t0001g0154a0001c0001t0001g0203a0001c0001t0001g0217others(152): Show | 175 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(172): Show |
intron_variant | MODIFIER | c.105-538G>A | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 2/26 | chr11 | 17532080 | ||||||
chr11:17532159
|
C | T | 11 | a0001c0001t0001g0154a0001c0001t0003g0206a0001c0003t0001g0150others(8): Show | 12 | HG00099.hp1 HG00323.hp2 HG00639.hp1 others(9): Show |
intron_variant | MODIFIER | c.105-617G>A | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 2/26 | chr11 | 17532159 | ||||||
chr11:17532160
|
G | A | 1 | a0001c0003t0001g0295 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.105-618C>T | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 2/26 | chr11 | 17532160 | ||||||
chr11:17532397
|
A | G | 2 | a0001c0003t0004g0030a0001c0003t0006g0031 | 2 | HG02258.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.105-855T>C | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 2/26 | chr11 | 17532397 | ||||||
chr11:17532458
|
C | T | 3 | a0001c0003t0001g0043a0001c0003t0004g0028a0001c0003t0005g0042 | 3 | HG00639.hp2 HG02559.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.104+797G>A | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 2/26 | chr11 | 17532458 | ||||||
chr11:17532582
|
G | A | 2 | a0002c0015t0002g0319a0002c0019t0002g0025 | 3 | HG02145.hp1 HG02647.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.104+673C>T | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 2/26 | chr11 | 17532582 | ||||||
chr11:17532713
|
G | A | 2 | a0002c0015t0002g0319a0002c0019t0002g0025 | 3 | HG02145.hp1 HG02647.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.104+542C>T | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 2/26 | chr11 | 17532713 | ||||||
chr11:17532867
|
T | C | 2 | a0002c0015t0002g0319a0002c0019t0002g0025 | 3 | HG02145.hp1 HG02647.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.104+388A>G | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 2/26 | chr11 | 17532867 | ||||||
chr11:17532882
|
A | C | 3 | a0001c0042t0001g0033a0002c0015t0001g0035a0002c0015t0002g0034 | 3 | HG01255.hp1 HG02486.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.104+373T>G | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 2/26 | chr11 | 17532882 | ||||||
chr11:17532901
|
G | A | 1 | a0002c0006t0002g0022 | 2 | HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.104+354C>T | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 2/26 | chr11 | 17532901 | ||||||
chr11:17532960
|
A | T | 3 | a0001c0003t0001g0043a0001c0003t0004g0028a0001c0003t0005g0042 | 3 | HG00639.hp2 HG02559.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.104+295T>A | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 2/26 | chr11 | 17532960 | ||||||
chr11:17532963
|
C | A | 149 | a0001c0001t0001g0154a0001c0001t0001g0203a0001c0001t0001g0217others(146): Show | 169 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(166): Show |
intron_variant | MODIFIER | c.104+292G>T | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 2/26 | chr11 | 17532963 | ||||||
chr11:17533363
|
A | AC | 32 | a0001c0001t0001g0287a0001c0001t0001g0291a0001c0001t0001g0292others(29): Show | 36 | HG00639.hp2 HG00741.hp2 HG01243.hp2 others(33): Show |
intron_variant | MODIFIER | c.37-42dupG | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 1/26 | chr11 | 17533363 | ||||||
chr11:17533363
|
A | ACC | 101 | a0001c0001t0001g0154a0001c0001t0001g0203a0001c0001t0001g0217others(98): Show | 115 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(112): Show |
intron_variant | MODIFIER | c.37-43_37-42dupGG | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 1/26 | chr11 | 17533363 | ||||||
chr11:17533363
|
A | ACCC | 17 | a0001c0001t0001g0228a0001c0001t0001g0297a0001c0001t0001g0307others(14): Show | 19 | HG00597.hp2 HG00735.hp1 HG01069.hp1 others(16): Show |
intron_variant | MODIFIER | c.37-44_37-42dupGGG | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 1/26 | chr11 | 17533363 | ||||||
chr11:17533366
|
C | A | 1 | a0005c0035t0004g0032 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.37-44G>T | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 1/26 | chr11 | 17533366 | ||||||
chr11:17533367
|
G | C | 204 | a0001c0001t0001g0016a0001c0001t0001g0154a0001c0001t0001g0166others(201): Show | 226 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(223): Show |
intron_variant | MODIFIER | c.37-45C>G | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 1/26 | chr11 | 17533367 | ||||||
chr11:17533369
|
C | A | 42 | a0001c0001t0001g0016a0001c0001t0001g0166a0001c0001t0001g0167others(39): Show | 43 | HG00099.hp2 HG01070.hp2 HG01243.hp1 others(40): Show |
intron_variant | MODIFIER | c.37-47G>T | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 1/26 | chr11 | 17533369 | ||||||
chr11:17533370
|
C | A | 6 | a0001c0003t0004g0030a0001c0003t0006g0031a0001c0021t0002g0162others(3): Show | 6 | HG01884.hp1 HG02258.hp2 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.37-48G>T | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 1/26 | chr11 | 17533370 | ||||||
chr11:17533370
|
C | CG | 2 | a0002c0015t0002g0319a0002c0019t0002g0025 | 3 | HG02145.hp1 HG02647.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.37-49_37-48insC | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 1/26 | chr11 | 17533370 | ||||||
chr11:17533383
|
T | C | 162 | a0001c0001t0001g0154a0001c0001t0001g0203a0001c0001t0001g0217others(159): Show | 183 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(180): Show |
intron_variant | MODIFIER | c.37-61A>G | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 1/26 | chr11 | 17533383 | ||||||
chr11:17533472
|
G | T | 2 | a0002c0015t0002g0319a0002c0019t0002g0025 | 3 | HG02145.hp1 HG02647.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.37-150C>A | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 1/26 | chr11 | 17533472 | ||||||
chr11:17533487
|
A | G | 1 | a0001c0001t0001g0073 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.37-165T>C | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 1/26 | chr11 | 17533487 | ||||||
chr11:17533565
|
T | C | 205 | a0001c0001t0001g0016a0001c0001t0001g0154a0001c0001t0001g0166others(202): Show | 227 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(224): Show |
intron_variant | MODIFIER | c.37-243A>G | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 1/26 | chr11 | 17533565 | ||||||
chr11:17533597
|
G | C | 1 | a0005c0035t0004g0032 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.37-275C>G | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 1/26 | chr11 | 17533597 | ||||||
chr11:17533672
|
C | T | 2 | a0001c0003t0001g0150a0001c0003t0001g0151 | 2 | HG00738.hp2 HG00741.hp1 |
intron_variant | MODIFIER | c.37-350G>A | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 1/26 | chr11 | 17533672 | ||||||
chr11:17533685
|
G | A | 7 | a0001c0001t0001g0297a0001c0001t0001g0302a0001c0004t0001g0003others(4): Show | 10 | HG02523.hp1 NA18943.hp2 NA18956.hp1 others(7): Show |
intron_variant | MODIFIER | c.37-363C>T | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 1/26 | chr11 | 17533685 | ||||||
chr11:17533738
|
C | T | 6 | a0001c0003t0004g0030a0001c0021t0002g0162a0002c0046t0002g0160others(3): Show | 6 | HG01884.hp1 HG02451.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.37-416G>A | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 1/26 | chr11 | 17533738 | ||||||
chr11:17533798
|
A | G | 1 | a0001c0008t0001g0221 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.37-476T>C | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 1/26 | chr11 | 17533798 | ||||||
chr11:17533803
|
C | T | 3 | a0001c0021t0001g0163a0001c0047t0001g0196a0002c0020t0002g0157 | 3 | HG03225.hp2 NA18522.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.37-481G>A | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 1/26 | chr11 | 17533803 | ||||||
chr11:17533851
|
C | T | 1 | a0001c0043t0006g0029 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.37-529G>A | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 1/26 | chr11 | 17533851 | ||||||
chr11:17533873
|
C | T | 1 | a0001c0021t0001g0163 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.37-551G>A | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 1/26 | chr11 | 17533873 | ||||||
chr11:17533927
|
C | T | 1 | a0001c0003t0001g0156 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.37-605G>A | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 1/26 | chr11 | 17533927 | ||||||
chr11:17533951
|
C | A | 162 | a0001c0001t0001g0154a0001c0001t0001g0203a0001c0001t0001g0217others(159): Show | 183 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(180): Show |
intron_variant | MODIFIER | c.37-629G>T | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 1/26 | chr11 | 17533951 | ||||||
chr11:17533981
|
C | A | 5 | a0001c0001t0001g0303a0001c0001t0001g0304a0001c0001t0001g0305others(2): Show | 5 | HG00558.hp1 HG00597.hp2 NA18947.hp2 others(2): Show |
intron_variant | MODIFIER | c.37-659G>T | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 1/26 | chr11 | 17533981 | ||||||
chr11:17534043
|
C | T | 38 | a0001c0001t0001g0016a0001c0001t0001g0166a0001c0001t0001g0167others(35): Show | 39 | HG00099.hp2 HG01070.hp2 HG01243.hp1 others(36): Show |
intron_variant | MODIFIER | c.37-721G>A | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 1/26 | chr11 | 17534043 | ||||||
chr11:17534044
|
G | A | 1 | a0002c0002t0002g0050 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.37-722C>T | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 1/26 | chr11 | 17534044 | ||||||
chr11:17534117
|
G | A | 1 | a0001c0021t0001g0163 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.37-795C>T | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 1/26 | chr11 | 17534117 | ||||||
chr11:17534126
|
C | T | 3 | a0001c0003t0001g0043a0001c0003t0004g0028a0001c0003t0005g0042 | 3 | HG00639.hp2 HG02559.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.37-804G>A | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 1/26 | chr11 | 17534126 | ||||||
chr11:17534187
|
C | T | 1 | a0002c0005t0001g0141 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.37-865G>A | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 1/26 | chr11 | 17534187 | ||||||
chr11:17534262
|
G | A | 7 | a0001c0003t0004g0030a0001c0003t0006g0031a0001c0021t0002g0162others(4): Show | 7 | HG01884.hp1 HG02258.hp2 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.37-940C>T | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 1/26 | chr11 | 17534262 | ||||||
chr11:17534318
|
G | A | 148 | a0001c0001t0001g0154a0001c0001t0001g0203a0001c0001t0001g0217others(145): Show | 169 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(166): Show |
intron_variant | MODIFIER | c.37-996C>T | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 1/26 | chr11 | 17534318 | ||||||
chr11:17534385
|
G | A | 1 | a0001c0001t0003g0132 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.37-1063C>T | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 1/26 | chr11 | 17534385 | ||||||
chr11:17534484
|
G | A | 20 | a0001c0007t0001g0176a0001c0007t0001g0177a0001c0007t0001g0187others(17): Show | 20 | HG00099.hp2 HG01070.hp2 HG02071.hp1 others(17): Show |
intron_variant | MODIFIER | c.37-1162C>T | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 1/26 | chr11 | 17534484 | ||||||
chr11:17534598
|
G | C | 38 | a0001c0001t0001g0016a0001c0001t0001g0166a0001c0001t0001g0167others(35): Show | 39 | HG00099.hp2 HG01070.hp2 HG01243.hp1 others(36): Show |
intron_variant | MODIFIER | c.37-1276C>G | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 1/26 | chr11 | 17534598 | ||||||
chr11:17534734
|
C | T | 1 | a0001c0001t0001g0052 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.37-1412G>A | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 1/26 | chr11 | 17534734 | ||||||
chr11:17534805
|
C | T | 7 | a0001c0003t0004g0030a0001c0003t0006g0031a0001c0021t0002g0162others(4): Show | 7 | HG01884.hp1 HG02258.hp2 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.37-1483G>A | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 1/26 | chr11 | 17534805 | ||||||
chr11:17534873
|
C | CA | 91 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0008others(88): Show | 105 | HG00280.hp1 HG00323.hp1 HG00438.hp2 others(102): Show |
intron_variant | MODIFIER | c.37-1552dupT | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 1/26 | chr11 | 17534873 | ||||||
chr11:17534873
|
CA | C | 183 | a0001c0001t0001g0016a0001c0001t0001g0154a0001c0001t0001g0166others(180): Show | 205 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(202): Show |
intron_variant | MODIFIER | c.37-1552delT | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 1/26 | chr11 | 17534873 | ||||||
chr11:17534891
|
A | C | 149 | a0001c0001t0001g0154a0001c0001t0001g0203a0001c0001t0001g0217others(146): Show | 170 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(167): Show |
intron_variant | MODIFIER | c.37-1569T>G | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 1/26 | chr11 | 17534891 | ||||||
chr11:17534930
|
G | A | 14 | a0001c0001t0001g0052a0001c0001t0001g0056a0001c0001t0001g0137others(11): Show | 14 | HG01167.hp1 HG01975.hp1 HG01978.hp1 others(11): Show |
intron_variant | MODIFIER | c.37-1608C>T | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 1/26 | chr11 | 17534930 | ||||||
chr11:17535155
|
G | A | 1 | a0002c0005t0002g0311 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.37-1833C>T | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 1/26 | chr11 | 17535155 | ||||||
chr11:17535204
|
C | T | 1 | a0002c0005t0002g0044 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.37-1882G>A | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 1/26 | chr11 | 17535204 | ||||||
chr11:17535270
|
C | T | 1 | a0004c0014t0005g0062 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.37-1948G>A | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 1/26 | chr11 | 17535270 | ||||||
chr11:17535294
|
C | G | 1 | a0004c0014t0005g0062 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.37-1972G>C | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 1/26 | chr11 | 17535294 | ||||||
chr11:17535367
|
G | T | 11 | a0001c0001t0001g0154a0001c0001t0003g0206a0001c0003t0001g0150others(8): Show | 12 | HG00099.hp1 HG00323.hp2 HG00639.hp1 others(9): Show |
intron_variant | MODIFIER | c.37-2045C>A | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 1/26 | chr11 | 17535367 | ||||||
chr11:17535447
|
C | T | 1 | a0002c0005t0013g0220 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.37-2125G>A | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 1/26 | chr11 | 17535447 | ||||||
chr11:17535463
|
C | A | 1 | a0001c0024t0001g0312 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.37-2141G>T | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 1/26 | chr11 | 17535463 | ||||||
chr11:17535469
|
C | T | 1 | a0001c0008t0001g0219 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.37-2147G>A | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 1/26 | chr11 | 17535469 | ||||||
chr11:17535470
|
A | G | 152 | a0001c0001t0001g0154a0001c0001t0001g0203a0001c0001t0001g0217others(149): Show | 173 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(170): Show |
intron_variant | MODIFIER | c.37-2148T>C | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 1/26 | chr11 | 17535470 | ||||||
chr11:17535546
|
G | A | 1 | a0002c0006t0002g0188 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.37-2224C>T | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 1/26 | chr11 | 17535546 | ||||||
chr11:17535734
|
T | A | 1 | a0001c0003t0001g0324 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.37-2412A>T | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 1/26 | chr11 | 17535734 | ||||||
chr11:17535824
|
G | A | 7 | a0001c0003t0004g0030a0001c0003t0006g0031a0001c0021t0002g0162others(4): Show | 7 | HG01884.hp1 HG02258.hp2 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.37-2502C>T | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 1/26 | chr11 | 17535824 | ||||||
chr11:17535908
|
C | T | 1 | a0002c0002t0002g0190 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.37-2586G>A | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 1/26 | chr11 | 17535908 | ||||||
chr11:17535931
|
G | A | 7 | a0001c0003t0004g0030a0001c0003t0006g0031a0001c0021t0002g0162others(4): Show | 7 | HG01884.hp1 HG02258.hp2 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.37-2609C>T | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 1/26 | chr11 | 17535931 | ||||||
chr11:17536000
|
T | C | 7 | a0001c0003t0004g0030a0001c0003t0006g0031a0001c0021t0002g0162others(4): Show | 7 | HG01884.hp1 HG02258.hp2 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.37-2678A>G | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 1/26 | chr11 | 17536000 | ||||||
chr11:17536144
|
G | T | 3 | a0001c0001t0001g0217a0001c0001t0002g0218a0002c0002t0001g0216 | 3 | HG00280.hp2 HG00642.hp2 HG01346.hp1 |
intron_variant | MODIFIER | c.37-2822C>A | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 1/26 | chr11 | 17536144 | ||||||
chr11:17536214
|
C | G | 1 | a0001c0004t0001g0215 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.37-2892G>C | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 1/26 | chr11 | 17536214 | ||||||
chr11:17536264
|
A | G | 7 | a0001c0003t0004g0030a0001c0003t0006g0031a0001c0021t0002g0162others(4): Show | 7 | HG01884.hp1 HG02258.hp2 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.37-2942T>C | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 1/26 | chr11 | 17536264 | ||||||
chr11:17536296
|
A | C | 1 | a0001c0043t0006g0029 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.37-2974T>G | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 1/26 | chr11 | 17536296 | ||||||
chr11:17536345
|
G | C | 2 | a0001c0001t0001g0139a0001c0001t0001g0147 | 2 | HG01074.hp2 HG01175.hp1 |
intron_variant | MODIFIER | c.37-3023C>G | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 1/26 | chr11 | 17536345 | ||||||
chr11:17536359
|
G | C | 3 | a0001c0042t0001g0033a0002c0015t0001g0035a0002c0015t0002g0034 | 3 | HG01255.hp1 HG02486.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.37-3037C>G | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 1/26 | chr11 | 17536359 | ||||||
chr11:17536631
|
G | A | 1 | a0001c0007t0001g0189 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.37-3309C>T | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 1/26 | chr11 | 17536631 | ||||||
chr11:17536698
|
G | T | 4 | a0001c0021t0001g0163a0001c0047t0001g0196a0002c0020t0001g0158others(1): Show | 4 | HG02280.hp2 HG03225.hp2 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.37-3376C>A | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 1/26 | chr11 | 17536698 | ||||||
chr11:17536767
|
C | A | 1 | a0002c0002t0002g0057 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.37-3445G>T | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 1/26 | chr11 | 17536767 | ||||||
chr11:17536832
|
T | C | 3 | a0001c0003t0001g0043a0001c0003t0004g0028a0001c0003t0005g0042 | 3 | HG00639.hp2 HG02559.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.37-3510A>G | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 1/26 | chr11 | 17536832 | ||||||
chr11:17536841
|
C | A | 195 | a0001c0001t0001g0016a0001c0001t0001g0154a0001c0001t0001g0166others(192): Show | 217 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(214): Show |
intron_variant | MODIFIER | c.37-3519G>T | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 1/26 | chr11 | 17536841 | ||||||
chr11:17537334
|
G | A | 7 | a0001c0003t0004g0030a0001c0003t0006g0031a0001c0021t0002g0162others(4): Show | 7 | HG01884.hp1 HG02258.hp2 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.37-4012C>T | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 1/26 | chr11 | 17537334 | ||||||
chr11:17537347
|
C | T | 1 | a0001c0003t0003g0165 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.37-4025G>A | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 1/26 | chr11 | 17537347 | ||||||
chr11:17537397
|
T | C | 1 | a0001c0001t0001g0140 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.37-4075A>G | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 1/26 | chr11 | 17537397 | ||||||
chr11:17537451
|
G | C | 1 | a0001c0018t0001g0149 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.37-4129C>G | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 1/26 | chr11 | 17537451 | ||||||
chr11:17537456
|
G | A | 7 | a0001c0003t0004g0030a0001c0003t0006g0031a0001c0021t0002g0162others(4): Show | 7 | HG01884.hp1 HG02258.hp2 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.37-4134C>T | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 1/26 | chr11 | 17537456 | ||||||
chr11:17537471
|
G | A | 150 | a0001c0001t0001g0154a0001c0001t0001g0203a0001c0001t0001g0217others(147): Show | 171 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(168): Show |
intron_variant | MODIFIER | c.37-4149C>T | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 1/26 | chr11 | 17537471 | ||||||
chr11:17537673
|
C | T | 3 | a0001c0001t0001g0059a0001c0001t0001g0060a0002c0002t0002g0061 | 3 | HG01256.hp1 HG01358.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.37-4351G>A | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 1/26 | chr11 | 17537673 | ||||||
chr11:17537714
|
G | A | 146 | a0001c0001t0001g0203a0001c0001t0001g0217a0001c0001t0001g0228others(143): Show | 166 | HG00280.hp2 HG00438.hp1 HG00558.hp1 others(163): Show |
intron_variant | MODIFIER | c.37-4392C>T | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 1/26 | chr11 | 17537714 | ||||||
chr11:17537857
|
G | A | 1 | a0001c0003t0004g0028 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.37-4535C>T | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 1/26 | chr11 | 17537857 | ||||||
chr11:17537962
|
T | A | 203 | a0001c0001t0001g0016a0001c0001t0001g0154a0001c0001t0001g0166others(200): Show | 225 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(222): Show |
intron_variant | MODIFIER | c.37-4640A>T | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 1/26 | chr11 | 17537962 | ||||||
chr11:17538000
|
TG | T | 7 | a0001c0003t0004g0030a0001c0003t0006g0031a0001c0021t0002g0162others(4): Show | 7 | HG01884.hp1 HG02258.hp2 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.37-4679delC | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 1/26 | chr11 | 17538000 | ||||||
chr11:17538043
|
G | T | 2 | a0001c0004t0001g0210a0001c0004t0001g0211 | 2 | NA18948.hp2 NA18994.hp1 |
intron_variant | MODIFIER | c.37-4721C>A | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 1/26 | chr11 | 17538043 | ||||||
chr11:17538086
|
C | T | 3 | a0001c0042t0001g0033a0002c0015t0001g0035a0002c0015t0002g0034 | 3 | HG01255.hp1 HG02486.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.37-4764G>A | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 1/26 | chr11 | 17538086 | ||||||
chr11:17538175
|
T | C | 1 | a0001c0007t0001g0194 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.37-4853A>G | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 1/26 | chr11 | 17538175 | ||||||
chr11:17538230
|
G | A | 1 | a0002c0002t0002g0190 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.37-4908C>T | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 1/26 | chr11 | 17538230 | ||||||
chr11:17538249
|
C | G | 7 | a0001c0003t0004g0030a0001c0003t0006g0031a0001c0021t0002g0162others(4): Show | 7 | HG01884.hp1 HG02258.hp2 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.37-4927G>C | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 1/26 | chr11 | 17538249 | ||||||
chr11:17538580
|
G | A | 190 | a0001c0001t0001g0016a0001c0001t0001g0166a0001c0001t0001g0167others(187): Show | 211 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(208): Show |
intron_variant | MODIFIER | c.37-5258C>T | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 1/26 | chr11 | 17538580 | ||||||
chr11:17538590
|
C | T | 2 | a0001c0003t0004g0030a0001c0003t0006g0031 | 2 | HG02258.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.37-5268G>A | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 1/26 | chr11 | 17538590 | ||||||
chr11:17538766
|
C | T | 2 | a0001c0001t0001g0008a0002c0002t0002g0058 | 3 | NA18950.hp2 NA18977.hp1 NA19067.hp2 |
intron_variant | MODIFIER | c.37-5444G>A | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 1/26 | chr11 | 17538766 | ||||||
chr11:17538805
|
C | T | 1 | a0001c0001t0003g0206 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.36+5467G>A | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 1/26 | chr11 | 17538805 | ||||||
chr11:17538870
|
T | C | 7 | a0001c0003t0004g0030a0001c0003t0006g0031a0001c0021t0002g0162others(4): Show | 7 | HG01884.hp1 HG02258.hp2 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.36+5402A>G | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 1/26 | chr11 | 17538870 | ||||||
chr11:17539127
|
A | C | 1 | a0006c0025t0001g0205 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.36+5145T>G | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 1/26 | chr11 | 17539127 | ||||||
chr11:17539193
|
A | G | 3 | a0001c0001t0001g0203a0001c0003t0001g0202a0001c0003t0001g0204 | 3 | NA18966.hp2 NA18984.hp1 NA19012.hp1 |
intron_variant | MODIFIER | c.36+5079T>C | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 1/26 | chr11 | 17539193 | ||||||
chr11:17539461
|
A | G | 7 | a0001c0001t0001g0052a0001c0001t0001g0056a0001c0001t0003g0055others(4): Show | 7 | HG01167.hp1 HG02027.hp2 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.36+4811T>C | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 1/26 | chr11 | 17539461 | ||||||
chr11:17539466
|
TG | T | 7 | a0001c0003t0004g0030a0001c0003t0006g0031a0001c0021t0002g0162others(4): Show | 7 | HG01884.hp1 HG02258.hp2 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.36+4805delC | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 1/26 | chr11 | 17539466 | ||||||
chr11:17539531
|
G | T | 1 | a0001c0001t0001g0051 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.36+4741C>A | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 1/26 | chr11 | 17539531 | ||||||
chr11:17539770
|
C | CTCTCTG | 7 | a0001c0003t0004g0030a0001c0003t0006g0031a0001c0021t0002g0162others(4): Show | 7 | HG01884.hp1 HG02258.hp2 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.36+4496_36+4501dup others(6): Show |
USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 1/26 | chr11 | 17539770 | ||||||
chr11:17539772
|
C | T | 1 | a0002c0009t0002g0201 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.36+4500G>A | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 1/26 | chr11 | 17539772 | ||||||
chr11:17539822
|
T | A | 7 | a0001c0003t0004g0030a0001c0003t0006g0031a0001c0021t0002g0162others(4): Show | 7 | HG01884.hp1 HG02258.hp2 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.36+4450A>T | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 1/26 | chr11 | 17539822 | ||||||
chr11:17539830
|
T | TC | 7 | a0001c0003t0004g0030a0001c0003t0006g0031a0001c0021t0002g0162others(4): Show | 7 | HG01884.hp1 HG02258.hp2 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.36+4441_36+4442ins others(1): Show |
USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 1/26 | chr11 | 17539830 | ||||||
chr11:17539833
|
C | CT | 11 | a0001c0001t0001g0046a0001c0001t0001g0048a0001c0001t0014g0047others(8): Show | 11 | HG00621.hp2 HG02080.hp2 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.36+4438dupA | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 1/26 | chr11 | 17539833 | ||||||
chr11:17539833
|
C | T | 7 | a0001c0003t0004g0030a0001c0003t0006g0031a0001c0021t0002g0162others(4): Show | 7 | HG01884.hp1 HG02258.hp2 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.36+4439G>A | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 1/26 | chr11 | 17539833 | ||||||
chr11:17539833
|
CT | C | 45 | a0001c0001t0001g0145a0001c0001t0001g0146a0001c0001t0001g0147others(42): Show | 46 | HG00099.hp2 HG00639.hp2 HG01070.hp2 others(43): Show |
intron_variant | MODIFIER | c.36+4438delA | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 1/26 | chr11 | 17539833 | ||||||
chr11:17539833
|
CTT | C | 147 | a0001c0001t0001g0016a0001c0001t0001g0203a0001c0001t0001g0212others(144): Show | 167 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(164): Show |
intron_variant | MODIFIER | c.36+4437_36+4438del others(2): Show |
USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 1/26 | chr11 | 17539833 | ||||||
chr11:17539836
|
T | C | 7 | a0001c0003t0004g0030a0001c0003t0006g0031a0001c0021t0002g0162others(4): Show | 7 | HG01884.hp1 HG02258.hp2 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.36+4436A>G | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 1/26 | chr11 | 17539836 | ||||||
chr11:17539913
|
G | A | 7 | a0001c0003t0004g0030a0001c0003t0006g0031a0001c0021t0002g0162others(4): Show | 7 | HG01884.hp1 HG02258.hp2 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.36+4359C>T | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 1/26 | chr11 | 17539913 | ||||||
chr11:17540032
|
A | C | 2 | a0001c0003t0001g0043a0001c0003t0005g0042 | 2 | HG00639.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.36+4240T>G | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 1/26 | chr11 | 17540032 | ||||||
chr11:17540189
|
T | C | 7 | a0001c0003t0004g0030a0001c0003t0006g0031a0001c0021t0002g0162others(4): Show | 7 | HG01884.hp1 HG02258.hp2 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.36+4083A>G | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 1/26 | chr11 | 17540189 | ||||||
chr11:17540349
|
G | A | 146 | a0001c0001t0001g0016a0001c0001t0001g0148a0001c0001t0001g0203others(143): Show | 166 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(163): Show |
intron_variant | MODIFIER | c.36+3923C>T | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 1/26 | chr11 | 17540349 | ||||||
chr11:17540411
|
C | A | 4 | a0001c0007t0001g0192a0001c0007t0001g0193a0001c0007t0001g0194others(1): Show | 4 | HG03490.hp1 NA18942.hp2 NA19057.hp2 others(1): Show |
intron_variant | MODIFIER | c.36+3861G>T | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 1/26 | chr11 | 17540411 | ||||||
chr11:17540416
|
G | A | 1 | a0001c0018t0001g0149 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.36+3856C>T | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 1/26 | chr11 | 17540416 | ||||||
chr11:17540482
|
T | A | 4 | a0001c0042t0001g0033a0002c0005t0001g0036a0002c0015t0001g0035others(1): Show | 4 | HG01255.hp1 HG02486.hp2 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.36+3790A>T | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 1/26 | chr11 | 17540482 | ||||||
chr11:17540566
|
G | A | 152 | a0001c0001t0001g0016a0001c0001t0001g0203a0001c0001t0001g0212others(149): Show | 173 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(170): Show |
intron_variant | MODIFIER | c.36+3706C>T | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 1/26 | chr11 | 17540566 | ||||||
chr11:17540576
|
T | TA | 3 | a0001c0003t0001g0043a0001c0003t0004g0028a0001c0003t0005g0042 | 3 | HG00639.hp2 HG02559.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.36+3695dupT | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 1/26 | chr11 | 17540576 | ||||||
chr11:17541021
|
G | A | 36 | a0001c0001t0001g0166a0001c0001t0001g0167a0001c0001t0001g0184others(33): Show | 36 | HG00099.hp2 HG01070.hp2 HG01243.hp1 others(33): Show |
intron_variant | MODIFIER | c.36+3251C>T | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 1/26 | chr11 | 17541021 | ||||||
chr11:17541089
|
T | A | 7 | a0001c0003t0004g0030a0001c0003t0006g0031a0001c0021t0002g0162others(4): Show | 7 | HG01884.hp1 HG02258.hp2 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.36+3183A>T | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 1/26 | chr11 | 17541089 | ||||||
chr11:17541091
|
T | C | 195 | a0001c0001t0001g0016a0001c0001t0001g0166a0001c0001t0001g0167others(192): Show | 216 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(213): Show |
intron_variant | MODIFIER | c.36+3181A>G | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 1/26 | chr11 | 17541091 | ||||||
chr11:17541102
|
T | C | 1 | a0002c0006t0002g0313 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.36+3170A>G | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 1/26 | chr11 | 17541102 | ||||||
chr11:17541144
|
T | A | 2 | a0001c0017t0001g0314a0001c0017t0001g0315 | 2 | HG02572.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.36+3128A>T | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 1/26 | chr11 | 17541144 | ||||||
chr11:17541175
|
C | T | 204 | a0001c0001t0001g0016a0001c0001t0001g0154a0001c0001t0001g0166others(201): Show | 226 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(223): Show |
intron_variant | MODIFIER | c.36+3097G>A | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 1/26 | chr11 | 17541175 | ||||||
chr11:17541337
|
A | G | 1 | a0005c0035t0004g0032 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.36+2935T>C | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 1/26 | chr11 | 17541337 | ||||||
chr11:17541399
|
A | G | 1 | a0001c0001t0001g0041 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.36+2873T>C | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 1/26 | chr11 | 17541399 | ||||||
chr11:17541407
|
C | G | 1 | a0002c0002t0002g0040 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.36+2865G>C | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 1/26 | chr11 | 17541407 | ||||||
chr11:17541488
|
C | G | 3 | a0001c0021t0001g0163a0002c0020t0001g0158a0002c0020t0002g0157 | 3 | HG02280.hp2 HG03225.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.36+2784G>C | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 1/26 | chr11 | 17541488 | ||||||
chr11:17541561
|
A | G | 197 | a0001c0001t0001g0016a0001c0001t0001g0166a0001c0001t0001g0167others(194): Show | 218 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(215): Show |
intron_variant | MODIFIER | c.36+2711T>C | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 1/26 | chr11 | 17541561 | ||||||
chr11:17541563
|
C | T | 4 | a0001c0042t0001g0033a0002c0005t0001g0036a0002c0015t0001g0035others(1): Show | 4 | HG01255.hp1 HG02486.hp2 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.36+2709G>A | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 1/26 | chr11 | 17541563 | ||||||
chr11:17541597
|
C | T | 1 | a0001c0004t0001g0199 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.36+2675G>A | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 1/26 | chr11 | 17541597 | ||||||
chr11:17541714
|
C | T | 2 | a0002c0015t0002g0319a0002c0019t0002g0025 | 3 | HG02145.hp1 HG02647.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.36+2558G>A | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 1/26 | chr11 | 17541714 | ||||||
chr11:17541856
|
C | T | 7 | a0001c0003t0004g0030a0001c0003t0006g0031a0001c0021t0002g0162others(4): Show | 7 | HG01884.hp1 HG02258.hp2 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.36+2416G>A | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 1/26 | chr11 | 17541856 | ||||||
chr11:17541912
|
C | T | 1 | a0001c0003t0001g0198 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.36+2360G>A | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 1/26 | chr11 | 17541912 | ||||||
chr11:17541942
|
T | C | 195 | a0001c0001t0001g0016a0001c0001t0001g0166a0001c0001t0001g0167others(192): Show | 216 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(213): Show |
intron_variant | MODIFIER | c.36+2330A>G | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 1/26 | chr11 | 17541942 | ||||||
chr11:17542094
|
T | C | 2 | a0002c0009t0001g0317a0002c0009t0002g0318 | 2 | HG02135.hp1 HG02165.hp2 |
intron_variant | MODIFIER | c.36+2178A>G | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 1/26 | chr11 | 17542094 | ||||||
chr11:17542146
|
A | G | 1 | a0001c0001t0001g0039 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.36+2126T>C | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 1/26 | chr11 | 17542146 | ||||||
chr11:17542231
|
G | T | 1 | a0001c0004t0001g0038 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.36+2041C>A | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 1/26 | chr11 | 17542231 | ||||||
chr11:17542387
|
G | A | 2 | a0002c0015t0002g0319a0002c0019t0002g0025 | 3 | HG02145.hp1 HG02647.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.36+1885C>T | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 1/26 | chr11 | 17542387 | ||||||
chr11:17542389
|
G | A | 36 | a0001c0001t0001g0166a0001c0001t0001g0167a0001c0001t0001g0184others(33): Show | 36 | HG00099.hp2 HG01070.hp2 HG01243.hp1 others(33): Show |
intron_variant | MODIFIER | c.36+1883C>T | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 1/26 | chr11 | 17542389 | ||||||
chr11:17542633
|
C | T | 2 | a0001c0001t0011g0027a0002c0044t0001g0197 | 2 | HG02109.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.36+1639G>A | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 1/26 | chr11 | 17542633 | ||||||
chr11:17542767
|
T | C | 1 | a0001c0003t0001g0320 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.36+1505A>G | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 1/26 | chr11 | 17542767 | ||||||
chr11:17542939
|
A | G | 195 | a0001c0001t0001g0016a0001c0001t0001g0166a0001c0001t0001g0167others(192): Show | 216 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(213): Show |
intron_variant | MODIFIER | c.36+1333T>C | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 1/26 | chr11 | 17542939 | ||||||
chr11:17543262
|
T | C | 7 | a0001c0001t0001g0154a0001c0003t0001g0150a0001c0003t0001g0151others(4): Show | 8 | HG00323.hp2 HG00738.hp2 HG00741.hp1 others(5): Show |
intron_variant | MODIFIER | c.36+1010A>G | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 1/26 | chr11 | 17543262 | ||||||
chr11:17543267
|
T | C | 194 | a0001c0001t0001g0016a0001c0001t0001g0166a0001c0001t0001g0167others(191): Show | 215 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(212): Show |
intron_variant | MODIFIER | c.36+1005A>G | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 1/26 | chr11 | 17543267 | ||||||
chr11:17543289
|
G | C | 1 | a0005c0035t0004g0032 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.36+983C>G | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 1/26 | chr11 | 17543289 | ||||||
chr11:17543296
|
C | T | 2 | a0002c0020t0001g0158a0002c0020t0002g0157 | 2 | HG02280.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.36+976G>A | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 1/26 | chr11 | 17543296 | ||||||
chr11:17543416
|
AC | A | 193 | a0001c0001t0001g0016a0001c0001t0001g0166a0001c0001t0001g0167others(190): Show | 214 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(211): Show |
intron_variant | MODIFIER | c.36+855delG | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 1/26 | chr11 | 17543416 | ||||||
chr11:17543423
|
C | A | 1 | a0001c0007t0001g0321 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.36+849G>T | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 1/26 | chr11 | 17543423 | ||||||
chr11:17543423
|
C | T | 4 | a0001c0042t0001g0033a0002c0005t0001g0036a0002c0015t0001g0035others(1): Show | 4 | HG01255.hp1 HG02486.hp2 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.36+849G>A | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 1/26 | chr11 | 17543423 | ||||||
chr11:17543429
|
G | A | 3 | a0001c0003t0004g0030a0001c0003t0006g0031a0005c0035t0004g0032 | 3 | HG02258.hp2 HG03486.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.36+843C>T | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 1/26 | chr11 | 17543429 | ||||||
chr11:17543462
|
CTTGGTGG others(5): Show |
C | 1 | a0002c0006t0002g0322 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.36+798_36+809delCT others(10): Show |
USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 1/26 | chr11 | 17543462 | ||||||
chr11:17543640
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G | A | 36 | a0001c0001t0001g0166a0001c0001t0001g0167a0001c0001t0001g0184others(33): Show | 36 | HG00099.hp2 HG01070.hp2 HG01243.hp1 others(33): Show |
intron_variant | MODIFIER | c.36+632C>T | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 1/26 | chr11 | 17543640 | ||||||
chr11:17543671
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C | T | 5 | a0001c0003t0004g0028a0001c0003t0004g0030a0001c0003t0006g0031others(2): Show | 5 | HG02258.hp2 HG02976.hp2 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.36+601G>A | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 1/26 | chr11 | 17543671 | ||||||
chr11:17543688
|
C | T | 4 | a0001c0042t0001g0033a0002c0005t0001g0036a0002c0015t0001g0035others(1): Show | 4 | HG01255.hp1 HG02486.hp2 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.36+584G>A | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 1/26 | chr11 | 17543688 | ||||||
chr11:17543919
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T | A | 1 | a0001c0047t0001g0196 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.36+353A>T | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 1/26 | chr11 | 17543919 | ||||||
chr11:17544058
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G | A | 145 | a0001c0001t0001g0016a0001c0001t0001g0203a0001c0001t0001g0212others(142): Show | 166 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(163): Show |
intron_variant | MODIFIER | c.36+214C>T | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 1/26 | chr11 | 17544058 | ||||||
chr11:17544086
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C | A | 2 | a0001c0003t0001g0323a0001c0003t0001g0324 | 2 | HG02155.hp2 NA18983.hp1 |
intron_variant | MODIFIER | c.36+186G>T | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 1/26 | chr11 | 17544086 |