Item | Value |
---|---|
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 | 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 | MDRKV others(894): Show |
chr11 | 17488900 | 17549416 |
a0002 | 0/0 | 899 | 128 | 30 | 22 | 50 | 8 | 18 | 37 | USH1C_chr11_17488900_17549416 | USH1C | MDRKV others(894): Show |
chr11 | 17488900 | 17549416 |
a0003 | 0/0 | 899 | 5 | 4 | 1 | 0 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | MDRKV others(894): Show |
chr11 | 17488900 | 17549416 |
a0004 | 0/0 | 899 | 3 | 2 | 1 | 0 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | MDRKV others(894): Show |
chr11 | 17488900 | 17549416 |
a0005 | 0/0 | 899 | 2 | 1 | 1 | 0 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | MDRKV others(894): Show |
chr11 | 17488900 | 17549416 |
a0006 | 0/0 | 899 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | MDRKV others(894): Show |
chr11 | 17488900 | 17549416 |
a0007 | 0/0 | 899 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | MDRKV others(894): Show |
chr11 | 17488900 | 17549416 |
a0008 | 0/0 | 899 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | MDRKV others(894): Show |
chr11 | 17488900 | 17549416 |
a0009 | 0/0 | 899 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | MDRKV others(894): Show |
chr11 | 17488900 | 17549416 |
a0010 | 0/0 | 899 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | MDRKV others(894): Show |
chr11 | 17488900 | 17549416 |
a0011 | 0/0 | 899 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | USH1C_chr11_17488900_17549416 | USH1C | MDRKV others(894): Show |
chr11 | 17488900 | 17549416 |
a0012 | 0/0 | 899 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | MDRKV others(894): Show |
chr11 | 17488900 | 17549416 |
a0013 | 0/0 | 899 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | MDRKV others(894): Show |
chr11 | 17488900 | 17549416 |
a0014 | 0/0 | 899 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | MDRKV others(894): Show |
chr11 | 17488900 | 17549416 |
a0015 | 0/0 | 899 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | USH1C_chr11_17488900_17549416 | USH1C | MDRKV others(894): Show |
chr11 | 17488900 | 17549416 |
a0016 | 0/0 | 899 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | MDRKV others(894): Show |
chr11 | 17488900 | 17549416 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 0/0 | 2697 | 102 | 18 | 23 | 52 | 3 | 6 | USH1C_chr11_17488900_17549416 | USH1C | ATGGA others(2692): Show |
chr11 | 17488900 | 17549416 | ||
a0001c0003 | 0/0 | 2697 | 39 | 19 | 7 | 10 | 0 | 3 | USH1C_chr11_17488900_17549416 | USH1C | ATGGA others(2692): Show |
chr11 | 17488900 | 17549416 | ||
a0001c0004 | 0/0 | 2697 | 26 | 0 | 4 | 20 | 1 | 1 | USH1C_chr11_17488900_17549416 | USH1C | ATGGA others(2692): Show |
chr11 | 17488900 | 17549416 | ||
a0001c0007 | 0/0 | 2697 | 12 | 0 | 2 | 7 | 0 | 3 | USH1C_chr11_17488900_17549416 | USH1C | ATGGA others(2692): Show |
chr11 | 17488900 | 17549416 | ||
a0001c0008 | 0/0 | 2697 | 11 | 1 | 2 | 6 | 0 | 2 | USH1C_chr11_17488900_17549416 | USH1C | ATGGA others(2692): Show |
chr11 | 17488900 | 17549416 | ||
a0001c0013 | 0/0 | 2697 | 4 | 0 | 0 | 4 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | ATGGA others(2692): Show |
chr11 | 17488900 | 17549416 | ||
a0001c0016 | 0/0 | 2697 | 2 | 0 | 0 | 2 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | ATGGA others(2692): Show |
chr11 | 17488900 | 17549416 | ||
a0001c0017 | 0/0 | 2697 | 2 | 2 | 0 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | ATGGA others(2692): Show |
chr11 | 17488900 | 17549416 | ||
a0001c0018 | 0/0 | 2697 | 2 | 0 | 0 | 1 | 0 | 1 | USH1C_chr11_17488900_17549416 | USH1C | ATGGA others(2692): Show |
chr11 | 17488900 | 17549416 | ||
a0001c0021 | 0/0 | 2697 | 2 | 2 | 0 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | ATGGA others(2692): Show |
chr11 | 17488900 | 17549416 | ||
a0001c0023 | 0/0 | 2697 | 1 | 0 | 0 | 1 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | ATGGA others(2692): Show |
chr11 | 17488900 | 17549416 | ||
a0001c0024 | 0/0 | 2697 | 1 | 0 | 0 | 0 | 0 | 1 | USH1C_chr11_17488900_17549416 | USH1C | ATGGA others(2692): Show |
chr11 | 17488900 | 17549416 | ||
a0001c0028 | 0/0 | 2697 | 1 | 0 | 0 | 1 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | ATGGA others(2692): Show |
chr11 | 17488900 | 17549416 | ||
a0001c0037 | 0/0 | 2697 | 1 | 0 | 0 | 1 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | ATGGA others(2692): Show |
chr11 | 17488900 | 17549416 | ||
a0001c0039 | 0/0 | 2697 | 1 | 0 | 0 | 1 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | ATGGA others(2692): Show |
chr11 | 17488900 | 17549416 | ||
a0001c0040 | 0/0 | 2697 | 1 | 0 | 0 | 1 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | ATGGA others(2692): Show |
chr11 | 17488900 | 17549416 | ||
a0001c0042 | 0/0 | 2697 | 1 | 0 | 1 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | ATGGA others(2692): Show |
chr11 | 17488900 | 17549416 | ||
a0001c0043 | 0/0 | 2697 | 1 | 1 | 0 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | ATGGA others(2692): Show |
chr11 | 17488900 | 17549416 | ||
a0001c0047 | 0/0 | 2697 | 1 | 1 | 0 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | ATGGA others(2692): Show |
chr11 | 17488900 | 17549416 | ||
a0002c0002 | 0/0 | 2697 | 46 | 2 | 11 | 21 | 4 | 8 | USH1C_chr11_17488900_17549416 | USH1C | ATGGA others(2692): Show |
chr11 | 17488900 | 17549416 | ||
a0002c0005 | 0/0 | 2697 | 25 | 18 | 3 | 2 | 0 | 2 | USH1C_chr11_17488900_17549416 | USH1C | ATGGA others(2692): Show |
chr11 | 17488900 | 17549416 | ||
a0002c0006 | 0/0 | 2697 | 22 | 0 | 6 | 10 | 1 | 5 | USH1C_chr11_17488900_17549416 | USH1C | ATGGA others(2692): Show |
chr11 | 17488900 | 17549416 | ||
a0002c0009 | 0/0 | 2697 | 9 | 0 | 0 | 9 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | ATGGA others(2692): Show |
chr11 | 17488900 | 17549416 | ||
a0002c0010 | 0/0 | 2697 | 9 | 0 | 2 | 5 | 2 | 0 | USH1C_chr11_17488900_17549416 | USH1C | ATGGA others(2692): Show |
chr11 | 17488900 | 17549416 | ||
a0002c0012 | 0/0 | 2697 | 5 | 1 | 0 | 0 | 1 | 3 | USH1C_chr11_17488900_17549416 | USH1C | ATGGA others(2692): Show |
chr11 | 17488900 | 17549416 | ||
a0002c0015 | 0/0 | 2697 | 3 | 3 | 0 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | ATGGA others(2692): Show |
chr11 | 17488900 | 17549416 | ||
a0002c0019 | 0/0 | 2697 | 2 | 2 | 0 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | ATGGA others(2692): Show |
chr11 | 17488900 | 17549416 | ||
a0002c0020 | 0/0 | 2697 | 2 | 2 | 0 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | ATGGA others(2692): Show |
chr11 | 17488900 | 17549416 | ||
a0002c0027 | 0/0 | 2697 | 1 | 0 | 0 | 1 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | ATGGA others(2692): Show |
chr11 | 17488900 | 17549416 | ||
a0002c0031 | 0/0 | 2697 | 1 | 0 | 0 | 1 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | ATGGA others(2692): Show |
chr11 | 17488900 | 17549416 | ||
a0002c0036 | 0/0 | 2697 | 1 | 0 | 0 | 1 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | ATGGA others(2692): Show |
chr11 | 17488900 | 17549416 | ||
a0002c0044 | 0/0 | 2697 | 1 | 1 | 0 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | ATGGA others(2692): Show |
chr11 | 17488900 | 17549416 | ||
a0002c0046 | 0/0 | 2697 | 1 | 1 | 0 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | ATGGA others(2692): Show |
chr11 | 17488900 | 17549416 | ||
a0003c0011 | 0/0 | 2697 | 5 | 4 | 1 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | ATGGA others(2692): Show |
chr11 | 17488900 | 17549416 | ||
a0004c0014 | 0/0 | 2697 | 3 | 2 | 1 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | ATGGA others(2692): Show |
chr11 | 17488900 | 17549416 | ||
a0005c0035 | 0/0 | 2697 | 1 | 1 | 0 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | ATGGA others(2692): Show |
chr11 | 17488900 | 17549416 | ||
a0005c0038 | 0/0 | 2697 | 1 | 0 | 1 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | ATGGA others(2692): Show |
chr11 | 17488900 | 17549416 | ||
a0006c0034 | 0/0 | 2697 | 1 | 0 | 1 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | ATGGA others(2692): Show |
chr11 | 17488900 | 17549416 | ||
a0007c0030 | 0/0 | 2697 | 1 | 0 | 1 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | ATGGA others(2692): Show |
chr11 | 17488900 | 17549416 | ||
a0008c0048 | 0/0 | 2697 | 1 | 1 | 0 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | ATGGA others(2692): Show |
chr11 | 17488900 | 17549416 | ||
a0009c0045 | 0/0 | 2697 | 1 | 1 | 0 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | ATGGA others(2692): Show |
chr11 | 17488900 | 17549416 | ||
a0010c0025 | 0/0 | 2697 | 1 | 1 | 0 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | ATGGA others(2692): Show |
chr11 | 17488900 | 17549416 | ||
a0011c0041 | 0/0 | 2697 | 1 | 0 | 0 | 0 | 0 | 1 | USH1C_chr11_17488900_17549416 | USH1C | ATGGA others(2692): Show |
chr11 | 17488900 | 17549416 | ||
a0012c0022 | 0/0 | 2697 | 1 | 1 | 0 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | ATGGA others(2692): Show |
chr11 | 17488900 | 17549416 | ||
a0013c0032 | 0/0 | 2697 | 1 | 1 | 0 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | ATGGA others(2692): Show |
chr11 | 17488900 | 17549416 | ||
a0014c0033 | 0/0 | 2697 | 1 | 1 | 0 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | ATGGA others(2692): Show |
chr11 | 17488900 | 17549416 | ||
a0015c0026 | 0/0 | 2697 | 1 | 0 | 0 | 1 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | ATGGA others(2692): Show |
chr11 | 17488900 | 17549416 | ||
a0016c0029 | 0/0 | 2697 | 1 | 1 | 0 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | ATGGA others(2692): Show |
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 | AGCTC others(3240): Show |
chr11 | 17488900 | 17549416 |
a0001c0001t0002 | 0/0 | 3245 | 2 | 0 | 2 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | AGCTC others(3240): Show |
chr11 | 17488900 | 17549416 |
a0001c0001t0003 | 0/0 | 3241 | 4 | 1 | 1 | 2 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | AGCTC others(3236): Show |
chr11 | 17488900 | 17549416 |
a0001c0001t0008 | 0/0 | 3245 | 1 | 1 | 0 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | AGCTC others(3240): Show |
chr11 | 17488900 | 17549416 |
a0001c0001t0009 | 0/0 | 3241 | 2 | 2 | 0 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | AGCTC others(3236): Show |
chr11 | 17488900 | 17549416 |
a0001c0001t0011 | 0/0 | 3245 | 1 | 1 | 0 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | AGCTC others(3240): Show |
chr11 | 17488900 | 17549416 |
a0001c0001t0014 | 0/0 | 3245 | 1 | 0 | 0 | 1 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | AGCTC others(3240): Show |
chr11 | 17488900 | 17549416 |
a0001c0003t0001 | 0/0 | 3245 | 30 | 13 | 5 | 10 | 0 | 2 | USH1C_chr11_17488900_17549416 | USH1C | AGCTC others(3240): Show |
chr11 | 17488900 | 17549416 |
a0001c0003t0002 | 0/0 | 3245 | 1 | 1 | 0 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | AGCTC others(3240): Show |
chr11 | 17488900 | 17549416 |
a0001c0003t0003 | 0/0 | 3241 | 3 | 0 | 2 | 0 | 0 | 1 | USH1C_chr11_17488900_17549416 | USH1C | AGCTC others(3236): Show |
chr11 | 17488900 | 17549416 |
a0001c0003t0004 | 0/0 | 3245 | 2 | 2 | 0 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | AGCTC others(3240): Show |
chr11 | 17488900 | 17549416 |
a0001c0003t0005 | 0/0 | 3245 | 1 | 1 | 0 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | AGCTC others(3240): Show |
chr11 | 17488900 | 17549416 |
a0001c0003t0006 | 0/0 | 3245 | 1 | 1 | 0 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | AGCTC others(3240): Show |
chr11 | 17488900 | 17549416 |
a0001c0003t0008 | 0/0 | 3245 | 1 | 1 | 0 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | AGCTC others(3240): Show |
chr11 | 17488900 | 17549416 |
a0001c0004t0001 | 0/0 | 3245 | 22 | 0 | 4 | 16 | 1 | 1 | USH1C_chr11_17488900_17549416 | USH1C | AGCTC others(3240): Show |
chr11 | 17488900 | 17549416 |
a0001c0004t0002 | 0/0 | 3245 | 1 | 0 | 0 | 1 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | AGCTC others(3240): Show |
chr11 | 17488900 | 17549416 |
a0001c0004t0003 | 0/0 | 3241 | 3 | 0 | 0 | 3 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | AGCTC others(3236): Show |
chr11 | 17488900 | 17549416 |
a0001c0007t0001 | 0/0 | 3245 | 10 | 0 | 2 | 5 | 0 | 3 | USH1C_chr11_17488900_17549416 | USH1C | AGCTC others(3240): Show |
chr11 | 17488900 | 17549416 |
a0001c0007t0003 | 0/0 | 3241 | 2 | 0 | 0 | 2 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | AGCTC others(3236): Show |
chr11 | 17488900 | 17549416 |
a0001c0008t0001 | 0/0 | 3245 | 11 | 1 | 2 | 6 | 0 | 2 | USH1C_chr11_17488900_17549416 | USH1C | AGCTC others(3240): Show |
chr11 | 17488900 | 17549416 |
a0001c0013t0001 | 0/0 | 3245 | 3 | 0 | 0 | 3 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | AGCTC others(3240): Show |
chr11 | 17488900 | 17549416 |
a0001c0013t0010 | 0/0 | 3245 | 1 | 0 | 0 | 1 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | AGCTC others(3240): Show |
chr11 | 17488900 | 17549416 |
a0001c0016t0001 | 0/0 | 3245 | 2 | 0 | 0 | 2 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | AGCTC others(3240): Show |
chr11 | 17488900 | 17549416 |
a0001c0017t0001 | 0/0 | 3245 | 2 | 2 | 0 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | AGCTC others(3240): Show |
chr11 | 17488900 | 17549416 |
a0001c0018t0001 | 0/0 | 3245 | 1 | 0 | 0 | 0 | 0 | 1 | USH1C_chr11_17488900_17549416 | USH1C | AGCTC others(3240): Show |
chr11 | 17488900 | 17549416 |
a0001c0018t0015 | 0/0 | 3245 | 1 | 0 | 0 | 1 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | AGCTC others(3240): Show |
chr11 | 17488900 | 17549416 |
a0001c0021t0001 | 0/0 | 3245 | 1 | 1 | 0 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | AGCTC others(3240): Show |
chr11 | 17488900 | 17549416 |
a0001c0021t0002 | 0/0 | 3245 | 1 | 1 | 0 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | AGCTC others(3240): Show |
chr11 | 17488900 | 17549416 |
a0001c0023t0017 | 0/0 | 3245 | 1 | 0 | 0 | 1 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | AGCTC others(3240): Show |
chr11 | 17488900 | 17549416 |
a0001c0024t0001 | 0/0 | 3245 | 1 | 0 | 0 | 0 | 0 | 1 | USH1C_chr11_17488900_17549416 | USH1C | AGCTC others(3240): Show |
chr11 | 17488900 | 17549416 |
a0001c0028t0003 | 0/0 | 3241 | 1 | 0 | 0 | 1 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | AGCTC others(3236): Show |
chr11 | 17488900 | 17549416 |
a0001c0037t0001 | 0/0 | 3245 | 1 | 0 | 0 | 1 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | AGCTC others(3240): Show |
chr11 | 17488900 | 17549416 |
a0001c0039t0001 | 0/0 | 3245 | 1 | 0 | 0 | 1 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | AGCTC others(3240): Show |
chr11 | 17488900 | 17549416 |
a0001c0040t0001 | 0/0 | 3245 | 1 | 0 | 0 | 1 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | AGCTC others(3240): Show |
chr11 | 17488900 | 17549416 |
a0001c0042t0001 | 0/0 | 3245 | 1 | 0 | 1 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | AGCTC others(3240): Show |
chr11 | 17488900 | 17549416 |
a0001c0043t0006 | 0/0 | 3245 | 1 | 1 | 0 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | AGCTC others(3240): Show |
chr11 | 17488900 | 17549416 |
a0001c0047t0001 | 0/0 | 3245 | 1 | 1 | 0 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | AGCTC others(3240): Show |
chr11 | 17488900 | 17549416 |
a0002c0002t0001 | 0/0 | 3245 | 4 | 1 | 1 | 0 | 2 | 0 | USH1C_chr11_17488900_17549416 | USH1C | AGCTC others(3240): Show |
chr11 | 17488900 | 17549416 |
a0002c0002t0002 | 0/0 | 3245 | 39 | 1 | 10 | 18 | 2 | 8 | USH1C_chr11_17488900_17549416 | USH1C | AGCTC others(3240): Show |
chr11 | 17488900 | 17549416 |
a0002c0002t0003 | 0/0 | 3241 | 1 | 0 | 0 | 1 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | AGCTC others(3236): Show |
chr11 | 17488900 | 17549416 |
a0002c0002t0007 | 0/0 | 3245 | 2 | 0 | 0 | 2 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | AGCTC others(3240): Show |
chr11 | 17488900 | 17549416 |
a0002c0005t0001 | 0/0 | 3245 | 8 | 8 | 0 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | AGCTC others(3240): Show |
chr11 | 17488900 | 17549416 |
a0002c0005t0002 | 0/0 | 3245 | 16 | 10 | 2 | 2 | 0 | 2 | USH1C_chr11_17488900_17549416 | USH1C | AGCTC others(3240): Show |
chr11 | 17488900 | 17549416 |
a0002c0005t0013 | 0/0 | 3245 | 1 | 0 | 1 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | AGCTC others(3240): Show |
chr11 | 17488900 | 17549416 |
a0002c0006t0001 | 0/0 | 3245 | 5 | 0 | 4 | 0 | 0 | 1 | USH1C_chr11_17488900_17549416 | USH1C | AGCTC others(3240): Show |
chr11 | 17488900 | 17549416 |
a0002c0006t0002 | 0/0 | 3245 | 17 | 0 | 2 | 10 | 1 | 4 | USH1C_chr11_17488900_17549416 | USH1C | AGCTC others(3240): Show |
chr11 | 17488900 | 17549416 |
a0002c0009t0001 | 0/0 | 3245 | 1 | 0 | 0 | 1 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | AGCTC others(3240): Show |
chr11 | 17488900 | 17549416 |
a0002c0009t0002 | 0/0 | 3245 | 8 | 0 | 0 | 8 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | AGCTC others(3240): Show |
chr11 | 17488900 | 17549416 |
a0002c0010t0001 | 0/0 | 3245 | 2 | 0 | 2 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | AGCTC others(3240): Show |
chr11 | 17488900 | 17549416 |
a0002c0010t0002 | 0/0 | 3245 | 7 | 0 | 0 | 5 | 2 | 0 | USH1C_chr11_17488900_17549416 | USH1C | AGCTC others(3240): Show |
chr11 | 17488900 | 17549416 |
a0002c0012t0001 | 0/0 | 3245 | 4 | 1 | 0 | 0 | 1 | 2 | USH1C_chr11_17488900_17549416 | USH1C | AGCTC others(3240): Show |
chr11 | 17488900 | 17549416 |
a0002c0012t0012 | 0/0 | 3245 | 1 | 0 | 0 | 0 | 0 | 1 | USH1C_chr11_17488900_17549416 | USH1C | AGCTC others(3240): Show |
chr11 | 17488900 | 17549416 |
a0002c0015t0001 | 0/0 | 3245 | 1 | 1 | 0 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | AGCTC others(3240): Show |
chr11 | 17488900 | 17549416 |
a0002c0015t0002 | 0/0 | 3245 | 2 | 2 | 0 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | AGCTC others(3240): Show |
chr11 | 17488900 | 17549416 |
a0002c0019t0002 | 0/0 | 3245 | 2 | 2 | 0 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | AGCTC others(3240): Show |
chr11 | 17488900 | 17549416 |
a0002c0020t0001 | 0/0 | 3245 | 1 | 1 | 0 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | AGCTC others(3240): Show |
chr11 | 17488900 | 17549416 |
a0002c0020t0002 | 0/0 | 3245 | 1 | 1 | 0 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | AGCTC others(3240): Show |
chr11 | 17488900 | 17549416 |
a0002c0027t0001 | 0/0 | 3245 | 1 | 0 | 0 | 1 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | AGCTC others(3240): Show |
chr11 | 17488900 | 17549416 |
a0002c0031t0002 | 0/0 | 3245 | 1 | 0 | 0 | 1 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | AGCTC others(3240): Show |
chr11 | 17488900 | 17549416 |
a0002c0036t0002 | 0/0 | 3245 | 1 | 0 | 0 | 1 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | AGCTC others(3240): Show |
chr11 | 17488900 | 17549416 |
a0002c0044t0001 | 0/0 | 3245 | 1 | 1 | 0 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | AGCTC others(3240): Show |
chr11 | 17488900 | 17549416 |
a0002c0046t0002 | 0/0 | 3245 | 1 | 1 | 0 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | AGCTC others(3240): Show |
chr11 | 17488900 | 17549416 |
a0003c0011t0001 | 0/0 | 3245 | 3 | 3 | 0 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | AGCTC others(3240): Show |
chr11 | 17488900 | 17549416 |
a0003c0011t0002 | 0/0 | 3245 | 2 | 1 | 1 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | AGCTC others(3240): Show |
chr11 | 17488900 | 17549416 |
a0004c0014t0001 | 0/0 | 3245 | 1 | 1 | 0 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | AGCTC others(3240): Show |
chr11 | 17488900 | 17549416 |
a0004c0014t0005 | 0/0 | 3245 | 2 | 1 | 1 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | AGCTC others(3240): Show |
chr11 | 17488900 | 17549416 |
a0005c0035t0004 | 0/0 | 3245 | 1 | 1 | 0 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | AGCTC others(3240): Show |
chr11 | 17488900 | 17549416 |
a0005c0038t0001 | 0/0 | 3245 | 1 | 0 | 1 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | AGCTC others(3240): Show |
chr11 | 17488900 | 17549416 |
a0006c0034t0002 | 0/0 | 3245 | 1 | 0 | 1 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | AGCTC others(3240): Show |
chr11 | 17488900 | 17549416 |
a0007c0030t0001 | 0/0 | 3245 | 1 | 0 | 1 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | AGCTC others(3240): Show |
chr11 | 17488900 | 17549416 |
a0008c0048t0001 | 0/0 | 3245 | 1 | 1 | 0 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | AGCTC others(3240): Show |
chr11 | 17488900 | 17549416 |
a0009c0045t0016 | 0/0 | 3241 | 1 | 1 | 0 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | AGCTC others(3236): Show |
chr11 | 17488900 | 17549416 |
a0010c0025t0001 | 0/0 | 3245 | 1 | 1 | 0 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | AGCTC others(3240): Show |
chr11 | 17488900 | 17549416 |
a0011c0041t0001 | 0/0 | 3245 | 1 | 0 | 0 | 0 | 0 | 1 | USH1C_chr11_17488900_17549416 | USH1C | AGCTC others(3240): Show |
chr11 | 17488900 | 17549416 |
a0012c0022t0002 | 0/0 | 3245 | 1 | 1 | 0 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | AGCTC others(3240): Show |
chr11 | 17488900 | 17549416 |
a0013c0032t0002 | 0/0 | 3245 | 1 | 1 | 0 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | AGCTC others(3240): Show |
chr11 | 17488900 | 17549416 |
a0014c0033t0001 | 0/0 | 3245 | 1 | 1 | 0 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | AGCTC others(3240): Show |
chr11 | 17488900 | 17549416 |
a0015c0026t0002 | 0/0 | 3245 | 1 | 0 | 0 | 1 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | AGCTC others(3240): Show |
chr11 | 17488900 | 17549416 |
a0016c0029t0001 | 0/0 | 3245 | 1 | 1 | 0 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | AGCTC others(3240): Show |
chr11 | 17488900 | 17549416 |
actghapid | grch38/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 |
a0001c0001t0001g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
a0001c0001t0001g0010 | 0/0 | 2 | 0 | 0 | 2 | 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 |
a0001c0001t0001g0012 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
a0001c0001t0001g0017 | 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 |
a0001c0001t0001g0049 | 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 |
a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 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 |
a0001c0001t0001g0084 | 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 |
a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
a0001c0001t0001g0099 | 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 |
a0001c0001t0001g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
a0001c0001t0001g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
a0001c0001t0001g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
a0001c0001t0001g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 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 | 0 | 0 | 1 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
a0001c0001t0001g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
a0001c0001t0001g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
a0001c0001t0001g0135 | 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 |
a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
a0001c0001t0001g0145 | 0/0 | 1 | 0 | 1 | 0 | 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 |
a0001c0001t0001g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
a0001c0001t0001g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
a0001c0001t0001g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
a0001c0001t0001g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
a0001c0001t0001g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
a0001c0001t0001g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
a0001c0001t0001g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
a0001c0001t0001g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
a0001c0001t0001g0243 | 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 |
a0001c0001t0001g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
a0001c0001t0001g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
a0001c0001t0001g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
a0001c0001t0001g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
a0001c0001t0001g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
a0001c0001t0001g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
a0001c0001t0001g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
a0001c0001t0001g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
a0001c0001t0001g0301 | 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 |
a0001c0001t0002g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
a0001c0001t0002g0216 | 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 |
a0001c0001t0003g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
a0001c0001t0003g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
a0001c0001t0003g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
a0001c0001t0008g0227 | 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 |
a0001c0001t0009g0121 | 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 |
a0001c0003t0001g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
a0001c0003t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
a0001c0003t0001g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
a0001c0003t0001g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
a0001c0003t0001g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
a0001c0003t0001g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
a0001c0003t0001g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
a0001c0003t0001g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
a0001c0003t0001g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
a0001c0003t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
a0001c0003t0001g0200 | 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 |
a0001c0003t0001g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
a0001c0003t0001g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
a0001c0003t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
a0001c0003t0001g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
a0001c0003t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
a0001c0003t0001g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
a0001c0003t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
a0001c0003t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
a0001c0003t0001g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
a0001c0003t0001g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
a0001c0003t0001g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
a0001c0003t0001g0293 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
a0001c0003t0001g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | 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 |
a0001c0003t0001g0321 | 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 |
a0001c0003t0003g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
a0001c0003t0003g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
a0001c0003t0003g0250 | 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 |
a0001c0003t0008g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
a0001c0004t0001g0004 | 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 |
a0001c0004t0001g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
a0001c0004t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
a0001c0004t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
a0001c0004t0001g0133 | 0/0 | 1 | 0 | 1 | 0 | 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 |
a0001c0004t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
a0001c0004t0001g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
a0001c0004t0001g0206 | 0/0 | 1 | 0 | 0 | 0 | 1 | 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 | 1 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
a0001c0004t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
a0001c0004t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
a0001c0004t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
a0001c0004t0001g0244 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
a0001c0004t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
a0001c0004t0001g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
a0001c0004t0001g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
a0001c0004t0002g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
a0001c0004t0003g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
a0001c0004t0003g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
a0001c0004t0003g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
a0001c0007t0001g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
a0001c0007t0001g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
a0001c0007t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
a0001c0007t0001g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
a0001c0007t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
a0001c0007t0001g0191 | 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 |
a0001c0007t0001g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
a0001c0007t0001g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
a0001c0007t0001g0318 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
a0001c0007t0003g0177 | 0/0 | 1 | 0 | 0 | 1 | 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 |
a0001c0008t0001g0006 | 0/0 | 3 | 0 | 2 | 1 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
a0001c0008t0001g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
a0001c0008t0001g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
a0001c0008t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | 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 |
a0001c0008t0001g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
a0001c0008t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
a0001c0008t0001g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
a0001c0008t0001g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
a0001c0013t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
a0001c0013t0001g0276 | 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 |
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 |
a0001c0016t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
a0001c0017t0001g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
a0001c0017t0001g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
a0001c0018t0001g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
a0001c0018t0015g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
a0001c0021t0001g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
a0001c0021t0002g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
a0001c0023t0017g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
a0001c0024t0001g0309 | 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 |
a0001c0037t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
a0001c0039t0001g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
a0001c0040t0001g0092 | 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 |
a0001c0047t0001g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
a0002c0002t0001g0101 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
a0002c0002t0001g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
a0002c0002t0001g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
a0002c0002t0001g0214 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
a0002c0002t0002g0002 | 0/0 | 5 | 0 | 0 | 0 | 0 | 5 | 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 |
a0002c0002t0002g0014 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
a0002c0002t0002g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
a0002c0002t0002g0020 | 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 |
a0002c0002t0002g0091 | 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 |
a0002c0002t0002g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
a0002c0002t0002g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
a0002c0002t0002g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
a0002c0002t0002g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
a0002c0002t0002g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
a0002c0002t0002g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
a0002c0002t0002g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
a0002c0002t0002g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
a0002c0002t0002g0183 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
a0002c0002t0002g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
a0002c0002t0002g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
a0002c0002t0002g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
a0002c0002t0002g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
a0002c0002t0002g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
a0002c0002t0002g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
a0002c0002t0002g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
a0002c0002t0003g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
a0002c0002t0007g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
a0002c0002t0007g0107 | 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 |
a0002c0005t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
a0002c0005t0001g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
a0002c0005t0001g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
a0002c0005t0001g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
a0002c0005t0001g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
a0002c0005t0001g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
a0002c0005t0002g0021 | 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 |
a0002c0005t0002g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
a0002c0005t0002g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
a0002c0005t0002g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
a0002c0005t0002g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
a0002c0005t0002g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
a0002c0005t0002g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
a0002c0005t0002g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
a0002c0005t0002g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
a0002c0005t0002g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
a0002c0005t0002g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
a0002c0005t0013g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
a0002c0006t0001g0007 | 0/0 | 3 | 0 | 2 | 0 | 0 | 1 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
a0002c0006t0001g0260 | 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 |
a0002c0006t0002g0003 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
a0002c0006t0002g0018 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
a0002c0006t0002g0019 | 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 |
a0002c0006t0002g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
a0002c0006t0002g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
a0002c0006t0002g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
a0002c0006t0002g0271 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
a0002c0006t0002g0285 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
a0002c0006t0002g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
a0002c0006t0002g0319 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
a0002c0009t0001g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
a0002c0009t0002g0008 | 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 |
a0002c0009t0002g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
a0002c0009t0002g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
a0002c0009t0002g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
a0002c0010t0001g0015 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
a0002c0010t0002g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
a0002c0010t0002g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
a0002c0010t0002g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
a0002c0010t0002g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
a0002c0010t0002g0153 | 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 |
a0002c0010t0002g0272 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
a0002c0012t0001g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
a0002c0012t0001g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
a0002c0012t0001g0176 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
a0002c0012t0001g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
a0002c0012t0012g0178 | 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 |
a0002c0015t0002g0316 | 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 |
a0002c0020t0001g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
a0002c0020t0002g0155 | 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 |
a0002c0031t0002g0255 | 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 |
a0002c0044t0001g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
a0002c0046t0002g0158 | 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 |
a0003c0011t0001g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
a0003c0011t0002g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
a0003c0011t0002g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
a0004c0014t0001g0266 | 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 |
a0004c0014t0005g0223 | 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 |
a0005c0038t0001g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
a0006c0034t0002g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
a0007c0030t0001g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
a0008c0048t0001g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
a0009c0045t0016g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
a0010c0025t0001g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
a0011c0041t0001g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
a0012c0022t0002g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
a0013c0032t0002g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
a0014c0033t0001g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
a0015c0026t0002g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
a0016c0029t0001g0290 | 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 | g0206 | EUR | GBR | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
HG00099 | hp2 | a0002 | c0012 | t0001 | g0176 | EUR | GBR | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
HG00280 | hp1 | a0001 | c0001 | t0001 | g0210 | EUR | FIN | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
HG00280 | hp2 | a0002 | c0002 | t0001 | g0214 | 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 | g0153 | EUR | FIN | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
HG00438 | hp1 | a0001 | c0008 | t0001 | g0261 | 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 | g0090 | 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 | g0020 | EAS | CHS | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
HG00597 | hp1 | a0001 | c0001 | t0001 | g0065 | EAS | CHS | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
HG00597 | hp2 | a0001 | c0001 | t0001 | g0304 | 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 | g0048 | EAS | CHS | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
HG00639 | hp1 | a0001 | c0001 | t0003 | g0204 | 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 | g0108 | AMR | PUR | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
HG00642 | hp2 | a0001 | c0001 | t0002 | g0216 | AMR | PUR | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
HG00673 | hp1 | a0002 | c0002 | t0002 | g0091 | EAS | CHS | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
HG00673 | hp2 | a0002 | c0031 | t0002 | g0255 | EAS | CHS | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
HG00733 | hp1 | a0002 | c0002 | t0002 | g0014 | 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 | g0223 | AMR | PUR | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
HG00735 | hp2 | a0001 | c0001 | t0001 | g0109 | 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 | g0148 | AMR | PUR | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
HG00741 | hp1 | a0001 | c0003 | t0001 | g0149 | AMR | PUR | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
HG00741 | hp2 | a0002 | c0006 | t0002 | g0285 | AMR | PUR | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
HG01069 | hp1 | a0002 | c0006 | t0002 | g0018 | AMR | PUR | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
HG01069 | hp2 | a0001 | c0001 | t0001 | g0011 | AMR | PUR | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
HG01070 | hp1 | a0001 | c0001 | t0001 | g0012 | AMR | PUR | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
HG01070 | hp2 | a0001 | c0007 | t0001 | g0175 | AMR | PUR | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
HG01071 | hp1 | a0001 | c0001 | t0001 | g0011 | AMR | PUR | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
HG01071 | hp2 | a0001 | c0001 | t0001 | g0012 | AMR | PUR | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
HG01074 | hp1 | a0002 | c0006 | t0001 | g0007 | AMR | PUR | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
HG01074 | hp2 | a0001 | c0001 | t0001 | g0145 | AMR | PUR | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
HG01081 | hp1 | a0002 | c0002 | t0002 | g0123 | AMR | PUR | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
HG01081 | hp2 | a0002 | c0006 | t0001 | g0263 | 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 | g0129 | AMR | PUR | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
HG01106 | hp1 | a0001 | c0003 | t0003 | g0232 | AMR | PUR | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
HG01106 | hp2 | a0002 | c0005 | t0002 | g0251 | AMR | PUR | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
HG01109 | hp1 | a0006 | c0034 | t0002 | g0258 | AMR | PUR | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
HG01109 | hp2 | a0001 | c0001 | t0001 | g0275 | AMR | PUR | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
HG01167 | hp1 | a0007 | c0030 | t0001 | g0140 | AMR | PUR | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
HG01167 | hp2 | a0005 | c0038 | t0001 | g0270 | AMR | PUR | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
HG01168 | hp1 | a0001 | c0003 | t0001 | g0265 | AMR | PUR | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
HG01168 | hp2 | a0002 | c0002 | t0001 | g0151 | AMR | PUR | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
HG01175 | hp1 | a0001 | c0001 | t0001 | g0137 | AMR | PUR | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
HG01175 | hp2 | a0002 | c0005 | t0002 | g0256 | AMR | PUR | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
HG01243 | hp1 | a0001 | c0001 | t0001 | g0164 | AMR | PUR | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
HG01243 | hp2 | a0003 | c0011 | t0002 | g0282 | 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 | g0013 | 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 | g0015 | AMR | CLM | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
HG01257 | hp1 | a0001 | c0004 | t0001 | g0207 | AMR | CLM | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
HG01257 | hp2 | a0002 | c0002 | t0002 | g0188 | AMR | CLM | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
HG01258 | hp1 | a0001 | c0004 | t0001 | g0205 | AMR | CLM | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
HG01258 | hp2 | a0002 | c0010 | t0001 | g0015 | AMR | CLM | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
HG01261 | hp1 | a0001 | c0001 | t0001 | g0105 | AMR | CLM | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
HG01261 | hp2 | a0002 | c0002 | t0002 | g0166 | AMR | CLM | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
HG01346 | hp1 | a0001 | c0001 | t0001 | g0215 | AMR | CLM | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
HG01346 | hp2 | a0002 | c0002 | t0002 | g0014 | 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 | g0125 | AMR | CLM | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
HG01433 | hp1 | a0002 | c0002 | t0002 | g0013 | AMR | CLM | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
HG01433 | hp2 | a0002 | c0002 | t0002 | g0124 | AMR | CLM | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
HG01496 | hp1 | a0001 | c0003 | t0003 | g0250 | AMR | CLM | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
HG01496 | hp2 | a0001 | c0007 | t0001 | g0318 | 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 | g0319 | EUR | IBS | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
HG01884 | hp1 | a0008 | c0048 | t0001 | g0159 | 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 | g0227 | 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 | g0152 | 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 | g0133 | AMR | PEL | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
HG01975 | hp2 | a0001 | c0003 | t0001 | g0246 | AMR | PEL | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
HG01978 | hp1 | a0001 | c0001 | t0001 | g0135 | AMR | PEL | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
HG01978 | hp2 | a0002 | c0005 | t0013 | g0218 | AMR | PEL | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
HG02004 | hp1 | a0001 | c0001 | t0001 | g0226 | AMR | PEL | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
HG02004 | hp2 | a0001 | c0004 | t0001 | g0082 | AMR | PEL | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
HG02015 | hp1 | a0002 | c0002 | t0003 | g0100 | EAS | KHV | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
HG02015 | hp2 | a0001 | c0003 | t0001 | g0257 | EAS | KHV | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
HG02027 | hp1 | a0001 | c0001 | t0001 | g0098 | 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 | g0120 | EAS | KHV | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
HG02040 | hp2 | a0001 | c0013 | t0001 | g0212 | EAS | KHV | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
HG02055 | hp1 | a0002 | c0002 | t0001 | g0127 | AFR | ACB | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
HG02055 | hp2 | a0001 | c0003 | t0001 | g0221 | 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 | g0225 | EAS | KHV | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
HG02071 | hp1 | a0001 | c0007 | t0001 | g0305 | EAS | KHV | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
HG02071 | hp2 | a0001 | c0001 | t0003 | g0130 | EAS | KHV | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
HG02074 | hp1 | a0002 | c0002 | t0002 | g0211 | EAS | KHV | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
HG02074 | hp2 | a0001 | c0001 | t0001 | g0083 | 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 | g0049 | EAS | KHV | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
HG02083 | hp1 | a0001 | c0003 | t0001 | g0264 | EAS | KHV | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
HG02083 | hp2 | a0002 | c0002 | t0002 | g0096 | EAS | KHV | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
HG02129 | hp1 | a0002 | c0002 | t0002 | g0239 | EAS | KHV | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
HG02129 | hp2 | a0001 | c0001 | t0003 | g0106 | EAS | KHV | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
HG02135 | hp1 | a0002 | c0009 | t0002 | g0315 | EAS | KHV | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
HG02135 | hp2 | a0001 | c0013 | t0001 | g0276 | EAS | KHV | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
HG02145 | hp1 | a0002 | c0015 | t0002 | g0316 | AFR | ACB | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
HG02145 | hp2 | a0001 | c0003 | t0001 | g0142 | AFR | ACB | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
HG02148 | hp1 | a0001 | c0001 | t0001 | g0116 | AMR | PEL | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
HG02148 | hp2 | a0002 | c0006 | t0001 | g0260 | AMR | PEL | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
HG02155 | hp1 | a0001 | c0001 | t0001 | g0087 | EAS | CDX | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
HG02155 | hp2 | a0001 | c0003 | t0001 | g0321 | EAS | CDX | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
HG02165 | hp1 | a0001 | c0004 | t0003 | g0136 | EAS | CDX | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
HG02165 | hp2 | a0002 | c0009 | t0001 | g0314 | 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 | g0233 | AFR | ACB | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
HG02280 | hp2 | a0002 | c0020 | t0001 | g0156 | AFR | ACB | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
HG02451 | hp1 | a0009 | c0045 | t0016 | g0157 | AFR | ACB | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
HG02451 | hp2 | a0010 | c0025 | t0001 | g0203 | AFR | ACB | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
HG02523 | hp1 | a0001 | c0004 | t0001 | g0297 | EAS | KHV | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
HG02523 | hp2 | a0002 | c0002 | t0002 | g0110 | EAS | KHV | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
HG02572 | hp1 | a0001 | c0017 | t0001 | g0311 | 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 | g0169 | SAS | PJL | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
HG02602 | hp2 | a0001 | c0001 | t0001 | g0113 | 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 | g0249 | 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 | g0292 | AFR | GWD | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
HG02723 | hp1 | a0002 | c0046 | t0002 | g0158 | AFR | GWD | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
HG02723 | hp2 | a0001 | c0017 | t0001 | g0312 | 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 | g0309 | SAS | PJL | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
HG02738 | hp1 | a0011 | c0041 | t0001 | g0181 | SAS | PJL | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
HG02738 | hp2 | a0001 | c0001 | t0001 | g0094 | SAS | PJL | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
HG02809 | hp1 | a0012 | c0022 | t0002 | g0220 | 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 | g0122 | AFR | GWD | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
HG02895 | hp1 | a0001 | c0003 | t0001 | g0168 | AFR | GWD | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
HG02895 | hp2 | a0001 | c0001 | t0001 | g0165 | AFR | GWD | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
HG02896 | hp1 | a0001 | c0001 | t0001 | g0229 | AFR | GWD | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
HG02896 | hp2 | a0002 | c0005 | t0002 | g0021 | AFR | GWD | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
HG02897 | hp1 | a0001 | c0001 | t0001 | g0228 | AFR | GWD | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
HG02897 | hp2 | a0001 | c0003 | t0001 | g0167 | AFR | GWD | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
HG02922 | hp1 | a0002 | c0005 | t0001 | g0139 | AFR | ESN | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
HG02922 | hp2 | a0001 | c0003 | t0001 | g0253 | AFR | ESN | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
HG02965 | hp1 | a0013 | c0032 | t0002 | g0247 | AFR | ESN | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
HG02965 | hp2 | a0003 | c0011 | t0001 | g0280 | 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 | g0266 | AFR | ESN | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
HG02976 | hp1 | a0001 | c0001 | t0001 | g0182 | 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 | g0173 | SAS | PJL | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
HG03041 | hp1 | a0001 | c0003 | t0001 | g0189 | AFR | GWD | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
HG03041 | hp2 | a0002 | c0005 | t0001 | g0234 | AFR | GWD | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
HG03098 | hp1 | a0001 | c0003 | t0001 | g0224 | AFR | MSL | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
HG03098 | hp2 | a0002 | c0005 | t0001 | g0222 | AFR | MSL | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
HG03130 | hp1 | a0002 | c0005 | t0002 | g0287 | AFR | ESN | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
HG03130 | hp2 | a0001 | c0001 | t0001 | g0111 | 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 | g0273 | AFR | ESN | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
HG03209 | hp1 | a0001 | c0003 | t0008 | g0269 | 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 | g0248 | AFR | MSL | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
HG03225 | hp2 | a0001 | c0021 | t0001 | g0161 | AFR | MSL | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
HG03453 | hp1 | a0001 | c0001 | t0009 | g0121 | AFR | MSL | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
HG03453 | hp2 | a0002 | c0005 | t0002 | g0021 | 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 | g0191 | 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 | g0002 | SAS | PJL | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
HG03491 | hp2 | a0002 | c0005 | t0002 | g0184 | 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 | g0002 | 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 | a0014 | c0033 | t0001 | g0230 | AFR | ESN | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
HG03540 | hp1 | a0001 | c0003 | t0001 | g0114 | AFR | GWD | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
HG03540 | hp2 | a0002 | c0012 | t0001 | g0141 | AFR | GWD | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
HG03579 | hp1 | a0001 | c0021 | t0002 | g0160 | 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 | g0147 | SAS | PJL | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
HG03669 | hp1 | a0002 | c0012 | t0012 | g0178 | 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 | g0293 | SAS | STU | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
HG03688 | hp2 | a0001 | c0001 | t0001 | g0126 | SAS | STU | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
HG03831 | hp1 | a0001 | c0007 | t0001 | g0187 | SAS | BEB | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
HG03831 | hp2 | a0001 | c0001 | t0001 | g0138 | SAS | BEB | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
HG03834 | hp1 | a0002 | c0006 | t0001 | g0007 | SAS | BEB | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
HG03834 | hp2 | a0001 | c0003 | t0003 | g0163 | SAS | BEB | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
HG04115 | hp1 | a0002 | c0002 | t0002 | g0002 | SAS | STU | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
HG04115 | hp2 | a0001 | c0004 | t0001 | g0244 | SAS | STU | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
HG04184 | hp1 | a0002 | c0002 | t0002 | g0162 | SAS | BEB | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
HG04184 | hp2 | a0002 | c0006 | t0002 | g0271 | SAS | BEB | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
HG04199 | hp1 | a0001 | c0007 | t0001 | g0174 | SAS | STU | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
HG04199 | hp2 | a0002 | c0006 | t0002 | g0186 | SAS | STU | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
HG04204 | hp1 | a0001 | c0003 | t0001 | g0154 | SAS | STU | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
HG04204 | hp2 | a0002 | c0005 | t0002 | g0170 | SAS | STU | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
HG04228 | hp1 | a0002 | c0012 | t0001 | g0180 | SAS | STU | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
HG04228 | hp2 | a0002 | c0002 | t0002 | g0002 | SAS | STU | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
NA18522 | hp1 | a0002 | c0005 | t0001 | g0267 | AFR | YRI | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
NA18522 | hp2 | a0002 | c0020 | t0002 | g0155 | 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 | g0308 | AFR | YRI | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
NA18940 | hp1 | a0001 | c0001 | t0001 | g0146 | EAS | JPT | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
NA18940 | hp2 | a0002 | c0006 | t0002 | g0018 | 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 | g0016 | EAS | JPT | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
NA18942 | hp1 | a0015 | c0026 | t0002 | g0131 | EAS | JPT | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
NA18942 | hp2 | a0001 | c0037 | t0001 | g0193 | EAS | JPT | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
NA18943 | hp1 | a0002 | c0006 | t0002 | g0310 | EAS | JPT | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
NA18943 | hp2 | a0001 | c0007 | t0001 | g0295 | EAS | JPT | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
NA18947 | hp1 | a0001 | c0001 | t0001 | g0288 | EAS | JPT | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
NA18947 | hp2 | a0001 | c0001 | t0001 | g0301 | EAS | JPT | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
NA18948 | hp1 | a0001 | c0023 | t0017 | g0278 | EAS | JPT | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
NA18948 | hp2 | a0001 | c0004 | t0001 | g0209 | EAS | JPT | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
NA18950 | hp1 | a0001 | c0001 | t0001 | g0086 | EAS | JPT | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
NA18950 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
NA18952 | hp1 | a0001 | c0001 | t0001 | g0245 | EAS | JPT | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
NA18952 | hp2 | a0002 | c0002 | t0002 | g0103 | EAS | JPT | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
NA18953 | hp1 | a0002 | c0010 | t0002 | g0088 | EAS | JPT | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
NA18953 | hp2 | a0001 | c0004 | t0001 | g0213 | EAS | JPT | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
NA18956 | hp1 | a0001 | c0004 | t0001 | g0004 | EAS | JPT | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
NA18956 | hp2 | a0002 | c0005 | t0002 | g0262 | EAS | JPT | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
NA18957 | hp1 | a0001 | c0039 | t0001 | g0306 | EAS | JPT | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
NA18957 | hp2 | a0001 | c0001 | t0001 | g0236 | EAS | JPT | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
NA18959 | hp1 | a0001 | c0007 | t0003 | g0177 | 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 | g0179 | EAS | JPT | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
NA18960 | hp2 | a0001 | c0001 | t0001 | g0115 | 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 | g0089 | EAS | JPT | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
NA18964 | hp1 | a0002 | c0002 | t0002 | g0020 | EAS | JPT | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
NA18964 | hp2 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
NA18965 | hp1 | a0002 | c0009 | t0002 | g0008 | EAS | JPT | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
NA18965 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
NA18966 | hp1 | a0001 | c0001 | t0001 | g0117 | EAS | JPT | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
NA18966 | hp2 | a0001 | c0003 | t0001 | g0202 | EAS | JPT | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
NA18968 | hp1 | a0001 | c0008 | t0001 | g0217 | EAS | JPT | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
NA18968 | hp2 | a0002 | c0010 | t0002 | g0102 | EAS | JPT | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
NA18969 | hp1 | a0001 | c0013 | t0001 | g0279 | EAS | JPT | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
NA18969 | hp2 | a0001 | c0001 | t0001 | g0243 | 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 | g0252 | EAS | JPT | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
NA18971 | hp1 | a0001 | c0018 | t0015 | g0307 | EAS | JPT | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
NA18971 | hp2 | a0001 | c0003 | t0001 | g0317 | EAS | JPT | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
NA18973 | hp1 | a0001 | c0008 | t0001 | g0286 | 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 | g0004 | EAS | JPT | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
NA18979 | hp1 | a0001 | c0004 | t0001 | g0134 | EAS | JPT | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
NA18979 | hp2 | a0002 | c0002 | t0007 | g0093 | EAS | JPT | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
NA18980 | hp1 | a0001 | c0001 | t0001 | g0284 | EAS | JPT | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
NA18980 | hp2 | a0002 | c0009 | t0002 | g0199 | 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 | g0240 | EAS | JPT | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
NA18983 | hp1 | a0001 | c0003 | t0001 | g0320 | EAS | JPT | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
NA18983 | hp2 | a0001 | c0001 | t0001 | g0242 | EAS | JPT | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
NA18984 | hp1 | a0001 | c0003 | t0001 | g0200 | EAS | JPT | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
NA18984 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
NA18987 | hp1 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
NA18987 | hp2 | a0001 | c0007 | t0001 | g0185 | EAS | JPT | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
NA18988 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
NA18988 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
NA18992 | hp1 | a0001 | c0004 | t0003 | g0298 | 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 | g0198 | EAS | JPT | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
NA18994 | hp1 | a0001 | c0004 | t0001 | g0208 | EAS | JPT | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
NA18994 | hp2 | a0001 | c0003 | t0001 | g0196 | EAS | JPT | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
NA18997 | hp1 | a0001 | c0001 | t0001 | g0294 | EAS | JPT | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
NA18997 | hp2 | a0001 | c0001 | t0001 | g0095 | 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 | g0231 | EAS | JPT | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
NA18999 | hp1 | a0001 | c0004 | t0001 | g0004 | EAS | JPT | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
NA18999 | hp2 | a0001 | c0001 | t0001 | g0300 | EAS | JPT | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
NA19000 | hp1 | a0001 | c0001 | t0001 | g0081 | EAS | JPT | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
NA19000 | hp2 | a0002 | c0002 | t0002 | g0241 | EAS | JPT | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
NA19002 | hp1 | a0001 | c0003 | t0001 | g0235 | EAS | JPT | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
NA19002 | hp2 | a0001 | c0008 | t0001 | g0219 | EAS | JPT | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
NA19005 | hp1 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
NA19005 | hp2 | a0002 | c0002 | t0002 | g0016 | EAS | JPT | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
NA19007 | hp1 | a0002 | c0006 | t0002 | g0003 | 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 | g0003 | EAS | JPT | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
NA19009 | hp2 | a0001 | c0001 | t0001 | g0099 | EAS | JPT | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
NA19010 | hp1 | a0001 | c0004 | t0001 | g0313 | EAS | JPT | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
NA19010 | hp2 | a0001 | c0001 | t0001 | g0084 | 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 | g0283 | EAS | JPT | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
NA19012 | hp1 | a0001 | c0001 | t0001 | g0201 | EAS | JPT | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
NA19012 | hp2 | a0002 | c0006 | t0002 | g0003 | EAS | JPT | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
NA19030 | hp1 | a0016 | c0029 | t0001 | g0290 | 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 | g0268 | AFR | LWK | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
NA19043 | hp2 | a0001 | c0047 | t0001 | g0194 | AFR | LWK | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
NA19057 | hp1 | a0002 | c0009 | t0002 | g0008 | EAS | JPT | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
NA19057 | hp2 | a0001 | c0007 | t0001 | g0192 | EAS | JPT | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
NA19060 | hp1 | a0001 | c0001 | t0001 | g0299 | 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 | g0289 | 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 | g0274 | EAS | JPT | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
NA19066 | hp1 | a0002 | c0006 | t0002 | g0003 | EAS | JPT | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
NA19066 | hp2 | a0002 | c0002 | t0007 | g0107 | EAS | JPT | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
NA19067 | hp1 | a0001 | c0004 | t0001 | g0197 | EAS | JPT | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
NA19067 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
NA19070 | hp1 | a0002 | c0005 | t0002 | g0150 | EAS | JPT | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
NA19070 | hp2 | a0001 | c0007 | t0001 | g0190 | EAS | JPT | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
NA19074 | hp1 | a0001 | c0001 | t0001 | g0119 | EAS | JPT | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
NA19074 | hp2 | a0002 | c0006 | t0002 | g0019 | EAS | JPT | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
NA19076 | hp1 | a0002 | c0009 | t0002 | g0277 | EAS | JPT | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
NA19076 | hp2 | a0001 | c0001 | t0001 | g0064 | EAS | JPT | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
NA19079 | hp1 | a0001 | c0004 | t0001 | g0085 | EAS | JPT | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
NA19079 | hp2 | a0002 | c0009 | t0002 | g0008 | EAS | JPT | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
NA19081 | hp1 | a0001 | c0040 | t0001 | g0092 | EAS | JPT | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
NA19081 | hp2 | a0001 | c0004 | t0002 | g0237 | EAS | JPT | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
NA19084 | hp1 | a0001 | c0004 | t0001 | g0004 | EAS | JPT | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
NA19084 | hp2 | a0002 | c0006 | t0002 | g0254 | EAS | JPT | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
NA19085 | hp1 | a0001 | c0004 | t0003 | g0296 | EAS | JPT | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
NA19085 | hp2 | a0001 | c0008 | t0001 | g0291 | EAS | JPT | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
NA19088 | hp1 | a0002 | c0002 | t0002 | g0097 | EAS | JPT | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
NA19088 | hp2 | a0001 | c0001 | t0001 | g0302 | EAS | JPT | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
NA19090 | hp1 | a0001 | c0004 | t0001 | g0132 | EAS | JPT | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
NA19090 | hp2 | a0001 | c0001 | t0001 | g0066 | 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 | g0101 | EUR | TSI | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
NA20752 | hp2 | a0002 | c0010 | t0002 | g0272 | 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 | g0183 | EUR | TSI | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
NA20905 | hp1 | a0001 | c0008 | t0001 | g0172 | SAS | GIH | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
NA20905 | hp2 | a0002 | c0002 | t0002 | g0002 | SAS | GIH | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
HG01123 | hp1 | a0001 | c0001 | t0002 | g0104 | AMR | CLM | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
HG01123 | hp2 | a0002 | c0006 | t0001 | g0007 | 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 | g0171 | 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 | g0281 | AFR | USA | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
NA18955 | hp1 | a0002 | c0006 | t0002 | g0019 | EAS | JPT | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
NA18955 | hp2 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
NA20300 | hp1 | a0002 | c0044 | t0001 | g0195 | AFR | USA | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
NA20300 | hp2 | a0001 | c0001 | t0001 | g0112 | AFR | USA | USH1C_chr11_17488900_17549416 | USH1C | chr11 | 17488900 | 17549416 |
NA21309 | hp1 | a0001 | c0008 | t0001 | g0259 | 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 |
view | 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 | a0006 | 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 | a0008 | 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 | a0002 a0003 a0006 others(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 | a0009 a0013 a0014 |
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 | a0007 | 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 | a0011 | 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 | a0016 | 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 | a0015 | 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 | a0003 a0010 |
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 | a0012 | 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 |
view | 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 | a0001c0004 a0001c0008 a0001c0013 others(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 | a0009c0045 a0010c0025 a0013c0032 others(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 | a0001c0007 a0001c0018 a0001c0037 others(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 | a0001c0001 a0001c0004 a0001c0016 others(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 | a0001c0042 a0001c0043 a0002c0015 others(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 | a0001c0016 a0001c0028 |
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 | a0001c0021 a0001c0047 a0002c0020 others(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 | a0001c0013 a0001c0023 a0002c0009 |
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 |
view | 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 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0008 others(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 | a0001c0001t0008 a0001c0003t0008 |
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 | a0001c0001t0002 a0001c0001t0008 a0001c0003t0002 others(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 | a0001c0001t0002 a0001c0001t0008 a0001c0003t0002 others(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 | a0001c0001t0002 a0001c0001t0008 a0001c0003t0002 others(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 | a0001c0003t0004 a0001c0003t0006 a0001c0043t0006 others(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 |
view | 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 | 87 | a0001c0001t0002g0216 a0001c0004t0002g0237 a0002c0002t0002g0002 others(84): 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 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0049 others(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 | 95 | a0001c0001t0002g0104 a0001c0001t0002g0216 a0001c0001t0008g0227 others(92): 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 | a0001c0001t0002g0104 a0001c0003t0002g0068 a0001c0021t0002g0160 others(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 | 301 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0009 others(298): 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 | a0004c0014t0005g0062 a0004c0014t0005g0223 |
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 | a0001c0003t0001g0149 | 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 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0049 others(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 | a0001c0001t0008g0227 a0001c0003t0008g0269 |
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 | a0001c0001t0002g0104 a0002c0002t0002g0110 |
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 | a0001c0001t0001g0005 a0001c0001t0001g0111 a0001c0001t0001g0112 others(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 | 88 | a0001c0001t0002g0216 a0001c0004t0002g0237 a0002c0002t0002g0002 others(85): 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 | a0001c0001t0001g0005 a0001c0001t0001g0111 a0001c0001t0001g0112 others(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 | a0001c0001t0001g0046 a0001c0001t0001g0051 a0001c0001t0001g0059 others(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 | a0001c0008t0001g0291 | 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 | 119 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0012 others(116): 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 | 188 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0010 others(185): 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 | 297 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0010 others(294): 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 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0049 others(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 | 123 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0012 others(120): 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 | a0001c0003t0001g0154 | 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 | a0002c0002t0002g0097 a0002c0002t0002g0241 |
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 | a0001c0004t0001g0132 | 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 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0012 others(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 | a0001c0001t0001g0128 | 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 | 123 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0012 others(120): 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 | a0013c0032t0002g0247 | 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 | a0002c0002t0002g0016 a0002c0002t0002g0198 |
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 | a0001c0001t0008g0227 a0001c0003t0001g0171 a0001c0003t0004g0030 others(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 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0046 others(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 | a0001c0001t0008g0227 a0001c0003t0008g0269 |
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 | a0001c0004t0001g0205 a0001c0004t0001g0207 |
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 | a0001c0021t0001g0161 | 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 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0049 others(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 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0049 others(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 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0012 others(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 | 190 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0010 others(187): 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 | a0002c0031t0002g0255 | 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 | a0001c0003t0001g0189 a0014c0033t0001g0230 |
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 | a0001c0001t0001g0060 a0001c0001t0001g0126 a0001c0003t0001g0224 others(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 | a0001c0001t0001g0009 a0001c0001t0001g0017 a0001c0001t0001g0084 others(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 | a0001c0001t0001g0126 | 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 | a0001c0003t0004g0030 a0001c0017t0001g0311 a0001c0017t0001g0312 |
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 | a0001c0001t0001g0112 | 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 | a0001c0003t0003g0250 a0002c0005t0001g0249 a0002c0005t0001g0267 |
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 | a0001c0001t0011g0027 a0001c0003t0001g0221 a0001c0003t0002g0068 others(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 | 82 | a0001c0003t0001g0114 a0001c0003t0001g0148 a0001c0003t0001g0149 others(79): 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 | a0001c0001t0001g0052 a0001c0001t0001g0152 a0001c0001t0001g0228 others(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 | a0001c0001t0001g0126 | 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 | a0001c0001t0001g0052 a0001c0001t0001g0152 a0001c0001t0001g0228 others(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 | a0001c0003t0001g0072 a0001c0003t0001g0142 |
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 | a0001c0003t0001g0072 a0001c0003t0001g0142 |
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 | a0013c0032t0002g0247 a0014c0033t0001g0230 |
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 | a0001c0001t0001g0094 | 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 | a0001c0003t0001g0154 a0001c0003t0001g0200 a0001c0003t0001g0202 others(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 | a0001c0003t0001g0189 a0001c0003t0001g0292 a0003c0011t0001g0024 others(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 | a0001c0001t0003g0106 | 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 | a0001c0003t0001g0171 | 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 | 181 | a0001c0001t0001g0052 a0001c0001t0001g0056 a0001c0001t0001g0152 others(178): 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 | a0001c0007t0001g0295 | 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 | a0001c0003t0001g0072 a0001c0003t0001g0142 a0004c0014t0001g0266 others(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 | a0001c0001t0001g0011 | 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 | a0009c0045t0016g0157 a0013c0032t0002g0247 a0014c0033t0001g0230 |
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 | a0001c0003t0001g0154 a0001c0003t0001g0221 a0001c0003t0001g0293 others(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 | a0001c0001t0001g0052 a0001c0001t0001g0056 a0001c0001t0001g0152 others(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 | a0001c0007t0001g0174 a0001c0007t0001g0175 a0001c0007t0001g0185 others(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 | a0001c0003t0003g0163 | 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 | a0007c0030t0001g0140 | 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 | a0001c0007t0003g0179 | 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 | a0001c0001t0001g0052 a0001c0001t0001g0056 a0001c0001t0001g0152 others(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 | a0001c0008t0001g0261 | 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 | a0001c0003t0001g0154 a0001c0003t0001g0221 a0001c0003t0001g0293 others(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 | a0001c0003t0008g0269 | 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 | a0001c0001t0011g0027 a0001c0003t0001g0072 a0001c0003t0001g0142 others(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 | a0001c0003t0001g0154 a0001c0003t0001g0293 |
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 | a0001c0008t0001g0169 | 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 | a0001c0001t0001g0052 a0001c0001t0001g0056 a0001c0001t0001g0152 others(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 | a0001c0003t0001g0072 a0001c0003t0001g0142 a0001c0003t0001g0221 others(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 | a0001c0001t0001g0052 a0001c0001t0001g0056 a0001c0001t0001g0152 others(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 | a0002c0002t0002g0123 | 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 | a0001c0003t0004g0028 a0003c0011t0001g0024 a0003c0011t0001g0280 others(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 | a0001c0001t0001g0005 a0001c0001t0001g0111 a0001c0001t0001g0112 |
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 | a0001c0003t0001g0154 a0001c0003t0001g0221 a0001c0003t0001g0293 others(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 | a0001c0042t0001g0033 a0002c0005t0001g0122 a0002c0005t0001g0139 others(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 | a0002c0020t0001g0156 a0002c0020t0002g0155 |
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 | a0001c0003t0004g0028 a0001c0008t0001g0286 a0003c0011t0001g0024 others(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 | a0001c0001t0001g0076 a0001c0001t0001g0117 |
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 | a0001c0001t0001g0125 a0001c0001t0001g0126 a0001c0001t0001g0129 others(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 | a0001c0001t0001g0049 | 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 | a0001c0003t0001g0154 a0001c0003t0001g0221 a0001c0003t0001g0293 others(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 | a0001c0001t0001g0115 | 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 | a0003c0011t0001g0024 a0003c0011t0001g0280 a0003c0011t0002g0282 |
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 | a0009c0045t0016g0157 a0010c0025t0001g0203 a0013c0032t0002g0247 others(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 | a0001c0003t0001g0072 a0001c0003t0001g0142 a0001c0017t0001g0311 others(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 | a0001c0013t0001g0279 | 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 | a0001c0004t0003g0296 | 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 | a0001c0001t0001g0065 | 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 | a0003c0011t0001g0024 a0003c0011t0001g0280 a0003c0011t0002g0282 |
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 | a0001c0003t0001g0072 a0001c0003t0001g0142 a0004c0014t0001g0266 others(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 | a0003c0011t0001g0024 a0003c0011t0001g0280 a0003c0011t0002g0282 |
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 | a0001c0001t0001g0052 a0001c0001t0001g0056 a0001c0001t0001g0152 others(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 | a0001c0003t0008g0269 | 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 | a0009c0045t0016g0157 a0010c0025t0001g0203 a0013c0032t0002g0247 others(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 | a0001c0004t0001g0244 | 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 | a0001c0024t0001g0309 | 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 | a0001c0021t0002g0160 | 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 | a0001c0003t0001g0072 a0001c0003t0001g0142 |
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 | a0001c0003t0001g0221 | 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 | a0001c0001t0001g0052 a0001c0001t0001g0056 a0001c0001t0001g0152 others(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 | a0009c0045t0016g0157 a0010c0025t0001g0203 a0013c0032t0002g0247 others(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 | a0001c0003t0001g0253 a0012c0022t0002g0220 |
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 | a0001c0042t0001g0033 a0002c0005t0001g0122 a0002c0005t0001g0139 others(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 | a0001c0003t0001g0072 a0001c0003t0001g0142 a0004c0014t0001g0266 others(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 | a0001c0001t0001g0128 | 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 | a0001c0003t0001g0189 a0001c0003t0001g0292 |
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 | a0001c0001t0001g0137 a0001c0001t0001g0145 |
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 | a0001c0008t0001g0172 a0002c0006t0002g0285 |
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 | a0001c0003t0001g0072 a0001c0003t0001g0142 a0001c0003t0002g0068 others(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 | a0001c0001t0003g0130 | 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 | a0001c0003t0001g0221 | 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 | a0001c0001t0001g0116 | 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 | a0001c0001t0001g0005 a0001c0001t0001g0017 a0001c0001t0001g0046 others(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 | 140 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0009 others(137): 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 | a0002c0005t0002g0248 | 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 | a0001c0003t0001g0320 a0001c0003t0001g0321 |
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 | 235 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0009 others(232): 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 | a0010c0025t0001g0203 a0013c0032t0002g0247 a0014c0033t0001g0230 |
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 | a0001c0004t0001g0274 | 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 | 147 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0009 others(144): 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 | a0001c0001t0001g0052 a0001c0001t0001g0056 a0001c0001t0001g0135 others(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 | a0003c0011t0001g0280 | 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 | 146 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0009 others(143): 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 | a0001c0007t0001g0192 a0001c0007t0001g0295 a0001c0037t0001g0193 |
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 | a0001c0003t0001g0072 a0001c0003t0001g0142 a0001c0003t0002g0068 others(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 | 154 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0009 others(151): 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 | a0001c0001t0001g0228 a0001c0001t0001g0229 a0001c0001t0008g0227 others(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 | a0002c0044t0001g0195 | 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 | 144 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0009 others(141): 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 | 241 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0009 others(238): 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 | a0001c0001t0001g0099 | 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 | a0001c0003t0001g0246 a0002c0005t0013g0218 |
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 | a0001c0001t0001g0098 a0001c0001t0001g0289 |
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 | a0001c0001t0001g0215 | 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 | a0001c0003t0001g0167 a0001c0003t0001g0168 a0001c0003t0001g0171 others(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 | a0001c0001t0001g0215 | 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 | 152 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0009 others(149): 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 | a0001c0003t0001g0167 a0001c0003t0001g0168 a0001c0003t0001g0171 others(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 | a0001c0003t0001g0200 | 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 | a0001c0017t0001g0311 a0001c0017t0001g0312 a0001c0042t0001g0033 others(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 | a0001c0003t0001g0167 a0001c0003t0001g0168 a0001c0003t0001g0171 others(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 | a0001c0001t0011g0027 a0001c0003t0005g0042 a0009c0045t0016g0157 others(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 | a0001c0001t0001g0152 a0002c0002t0002g0053 |
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 | a0001c0001t0001g0228 a0001c0001t0001g0229 a0001c0001t0008g0227 others(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 | a0001c0001t0001g0052 a0001c0001t0001g0056 a0001c0001t0001g0135 others(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 | a0002c0005t0001g0070 a0005c0035t0004g0032 |
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 | a0002c0005t0002g0044 a0002c0005t0002g0045 |
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 | a0002c0002t0002g0123 | 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 | a0001c0003t0001g0235 | 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 | a0001c0001t0001g0052 a0001c0001t0001g0056 a0001c0001t0001g0135 others(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 | a0001c0003t0001g0072 a0001c0003t0001g0142 a0001c0003t0002g0068 others(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 | 198 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0009 others(195): 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 | a0001c0007t0001g0190 a0001c0007t0001g0191 a0001c0007t0001g0305 others(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 | 153 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0009 others(150): 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 | a0002c0002t0002g0013 | 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 | a0002c0012t0012g0178 | 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 | a0001c0001t0003g0130 a0001c0003t0001g0200 a0001c0003t0001g0202 others(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 | a0001c0017t0001g0311 a0001c0017t0001g0312 a0001c0042t0001g0033 others(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 | 153 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0009 others(150): 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 | 153 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0009 others(150): 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 | a0001c0003t0001g0200 a0001c0003t0001g0202 a0001c0003t0001g0246 others(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 | a0001c0001t0001g0052 a0001c0001t0001g0056 a0001c0001t0001g0135 others(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 | a0001c0003t0001g0072 a0001c0003t0001g0142 |
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 | 153 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0009 others(150): 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 | a0002c0044t0001g0195 | 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 | a0001c0001t0001g0245 | 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 | a0001c0003t0001g0142 a0001c0003t0002g0068 a0002c0005t0002g0067 others(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 | a0001c0001t0001g0229 a0001c0003t0001g0168 a0001c0004t0001g0207 others(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 | 149 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0009 others(146): 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 | a0001c0003t0001g0054 a0002c0005t0002g0044 a0002c0005t0002g0045 |
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 | 149 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0009 others(146): 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 | a0001c0001t0001g0128 | 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 | a0009c0045t0016g0157 a0010c0025t0001g0203 a0013c0032t0002g0247 others(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 | 154 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0009 others(151): 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 | 250 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0009 others(247): 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 | 250 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0009 others(247): 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 | 154 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0009 others(151): 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 | a0001c0017t0001g0311 a0001c0017t0001g0312 |
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 | a0001c0001t0001g0052 a0001c0001t0001g0056 a0001c0001t0001g0135 others(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 | 252 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0009 others(249): 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 | a0001c0017t0001g0311 a0001c0017t0001g0312 a0001c0042t0001g0033 others(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 | a0001c0001t0001g0046 a0001c0001t0001g0164 a0001c0001t0001g0165 others(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 | a0001c0001t0001g0005 a0001c0001t0001g0017 a0001c0001t0001g0046 others(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 | a0002c0002t0002g0097 | 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 | a0001c0001t0001g0005 a0001c0001t0001g0017 a0001c0001t0001g0046 others(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 | a0001c0001t0001g0119 | 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 | 248 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0009 others(245): 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 | a0001c0003t0003g0232 | 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 | a0009c0045t0016g0157 | 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 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0017 others(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 | a0001c0001t0001g0005 a0001c0001t0001g0017 a0001c0001t0001g0046 others(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 | a0002c0005t0001g0222 | 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 | a0001c0017t0001g0311 a0001c0017t0001g0312 a0001c0042t0001g0033 others(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 | a0001c0013t0001g0212 a0001c0013t0001g0276 a0001c0013t0001g0279 others(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 | a0001c0017t0001g0311 a0001c0017t0001g0312 a0001c0042t0001g0033 others(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 | a0002c0005t0002g0044 a0002c0005t0002g0045 |
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 | 206 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0009 others(203): 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 | a0001c0001t0001g0052 a0001c0001t0001g0056 a0001c0001t0001g0135 others(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 | a0001c0001t0001g0052 a0001c0001t0001g0056 a0001c0001t0001g0135 others(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 | 255 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0009 others(252): 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 | a0001c0001t0001g0245 | 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 | a0001c0003t0001g0154 a0001c0003t0001g0167 a0001c0003t0001g0168 others(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 | a0001c0003t0001g0142 | 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 | a0001c0001t0001g0111 | 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 | a0001c0003t0001g0072 a0001c0003t0001g0142 a0001c0003t0002g0068 others(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 | a0001c0001t0011g0027 a0001c0003t0005g0042 a0009c0045t0016g0157 others(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 | a0001c0003t0001g0114 | 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 | a0001c0003t0001g0114 | 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 | a0001c0003t0001g0114 | 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 | a0001c0017t0001g0311 a0001c0017t0001g0312 a0001c0042t0001g0033 others(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 | 155 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0010 others(152): 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 | a0002c0005t0001g0036 a0008c0048t0001g0159 |
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 | a0001c0003t0001g0167 a0001c0003t0001g0168 a0001c0003t0001g0171 others(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 | a0001c0001t0011g0027 a0001c0003t0005g0042 a0009c0045t0016g0157 others(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 | a0001c0003t0001g0221 | 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 | a0001c0001t0001g0052 a0001c0001t0001g0056 a0001c0001t0001g0135 others(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 | a0001c0001t0011g0027 a0001c0003t0005g0042 a0001c0043t0006g0029 others(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 | a0001c0001t0001g0236 | 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 | a0001c0001t0011g0027 a0001c0003t0005g0042 a0009c0045t0016g0157 others(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 | a0001c0003t0001g0167 a0001c0003t0001g0168 a0001c0003t0001g0171 others(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 | a0001c0013t0001g0279 a0001c0013t0010g0026 a0002c0009t0001g0314 others(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 | a0011c0041t0001g0181 | 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 | a0001c0001t0011g0027 a0001c0003t0005g0042 |
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 | a0001c0001t0001g0052 a0001c0001t0001g0056 a0001c0001t0001g0135 others(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 | a0001c0001t0001g0052 a0001c0001t0001g0056 a0001c0001t0001g0135 others(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 | a0001c0001t0001g0052 a0001c0001t0001g0056 a0001c0001t0001g0135 others(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 | a0001c0001t0011g0027 a0001c0003t0001g0167 a0001c0003t0001g0168 others(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 | a0001c0003t0001g0072 a0001c0003t0001g0142 a0001c0003t0002g0068 others(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 | a0010c0025t0001g0203 | 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 | a0001c0001t0001g0120 | 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 | a0001c0001t0001g0052 a0001c0001t0001g0056 a0001c0001t0001g0135 others(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 | a0001c0047t0001g0194 | 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 | a0001c0001t0001g0056 a0001c0001t0001g0113 a0001c0001t0001g0135 others(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 | a0001c0001t0001g0012 | 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 | a0009c0045t0016g0157 a0010c0025t0001g0203 a0013c0032t0002g0247 |
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 | a0001c0003t0004g0030 a0001c0003t0005g0042 a0001c0043t0006g0029 others(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 | a0002c0006t0002g0319 | 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 | a0001c0001t0001g0052 a0001c0001t0001g0056 a0001c0001t0001g0135 others(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 | 217 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0009 others(214): 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 | 217 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0009 others(214): 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 | 210 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0009 others(207): 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 | a0002c0005t0002g0021 a0002c0005t0002g0248 a0014c0033t0001g0230 |
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 | 148 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0009 others(145): 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 | a0002c0020t0001g0156 a0002c0020t0002g0155 |
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 | a0001c0003t0001g0167 a0001c0003t0001g0168 a0001c0003t0001g0171 others(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 | a0001c0003t0001g0224 a0013c0032t0002g0247 |
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 | a0016c0029t0001g0290 | 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 | a0002c0005t0001g0070 a0005c0035t0004g0032 |
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 | a0001c0001t0001g0049 a0002c0002t0002g0050 a0002c0010t0002g0048 |
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 | a0001c0001t0001g0109 a0002c0002t0002g0108 |
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 | a0001c0003t0001g0167 a0001c0003t0001g0168 a0001c0003t0001g0171 others(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 | a0001c0003t0001g0200 a0001c0003t0001g0202 a0001c0003t0001g0246 others(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 | a0002c0002t0001g0214 | 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 | a0002c0002t0002g0110 | 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 | a0001c0021t0002g0160 a0002c0046t0002g0158 a0008c0048t0001g0159 others(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 | a0001c0008t0001g0291 | 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 | a0002c0002t0001g0151 | 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 | 203 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0009 others(200): 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 | a0001c0001t0001g0052 a0001c0001t0001g0056 a0001c0001t0001g0135 others(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 | a0001c0042t0001g0033 a0002c0015t0001g0035 a0002c0015t0002g0034 |
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 | a0002c0012t0001g0173 | 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 | a0002c0012t0001g0173 | 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 | a0001c0003t0001g0189 | 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 | a0001c0013t0001g0276 | 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 | a0001c0001t0001g0081 | 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 | a0001c0001t0001g0052 a0001c0001t0001g0056 a0001c0001t0001g0135 others(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 | a0001c0001t0001g0052 a0001c0001t0001g0056 a0001c0001t0001g0135 others(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 | a0001c0003t0004g0030 a0001c0021t0002g0160 a0002c0046t0002g0158 others(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 | a0001c0043t0006g0029 a0005c0035t0004g0032 |
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 | a0001c0003t0001g0224 | 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 | a0002c0002t0002g0110 | 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 | a0001c0001t0001g0052 a0001c0001t0001g0056 a0001c0001t0003g0055 others(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 | a0001c0021t0002g0160 a0002c0046t0002g0158 a0008c0048t0001g0159 others(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 | a0001c0042t0001g0033 a0001c0043t0006g0029 a0002c0015t0001g0035 others(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 | a0001c0042t0001g0033 a0001c0043t0006g0029 a0002c0015t0001g0035 others(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 | a0001c0042t0001g0033 a0001c0043t0006g0029 a0002c0015t0001g0035 others(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 | 236 | a0001c0001t0001g0005 a0001c0001t0001g0017 a0001c0001t0001g0046 others(233): 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 | a0001c0042t0001g0033 a0001c0043t0006g0029 a0002c0015t0001g0035 others(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 | a0001c0042t0001g0033 a0001c0043t0006g0029 a0002c0015t0001g0035 others(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 | a0001c0001t0001g0011 | 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 | a0001c0001t0009g0071 a0001c0003t0001g0142 a0002c0005t0001g0070 others(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 | a0001c0001t0001g0066 a0001c0001t0001g0073 a0001c0001t0001g0115 others(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 | a0001c0042t0001g0033 a0001c0043t0006g0029 a0002c0015t0001g0035 others(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 | a0001c0042t0001g0033 a0001c0043t0006g0029 a0002c0015t0001g0035 others(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 | a0001c0042t0001g0033 a0001c0043t0006g0029 a0002c0015t0001g0035 others(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 | a0002c0005t0002g0044 a0002c0005t0002g0045 |
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 | a0001c0042t0001g0033 a0001c0043t0006g0029 a0002c0015t0001g0035 others(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 | a0001c0042t0001g0033 a0001c0043t0006g0029 a0002c0015t0001g0035 others(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 | a0001c0042t0001g0033 a0001c0043t0006g0029 a0002c0015t0001g0035 others(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 | a0001c0042t0001g0033 a0001c0043t0006g0029 a0002c0015t0001g0035 others(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 | a0001c0042t0001g0033 a0002c0015t0001g0035 a0002c0015t0002g0034 |
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 | a0001c0001t0001g0017 a0001c0001t0001g0164 a0001c0001t0001g0165 others(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 | a0001c0042t0001g0033 a0001c0043t0006g0029 a0002c0015t0001g0035 others(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 | a0001c0003t0001g0043 a0001c0003t0005g0042 |
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 | a0001c0042t0001g0033 a0001c0043t0006g0029 a0002c0015t0001g0035 others(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 | a0001c0042t0001g0033 a0001c0043t0006g0029 a0002c0015t0001g0035 others(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 | a0001c0042t0001g0033 a0001c0043t0006g0029 a0002c0015t0001g0035 others(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 | a0001c0042t0001g0033 a0001c0043t0006g0029 a0002c0015t0001g0035 others(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 | a0001c0042t0001g0033 a0001c0043t0006g0029 a0002c0015t0001g0035 others(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 | a0001c0042t0001g0033 a0001c0043t0006g0029 a0002c0015t0001g0035 others(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 | a0001c0042t0001g0033 a0001c0043t0006g0029 a0002c0015t0001g0035 others(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 | a0001c0003t0001g0043 a0001c0003t0004g0028 a0001c0003t0005g0042 others(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 | a0001c0042t0001g0033 a0001c0043t0006g0029 a0002c0015t0001g0035 others(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 | a0001c0042t0001g0033 a0001c0043t0006g0029 a0002c0015t0001g0035 others(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 | a0001c0042t0001g0033 a0001c0043t0006g0029 a0002c0015t0001g0035 others(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 | a0001c0042t0001g0033 a0001c0043t0006g0029 a0002c0015t0001g0035 others(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 | a0001c0004t0001g0197 a0002c0010t0002g0238 |
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 | a0001c0042t0001g0033 a0001c0043t0006g0029 a0002c0015t0001g0035 others(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 | a0001c0042t0001g0033 a0001c0043t0006g0029 a0002c0015t0001g0035 others(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 | a0001c0042t0001g0033 a0001c0043t0006g0029 a0002c0015t0001g0035 others(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 | a0001c0017t0001g0311 a0001c0017t0001g0312 |
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 | a0001c0001t0001g0046 a0001c0001t0001g0201 a0001c0001t0001g0215 others(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 | a0001c0003t0003g0163 | 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 | a0001c0042t0001g0033 a0001c0043t0006g0029 a0002c0015t0001g0035 others(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 | a0001c0042t0001g0033 a0001c0043t0006g0029 a0002c0015t0001g0035 others(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 | a0001c0042t0001g0033 a0001c0043t0006g0029 a0002c0015t0001g0035 others(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 | a0001c0042t0001g0033 a0001c0043t0006g0029 a0002c0015t0001g0035 others(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 | a0001c0042t0001g0033 a0001c0043t0006g0029 a0002c0015t0001g0035 others(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 | a0001c0001t0001g0017 a0001c0001t0001g0152 a0001c0001t0001g0164 others(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 | 123 | a0001c0001t0001g0046 a0001c0001t0001g0201 a0001c0001t0001g0215 others(120): 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 | a0001c0001t0001g0017 a0001c0001t0001g0164 a0001c0001t0001g0165 others(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 | a0001c0001t0001g0094 | 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 | a0002c0002t0002g0096 | 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 | a0001c0001t0001g0064 a0001c0001t0001g0095 a0001c0001t0001g0146 |
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 | a0001c0001t0014g0047 a0001c0040t0001g0092 a0002c0002t0007g0093 |
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 | a0001c0001t0001g0010 a0001c0001t0001g0081 a0001c0001t0001g0083 others(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 | a0001c0001t0001g0046 a0001c0001t0001g0135 a0001c0001t0001g0303 others(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 | a0001c0023t0017g0278 | 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 | a0002c0006t0001g0007 | 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 | a0002c0005t0002g0150 | 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 | a0002c0002t0002g0002 a0002c0002t0002g0013 a0002c0002t0003g0100 others(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 | a0001c0001t0001g0041 a0001c0001t0001g0049 a0001c0001t0001g0116 others(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 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0012 others(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 | a0001c0001t0001g0126 a0001c0016t0001g0075 |
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 | a0001c0001t0001g0105 | 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 | a0001c0001t0001g0129 | 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 | a0001c0001t0001g0011 | 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 | a0002c0002t0002g0002 | 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 | a0001c0001t0001g0010 a0001c0001t0001g0064 a0001c0001t0001g0081 others(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 | 140 | a0001c0001t0001g0056 a0001c0001t0001g0113 a0001c0001t0001g0152 others(137): 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 | a0001c0001t0001g0138 | 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 | a0001c0001t0009g0121 | 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 | a0001c0047t0001g0194 | 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 | a0001c0003t0001g0154 | 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 | a0001c0003t0001g0292 | 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 | a0002c0006t0002g0019 | 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 | a0001c0001t0001g0076 a0001c0001t0001g0077 a0001c0001t0001g0078 others(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 | a0002c0015t0002g0316 a0002c0019t0002g0025 |
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 | a0001c0001t0001g0275 | 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 | a0002c0015t0002g0316 a0002c0019t0002g0025 |
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 | a0001c0043t0006g0029 a0002c0015t0002g0316 a0002c0019t0002g0025 |
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 | a0001c0001t0001g0017 a0001c0001t0001g0164 a0001c0001t0001g0165 others(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 | a0001c0003t0001g0043 a0001c0003t0004g0028 a0001c0003t0005g0042 others(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 | a0001c0001t0001g0226 | 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 | a0001c0004t0001g0213 | 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 | a0001c0001t0001g0017 a0001c0001t0001g0164 a0001c0001t0001g0165 others(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 | a0001c0003t0001g0043 a0001c0003t0004g0028 a0001c0003t0005g0042 |
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 | a0014c0033t0001g0230 | 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 | a0001c0001t0001g0017 a0001c0001t0001g0164 a0001c0001t0001g0165 others(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 | a0001c0021t0001g0161 a0002c0020t0001g0156 a0002c0020t0002g0155 |
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 | a0001c0013t0001g0279 a0001c0013t0010g0026 |
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 | a0001c0013t0001g0279 a0001c0013t0010g0026 |
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 | 229 | a0001c0001t0001g0017 a0001c0001t0001g0046 a0001c0001t0001g0052 others(226): 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 | a0001c0003t0004g0030 a0001c0003t0006g0031 |
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 | a0001c0003t0004g0030 a0001c0003t0006g0031 a0001c0016t0001g0075 others(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 | 151 | a0001c0001t0001g0152 a0001c0001t0001g0201 a0001c0001t0001g0215 others(148): 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 | a0001c0003t0004g0030 a0001c0003t0006g0031 |
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 | a0001c0001t0001g0010 | 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 | a0002c0009t0002g0008 | 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 | a0001c0003t0004g0030 a0001c0003t0006g0031 |
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 | 144 | a0001c0001t0001g0152 a0001c0001t0001g0201 a0001c0001t0001g0215 others(141): 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 | a0001c0001t0001g0164 a0001c0001t0001g0165 a0001c0001t0001g0182 others(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 | a0001c0001t0001g0017 a0002c0002t0002g0188 a0002c0002t0002g0211 |
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 | a0001c0017t0001g0311 a0001c0017t0001g0312 |
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 | a0001c0021t0002g0160 a0002c0046t0002g0158 a0008c0048t0001g0159 |
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 | a0001c0001t0001g0052 a0001c0001t0003g0055 a0001c0008t0001g0291 others(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 | a0001c0001t0001g0017 a0001c0001t0001g0164 a0001c0001t0001g0165 others(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 | a0001c0001t0008g0227 | 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 | a0001c0001t0001g0125 a0001c0001t0001g0126 a0001c0001t0001g0129 others(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 | a0001c0003t0004g0030 a0001c0003t0006g0031 a0005c0035t0004g0032 |
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 | a0001c0003t0004g0030 a0001c0003t0006g0031 a0005c0035t0004g0032 |
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 | a0001c0017t0001g0311 a0001c0017t0001g0312 |
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 | a0001c0003t0004g0030 a0001c0003t0006g0031 a0005c0035t0004g0032 |
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 | a0002c0005t0002g0308 | 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 | a0001c0001t0001g0017 a0001c0001t0001g0164 a0001c0001t0001g0165 others(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 | a0001c0003t0001g0171 | 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 | a0001c0003t0004g0030 a0001c0003t0006g0031 a0005c0035t0004g0032 |
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 | a0001c0003t0004g0030 a0001c0003t0006g0031 a0005c0035t0004g0032 |
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 | a0001c0003t0001g0200 | 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 | a0001c0001t0001g0128 | 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 | a0001c0001t0001g0046 a0002c0005t0002g0044 a0002c0005t0002g0045 |
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 | 146 | a0001c0001t0001g0152 a0001c0001t0001g0201 a0001c0001t0001g0215 others(143): 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 | a0001c0001t0001g0056 a0001c0003t0004g0028 |
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 | a0001c0003t0004g0030 a0001c0003t0006g0031 a0005c0035t0004g0032 |
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 | a0001c0001t0001g0129 | 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 | 154 | a0001c0001t0001g0152 a0001c0001t0001g0201 a0001c0001t0001g0215 others(151): 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 | a0001c0001t0001g0152 a0001c0001t0003g0204 a0001c0003t0001g0148 others(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 | a0001c0003t0001g0292 | 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 | a0001c0003t0004g0030 a0001c0003t0006g0031 |
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 | a0001c0003t0001g0043 a0001c0003t0004g0028 a0001c0003t0005g0042 |
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 | a0002c0015t0002g0316 a0002c0019t0002g0025 |
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 | a0002c0015t0002g0316 a0002c0019t0002g0025 |
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 | a0002c0015t0002g0316 a0002c0019t0002g0025 |
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 | a0001c0042t0001g0033 a0002c0015t0001g0035 a0002c0015t0002g0034 |
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 | a0001c0003t0001g0043 a0001c0003t0004g0028 a0001c0003t0005g0042 |
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 | 148 | a0001c0001t0001g0152 a0001c0001t0001g0201 a0001c0001t0001g0215 others(145): 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 | a0001c0001t0001g0284 a0001c0001t0001g0288 a0001c0001t0001g0289 others(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 | 100 | a0001c0001t0001g0152 a0001c0001t0001g0201 a0001c0001t0001g0215 others(97): 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 | a0001c0001t0001g0226 a0001c0001t0001g0294 a0001c0001t0001g0304 others(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 | 203 | a0001c0001t0001g0017 a0001c0001t0001g0152 a0001c0001t0001g0164 others(200): 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 | a0001c0001t0001g0017 a0001c0001t0001g0164 a0001c0001t0001g0165 others(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 | a0001c0003t0004g0030 a0001c0003t0006g0031 a0001c0021t0002g0160 others(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 | a0002c0015t0002g0316 a0002c0019t0002g0025 |
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 | 161 | a0001c0001t0001g0152 a0001c0001t0001g0201 a0001c0001t0001g0215 others(158): 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 | a0002c0015t0002g0316 a0002c0019t0002g0025 |
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 | 204 | a0001c0001t0001g0017 a0001c0001t0001g0152 a0001c0001t0001g0164 others(201): 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 | a0001c0003t0001g0148 a0001c0003t0001g0149 |
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 | a0001c0001t0001g0294 a0001c0001t0001g0299 a0001c0004t0001g0004 others(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 | a0001c0003t0004g0030 a0001c0021t0002g0160 a0002c0046t0002g0158 others(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 | a0001c0008t0001g0219 | 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 | a0001c0021t0001g0161 a0001c0047t0001g0194 a0002c0020t0002g0155 |
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 | a0001c0021t0001g0161 | 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 | a0001c0003t0001g0154 | 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 | 161 | a0001c0001t0001g0152 a0001c0001t0001g0201 a0001c0001t0001g0215 others(158): 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 | a0001c0001t0001g0300 a0001c0001t0001g0301 a0001c0001t0001g0302 others(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 | a0001c0001t0001g0017 a0001c0001t0001g0164 a0001c0001t0001g0165 others(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 | a0001c0021t0001g0161 | 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 | a0001c0003t0001g0043 a0001c0003t0004g0028 a0001c0003t0005g0042 |
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 | a0002c0005t0001g0139 | 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 | a0001c0003t0004g0030 a0001c0003t0006g0031 a0001c0021t0002g0160 others(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 | 147 | a0001c0001t0001g0152 a0001c0001t0001g0201 a0001c0001t0001g0215 others(144): 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 | a0001c0001t0003g0130 | 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 | a0001c0007t0001g0174 a0001c0007t0001g0175 a0001c0007t0001g0185 others(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 | a0001c0001t0001g0017 a0001c0001t0001g0164 a0001c0001t0001g0165 others(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 | a0001c0003t0004g0030 a0001c0003t0006g0031 a0001c0021t0002g0160 others(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 | 89 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0009 others(86): 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 | 182 | a0001c0001t0001g0017 a0001c0001t0001g0152 a0001c0001t0001g0164 others(179): 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 | 148 | a0001c0001t0001g0152 a0001c0001t0001g0201 a0001c0001t0001g0215 others(145): 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 | a0001c0001t0001g0052 a0001c0001t0001g0056 a0001c0001t0001g0135 others(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 | a0002c0005t0002g0308 | 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 | a0001c0001t0001g0152 a0001c0001t0003g0204 a0001c0003t0001g0148 others(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 | a0002c0005t0013g0218 | 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 | a0001c0024t0001g0309 | 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 | a0001c0008t0001g0217 | 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 | 151 | a0001c0001t0001g0152 a0001c0001t0001g0201 a0001c0001t0001g0215 others(148): 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 | a0002c0006t0002g0186 | 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 | a0001c0003t0001g0321 | 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 | a0001c0003t0004g0030 a0001c0003t0006g0031 a0001c0021t0002g0160 others(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 | a0002c0002t0002g0188 | 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 | a0001c0003t0004g0030 a0001c0003t0006g0031 a0001c0021t0002g0160 others(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 | a0001c0003t0004g0030 a0001c0003t0006g0031 a0001c0021t0002g0160 others(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 | a0001c0001t0001g0215 a0001c0001t0002g0216 a0002c0002t0001g0214 |
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 | a0001c0004t0001g0213 | 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 | a0001c0003t0004g0030 a0001c0003t0006g0031 a0001c0021t0002g0160 others(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 | a0001c0001t0001g0137 a0001c0001t0001g0145 |
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 | a0001c0042t0001g0033 a0002c0015t0001g0035 a0002c0015t0002g0034 |
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 | a0001c0007t0001g0187 | 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 | a0001c0021t0001g0161 a0001c0047t0001g0194 a0002c0020t0001g0156 others(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 | a0001c0003t0001g0043 a0001c0003t0004g0028 a0001c0003t0005g0042 |
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 | 194 | a0001c0001t0001g0017 a0001c0001t0001g0152 a0001c0001t0001g0164 others(191): 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 | a0001c0003t0004g0030 a0001c0003t0006g0031 a0001c0021t0002g0160 others(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 | a0001c0003t0003g0163 | 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 | a0001c0001t0001g0138 | 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 | a0001c0018t0001g0147 | 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 | a0001c0003t0004g0030 a0001c0003t0006g0031 a0001c0021t0002g0160 others(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 | 149 | a0001c0001t0001g0152 a0001c0001t0001g0201 a0001c0001t0001g0215 others(146): 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 | a0001c0001t0001g0059 a0001c0001t0001g0060 a0002c0002t0002g0061 |
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 | 145 | a0001c0001t0001g0201 a0001c0001t0001g0215 a0001c0001t0001g0226 others(142): 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 | 202 | a0001c0001t0001g0017 a0001c0001t0001g0152 a0001c0001t0001g0164 others(199): 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 | a0001c0003t0004g0030 a0001c0003t0006g0031 a0001c0021t0002g0160 others(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 | a0001c0004t0001g0208 a0001c0004t0001g0209 |
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 | a0001c0042t0001g0033 a0002c0015t0001g0035 a0002c0015t0002g0034 |
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 | a0001c0007t0001g0192 | 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 | a0002c0002t0002g0188 | 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 | a0001c0003t0004g0030 a0001c0003t0006g0031 a0001c0021t0002g0160 others(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 | 189 | a0001c0001t0001g0017 a0001c0001t0001g0164 a0001c0001t0001g0165 others(186): 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 | a0001c0003t0004g0030 a0001c0003t0006g0031 |
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 | a0001c0001t0001g0009 a0002c0002t0002g0058 |
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 | a0001c0001t0003g0204 | 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 | a0001c0003t0004g0030 a0001c0003t0006g0031 a0001c0021t0002g0160 others(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 | a0010c0025t0001g0203 | 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 | a0001c0001t0001g0201 a0001c0003t0001g0200 a0001c0003t0001g0202 |
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 | a0001c0001t0001g0052 a0001c0001t0001g0056 a0001c0001t0003g0055 others(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 | a0001c0003t0004g0030 a0001c0003t0006g0031 a0001c0021t0002g0160 others(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 | a0001c0003t0004g0030 a0001c0003t0006g0031 a0001c0021t0002g0160 others(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 | a0002c0009t0002g0199 | 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 | a0001c0003t0004g0030 a0001c0003t0006g0031 a0001c0021t0002g0160 others(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 | a0001c0003t0004g0030 a0001c0003t0006g0031 a0001c0021t0002g0160 others(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 | a0001c0001t0001g0046 a0001c0001t0001g0049 a0001c0001t0014g0047 others(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 | a0001c0003t0004g0030 a0001c0003t0006g0031 a0001c0021t0002g0160 others(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 | a0001c0001t0001g0143 a0001c0001t0001g0144 a0001c0001t0001g0145 others(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 | 146 | a0001c0001t0001g0017 a0001c0001t0001g0201 a0001c0001t0001g0210 others(143): 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 | a0001c0003t0004g0030 a0001c0003t0006g0031 a0001c0021t0002g0160 others(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 | a0001c0003t0004g0030 a0001c0003t0006g0031 a0001c0021t0002g0160 others(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 | a0001c0003t0001g0043 a0001c0003t0005g0042 |
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 | a0001c0003t0004g0030 a0001c0003t0006g0031 a0001c0021t0002g0160 others(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 | 145 | a0001c0001t0001g0017 a0001c0001t0001g0146 a0001c0001t0001g0201 others(142): 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 | a0001c0007t0001g0190 a0001c0007t0001g0191 a0001c0007t0001g0192 others(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 | a0001c0018t0001g0147 | 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 | a0001c0042t0001g0033 a0002c0005t0001g0036 a0002c0015t0001g0035 others(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 | 151 | a0001c0001t0001g0017 a0001c0001t0001g0201 a0001c0001t0001g0210 others(148): 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 | a0001c0003t0001g0043 a0001c0003t0004g0028 a0001c0003t0005g0042 |
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 | a0001c0001t0001g0164 a0001c0001t0001g0165 a0001c0001t0001g0182 others(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 | a0001c0003t0004g0030 a0001c0003t0006g0031 a0001c0021t0002g0160 others(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 | 194 | a0001c0001t0001g0017 a0001c0001t0001g0164 a0001c0001t0001g0165 others(191): 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 | a0002c0006t0002g0310 | 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 | a0001c0017t0001g0311 a0001c0017t0001g0312 |
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 | 203 | a0001c0001t0001g0017 a0001c0001t0001g0152 a0001c0001t0001g0164 others(200): 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 | a0001c0021t0001g0161 a0002c0020t0001g0156 a0002c0020t0002g0155 |
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 | 196 | a0001c0001t0001g0017 a0001c0001t0001g0164 a0001c0001t0001g0165 others(193): 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 | a0001c0042t0001g0033 a0002c0005t0001g0036 a0002c0015t0001g0035 others(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 | a0001c0004t0001g0197 | 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 | a0002c0015t0002g0316 a0002c0019t0002g0025 |
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 | a0001c0003t0004g0030 a0001c0003t0006g0031 a0001c0021t0002g0160 others(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 | a0001c0003t0001g0196 | 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 | 194 | a0001c0001t0001g0017 a0001c0001t0001g0164 a0001c0001t0001g0165 others(191): 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 | a0002c0009t0001g0314 a0002c0009t0002g0315 |
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 | a0002c0015t0002g0316 a0002c0019t0002g0025 |
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 | a0001c0001t0001g0164 a0001c0001t0001g0165 a0001c0001t0001g0182 others(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 | a0001c0001t0011g0027 a0002c0044t0001g0195 |
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 | a0001c0003t0001g0317 | 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 | 194 | a0001c0001t0001g0017 a0001c0001t0001g0164 a0001c0001t0001g0165 others(191): 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 | a0001c0001t0001g0152 a0001c0003t0001g0148 a0001c0003t0001g0149 others(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 | 193 | a0001c0001t0001g0017 a0001c0001t0001g0164 a0001c0001t0001g0165 others(190): 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 | a0002c0020t0001g0156 a0002c0020t0002g0155 |
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 | 192 | a0001c0001t0001g0017 a0001c0001t0001g0164 a0001c0001t0001g0165 others(189): 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 | a0001c0007t0001g0318 | 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 | a0001c0042t0001g0033 a0002c0005t0001g0036 a0002c0015t0001g0035 others(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 | a0001c0003t0004g0030 a0001c0003t0006g0031 a0005c0035t0004g0032 |
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 | a0002c0006t0002g0319 | 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 | G | A | 36 | a0001c0001t0001g0164 a0001c0001t0001g0165 a0001c0001t0001g0182 others(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 | C | T | 5 | a0001c0003t0004g0028 a0001c0003t0004g0030 a0001c0003t0006g0031 others(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 | a0001c0042t0001g0033 a0002c0005t0001g0036 a0002c0015t0001g0035 others(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 | T | A | 1 | a0001c0047t0001g0194 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.36+353A>T | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 1/26 | chr11 | 17543919 | |||||||
chr11:17544058 | G | A | 144 | a0001c0001t0001g0017 a0001c0001t0001g0201 a0001c0001t0001g0210 others(141): 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 | C | A | 2 | a0001c0003t0001g0320 a0001c0003t0001g0321 |
2 | HG02155.hp2 NA18983.hp1 |
intron_variant | MODIFIER | c.36+186G>T | USH1C | ENSG00000006611.17 | transcript | ENST00000005226.12 | protein_coding | 1/26 | chr11 | 17544086 |