Item | Value |
---|---|
geneid | 4648 |
ensemblid | ENSG00000169994.20 |
hgncid | 7607 |
symbol | MYO7B |
name | myosin VIIB |
refseq_nuc | NM_001393586.1 |
refseq_prot | NP_001380515.1 |
ensembl_nuc | ENST00000409816.8 |
ensembl_prot | ENSP00000386461.3 |
mane_status | MANE Select |
chr | chr2 |
start | 127535683 |
end | 127637726 |
strand | + |
ver | v1.2 |
region | chr2:127535683-127637726 |
region5000 | chr2:127530683-127642726 |
regionname0 | MYO7B_chr2_127535683_127637726 |
regionname5000 | MYO7B_chr2_127530683_127642726 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/0 | 2142 | 91 | 40 | 17 | 25 | 0 | 8 | 21 | MYO7B_chr2_127530683_127642726 | MYO7B | MSGFR others(2137): Show |
chr2 | 127530683 | 127642726 |
a0002 | 0/1 | 2142 | 61 | 3 | 19 | 24 | 5 | 9 | 17 | MYO7B_chr2_127530683_127642726 | MYO7B | MSGFR others(2137): Show |
chr2 | 127530683 | 127642726 |
a0003 | 0/0 | 2142 | 33 | 3 | 7 | 15 | 2 | 6 | 11 | MYO7B_chr2_127530683_127642726 | MYO7B | MSGFR others(2137): Show |
chr2 | 127530683 | 127642726 |
a0004 | 0/0 | 2142 | 15 | 2 | 9 | 1 | 2 | 1 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | MSGFR others(2137): Show |
chr2 | 127530683 | 127642726 |
a0005 | 0/0 | 2142 | 9 | 6 | 1 | 1 | 0 | 1 | 1 | MYO7B_chr2_127530683_127642726 | MYO7B | MSGFR others(2137): Show |
chr2 | 127530683 | 127642726 |
a0006 | 0/0 | 2142 | 8 | 0 | 2 | 0 | 2 | 4 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | MSGFR others(2137): Show |
chr2 | 127530683 | 127642726 |
a0007 | 0/0 | 2142 | 7 | 4 | 0 | 1 | 1 | 1 | 1 | MYO7B_chr2_127530683_127642726 | MYO7B | MSGFR others(2137): Show |
chr2 | 127530683 | 127642726 |
a0008 | 0/0 | 2142 | 6 | 5 | 1 | 0 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | MSGFR others(2137): Show |
chr2 | 127530683 | 127642726 |
a0009 | 0/0 | 2142 | 4 | 4 | 0 | 0 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | MSGFR others(2137): Show |
chr2 | 127530683 | 127642726 |
a0010 | 0/0 | 2142 | 3 | 0 | 1 | 0 | 0 | 2 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | MSGFR others(2137): Show |
chr2 | 127530683 | 127642726 |
a0011 | 0/0 | 2142 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | MSGFR others(2137): Show |
chr2 | 127530683 | 127642726 |
a0012 | 0/0 | 2142 | 2 | 0 | 2 | 0 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | MSGFR others(2137): Show |
chr2 | 127530683 | 127642726 |
a0013 | 0/0 | 2142 | 2 | 0 | 2 | 0 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | MSGFR others(2137): Show |
chr2 | 127530683 | 127642726 |
a0014 | 0/0 | 2142 | 2 | 0 | 1 | 1 | 0 | 0 | 1 | MYO7B_chr2_127530683_127642726 | MYO7B | MSGFR others(2137): Show |
chr2 | 127530683 | 127642726 |
a0015 | 0/0 | 2142 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | MSGFR others(2137): Show |
chr2 | 127530683 | 127642726 |
a0016 | 0/0 | 2142 | 2 | 1 | 1 | 0 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | MSGFR others(2137): Show |
chr2 | 127530683 | 127642726 |
a0017 | 0/0 | 2142 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | MSGFR others(2137): Show |
chr2 | 127530683 | 127642726 |
a0018 | 0/0 | 2142 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | MSGFR others(2137): Show |
chr2 | 127530683 | 127642726 |
a0019 | 0/0 | 2142 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | MSGFR others(2137): Show |
chr2 | 127530683 | 127642726 |
a0020 | 0/0 | 2142 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | MSGFR others(2137): Show |
chr2 | 127530683 | 127642726 |
a0021 | 0/0 | 2142 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | MSGFR others(2137): Show |
chr2 | 127530683 | 127642726 |
a0022 | 0/0 | 2142 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | MSGFR others(2137): Show |
chr2 | 127530683 | 127642726 |
a0023 | 0/0 | 2142 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | MSGFR others(2137): Show |
chr2 | 127530683 | 127642726 |
a0024 | 0/0 | 2142 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | MSGFR others(2137): Show |
chr2 | 127530683 | 127642726 |
a0025 | 0/0 | 2142 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | MSGFR others(2137): Show |
chr2 | 127530683 | 127642726 |
a0026 | 0/0 | 2142 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | MSGFR others(2137): Show |
chr2 | 127530683 | 127642726 |
a0027 | 0/0 | 2142 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | MSGFR others(2137): Show |
chr2 | 127530683 | 127642726 |
a0028 | 0/0 | 2142 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | MSGFR others(2137): Show |
chr2 | 127530683 | 127642726 |
a0029 | 0/0 | 2142 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | MSGFR others(2137): Show |
chr2 | 127530683 | 127642726 |
a0030 | 0/0 | 2142 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | MSGFR others(2137): Show |
chr2 | 127530683 | 127642726 |
a0031 | 0/0 | 2142 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | MSGFR others(2137): Show |
chr2 | 127530683 | 127642726 |
a0032 | 0/0 | 2142 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | MSGFR others(2137): Show |
chr2 | 127530683 | 127642726 |
a0033 | 0/0 | 2142 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | MSGFR others(2137): Show |
chr2 | 127530683 | 127642726 |
a0034 | 0/0 | 2142 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | MSGFR others(2137): Show |
chr2 | 127530683 | 127642726 |
a0035 | 0/0 | 2142 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | MSGFR others(2137): Show |
chr2 | 127530683 | 127642726 |
a0036 | 0/0 | 2142 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | MSGFR others(2137): Show |
chr2 | 127530683 | 127642726 |
a0037 | 0/0 | 2142 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | MYO7B_chr2_127530683_127642726 | MYO7B | MSGFR others(2137): Show |
chr2 | 127530683 | 127642726 |
a0038 | 0/0 | 2142 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | MYO7B_chr2_127530683_127642726 | MYO7B | MSGFR others(2137): Show |
chr2 | 127530683 | 127642726 |
a0039 | 0/0 | 2142 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | MYO7B_chr2_127530683_127642726 | MYO7B | MSGFR others(2137): Show |
chr2 | 127530683 | 127642726 |
a0040 | 0/0 | 2142 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | MYO7B_chr2_127530683_127642726 | MYO7B | MSGFR others(2137): Show |
chr2 | 127530683 | 127642726 |
a0041 | 0/0 | 2142 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | MYO7B_chr2_127530683_127642726 | MYO7B | MSGFR others(2137): Show |
chr2 | 127530683 | 127642726 |
a0042 | 0/0 | 2142 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | MYO7B_chr2_127530683_127642726 | MYO7B | MSGFR others(2137): Show |
chr2 | 127530683 | 127642726 |
a0043 | 0/0 | 2142 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | MYO7B_chr2_127530683_127642726 | MYO7B | MSGFR others(2137): Show |
chr2 | 127530683 | 127642726 |
a0044 | 0/0 | 2142 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | MSGFR others(2137): Show |
chr2 | 127530683 | 127642726 |
a0045 | 0/0 | 2142 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | MSGFR others(2137): Show |
chr2 | 127530683 | 127642726 |
a0046 | 0/0 | 2142 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | MSGFR others(2137): Show |
chr2 | 127530683 | 127642726 |
a0047 | 0/0 | 2142 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | MYO7B_chr2_127530683_127642726 | MYO7B | MSGFR others(2137): Show |
chr2 | 127530683 | 127642726 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0002 | 0/0 | 6426 | 36 | 19 | 8 | 8 | 0 | 1 | MYO7B_chr2_127530683_127642726 | MYO7B | ATGTC others(6421): Show |
chr2 | 127530683 | 127642726 | ||
a0001c0004 | 1/0 | 6426 | 18 | 0 | 3 | 9 | 0 | 5 | MYO7B_chr2_127530683_127642726 | MYO7B | ATGTC others(6421): Show |
chr2 | 127530683 | 127642726 | ||
a0001c0005 | 0/0 | 6426 | 15 | 2 | 4 | 7 | 0 | 2 | MYO7B_chr2_127530683_127642726 | MYO7B | ATGTC others(6421): Show |
chr2 | 127530683 | 127642726 | ||
a0001c0010 | 0/0 | 6426 | 6 | 5 | 1 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | ATGTC others(6421): Show |
chr2 | 127530683 | 127642726 | ||
a0001c0013 | 0/0 | 6426 | 5 | 4 | 1 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | ATGTC others(6421): Show |
chr2 | 127530683 | 127642726 | ||
a0001c0017 | 0/0 | 6426 | 3 | 3 | 0 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | ATGTC others(6421): Show |
chr2 | 127530683 | 127642726 | ||
a0001c0018 | 0/0 | 6426 | 3 | 3 | 0 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | ATGTC others(6421): Show |
chr2 | 127530683 | 127642726 | ||
a0001c0044 | 0/0 | 6426 | 1 | 1 | 0 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | ATGTC others(6421): Show |
chr2 | 127530683 | 127642726 | ||
a0001c0045 | 0/0 | 6426 | 1 | 1 | 0 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | ATGTC others(6421): Show |
chr2 | 127530683 | 127642726 | ||
a0001c0058 | 0/0 | 6426 | 1 | 0 | 0 | 1 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | ATGTC others(6421): Show |
chr2 | 127530683 | 127642726 | ||
a0001c0061 | 0/0 | 6426 | 1 | 1 | 0 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | ATGTC others(6421): Show |
chr2 | 127530683 | 127642726 | ||
a0001c0068 | 0/0 | 6426 | 1 | 1 | 0 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | ATGTC others(6421): Show |
chr2 | 127530683 | 127642726 | ||
a0002c0001 | 0/1 | 6426 | 38 | 1 | 13 | 16 | 1 | 6 | MYO7B_chr2_127530683_127642726 | MYO7B | ATGTC others(6421): Show |
chr2 | 127530683 | 127642726 | ||
a0002c0006 | 0/0 | 6426 | 13 | 1 | 6 | 1 | 4 | 1 | MYO7B_chr2_127530683_127642726 | MYO7B | ATGTC others(6421): Show |
chr2 | 127530683 | 127642726 | ||
a0002c0011 | 0/0 | 6426 | 5 | 1 | 0 | 2 | 0 | 2 | MYO7B_chr2_127530683_127642726 | MYO7B | ATGTC others(6421): Show |
chr2 | 127530683 | 127642726 | ||
a0002c0012 | 0/0 | 6426 | 5 | 0 | 0 | 5 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | ATGTC others(6421): Show |
chr2 | 127530683 | 127642726 | ||
a0003c0003 | 0/0 | 6426 | 30 | 3 | 7 | 12 | 2 | 6 | MYO7B_chr2_127530683_127642726 | MYO7B | ATGTC others(6421): Show |
chr2 | 127530683 | 127642726 | ||
a0003c0026 | 0/0 | 6426 | 2 | 0 | 0 | 2 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | ATGTC others(6421): Show |
chr2 | 127530683 | 127642726 | ||
a0003c0069 | 0/0 | 6426 | 1 | 0 | 0 | 1 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | ATGTC others(6421): Show |
chr2 | 127530683 | 127642726 | ||
a0004c0007 | 0/0 | 6426 | 12 | 2 | 6 | 1 | 2 | 1 | MYO7B_chr2_127530683_127642726 | MYO7B | ATGTC others(6421): Show |
chr2 | 127530683 | 127642726 | ||
a0004c0021 | 0/0 | 6426 | 2 | 0 | 2 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | ATGTC others(6421): Show |
chr2 | 127530683 | 127642726 | ||
a0004c0054 | 0/0 | 6426 | 1 | 0 | 1 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | ATGTC others(6421): Show |
chr2 | 127530683 | 127642726 | ||
a0005c0008 | 0/0 | 6426 | 9 | 6 | 1 | 1 | 0 | 1 | MYO7B_chr2_127530683_127642726 | MYO7B | ATGTC others(6421): Show |
chr2 | 127530683 | 127642726 | ||
a0006c0009 | 0/0 | 6426 | 8 | 0 | 2 | 0 | 2 | 4 | MYO7B_chr2_127530683_127642726 | MYO7B | ATGTC others(6421): Show |
chr2 | 127530683 | 127642726 | ||
a0007c0023 | 0/0 | 6426 | 2 | 2 | 0 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | ATGTC others(6421): Show |
chr2 | 127530683 | 127642726 | ||
a0007c0024 | 0/0 | 6426 | 2 | 2 | 0 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | ATGTC others(6421): Show |
chr2 | 127530683 | 127642726 | ||
a0007c0025 | 0/0 | 6426 | 2 | 0 | 0 | 0 | 1 | 1 | MYO7B_chr2_127530683_127642726 | MYO7B | ATGTC others(6421): Show |
chr2 | 127530683 | 127642726 | ||
a0007c0062 | 0/0 | 6426 | 1 | 0 | 0 | 1 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | ATGTC others(6421): Show |
chr2 | 127530683 | 127642726 | ||
a0008c0015 | 0/0 | 6426 | 4 | 3 | 1 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | ATGTC others(6421): Show |
chr2 | 127530683 | 127642726 | ||
a0008c0042 | 0/0 | 6426 | 1 | 1 | 0 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | ATGTC others(6421): Show |
chr2 | 127530683 | 127642726 | ||
a0008c0063 | 0/0 | 6426 | 1 | 1 | 0 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | ATGTC others(6421): Show |
chr2 | 127530683 | 127642726 | ||
a0009c0014 | 0/0 | 6426 | 4 | 4 | 0 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | ATGTC others(6421): Show |
chr2 | 127530683 | 127642726 | ||
a0010c0020 | 0/0 | 6426 | 2 | 0 | 0 | 0 | 0 | 2 | MYO7B_chr2_127530683_127642726 | MYO7B | ATGTC others(6421): Show |
chr2 | 127530683 | 127642726 | ||
a0010c0036 | 0/0 | 6426 | 1 | 0 | 1 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | ATGTC others(6421): Show |
chr2 | 127530683 | 127642726 | ||
a0011c0016 | 0/0 | 6426 | 3 | 3 | 0 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | ATGTC others(6421): Show |
chr2 | 127530683 | 127642726 | ||
a0012c0022 | 0/0 | 6426 | 2 | 0 | 2 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | ATGTC others(6421): Show |
chr2 | 127530683 | 127642726 | ||
a0013c0019 | 0/0 | 6426 | 2 | 0 | 2 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | ATGTC others(6421): Show |
chr2 | 127530683 | 127642726 | ||
a0014c0031 | 0/0 | 6426 | 1 | 0 | 1 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | ATGTC others(6421): Show |
chr2 | 127530683 | 127642726 | ||
a0014c0040 | 0/0 | 6426 | 1 | 0 | 0 | 1 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | ATGTC others(6421): Show |
chr2 | 127530683 | 127642726 | ||
a0015c0066 | 0/0 | 6426 | 1 | 1 | 0 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | ATGTC others(6421): Show |
chr2 | 127530683 | 127642726 | ||
a0015c0071 | 0/0 | 6426 | 1 | 1 | 0 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | ATGTC others(6421): Show |
chr2 | 127530683 | 127642726 | ||
a0016c0027 | 0/0 | 6426 | 2 | 1 | 1 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | ATGTC others(6421): Show |
chr2 | 127530683 | 127642726 | ||
a0017c0053 | 0/0 | 6426 | 1 | 1 | 0 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | ATGTC others(6421): Show |
chr2 | 127530683 | 127642726 | ||
a0017c0072 | 0/0 | 6426 | 1 | 1 | 0 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | ATGTC others(6421): Show |
chr2 | 127530683 | 127642726 | ||
a0018c0047 | 0/0 | 6426 | 1 | 0 | 0 | 1 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | ATGTC others(6421): Show |
chr2 | 127530683 | 127642726 | ||
a0019c0039 | 0/0 | 6426 | 1 | 0 | 1 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | ATGTC others(6421): Show |
chr2 | 127530683 | 127642726 | ||
a0020c0055 | 0/0 | 6426 | 1 | 0 | 1 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | ATGTC others(6421): Show |
chr2 | 127530683 | 127642726 | ||
a0021c0046 | 0/0 | 6426 | 1 | 1 | 0 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | ATGTC others(6421): Show |
chr2 | 127530683 | 127642726 | ||
a0022c0049 | 0/0 | 6426 | 1 | 0 | 1 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | ATGTC others(6421): Show |
chr2 | 127530683 | 127642726 | ||
a0023c0037 | 0/0 | 6426 | 1 | 0 | 0 | 1 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | ATGTC others(6421): Show |
chr2 | 127530683 | 127642726 | ||
a0024c0070 | 0/0 | 6426 | 1 | 1 | 0 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | ATGTC others(6421): Show |
chr2 | 127530683 | 127642726 | ||
a0025c0041 | 0/0 | 6426 | 1 | 1 | 0 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | ATGTC others(6421): Show |
chr2 | 127530683 | 127642726 | ||
a0026c0035 | 0/0 | 6426 | 1 | 0 | 0 | 1 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | ATGTC others(6421): Show |
chr2 | 127530683 | 127642726 | ||
a0027c0057 | 0/0 | 6426 | 1 | 1 | 0 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | ATGTC others(6421): Show |
chr2 | 127530683 | 127642726 | ||
a0028c0064 | 0/0 | 6426 | 1 | 1 | 0 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | ATGTC others(6421): Show |
chr2 | 127530683 | 127642726 | ||
a0029c0048 | 0/0 | 6426 | 1 | 1 | 0 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | ATGTC others(6421): Show |
chr2 | 127530683 | 127642726 | ||
a0030c0052 | 0/0 | 6426 | 1 | 0 | 0 | 0 | 0 | 1 | MYO7B_chr2_127530683_127642726 | MYO7B | ATGTC others(6421): Show |
chr2 | 127530683 | 127642726 | ||
a0031c0074 | 0/0 | 6426 | 1 | 0 | 0 | 0 | 0 | 1 | MYO7B_chr2_127530683_127642726 | MYO7B | ATGTC others(6421): Show |
chr2 | 127530683 | 127642726 | ||
a0032c0038 | 0/0 | 6426 | 1 | 0 | 0 | 0 | 0 | 1 | MYO7B_chr2_127530683_127642726 | MYO7B | ATGTC others(6421): Show |
chr2 | 127530683 | 127642726 | ||
a0033c0029 | 0/0 | 6426 | 1 | 0 | 0 | 0 | 0 | 1 | MYO7B_chr2_127530683_127642726 | MYO7B | ATGTC others(6421): Show |
chr2 | 127530683 | 127642726 | ||
a0034c0059 | 0/0 | 6426 | 1 | 0 | 0 | 0 | 0 | 1 | MYO7B_chr2_127530683_127642726 | MYO7B | ATGTC others(6421): Show |
chr2 | 127530683 | 127642726 | ||
a0035c0067 | 0/0 | 6426 | 1 | 0 | 0 | 0 | 0 | 1 | MYO7B_chr2_127530683_127642726 | MYO7B | ATGTC others(6421): Show |
chr2 | 127530683 | 127642726 | ||
a0036c0050 | 0/0 | 6426 | 1 | 0 | 0 | 1 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | ATGTC others(6421): Show |
chr2 | 127530683 | 127642726 | ||
a0037c0043 | 0/0 | 6426 | 1 | 0 | 0 | 1 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | ATGTC others(6421): Show |
chr2 | 127530683 | 127642726 | ||
a0038c0033 | 0/0 | 6426 | 1 | 0 | 0 | 1 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | ATGTC others(6421): Show |
chr2 | 127530683 | 127642726 | ||
a0039c0051 | 0/0 | 6426 | 1 | 0 | 0 | 1 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | ATGTC others(6421): Show |
chr2 | 127530683 | 127642726 | ||
a0040c0060 | 0/0 | 6426 | 1 | 0 | 0 | 1 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | ATGTC others(6421): Show |
chr2 | 127530683 | 127642726 | ||
a0041c0028 | 0/0 | 6426 | 1 | 0 | 0 | 1 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | ATGTC others(6421): Show |
chr2 | 127530683 | 127642726 | ||
a0042c0030 | 0/0 | 6426 | 1 | 0 | 0 | 1 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | ATGTC others(6421): Show |
chr2 | 127530683 | 127642726 | ||
a0043c0056 | 0/0 | 6426 | 1 | 0 | 0 | 1 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | ATGTC others(6421): Show |
chr2 | 127530683 | 127642726 | ||
a0044c0034 | 0/0 | 6426 | 1 | 1 | 0 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | ATGTC others(6421): Show |
chr2 | 127530683 | 127642726 | ||
a0045c0065 | 0/0 | 6426 | 1 | 1 | 0 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | ATGTC others(6421): Show |
chr2 | 127530683 | 127642726 | ||
a0046c0073 | 0/0 | 6426 | 1 | 1 | 0 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | ATGTC others(6421): Show |
chr2 | 127530683 | 127642726 | ||
a0047c0032 | 0/0 | 6426 | 1 | 0 | 0 | 1 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | ATGTC others(6421): Show |
chr2 | 127530683 | 127642726 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0002t0001 | 0/0 | 6910 | 34 | 17 | 8 | 8 | 0 | 1 | MYO7B_chr2_127530683_127642726 | MYO7B | AGTCA others(6905): Show |
chr2 | 127530683 | 127642726 |
a0001c0002t0003 | 0/0 | 6910 | 1 | 1 | 0 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | AGTCA others(6905): Show |
chr2 | 127530683 | 127642726 |
a0001c0002t0005 | 0/0 | 6910 | 1 | 1 | 0 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | AGTCA others(6905): Show |
chr2 | 127530683 | 127642726 |
a0001c0004t0001 | 1/0 | 6910 | 18 | 0 | 3 | 9 | 0 | 5 | MYO7B_chr2_127530683_127642726 | MYO7B | AGTCA others(6905): Show |
chr2 | 127530683 | 127642726 |
a0001c0005t0001 | 0/0 | 6910 | 2 | 0 | 0 | 1 | 0 | 1 | MYO7B_chr2_127530683_127642726 | MYO7B | AGTCA others(6905): Show |
chr2 | 127530683 | 127642726 |
a0001c0005t0002 | 0/0 | 6910 | 12 | 2 | 4 | 6 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | AGTCA others(6905): Show |
chr2 | 127530683 | 127642726 |
a0001c0005t0003 | 0/0 | 6910 | 1 | 0 | 0 | 0 | 0 | 1 | MYO7B_chr2_127530683_127642726 | MYO7B | AGTCA others(6905): Show |
chr2 | 127530683 | 127642726 |
a0001c0010t0001 | 0/0 | 6910 | 6 | 5 | 1 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | AGTCA others(6905): Show |
chr2 | 127530683 | 127642726 |
a0001c0013t0001 | 0/0 | 6910 | 5 | 4 | 1 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | AGTCA others(6905): Show |
chr2 | 127530683 | 127642726 |
a0001c0017t0004 | 0/0 | 6910 | 3 | 3 | 0 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | AGTCA others(6905): Show |
chr2 | 127530683 | 127642726 |
a0001c0018t0001 | 0/0 | 6910 | 3 | 3 | 0 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | AGTCA others(6905): Show |
chr2 | 127530683 | 127642726 |
a0001c0044t0003 | 0/0 | 6910 | 1 | 1 | 0 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | AGTCA others(6905): Show |
chr2 | 127530683 | 127642726 |
a0001c0045t0001 | 0/0 | 6910 | 1 | 1 | 0 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | AGTCA others(6905): Show |
chr2 | 127530683 | 127642726 |
a0001c0058t0002 | 0/0 | 6910 | 1 | 0 | 0 | 1 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | AGTCA others(6905): Show |
chr2 | 127530683 | 127642726 |
a0001c0061t0001 | 0/0 | 6910 | 1 | 1 | 0 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | AGTCA others(6905): Show |
chr2 | 127530683 | 127642726 |
a0001c0068t0001 | 0/0 | 6910 | 1 | 1 | 0 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | AGTCA others(6905): Show |
chr2 | 127530683 | 127642726 |
a0002c0001t0001 | 0/1 | 6910 | 36 | 1 | 13 | 15 | 0 | 6 | MYO7B_chr2_127530683_127642726 | MYO7B | AGTCA others(6905): Show |
chr2 | 127530683 | 127642726 |
a0002c0001t0006 | 0/0 | 6910 | 1 | 0 | 0 | 0 | 1 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | AGTCA others(6905): Show |
chr2 | 127530683 | 127642726 |
a0002c0001t0008 | 0/0 | 6910 | 1 | 0 | 0 | 1 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | AGTCA others(6905): Show |
chr2 | 127530683 | 127642726 |
a0002c0006t0001 | 0/0 | 6910 | 12 | 1 | 6 | 0 | 4 | 1 | MYO7B_chr2_127530683_127642726 | MYO7B | AGTCA others(6905): Show |
chr2 | 127530683 | 127642726 |
a0002c0006t0007 | 0/0 | 6910 | 1 | 0 | 0 | 1 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | AGTCA others(6905): Show |
chr2 | 127530683 | 127642726 |
a0002c0011t0002 | 0/0 | 6910 | 5 | 1 | 0 | 2 | 0 | 2 | MYO7B_chr2_127530683_127642726 | MYO7B | AGTCA others(6905): Show |
chr2 | 127530683 | 127642726 |
a0002c0012t0001 | 0/0 | 6910 | 5 | 0 | 0 | 5 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | AGTCA others(6905): Show |
chr2 | 127530683 | 127642726 |
a0003c0003t0001 | 0/0 | 6910 | 30 | 3 | 7 | 12 | 2 | 6 | MYO7B_chr2_127530683_127642726 | MYO7B | AGTCA others(6905): Show |
chr2 | 127530683 | 127642726 |
a0003c0026t0001 | 0/0 | 6910 | 2 | 0 | 0 | 2 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | AGTCA others(6905): Show |
chr2 | 127530683 | 127642726 |
a0003c0069t0001 | 0/0 | 6910 | 1 | 0 | 0 | 1 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | AGTCA others(6905): Show |
chr2 | 127530683 | 127642726 |
a0004c0007t0001 | 0/0 | 6910 | 6 | 1 | 5 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | AGTCA others(6905): Show |
chr2 | 127530683 | 127642726 |
a0004c0007t0003 | 0/0 | 6910 | 6 | 1 | 1 | 1 | 2 | 1 | MYO7B_chr2_127530683_127642726 | MYO7B | AGTCA others(6905): Show |
chr2 | 127530683 | 127642726 |
a0004c0021t0003 | 0/0 | 6910 | 2 | 0 | 2 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | AGTCA others(6905): Show |
chr2 | 127530683 | 127642726 |
a0004c0054t0001 | 0/0 | 6910 | 1 | 0 | 1 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | AGTCA others(6905): Show |
chr2 | 127530683 | 127642726 |
a0005c0008t0001 | 0/0 | 6910 | 9 | 6 | 1 | 1 | 0 | 1 | MYO7B_chr2_127530683_127642726 | MYO7B | AGTCA others(6905): Show |
chr2 | 127530683 | 127642726 |
a0006c0009t0001 | 0/0 | 6910 | 8 | 0 | 2 | 0 | 2 | 4 | MYO7B_chr2_127530683_127642726 | MYO7B | AGTCA others(6905): Show |
chr2 | 127530683 | 127642726 |
a0007c0023t0001 | 0/0 | 6910 | 2 | 2 | 0 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | AGTCA others(6905): Show |
chr2 | 127530683 | 127642726 |
a0007c0024t0001 | 0/0 | 6910 | 2 | 2 | 0 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | AGTCA others(6905): Show |
chr2 | 127530683 | 127642726 |
a0007c0025t0001 | 0/0 | 6910 | 2 | 0 | 0 | 0 | 1 | 1 | MYO7B_chr2_127530683_127642726 | MYO7B | AGTCA others(6905): Show |
chr2 | 127530683 | 127642726 |
a0007c0062t0001 | 0/0 | 6910 | 1 | 0 | 0 | 1 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | AGTCA others(6905): Show |
chr2 | 127530683 | 127642726 |
a0008c0015t0001 | 0/0 | 6910 | 4 | 3 | 1 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | AGTCA others(6905): Show |
chr2 | 127530683 | 127642726 |
a0008c0042t0001 | 0/0 | 6910 | 1 | 1 | 0 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | AGTCA others(6905): Show |
chr2 | 127530683 | 127642726 |
a0008c0063t0001 | 0/0 | 6910 | 1 | 1 | 0 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | AGTCA others(6905): Show |
chr2 | 127530683 | 127642726 |
a0009c0014t0001 | 0/0 | 6910 | 4 | 4 | 0 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | AGTCA others(6905): Show |
chr2 | 127530683 | 127642726 |
a0010c0020t0001 | 0/0 | 6910 | 2 | 0 | 0 | 0 | 0 | 2 | MYO7B_chr2_127530683_127642726 | MYO7B | AGTCA others(6905): Show |
chr2 | 127530683 | 127642726 |
a0010c0036t0001 | 0/0 | 6910 | 1 | 0 | 1 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | AGTCA others(6905): Show |
chr2 | 127530683 | 127642726 |
a0011c0016t0001 | 0/0 | 6910 | 3 | 3 | 0 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | AGTCA others(6905): Show |
chr2 | 127530683 | 127642726 |
a0012c0022t0001 | 0/0 | 6910 | 2 | 0 | 2 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | AGTCA others(6905): Show |
chr2 | 127530683 | 127642726 |
a0013c0019t0001 | 0/0 | 6910 | 2 | 0 | 2 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | AGTCA others(6905): Show |
chr2 | 127530683 | 127642726 |
a0014c0031t0001 | 0/0 | 6910 | 1 | 0 | 1 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | AGTCA others(6905): Show |
chr2 | 127530683 | 127642726 |
a0014c0040t0001 | 0/0 | 6910 | 1 | 0 | 0 | 1 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | AGTCA others(6905): Show |
chr2 | 127530683 | 127642726 |
a0015c0066t0001 | 0/0 | 6910 | 1 | 1 | 0 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | AGTCA others(6905): Show |
chr2 | 127530683 | 127642726 |
a0015c0071t0001 | 0/0 | 6910 | 1 | 1 | 0 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | AGTCA others(6905): Show |
chr2 | 127530683 | 127642726 |
a0016c0027t0001 | 0/0 | 6910 | 2 | 1 | 1 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | AGTCA others(6905): Show |
chr2 | 127530683 | 127642726 |
a0017c0053t0001 | 0/0 | 6910 | 1 | 1 | 0 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | AGTCA others(6905): Show |
chr2 | 127530683 | 127642726 |
a0017c0072t0001 | 0/0 | 6910 | 1 | 1 | 0 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | AGTCA others(6905): Show |
chr2 | 127530683 | 127642726 |
a0018c0047t0001 | 0/0 | 6910 | 1 | 0 | 0 | 1 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | AGTCA others(6905): Show |
chr2 | 127530683 | 127642726 |
a0019c0039t0001 | 0/0 | 6910 | 1 | 0 | 1 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | AGTCA others(6905): Show |
chr2 | 127530683 | 127642726 |
a0020c0055t0001 | 0/0 | 6910 | 1 | 0 | 1 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | AGTCA others(6905): Show |
chr2 | 127530683 | 127642726 |
a0021c0046t0003 | 0/0 | 6910 | 1 | 1 | 0 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | AGTCA others(6905): Show |
chr2 | 127530683 | 127642726 |
a0022c0049t0001 | 0/0 | 6910 | 1 | 0 | 1 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | AGTCA others(6905): Show |
chr2 | 127530683 | 127642726 |
a0023c0037t0001 | 0/0 | 6910 | 1 | 0 | 0 | 1 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | AGTCA others(6905): Show |
chr2 | 127530683 | 127642726 |
a0024c0070t0001 | 0/0 | 6910 | 1 | 1 | 0 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | AGTCA others(6905): Show |
chr2 | 127530683 | 127642726 |
a0025c0041t0004 | 0/0 | 6910 | 1 | 1 | 0 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | AGTCA others(6905): Show |
chr2 | 127530683 | 127642726 |
a0026c0035t0001 | 0/0 | 6910 | 1 | 0 | 0 | 1 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | AGTCA others(6905): Show |
chr2 | 127530683 | 127642726 |
a0027c0057t0001 | 0/0 | 6910 | 1 | 1 | 0 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | AGTCA others(6905): Show |
chr2 | 127530683 | 127642726 |
a0028c0064t0002 | 0/0 | 6910 | 1 | 1 | 0 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | AGTCA others(6905): Show |
chr2 | 127530683 | 127642726 |
a0029c0048t0001 | 0/0 | 6910 | 1 | 1 | 0 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | AGTCA others(6905): Show |
chr2 | 127530683 | 127642726 |
a0030c0052t0001 | 0/0 | 6910 | 1 | 0 | 0 | 0 | 0 | 1 | MYO7B_chr2_127530683_127642726 | MYO7B | AGTCA others(6905): Show |
chr2 | 127530683 | 127642726 |
a0031c0074t0001 | 0/0 | 6910 | 1 | 0 | 0 | 0 | 0 | 1 | MYO7B_chr2_127530683_127642726 | MYO7B | AGTCA others(6905): Show |
chr2 | 127530683 | 127642726 |
a0032c0038t0002 | 0/0 | 6910 | 1 | 0 | 0 | 0 | 0 | 1 | MYO7B_chr2_127530683_127642726 | MYO7B | AGTCA others(6905): Show |
chr2 | 127530683 | 127642726 |
a0033c0029t0001 | 0/0 | 6910 | 1 | 0 | 0 | 0 | 0 | 1 | MYO7B_chr2_127530683_127642726 | MYO7B | AGTCA others(6905): Show |
chr2 | 127530683 | 127642726 |
a0034c0059t0001 | 0/0 | 6910 | 1 | 0 | 0 | 0 | 0 | 1 | MYO7B_chr2_127530683_127642726 | MYO7B | AGTCA others(6905): Show |
chr2 | 127530683 | 127642726 |
a0035c0067t0001 | 0/0 | 6910 | 1 | 0 | 0 | 0 | 0 | 1 | MYO7B_chr2_127530683_127642726 | MYO7B | AGTCA others(6905): Show |
chr2 | 127530683 | 127642726 |
a0036c0050t0001 | 0/0 | 6910 | 1 | 0 | 0 | 1 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | AGTCA others(6905): Show |
chr2 | 127530683 | 127642726 |
a0037c0043t0001 | 0/0 | 6910 | 1 | 0 | 0 | 1 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | AGTCA others(6905): Show |
chr2 | 127530683 | 127642726 |
a0038c0033t0001 | 0/0 | 6910 | 1 | 0 | 0 | 1 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | AGTCA others(6905): Show |
chr2 | 127530683 | 127642726 |
a0039c0051t0001 | 0/0 | 6910 | 1 | 0 | 0 | 1 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | AGTCA others(6905): Show |
chr2 | 127530683 | 127642726 |
a0040c0060t0001 | 0/0 | 6910 | 1 | 0 | 0 | 1 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | AGTCA others(6905): Show |
chr2 | 127530683 | 127642726 |
a0041c0028t0001 | 0/0 | 6910 | 1 | 0 | 0 | 1 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | AGTCA others(6905): Show |
chr2 | 127530683 | 127642726 |
a0042c0030t0001 | 0/0 | 6910 | 1 | 0 | 0 | 1 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | AGTCA others(6905): Show |
chr2 | 127530683 | 127642726 |
a0043c0056t0001 | 0/0 | 6910 | 1 | 0 | 0 | 1 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | AGTCA others(6905): Show |
chr2 | 127530683 | 127642726 |
a0044c0034t0001 | 0/0 | 6910 | 1 | 1 | 0 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | AGTCA others(6905): Show |
chr2 | 127530683 | 127642726 |
a0045c0065t0001 | 0/0 | 6910 | 1 | 1 | 0 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | AGTCA others(6905): Show |
chr2 | 127530683 | 127642726 |
a0046c0073t0001 | 0/0 | 6910 | 1 | 1 | 0 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | AGTCA others(6905): Show |
chr2 | 127530683 | 127642726 |
a0047c0032t0001 | 0/0 | 6910 | 1 | 0 | 0 | 1 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | AGTCA others(6905): Show |
chr2 | 127530683 | 127642726 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0002t0001g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
a0001c0002t0001g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
a0001c0002t0001g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
a0001c0002t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
a0001c0002t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
a0001c0002t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
a0001c0002t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
a0001c0002t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
a0001c0002t0001g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
a0001c0002t0001g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
a0001c0002t0001g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
a0001c0002t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
a0001c0002t0001g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
a0001c0002t0001g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
a0001c0002t0001g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
a0001c0002t0001g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
a0001c0002t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
a0001c0002t0001g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
a0001c0002t0001g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
a0001c0002t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
a0001c0002t0001g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
a0001c0002t0001g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
a0001c0002t0001g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
a0001c0002t0001g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
a0001c0002t0001g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
a0001c0002t0001g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
a0001c0002t0001g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
a0001c0002t0001g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
a0001c0002t0001g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
a0001c0002t0001g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
a0001c0002t0001g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
a0001c0002t0001g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
a0001c0002t0001g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
a0001c0002t0001g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
a0001c0002t0003g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
a0001c0002t0005g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
a0001c0004t0001g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
a0001c0004t0001g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
a0001c0004t0001g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
a0001c0004t0001g0022 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
a0001c0004t0001g0023 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
a0001c0004t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
a0001c0004t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
a0001c0004t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
a0001c0004t0001g0073 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
a0001c0004t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
a0001c0004t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
a0001c0004t0001g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
a0001c0004t0001g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
a0001c0004t0001g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
a0001c0004t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
a0001c0004t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
a0001c0004t0001g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
a0001c0004t0001g0254 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
a0001c0005t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
a0001c0005t0001g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
a0001c0005t0002g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
a0001c0005t0002g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
a0001c0005t0002g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
a0001c0005t0002g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
a0001c0005t0002g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
a0001c0005t0002g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
a0001c0005t0002g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
a0001c0005t0002g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
a0001c0005t0002g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
a0001c0005t0002g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
a0001c0005t0002g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
a0001c0005t0002g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
a0001c0005t0003g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
a0001c0010t0001g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
a0001c0010t0001g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
a0001c0010t0001g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
a0001c0010t0001g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
a0001c0010t0001g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
a0001c0010t0001g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
a0001c0013t0001g0005 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
a0001c0013t0001g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
a0001c0013t0001g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
a0001c0013t0001g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
a0001c0017t0004g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
a0001c0017t0004g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
a0001c0017t0004g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
a0001c0018t0001g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
a0001c0018t0001g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
a0001c0018t0001g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
a0001c0044t0003g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
a0001c0045t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
a0001c0058t0002g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
a0001c0061t0001g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
a0001c0068t0001g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
a0002c0001t0001g0001 | 0/0 | 4 | 0 | 4 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
a0002c0001t0001g0002 | 0/0 | 3 | 0 | 1 | 0 | 0 | 2 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
a0002c0001t0001g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
a0002c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
a0002c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
a0002c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
a0002c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
a0002c0001t0001g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
a0002c0001t0001g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
a0002c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
a0002c0001t0001g0147 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
a0002c0001t0001g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
a0002c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
a0002c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
a0002c0001t0001g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
a0002c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
a0002c0001t0001g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
a0002c0001t0001g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
a0002c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
a0002c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
a0002c0001t0001g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
a0002c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
a0002c0001t0001g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
a0002c0001t0001g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
a0002c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
a0002c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
a0002c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
a0002c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
a0002c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
a0002c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
a0002c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
a0002c0001t0006g0180 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
a0002c0001t0008g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
a0002c0006t0001g0004 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
a0002c0006t0001g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
a0002c0006t0001g0014 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
a0002c0006t0001g0015 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
a0002c0006t0001g0016 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
a0002c0006t0001g0018 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
a0002c0006t0001g0019 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
a0002c0006t0001g0156 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
a0002c0006t0001g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
a0002c0006t0001g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
a0002c0006t0001g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
a0002c0006t0007g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
a0002c0011t0002g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
a0002c0011t0002g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
a0002c0011t0002g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
a0002c0011t0002g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
a0002c0011t0002g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
a0002c0012t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
a0002c0012t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
a0002c0012t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
a0002c0012t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
a0002c0012t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
a0003c0003t0001g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
a0003c0003t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
a0003c0003t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
a0003c0003t0001g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
a0003c0003t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
a0003c0003t0001g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
a0003c0003t0001g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
a0003c0003t0001g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
a0003c0003t0001g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
a0003c0003t0001g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
a0003c0003t0001g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
a0003c0003t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
a0003c0003t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
a0003c0003t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
a0003c0003t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
a0003c0003t0001g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
a0003c0003t0001g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
a0003c0003t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
a0003c0003t0001g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
a0003c0003t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
a0003c0003t0001g0241 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
a0003c0003t0001g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
a0003c0003t0001g0244 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
a0003c0003t0001g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
a0003c0003t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
a0003c0003t0001g0248 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
a0003c0003t0001g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
a0003c0003t0001g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
a0003c0003t0001g0255 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
a0003c0003t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
a0003c0026t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
a0003c0026t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
a0003c0069t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
a0004c0007t0001g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
a0004c0007t0001g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
a0004c0007t0001g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
a0004c0007t0001g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
a0004c0007t0001g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
a0004c0007t0001g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
a0004c0007t0003g0007 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
a0004c0007t0003g0010 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
a0004c0007t0003g0072 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
a0004c0007t0003g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
a0004c0007t0003g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
a0004c0007t0003g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
a0004c0021t0003g0007 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
a0004c0021t0003g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
a0004c0054t0001g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
a0005c0008t0001g0003 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
a0005c0008t0001g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
a0005c0008t0001g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
a0005c0008t0001g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
a0005c0008t0001g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
a0005c0008t0001g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
a0005c0008t0001g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
a0005c0008t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
a0006c0009t0001g0020 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
a0006c0009t0001g0037 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
a0006c0009t0001g0051 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
a0006c0009t0001g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
a0006c0009t0001g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
a0006c0009t0001g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
a0006c0009t0001g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
a0006c0009t0001g0097 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
a0007c0023t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
a0007c0023t0001g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
a0007c0024t0001g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
a0007c0024t0001g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
a0007c0025t0001g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
a0007c0025t0001g0211 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
a0007c0062t0001g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
a0008c0015t0001g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
a0008c0015t0001g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
a0008c0015t0001g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
a0008c0015t0001g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
a0008c0042t0001g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
a0008c0063t0001g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
a0009c0014t0001g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
a0009c0014t0001g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
a0009c0014t0001g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
a0009c0014t0001g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
a0010c0020t0001g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
a0010c0020t0001g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
a0010c0036t0001g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
a0011c0016t0001g0008 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
a0011c0016t0001g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
a0012c0022t0001g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
a0012c0022t0001g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
a0013c0019t0001g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
a0013c0019t0001g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
a0014c0031t0001g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
a0014c0040t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
a0015c0066t0001g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
a0015c0071t0001g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
a0016c0027t0001g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
a0016c0027t0001g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
a0017c0053t0001g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
a0017c0072t0001g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
a0018c0047t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
a0019c0039t0001g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
a0020c0055t0001g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
a0021c0046t0003g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
a0022c0049t0001g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
a0023c0037t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
a0024c0070t0001g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
a0025c0041t0004g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
a0026c0035t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
a0027c0057t0001g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
a0028c0064t0002g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
a0029c0048t0001g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
a0030c0052t0001g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
a0031c0074t0001g0026 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
a0032c0038t0002g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
a0033c0029t0001g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
a0034c0059t0001g0031 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
a0035c0067t0001g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
a0036c0050t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
a0037c0043t0001g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
a0038c0033t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
a0039c0051t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
a0040c0060t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
a0041c0028t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
a0042c0030t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
a0043c0056t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
a0044c0034t0001g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
a0045c0065t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
a0046c0073t0001g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
a0047c0032t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0002 | c0006 | t0001 | g0018 | EUR | GBR | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
HG00099 | hp2 | a0002 | c0001 | t0006 | g0180 | EUR | GBR | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
HG00280 | hp1 | a0003 | c0003 | t0001 | g0255 | EUR | FIN | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
HG00280 | hp2 | a0004 | c0007 | t0003 | g0007 | EUR | FIN | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
HG00323 | hp1 | a0003 | c0003 | t0001 | g0241 | EUR | FIN | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
HG00323 | hp2 | a0006 | c0009 | t0001 | g0097 | EUR | FIN | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
HG00621 | hp1 | a0018 | c0047 | t0001 | g0130 | EAS | CHS | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
HG00621 | hp2 | a0003 | c0003 | t0001 | g0033 | EAS | CHS | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
HG00642 | hp1 | a0001 | c0002 | t0001 | g0100 | AMR | PUR | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
HG00642 | hp2 | a0004 | c0007 | t0003 | g0121 | AMR | PUR | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
HG00733 | hp1 | a0003 | c0003 | t0001 | g0237 | AMR | PUR | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
HG00733 | hp2 | a0006 | c0009 | t0001 | g0061 | AMR | PUR | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
HG00735 | hp1 | a0002 | c0001 | t0001 | g0001 | AMR | PUR | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
HG00735 | hp2 | a0004 | c0007 | t0001 | g0162 | AMR | PUR | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
HG00738 | hp1 | a0002 | c0006 | t0001 | g0004 | AMR | PUR | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
HG00738 | hp2 | a0002 | c0001 | t0001 | g0189 | AMR | PUR | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
HG00741 | hp1 | a0002 | c0006 | t0001 | g0016 | AMR | PUR | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
HG00741 | hp2 | a0002 | c0006 | t0001 | g0160 | AMR | PUR | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
HG01069 | hp1 | a0012 | c0022 | t0001 | g0217 | AMR | PUR | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
HG01069 | hp2 | a0001 | c0002 | t0001 | g0225 | AMR | PUR | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
HG01070 | hp1 | a0001 | c0005 | t0002 | g0208 | AMR | PUR | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
HG01070 | hp2 | a0002 | c0006 | t0001 | g0158 | AMR | PUR | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
HG01071 | hp1 | a0012 | c0022 | t0001 | g0120 | AMR | PUR | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
HG01071 | hp2 | a0002 | c0006 | t0001 | g0004 | AMR | PUR | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
HG01081 | hp1 | a0002 | c0001 | t0001 | g0194 | AMR | PUR | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
HG01081 | hp2 | a0019 | c0039 | t0001 | g0017 | AMR | PUR | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
HG01099 | hp1 | a0001 | c0002 | t0001 | g0027 | AMR | PUR | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
HG01099 | hp2 | a0002 | c0001 | t0001 | g0001 | AMR | PUR | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
HG01106 | hp1 | a0006 | c0009 | t0001 | g0058 | AMR | PUR | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
HG01106 | hp2 | a0004 | c0007 | t0001 | g0261 | AMR | PUR | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
HG01109 | hp1 | a0003 | c0003 | t0001 | g0118 | AMR | PUR | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
HG01109 | hp2 | a0002 | c0001 | t0001 | g0116 | AMR | PUR | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
HG01168 | hp1 | a0004 | c0021 | t0003 | g0007 | AMR | PUR | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
HG01168 | hp2 | a0002 | c0001 | t0001 | g0183 | AMR | PUR | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
HG01169 | hp1 | a0013 | c0019 | t0001 | g0179 | AMR | PUR | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
HG01169 | hp2 | a0004 | c0021 | t0003 | g0219 | AMR | PUR | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
HG01175 | hp1 | a0001 | c0002 | t0001 | g0145 | AMR | PUR | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
HG01175 | hp2 | a0004 | c0054 | t0001 | g0165 | AMR | PUR | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
HG01192 | hp1 | a0010 | c0036 | t0001 | g0157 | AMR | PUR | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
HG01192 | hp2 | a0001 | c0004 | t0001 | g0214 | AMR | PUR | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
HG01243 | hp1 | a0001 | c0013 | t0001 | g0167 | AMR | PUR | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
HG01243 | hp2 | a0008 | c0015 | t0001 | g0047 | AMR | PUR | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
HG01255 | hp1 | a0004 | c0007 | t0001 | g0259 | AMR | CLM | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
HG01255 | hp2 | a0003 | c0003 | t0001 | g0239 | AMR | CLM | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
HG01256 | hp1 | a0001 | c0005 | t0002 | g0095 | AMR | CLM | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
HG01256 | hp2 | a0005 | c0008 | t0001 | g0209 | AMR | CLM | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
HG01257 | hp1 | a0002 | c0001 | t0001 | g0002 | AMR | CLM | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
HG01257 | hp2 | a0004 | c0007 | t0001 | g0220 | AMR | CLM | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
HG01258 | hp1 | a0004 | c0007 | t0001 | g0222 | AMR | CLM | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
HG01258 | hp2 | a0001 | c0005 | t0002 | g0052 | AMR | CLM | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
HG01346 | hp1 | a0001 | c0010 | t0001 | g0163 | AMR | CLM | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
HG01346 | hp2 | a0001 | c0005 | t0002 | g0050 | AMR | CLM | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
HG01358 | hp1 | a0014 | c0031 | t0001 | g0193 | AMR | CLM | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
HG01358 | hp2 | a0020 | c0055 | t0001 | g0260 | AMR | CLM | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
HG01361 | hp1 | a0002 | c0006 | t0001 | g0159 | AMR | CLM | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
HG01361 | hp2 | a0002 | c0001 | t0001 | g0181 | AMR | CLM | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
HG01433 | hp1 | a0003 | c0003 | t0001 | g0251 | AMR | CLM | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
HG01433 | hp2 | a0003 | c0003 | t0001 | g0210 | AMR | CLM | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
HG01515 | hp1 | a0002 | c0006 | t0001 | g0014 | EUR | IBS | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
HG01515 | hp2 | a0002 | c0006 | t0001 | g0156 | EUR | IBS | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
HG01516 | hp1 | a0007 | c0025 | t0001 | g0211 | EUR | IBS | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
HG01516 | hp2 | a0002 | c0006 | t0001 | g0019 | EUR | IBS | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
HG01884 | hp1 | a0015 | c0066 | t0001 | g0067 | AFR | ACB | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
HG01884 | hp2 | a0001 | c0002 | t0001 | g0155 | AFR | ACB | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
HG01891 | hp1 | a0016 | c0027 | t0001 | g0226 | AFR | ACB | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
HG01891 | hp2 | a0021 | c0046 | t0003 | g0078 | AFR | ACB | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
HG01943 | hp1 | a0001 | c0002 | t0001 | g0084 | AMR | PEL | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
HG01943 | hp2 | a0001 | c0004 | t0001 | g0021 | AMR | PEL | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
HG01952 | hp1 | a0002 | c0001 | t0001 | g0001 | AMR | PEL | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
HG01952 | hp2 | a0001 | c0002 | t0001 | g0083 | AMR | PEL | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
HG01975 | hp1 | a0016 | c0027 | t0001 | g0082 | AMR | PEL | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
HG01975 | hp2 | a0003 | c0003 | t0001 | g0243 | AMR | PEL | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
HG01981 | hp1 | a0002 | c0001 | t0001 | g0175 | AMR | PEL | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
HG01981 | hp2 | a0022 | c0049 | t0001 | g0252 | AMR | PEL | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
HG02027 | hp1 | a0001 | c0004 | t0001 | g0057 | EAS | KHV | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
HG02027 | hp2 | a0002 | c0011 | t0002 | g0187 | EAS | KHV | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
HG02055 | hp1 | a0001 | c0013 | t0001 | g0090 | AFR | ACB | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
HG02055 | hp2 | a0001 | c0002 | t0001 | g0106 | AFR | ACB | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
HG02071 | hp1 | a0002 | c0001 | t0001 | g0117 | EAS | KHV | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
HG02071 | hp2 | a0003 | c0003 | t0001 | g0109 | EAS | KHV | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
HG02074 | hp1 | a0001 | c0005 | t0002 | g0054 | EAS | KHV | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
HG02074 | hp2 | a0003 | c0003 | t0001 | g0125 | EAS | KHV | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
HG02132 | hp1 | a0004 | c0007 | t0003 | g0256 | EAS | KHV | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
HG02132 | hp2 | a0002 | c0001 | t0001 | g0199 | EAS | KHV | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
HG02135 | hp1 | a0003 | c0003 | t0001 | g0238 | EAS | KHV | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
HG02135 | hp2 | a0002 | c0001 | t0008 | g0006 | EAS | KHV | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
HG02145 | hp1 | a0008 | c0015 | t0001 | g0107 | AFR | ACB | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
HG02145 | hp2 | a0001 | c0002 | t0001 | g0089 | AFR | ACB | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
HG02148 | hp1 | a0001 | c0002 | t0001 | g0041 | AMR | PEL | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
HG02148 | hp2 | a0002 | c0001 | t0001 | g0196 | AMR | PEL | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
HG02165 | hp1 | a0023 | c0037 | t0001 | g0212 | EAS | CDX | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
HG02165 | hp2 | a0001 | c0005 | t0002 | g0094 | EAS | CDX | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
HG02257 | hp1 | a0001 | c0002 | t0001 | g0144 | AFR | ACB | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
HG02257 | hp2 | a0024 | c0070 | t0001 | g0028 | AFR | ACB | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
HG02258 | hp1 | a0004 | c0007 | t0001 | g0164 | AFR | ACB | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
HG02258 | hp2 | a0025 | c0041 | t0004 | g0076 | AFR | ACB | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
HG02280 | hp1 | a0008 | c0015 | t0001 | g0168 | AFR | ACB | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
HG02280 | hp2 | a0001 | c0005 | t0002 | g0131 | AFR | ACB | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
HG02293 | hp1 | a0001 | c0004 | t0001 | g0218 | AMR | PEL | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
HG02293 | hp2 | a0001 | c0002 | t0001 | g0034 | AMR | PEL | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
HG02300 | hp1 | a0002 | c0001 | t0001 | g0113 | AMR | PEL | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
HG02300 | hp2 | a0013 | c0019 | t0001 | g0178 | AMR | PEL | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
HG02451 | hp1 | a0001 | c0010 | t0001 | g0265 | AFR | ACB | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
HG02451 | hp2 | a0001 | c0002 | t0001 | g0088 | AFR | ACB | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
HG02523 | hp1 | a0002 | c0001 | t0001 | g0110 | EAS | KHV | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
HG02523 | hp2 | a0026 | c0035 | t0001 | g0114 | EAS | KHV | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
HG02572 | hp1 | a0017 | c0053 | t0001 | g0271 | AFR | GWD | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
HG02572 | hp2 | a0009 | c0014 | t0001 | g0104 | AFR | GWD | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
HG02602 | hp1 | a0005 | c0008 | t0001 | g0161 | SAS | PJL | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
HG02602 | hp2 | a0003 | c0003 | t0001 | g0129 | SAS | PJL | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
HG02622 | hp1 | a0001 | c0018 | t0001 | g0266 | AFR | GWD | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
HG02622 | hp2 | a0007 | c0023 | t0001 | g0122 | AFR | GWD | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
HG02630 | hp1 | a0011 | c0016 | t0001 | g0008 | AFR | GWD | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
HG02630 | hp2 | a0001 | c0017 | t0004 | g0025 | AFR | GWD | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
HG02647 | hp1 | a0001 | c0002 | t0001 | g0269 | AFR | GWD | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
HG02647 | hp2 | a0001 | c0002 | t0001 | g0048 | AFR | GWD | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
HG02683 | hp1 | a0003 | c0003 | t0001 | g0244 | SAS | PJL | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
HG02683 | hp2 | a0001 | c0005 | t0001 | g0098 | SAS | PJL | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
HG02698 | hp1 | a0001 | c0004 | t0001 | g0246 | SAS | PJL | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
HG02698 | hp2 | a0002 | c0001 | t0001 | g0002 | SAS | PJL | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
HG02717 | hp1 | a0005 | c0008 | t0001 | g0003 | AFR | GWD | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
HG02717 | hp2 | a0001 | c0002 | t0003 | g0046 | AFR | GWD | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
HG02723 | hp1 | a0003 | c0003 | t0001 | g0245 | AFR | GWD | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
HG02723 | hp2 | a0027 | c0057 | t0001 | g0079 | AFR | GWD | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
HG02809 | hp1 | a0001 | c0013 | t0001 | g0166 | AFR | GWD | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
HG02809 | hp2 | a0001 | c0044 | t0003 | g0080 | AFR | GWD | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
HG02818 | hp1 | a0001 | c0061 | t0001 | g0099 | AFR | GWD | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
HG02818 | hp2 | a0009 | c0014 | t0001 | g0148 | AFR | GWD | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
HG02886 | hp1 | a0002 | c0001 | t0001 | g0184 | AFR | GWD | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
HG02886 | hp2 | a0001 | c0002 | t0001 | g0262 | AFR | GWD | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
HG02895 | hp1 | a0001 | c0045 | t0001 | g0142 | AFR | GWD | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
HG02895 | hp2 | a0001 | c0018 | t0001 | g0268 | AFR | GWD | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
HG02896 | hp1 | a0005 | c0008 | t0001 | g0154 | AFR | GWD | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
HG02896 | hp2 | a0001 | c0002 | t0001 | g0092 | AFR | GWD | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
HG02897 | hp1 | a0005 | c0008 | t0001 | g0153 | AFR | GWD | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
HG02897 | hp2 | a0001 | c0018 | t0001 | g0267 | AFR | GWD | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
HG02922 | hp1 | a0005 | c0008 | t0001 | g0170 | AFR | ESN | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
HG02922 | hp2 | a0017 | c0072 | t0001 | g0012 | AFR | ESN | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
HG02965 | hp1 | a0001 | c0002 | t0001 | g0045 | AFR | ESN | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
HG02965 | hp2 | a0002 | c0011 | t0002 | g0270 | AFR | ESN | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
HG02970 | hp1 | a0001 | c0002 | t0001 | g0133 | AFR | ESN | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
HG02970 | hp2 | a0009 | c0014 | t0001 | g0136 | AFR | ESN | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
HG03017 | hp1 | a0002 | c0001 | t0001 | g0176 | SAS | PJL | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
HG03017 | hp2 | a0002 | c0011 | t0002 | g0186 | SAS | PJL | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
HG03041 | hp1 | a0011 | c0016 | t0001 | g0008 | AFR | GWD | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
HG03041 | hp2 | a0001 | c0017 | t0004 | g0024 | AFR | GWD | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
HG03130 | hp1 | a0001 | c0010 | t0001 | g0264 | AFR | ESN | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
HG03130 | hp2 | a0001 | c0013 | t0001 | g0005 | AFR | ESN | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
HG03139 | hp1 | a0005 | c0008 | t0001 | g0003 | AFR | ESN | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
HG03139 | hp2 | a0001 | c0068 | t0001 | g0093 | AFR | ESN | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
HG03195 | hp1 | a0001 | c0010 | t0001 | g0228 | AFR | ESN | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
HG03195 | hp2 | a0007 | c0024 | t0001 | g0086 | AFR | ESN | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
HG03209 | hp1 | a0028 | c0064 | t0002 | g0143 | AFR | MSL | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
HG03209 | hp2 | a0008 | c0042 | t0001 | g0064 | AFR | MSL | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
HG03225 | hp1 | a0001 | c0002 | t0001 | g0135 | AFR | MSL | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
HG03225 | hp2 | a0029 | c0048 | t0001 | g0132 | AFR | MSL | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
HG03239 | hp1 | a0006 | c0009 | t0001 | g0059 | SAS | PJL | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
HG03239 | hp2 | a0002 | c0006 | t0001 | g0015 | SAS | PJL | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
HG03453 | hp1 | a0015 | c0071 | t0001 | g0123 | AFR | MSL | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
HG03453 | hp2 | a0001 | c0005 | t0002 | g0065 | AFR | MSL | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
HG03490 | hp1 | a0001 | c0004 | t0001 | g0254 | SAS | PJL | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
HG03490 | hp2 | a0002 | c0001 | t0001 | g0182 | SAS | PJL | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
HG03492 | hp1 | a0002 | c0001 | t0001 | g0002 | SAS | PJL | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
HG03492 | hp2 | a0030 | c0052 | t0001 | g0087 | SAS | PJL | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
HG03516 | hp1 | a0011 | c0016 | t0001 | g0141 | AFR | ESN | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
HG03516 | hp2 | a0001 | c0002 | t0005 | g0074 | AFR | ESN | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
HG03654 | hp1 | a0031 | c0074 | t0001 | g0026 | SAS | PJL | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
HG03654 | hp2 | a0001 | c0004 | t0001 | g0221 | SAS | PJL | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
HG03669 | hp1 | a0003 | c0003 | t0001 | g0128 | SAS | PJL | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
HG03669 | hp2 | a0001 | c0004 | t0001 | g0022 | SAS | PJL | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
HG03688 | hp1 | a0004 | c0007 | t0003 | g0010 | SAS | STU | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
HG03688 | hp2 | a0006 | c0009 | t0001 | g0020 | SAS | STU | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
HG03710 | hp1 | a0007 | c0025 | t0001 | g0042 | SAS | PJL | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
HG03710 | hp2 | a0010 | c0020 | t0001 | g0151 | SAS | PJL | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
HG03831 | hp1 | a0001 | c0004 | t0001 | g0023 | SAS | BEB | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
HG03831 | hp2 | a0001 | c0005 | t0003 | g0063 | SAS | BEB | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
HG03927 | hp1 | a0006 | c0009 | t0001 | g0037 | SAS | BEB | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
HG03927 | hp2 | a0001 | c0002 | t0001 | g0060 | SAS | BEB | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
HG03942 | hp1 | a0032 | c0038 | t0002 | g0105 | SAS | BEB | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
HG03942 | hp2 | a0002 | c0001 | t0001 | g0112 | SAS | BEB | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
HG04115 | hp1 | a0003 | c0003 | t0001 | g0126 | SAS | STU | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
HG04115 | hp2 | a0033 | c0029 | t0001 | g0201 | SAS | STU | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
HG04184 | hp1 | a0003 | c0003 | t0001 | g0127 | SAS | BEB | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
HG04184 | hp2 | a0002 | c0011 | t0002 | g0108 | SAS | BEB | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
HG04199 | hp1 | a0003 | c0003 | t0001 | g0248 | SAS | STU | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
HG04199 | hp2 | a0006 | c0009 | t0001 | g0056 | SAS | STU | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
HG04204 | hp1 | a0010 | c0020 | t0001 | g0150 | SAS | STU | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
HG04204 | hp2 | a0002 | c0001 | t0001 | g0111 | SAS | STU | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
HG04228 | hp1 | a0034 | c0059 | t0001 | g0031 | SAS | STU | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
HG04228 | hp2 | a0035 | c0067 | t0001 | g0119 | SAS | STU | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
NA18522 | hp1 | a0001 | c0017 | t0004 | g0075 | AFR | YRI | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
NA18522 | hp2 | a0001 | c0002 | t0001 | g0091 | AFR | YRI | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
NA18612 | hp1 | a0002 | c0006 | t0007 | g0216 | EAS | CHB | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
NA18612 | hp2 | a0001 | c0004 | t0001 | g0124 | EAS | CHB | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
NA18747 | hp1 | a0002 | c0001 | t0001 | g0192 | EAS | CHB | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
NA18747 | hp2 | a0036 | c0050 | t0001 | g0231 | EAS | CHB | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
NA18906 | hp1 | a0001 | c0002 | t0001 | g0101 | AFR | YRI | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
NA18906 | hp2 | a0008 | c0063 | t0001 | g0257 | AFR | YRI | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
NA18941 | hp1 | a0002 | c0012 | t0001 | g0171 | EAS | JPT | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
NA18941 | hp2 | a0003 | c0003 | t0001 | g0263 | EAS | JPT | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
NA18942 | hp1 | a0001 | c0002 | t0001 | g0032 | EAS | JPT | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
NA18942 | hp2 | a0001 | c0004 | t0001 | g0232 | EAS | JPT | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
NA18947 | hp1 | a0002 | c0001 | t0001 | g0204 | EAS | JPT | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
NA18947 | hp2 | a0003 | c0003 | t0001 | g0247 | EAS | JPT | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
NA18949 | hp1 | a0002 | c0001 | t0001 | g0188 | EAS | JPT | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
NA18949 | hp2 | a0037 | c0043 | t0001 | g0030 | EAS | JPT | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
NA18950 | hp1 | a0002 | c0001 | t0001 | g0205 | EAS | JPT | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
NA18950 | hp2 | a0003 | c0003 | t0001 | g0230 | EAS | JPT | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
NA18957 | hp1 | a0001 | c0058 | t0002 | g0103 | EAS | JPT | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
NA18957 | hp2 | a0002 | c0012 | t0001 | g0206 | EAS | JPT | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
NA18959 | hp1 | a0014 | c0040 | t0001 | g0190 | EAS | JPT | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
NA18959 | hp2 | a0003 | c0003 | t0001 | g0229 | EAS | JPT | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
NA18962 | hp1 | a0038 | c0033 | t0001 | g0069 | EAS | JPT | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
NA18962 | hp2 | a0001 | c0004 | t0001 | g0043 | EAS | JPT | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
NA18964 | hp1 | a0002 | c0001 | t0001 | g0185 | EAS | JPT | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
NA18964 | hp2 | a0001 | c0002 | t0001 | g0035 | EAS | JPT | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
NA18966 | hp1 | a0002 | c0001 | t0001 | g0006 | EAS | JPT | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
NA18966 | hp2 | a0003 | c0003 | t0001 | g0233 | EAS | JPT | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
NA18967 | hp1 | a0001 | c0002 | t0001 | g0040 | EAS | JPT | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
NA18967 | hp2 | a0002 | c0001 | t0001 | g0215 | EAS | JPT | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
NA18968 | hp1 | a0001 | c0004 | t0001 | g0197 | EAS | JPT | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
NA18968 | hp2 | a0001 | c0005 | t0002 | g0044 | EAS | JPT | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
NA18972 | hp1 | a0003 | c0026 | t0001 | g0146 | EAS | JPT | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
NA18972 | hp2 | a0001 | c0004 | t0001 | g0242 | EAS | JPT | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
NA18975 | hp1 | a0039 | c0051 | t0001 | g0234 | EAS | JPT | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
NA18975 | hp2 | a0001 | c0005 | t0001 | g0049 | EAS | JPT | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
NA18980 | hp1 | a0040 | c0060 | t0001 | g0055 | EAS | JPT | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
NA18980 | hp2 | a0001 | c0004 | t0001 | g0011 | EAS | JPT | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
NA18981 | hp1 | a0001 | c0002 | t0001 | g0085 | EAS | JPT | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
NA18981 | hp2 | a0041 | c0028 | t0001 | g0195 | EAS | JPT | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
NA18983 | hp1 | a0003 | c0003 | t0001 | g0081 | EAS | JPT | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
NA18983 | hp2 | a0001 | c0002 | t0001 | g0038 | EAS | JPT | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
NA18984 | hp1 | a0042 | c0030 | t0001 | g0202 | EAS | JPT | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
NA18984 | hp2 | a0001 | c0005 | t0002 | g0096 | EAS | JPT | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
NA18985 | hp1 | a0002 | c0001 | t0001 | g0071 | EAS | JPT | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
NA18985 | hp2 | a0003 | c0003 | t0001 | g0240 | EAS | JPT | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
NA18986 | hp1 | a0001 | c0005 | t0002 | g0062 | EAS | JPT | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
NA18986 | hp2 | a0002 | c0001 | t0001 | g0198 | EAS | JPT | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
NA18995 | hp1 | a0043 | c0056 | t0001 | g0258 | EAS | JPT | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
NA18995 | hp2 | a0002 | c0001 | t0001 | g0177 | EAS | JPT | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
NA19000 | hp1 | a0007 | c0062 | t0001 | g0029 | EAS | JPT | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
NA19000 | hp2 | a0002 | c0012 | t0001 | g0115 | EAS | JPT | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
NA19007 | hp1 | a0002 | c0001 | t0001 | g0203 | EAS | JPT | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
NA19007 | hp2 | a0001 | c0005 | t0002 | g0102 | EAS | JPT | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
NA19010 | hp1 | a0001 | c0004 | t0001 | g0009 | EAS | JPT | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
NA19010 | hp2 | a0002 | c0001 | t0001 | g0200 | EAS | JPT | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
NA19030 | hp1 | a0044 | c0034 | t0001 | g0070 | AFR | LWK | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
NA19030 | hp2 | a0001 | c0002 | t0001 | g0077 | AFR | LWK | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
NA19043 | hp1 | a0045 | c0065 | t0001 | g0140 | AFR | LWK | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
NA19043 | hp2 | a0046 | c0073 | t0001 | g0068 | AFR | LWK | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
NA19056 | hp1 | a0002 | c0012 | t0001 | g0173 | EAS | JPT | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
NA19056 | hp2 | a0001 | c0002 | t0001 | g0036 | EAS | JPT | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
NA19060 | hp1 | a0003 | c0026 | t0001 | g0253 | EAS | JPT | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
NA19060 | hp2 | a0001 | c0002 | t0001 | g0039 | EAS | JPT | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
NA19063 | hp1 | a0001 | c0002 | t0001 | g0053 | EAS | JPT | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
NA19063 | hp2 | a0002 | c0011 | t0002 | g0207 | EAS | JPT | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
NA19070 | hp1 | a0001 | c0004 | t0001 | g0066 | EAS | JPT | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
NA19070 | hp2 | a0005 | c0008 | t0001 | g0213 | EAS | JPT | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
NA19074 | hp1 | a0047 | c0032 | t0001 | g0172 | EAS | JPT | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
NA19074 | hp2 | a0003 | c0003 | t0001 | g0235 | EAS | JPT | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
NA19079 | hp1 | a0002 | c0012 | t0001 | g0191 | EAS | JPT | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
NA19079 | hp2 | a0003 | c0069 | t0001 | g0250 | EAS | JPT | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
NA20129 | hp1 | a0001 | c0002 | t0001 | g0134 | AFR | ASW | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
NA20129 | hp2 | a0001 | c0010 | t0001 | g0138 | AFR | ASW | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
NA20752 | hp1 | a0004 | c0007 | t0003 | g0072 | EUR | TSI | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
NA20752 | hp2 | a0006 | c0009 | t0001 | g0051 | EUR | TSI | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
HG01123 | hp1 | a0002 | c0001 | t0001 | g0001 | AMR | CLM | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
HG01123 | hp2 | a0003 | c0003 | t0001 | g0224 | AMR | CLM | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
HG02109 | hp1 | a0007 | c0023 | t0001 | g0149 | AFR | ACB | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
HG02109 | hp2 | a0001 | c0010 | t0001 | g0139 | AFR | ACB | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
HG02486 | hp1 | a0003 | c0003 | t0001 | g0236 | AFR | ACB | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
HG02486 | hp2 | a0009 | c0014 | t0001 | g0174 | AFR | ACB | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
HG02559 | hp1 | a0003 | c0003 | t0001 | g0249 | AFR | ACB | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
HG02559 | hp2 | a0008 | c0015 | t0001 | g0169 | AFR | ACB | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
HG03471 | hp1 | a0002 | c0006 | t0001 | g0013 | AFR | MSL | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
HG03471 | hp2 | a0005 | c0008 | t0001 | g0152 | AFR | MSL | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
HG06807 | hp1 | a0001 | c0013 | t0001 | g0005 | AFR | USA | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
HG06807 | hp2 | a0007 | c0024 | t0001 | g0227 | AFR | USA | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
NA21309 | hp1 | a0001 | c0002 | t0001 | g0137 | AFR | LWK | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
NA21309 | hp2 | a0004 | c0007 | t0003 | g0223 | AFR | LWK | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
homoSapiens | chm13v2 | a0002 | c0001 | t0001 | g0147 | REF | REF | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
homoSapiens | grch38p0 | a0001 | c0004 | t0001 | g0073 | REF | REF | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:127564195 | G | A | 15 | a0002 a0005 a0010 others(12): Show |
86 | HG00099.hp1 HG00099.hp2 HG00735.hp1 others(83): Show |
missense_variant | MODERATE | c.61G>A | p.Gly21Ser | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 3/48 | 233/6910 | 61/6429 | 21/2142 | chr2 | 127564195 | |||
chr2:127564211 | G | A | 1 | a0025 | 1 | HG02258.hp2 | missense_variant | MODERATE | c.77G>A | p.Gly26Asp | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 3/48 | 249/6910 | 77/6429 | 26/2142 | chr2 | 127564211 | |||
chr2:127569812 | C | T | 1 | a0019 | 1 | HG01081.hp2 | missense_variant | MODERATE | c.494C>T | p.Thr165Met | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 6/48 | 666/6910 | 494/6429 | 165/2142 | chr2 | 127569812 | |||
chr2:127573931 | G | T | 1 | a0031 | 1 | HG03654.hp1 | missense_variant | MODERATE | c.604G>T | p.Ala202Ser | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 7/48 | 776/6910 | 604/6429 | 202/2142 | chr2 | 127573931 | |||
chr2:127574003 | G | T | 1 | a0032 | 1 | HG03942.hp1 | missense_variant | MODERATE | c.676G>T | p.Val226Leu | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 7/48 | 848/6910 | 676/6429 | 226/2142 | chr2 | 127574003 | |||
chr2:127574018 | C | T | 1 | a0016 | 2 | HG01891.hp1 HG01975.hp1 |
missense_variant | MODERATE | c.691C>T | p.Arg231Cys | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 7/48 | 863/6910 | 691/6429 | 231/2142 | chr2 | 127574018 | |||
chr2:127578178 | G | C | 1 | a0037 | 1 | NA18949.hp2 | missense_variant | MODERATE | c.895G>C | p.Ala299Pro | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 9/48 | 1067/6910 | 895/6429 | 299/2142 | chr2 | 127578178 | |||
chr2:127590134 | T | G | 1 | a0041 | 1 | NA18981.hp2 | missense_variant | MODERATE | c.1897T>G | p.Phe633Val | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 16/48 | 2069/6910 | 1897/6429 | 633/2142 | chr2 | 127590134 | |||
chr2:127590183 | C | G | 1 | a0035 | 1 | HG04228.hp2 | missense_variant | MODERATE | c.1946C>G | p.Pro649Arg | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 16/48 | 2118/6910 | 1946/6429 | 649/2142 | chr2 | 127590183 | |||
chr2:127593588 | G | A | 1 | a0024 | 1 | HG02257.hp2 | missense_variant | MODERATE | c.2188G>A | p.Val730Met | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 18/48 | 2360/6910 | 2188/6429 | 730/2142 | chr2 | 127593588 | |||
chr2:127593608 | A | C | 1 | a0015 | 2 | HG01884.hp1 HG03453.hp1 |
missense_variant | MODERATE | c.2208A>C | p.Lys736Asn | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 18/48 | 2380/6910 | 2208/6429 | 736/2142 | chr2 | 127593608 | |||
chr2:127607225 | G | A | 1 | a0021 | 1 | HG01891.hp2 | missense_variant | MODERATE | c.2444G>A | p.Arg815His | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 21/48 | 2616/6910 | 2444/6429 | 815/2142 | chr2 | 127607225 | |||
chr2:127607399 | G | A | 1 | a0018 | 1 | HG00621.hp1 | missense_variant | MODERATE | c.2618G>A | p.Arg873His | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 21/48 | 2790/6910 | 2618/6429 | 873/2142 | chr2 | 127607399 | |||
chr2:127609573 | C | T | 1 | a0028 | 1 | HG03209.hp1 | missense_variant | MODERATE | c.2882C>T | p.Pro961Leu | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 23/48 | 3054/6910 | 2882/6429 | 961/2142 | chr2 | 127609573 | |||
chr2:127609858 | G | A | 2 | a0011 a0029 |
4 | HG02630.hp1 HG03041.hp1 HG03225.hp2 others(1): Show |
missense_variant | MODERATE | c.3034G>A | p.Val1012Ile | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 24/48 | 3206/6910 | 3034/6429 | 1012/2142 | chr2 | 127609858 | |||
chr2:127609981 | G | A | 1 | a0011 | 3 | HG02630.hp1 HG03041.hp1 HG03516.hp1 |
missense_variant | MODERATE | c.3157G>A | p.Gly1053Ser | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 24/48 | 3329/6910 | 3157/6429 | 1053/2142 | chr2 | 127609981 | |||
chr2:127612590 | C | T | 1 | a0021 | 1 | HG01891.hp2 | missense_variant | MODERATE | c.3385C>T | p.Arg1129Trp | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 26/48 | 3557/6910 | 3385/6429 | 1129/2142 | chr2 | 127612590 | |||
chr2:127620434 | G | A | 1 | a0011 | 3 | HG02630.hp1 HG03041.hp1 HG03516.hp1 |
missense_variant | MODERATE | c.3493G>A | p.Gly1165Ser | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 27/48 | 3665/6910 | 3493/6429 | 1165/2142 | chr2 | 127620434 | |||
chr2:127621988 | C | G | 4 | a0004 a0020 a0031 others(1): Show |
18 | HG00280.hp2 HG00642.hp2 HG00735.hp2 others(15): Show |
missense_variant | MODERATE | c.3532C>G | p.Leu1178Val | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 28/48 | 3704/6910 | 3532/6429 | 1178/2142 | chr2 | 127621988 | |||
chr2:127622034 | C | T | 1 | a0009 | 4 | HG02486.hp2 HG02572.hp2 HG02818.hp2 others(1): Show |
missense_variant | MODERATE | c.3578C>T | p.Ala1193Val | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 28/48 | 3750/6910 | 3578/6429 | 1193/2142 | chr2 | 127622034 | |||
chr2:127622040 | G | A | 1 | a0012 | 2 | HG01069.hp1 HG01071.hp1 |
missense_variant | MODERATE | c.3584G>A | p.Arg1195His | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 28/48 | 3756/6910 | 3584/6429 | 1195/2142 | chr2 | 127622040 | |||
chr2:127624142 | G | A | 3 | a0011 a0024 a0029 |
5 | HG02257.hp2 HG02630.hp1 HG03041.hp1 others(2): Show |
missense_variant | MODERATE | c.3869G>A | p.Arg1290Gln | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 30/48 | 4041/6910 | 3869/6429 | 1290/2142 | chr2 | 127624142 | |||
chr2:127624156 | G | A | 1 | a0034 | 1 | HG04228.hp1 | missense_variant | MODERATE | c.3883G>A | p.Ala1295Thr | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 30/48 | 4055/6910 | 3883/6429 | 1295/2142 | chr2 | 127624156 | |||
chr2:127624198 | A | G | 1 | a0008 | 6 | HG01243.hp2 HG02145.hp1 HG02280.hp1 others(3): Show |
missense_variant | MODERATE | c.3925A>G | p.Ile1309Val | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 30/48 | 4097/6910 | 3925/6429 | 1309/2142 | chr2 | 127624198 | |||
chr2:127624286 | G | A | 2 | a0011 a0029 |
4 | HG02630.hp1 HG03041.hp1 HG03225.hp2 others(1): Show |
missense_variant | MODERATE | c.4013G>A | p.Arg1338Gln | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 30/48 | 4185/6910 | 4013/6429 | 1338/2142 | chr2 | 127624286 | |||
chr2:127627015 | G | A | 1 | a0025 | 1 | HG02258.hp2 | missense_variant | MODERATE | c.4256G>A | p.Arg1419Gln | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 32/48 | 4428/6910 | 4256/6429 | 1419/2142 | chr2 | 127627015 | |||
chr2:127627038 | C | T | 1 | a0026 | 1 | HG02523.hp2 | missense_variant | MODERATE | c.4279C>T | p.Arg1427Cys | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 32/48 | 4451/6910 | 4279/6429 | 1427/2142 | chr2 | 127627038 | |||
chr2:127628407 | C | T | 2 | a0017 a0046 |
3 | HG02572.hp1 HG02922.hp2 NA19043.hp2 |
missense_variant | MODERATE | c.4496C>T | p.Thr1499Met | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 34/48 | 4668/6910 | 4496/6429 | 1499/2142 | chr2 | 127628407 | |||
chr2:127629686 | G | A | 2 | a0013 a0043 |
3 | HG01169.hp1 HG02300.hp2 NA18995.hp1 |
missense_variant | MODERATE | c.4666G>A | p.Val1556Ile | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 35/48 | 4838/6910 | 4666/6429 | 1556/2142 | chr2 | 127629686 | |||
chr2:127630832 | T | C | 1 | a0037 | 1 | NA18949.hp2 | missense_variant | MODERATE | c.4861T>C | p.Phe1621Leu | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 36/48 | 5033/6910 | 4861/6429 | 1621/2142 | chr2 | 127630832 | |||
chr2:127630862 | A | C | 3 | a0006 a0010 a0023 |
12 | HG00323.hp2 HG00733.hp2 HG01106.hp1 others(9): Show |
missense_variant | MODERATE | c.4891A>C | p.Lys1631Gln | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 36/48 | 5063/6910 | 4891/6429 | 1631/2142 | chr2 | 127630862 | |||
chr2:127631219 | G | A | 1 | a0045 | 1 | NA19043.hp1 | missense_variant | MODERATE | c.4951G>A | p.Asp1651Asn | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 37/48 | 5123/6910 | 4951/6429 | 1651/2142 | chr2 | 127631219 | |||
chr2:127631237 | G | A | 1 | a0011 | 3 | HG02630.hp1 HG03041.hp1 HG03516.hp1 |
missense_variant | MODERATE | c.4969G>A | p.Val1657Met | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 37/48 | 5141/6910 | 4969/6429 | 1657/2142 | chr2 | 127631237 | |||
chr2:127631287 | G | C | 7 | a0003 a0005 a0022 others(4): Show |
47 | HG00280.hp1 HG00323.hp1 HG00621.hp2 others(44): Show |
missense_variant | MODERATE | c.5019G>C | p.Glu1673Asp | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 37/48 | 5191/6910 | 5019/6429 | 1673/2142 | chr2 | 127631287 | |||
chr2:127632259 | C | T | 1 | a0044 | 1 | NA19030.hp1 | missense_variant | MODERATE | c.5263C>T | p.Arg1755Trp | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 39/48 | 5435/6910 | 5263/6429 | 1755/2142 | chr2 | 127632259 | |||
chr2:127632260 | G | A | 1 | a0022 | 1 | HG01981.hp2 | missense_variant | MODERATE | c.5264G>A | p.Arg1755Gln | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 39/48 | 5436/6910 | 5264/6429 | 1755/2142 | chr2 | 127632260 | |||
chr2:127634620 | T | G | 1 | a0042 | 1 | NA18984.hp1 | missense_variant | MODERATE | c.5650T>G | p.Phe1884Val | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 42/48 | 5822/6910 | 5650/6429 | 1884/2142 | chr2 | 127634620 | |||
chr2:127634621 | T | A | 1 | a0042 | 1 | NA18984.hp1 | missense_variant | MODERATE | c.5651T>A | p.Phe1884Tyr | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 42/48 | 5823/6910 | 5651/6429 | 1884/2142 | chr2 | 127634621 | |||
chr2:127634639 | G | T | 1 | a0038 | 1 | NA18962.hp1 | missense_variant | MODERATE | c.5669G>T | p.Arg1890Met | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 42/48 | 5841/6910 | 5669/6429 | 1890/2142 | chr2 | 127634639 | |||
chr2:127635123 | C | T | 1 | a0026 | 1 | HG02523.hp2 | missense_variant | MODERATE | c.5717C>T | p.Ala1906Val | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 43/48 | 5889/6910 | 5717/6429 | 1906/2142 | chr2 | 127635123 | |||
chr2:127635740 | C | T | 1 | a0030 | 1 | HG03492.hp2 | missense_variant | MODERATE | c.5839C>T | p.Arg1947Cys | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 44/48 | 6011/6910 | 5839/6429 | 1947/2142 | chr2 | 127635740 | |||
chr2:127635818 | C | T | 1 | a0027 | 1 | HG02723.hp2 | missense_variant | MODERATE | c.5917C>T | p.Arg1973Trp | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 44/48 | 6089/6910 | 5917/6429 | 1973/2142 | chr2 | 127635818 | |||
chr2:127635872 | C | T | 1 | a0020 | 1 | HG01358.hp2 | missense_variant | MODERATE | c.5971C>T | p.Leu1991Phe | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 44/48 | 6143/6910 | 5971/6429 | 1991/2142 | chr2 | 127635872 | |||
chr2:127635878 | C | T | 1 | a0039 | 1 | NA18975.hp1 | missense_variant | MODERATE | c.5977C>T | p.Arg1993Cys | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 44/48 | 6149/6910 | 5977/6429 | 1993/2142 | chr2 | 127635878 | |||
chr2:127636287 | G | A | 1 | a0034 | 1 | HG04228.hp1 | missense_variant | MODERATE | c.6086G>A | p.Arg2029Gln | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 45/48 | 6258/6910 | 6086/6429 | 2029/2142 | chr2 | 127636287 | |||
chr2:127636560 | T | G | 1 | a0040 | 1 | NA18980.hp1 | missense_variant | MODERATE | c.6139T>G | p.Ser2047Ala | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 46/48 | 6311/6910 | 6139/6429 | 2047/2142 | chr2 | 127636560 | |||
chr2:127637332 | A | G | 1 | a0047 | 1 | NA19074.hp1 | missense_variant | MODERATE | c.6344A>G | p.Asp2115Gly | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 48/48 | 6516/6910 | 6344/6429 | 2115/2142 | chr2 | 127637332 | |||
chr2:127637380 | A | G | 13 | a0003 a0005 a0007 others(10): Show |
61 | HG00280.hp1 HG00323.hp1 HG00621.hp2 others(58): Show |
missense_variant | MODERATE | c.6392A>G | p.Gln2131Arg | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 48/48 | 6564/6910 | 6392/6429 | 2131/2142 | chr2 | 127637380 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:127566753 | G | A | 1 | a0008c0042 | 1 | HG03209.hp2 | synonymous_variant | LOW | c.396G>A | p.Pro132Pro | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 5/48 | 568/6910 | 396/6429 | 132/2142 | chr2 | 127566753 | |||
chr2:127566783 | C | T | 2 | a0002c0012 a0014c0040 |
6 | NA18941.hp1 NA18957.hp2 NA18959.hp1 others(3): Show |
synonymous_variant | LOW | c.426C>T | p.Tyr142Tyr | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 5/48 | 598/6910 | 426/6429 | 142/2142 | chr2 | 127566783 | |||
chr2:127574029 | A | G | 2 | a0017c0072 a0046c0073 |
2 | HG02922.hp2 NA19043.hp2 |
synonymous_variant | LOW | c.702A>G | p.Gln234Gln | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 7/48 | 874/6910 | 702/6429 | 234/2142 | chr2 | 127574029 | |||
chr2:127580768 | C | T | 2 | a0015c0071 a0024c0070 |
2 | HG02257.hp2 HG03453.hp1 |
synonymous_variant | LOW | c.1026C>T | p.Asp342Asp | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 10/48 | 1198/6910 | 1026/6429 | 342/2142 | chr2 | 127580768 | |||
chr2:127584215 | G | A | 1 | a0004c0021 | 2 | HG01168.hp1 HG01169.hp2 |
synonymous_variant | LOW | c.1437G>A | p.Ser479Ser | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 13/48 | 1609/6910 | 1437/6429 | 479/2142 | chr2 | 127584215 | |||
chr2:127584227 | C | T | 1 | a0003c0069 | 1 | NA19079.hp2 | synonymous_variant | LOW | c.1449C>T | p.Ser483Ser | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 13/48 | 1621/6910 | 1449/6429 | 483/2142 | chr2 | 127584227 | |||
chr2:127584308 | G | A | 1 | a0001c0044 | 1 | HG02809.hp2 | synonymous_variant | LOW | c.1530G>A | p.Leu510Leu | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 13/48 | 1702/6910 | 1530/6429 | 510/2142 | chr2 | 127584308 | |||
chr2:127584329 | G | A | 2 | a0001c0045 a0011c0016 |
4 | HG02630.hp1 HG02895.hp1 HG03041.hp1 others(1): Show |
synonymous_variant | LOW | c.1551G>A | p.Pro517Pro | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 13/48 | 1723/6910 | 1551/6429 | 517/2142 | chr2 | 127584329 | |||
chr2:127584801 | A | G | 1 | a0001c0068 | 1 | HG03139.hp2 | synonymous_variant | LOW | c.1578A>G | p.Gln526Gln | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 14/48 | 1750/6910 | 1578/6429 | 526/2142 | chr2 | 127584801 | |||
chr2:127592889 | G | T | 1 | a0001c0018 | 3 | HG02622.hp1 HG02895.hp2 HG02897.hp2 |
synonymous_variant | LOW | c.2088G>T | p.Thr696Thr | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 17/48 | 2260/6910 | 2088/6429 | 696/2142 | chr2 | 127592889 | |||
chr2:127607305 | C | T | 2 | a0003c0026 a0003c0069 |
3 | NA18972.hp1 NA19060.hp1 NA19079.hp2 |
synonymous_variant | LOW | c.2524C>T | p.Leu842Leu | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 21/48 | 2696/6910 | 2524/6429 | 842/2142 | chr2 | 127607305 | |||
chr2:127608788 | C | T | 1 | a0045c0065 | 1 | NA19043.hp1 | synonymous_variant | LOW | c.2724C>T | p.Thr908Thr | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 22/48 | 2896/6910 | 2724/6429 | 908/2142 | chr2 | 127608788 | |||
chr2:127609517 | G | A | 32 | a0001c0010 a0001c0017 a0001c0018 others(29): Show |
98 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(95): Show |
synonymous_variant | LOW | c.2826G>A | p.Ser942Ser | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 23/48 | 2998/6910 | 2826/6429 | 942/2142 | chr2 | 127609517 | |||
chr2:127612321 | A | G | 58 | a0001c0002 a0001c0005 a0001c0010 others(55): Show |
207 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(204): Show |
synonymous_variant | LOW | c.3264A>G | p.Thr1088Thr | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 25/48 | 3436/6910 | 3264/6429 | 1088/2142 | chr2 | 127612321 | |||
chr2:127622035 | C | T | 1 | a0008c0063 | 1 | NA18906.hp2 | synonymous_variant | LOW | c.3579C>T | p.Ala1193Ala | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 28/48 | 3751/6910 | 3579/6429 | 1193/2142 | chr2 | 127622035 | |||
chr2:127623204 | T | G | 1 | a0010c0036 | 1 | HG01192.hp1 | splice_region_variant&synonymous_variant | LOW | c.3648T>G | p.Ala1216Ala | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 29/48 | 3820/6910 | 3648/6429 | 1216/2142 | chr2 | 127623204 | |||
chr2:127624233 | C | T | 13 | a0001c0005 a0001c0058 a0002c0011 others(10): Show |
44 | HG00280.hp2 HG00642.hp2 HG00735.hp2 others(41): Show |
synonymous_variant | LOW | c.3960C>T | p.His1320His | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 30/48 | 4132/6910 | 3960/6429 | 1320/2142 | chr2 | 127624233 | |||
chr2:127624314 | C | T | 1 | a0029c0048 | 1 | HG03225.hp2 | synonymous_variant | LOW | c.4041C>T | p.Phe1347Phe | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 30/48 | 4213/6910 | 4041/6429 | 1347/2142 | chr2 | 127624314 | |||
chr2:127631215 | G | A | 9 | a0003c0003 a0003c0026 a0003c0069 others(6): Show |
47 | HG00280.hp1 HG00323.hp1 HG00621.hp2 others(44): Show |
synonymous_variant | LOW | c.4947G>A | p.Glu1649Glu | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 37/48 | 5119/6910 | 4947/6429 | 1649/2142 | chr2 | 127631215 | |||
chr2:127633261 | G | A | 1 | a0024c0070 | 1 | HG02257.hp2 | synonymous_variant | LOW | c.5409G>A | p.Thr1803Thr | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 40/48 | 5581/6910 | 5409/6429 | 1803/2142 | chr2 | 127633261 | |||
chr2:127634598 | C | T | 2 | a0001c0017 a0025c0041 |
4 | HG02258.hp2 HG02630.hp2 HG03041.hp2 others(1): Show |
splice_region_variant&synonymous_variant | LOW | c.5628C>T | p.Val1876Val | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 42/48 | 5800/6910 | 5628/6429 | 1876/2142 | chr2 | 127634598 | |||
chr2:127635784 | G | A | 1 | a0045c0065 | 1 | NA19043.hp1 | synonymous_variant | LOW | c.5883G>A | p.Ala1961Ala | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 44/48 | 6055/6910 | 5883/6429 | 1961/2142 | chr2 | 127635784 | |||
chr2:127636225 | T | C | 20 | a0001c0013 a0003c0003 a0003c0026 others(17): Show |
65 | HG00280.hp1 HG00323.hp1 HG00621.hp2 others(62): Show |
synonymous_variant | LOW | c.6024T>C | p.Tyr2008Tyr | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 45/48 | 6196/6910 | 6024/6429 | 2008/2142 | chr2 | 127636225 | |||
chr2:127636306 | C | T | 1 | a0001c0061 | 1 | HG02818.hp1 | synonymous_variant | LOW | c.6105C>T | p.Ser2035Ser | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 45/48 | 6277/6910 | 6105/6429 | 2035/2142 | chr2 | 127636306 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:127535770 | G | A | 3 | a0001c0002t0005 a0001c0017t0004 a0025c0041t0004 |
5 | HG02258.hp2 HG02630.hp2 HG03041.hp2 others(2): Show |
5_prime_UTR_variant | MODIFIER | c.-85G>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/48 | 23953 | chr2 | 127535770 | ||||||
chr2:127637469 | C | T | 1 | a0002c0001t0008 | 1 | HG02135.hp2 | 3_prime_UTR_variant | MODIFIER | c.*52C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 48/48 | 52 | chr2 | 127637469 | ||||||
chr2:127637563 | G | A | 5 | a0001c0005t0002 a0001c0058t0002 a0002c0011t0002 others(2): Show |
20 | HG01070.hp1 HG01256.hp1 HG01258.hp2 others(17): Show |
3_prime_UTR_variant | MODIFIER | c.*146G>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 48/48 | 146 | chr2 | 127637563 | ||||||
chr2:127637620 | T | G | 1 | a0002c0001t0006 | 1 | HG00099.hp2 | 3_prime_UTR_variant | MODIFIER | c.*203T>G | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 48/48 | 203 | chr2 | 127637620 | ||||||
chr2:127637622 | G | A | 8 | a0001c0002t0003 a0001c0005t0003 a0001c0017t0004 others(5): Show |
16 | HG00280.hp2 HG00642.hp2 HG01168.hp1 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*205G>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 48/48 | 205 | chr2 | 127637622 | ||||||
chr2:127637717 | T | A | 1 | a0002c0006t0007 | 1 | NA18612.hp1 | 3_prime_UTR_variant | MODIFIER | c.*300T>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 48/48 | 300 | chr2 | 127637717 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:127535896 | G | A | 3 | a0001c0004t0001g0009 a0001c0004t0001g0011 a0004c0007t0003g0010 |
3 | HG03688.hp1 NA18980.hp2 NA19010.hp1 |
intron_variant | MODIFIER | c.-24+65G>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | chr2 | 127535896 | |||||||
chr2:127535973 | C | G | 8 | a0001c0002t0001g0269 a0001c0010t0001g0264 a0001c0010t0001g0265 others(5): Show |
8 | HG02451.hp1 HG02572.hp1 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.-24+142C>G | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | chr2 | 127535973 | |||||||
chr2:127535989 | C | T | 1 | a0003c0003t0001g0263 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.-24+158C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | chr2 | 127535989 | |||||||
chr2:127536139 | G | A | 1 | a0017c0072t0001g0012 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.-24+308G>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | chr2 | 127536139 | |||||||
chr2:127536206 | T | A | 7 | a0002c0006t0001g0013 a0002c0006t0001g0014 a0002c0006t0001g0015 others(4): Show |
7 | HG00099.hp1 HG00741.hp1 HG01081.hp2 others(4): Show |
intron_variant | MODIFIER | c.-24+375T>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | chr2 | 127536206 | |||||||
chr2:127536287 | A | C | 1 | a0001c0002t0001g0262 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-24+456A>C | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | chr2 | 127536287 | |||||||
chr2:127536379 | G | A | 5 | a0001c0010t0001g0264 a0001c0010t0001g0265 a0001c0018t0001g0266 others(2): Show |
5 | HG02451.hp1 HG02622.hp1 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.-24+548G>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | chr2 | 127536379 | |||||||
chr2:127536442 | G | A | 1 | a0006c0009t0001g0020 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.-24+611G>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | chr2 | 127536442 | |||||||
chr2:127536467 | T | TG | 45 | a0001c0002t0001g0027 a0001c0002t0001g0032 a0001c0002t0001g0034 others(42): Show |
45 | HG00621.hp2 HG00733.hp2 HG01099.hp1 others(42): Show |
intron_variant | MODIFIER | c.-24+647dupG | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | INFO_REALIGN_3_PRIME | chr2 | 127536467 | ||||||
chr2:127536467 | TG | T | 37 | a0001c0002t0001g0106 a0001c0002t0001g0133 a0001c0002t0001g0134 others(34): Show |
37 | HG00621.hp1 HG00642.hp2 HG01071.hp1 others(34): Show |
intron_variant | MODIFIER | c.-24+647delG | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | INFO_REALIGN_3_PRIME | chr2 | 127536467 | ||||||
chr2:127536467 | TGG | T | 147 | a0001c0002t0001g0135 a0001c0002t0001g0137 a0001c0002t0001g0144 others(144): Show |
156 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(153): Show |
intron_variant | MODIFIER | c.-24+646_-24+647del others(2): Show |
MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | INFO_REALIGN_3_PRIME | chr2 | 127536467 | ||||||
chr2:127536476 | G | T | 3 | a0004c0007t0001g0259 a0004c0007t0001g0261 a0020c0055t0001g0260 |
3 | HG01106.hp2 HG01255.hp1 HG01358.hp2 |
intron_variant | MODIFIER | c.-24+645G>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | chr2 | 127536476 | |||||||
chr2:127536588 | C | T | 78 | a0001c0002t0001g0027 a0001c0002t0001g0032 a0001c0002t0001g0034 others(75): Show |
78 | HG00323.hp2 HG00621.hp2 HG00642.hp1 others(75): Show |
intron_variant | MODIFIER | c.-24+757C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | chr2 | 127536588 | |||||||
chr2:127536677 | C | T | 2 | a0011c0016t0001g0008 a0029c0048t0001g0132 |
3 | HG02630.hp1 HG03041.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.-24+846C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | chr2 | 127536677 | |||||||
chr2:127536820 | A | G | 1 | a0043c0056t0001g0258 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.-24+989A>G | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | chr2 | 127536820 | |||||||
chr2:127536854 | G | A | 3 | a0001c0002t0001g0135 a0001c0005t0002g0065 a0009c0014t0001g0136 |
3 | HG02970.hp2 HG03225.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.-24+1023G>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | chr2 | 127536854 | |||||||
chr2:127536861 | G | A | 5 | a0001c0002t0005g0074 a0001c0017t0004g0024 a0001c0017t0004g0025 others(2): Show |
5 | HG02258.hp2 HG02630.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.-24+1030G>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | chr2 | 127536861 | |||||||
chr2:127536868 | C | A | 89 | a0001c0002t0001g0027 a0001c0002t0001g0032 a0001c0002t0001g0034 others(86): Show |
90 | HG00323.hp2 HG00621.hp2 HG00642.hp1 others(87): Show |
intron_variant | MODIFIER | c.-24+1037C>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | chr2 | 127536868 | |||||||
chr2:127536958 | C | A | 2 | a0001c0004t0001g0066 a0003c0026t0001g0146 |
2 | NA18972.hp1 NA19070.hp1 |
intron_variant | MODIFIER | c.-24+1127C>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | chr2 | 127536958 | |||||||
chr2:127537479 | C | A | 210 | a0001c0002t0001g0027 a0001c0002t0001g0032 a0001c0002t0001g0034 others(207): Show |
219 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(216): Show |
intron_variant | MODIFIER | c.-24+1648C>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | chr2 | 127537479 | |||||||
chr2:127537709 | G | A | 247 | a0001c0002t0001g0027 a0001c0002t0001g0032 a0001c0002t0001g0034 others(244): Show |
256 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(253): Show |
intron_variant | MODIFIER | c.-24+1878G>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | chr2 | 127537709 | |||||||
chr2:127537743 | A | C | 67 | a0001c0004t0001g0197 a0001c0004t0001g0214 a0001c0005t0002g0208 others(64): Show |
72 | HG00099.hp2 HG00735.hp1 HG00738.hp2 others(69): Show |
intron_variant | MODIFIER | c.-24+1912A>C | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | chr2 | 127537743 | |||||||
chr2:127537747 | T | G | 1 | a0002c0012t0001g0171 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.-24+1916T>G | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | chr2 | 127537747 | |||||||
chr2:127537860 | A | G | 251 | a0001c0002t0001g0027 a0001c0002t0001g0032 a0001c0002t0001g0034 others(248): Show |
260 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(257): Show |
intron_variant | MODIFIER | c.-24+2029A>G | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | chr2 | 127537860 | |||||||
chr2:127537931 | G | A | 1 | a0031c0074t0001g0026 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.-24+2100G>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | chr2 | 127537931 | |||||||
chr2:127537985 | C | T | 2 | a0001c0005t0002g0131 a0008c0063t0001g0257 |
2 | HG02280.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.-24+2154C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | chr2 | 127537985 | |||||||
chr2:127538053 | G | A | 3 | a0001c0002t0001g0027 a0001c0002t0001g0137 a0003c0003t0001g0229 |
3 | HG01099.hp1 NA18959.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.-24+2222G>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | chr2 | 127538053 | |||||||
chr2:127538119 | A | T | 1 | a0002c0006t0001g0013 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-24+2288A>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | chr2 | 127538119 | |||||||
chr2:127538209 | A | C | 1 | a0004c0007t0003g0256 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.-24+2378A>C | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | chr2 | 127538209 | |||||||
chr2:127538262 | C | CGGT | 16 | a0001c0002t0001g0077 a0001c0002t0001g0135 a0001c0002t0001g0269 others(13): Show |
16 | HG01891.hp2 HG02257.hp2 HG02451.hp1 others(13): Show |
intron_variant | MODIFIER | c.-24+2432_-24+2434d others(5): Show |
MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | INFO_REALIGN_3_PRIME | chr2 | 127538262 | ||||||
chr2:127538296 | G | A | 7 | a0001c0004t0001g0218 a0002c0011t0002g0108 a0004c0007t0003g0007 others(4): Show |
7 | HG00280.hp2 HG00642.hp2 HG01168.hp1 others(4): Show |
intron_variant | MODIFIER | c.-24+2465G>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | chr2 | 127538296 | |||||||
chr2:127538346 | A | T | 1 | a0005c0008t0001g0170 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-24+2515A>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | chr2 | 127538346 | |||||||
chr2:127538436 | C | T | 3 | a0015c0066t0001g0067 a0017c0072t0001g0012 a0046c0073t0001g0068 |
3 | HG01884.hp1 HG02922.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.-24+2605C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | chr2 | 127538436 | |||||||
chr2:127538477 | A | G | 1 | a0001c0044t0003g0080 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.-24+2646A>G | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | chr2 | 127538477 | |||||||
chr2:127538485 | T | C | 2 | a0001c0010t0001g0138 a0009c0014t0001g0104 |
2 | HG02572.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.-24+2654T>C | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | chr2 | 127538485 | |||||||
chr2:127538527 | C | T | 103 | a0001c0002t0001g0106 a0001c0002t0001g0155 a0001c0004t0001g0197 others(100): Show |
111 | HG00099.hp1 HG00099.hp2 HG00735.hp1 others(108): Show |
intron_variant | MODIFIER | c.-24+2696C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | chr2 | 127538527 | |||||||
chr2:127538570 | C | CT | 5 | a0001c0005t0003g0063 a0002c0001t0001g0215 a0002c0006t0007g0216 others(2): Show |
5 | HG01069.hp1 HG01071.hp1 HG03831.hp2 others(2): Show |
intron_variant | MODIFIER | c.-24+2752dupT | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | INFO_REALIGN_3_PRIME | chr2 | 127538570 | ||||||
chr2:127538690 | C | T | 3 | a0001c0002t0001g0135 a0001c0005t0002g0065 a0009c0014t0001g0136 |
3 | HG02970.hp2 HG03225.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.-24+2859C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | chr2 | 127538690 | |||||||
chr2:127539007 | C | A | 3 | a0015c0066t0001g0067 a0017c0072t0001g0012 a0046c0073t0001g0068 |
3 | HG01884.hp1 HG02922.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.-24+3176C>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | chr2 | 127539007 | |||||||
chr2:127539054 | G | C | 12 | a0001c0002t0001g0137 a0001c0002t0001g0144 a0001c0002t0001g0145 others(9): Show |
13 | HG01175.hp1 HG02109.hp2 HG02257.hp1 others(10): Show |
intron_variant | MODIFIER | c.-24+3223G>C | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | chr2 | 127539054 | |||||||
chr2:127539119 | A | G | 3 | a0001c0002t0001g0135 a0001c0005t0002g0065 a0009c0014t0001g0136 |
3 | HG02970.hp2 HG03225.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.-24+3288A>G | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | chr2 | 127539119 | |||||||
chr2:127539255 | A | G | 3 | a0001c0004t0001g0214 a0005c0008t0001g0213 a0023c0037t0001g0212 |
3 | HG01192.hp2 HG02165.hp1 NA19070.hp2 |
intron_variant | MODIFIER | c.-24+3424A>G | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | chr2 | 127539255 | |||||||
chr2:127539597 | CA | C | 8 | a0001c0005t0002g0208 a0003c0003t0001g0118 a0003c0003t0001g0210 others(5): Show |
8 | HG01069.hp1 HG01070.hp1 HG01071.hp1 others(5): Show |
intron_variant | MODIFIER | c.-24+3767delA | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | chr2 | 127539597 | |||||||
chr2:127539657 | G | A | 3 | a0001c0010t0001g0138 a0001c0010t0001g0139 a0009c0014t0001g0104 |
3 | HG02109.hp2 HG02572.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.-24+3826G>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | chr2 | 127539657 | |||||||
chr2:127539682 | TA | T | 96 | a0001c0002t0001g0027 a0001c0002t0001g0032 a0001c0002t0001g0034 others(93): Show |
97 | HG00323.hp2 HG00621.hp2 HG00642.hp1 others(94): Show |
intron_variant | MODIFIER | c.-24+3862delA | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | INFO_REALIGN_3_PRIME | chr2 | 127539682 | ||||||
chr2:127539697 | C | A | 136 | a0001c0002t0001g0027 a0001c0002t0001g0032 a0001c0002t0001g0034 others(133): Show |
137 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(134): Show |
intron_variant | MODIFIER | c.-24+3866C>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | chr2 | 127539697 | |||||||
chr2:127540151 | T | G | 251 | a0001c0002t0001g0027 a0001c0002t0001g0032 a0001c0002t0001g0034 others(248): Show |
260 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(257): Show |
intron_variant | MODIFIER | c.-24+4320T>G | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | chr2 | 127540151 | |||||||
chr2:127540164 | G | GT | 3 | a0001c0002t0001g0135 a0001c0005t0002g0065 a0009c0014t0001g0136 |
3 | HG02970.hp2 HG03225.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.-24+4337dupT | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | INFO_REALIGN_3_PRIME | chr2 | 127540164 | ||||||
chr2:127540168 | T | A | 1 | a0002c0012t0001g0171 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.-24+4337T>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | chr2 | 127540168 | |||||||
chr2:127540169 | A | AT | 67 | a0001c0002t0005g0074 a0001c0004t0001g0197 a0001c0004t0001g0214 others(64): Show |
72 | HG00099.hp2 HG00735.hp1 HG00738.hp2 others(69): Show |
intron_variant | MODIFIER | c.-24+4350dupT | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | INFO_REALIGN_3_PRIME | chr2 | 127540169 | ||||||
chr2:127540169 | A | ATT | 66 | a0001c0002t0001g0027 a0001c0002t0001g0032 a0001c0002t0001g0034 others(63): Show |
66 | HG00323.hp2 HG00621.hp2 HG00642.hp1 others(63): Show |
intron_variant | MODIFIER | c.-24+4349_-24+4350d others(4): Show |
MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | INFO_REALIGN_3_PRIME | chr2 | 127540169 | ||||||
chr2:127540169 | A | T | 4 | a0001c0002t0001g0135 a0001c0005t0002g0065 a0002c0012t0001g0171 others(1): Show |
4 | HG02970.hp2 HG03225.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.-24+4338A>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | chr2 | 127540169 | |||||||
chr2:127540383 | C | T | 40 | a0001c0004t0001g0066 a0001c0004t0001g0124 a0001c0004t0001g0232 others(37): Show |
40 | HG00280.hp1 HG00323.hp1 HG00621.hp1 others(37): Show |
intron_variant | MODIFIER | c.-24+4552C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | chr2 | 127540383 | |||||||
chr2:127540454 | G | A | 1 | a0034c0059t0001g0031 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.-24+4623G>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | chr2 | 127540454 | |||||||
chr2:127540664 | A | G | 1 | a0003c0003t0001g0255 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.-24+4833A>G | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | chr2 | 127540664 | |||||||
chr2:127540762 | G | C | 17 | a0001c0002t0001g0027 a0001c0002t0001g0032 a0001c0002t0001g0034 others(14): Show |
17 | HG00621.hp2 HG01099.hp1 HG01943.hp1 others(14): Show |
intron_variant | MODIFIER | c.-24+4931G>C | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | chr2 | 127540762 | |||||||
chr2:127540863 | G | C | 37 | a0001c0002t0001g0106 a0001c0002t0001g0155 a0001c0010t0001g0163 others(34): Show |
40 | HG00099.hp1 HG00735.hp2 HG00738.hp1 others(37): Show |
intron_variant | MODIFIER | c.-24+5032G>C | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | chr2 | 127540863 | |||||||
chr2:127540948 | A | C | 2 | a0001c0018t0001g0267 a0001c0018t0001g0268 |
2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.-24+5117A>C | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | chr2 | 127540948 | |||||||
chr2:127540994 | T | C | 3 | a0001c0002t0001g0135 a0001c0005t0002g0065 a0009c0014t0001g0136 |
3 | HG02970.hp2 HG03225.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.-24+5163T>C | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | chr2 | 127540994 | |||||||
chr2:127541057 | A | T | 1 | a0001c0002t0001g0269 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.-24+5226A>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | chr2 | 127541057 | |||||||
chr2:127541068 | A | T | 40 | a0001c0004t0001g0066 a0001c0004t0001g0124 a0001c0004t0001g0232 others(37): Show |
40 | HG00280.hp1 HG00323.hp1 HG00621.hp1 others(37): Show |
intron_variant | MODIFIER | c.-24+5237A>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | chr2 | 127541068 | |||||||
chr2:127541079 | G | A | 1 | a0001c0010t0001g0139 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.-24+5248G>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | chr2 | 127541079 | |||||||
chr2:127541090 | ATCTGCTG others(25): Show |
A | 3 | a0001c0005t0002g0062 a0001c0005t0002g0102 a0001c0058t0002g0103 |
3 | NA18957.hp1 NA18986.hp1 NA19007.hp2 |
intron_variant | MODIFIER | c.-24+5291_-24+5322d others(34): Show |
MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | INFO_REALIGN_3_PRIME | chr2 | 127541090 | ||||||
chr2:127541121 | C | T | 8 | a0001c0002t0001g0077 a0001c0002t0001g0269 a0001c0044t0003g0080 others(5): Show |
8 | HG01891.hp2 HG02257.hp2 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.-24+5290C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | chr2 | 127541121 | |||||||
chr2:127541353 | C | T | 5 | a0001c0010t0001g0264 a0001c0010t0001g0265 a0001c0018t0001g0266 others(2): Show |
5 | HG02451.hp1 HG02622.hp1 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.-24+5522C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | chr2 | 127541353 | |||||||
chr2:127541436 | C | T | 113 | a0001c0002t0001g0106 a0001c0002t0001g0155 a0001c0004t0001g0009 others(110): Show |
121 | HG00099.hp1 HG00099.hp2 HG00735.hp1 others(118): Show |
intron_variant | MODIFIER | c.-24+5605C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | chr2 | 127541436 | |||||||
chr2:127541441 | C | T | 256 | a0001c0002t0001g0027 a0001c0002t0001g0032 a0001c0002t0001g0034 others(253): Show |
265 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(262): Show |
intron_variant | MODIFIER | c.-24+5610C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | chr2 | 127541441 | |||||||
chr2:127541476 | G | C | 1 | a0002c0012t0001g0173 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.-24+5645G>C | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | chr2 | 127541476 | |||||||
chr2:127541503 | A | G | 248 | a0001c0002t0001g0027 a0001c0002t0001g0032 a0001c0002t0001g0034 others(245): Show |
257 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(254): Show |
intron_variant | MODIFIER | c.-24+5672A>G | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | chr2 | 127541503 | |||||||
chr2:127541537 | G | C | 5 | a0001c0002t0001g0225 a0001c0010t0001g0228 a0007c0024t0001g0227 others(2): Show |
5 | HG01069.hp2 HG01891.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.-24+5706G>C | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | chr2 | 127541537 | |||||||
chr2:127541602 | C | T | 1 | a0006c0009t0001g0061 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.-24+5771C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | chr2 | 127541602 | |||||||
chr2:127541625 | C | CT | 3 | a0001c0002t0001g0100 a0001c0002t0001g0101 a0001c0002t0001g0262 |
3 | HG00642.hp1 HG02886.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.-24+5795dupT | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | INFO_REALIGN_3_PRIME | chr2 | 127541625 | ||||||
chr2:127541828 | A | T | 40 | a0001c0004t0001g0066 a0001c0004t0001g0124 a0001c0004t0001g0232 others(37): Show |
40 | HG00280.hp1 HG00323.hp1 HG00621.hp1 others(37): Show |
intron_variant | MODIFIER | c.-24+5997A>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | chr2 | 127541828 | |||||||
chr2:127541843 | G | T | 102 | a0001c0002t0001g0106 a0001c0002t0001g0155 a0001c0004t0001g0197 others(99): Show |
110 | HG00099.hp1 HG00099.hp2 HG00735.hp1 others(107): Show |
intron_variant | MODIFIER | c.-24+6012G>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | chr2 | 127541843 | |||||||
chr2:127541852 | G | A | 3 | a0015c0066t0001g0067 a0017c0072t0001g0012 a0046c0073t0001g0068 |
3 | HG01884.hp1 HG02922.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.-24+6021G>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | chr2 | 127541852 | |||||||
chr2:127541951 | C | A | 253 | a0001c0002t0001g0027 a0001c0002t0001g0032 a0001c0002t0001g0034 others(250): Show |
262 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(259): Show |
intron_variant | MODIFIER | c.-24+6120C>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | chr2 | 127541951 | |||||||
chr2:127542005 | T | C | 2 | a0010c0020t0001g0150 a0010c0020t0001g0151 |
2 | HG03710.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.-24+6174T>C | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | chr2 | 127542005 | |||||||
chr2:127542085 | C | T | 80 | a0001c0002t0001g0027 a0001c0002t0001g0032 a0001c0002t0001g0034 others(77): Show |
81 | HG00323.hp2 HG00621.hp2 HG00642.hp1 others(78): Show |
intron_variant | MODIFIER | c.-24+6254C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | chr2 | 127542085 | |||||||
chr2:127542124 | A | G | 3 | a0008c0015t0001g0107 a0008c0015t0001g0168 a0008c0015t0001g0169 |
3 | HG02145.hp1 HG02280.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.-24+6293A>G | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | chr2 | 127542124 | |||||||
chr2:127542237 | C | T | 1 | a0001c0002t0001g0137 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-24+6406C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | chr2 | 127542237 | |||||||
chr2:127542344 | C | A | 3 | a0001c0004t0001g0009 a0001c0004t0001g0011 a0004c0007t0003g0010 |
3 | HG03688.hp1 NA18980.hp2 NA19010.hp1 |
intron_variant | MODIFIER | c.-24+6513C>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | chr2 | 127542344 | |||||||
chr2:127542429 | G | A | 9 | a0001c0002t0001g0137 a0001c0002t0001g0144 a0001c0002t0001g0145 others(6): Show |
10 | HG01175.hp1 HG02257.hp1 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.-24+6598G>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | chr2 | 127542429 | |||||||
chr2:127542538 | A | T | 1 | a0002c0001t0001g0116 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.-24+6707A>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | chr2 | 127542538 | |||||||
chr2:127542565 | T | C | 71 | a0001c0002t0001g0027 a0001c0002t0001g0032 a0001c0002t0001g0034 others(68): Show |
71 | HG00323.hp2 HG00621.hp2 HG00642.hp1 others(68): Show |
intron_variant | MODIFIER | c.-24+6734T>C | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | chr2 | 127542565 | |||||||
chr2:127542615 | C | T | 3 | a0001c0002t0001g0060 a0006c0009t0001g0058 a0006c0009t0001g0059 |
3 | HG01106.hp1 HG03239.hp1 HG03927.hp2 |
intron_variant | MODIFIER | c.-24+6784C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | chr2 | 127542615 | |||||||
chr2:127542616 | G | A | 1 | a0002c0001t0001g0117 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.-24+6785G>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | chr2 | 127542616 | |||||||
chr2:127542664 | T | G | 40 | a0001c0004t0001g0066 a0001c0004t0001g0124 a0001c0004t0001g0232 others(37): Show |
40 | HG00280.hp1 HG00323.hp1 HG00621.hp1 others(37): Show |
intron_variant | MODIFIER | c.-24+6833T>G | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | chr2 | 127542664 | |||||||
chr2:127542694 | C | T | 1 | a0001c0004t0001g0214 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.-24+6863C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | chr2 | 127542694 | |||||||
chr2:127542780 | A | G | 142 | a0001c0002t0001g0027 a0001c0002t0001g0032 a0001c0002t0001g0034 others(139): Show |
143 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(140): Show |
intron_variant | MODIFIER | c.-24+6949A>G | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | chr2 | 127542780 | |||||||
chr2:127542827 | A | G | 1 | a0004c0007t0003g0072 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.-24+6996A>G | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | chr2 | 127542827 | |||||||
chr2:127542874 | A | C | 1 | a0001c0002t0001g0137 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-24+7043A>C | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | chr2 | 127542874 | |||||||
chr2:127542880 | A | G | 1 | a0001c0004t0001g0254 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.-24+7049A>G | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | chr2 | 127542880 | |||||||
chr2:127543145 | T | C | 3 | a0001c0002t0001g0135 a0001c0005t0002g0065 a0009c0014t0001g0136 |
3 | HG02970.hp2 HG03225.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.-24+7314T>C | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | chr2 | 127543145 | |||||||
chr2:127543186 | A | G | 3 | a0001c0002t0001g0269 a0002c0011t0002g0270 a0017c0053t0001g0271 |
3 | HG02572.hp1 HG02647.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.-24+7355A>G | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | chr2 | 127543186 | |||||||
chr2:127543193 | G | A | 9 | a0001c0002t0001g0137 a0001c0002t0001g0144 a0001c0002t0001g0145 others(6): Show |
10 | HG01175.hp1 HG02257.hp1 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.-24+7362G>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | chr2 | 127543193 | |||||||
chr2:127543325 | CT | C | 5 | a0001c0002t0001g0135 a0001c0005t0002g0065 a0001c0005t0002g0131 others(2): Show |
5 | HG02280.hp2 HG02970.hp2 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.-24+7505delT | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | INFO_REALIGN_3_PRIME | chr2 | 127543325 | ||||||
chr2:127543473 | A | G | 3 | a0001c0004t0001g0009 a0001c0004t0001g0011 a0004c0007t0003g0010 |
3 | HG03688.hp1 NA18980.hp2 NA19010.hp1 |
intron_variant | MODIFIER | c.-24+7642A>G | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | chr2 | 127543473 | |||||||
chr2:127543643 | G | A | 2 | a0001c0002t0001g0077 a0001c0044t0003g0080 |
2 | HG02809.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.-24+7812G>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | chr2 | 127543643 | |||||||
chr2:127543739 | C | CAT | 66 | a0001c0002t0001g0027 a0001c0002t0001g0032 a0001c0002t0001g0034 others(63): Show |
66 | HG00323.hp2 HG00621.hp2 HG00642.hp1 others(63): Show |
intron_variant | MODIFIER | c.-24+7921_-24+7922d others(4): Show |
MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | INFO_REALIGN_3_PRIME | chr2 | 127543739 | ||||||
chr2:127543752 | A | T | 5 | a0002c0001t0001g0071 a0002c0001t0001g0203 a0002c0001t0001g0204 others(2): Show |
5 | NA18947.hp1 NA18950.hp1 NA18984.hp1 others(2): Show |
intron_variant | MODIFIER | c.-24+7921A>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | chr2 | 127543752 | |||||||
chr2:127543754 | T | A | 109 | a0001c0002t0001g0027 a0001c0002t0001g0032 a0001c0002t0001g0034 others(106): Show |
110 | HG00323.hp2 HG00621.hp2 HG00642.hp1 others(107): Show |
intron_variant | MODIFIER | c.-24+7923T>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | chr2 | 127543754 | |||||||
chr2:127543756 | T | A | 82 | a0001c0002t0001g0027 a0001c0002t0001g0032 a0001c0002t0001g0034 others(79): Show |
83 | HG00323.hp2 HG00621.hp2 HG00642.hp1 others(80): Show |
intron_variant | MODIFIER | c.-24+7925T>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | chr2 | 127543756 | |||||||
chr2:127543784 | A | G | 251 | a0001c0002t0001g0027 a0001c0002t0001g0032 a0001c0002t0001g0034 others(248): Show |
260 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(257): Show |
intron_variant | MODIFIER | c.-24+7953A>G | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | chr2 | 127543784 | |||||||
chr2:127543822 | G | A | 1 | a0002c0001t0001g0176 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.-24+7991G>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | chr2 | 127543822 | |||||||
chr2:127543828 | T | A | 102 | a0001c0002t0001g0106 a0001c0002t0001g0155 a0001c0004t0001g0197 others(99): Show |
110 | HG00099.hp1 HG00099.hp2 HG00735.hp1 others(107): Show |
intron_variant | MODIFIER | c.-24+7997T>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | chr2 | 127543828 | |||||||
chr2:127543831 | C | G | 251 | a0001c0002t0001g0027 a0001c0002t0001g0032 a0001c0002t0001g0034 others(248): Show |
260 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(257): Show |
intron_variant | MODIFIER | c.-24+8000C>G | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | chr2 | 127543831 | |||||||
chr2:127543835 | G | C | 251 | a0001c0002t0001g0027 a0001c0002t0001g0032 a0001c0002t0001g0034 others(248): Show |
260 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(257): Show |
intron_variant | MODIFIER | c.-24+8004G>C | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | chr2 | 127543835 | |||||||
chr2:127543882 | C | A | 3 | a0015c0066t0001g0067 a0017c0072t0001g0012 a0046c0073t0001g0068 |
3 | HG01884.hp1 HG02922.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.-24+8051C>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | chr2 | 127543882 | |||||||
chr2:127543938 | G | T | 3 | a0001c0004t0001g0009 a0001c0004t0001g0011 a0004c0007t0003g0010 |
3 | HG03688.hp1 NA18980.hp2 NA19010.hp1 |
intron_variant | MODIFIER | c.-24+8107G>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | chr2 | 127543938 | |||||||
chr2:127543946 | C | T | 1 | a0007c0025t0001g0211 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.-24+8115C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | chr2 | 127543946 | |||||||
chr2:127543981 | G | C | 3 | a0015c0066t0001g0067 a0017c0072t0001g0012 a0046c0073t0001g0068 |
3 | HG01884.hp1 HG02922.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.-24+8150G>C | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | chr2 | 127543981 | |||||||
chr2:127543997 | T | C | 3 | a0008c0015t0001g0107 a0008c0015t0001g0168 a0008c0015t0001g0169 |
3 | HG02145.hp1 HG02280.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.-24+8166T>C | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | chr2 | 127543997 | |||||||
chr2:127544107 | T | C | 3 | a0001c0002t0001g0135 a0001c0005t0002g0065 a0009c0014t0001g0136 |
3 | HG02970.hp2 HG03225.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.-24+8276T>C | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | chr2 | 127544107 | |||||||
chr2:127544289 | T | C | 5 | a0001c0002t0005g0074 a0001c0017t0004g0024 a0001c0017t0004g0025 others(2): Show |
5 | HG02258.hp2 HG02630.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.-24+8458T>C | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | chr2 | 127544289 | |||||||
chr2:127544462 | G | A | 5 | a0005c0008t0001g0003 a0005c0008t0001g0152 a0005c0008t0001g0153 others(2): Show |
6 | HG02717.hp1 HG02896.hp1 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.-24+8631G>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | chr2 | 127544462 | |||||||
chr2:127544565 | C | T | 37 | a0001c0002t0001g0106 a0001c0002t0001g0155 a0001c0010t0001g0163 others(34): Show |
40 | HG00099.hp1 HG00735.hp2 HG00738.hp1 others(37): Show |
intron_variant | MODIFIER | c.-24+8734C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | chr2 | 127544565 | |||||||
chr2:127544571 | G | C | 37 | a0001c0002t0001g0106 a0001c0002t0001g0155 a0001c0010t0001g0163 others(34): Show |
40 | HG00099.hp1 HG00735.hp2 HG00738.hp1 others(37): Show |
intron_variant | MODIFIER | c.-24+8740G>C | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | chr2 | 127544571 | |||||||
chr2:127544575 | A | AT | 154 | a0001c0002t0001g0027 a0001c0002t0001g0034 a0001c0002t0001g0035 others(151): Show |
157 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(154): Show |
intron_variant | MODIFIER | c.-24+8767dupT | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | INFO_REALIGN_3_PRIME | chr2 | 127544575 | ||||||
chr2:127544575 | A | ATT | 17 | a0001c0002t0001g0041 a0001c0002t0001g0085 a0001c0002t0001g0101 others(14): Show |
17 | HG00621.hp1 HG01106.hp2 HG02027.hp1 others(14): Show |
intron_variant | MODIFIER | c.-24+8766_-24+8767d others(4): Show |
MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | INFO_REALIGN_3_PRIME | chr2 | 127544575 | ||||||
chr2:127544575 | AT | A | 6 | a0001c0002t0001g0225 a0001c0004t0001g0009 a0001c0004t0001g0011 others(3): Show |
6 | HG01069.hp2 NA18950.hp2 NA18980.hp2 others(3): Show |
intron_variant | MODIFIER | c.-24+8767delT | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | INFO_REALIGN_3_PRIME | chr2 | 127544575 | ||||||
chr2:127544575 | ATTTTTTT others(5): Show |
A | 9 | a0001c0002t0001g0137 a0001c0002t0001g0144 a0001c0002t0001g0145 others(6): Show |
10 | HG01175.hp1 HG02257.hp1 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.-24+8756_-24+8767d others(14): Show |
MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | INFO_REALIGN_3_PRIME | chr2 | 127544575 | ||||||
chr2:127544641 | C | T | 1 | a0003c0026t0001g0253 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.-24+8810C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | chr2 | 127544641 | |||||||
chr2:127544647 | C | T | 65 | a0001c0004t0001g0197 a0001c0004t0001g0214 a0001c0005t0002g0208 others(62): Show |
70 | HG00099.hp2 HG00735.hp1 HG00738.hp2 others(67): Show |
intron_variant | MODIFIER | c.-24+8816C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | chr2 | 127544647 | |||||||
chr2:127544870 | G | A | 1 | a0045c0065t0001g0140 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-24+9039G>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | chr2 | 127544870 | |||||||
chr2:127544891 | A | AT | 9 | a0001c0002t0001g0137 a0001c0002t0001g0144 a0001c0002t0001g0145 others(6): Show |
10 | HG01175.hp1 HG02257.hp1 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.-24+9067dupT | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | INFO_REALIGN_3_PRIME | chr2 | 127544891 | ||||||
chr2:127544961 | A | G | 37 | a0001c0002t0001g0106 a0001c0002t0001g0155 a0001c0010t0001g0163 others(34): Show |
40 | HG00099.hp1 HG00735.hp2 HG00738.hp1 others(37): Show |
intron_variant | MODIFIER | c.-24+9130A>G | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | chr2 | 127544961 | |||||||
chr2:127545006 | T | C | 9 | a0001c0002t0001g0137 a0001c0002t0001g0144 a0001c0002t0001g0145 others(6): Show |
10 | HG01175.hp1 HG02257.hp1 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.-24+9175T>C | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | chr2 | 127545006 | |||||||
chr2:127545014 | C | T | 1 | a0040c0060t0001g0055 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.-24+9183C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | chr2 | 127545014 | |||||||
chr2:127545017 | A | G | 3 | a0001c0002t0001g0135 a0001c0005t0002g0065 a0009c0014t0001g0136 |
3 | HG02970.hp2 HG03225.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.-24+9186A>G | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | chr2 | 127545017 | |||||||
chr2:127545352 | C | T | 102 | a0001c0002t0001g0106 a0001c0002t0001g0155 a0001c0004t0001g0197 others(99): Show |
110 | HG00099.hp1 HG00099.hp2 HG00735.hp1 others(107): Show |
intron_variant | MODIFIER | c.-24+9521C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | chr2 | 127545352 | |||||||
chr2:127545428 | G | A | 102 | a0001c0002t0001g0106 a0001c0002t0001g0155 a0001c0004t0001g0197 others(99): Show |
110 | HG00099.hp1 HG00099.hp2 HG00735.hp1 others(107): Show |
intron_variant | MODIFIER | c.-24+9597G>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | chr2 | 127545428 | |||||||
chr2:127545509 | G | C | 2 | a0001c0010t0001g0138 a0009c0014t0001g0104 |
2 | HG02572.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.-24+9678G>C | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | chr2 | 127545509 | |||||||
chr2:127545614 | G | T | 1 | a0004c0007t0003g0256 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.-24+9783G>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | chr2 | 127545614 | |||||||
chr2:127545647 | G | C | 3 | a0001c0002t0001g0135 a0001c0005t0002g0065 a0009c0014t0001g0136 |
3 | HG02970.hp2 HG03225.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.-24+9816G>C | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | chr2 | 127545647 | |||||||
chr2:127545789 | G | A | 71 | a0001c0002t0001g0027 a0001c0002t0001g0032 a0001c0002t0001g0034 others(68): Show |
71 | HG00323.hp2 HG00621.hp2 HG00642.hp1 others(68): Show |
intron_variant | MODIFIER | c.-24+9958G>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | chr2 | 127545789 | |||||||
chr2:127545957 | G | A | 1 | a0007c0024t0001g0086 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.-24+10126G>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | chr2 | 127545957 | |||||||
chr2:127546029 | C | T | 1 | a0040c0060t0001g0055 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.-24+10198C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | chr2 | 127546029 | |||||||
chr2:127546106 | T | A | 3 | a0001c0002t0001g0135 a0001c0005t0002g0065 a0009c0014t0001g0136 |
3 | HG02970.hp2 HG03225.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.-24+10275T>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | chr2 | 127546106 | |||||||
chr2:127546238 | C | T | 3 | a0001c0002t0001g0135 a0001c0005t0002g0065 a0009c0014t0001g0136 |
3 | HG02970.hp2 HG03225.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.-24+10407C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | chr2 | 127546238 | |||||||
chr2:127546283 | T | C | 1 | a0045c0065t0001g0140 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-24+10452T>C | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | chr2 | 127546283 | |||||||
chr2:127546327 | G | A | 1 | a0007c0025t0001g0042 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.-24+10496G>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | chr2 | 127546327 | |||||||
chr2:127546762 | G | GTCCA | 86 | a0001c0002t0001g0045 a0001c0002t0001g0048 a0001c0002t0001g0053 others(83): Show |
88 | HG00323.hp1 HG00323.hp2 HG00621.hp1 others(85): Show |
intron_variant | MODIFIER | c.-24+10970_-24+1097 others(8): Show |
MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | INFO_REALIGN_3_PRIME | chr2 | 127546762 | ||||||
chr2:127546762 | G | GTCCATCC others(1): Show |
6 | a0001c0002t0001g0144 a0001c0002t0001g0145 a0001c0005t0001g0098 others(3): Show |
6 | HG01175.hp1 HG02257.hp1 HG02683.hp2 others(3): Show |
intron_variant | MODIFIER | c.-24+10966_-24+1097 others(12): Show |
MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | INFO_REALIGN_3_PRIME | chr2 | 127546762 | ||||||
chr2:127546762 | GTCCA | G | 17 | a0001c0004t0001g0009 a0001c0004t0001g0011 a0001c0005t0002g0208 others(14): Show |
17 | HG00621.hp2 HG01069.hp1 HG01070.hp1 others(14): Show |
intron_variant | MODIFIER | c.-24+10970_-24+1097 others(8): Show |
MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | INFO_REALIGN_3_PRIME | chr2 | 127546762 | ||||||
chr2:127546762 | GTCCATCC others(13): Show |
G | 1 | a0002c0001t0001g0071 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.-24+10954_-24+1097 others(24): Show |
MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | INFO_REALIGN_3_PRIME | chr2 | 127546762 | ||||||
chr2:127546779 | T | TCCAC | 3 | a0021c0046t0003g0078 a0024c0070t0001g0028 a0027c0057t0001g0079 |
3 | HG01891.hp2 HG02257.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.-24+10951_-24+1095 others(8): Show |
MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | INFO_REALIGN_3_PRIME | chr2 | 127546779 | ||||||
chr2:127546816 | CTGTTTGT others(3): Show |
C | 1 | a0002c0006t0001g0019 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.-24+10987_-24+1099 others(14): Show |
MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | INFO_REALIGN_3_PRIME | chr2 | 127546816 | ||||||
chr2:127546915 | C | T | 40 | a0001c0004t0001g0066 a0001c0004t0001g0124 a0001c0004t0001g0232 others(37): Show |
40 | HG00280.hp1 HG00323.hp1 HG00621.hp1 others(37): Show |
intron_variant | MODIFIER | c.-24+11084C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | chr2 | 127546915 | |||||||
chr2:127546944 | C | T | 1 | a0025c0041t0004g0076 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.-24+11113C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | chr2 | 127546944 | |||||||
chr2:127547243 | G | A | 1 | a0003c0003t0001g0240 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.-24+11412G>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | chr2 | 127547243 | |||||||
chr2:127547533 | G | A | 3 | a0001c0002t0001g0135 a0001c0005t0002g0065 a0009c0014t0001g0136 |
3 | HG02970.hp2 HG03225.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.-24+11702G>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | chr2 | 127547533 | |||||||
chr2:127547621 | T | C | 251 | a0001c0002t0001g0027 a0001c0002t0001g0032 a0001c0002t0001g0034 others(248): Show |
260 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(257): Show |
intron_variant | MODIFIER | c.-24+11790T>C | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | chr2 | 127547621 | |||||||
chr2:127547699 | C | T | 3 | a0001c0002t0001g0135 a0001c0005t0002g0065 a0009c0014t0001g0136 |
3 | HG02970.hp2 HG03225.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.-24+11868C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | chr2 | 127547699 | |||||||
chr2:127547884 | A | G | 1 | a0001c0002t0001g0101 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.-23-11816A>G | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | chr2 | 127547884 | |||||||
chr2:127547987 | C | T | 9 | a0001c0002t0001g0137 a0001c0002t0001g0144 a0001c0002t0001g0145 others(6): Show |
10 | HG01175.hp1 HG02257.hp1 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.-23-11713C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | chr2 | 127547987 | |||||||
chr2:127548168 | C | T | 9 | a0001c0002t0001g0137 a0001c0002t0001g0144 a0001c0002t0001g0145 others(6): Show |
10 | HG01175.hp1 HG02257.hp1 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.-23-11532C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | chr2 | 127548168 | |||||||
chr2:127548419 | C | CT | 24 | a0001c0002t0001g0077 a0001c0002t0001g0106 a0001c0002t0001g0137 others(21): Show |
25 | HG01175.hp1 HG01891.hp2 HG02055.hp2 others(22): Show |
intron_variant | MODIFIER | c.-23-11266dupT | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | INFO_REALIGN_3_PRIME | chr2 | 127548419 | ||||||
chr2:127548478 | G | A | 90 | a0001c0002t0001g0027 a0001c0002t0001g0032 a0001c0002t0001g0034 others(87): Show |
90 | HG00323.hp2 HG00621.hp2 HG00642.hp1 others(87): Show |
intron_variant | MODIFIER | c.-23-11222G>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | chr2 | 127548478 | |||||||
chr2:127548492 | T | C | 3 | a0001c0002t0001g0135 a0001c0005t0002g0065 a0009c0014t0001g0136 |
3 | HG02970.hp2 HG03225.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.-23-11208T>C | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | chr2 | 127548492 | |||||||
chr2:127548562 | C | T | 3 | a0015c0066t0001g0067 a0017c0072t0001g0012 a0046c0073t0001g0068 |
3 | HG01884.hp1 HG02922.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.-23-11138C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | chr2 | 127548562 | |||||||
chr2:127548563 | G | A | 5 | a0001c0002t0005g0074 a0001c0017t0004g0024 a0001c0017t0004g0025 others(2): Show |
5 | HG02258.hp2 HG02630.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.-23-11137G>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | chr2 | 127548563 | |||||||
chr2:127548659 | C | T | 3 | a0001c0002t0001g0135 a0001c0005t0002g0065 a0009c0014t0001g0136 |
3 | HG02970.hp2 HG03225.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.-23-11041C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | chr2 | 127548659 | |||||||
chr2:127548668 | C | A | 3 | a0001c0002t0001g0135 a0001c0005t0002g0065 a0009c0014t0001g0136 |
3 | HG02970.hp2 HG03225.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.-23-11032C>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | chr2 | 127548668 | |||||||
chr2:127548710 | G | C | 4 | a0001c0002t0001g0106 a0001c0013t0001g0005 a0001c0013t0001g0166 others(1): Show |
5 | HG01243.hp1 HG02055.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.-23-10990G>C | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | chr2 | 127548710 | |||||||
chr2:127548927 | T | TGG | 9 | a0001c0002t0001g0137 a0001c0002t0001g0144 a0001c0002t0001g0145 others(6): Show |
10 | HG01175.hp1 HG02257.hp1 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.-23-10773_-23-1077 others(6): Show |
MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | chr2 | 127548927 | |||||||
chr2:127548931 | TCC | T | 9 | a0001c0002t0001g0137 a0001c0002t0001g0144 a0001c0002t0001g0145 others(6): Show |
10 | HG01175.hp1 HG02257.hp1 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.-23-10768_-23-1076 others(6): Show |
MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | chr2 | 127548931 | |||||||
chr2:127549127 | TTCTC | T | 3 | a0001c0002t0001g0269 a0002c0011t0002g0270 a0017c0053t0001g0271 |
3 | HG02572.hp1 HG02647.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.-23-10569_-23-1056 others(8): Show |
MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | INFO_REALIGN_3_PRIME | chr2 | 127549127 | ||||||
chr2:127549133 | CTT | C | 3 | a0001c0002t0001g0135 a0001c0005t0002g0065 a0009c0014t0001g0136 |
3 | HG02970.hp2 HG03225.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.-23-10565_-23-1056 others(6): Show |
MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | INFO_REALIGN_3_PRIME | chr2 | 127549133 | ||||||
chr2:127549155 | CCTTCCTT others(5): Show |
C | 3 | a0001c0002t0001g0135 a0001c0005t0002g0065 a0009c0014t0001g0136 |
3 | HG02970.hp2 HG03225.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.-23-10541_-23-1053 others(16): Show |
MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | INFO_REALIGN_3_PRIME | chr2 | 127549155 | ||||||
chr2:127549159 | CCTTCCTT others(1): Show |
C | 102 | a0001c0002t0001g0106 a0001c0002t0001g0155 a0001c0004t0001g0197 others(99): Show |
110 | HG00099.hp1 HG00099.hp2 HG00735.hp1 others(107): Show |
intron_variant | MODIFIER | c.-23-10537_-23-1053 others(12): Show |
MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | INFO_REALIGN_3_PRIME | chr2 | 127549159 | ||||||
chr2:127549159 | CCTTCCTT others(5): Show |
C | 1 | a0002c0011t0002g0186 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.-23-10537_-23-1052 others(16): Show |
MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | INFO_REALIGN_3_PRIME | chr2 | 127549159 | ||||||
chr2:127549163 | CCTTT | C | 56 | a0001c0002t0001g0225 a0001c0004t0001g0009 a0001c0004t0001g0011 others(53): Show |
56 | HG00280.hp1 HG00323.hp1 HG00621.hp1 others(53): Show |
intron_variant | MODIFIER | c.-23-10518_-23-1051 others(8): Show |
MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | INFO_REALIGN_3_PRIME | chr2 | 127549163 | ||||||
chr2:127549163 | CCTTTCTT others(1): Show |
C | 5 | a0001c0010t0001g0264 a0001c0010t0001g0265 a0001c0018t0001g0266 others(2): Show |
5 | HG02451.hp1 HG02622.hp1 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.-23-10522_-23-1051 others(12): Show |
MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | INFO_REALIGN_3_PRIME | chr2 | 127549163 | ||||||
chr2:127549167 | T | C | 1 | a0006c0009t0001g0097 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.-23-10533T>C | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | chr2 | 127549167 | |||||||
chr2:127549174 | TTCTTTCT others(5): Show |
T | 2 | a0009c0014t0001g0174 a0040c0060t0001g0055 |
2 | HG02486.hp2 NA18980.hp1 |
intron_variant | MODIFIER | c.-23-10514_-23-1050 others(16): Show |
MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | INFO_REALIGN_3_PRIME | chr2 | 127549174 | ||||||
chr2:127549178 | TTCTTTCT others(1): Show |
T | 83 | a0001c0002t0001g0027 a0001c0002t0001g0032 a0001c0002t0001g0034 others(80): Show |
84 | HG00323.hp2 HG00621.hp2 HG00642.hp1 others(81): Show |
intron_variant | MODIFIER | c.-23-10514_-23-1050 others(12): Show |
MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | INFO_REALIGN_3_PRIME | chr2 | 127549178 | ||||||
chr2:127549182 | TTCTC | T | 5 | a0001c0002t0001g0045 a0001c0002t0001g0088 a0001c0002t0001g0091 others(2): Show |
5 | HG02451.hp2 HG02896.hp2 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.-23-10514_-23-1051 others(8): Show |
MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | INFO_REALIGN_3_PRIME | chr2 | 127549182 | ||||||
chr2:127549186 | C | T | 2 | a0001c0010t0001g0139 a0002c0011t0002g0186 |
2 | HG02109.hp2 HG03017.hp2 |
intron_variant | MODIFIER | c.-23-10514C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | chr2 | 127549186 | |||||||
chr2:127549213 | T | A | 2 | a0001c0004t0001g0043 a0001c0005t0002g0044 |
2 | NA18962.hp2 NA18968.hp2 |
intron_variant | MODIFIER | c.-23-10487T>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | chr2 | 127549213 | |||||||
chr2:127549334 | G | T | 3 | a0001c0010t0001g0163 a0004c0007t0001g0164 a0004c0054t0001g0165 |
3 | HG01175.hp2 HG01346.hp1 HG02258.hp1 |
intron_variant | MODIFIER | c.-23-10366G>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | chr2 | 127549334 | |||||||
chr2:127550012 | C | T | 5 | a0001c0002t0001g0225 a0001c0010t0001g0228 a0007c0024t0001g0227 others(2): Show |
5 | HG01069.hp2 HG01891.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.-23-9688C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | chr2 | 127550012 | |||||||
chr2:127550016 | G | T | 40 | a0001c0004t0001g0066 a0001c0004t0001g0124 a0001c0004t0001g0232 others(37): Show |
40 | HG00280.hp1 HG00323.hp1 HG00621.hp1 others(37): Show |
intron_variant | MODIFIER | c.-23-9684G>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | chr2 | 127550016 | |||||||
chr2:127550131 | C | T | 1 | a0001c0005t0002g0131 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.-23-9569C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | chr2 | 127550131 | |||||||
chr2:127550200 | T | C | 3 | a0001c0002t0001g0135 a0001c0005t0002g0065 a0009c0014t0001g0136 |
3 | HG02970.hp2 HG03225.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.-23-9500T>C | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | chr2 | 127550200 | |||||||
chr2:127550289 | G | A | 2 | a0001c0002t0001g0225 a0015c0071t0001g0123 |
2 | HG01069.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.-23-9411G>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | chr2 | 127550289 | |||||||
chr2:127550343 | C | A | 248 | a0001c0002t0001g0027 a0001c0002t0001g0032 a0001c0002t0001g0034 others(245): Show |
257 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(254): Show |
intron_variant | MODIFIER | c.-23-9357C>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | chr2 | 127550343 | |||||||
chr2:127550558 | CA | C | 246 | a0001c0002t0001g0027 a0001c0002t0001g0032 a0001c0002t0001g0034 others(243): Show |
255 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(252): Show |
intron_variant | MODIFIER | c.-23-9129delA | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | INFO_REALIGN_3_PRIME | chr2 | 127550558 | ||||||
chr2:127550592 | G | T | 146 | a0001c0002t0001g0106 a0001c0002t0001g0155 a0001c0004t0001g0009 others(143): Show |
154 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(151): Show |
intron_variant | MODIFIER | c.-23-9108G>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | chr2 | 127550592 | |||||||
chr2:127550618 | A | C | 1 | a0001c0002t0001g0145 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.-23-9082A>C | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | chr2 | 127550618 | |||||||
chr2:127550840 | C | T | 6 | a0001c0010t0001g0163 a0004c0007t0001g0164 a0004c0007t0001g0259 others(3): Show |
6 | HG01106.hp2 HG01175.hp2 HG01255.hp1 others(3): Show |
intron_variant | MODIFIER | c.-23-8860C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | chr2 | 127550840 | |||||||
chr2:127550867 | T | A | 2 | a0013c0019t0001g0178 a0013c0019t0001g0179 |
2 | HG01169.hp1 HG02300.hp2 |
intron_variant | MODIFIER | c.-23-8833T>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | chr2 | 127550867 | |||||||
chr2:127550869 | A | AG | 253 | a0001c0002t0001g0027 a0001c0002t0001g0032 a0001c0002t0001g0034 others(250): Show |
262 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(259): Show |
intron_variant | MODIFIER | c.-23-8828dupG | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | INFO_REALIGN_3_PRIME | chr2 | 127550869 | ||||||
chr2:127551110 | T | C | 5 | a0001c0002t0005g0074 a0001c0017t0004g0024 a0001c0017t0004g0025 others(2): Show |
5 | HG02258.hp2 HG02630.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.-23-8590T>C | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | chr2 | 127551110 | |||||||
chr2:127551271 | T | C | 47 | a0001c0004t0001g0009 a0001c0004t0001g0011 a0001c0004t0001g0066 others(44): Show |
47 | HG00280.hp1 HG00323.hp1 HG00621.hp1 others(44): Show |
intron_variant | MODIFIER | c.-23-8429T>C | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | chr2 | 127551271 | |||||||
chr2:127551302 | T | C | 3 | a0011c0016t0001g0008 a0011c0016t0001g0141 a0029c0048t0001g0132 |
4 | HG02630.hp1 HG03041.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.-23-8398T>C | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | chr2 | 127551302 | |||||||
chr2:127551443 | C | A | 5 | a0001c0002t0001g0225 a0001c0010t0001g0228 a0007c0024t0001g0227 others(2): Show |
5 | HG01069.hp2 HG01891.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.-23-8257C>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | chr2 | 127551443 | |||||||
chr2:127551689 | G | A | 7 | a0001c0004t0001g0009 a0001c0004t0001g0011 a0001c0005t0002g0131 others(4): Show |
7 | HG02109.hp1 HG02280.hp2 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.-23-8011G>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | chr2 | 127551689 | |||||||
chr2:127551894 | G | C | 99 | a0001c0002t0001g0106 a0001c0002t0001g0155 a0001c0004t0001g0197 others(96): Show |
107 | HG00099.hp1 HG00099.hp2 HG00735.hp1 others(104): Show |
intron_variant | MODIFIER | c.-23-7806G>C | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | chr2 | 127551894 | |||||||
chr2:127552056 | G | A | 71 | a0001c0002t0001g0027 a0001c0002t0001g0032 a0001c0002t0001g0034 others(68): Show |
71 | HG00323.hp2 HG00621.hp2 HG00642.hp1 others(68): Show |
intron_variant | MODIFIER | c.-23-7644G>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | chr2 | 127552056 | |||||||
chr2:127552162 | C | G | 1 | a0001c0061t0001g0099 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.-23-7538C>G | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | chr2 | 127552162 | |||||||
chr2:127552408 | C | T | 5 | a0001c0004t0001g0009 a0001c0004t0001g0011 a0004c0007t0003g0010 others(2): Show |
5 | HG02109.hp1 HG02818.hp2 HG03688.hp1 others(2): Show |
intron_variant | MODIFIER | c.-23-7292C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | chr2 | 127552408 | |||||||
chr2:127552422 | C | G | 2 | a0001c0002t0001g0039 a0001c0002t0001g0040 |
2 | NA18967.hp1 NA19060.hp2 |
intron_variant | MODIFIER | c.-23-7278C>G | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | chr2 | 127552422 | |||||||
chr2:127552446 | A | G | 253 | a0001c0002t0001g0027 a0001c0002t0001g0032 a0001c0002t0001g0034 others(250): Show |
262 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(259): Show |
intron_variant | MODIFIER | c.-23-7254A>G | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | chr2 | 127552446 | |||||||
chr2:127552463 | C | A | 40 | a0001c0004t0001g0066 a0001c0004t0001g0124 a0001c0004t0001g0232 others(37): Show |
40 | HG00280.hp1 HG00323.hp1 HG00621.hp1 others(37): Show |
intron_variant | MODIFIER | c.-23-7237C>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | chr2 | 127552463 | |||||||
chr2:127552468 | G | C | 3 | a0015c0066t0001g0067 a0017c0072t0001g0012 a0046c0073t0001g0068 |
3 | HG01884.hp1 HG02922.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.-23-7232G>C | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | chr2 | 127552468 | |||||||
chr2:127552473 | T | A | 1 | a0001c0002t0001g0137 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-23-7227T>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | chr2 | 127552473 | |||||||
chr2:127552527 | C | T | 1 | a0006c0009t0001g0097 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.-23-7173C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | chr2 | 127552527 | |||||||
chr2:127552529 | C | T | 1 | a0013c0019t0001g0179 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.-23-7171C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | chr2 | 127552529 | |||||||
chr2:127552571 | A | G | 1 | a0007c0023t0001g0122 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.-23-7129A>G | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | chr2 | 127552571 | |||||||
chr2:127552770 | G | A | 9 | a0001c0002t0001g0137 a0001c0002t0001g0144 a0001c0002t0001g0145 others(6): Show |
10 | HG01175.hp1 HG02257.hp1 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.-23-6930G>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | chr2 | 127552770 | |||||||
chr2:127552805 | C | G | 83 | a0001c0002t0001g0027 a0001c0002t0001g0032 a0001c0002t0001g0034 others(80): Show |
83 | HG00323.hp2 HG00621.hp2 HG00642.hp1 others(80): Show |
intron_variant | MODIFIER | c.-23-6895C>G | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | chr2 | 127552805 | |||||||
chr2:127552806 | C | A | 40 | a0001c0004t0001g0066 a0001c0004t0001g0124 a0001c0004t0001g0232 others(37): Show |
40 | HG00280.hp1 HG00323.hp1 HG00621.hp1 others(37): Show |
intron_variant | MODIFIER | c.-23-6894C>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | chr2 | 127552806 | |||||||
chr2:127552977 | GTCTCAGC others(3): Show |
G | 7 | a0001c0002t0001g0100 a0001c0002t0001g0101 a0001c0002t0001g0262 others(4): Show |
7 | HG00099.hp1 HG00642.hp1 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.-23-6706_-23-6697d others(12): Show |
MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | INFO_REALIGN_3_PRIME | chr2 | 127552977 | ||||||
chr2:127553055 | C | T | 3 | a0001c0004t0001g0009 a0001c0004t0001g0011 a0004c0007t0003g0010 |
3 | HG03688.hp1 NA18980.hp2 NA19010.hp1 |
intron_variant | MODIFIER | c.-23-6645C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | chr2 | 127553055 | |||||||
chr2:127553106 | C | T | 3 | a0001c0002t0001g0269 a0002c0011t0002g0270 a0017c0053t0001g0271 |
3 | HG02572.hp1 HG02647.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.-23-6594C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | chr2 | 127553106 | |||||||
chr2:127553145 | T | C | 1 | a0045c0065t0001g0140 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-23-6555T>C | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | chr2 | 127553145 | |||||||
chr2:127553170 | G | C | 1 | a0023c0037t0001g0212 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.-23-6530G>C | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | chr2 | 127553170 | |||||||
chr2:127553243 | A | C | 3 | a0001c0002t0001g0135 a0001c0005t0002g0065 a0009c0014t0001g0136 |
3 | HG02970.hp2 HG03225.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.-23-6457A>C | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | chr2 | 127553243 | |||||||
chr2:127553355 | G | A | 1 | a0001c0013t0001g0166 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.-23-6345G>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | chr2 | 127553355 | |||||||
chr2:127553487 | T | G | 93 | a0001c0002t0001g0027 a0001c0002t0001g0032 a0001c0002t0001g0034 others(90): Show |
94 | HG00323.hp2 HG00621.hp2 HG00642.hp1 others(91): Show |
intron_variant | MODIFIER | c.-23-6213T>G | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | chr2 | 127553487 | |||||||
chr2:127553491 | T | C | 248 | a0001c0002t0001g0027 a0001c0002t0001g0032 a0001c0002t0001g0034 others(245): Show |
257 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(254): Show |
intron_variant | MODIFIER | c.-23-6209T>C | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | chr2 | 127553491 | |||||||
chr2:127553593 | G | C | 3 | a0001c0002t0001g0135 a0001c0005t0002g0065 a0009c0014t0001g0136 |
3 | HG02970.hp2 HG03225.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.-23-6107G>C | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | chr2 | 127553593 | |||||||
chr2:127553615 | G | A | 2 | a0004c0007t0001g0259 a0004c0007t0001g0261 |
2 | HG01106.hp2 HG01255.hp1 |
intron_variant | MODIFIER | c.-23-6085G>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | chr2 | 127553615 | |||||||
chr2:127553731 | G | A | 3 | a0001c0004t0001g0009 a0001c0004t0001g0011 a0004c0007t0003g0010 |
3 | HG03688.hp1 NA18980.hp2 NA19010.hp1 |
intron_variant | MODIFIER | c.-23-5969G>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | chr2 | 127553731 | |||||||
chr2:127553886 | C | T | 79 | a0001c0002t0001g0027 a0001c0002t0001g0032 a0001c0002t0001g0034 others(76): Show |
79 | HG00323.hp2 HG00621.hp2 HG00642.hp1 others(76): Show |
intron_variant | MODIFIER | c.-23-5814C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | chr2 | 127553886 | |||||||
chr2:127553922 | G | C | 1 | a0001c0002t0001g0137 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-23-5778G>C | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | chr2 | 127553922 | |||||||
chr2:127553979 | T | C | 2 | a0001c0002t0001g0077 a0001c0044t0003g0080 |
2 | HG02809.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.-23-5721T>C | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | chr2 | 127553979 | |||||||
chr2:127553991 | C | T | 3 | a0015c0066t0001g0067 a0017c0072t0001g0012 a0046c0073t0001g0068 |
3 | HG01884.hp1 HG02922.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.-23-5709C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | chr2 | 127553991 | |||||||
chr2:127554040 | A | G | 2 | a0001c0002t0001g0032 a0001c0002t0001g0038 |
2 | NA18942.hp1 NA18983.hp2 |
intron_variant | MODIFIER | c.-23-5660A>G | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | chr2 | 127554040 | |||||||
chr2:127554056 | A | C | 1 | a0003c0003t0001g0239 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.-23-5644A>C | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | chr2 | 127554056 | |||||||
chr2:127554096 | C | T | 1 | a0007c0024t0001g0086 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.-23-5604C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | chr2 | 127554096 | |||||||
chr2:127554275 | T | A | 1 | a0029c0048t0001g0132 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.-23-5425T>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | chr2 | 127554275 | |||||||
chr2:127554511 | A | G | 2 | a0010c0020t0001g0150 a0010c0020t0001g0151 |
2 | HG03710.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.-23-5189A>G | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | chr2 | 127554511 | |||||||
chr2:127554519 | C | G | 1 | a0038c0033t0001g0069 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.-23-5181C>G | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | chr2 | 127554519 | |||||||
chr2:127554656 | G | C | 5 | a0001c0002t0005g0074 a0001c0017t0004g0024 a0001c0017t0004g0025 others(2): Show |
5 | HG02258.hp2 HG02630.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.-23-5044G>C | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | chr2 | 127554656 | |||||||
chr2:127554949 | A | AT | 7 | a0001c0002t0001g0106 a0001c0002t0001g0137 a0001c0004t0001g0023 others(4): Show |
7 | HG02055.hp2 HG02895.hp1 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.-23-4735dupT | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | INFO_REALIGN_3_PRIME | chr2 | 127554949 | ||||||
chr2:127555196 | C | T | 40 | a0001c0004t0001g0066 a0001c0004t0001g0124 a0001c0004t0001g0232 others(37): Show |
40 | HG00280.hp1 HG00323.hp1 HG00621.hp1 others(37): Show |
intron_variant | MODIFIER | c.-23-4504C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | chr2 | 127555196 | |||||||
chr2:127555252 | A | G | 3 | a0015c0066t0001g0067 a0017c0072t0001g0012 a0046c0073t0001g0068 |
3 | HG01884.hp1 HG02922.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.-23-4448A>G | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | chr2 | 127555252 | |||||||
chr2:127555367 | T | A | 40 | a0001c0004t0001g0066 a0001c0004t0001g0124 a0001c0004t0001g0232 others(37): Show |
40 | HG00280.hp1 HG00323.hp1 HG00621.hp1 others(37): Show |
intron_variant | MODIFIER | c.-23-4333T>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | chr2 | 127555367 | |||||||
chr2:127555534 | G | A | 5 | a0001c0010t0001g0264 a0001c0010t0001g0265 a0001c0018t0001g0266 others(2): Show |
5 | HG02451.hp1 HG02622.hp1 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.-23-4166G>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | chr2 | 127555534 | |||||||
chr2:127555653 | C | T | 3 | a0001c0002t0001g0089 a0001c0002t0001g0133 a0001c0013t0001g0090 |
3 | HG02055.hp1 HG02145.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.-23-4047C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | chr2 | 127555653 | |||||||
chr2:127555719 | T | C | 2 | a0003c0003t0001g0033 a0003c0003t0001g0081 |
2 | HG00621.hp2 NA18983.hp1 |
intron_variant | MODIFIER | c.-23-3981T>C | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | chr2 | 127555719 | |||||||
chr2:127555721 | G | A | 9 | a0001c0002t0001g0137 a0001c0002t0001g0144 a0001c0002t0001g0145 others(6): Show |
10 | HG01175.hp1 HG02257.hp1 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.-23-3979G>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | chr2 | 127555721 | |||||||
chr2:127555793 | T | C | 3 | a0021c0046t0003g0078 a0024c0070t0001g0028 a0027c0057t0001g0079 |
3 | HG01891.hp2 HG02257.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.-23-3907T>C | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | chr2 | 127555793 | |||||||
chr2:127555978 | A | G | 2 | a0007c0023t0001g0149 a0009c0014t0001g0148 |
2 | HG02109.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.-23-3722A>G | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | chr2 | 127555978 | |||||||
chr2:127556229 | T | A | 3 | a0015c0066t0001g0067 a0017c0072t0001g0012 a0046c0073t0001g0068 |
3 | HG01884.hp1 HG02922.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.-23-3471T>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | chr2 | 127556229 | |||||||
chr2:127556325 | G | T | 1 | a0009c0014t0001g0136 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.-23-3375G>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | chr2 | 127556325 | |||||||
chr2:127556736 | A | G | 1 | a0002c0011t0002g0270 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-23-2964A>G | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | chr2 | 127556736 | |||||||
chr2:127556909 | T | C | 45 | a0001c0004t0001g0009 a0001c0004t0001g0011 a0001c0004t0001g0066 others(42): Show |
45 | HG00280.hp1 HG00323.hp1 HG00621.hp1 others(42): Show |
intron_variant | MODIFIER | c.-23-2791T>C | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | chr2 | 127556909 | |||||||
chr2:127556927 | A | T | 5 | a0001c0002t0001g0135 a0001c0005t0002g0065 a0001c0005t0002g0131 others(2): Show |
5 | HG02280.hp2 HG02970.hp2 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.-23-2773A>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | chr2 | 127556927 | |||||||
chr2:127557044 | A | G | 5 | a0003c0003t0001g0125 a0003c0003t0001g0230 a0003c0003t0001g0233 others(2): Show |
5 | HG02074.hp2 HG02135.hp1 NA18747.hp2 others(2): Show |
intron_variant | MODIFIER | c.-23-2656A>G | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | chr2 | 127557044 | |||||||
chr2:127557213 | G | T | 40 | a0001c0004t0001g0066 a0001c0004t0001g0124 a0001c0004t0001g0232 others(37): Show |
40 | HG00280.hp1 HG00323.hp1 HG00621.hp1 others(37): Show |
intron_variant | MODIFIER | c.-23-2487G>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | chr2 | 127557213 | |||||||
chr2:127557255 | G | A | 5 | a0001c0002t0001g0225 a0001c0010t0001g0228 a0007c0024t0001g0227 others(2): Show |
5 | HG01069.hp2 HG01891.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.-23-2445G>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | chr2 | 127557255 | |||||||
chr2:127557341 | C | T | 1 | a0040c0060t0001g0055 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.-23-2359C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | chr2 | 127557341 | |||||||
chr2:127557414 | C | A | 5 | a0001c0002t0001g0225 a0001c0010t0001g0228 a0007c0024t0001g0227 others(2): Show |
5 | HG01069.hp2 HG01891.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.-23-2286C>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | chr2 | 127557414 | |||||||
chr2:127557654 | C | T | 71 | a0001c0002t0001g0027 a0001c0002t0001g0032 a0001c0002t0001g0034 others(68): Show |
71 | HG00323.hp2 HG00621.hp2 HG00642.hp1 others(68): Show |
intron_variant | MODIFIER | c.-23-2046C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | chr2 | 127557654 | |||||||
chr2:127557891 | C | A | 2 | a0003c0003t0001g0128 a0003c0003t0001g0241 |
2 | HG00323.hp1 HG03669.hp1 |
intron_variant | MODIFIER | c.-23-1809C>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | chr2 | 127557891 | |||||||
chr2:127557992 | G | C | 4 | a0001c0045t0001g0142 a0011c0016t0001g0008 a0011c0016t0001g0141 others(1): Show |
5 | HG02630.hp1 HG02895.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.-23-1708G>C | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | chr2 | 127557992 | |||||||
chr2:127558004 | T | C | 99 | a0001c0002t0001g0106 a0001c0002t0001g0155 a0001c0004t0001g0197 others(96): Show |
107 | HG00099.hp1 HG00099.hp2 HG00735.hp1 others(104): Show |
intron_variant | MODIFIER | c.-23-1696T>C | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | chr2 | 127558004 | |||||||
chr2:127558433 | T | C | 7 | a0001c0004t0001g0009 a0001c0004t0001g0011 a0001c0005t0002g0131 others(4): Show |
7 | HG02109.hp1 HG02280.hp2 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.-23-1267T>C | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | chr2 | 127558433 | |||||||
chr2:127558451 | A | G | 4 | a0001c0002t0001g0077 a0001c0010t0001g0138 a0001c0044t0003g0080 others(1): Show |
4 | HG02572.hp2 HG02809.hp2 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.-23-1249A>G | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | chr2 | 127558451 | |||||||
chr2:127558545 | C | T | 2 | a0001c0005t0002g0131 a0008c0063t0001g0257 |
2 | HG02280.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.-23-1155C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | chr2 | 127558545 | |||||||
chr2:127558598 | A | C | 18 | a0001c0002t0001g0027 a0001c0002t0001g0032 a0001c0002t0001g0034 others(15): Show |
18 | HG00621.hp2 HG01099.hp1 HG01943.hp1 others(15): Show |
intron_variant | MODIFIER | c.-23-1102A>C | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | chr2 | 127558598 | |||||||
chr2:127558652 | T | C | 2 | a0001c0010t0001g0138 a0009c0014t0001g0104 |
2 | HG02572.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.-23-1048T>C | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | chr2 | 127558652 | |||||||
chr2:127558741 | G | A | 1 | a0007c0023t0001g0122 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.-23-959G>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | chr2 | 127558741 | |||||||
chr2:127558759 | T | G | 250 | a0001c0002t0001g0027 a0001c0002t0001g0032 a0001c0002t0001g0034 others(247): Show |
259 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(256): Show |
intron_variant | MODIFIER | c.-23-941T>G | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | chr2 | 127558759 | |||||||
chr2:127558856 | G | A | 5 | a0001c0002t0005g0074 a0001c0017t0004g0024 a0001c0017t0004g0025 others(2): Show |
5 | HG02258.hp2 HG02630.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.-23-844G>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | chr2 | 127558856 | |||||||
chr2:127558915 | T | C | 3 | a0001c0004t0001g0009 a0001c0004t0001g0011 a0004c0007t0003g0010 |
3 | HG03688.hp1 NA18980.hp2 NA19010.hp1 |
intron_variant | MODIFIER | c.-23-785T>C | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | chr2 | 127558915 | |||||||
chr2:127558983 | C | T | 2 | a0007c0023t0001g0149 a0009c0014t0001g0148 |
2 | HG02109.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.-23-717C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | chr2 | 127558983 | |||||||
chr2:127559315 | G | T | 1 | a0001c0002t0001g0269 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.-23-385G>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | chr2 | 127559315 | |||||||
chr2:127559325 | G | A | 40 | a0001c0004t0001g0066 a0001c0004t0001g0124 a0001c0004t0001g0232 others(37): Show |
40 | HG00280.hp1 HG00323.hp1 HG00621.hp1 others(37): Show |
intron_variant | MODIFIER | c.-23-375G>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | chr2 | 127559325 | |||||||
chr2:127559438 | C | A | 2 | a0007c0023t0001g0149 a0009c0014t0001g0148 |
2 | HG02109.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.-23-262C>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | chr2 | 127559438 | |||||||
chr2:127559511 | G | A | 1 | a0001c0002t0001g0089 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.-23-189G>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | chr2 | 127559511 | |||||||
chr2:127559533 | G | A | 1 | a0001c0002t0001g0137 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-23-167G>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | chr2 | 127559533 | |||||||
chr2:127559619 | A | C | 8 | a0001c0002t0001g0077 a0001c0002t0001g0269 a0001c0010t0001g0138 others(5): Show |
8 | HG02109.hp2 HG02572.hp1 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.-23-81A>C | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | chr2 | 127559619 | |||||||
chr2:127559841 | T | C | 3 | a0001c0002t0001g0144 a0001c0002t0001g0145 a0028c0064t0002g0143 |
3 | HG01175.hp1 HG02257.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.18+101T>C | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 2/47 | chr2 | 127559841 | |||||||
chr2:127560006 | ATTTCTTT others(3): Show |
A | 1 | a0002c0011t0002g0270 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.18+285_18+294delCT others(8): Show |
MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 2/47 | INFO_REALIGN_3_PRIME | chr2 | 127560006 | ||||||
chr2:127560030 | C | CT | 15 | a0001c0002t0001g0137 a0001c0002t0001g0144 a0001c0002t0001g0145 others(12): Show |
16 | HG01175.hp1 HG02257.hp1 HG02451.hp1 others(13): Show |
intron_variant | MODIFIER | c.18+304dupT | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 2/47 | INFO_REALIGN_3_PRIME | chr2 | 127560030 | ||||||
chr2:127560030 | CT | C | 111 | a0001c0002t0001g0106 a0001c0002t0001g0155 a0001c0002t0005g0074 others(108): Show |
119 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(116): Show |
intron_variant | MODIFIER | c.18+304delT | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 2/47 | INFO_REALIGN_3_PRIME | chr2 | 127560030 | ||||||
chr2:127560102 | C | T | 2 | a0001c0005t0002g0131 a0008c0063t0001g0257 |
2 | HG02280.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.18+362C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 2/47 | chr2 | 127560102 | |||||||
chr2:127560349 | G | A | 3 | a0001c0005t0002g0102 a0001c0010t0001g0139 a0001c0058t0002g0103 |
3 | HG02109.hp2 NA18957.hp1 NA19007.hp2 |
intron_variant | MODIFIER | c.18+609G>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 2/47 | chr2 | 127560349 | |||||||
chr2:127560451 | C | T | 5 | a0001c0002t0001g0225 a0001c0010t0001g0228 a0007c0024t0001g0227 others(2): Show |
5 | HG01069.hp2 HG01891.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.18+711C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 2/47 | chr2 | 127560451 | |||||||
chr2:127560546 | A | G | 96 | a0001c0002t0001g0027 a0001c0002t0001g0032 a0001c0002t0001g0034 others(93): Show |
97 | HG00323.hp2 HG00621.hp2 HG00642.hp1 others(94): Show |
intron_variant | MODIFIER | c.18+806A>G | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 2/47 | chr2 | 127560546 | |||||||
chr2:127560560 | T | C | 1 | a0003c0003t0001g0241 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.18+820T>C | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 2/47 | chr2 | 127560560 | |||||||
chr2:127560584 | G | T | 1 | a0001c0005t0002g0044 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.18+844G>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 2/47 | chr2 | 127560584 | |||||||
chr2:127560873 | C | A | 3 | a0021c0046t0003g0078 a0024c0070t0001g0028 a0027c0057t0001g0079 |
3 | HG01891.hp2 HG02257.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.18+1133C>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 2/47 | chr2 | 127560873 | |||||||
chr2:127560889 | C | A | 3 | a0021c0046t0003g0078 a0024c0070t0001g0028 a0027c0057t0001g0079 |
3 | HG01891.hp2 HG02257.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.18+1149C>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 2/47 | chr2 | 127560889 | |||||||
chr2:127561023 | G | A | 14 | a0001c0002t0001g0137 a0001c0002t0001g0144 a0001c0002t0001g0145 others(11): Show |
15 | HG01175.hp1 HG02257.hp1 HG02451.hp1 others(12): Show |
intron_variant | MODIFIER | c.18+1283G>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 2/47 | chr2 | 127561023 | |||||||
chr2:127561320 | G | A | 1 | a0030c0052t0001g0087 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.18+1580G>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 2/47 | chr2 | 127561320 | |||||||
chr2:127561327 | C | T | 14 | a0001c0002t0001g0137 a0001c0002t0001g0144 a0001c0002t0001g0145 others(11): Show |
15 | HG01175.hp1 HG02257.hp1 HG02451.hp1 others(12): Show |
intron_variant | MODIFIER | c.18+1587C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 2/47 | chr2 | 127561327 | |||||||
chr2:127561343 | C | T | 1 | a0001c0002t0001g0137 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.18+1603C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 2/47 | chr2 | 127561343 | |||||||
chr2:127561354 | G | T | 7 | a0001c0010t0001g0163 a0004c0007t0001g0162 a0004c0007t0001g0164 others(4): Show |
7 | HG00735.hp2 HG01106.hp2 HG01175.hp2 others(4): Show |
intron_variant | MODIFIER | c.18+1614G>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 2/47 | chr2 | 127561354 | |||||||
chr2:127561360 | G | A | 71 | a0001c0002t0001g0027 a0001c0002t0001g0032 a0001c0002t0001g0034 others(68): Show |
71 | HG00323.hp2 HG00621.hp2 HG00642.hp1 others(68): Show |
intron_variant | MODIFIER | c.18+1620G>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 2/47 | chr2 | 127561360 | |||||||
chr2:127561373 | C | T | 4 | a0003c0003t0001g0236 a0003c0003t0001g0237 a0003c0003t0001g0239 others(1): Show |
4 | HG00280.hp1 HG00733.hp1 HG01255.hp2 others(1): Show |
intron_variant | MODIFIER | c.18+1633C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 2/47 | chr2 | 127561373 | |||||||
chr2:127561541 | G | C | 79 | a0001c0002t0001g0027 a0001c0002t0001g0032 a0001c0002t0001g0034 others(76): Show |
79 | HG00323.hp2 HG00621.hp2 HG00642.hp1 others(76): Show |
intron_variant | MODIFIER | c.18+1801G>C | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 2/47 | chr2 | 127561541 | |||||||
chr2:127561620 | G | A | 79 | a0001c0002t0001g0027 a0001c0002t0001g0032 a0001c0002t0001g0034 others(76): Show |
79 | HG00323.hp2 HG00621.hp2 HG00642.hp1 others(76): Show |
intron_variant | MODIFIER | c.18+1880G>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 2/47 | chr2 | 127561620 | |||||||
chr2:127561637 | G | A | 2 | a0001c0005t0002g0131 a0008c0063t0001g0257 |
2 | HG02280.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.18+1897G>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 2/47 | chr2 | 127561637 | |||||||
chr2:127561729 | G | A | 4 | a0001c0002t0001g0155 a0008c0015t0001g0107 a0008c0015t0001g0168 others(1): Show |
4 | HG01884.hp2 HG02145.hp1 HG02280.hp1 others(1): Show |
intron_variant | MODIFIER | c.18+1989G>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 2/47 | chr2 | 127561729 | |||||||
chr2:127561849 | G | A | 10 | a0002c0001t0001g0002 a0002c0001t0001g0111 a0002c0001t0001g0116 others(7): Show |
12 | HG00099.hp2 HG01109.hp2 HG01168.hp2 others(9): Show |
intron_variant | MODIFIER | c.18+2109G>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 2/47 | chr2 | 127561849 | |||||||
chr2:127561878 | A | G | 5 | a0001c0010t0001g0264 a0001c0010t0001g0265 a0001c0018t0001g0266 others(2): Show |
5 | HG02451.hp1 HG02622.hp1 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.18+2138A>G | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 2/47 | chr2 | 127561878 | |||||||
chr2:127561981 | T | G | 247 | a0001c0002t0001g0027 a0001c0002t0001g0032 a0001c0002t0001g0034 others(244): Show |
256 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(253): Show |
intron_variant | MODIFIER | c.19-2172T>G | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 2/47 | chr2 | 127561981 | |||||||
chr2:127562028 | G | GGA | 47 | a0001c0004t0001g0009 a0001c0004t0001g0011 a0001c0004t0001g0066 others(44): Show |
47 | HG00280.hp1 HG00323.hp1 HG00621.hp1 others(44): Show |
intron_variant | MODIFIER | c.19-2113_19-2112dup others(2): Show |
MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 2/47 | INFO_REALIGN_3_PRIME | chr2 | 127562028 | ||||||
chr2:127562072 | C | T | 2 | a0001c0004t0001g0043 a0001c0005t0002g0044 |
2 | NA18962.hp2 NA18968.hp2 |
intron_variant | MODIFIER | c.19-2081C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 2/47 | chr2 | 127562072 | |||||||
chr2:127562220 | A | C | 78 | a0001c0002t0001g0027 a0001c0002t0001g0032 a0001c0002t0001g0034 others(75): Show |
78 | HG00323.hp2 HG00621.hp2 HG00642.hp1 others(75): Show |
intron_variant | MODIFIER | c.19-1933A>C | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 2/47 | chr2 | 127562220 | |||||||
chr2:127562266 | C | T | 1 | a0008c0063t0001g0257 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.19-1887C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 2/47 | chr2 | 127562266 | |||||||
chr2:127562359 | C | A | 1 | a0029c0048t0001g0132 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.19-1794C>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 2/47 | chr2 | 127562359 | |||||||
chr2:127562430 | G | A | 4 | a0001c0002t0001g0077 a0001c0010t0001g0138 a0001c0044t0003g0080 others(1): Show |
4 | HG02572.hp2 HG02809.hp2 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.19-1723G>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 2/47 | chr2 | 127562430 | |||||||
chr2:127562441 | C | T | 1 | a0001c0002t0001g0134 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.19-1712C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 2/47 | chr2 | 127562441 | |||||||
chr2:127562482 | G | GTTT | 27 | a0001c0004t0001g0232 a0001c0004t0001g0246 a0001c0004t0001g0254 others(24): Show |
27 | HG00280.hp1 HG00323.hp1 HG00621.hp1 others(24): Show |
intron_variant | MODIFIER | c.19-1649_19-1647dup others(3): Show |
MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 2/47 | INFO_REALIGN_3_PRIME | chr2 | 127562482 | ||||||
chr2:127562482 | G | GTTTT | 8 | a0003c0003t0001g0126 a0003c0003t0001g0127 a0003c0003t0001g0128 others(5): Show |
8 | HG01433.hp1 HG01981.hp2 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.19-1650_19-1647dup others(4): Show |
MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 2/47 | INFO_REALIGN_3_PRIME | chr2 | 127562482 | ||||||
chr2:127562482 | GT | G | 144 | a0001c0002t0001g0027 a0001c0002t0001g0032 a0001c0002t0001g0034 others(141): Show |
153 | HG00099.hp1 HG00099.hp2 HG00621.hp2 others(150): Show |
intron_variant | MODIFIER | c.19-1647delT | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 2/47 | INFO_REALIGN_3_PRIME | chr2 | 127562482 | ||||||
chr2:127562484 | T | G | 1 | a0001c0002t0001g0145 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.19-1669T>G | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 2/47 | chr2 | 127562484 | |||||||
chr2:127562485 | T | G | 13 | a0001c0002t0001g0137 a0001c0002t0001g0144 a0001c0010t0001g0264 others(10): Show |
14 | HG02257.hp1 HG02451.hp1 HG02622.hp1 others(11): Show |
intron_variant | MODIFIER | c.19-1668T>G | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 2/47 | chr2 | 127562485 | |||||||
chr2:127562558 | G | A | 1 | a0001c0005t0001g0049 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.19-1595G>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 2/47 | chr2 | 127562558 | |||||||
chr2:127562602 | G | C | 14 | a0001c0002t0001g0137 a0001c0002t0001g0144 a0001c0002t0001g0145 others(11): Show |
15 | HG01175.hp1 HG02257.hp1 HG02451.hp1 others(12): Show |
intron_variant | MODIFIER | c.19-1551G>C | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 2/47 | chr2 | 127562602 | |||||||
chr2:127562635 | T | G | 247 | a0001c0002t0001g0027 a0001c0002t0001g0032 a0001c0002t0001g0034 others(244): Show |
256 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(253): Show |
intron_variant | MODIFIER | c.19-1518T>G | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 2/47 | chr2 | 127562635 | |||||||
chr2:127562733 | G | A | 2 | a0001c0004t0001g0254 a0001c0010t0001g0139 |
2 | HG02109.hp2 HG03490.hp1 |
intron_variant | MODIFIER | c.19-1420G>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 2/47 | chr2 | 127562733 | |||||||
chr2:127562900 | C | T | 3 | a0021c0046t0003g0078 a0024c0070t0001g0028 a0027c0057t0001g0079 |
3 | HG01891.hp2 HG02257.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.19-1253C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 2/47 | chr2 | 127562900 | |||||||
chr2:127562914 | T | C | 7 | a0001c0004t0001g0009 a0001c0004t0001g0011 a0001c0005t0002g0131 others(4): Show |
7 | HG02109.hp1 HG02280.hp2 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.19-1239T>C | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 2/47 | chr2 | 127562914 | |||||||
chr2:127563087 | C | T | 1 | a0002c0006t0001g0013 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.19-1066C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 2/47 | chr2 | 127563087 | |||||||
chr2:127563091 | T | G | 2 | a0001c0010t0001g0138 a0009c0014t0001g0104 |
2 | HG02572.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.19-1062T>G | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 2/47 | chr2 | 127563091 | |||||||
chr2:127563133 | G | C | 2 | a0002c0006t0001g0015 a0002c0006t0001g0016 |
2 | HG00741.hp1 HG03239.hp2 |
intron_variant | MODIFIER | c.19-1020G>C | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 2/47 | chr2 | 127563133 | |||||||
chr2:127563411 | T | C | 1 | a0002c0001t0001g0198 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.19-742T>C | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 2/47 | chr2 | 127563411 | |||||||
chr2:127563503 | TCCTGCAA others(10): Show |
T | 1 | a0027c0057t0001g0079 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.19-636_19-620delAA others(15): Show |
MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 2/47 | INFO_REALIGN_3_PRIME | chr2 | 127563503 | ||||||
chr2:127563592 | C | T | 1 | a0001c0002t0001g0101 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.19-561C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 2/47 | chr2 | 127563592 | |||||||
chr2:127563715 | G | A | 3 | a0015c0066t0001g0067 a0017c0072t0001g0012 a0046c0073t0001g0068 |
3 | HG01884.hp1 HG02922.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.19-438G>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 2/47 | chr2 | 127563715 | |||||||
chr2:127563792 | C | T | 3 | a0021c0046t0003g0078 a0024c0070t0001g0028 a0027c0057t0001g0079 |
3 | HG01891.hp2 HG02257.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.19-361C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 2/47 | chr2 | 127563792 | |||||||
chr2:127563838 | A | G | 1 | a0001c0005t0002g0054 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.19-315A>G | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 2/47 | chr2 | 127563838 | |||||||
chr2:127564002 | A | G | 2 | a0001c0002t0001g0135 a0009c0014t0001g0136 |
2 | HG02970.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.19-151A>G | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 2/47 | chr2 | 127564002 | |||||||
chr2:127564106 | G | T | 1 | a0002c0001t0001g0205 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.19-47G>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 2/47 | chr2 | 127564106 | |||||||
chr2:127564108 | A | G | 4 | a0002c0001t0001g0071 a0002c0001t0001g0203 a0002c0001t0001g0204 others(1): Show |
4 | NA18947.hp1 NA18950.hp1 NA18985.hp1 others(1): Show |
intron_variant | MODIFIER | c.19-45A>G | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 2/47 | chr2 | 127564108 | |||||||
chr2:127564274 | T | C | 2 | a0007c0023t0001g0149 a0009c0014t0001g0148 |
2 | HG02109.hp1 HG02818.hp2 |
splice_region_variant&intron_variant | LOW | c.132+8T>C | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 3/47 | chr2 | 127564274 | |||||||
chr2:127564300 | C | T | 1 | a0001c0005t0002g0208 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.132+34C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 3/47 | chr2 | 127564300 | |||||||
chr2:127564578 | G | A | 1 | a0001c0002t0001g0137 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.132+312G>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 3/47 | chr2 | 127564578 | |||||||
chr2:127564752 | GGCTTAGC others(6): Show |
G | 2 | a0001c0002t0001g0077 a0001c0044t0003g0080 |
2 | HG02809.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.133-479_133-467del others(13): Show |
MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 3/47 | INFO_REALIGN_3_PRIME | chr2 | 127564752 | ||||||
chr2:127564925 | C | T | 1 | a0001c0005t0002g0054 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.133-308C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 3/47 | chr2 | 127564925 | |||||||
chr2:127565088 | G | T | 3 | a0007c0024t0001g0227 a0017c0072t0001g0012 a0046c0073t0001g0068 |
3 | HG02922.hp2 HG06807.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.133-145G>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 3/47 | chr2 | 127565088 | |||||||
chr2:127565613 | G | T | 6 | a0001c0004t0001g0009 a0001c0004t0001g0011 a0004c0007t0003g0010 others(3): Show |
6 | HG02922.hp2 HG03688.hp1 HG06807.hp2 others(3): Show |
intron_variant | MODIFIER | c.285+228G>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 4/47 | chr2 | 127565613 | |||||||
chr2:127565760 | C | A | 11 | a0001c0002t0001g0137 a0001c0002t0001g0144 a0001c0002t0001g0145 others(8): Show |
12 | HG01175.hp1 HG02257.hp1 HG02572.hp2 others(9): Show |
intron_variant | MODIFIER | c.285+375C>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 4/47 | chr2 | 127565760 | |||||||
chr2:127565782 | C | G | 1 | a0001c0010t0001g0139 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.285+397C>G | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 4/47 | chr2 | 127565782 | |||||||
chr2:127565921 | G | A | 8 | a0001c0010t0001g0228 a0001c0010t0001g0264 a0001c0010t0001g0265 others(5): Show |
8 | HG01891.hp1 HG02451.hp1 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.285+536G>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 4/47 | chr2 | 127565921 | |||||||
chr2:127566142 | T | C | 6 | a0001c0010t0001g0139 a0002c0001t0001g0006 a0002c0001t0001g0177 others(3): Show |
6 | HG02109.hp2 HG02135.hp2 NA18962.hp1 others(3): Show |
intron_variant | MODIFIER | c.286-501T>C | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 4/47 | chr2 | 127566142 | |||||||
chr2:127566230 | C | T | 1 | a0004c0007t0003g0223 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.286-413C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 4/47 | chr2 | 127566230 | |||||||
chr2:127566354 | C | T | 1 | a0008c0042t0001g0064 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.286-289C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 4/47 | chr2 | 127566354 | |||||||
chr2:127566363 | T | C | 3 | a0001c0002t0001g0091 a0001c0002t0001g0092 a0001c0002t0001g0225 |
3 | HG01069.hp2 HG02896.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.286-280T>C | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 4/47 | chr2 | 127566363 | |||||||
chr2:127566431 | C | T | 1 | a0041c0028t0001g0195 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.286-212C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 4/47 | chr2 | 127566431 | |||||||
chr2:127566457 | C | T | 1 | a0003c0003t0001g0243 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.286-186C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 4/47 | chr2 | 127566457 | |||||||
chr2:127566475 | G | A | 5 | a0001c0002t0005g0074 a0001c0017t0004g0024 a0001c0017t0004g0025 others(2): Show |
5 | HG02258.hp2 HG02630.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.286-168G>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 4/47 | chr2 | 127566475 | |||||||
chr2:127566550 | C | CT | 248 | a0001c0002t0001g0027 a0001c0002t0001g0032 a0001c0002t0001g0034 others(245): Show |
257 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(254): Show |
intron_variant | MODIFIER | c.286-93_286-92insT | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 4/47 | chr2 | 127566550 | |||||||
chr2:127566936 | C | T | 2 | a0001c0002t0001g0135 a0009c0014t0001g0136 |
2 | HG02970.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.470+109C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 5/47 | chr2 | 127566936 | |||||||
chr2:127566991 | C | T | 1 | a0008c0042t0001g0064 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.470+164C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 5/47 | chr2 | 127566991 | |||||||
chr2:127567306 | G | A | 1 | a0002c0001t0001g0112 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.470+479G>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 5/47 | chr2 | 127567306 | |||||||
chr2:127567319 | C | CA | 67 | a0001c0002t0001g0027 a0001c0002t0001g0032 a0001c0002t0001g0034 others(64): Show |
67 | HG00323.hp2 HG00621.hp2 HG00642.hp1 others(64): Show |
intron_variant | MODIFIER | c.470+501dupA | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 5/47 | INFO_REALIGN_3_PRIME | chr2 | 127567319 | ||||||
chr2:127567330 | A | T | 251 | a0001c0002t0001g0027 a0001c0002t0001g0032 a0001c0002t0001g0034 others(248): Show |
260 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(257): Show |
intron_variant | MODIFIER | c.470+503A>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 5/47 | chr2 | 127567330 | |||||||
chr2:127567345 | G | A | 2 | a0001c0002t0001g0135 a0009c0014t0001g0136 |
2 | HG02970.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.470+518G>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 5/47 | chr2 | 127567345 | |||||||
chr2:127567561 | C | A | 3 | a0001c0010t0001g0228 a0015c0071t0001g0123 a0016c0027t0001g0226 |
3 | HG01891.hp1 HG03195.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.470+734C>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 5/47 | chr2 | 127567561 | |||||||
chr2:127567598 | T | C | 1 | a0002c0001t0001g0199 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.470+771T>C | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 5/47 | chr2 | 127567598 | |||||||
chr2:127567662 | GATTC | G | 3 | a0011c0016t0001g0008 a0011c0016t0001g0141 a0029c0048t0001g0132 |
4 | HG02630.hp1 HG03041.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.470+861_470+864del others(4): Show |
MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 5/47 | INFO_REALIGN_3_PRIME | chr2 | 127567662 | ||||||
chr2:127567832 | G | A | 1 | a0001c0010t0001g0139 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.470+1005G>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 5/47 | chr2 | 127567832 | |||||||
chr2:127567835 | C | T | 35 | a0001c0004t0001g0246 a0001c0004t0001g0254 a0003c0003t0001g0109 others(32): Show |
35 | HG00280.hp1 HG00323.hp1 HG00621.hp1 others(32): Show |
intron_variant | MODIFIER | c.470+1008C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 5/47 | chr2 | 127567835 | |||||||
chr2:127567899 | C | T | 4 | a0001c0002t0001g0106 a0001c0013t0001g0005 a0001c0013t0001g0166 others(1): Show |
5 | HG01243.hp1 HG02055.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.470+1072C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 5/47 | chr2 | 127567899 | |||||||
chr2:127568574 | G | C | 1 | a0006c0009t0001g0059 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.471-1215G>C | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 5/47 | chr2 | 127568574 | |||||||
chr2:127568624 | C | T | 3 | a0001c0002t0001g0144 a0001c0002t0001g0145 a0028c0064t0002g0143 |
3 | HG01175.hp1 HG02257.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.471-1165C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 5/47 | chr2 | 127568624 | |||||||
chr2:127568725 | C | T | 3 | a0001c0002t0001g0060 a0006c0009t0001g0058 a0006c0009t0001g0059 |
3 | HG01106.hp1 HG03239.hp1 HG03927.hp2 |
intron_variant | MODIFIER | c.471-1064C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 5/47 | chr2 | 127568725 | |||||||
chr2:127568795 | G | A | 71 | a0001c0002t0001g0077 a0001c0002t0001g0269 a0001c0004t0001g0066 others(68): Show |
76 | HG00099.hp2 HG00735.hp1 HG00738.hp2 others(73): Show |
intron_variant | MODIFIER | c.471-994G>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 5/47 | chr2 | 127568795 | |||||||
chr2:127568814 | T | A | 5 | a0001c0010t0001g0264 a0001c0010t0001g0265 a0001c0018t0001g0266 others(2): Show |
5 | HG02451.hp1 HG02622.hp1 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.471-975T>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 5/47 | chr2 | 127568814 | |||||||
chr2:127568861 | G | T | 5 | a0001c0010t0001g0264 a0001c0010t0001g0265 a0001c0018t0001g0266 others(2): Show |
5 | HG02451.hp1 HG02622.hp1 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.471-928G>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 5/47 | chr2 | 127568861 | |||||||
chr2:127568862 | C | T | 5 | a0001c0010t0001g0264 a0001c0010t0001g0265 a0001c0018t0001g0266 others(2): Show |
5 | HG02451.hp1 HG02622.hp1 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.471-927C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 5/47 | chr2 | 127568862 | |||||||
chr2:127568866 | C | G | 5 | a0001c0010t0001g0264 a0001c0010t0001g0265 a0001c0018t0001g0266 others(2): Show |
5 | HG02451.hp1 HG02622.hp1 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.471-923C>G | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 5/47 | chr2 | 127568866 | |||||||
chr2:127568959 | G | A | 2 | a0017c0072t0001g0012 a0046c0073t0001g0068 |
2 | HG02922.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.471-830G>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 5/47 | chr2 | 127568959 | |||||||
chr2:127568973 | C | T | 1 | a0001c0002t0001g0089 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.471-816C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 5/47 | chr2 | 127568973 | |||||||
chr2:127569144 | G | A | 1 | a0001c0002t0001g0089 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.471-645G>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 5/47 | chr2 | 127569144 | |||||||
chr2:127569207 | C | CA | 159 | a0001c0002t0001g0027 a0001c0002t0001g0032 a0001c0002t0001g0035 others(156): Show |
163 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(160): Show |
intron_variant | MODIFIER | c.471-562dupA | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 5/47 | INFO_REALIGN_3_PRIME | chr2 | 127569207 | ||||||
chr2:127569207 | C | CAA | 13 | a0001c0002t0001g0034 a0001c0002t0001g0101 a0001c0004t0001g0242 others(10): Show |
13 | HG00741.hp1 HG02293.hp2 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.471-563_471-562dup others(2): Show |
MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 5/47 | INFO_REALIGN_3_PRIME | chr2 | 127569207 | ||||||
chr2:127569207 | CA | C | 7 | a0001c0010t0001g0228 a0002c0001t0001g0182 a0002c0001t0001g0183 others(4): Show |
7 | HG01168.hp2 HG01169.hp2 HG01256.hp2 others(4): Show |
intron_variant | MODIFIER | c.471-562delA | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 5/47 | INFO_REALIGN_3_PRIME | chr2 | 127569207 | ||||||
chr2:127569282 | C | T | 1 | a0008c0042t0001g0064 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.471-507C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 5/47 | chr2 | 127569282 | |||||||
chr2:127569431 | C | T | 1 | a0009c0014t0001g0174 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.471-358C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 5/47 | chr2 | 127569431 | |||||||
chr2:127569504 | G | A | 1 | a0001c0002t0001g0137 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.471-285G>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 5/47 | chr2 | 127569504 | |||||||
chr2:127569522 | C | T | 3 | a0002c0006t0001g0013 a0007c0023t0001g0149 a0009c0014t0001g0148 |
3 | HG02109.hp1 HG02818.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.471-267C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 5/47 | chr2 | 127569522 | |||||||
chr2:127569917 | A | C | 1 | a0001c0004t0001g0022 | 1 | HG03669.hp2 | splice_region_variant&intron_variant | LOW | c.592+7A>C | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 6/47 | chr2 | 127569917 | |||||||
chr2:127569923 | C | G | 1 | a0002c0001t0001g0176 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.592+13C>G | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 6/47 | chr2 | 127569923 | |||||||
chr2:127569934 | C | A | 1 | a0007c0024t0001g0227 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.592+24C>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 6/47 | chr2 | 127569934 | |||||||
chr2:127569994 | T | G | 6 | a0001c0004t0001g0218 a0004c0007t0003g0007 a0004c0007t0003g0072 others(3): Show |
6 | HG00280.hp2 HG00642.hp2 HG01168.hp1 others(3): Show |
intron_variant | MODIFIER | c.592+84T>G | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 6/47 | chr2 | 127569994 | |||||||
chr2:127570091 | G | A | 1 | a0008c0063t0001g0257 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.592+181G>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 6/47 | chr2 | 127570091 | |||||||
chr2:127570154 | T | C | 11 | a0001c0002t0001g0144 a0001c0002t0001g0145 a0001c0005t0002g0065 others(8): Show |
12 | HG01175.hp1 HG02257.hp1 HG02572.hp2 others(9): Show |
intron_variant | MODIFIER | c.592+244T>C | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 6/47 | chr2 | 127570154 | |||||||
chr2:127570367 | G | A | 1 | a0010c0020t0001g0150 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.592+457G>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 6/47 | chr2 | 127570367 | |||||||
chr2:127570527 | A | G | 1 | a0006c0009t0001g0020 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.592+617A>G | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 6/47 | chr2 | 127570527 | |||||||
chr2:127570583 | C | T | 1 | a0001c0018t0001g0266 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.592+673C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 6/47 | chr2 | 127570583 | |||||||
chr2:127570743 | C | T | 1 | a0001c0004t0001g0254 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.592+833C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 6/47 | chr2 | 127570743 | |||||||
chr2:127570783 | C | T | 7 | a0001c0002t0001g0077 a0001c0044t0003g0080 a0002c0006t0001g0013 others(4): Show |
7 | HG02109.hp1 HG02809.hp2 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.592+873C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 6/47 | chr2 | 127570783 | |||||||
chr2:127570800 | C | T | 74 | a0001c0002t0001g0053 a0001c0002t0001g0269 a0001c0004t0001g0009 others(71): Show |
79 | HG00099.hp2 HG00735.hp1 HG00738.hp2 others(76): Show |
intron_variant | MODIFIER | c.592+890C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 6/47 | chr2 | 127570800 | |||||||
chr2:127570866 | T | G | 3 | a0001c0005t0002g0131 a0001c0010t0001g0139 a0008c0063t0001g0257 |
3 | HG02109.hp2 HG02280.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.592+956T>G | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 6/47 | chr2 | 127570866 | |||||||
chr2:127570882 | T | C | 9 | a0001c0002t0001g0144 a0001c0002t0001g0145 a0001c0005t0002g0065 others(6): Show |
10 | HG01175.hp1 HG02257.hp1 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.592+972T>C | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 6/47 | chr2 | 127570882 | |||||||
chr2:127571011 | C | T | 1 | a0034c0059t0001g0031 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.592+1101C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 6/47 | chr2 | 127571011 | |||||||
chr2:127571029 | G | T | 3 | a0001c0005t0002g0131 a0001c0010t0001g0139 a0008c0063t0001g0257 |
3 | HG02109.hp2 HG02280.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.592+1119G>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 6/47 | chr2 | 127571029 | |||||||
chr2:127571190 | C | T | 5 | a0004c0007t0001g0164 a0004c0007t0001g0259 a0004c0007t0001g0261 others(2): Show |
5 | HG01106.hp2 HG01175.hp2 HG01255.hp1 others(2): Show |
intron_variant | MODIFIER | c.592+1280C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 6/47 | chr2 | 127571190 | |||||||
chr2:127571199 | C | T | 1 | a0007c0024t0001g0227 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.592+1289C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 6/47 | chr2 | 127571199 | |||||||
chr2:127571247 | G | A | 3 | a0001c0005t0002g0131 a0001c0010t0001g0139 a0008c0063t0001g0257 |
3 | HG02109.hp2 HG02280.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.592+1337G>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 6/47 | chr2 | 127571247 | |||||||
chr2:127571261 | C | A | 251 | a0001c0002t0001g0027 a0001c0002t0001g0032 a0001c0002t0001g0034 others(248): Show |
260 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(257): Show |
intron_variant | MODIFIER | c.592+1351C>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 6/47 | chr2 | 127571261 | |||||||
chr2:127571410 | A | G | 4 | a0002c0006t0001g0004 a0002c0006t0001g0158 a0002c0006t0001g0159 others(1): Show |
5 | HG00738.hp1 HG00741.hp2 HG01070.hp2 others(2): Show |
intron_variant | MODIFIER | c.592+1500A>G | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 6/47 | chr2 | 127571410 | |||||||
chr2:127571442 | G | GT | 5 | a0001c0010t0001g0264 a0001c0010t0001g0265 a0006c0009t0001g0058 others(2): Show |
5 | HG01106.hp1 HG02451.hp1 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.592+1549dupT | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 6/47 | INFO_REALIGN_3_PRIME | chr2 | 127571442 | ||||||
chr2:127571442 | G | GTTTTTT | 12 | a0003c0003t0001g0125 a0003c0003t0001g0128 a0003c0003t0001g0230 others(9): Show |
13 | HG00323.hp1 HG01433.hp1 HG01975.hp2 others(10): Show |
intron_variant | MODIFIER | c.592+1544_592+1549d others(8): Show |
MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 6/47 | INFO_REALIGN_3_PRIME | chr2 | 127571442 | ||||||
chr2:127571442 | G | GTTTTTTT others(2): Show |
5 | a0001c0002t0001g0036 a0001c0002t0001g0101 a0001c0002t0001g0137 others(2): Show |
5 | HG02109.hp2 HG02647.hp1 NA18906.hp1 others(2): Show |
intron_variant | MODIFIER | c.592+1541_592+1549d others(11): Show |
MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 6/47 | INFO_REALIGN_3_PRIME | chr2 | 127571442 | ||||||
chr2:127571442 | G | GTTTTTTT others(3): Show |
20 | a0001c0002t0001g0027 a0001c0002t0001g0034 a0001c0002t0001g0045 others(17): Show |
20 | HG00621.hp2 HG00642.hp1 HG01069.hp2 others(17): Show |
intron_variant | MODIFIER | c.592+1540_592+1549d others(12): Show |
MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 6/47 | INFO_REALIGN_3_PRIME | chr2 | 127571442 | ||||||
chr2:127571442 | G | GTTTTTTT others(11): Show |
5 | a0001c0010t0001g0163 a0005c0008t0001g0209 a0012c0022t0001g0120 others(2): Show |
5 | HG01069.hp1 HG01071.hp1 HG01256.hp2 others(2): Show |
intron_variant | MODIFIER | c.592+1542_592+1543i others(20): Show |
MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 6/47 | INFO_REALIGN_3_PRIME | chr2 | 127571442 | ||||||
chr2:127571442 | G | GTTTTTTT others(12): Show |
22 | a0001c0013t0001g0005 a0001c0013t0001g0166 a0001c0013t0001g0167 others(19): Show |
23 | HG00099.hp1 HG00741.hp1 HG00741.hp2 others(20): Show |
intron_variant | MODIFIER | c.592+1542_592+1543i others(21): Show |
MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 6/47 | INFO_REALIGN_3_PRIME | chr2 | 127571442 | ||||||
chr2:127571442 | G | GTTTTTTT others(13): Show |
13 | a0001c0002t0001g0106 a0001c0002t0001g0155 a0001c0017t0004g0024 others(10): Show |
13 | HG00735.hp2 HG00738.hp1 HG01081.hp2 others(10): Show |
intron_variant | MODIFIER | c.592+1542_592+1543i others(22): Show |
MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 6/47 | INFO_REALIGN_3_PRIME | chr2 | 127571442 | ||||||
chr2:127571442 | G | GTTTTTTT others(4): Show |
35 | a0001c0002t0001g0032 a0001c0002t0001g0035 a0001c0002t0001g0038 others(32): Show |
35 | HG01175.hp1 HG01255.hp2 HG01952.hp2 others(32): Show |
intron_variant | MODIFIER | c.592+1539_592+1549d others(13): Show |
MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 6/47 | INFO_REALIGN_3_PRIME | chr2 | 127571442 | ||||||
chr2:127571442 | G | GTTTTTTT others(13): Show |
1 | a0010c0020t0001g0150 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.592+1543_592+1544i others(22): Show |
MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 6/47 | INFO_REALIGN_3_PRIME | chr2 | 127571442 | ||||||
chr2:127571442 | G | GTTTTTTT others(14): Show |
1 | a0010c0020t0001g0151 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.592+1543_592+1544i others(23): Show |
MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 6/47 | INFO_REALIGN_3_PRIME | chr2 | 127571442 | ||||||
chr2:127571442 | G | GTTTTTTT others(5): Show |
7 | a0001c0002t0001g0040 a0001c0002t0001g0134 a0003c0003t0001g0237 others(4): Show |
7 | HG00280.hp1 HG00621.hp1 HG00733.hp1 others(4): Show |
intron_variant | MODIFIER | c.592+1538_592+1549d others(14): Show |
MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 6/47 | INFO_REALIGN_3_PRIME | chr2 | 127571442 | ||||||
chr2:127571442 | G | GTTTTTTT others(6): Show |
2 | a0001c0002t0001g0144 a0009c0014t0001g0148 |
2 | HG02257.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.592+1537_592+1549d others(15): Show |
MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 6/47 | INFO_REALIGN_3_PRIME | chr2 | 127571442 | ||||||
chr2:127571442 | G | GTTTTTTT others(9): Show |
2 | a0002c0001t0001g0198 a0002c0012t0001g0171 |
2 | NA18941.hp1 NA18986.hp2 |
intron_variant | MODIFIER | c.592+1534_592+1549d others(18): Show |
MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 6/47 | INFO_REALIGN_3_PRIME | chr2 | 127571442 | ||||||
chr2:127571442 | G | GTTTTTTT others(10): Show |
2 | a0001c0004t0001g0214 a0002c0012t0001g0173 |
2 | HG01192.hp2 NA19056.hp1 |
intron_variant | MODIFIER | c.592+1533_592+1549d others(19): Show |
MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 6/47 | INFO_REALIGN_3_PRIME | chr2 | 127571442 | ||||||
chr2:127571442 | G | GTTTTTTT others(11): Show |
16 | a0001c0002t0001g0053 a0001c0004t0001g0124 a0001c0004t0001g0197 others(13): Show |
17 | HG00099.hp2 HG01109.hp2 HG01123.hp1 others(14): Show |
intron_variant | MODIFIER | c.592+1549_592+1550i others(20): Show |
MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 6/47 | INFO_REALIGN_3_PRIME | chr2 | 127571442 | ||||||
chr2:127571442 | G | GTTTTTTT others(12): Show |
27 | a0001c0004t0001g0009 a0001c0004t0001g0011 a0001c0004t0001g0066 others(24): Show |
28 | HG00735.hp1 HG00738.hp2 HG01081.hp1 others(25): Show |
intron_variant | MODIFIER | c.592+1549_592+1550i others(21): Show |
MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 6/47 | INFO_REALIGN_3_PRIME | chr2 | 127571442 | ||||||
chr2:127571442 | G | GTTTTTTT others(13): Show |
11 | a0002c0001t0001g0071 a0002c0001t0001g0112 a0002c0001t0001g0184 others(8): Show |
11 | HG01358.hp1 HG02132.hp2 HG02886.hp1 others(8): Show |
intron_variant | MODIFIER | c.592+1549_592+1550i others(22): Show |
MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 6/47 | INFO_REALIGN_3_PRIME | chr2 | 127571442 | ||||||
chr2:127571442 | G | GTTTTTTT others(14): Show |
5 | a0001c0004t0001g0057 a0001c0004t0001g0242 a0002c0001t0001g0196 others(2): Show |
5 | HG02027.hp1 HG02027.hp2 HG02148.hp2 others(2): Show |
intron_variant | MODIFIER | c.592+1549_592+1550i others(23): Show |
MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 6/47 | INFO_REALIGN_3_PRIME | chr2 | 127571442 | ||||||
chr2:127571442 | G | GTTTTTTT others(15): Show |
1 | a0002c0001t0001g0117 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.592+1549_592+1550i others(24): Show |
MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 6/47 | INFO_REALIGN_3_PRIME | chr2 | 127571442 | ||||||
chr2:127571442 | G | GTTTTTTT others(21): Show |
1 | a0041c0028t0001g0195 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.592+1549_592+1550i others(30): Show |
MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 6/47 | INFO_REALIGN_3_PRIME | chr2 | 127571442 | ||||||
chr2:127571442 | GT | G | 5 | a0001c0005t0001g0049 a0001c0010t0001g0228 a0001c0058t0002g0103 others(2): Show |
5 | HG01891.hp1 HG03195.hp1 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.592+1549delT | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 6/47 | INFO_REALIGN_3_PRIME | chr2 | 127571442 | ||||||
chr2:127571513 | T | C | 2 | a0001c0002t0001g0045 a0001c0002t0001g0088 |
2 | HG02451.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.592+1603T>C | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 6/47 | chr2 | 127571513 | |||||||
chr2:127571573 | T | C | 3 | a0001c0002t0001g0100 a0001c0002t0001g0101 a0001c0002t0001g0262 |
3 | HG00642.hp1 HG02886.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.592+1663T>C | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 6/47 | chr2 | 127571573 | |||||||
chr2:127571584 | G | A | 1 | a0007c0024t0001g0227 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.592+1674G>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 6/47 | chr2 | 127571584 | |||||||
chr2:127571606 | G | A | 3 | a0001c0002t0001g0027 a0013c0019t0001g0178 a0013c0019t0001g0179 |
3 | HG01099.hp1 HG01169.hp1 HG02300.hp2 |
intron_variant | MODIFIER | c.592+1696G>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 6/47 | chr2 | 127571606 | |||||||
chr2:127571668 | C | T | 1 | a0001c0002t0001g0077 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.592+1758C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 6/47 | chr2 | 127571668 | |||||||
chr2:127571708 | G | A | 1 | a0040c0060t0001g0055 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.592+1798G>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 6/47 | chr2 | 127571708 | |||||||
chr2:127571726 | C | T | 1 | a0007c0024t0001g0227 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.592+1816C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 6/47 | chr2 | 127571726 | |||||||
chr2:127571727 | G | A | 28 | a0001c0002t0001g0060 a0001c0004t0001g0043 a0001c0005t0001g0049 others(25): Show |
28 | HG00323.hp2 HG00733.hp2 HG01070.hp1 others(25): Show |
intron_variant | MODIFIER | c.592+1817G>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 6/47 | chr2 | 127571727 | |||||||
chr2:127571760 | G | A | 3 | a0021c0046t0003g0078 a0024c0070t0001g0028 a0027c0057t0001g0079 |
3 | HG01891.hp2 HG02257.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.592+1850G>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 6/47 | chr2 | 127571760 | |||||||
chr2:127571887 | T | C | 2 | a0001c0002t0001g0077 a0001c0044t0003g0080 |
2 | HG02809.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.592+1977T>C | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 6/47 | chr2 | 127571887 | |||||||
chr2:127571962 | T | C | 1 | a0001c0005t0002g0050 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.593-1958T>C | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 6/47 | chr2 | 127571962 | |||||||
chr2:127571995 | C | A | 1 | a0006c0009t0001g0097 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.593-1925C>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 6/47 | chr2 | 127571995 | |||||||
chr2:127572089 | G | A | 2 | a0001c0002t0001g0077 a0001c0044t0003g0080 |
2 | HG02809.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.593-1831G>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 6/47 | chr2 | 127572089 | |||||||
chr2:127572277 | A | G | 1 | a0025c0041t0004g0076 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.593-1643A>G | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 6/47 | chr2 | 127572277 | |||||||
chr2:127572349 | G | A | 1 | a0002c0001t0001g0175 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.593-1571G>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 6/47 | chr2 | 127572349 | |||||||
chr2:127572367 | C | T | 4 | a0001c0045t0001g0142 a0011c0016t0001g0008 a0011c0016t0001g0141 others(1): Show |
5 | HG02630.hp1 HG02895.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.593-1553C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 6/47 | chr2 | 127572367 | |||||||
chr2:127572368 | G | A | 1 | a0007c0023t0001g0122 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.593-1552G>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 6/47 | chr2 | 127572368 | |||||||
chr2:127572416 | C | CA | 130 | a0001c0002t0001g0027 a0001c0002t0001g0032 a0001c0002t0001g0034 others(127): Show |
132 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(129): Show |
intron_variant | MODIFIER | c.593-1489dupA | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 6/47 | INFO_REALIGN_3_PRIME | chr2 | 127572416 | ||||||
chr2:127572416 | C | CAA | 10 | a0001c0004t0001g0242 a0001c0005t0002g0131 a0001c0010t0001g0139 others(7): Show |
10 | HG01243.hp1 HG01891.hp1 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.593-1490_593-1489d others(4): Show |
MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 6/47 | INFO_REALIGN_3_PRIME | chr2 | 127572416 | ||||||
chr2:127572416 | C | CAAA | 95 | a0001c0002t0001g0053 a0001c0002t0001g0155 a0001c0004t0001g0009 others(92): Show |
102 | HG00099.hp1 HG00099.hp2 HG00735.hp1 others(99): Show |
intron_variant | MODIFIER | c.593-1491_593-1489d others(5): Show |
MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 6/47 | INFO_REALIGN_3_PRIME | chr2 | 127572416 | ||||||
chr2:127572468 | C | CTTTTCTC others(14): Show |
5 | a0003c0003t0001g0127 a0003c0003t0001g0129 a0004c0007t0003g0010 others(2): Show |
5 | HG02132.hp1 HG02602.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.593-1335_593-1315d others(23): Show |
MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 6/47 | INFO_REALIGN_3_PRIME | chr2 | 127572468 | ||||||
chr2:127572468 | C | CTTTTCTC others(56): Show |
1 | a0041c0028t0001g0195 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.593-1377_593-1315d others(65): Show |
MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 6/47 | INFO_REALIGN_3_PRIME | chr2 | 127572468 | ||||||
chr2:127572468 | CTTTTCTC others(14): Show |
C | 10 | a0001c0002t0001g0048 a0001c0002t0001g0091 a0001c0002t0001g0092 others(7): Show |
10 | HG01243.hp2 HG01884.hp1 HG02109.hp1 others(7): Show |
intron_variant | MODIFIER | c.593-1335_593-1315d others(23): Show |
MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 6/47 | INFO_REALIGN_3_PRIME | chr2 | 127572468 | ||||||
chr2:127572468 | CTTTTCTC others(35): Show |
C | 6 | a0001c0005t0002g0131 a0001c0010t0001g0139 a0001c0010t0001g0228 others(3): Show |
6 | HG01891.hp1 HG02109.hp2 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.593-1356_593-1315d others(44): Show |
MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 6/47 | INFO_REALIGN_3_PRIME | chr2 | 127572468 | ||||||
chr2:127572722 | A | G | 2 | a0017c0072t0001g0012 a0046c0073t0001g0068 |
2 | HG02922.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.593-1198A>G | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 6/47 | chr2 | 127572722 | |||||||
chr2:127572750 | T | TTATC | 2 | a0001c0002t0001g0144 a0028c0064t0002g0143 |
2 | HG02257.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.593-1168_593-1165d others(6): Show |
MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 6/47 | INFO_REALIGN_3_PRIME | chr2 | 127572750 | ||||||
chr2:127572757 | C | A | 5 | a0003c0003t0001g0127 a0003c0003t0001g0129 a0004c0007t0003g0010 others(2): Show |
5 | HG02132.hp1 HG02602.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.593-1163C>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 6/47 | chr2 | 127572757 | |||||||
chr2:127572883 | A | C | 240 | a0001c0002t0001g0027 a0001c0002t0001g0032 a0001c0002t0001g0034 others(237): Show |
248 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(245): Show |
intron_variant | MODIFIER | c.593-1037A>C | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 6/47 | chr2 | 127572883 | |||||||
chr2:127572935 | C | CA | 81 | a0001c0002t0001g0060 a0001c0002t0001g0077 a0001c0002t0001g0144 others(78): Show |
81 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(78): Show |
intron_variant | MODIFIER | c.593-972dupA | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 6/47 | INFO_REALIGN_3_PRIME | chr2 | 127572935 | ||||||
chr2:127573300 | A | G | 1 | a0002c0011t0002g0270 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.593-620A>G | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 6/47 | chr2 | 127573300 | |||||||
chr2:127573530 | C | T | 1 | a0001c0002t0001g0144 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.593-390C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 6/47 | chr2 | 127573530 | |||||||
chr2:127573596 | C | T | 1 | a0017c0072t0001g0012 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.593-324C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 6/47 | chr2 | 127573596 | |||||||
chr2:127573752 | G | T | 1 | a0001c0002t0001g0053 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.593-168G>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 6/47 | chr2 | 127573752 | |||||||
chr2:127573903 | C | T | 1 | a0002c0006t0001g0014 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.593-17C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 6/47 | chr2 | 127573903 | |||||||
chr2:127573904 | G | A | 1 | a0001c0004t0001g0214 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.593-16G>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 6/47 | chr2 | 127573904 | |||||||
chr2:127574069 | C | G | 1 | a0001c0004t0001g0057 | 1 | HG02027.hp1 | splice_region_variant&intron_variant | LOW | c.735+7C>G | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 7/47 | chr2 | 127574069 | |||||||
chr2:127574070 | C | A | 30 | a0001c0002t0001g0060 a0001c0004t0001g0043 a0001c0005t0001g0049 others(27): Show |
30 | HG00323.hp2 HG00733.hp2 HG01070.hp1 others(27): Show |
splice_region_variant&intron_variant | LOW | c.735+8C>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 7/47 | chr2 | 127574070 | |||||||
chr2:127574205 | C | T | 1 | a0010c0036t0001g0157 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.735+143C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 7/47 | chr2 | 127574205 | |||||||
chr2:127574405 | T | C | 1 | a0001c0002t0001g0137 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.735+343T>C | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 7/47 | chr2 | 127574405 | |||||||
chr2:127574459 | G | A | 1 | a0004c0007t0003g0223 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.735+397G>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 7/47 | chr2 | 127574459 | |||||||
chr2:127574738 | T | C | 40 | a0001c0002t0001g0027 a0001c0002t0001g0032 a0001c0002t0001g0034 others(37): Show |
40 | HG00621.hp2 HG00642.hp1 HG01069.hp2 others(37): Show |
intron_variant | MODIFIER | c.735+676T>C | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 7/47 | chr2 | 127574738 | |||||||
chr2:127574869 | C | G | 1 | a0008c0063t0001g0257 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.735+807C>G | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 7/47 | chr2 | 127574869 | |||||||
chr2:127574988 | A | G | 2 | a0001c0005t0003g0063 a0007c0025t0001g0042 |
2 | HG03710.hp1 HG03831.hp2 |
intron_variant | MODIFIER | c.735+926A>G | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 7/47 | chr2 | 127574988 | |||||||
chr2:127574999 | C | T | 7 | a0001c0017t0004g0024 a0001c0017t0004g0025 a0001c0017t0004g0075 others(4): Show |
7 | HG01891.hp2 HG02257.hp2 HG02258.hp2 others(4): Show |
intron_variant | MODIFIER | c.735+937C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 7/47 | chr2 | 127574999 | |||||||
chr2:127575079 | G | A | 40 | a0001c0002t0001g0027 a0001c0002t0001g0032 a0001c0002t0001g0034 others(37): Show |
40 | HG00621.hp2 HG00642.hp1 HG01069.hp2 others(37): Show |
intron_variant | MODIFIER | c.735+1017G>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 7/47 | chr2 | 127575079 | |||||||
chr2:127575160 | A | G | 1 | a0008c0042t0001g0064 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.735+1098A>G | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 7/47 | chr2 | 127575160 | |||||||
chr2:127575240 | T | C | 2 | a0001c0002t0001g0077 a0001c0044t0003g0080 |
2 | HG02809.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.735+1178T>C | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 7/47 | chr2 | 127575240 | |||||||
chr2:127575335 | A | AGT | 3 | a0001c0010t0001g0228 a0015c0071t0001g0123 a0016c0027t0001g0226 |
3 | HG01891.hp1 HG03195.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.736-1258_736-1257d others(4): Show |
MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 7/47 | INFO_REALIGN_3_PRIME | chr2 | 127575335 | ||||||
chr2:127575398 | C | T | 1 | a0002c0011t0002g0207 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.736-1197C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 7/47 | chr2 | 127575398 | |||||||
chr2:127575489 | T | C | 4 | a0002c0006t0001g0018 a0002c0006t0001g0019 a0002c0006t0001g0156 others(1): Show |
4 | HG00099.hp1 HG01081.hp2 HG01515.hp2 others(1): Show |
intron_variant | MODIFIER | c.736-1106T>C | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 7/47 | chr2 | 127575489 | |||||||
chr2:127575549 | C | A | 1 | a0008c0063t0001g0257 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.736-1046C>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 7/47 | chr2 | 127575549 | |||||||
chr2:127575618 | A | G | 4 | a0001c0002t0001g0027 a0001c0002t0001g0034 a0001c0002t0001g0041 others(1): Show |
4 | HG01099.hp1 HG01943.hp1 HG02148.hp1 others(1): Show |
intron_variant | MODIFIER | c.736-977A>G | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 7/47 | chr2 | 127575618 | |||||||
chr2:127575635 | T | A | 1 | a0007c0023t0001g0149 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.736-960T>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 7/47 | chr2 | 127575635 | |||||||
chr2:127575663 | G | T | 1 | a0001c0004t0001g0057 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.736-932G>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 7/47 | chr2 | 127575663 | |||||||
chr2:127575948 | G | T | 2 | a0009c0014t0001g0148 a0009c0014t0001g0174 |
2 | HG02486.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.736-647G>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 7/47 | chr2 | 127575948 | |||||||
chr2:127576056 | G | A | 4 | a0002c0001t0001g0196 a0004c0007t0003g0010 a0004c0007t0003g0256 others(1): Show |
4 | HG02132.hp1 HG02148.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.736-539G>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 7/47 | chr2 | 127576056 | |||||||
chr2:127576107 | G | A | 33 | a0001c0004t0001g0246 a0001c0004t0001g0254 a0003c0003t0001g0109 others(30): Show |
33 | HG00280.hp1 HG00323.hp1 HG00621.hp1 others(30): Show |
intron_variant | MODIFIER | c.736-488G>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 7/47 | chr2 | 127576107 | |||||||
chr2:127576413 | G | A | 1 | a0001c0005t0002g0131 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.736-182G>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 7/47 | chr2 | 127576413 | |||||||
chr2:127576413 | G | T | 6 | a0004c0007t0001g0162 a0004c0007t0001g0164 a0004c0007t0001g0259 others(3): Show |
6 | HG00735.hp2 HG01106.hp2 HG01175.hp2 others(3): Show |
intron_variant | MODIFIER | c.736-182G>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 7/47 | chr2 | 127576413 | |||||||
chr2:127576727 | G | A | 1 | a0003c0003t0001g0244 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.849+19G>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 8/47 | chr2 | 127576727 | |||||||
chr2:127576770 | G | T | 1 | a0007c0023t0001g0122 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.849+62G>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 8/47 | chr2 | 127576770 | |||||||
chr2:127576780 | C | T | 5 | a0004c0007t0001g0164 a0004c0007t0001g0259 a0004c0007t0001g0261 others(2): Show |
5 | HG01106.hp2 HG01175.hp2 HG01255.hp1 others(2): Show |
intron_variant | MODIFIER | c.849+72C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 8/47 | chr2 | 127576780 | |||||||
chr2:127576817 | C | T | 1 | a0001c0068t0001g0093 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.849+109C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 8/47 | chr2 | 127576817 | |||||||
chr2:127576838 | C | T | 40 | a0001c0004t0001g0246 a0001c0005t0003g0063 a0003c0003t0001g0033 others(37): Show |
41 | HG00280.hp1 HG00323.hp1 HG00621.hp1 others(38): Show |
intron_variant | MODIFIER | c.849+130C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 8/47 | chr2 | 127576838 | |||||||
chr2:127576851 | C | T | 5 | a0002c0001t0001g0117 a0002c0001t0001g0192 a0002c0001t0001g0194 others(2): Show |
5 | HG01081.hp1 HG01358.hp1 HG02071.hp1 others(2): Show |
intron_variant | MODIFIER | c.849+143C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 8/47 | chr2 | 127576851 | |||||||
chr2:127576866 | G | C | 1 | a0039c0051t0001g0234 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.849+158G>C | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 8/47 | chr2 | 127576866 | |||||||
chr2:127576887 | G | A | 1 | a0001c0002t0001g0060 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.849+179G>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 8/47 | chr2 | 127576887 | |||||||
chr2:127576895 | C | T | 61 | a0001c0002t0001g0027 a0001c0002t0001g0032 a0001c0002t0001g0034 others(58): Show |
63 | HG00099.hp1 HG00642.hp1 HG00738.hp1 others(60): Show |
intron_variant | MODIFIER | c.849+187C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 8/47 | chr2 | 127576895 | |||||||
chr2:127576922 | C | T | 1 | a0002c0006t0007g0216 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.849+214C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 8/47 | chr2 | 127576922 | |||||||
chr2:127576951 | A | G | 72 | a0001c0002t0001g0144 a0001c0004t0001g0009 a0001c0004t0001g0011 others(69): Show |
77 | HG00099.hp2 HG00735.hp1 HG00738.hp2 others(74): Show |
intron_variant | MODIFIER | c.849+243A>G | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 8/47 | chr2 | 127576951 | |||||||
chr2:127576991 | G | C | 1 | a0001c0005t0002g0065 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.849+283G>C | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 8/47 | chr2 | 127576991 | |||||||
chr2:127577148 | C | A | 1 | a0003c0026t0001g0146 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.849+440C>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 8/47 | chr2 | 127577148 | |||||||
chr2:127577164 | G | A | 3 | a0001c0002t0001g0091 a0001c0002t0001g0092 a0001c0061t0001g0099 |
3 | HG02818.hp1 HG02896.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.849+456G>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 8/47 | chr2 | 127577164 | |||||||
chr2:127577271 | C | T | 1 | a0001c0005t0002g0065 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.849+563C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 8/47 | chr2 | 127577271 | |||||||
chr2:127577302 | C | T | 2 | a0017c0072t0001g0012 a0046c0073t0001g0068 |
2 | HG02922.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.849+594C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 8/47 | chr2 | 127577302 | |||||||
chr2:127577338 | G | A | 1 | a0001c0002t0001g0137 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.849+630G>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 8/47 | chr2 | 127577338 | |||||||
chr2:127577388 | C | T | 3 | a0007c0023t0001g0149 a0007c0024t0001g0227 a0017c0053t0001g0271 |
3 | HG02109.hp1 HG02572.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.849+680C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 8/47 | chr2 | 127577388 | |||||||
chr2:127577554 | C | T | 1 | a0002c0001t0001g0183 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.850-579C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 8/47 | chr2 | 127577554 | |||||||
chr2:127577633 | C | T | 1 | a0007c0023t0001g0122 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.850-500C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 8/47 | chr2 | 127577633 | |||||||
chr2:127577696 | C | T | 3 | a0003c0003t0001g0118 a0003c0003t0001g0210 a0035c0067t0001g0119 |
3 | HG01109.hp1 HG01433.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.850-437C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 8/47 | chr2 | 127577696 | |||||||
chr2:127577697 | G | A | 9 | a0001c0010t0001g0138 a0001c0010t0001g0139 a0001c0010t0001g0264 others(6): Show |
9 | HG02109.hp2 HG02451.hp1 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.850-436G>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 8/47 | chr2 | 127577697 | |||||||
chr2:127577806 | T | C | 83 | a0001c0002t0001g0060 a0001c0004t0001g0043 a0001c0004t0001g0246 others(80): Show |
84 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(81): Show |
intron_variant | MODIFIER | c.850-327T>C | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 8/47 | chr2 | 127577806 | |||||||
chr2:127577875 | C | T | 1 | a0001c0005t0002g0054 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.850-258C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 8/47 | chr2 | 127577875 | |||||||
chr2:127577896 | GAGA | G | 5 | a0001c0002t0001g0144 a0001c0005t0002g0065 a0007c0023t0001g0149 others(2): Show |
5 | HG02109.hp1 HG02257.hp1 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.850-231_850-229del others(3): Show |
MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 8/47 | INFO_REALIGN_3_PRIME | chr2 | 127577896 | ||||||
chr2:127578304 | C | G | 1 | a0001c0005t0002g0065 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1003+18C>G | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 9/47 | chr2 | 127578304 | |||||||
chr2:127578444 | TC | T | 9 | a0001c0010t0001g0138 a0001c0010t0001g0139 a0001c0010t0001g0264 others(6): Show |
9 | HG02109.hp2 HG02451.hp1 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.1003+159delC | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 9/47 | chr2 | 127578444 | |||||||
chr2:127578483 | C | A | 1 | a0007c0023t0001g0122 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1003+197C>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 9/47 | chr2 | 127578483 | |||||||
chr2:127578509 | C | T | 1 | a0006c0009t0001g0056 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.1003+223C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 9/47 | chr2 | 127578509 | |||||||
chr2:127578569 | A | T | 1 | a0037c0043t0001g0030 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.1003+283A>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 9/47 | chr2 | 127578569 | |||||||
chr2:127578614 | T | C | 259 | a0001c0002t0001g0027 a0001c0002t0001g0032 a0001c0002t0001g0034 others(256): Show |
268 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(265): Show |
intron_variant | MODIFIER | c.1003+328T>C | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 9/47 | chr2 | 127578614 | |||||||
chr2:127578652 | C | G | 9 | a0001c0002t0001g0048 a0001c0002t0001g0091 a0001c0002t0001g0092 others(6): Show |
9 | HG00642.hp1 HG02647.hp2 HG02717.hp2 others(6): Show |
intron_variant | MODIFIER | c.1003+366C>G | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 9/47 | chr2 | 127578652 | |||||||
chr2:127578653 | C | A | 1 | a0037c0043t0001g0030 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.1003+367C>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 9/47 | chr2 | 127578653 | |||||||
chr2:127578692 | A | G | 250 | a0001c0002t0001g0027 a0001c0002t0001g0032 a0001c0002t0001g0034 others(247): Show |
258 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(255): Show |
intron_variant | MODIFIER | c.1003+406A>G | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 9/47 | chr2 | 127578692 | |||||||
chr2:127578766 | G | C | 1 | a0007c0023t0001g0122 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1003+480G>C | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 9/47 | chr2 | 127578766 | |||||||
chr2:127578975 | C | T | 1 | a0001c0002t0001g0137 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1003+689C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 9/47 | chr2 | 127578975 | |||||||
chr2:127578976 | A | G | 254 | a0001c0002t0001g0027 a0001c0002t0001g0032 a0001c0002t0001g0034 others(251): Show |
263 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(260): Show |
intron_variant | MODIFIER | c.1003+690A>G | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 9/47 | chr2 | 127578976 | |||||||
chr2:127579013 | A | T | 9 | a0001c0010t0001g0138 a0001c0010t0001g0139 a0001c0010t0001g0264 others(6): Show |
9 | HG02109.hp2 HG02451.hp1 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.1003+727A>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 9/47 | chr2 | 127579013 | |||||||
chr2:127579022 | A | C | 4 | a0001c0017t0004g0024 a0001c0017t0004g0025 a0001c0017t0004g0075 others(1): Show |
4 | HG02258.hp2 HG02630.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.1003+736A>C | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 9/47 | chr2 | 127579022 | |||||||
chr2:127579113 | T | G | 83 | a0001c0002t0001g0060 a0001c0004t0001g0043 a0001c0004t0001g0246 others(80): Show |
84 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(81): Show |
intron_variant | MODIFIER | c.1003+827T>G | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 9/47 | chr2 | 127579113 | |||||||
chr2:127579231 | G | C | 183 | a0001c0002t0001g0027 a0001c0002t0001g0032 a0001c0002t0001g0034 others(180): Show |
186 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(183): Show |
intron_variant | MODIFIER | c.1003+945G>C | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 9/47 | chr2 | 127579231 | |||||||
chr2:127579346 | T | C | 1 | a0001c0044t0003g0080 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1003+1060T>C | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 9/47 | chr2 | 127579346 | |||||||
chr2:127579381 | C | T | 7 | a0001c0002t0001g0155 a0002c0011t0002g0270 a0008c0015t0001g0047 others(4): Show |
7 | HG01243.hp2 HG01884.hp2 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.1003+1095C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 9/47 | chr2 | 127579381 | |||||||
chr2:127579382 | A | G | 254 | a0001c0002t0001g0027 a0001c0002t0001g0032 a0001c0002t0001g0034 others(251): Show |
263 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(260): Show |
intron_variant | MODIFIER | c.1003+1096A>G | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 9/47 | chr2 | 127579382 | |||||||
chr2:127579491 | C | T | 1 | a0001c0005t0002g0065 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1003+1205C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 9/47 | chr2 | 127579491 | |||||||
chr2:127579574 | A | ATTTG | 159 | a0001c0002t0001g0027 a0001c0002t0001g0032 a0001c0002t0001g0034 others(156): Show |
162 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(159): Show |
intron_variant | MODIFIER | c.1004-1148_1004-114 others(8): Show |
MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 9/47 | INFO_REALIGN_3_PRIME | chr2 | 127579574 | ||||||
chr2:127579574 | A | ATTTGTTT others(1): Show |
3 | a0001c0002t0001g0137 a0015c0066t0001g0067 a0021c0046t0003g0078 |
3 | HG01884.hp1 HG01891.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.1004-1152_1004-114 others(12): Show |
MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 9/47 | INFO_REALIGN_3_PRIME | chr2 | 127579574 | ||||||
chr2:127579574 | A | ATTTGTTT others(5): Show |
1 | a0001c0005t0002g0131 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1004-1156_1004-114 others(16): Show |
MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 9/47 | INFO_REALIGN_3_PRIME | chr2 | 127579574 | ||||||
chr2:127579574 | ATTTG | A | 10 | a0001c0002t0001g0144 a0001c0005t0002g0065 a0001c0045t0001g0142 others(7): Show |
11 | HG02109.hp1 HG02257.hp1 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.1004-1148_1004-114 others(8): Show |
MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 9/47 | INFO_REALIGN_3_PRIME | chr2 | 127579574 | ||||||
chr2:127579700 | C | G | 1 | a0001c0002t0001g0053 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.1004-1046C>G | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 9/47 | chr2 | 127579700 | |||||||
chr2:127579841 | C | T | 1 | a0002c0006t0001g0013 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1004-905C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 9/47 | chr2 | 127579841 | |||||||
chr2:127579931 | G | A | 1 | a0001c0058t0002g0103 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.1004-815G>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 9/47 | chr2 | 127579931 | |||||||
chr2:127579937 | A | G | 152 | a0001c0002t0001g0027 a0001c0002t0001g0032 a0001c0002t0001g0034 others(149): Show |
155 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(152): Show |
intron_variant | MODIFIER | c.1004-809A>G | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 9/47 | chr2 | 127579937 | |||||||
chr2:127579970 | C | T | 16 | a0001c0002t0001g0137 a0001c0002t0001g0144 a0001c0002t0001g0155 others(13): Show |
16 | HG01243.hp2 HG01884.hp2 HG02109.hp1 others(13): Show |
intron_variant | MODIFIER | c.1004-776C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 9/47 | chr2 | 127579970 | |||||||
chr2:127580046 | A | C | 1 | a0007c0023t0001g0122 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1004-700A>C | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 9/47 | chr2 | 127580046 | |||||||
chr2:127580122 | C | G | 1 | a0015c0066t0001g0067 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1004-624C>G | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 9/47 | chr2 | 127580122 | |||||||
chr2:127580170 | A | C | 1 | a0009c0014t0001g0136 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1004-576A>C | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 9/47 | chr2 | 127580170 | |||||||
chr2:127580204 | G | A | 2 | a0002c0001t0001g0117 a0002c0011t0002g0207 |
2 | HG02071.hp1 NA19063.hp2 |
intron_variant | MODIFIER | c.1004-542G>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 9/47 | chr2 | 127580204 | |||||||
chr2:127580206 | C | A | 9 | a0001c0010t0001g0138 a0001c0010t0001g0139 a0001c0010t0001g0264 others(6): Show |
9 | HG02109.hp2 HG02451.hp1 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.1004-540C>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 9/47 | chr2 | 127580206 | |||||||
chr2:127580583 | G | A | 2 | a0001c0002t0001g0089 a0023c0037t0001g0212 |
2 | HG02145.hp2 HG02165.hp1 |
intron_variant | MODIFIER | c.1004-163G>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 9/47 | chr2 | 127580583 | |||||||
chr2:127580627 | C | T | 2 | a0003c0003t0001g0127 a0003c0003t0001g0129 |
2 | HG02602.hp2 HG04184.hp1 |
intron_variant | MODIFIER | c.1004-119C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 9/47 | chr2 | 127580627 | |||||||
chr2:127580628 | G | A | 11 | a0001c0010t0001g0138 a0001c0010t0001g0139 a0001c0010t0001g0264 others(8): Show |
11 | HG02109.hp2 HG02257.hp2 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.1004-118G>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 9/47 | chr2 | 127580628 | |||||||
chr2:127580923 | C | T | 3 | a0001c0002t0001g0144 a0028c0064t0002g0143 a0029c0048t0001g0132 |
3 | HG02257.hp1 HG03209.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.1080+101C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 10/47 | chr2 | 127580923 | |||||||
chr2:127580924 | C | CA | 9 | a0001c0002t0001g0048 a0001c0002t0001g0091 a0001c0002t0001g0092 others(6): Show |
9 | HG00642.hp1 HG02647.hp2 HG02717.hp2 others(6): Show |
intron_variant | MODIFIER | c.1080+103dupA | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 10/47 | INFO_REALIGN_3_PRIME | chr2 | 127580924 | ||||||
chr2:127580944 | T | G | 71 | a0001c0004t0001g0009 a0001c0004t0001g0011 a0001c0004t0001g0057 others(68): Show |
77 | HG00099.hp2 HG00621.hp1 HG00735.hp1 others(74): Show |
intron_variant | MODIFIER | c.1080+122T>G | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 10/47 | chr2 | 127580944 | |||||||
chr2:127580959 | C | G | 3 | a0005c0008t0001g0003 a0005c0008t0001g0153 a0005c0008t0001g0154 |
4 | HG02717.hp1 HG02896.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.1080+137C>G | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 10/47 | chr2 | 127580959 | |||||||
chr2:127581138 | C | T | 7 | a0001c0002t0001g0155 a0002c0011t0002g0270 a0008c0015t0001g0047 others(4): Show |
7 | HG01243.hp2 HG01884.hp2 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.1080+316C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 10/47 | chr2 | 127581138 | |||||||
chr2:127581139 | A | G | 101 | a0001c0002t0001g0137 a0001c0002t0001g0144 a0001c0002t0001g0155 others(98): Show |
107 | HG00099.hp2 HG00621.hp1 HG00735.hp1 others(104): Show |
intron_variant | MODIFIER | c.1080+317A>G | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 10/47 | chr2 | 127581139 | |||||||
chr2:127581166 | T | C | 74 | a0001c0004t0001g0009 a0001c0004t0001g0011 a0001c0004t0001g0057 others(71): Show |
80 | HG00099.hp2 HG00621.hp1 HG00735.hp1 others(77): Show |
intron_variant | MODIFIER | c.1080+344T>C | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 10/47 | chr2 | 127581166 | |||||||
chr2:127581203 | C | T | 1 | a0024c0070t0001g0028 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1080+381C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 10/47 | chr2 | 127581203 | |||||||
chr2:127581222 | G | T | 3 | a0005c0008t0001g0003 a0005c0008t0001g0153 a0005c0008t0001g0154 |
4 | HG02717.hp1 HG02896.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.1080+400G>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 10/47 | chr2 | 127581222 | |||||||
chr2:127581307 | A | C | 1 | a0001c0002t0001g0134 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1080+485A>C | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 10/47 | chr2 | 127581307 | |||||||
chr2:127581486 | G | A | 3 | a0007c0023t0001g0149 a0007c0024t0001g0227 a0017c0053t0001g0271 |
3 | HG02109.hp1 HG02572.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.1081-405G>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 10/47 | chr2 | 127581486 | |||||||
chr2:127581590 | G | T | 1 | a0002c0006t0001g0156 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.1081-301G>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 10/47 | chr2 | 127581590 | |||||||
chr2:127581636 | A | G | 267 | a0001c0002t0001g0027 a0001c0002t0001g0032 a0001c0002t0001g0034 others(264): Show |
276 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(273): Show |
intron_variant | MODIFIER | c.1081-255A>G | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 10/47 | chr2 | 127581636 | |||||||
chr2:127581651 | G | C | 74 | a0001c0004t0001g0009 a0001c0004t0001g0011 a0001c0004t0001g0057 others(71): Show |
80 | HG00099.hp2 HG00621.hp1 HG00735.hp1 others(77): Show |
intron_variant | MODIFIER | c.1081-240G>C | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 10/47 | chr2 | 127581651 | |||||||
chr2:127581710 | G | A | 7 | a0001c0002t0001g0155 a0002c0011t0002g0270 a0008c0015t0001g0047 others(4): Show |
7 | HG01243.hp2 HG01884.hp2 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.1081-181G>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 10/47 | chr2 | 127581710 | |||||||
chr2:127581800 | C | T | 4 | a0001c0044t0003g0080 a0001c0045t0001g0142 a0011c0016t0001g0008 others(1): Show |
5 | HG02630.hp1 HG02809.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.1081-91C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 10/47 | chr2 | 127581800 | |||||||
chr2:127581864 | C | T | 4 | a0001c0002t0001g0144 a0001c0005t0002g0131 a0028c0064t0002g0143 others(1): Show |
4 | HG02257.hp1 HG02280.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.1081-27C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 10/47 | chr2 | 127581864 | |||||||
chr2:127581881 | G | T | 66 | a0001c0004t0001g0009 a0001c0004t0001g0011 a0001c0004t0001g0057 others(63): Show |
71 | HG00099.hp2 HG00621.hp1 HG00735.hp1 others(68): Show |
intron_variant | MODIFIER | c.1081-10G>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 10/47 | chr2 | 127581881 | |||||||
chr2:127582183 | C | G | 153 | a0001c0002t0001g0027 a0001c0002t0001g0032 a0001c0002t0001g0034 others(150): Show |
156 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(153): Show |
intron_variant | MODIFIER | c.1201-121C>G | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 11/47 | chr2 | 127582183 | |||||||
chr2:127582211 | G | A | 1 | a0001c0005t0002g0054 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.1201-93G>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 11/47 | chr2 | 127582211 | |||||||
chr2:127582256 | C | T | 2 | a0001c0004t0001g0009 a0001c0004t0001g0011 |
2 | NA18980.hp2 NA19010.hp1 |
intron_variant | MODIFIER | c.1201-48C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 11/47 | chr2 | 127582256 | |||||||
chr2:127582468 | G | A | 10 | a0001c0005t0002g0062 a0001c0005t0002g0094 a0001c0005t0002g0096 others(7): Show |
10 | HG01070.hp1 HG01516.hp1 HG02165.hp2 others(7): Show |
intron_variant | MODIFIER | c.1343+22G>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 12/47 | chr2 | 127582468 | |||||||
chr2:127582535 | G | A | 1 | a0042c0030t0001g0202 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.1343+89G>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 12/47 | chr2 | 127582535 | |||||||
chr2:127582551 | G | A | 1 | a0009c0014t0001g0136 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1343+105G>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 12/47 | chr2 | 127582551 | |||||||
chr2:127582678 | T | C | 254 | a0001c0002t0001g0027 a0001c0002t0001g0032 a0001c0002t0001g0034 others(251): Show |
263 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(260): Show |
intron_variant | MODIFIER | c.1343+232T>C | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 12/47 | chr2 | 127582678 | |||||||
chr2:127582702 | T | C | 1 | a0003c0003t0001g0236 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1343+256T>C | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 12/47 | chr2 | 127582702 | |||||||
chr2:127582741 | CAG | C | 153 | a0001c0002t0001g0027 a0001c0002t0001g0032 a0001c0002t0001g0034 others(150): Show |
156 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(153): Show |
intron_variant | MODIFIER | c.1343+297_1343+298d others(4): Show |
MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 12/47 | INFO_REALIGN_3_PRIME | chr2 | 127582741 | ||||||
chr2:127582975 | G | T | 153 | a0001c0002t0001g0027 a0001c0002t0001g0032 a0001c0002t0001g0034 others(150): Show |
156 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(153): Show |
intron_variant | MODIFIER | c.1343+529G>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 12/47 | chr2 | 127582975 | |||||||
chr2:127582996 | G | T | 1 | a0002c0001t0001g0181 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.1343+550G>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 12/47 | chr2 | 127582996 | |||||||
chr2:127583033 | T | G | 3 | a0007c0023t0001g0149 a0007c0024t0001g0227 a0017c0053t0001g0271 |
3 | HG02109.hp1 HG02572.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.1343+587T>G | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 12/47 | chr2 | 127583033 | |||||||
chr2:127583076 | G | A | 1 | a0016c0027t0001g0082 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.1343+630G>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 12/47 | chr2 | 127583076 | |||||||
chr2:127583146 | T | A | 6 | a0002c0001t0001g0002 a0002c0001t0001g0181 a0002c0001t0001g0182 others(3): Show |
8 | HG01168.hp2 HG01257.hp1 HG01361.hp2 others(5): Show |
intron_variant | MODIFIER | c.1343+700T>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 12/47 | chr2 | 127583146 | |||||||
chr2:127583157 | G | C | 2 | a0007c0024t0001g0227 a0017c0053t0001g0271 |
2 | HG02572.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.1343+711G>C | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 12/47 | chr2 | 127583157 | |||||||
chr2:127583191 | C | T | 1 | a0007c0023t0001g0122 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1343+745C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 12/47 | chr2 | 127583191 | |||||||
chr2:127583224 | C | T | 1 | a0002c0006t0001g0013 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1343+778C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 12/47 | chr2 | 127583224 | |||||||
chr2:127583280 | G | A | 58 | a0001c0002t0001g0045 a0001c0002t0001g0048 a0001c0002t0001g0060 others(55): Show |
60 | HG00099.hp1 HG00323.hp2 HG00642.hp1 others(57): Show |
intron_variant | MODIFIER | c.1343+834G>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 12/47 | chr2 | 127583280 | |||||||
chr2:127583286 | C | A | 1 | a0007c0023t0001g0122 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1344-836C>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 12/47 | chr2 | 127583286 | |||||||
chr2:127583326 | C | T | 71 | a0001c0004t0001g0009 a0001c0004t0001g0011 a0001c0004t0001g0057 others(68): Show |
77 | HG00099.hp2 HG00621.hp1 HG00735.hp1 others(74): Show |
intron_variant | MODIFIER | c.1344-796C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 12/47 | chr2 | 127583326 | |||||||
chr2:127583327 | G | A | 1 | a0002c0006t0001g0014 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.1344-795G>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 12/47 | chr2 | 127583327 | |||||||
chr2:127583347 | G | A | 2 | a0017c0072t0001g0012 a0046c0073t0001g0068 |
2 | HG02922.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1344-775G>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 12/47 | chr2 | 127583347 | |||||||
chr2:127583415 | G | A | 1 | a0004c0007t0003g0256 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.1344-707G>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 12/47 | chr2 | 127583415 | |||||||
chr2:127583436 | G | A | 1 | a0004c0054t0001g0165 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.1344-686G>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 12/47 | chr2 | 127583436 | |||||||
chr2:127583567 | C | G | 66 | a0001c0004t0001g0009 a0001c0004t0001g0011 a0001c0004t0001g0057 others(63): Show |
71 | HG00099.hp2 HG00621.hp1 HG00735.hp1 others(68): Show |
intron_variant | MODIFIER | c.1344-555C>G | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 12/47 | chr2 | 127583567 | |||||||
chr2:127583910 | G | T | 16 | a0001c0002t0001g0027 a0001c0002t0001g0032 a0001c0002t0001g0034 others(13): Show |
16 | HG01099.hp1 HG01943.hp1 HG01952.hp2 others(13): Show |
intron_variant | MODIFIER | c.1344-212G>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 12/47 | chr2 | 127583910 | |||||||
chr2:127583956 | AGT | A | 71 | a0001c0004t0001g0009 a0001c0004t0001g0011 a0001c0004t0001g0057 others(68): Show |
77 | HG00099.hp2 HG00621.hp1 HG00735.hp1 others(74): Show |
intron_variant | MODIFIER | c.1344-162_1344-161d others(4): Show |
MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 12/47 | INFO_REALIGN_3_PRIME | chr2 | 127583956 | ||||||
chr2:127584028 | T | G | 71 | a0001c0004t0001g0009 a0001c0004t0001g0011 a0001c0004t0001g0057 others(68): Show |
77 | HG00099.hp2 HG00621.hp1 HG00735.hp1 others(74): Show |
intron_variant | MODIFIER | c.1344-94T>G | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 12/47 | chr2 | 127584028 | |||||||
chr2:127584446 | T | C | 1 | a0001c0002t0001g0137 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1554+114T>C | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 13/47 | chr2 | 127584446 | |||||||
chr2:127584650 | T | C | 7 | a0001c0002t0001g0155 a0002c0011t0002g0270 a0008c0015t0001g0047 others(4): Show |
7 | HG01243.hp2 HG01884.hp2 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.1555-128T>C | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 13/47 | chr2 | 127584650 | |||||||
chr2:127584972 | G | A | 254 | a0001c0002t0001g0027 a0001c0002t0001g0032 a0001c0002t0001g0034 others(251): Show |
263 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(260): Show |
intron_variant | MODIFIER | c.1690+59G>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 14/47 | chr2 | 127584972 | |||||||
chr2:127585100 | A | G | 75 | a0001c0002t0001g0027 a0001c0002t0001g0032 a0001c0002t0001g0034 others(72): Show |
77 | HG00099.hp1 HG00323.hp2 HG00642.hp1 others(74): Show |
intron_variant | MODIFIER | c.1690+187A>G | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 14/47 | chr2 | 127585100 | |||||||
chr2:127585160 | T | C | 66 | a0001c0004t0001g0009 a0001c0004t0001g0011 a0001c0004t0001g0057 others(63): Show |
71 | HG00099.hp2 HG00621.hp1 HG00735.hp1 others(68): Show |
intron_variant | MODIFIER | c.1690+247T>C | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 14/47 | chr2 | 127585160 | |||||||
chr2:127585232 | C | T | 30 | a0001c0004t0001g0043 a0001c0005t0001g0049 a0001c0005t0001g0098 others(27): Show |
30 | HG01070.hp1 HG01256.hp1 HG01258.hp2 others(27): Show |
intron_variant | MODIFIER | c.1690+319C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 14/47 | chr2 | 127585232 | |||||||
chr2:127585290 | C | G | 1 | a0027c0057t0001g0079 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1690+377C>G | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 14/47 | chr2 | 127585290 | |||||||
chr2:127585343 | T | C | 1 | a0002c0001t0001g0215 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.1690+430T>C | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 14/47 | chr2 | 127585343 | |||||||
chr2:127585452 | T | C | 3 | a0001c0010t0001g0163 a0012c0022t0001g0120 a0012c0022t0001g0217 |
3 | HG01069.hp1 HG01071.hp1 HG01346.hp1 |
intron_variant | MODIFIER | c.1690+539T>C | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 14/47 | chr2 | 127585452 | |||||||
chr2:127585732 | C | T | 1 | a0001c0002t0001g0137 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1690+819C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 14/47 | chr2 | 127585732 | |||||||
chr2:127585790 | C | T | 1 | a0006c0009t0001g0051 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.1690+877C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 14/47 | chr2 | 127585790 | |||||||
chr2:127585969 | A | G | 1 | a0002c0011t0002g0187 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.1690+1056A>G | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 14/47 | chr2 | 127585969 | |||||||
chr2:127585990 | A | C | 2 | a0002c0001t0001g0204 a0002c0001t0001g0205 |
2 | NA18947.hp1 NA18950.hp1 |
intron_variant | MODIFIER | c.1690+1077A>C | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 14/47 | chr2 | 127585990 | |||||||
chr2:127585991 | A | T | 16 | a0001c0002t0001g0027 a0001c0002t0001g0032 a0001c0002t0001g0034 others(13): Show |
16 | HG01099.hp1 HG01943.hp1 HG01952.hp2 others(13): Show |
intron_variant | MODIFIER | c.1690+1078A>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 14/47 | chr2 | 127585991 | |||||||
chr2:127586194 | G | A | 10 | a0001c0002t0001g0106 a0001c0013t0001g0005 a0001c0013t0001g0166 others(7): Show |
11 | HG00735.hp2 HG01106.hp2 HG01175.hp2 others(8): Show |
intron_variant | MODIFIER | c.1690+1281G>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 14/47 | chr2 | 127586194 | |||||||
chr2:127586234 | T | C | 1 | a0007c0024t0001g0086 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1690+1321T>C | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 14/47 | chr2 | 127586234 | |||||||
chr2:127586487 | T | A | 7 | a0001c0002t0001g0155 a0002c0011t0002g0270 a0008c0015t0001g0047 others(4): Show |
7 | HG01243.hp2 HG01884.hp2 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.1690+1574T>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 14/47 | chr2 | 127586487 | |||||||
chr2:127586784 | C | T | 1 | a0007c0023t0001g0122 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1691-1608C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 14/47 | chr2 | 127586784 | |||||||
chr2:127586785 | T | C | 1 | a0007c0023t0001g0122 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1691-1607T>C | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 14/47 | chr2 | 127586785 | |||||||
chr2:127586814 | G | T | 10 | a0001c0010t0001g0138 a0001c0010t0001g0139 a0001c0010t0001g0264 others(7): Show |
10 | HG02109.hp2 HG02257.hp2 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.1691-1578G>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 14/47 | chr2 | 127586814 | |||||||
chr2:127586854 | C | A | 1 | a0007c0025t0001g0042 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1691-1538C>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 14/47 | chr2 | 127586854 | |||||||
chr2:127586907 | T | C | 66 | a0001c0004t0001g0009 a0001c0004t0001g0011 a0001c0004t0001g0057 others(63): Show |
71 | HG00099.hp2 HG00621.hp1 HG00735.hp1 others(68): Show |
intron_variant | MODIFIER | c.1691-1485T>C | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 14/47 | chr2 | 127586907 | |||||||
chr2:127587265 | G | A | 3 | a0001c0002t0001g0060 a0006c0009t0001g0058 a0006c0009t0001g0059 |
3 | HG01106.hp1 HG03239.hp1 HG03927.hp2 |
intron_variant | MODIFIER | c.1691-1127G>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 14/47 | chr2 | 127587265 | |||||||
chr2:127587293 | G | A | 2 | a0001c0002t0001g0155 a0002c0011t0002g0270 |
2 | HG01884.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.1691-1099G>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 14/47 | chr2 | 127587293 | |||||||
chr2:127587523 | T | C | 254 | a0001c0002t0001g0027 a0001c0002t0001g0032 a0001c0002t0001g0034 others(251): Show |
263 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(260): Show |
intron_variant | MODIFIER | c.1691-869T>C | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 14/47 | chr2 | 127587523 | |||||||
chr2:127587545 | C | A | 1 | a0007c0025t0001g0042 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1691-847C>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 14/47 | chr2 | 127587545 | |||||||
chr2:127587568 | C | CT | 26 | a0001c0002t0001g0039 a0001c0002t0001g0041 a0001c0002t0001g0060 others(23): Show |
27 | HG01175.hp2 HG01884.hp2 HG01981.hp2 others(24): Show |
intron_variant | MODIFIER | c.1691-806dupT | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 14/47 | INFO_REALIGN_3_PRIME | chr2 | 127587568 | ||||||
chr2:127587568 | CT | C | 68 | a0001c0004t0001g0009 a0001c0004t0001g0011 a0001c0004t0001g0057 others(65): Show |
73 | HG00099.hp2 HG00621.hp1 HG00735.hp1 others(70): Show |
intron_variant | MODIFIER | c.1691-806delT | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 14/47 | INFO_REALIGN_3_PRIME | chr2 | 127587568 | ||||||
chr2:127587572 | T | C | 1 | a0001c0013t0001g0090 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1691-820T>C | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 14/47 | chr2 | 127587572 | |||||||
chr2:127587625 | A | G | 2 | a0002c0012t0001g0115 a0002c0012t0001g0191 |
2 | NA19000.hp2 NA19079.hp1 |
intron_variant | MODIFIER | c.1691-767A>G | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 14/47 | chr2 | 127587625 | |||||||
chr2:127587694 | G | A | 4 | a0001c0044t0003g0080 a0001c0045t0001g0142 a0011c0016t0001g0008 others(1): Show |
5 | HG02630.hp1 HG02809.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.1691-698G>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 14/47 | chr2 | 127587694 | |||||||
chr2:127587881 | T | C | 3 | a0001c0010t0001g0138 a0001c0010t0001g0139 a0009c0014t0001g0104 |
3 | HG02109.hp2 HG02572.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.1691-511T>C | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 14/47 | chr2 | 127587881 | |||||||
chr2:127587939 | A | T | 2 | a0002c0006t0001g0018 a0002c0006t0001g0019 |
2 | HG00099.hp1 HG01516.hp2 |
intron_variant | MODIFIER | c.1691-453A>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 14/47 | chr2 | 127587939 | |||||||
chr2:127588146 | A | G | 2 | a0002c0001t0001g0177 a0043c0056t0001g0258 |
2 | NA18995.hp1 NA18995.hp2 |
intron_variant | MODIFIER | c.1691-246A>G | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 14/47 | chr2 | 127588146 | |||||||
chr2:127588191 | T | C | 1 | a0007c0023t0001g0122 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1691-201T>C | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 14/47 | chr2 | 127588191 | |||||||
chr2:127588385 | T | C | 83 | a0001c0002t0001g0137 a0001c0002t0001g0144 a0001c0002t0001g0155 others(80): Show |
89 | HG00099.hp2 HG00621.hp1 HG00735.hp1 others(86): Show |
splice_region_variant&intron_variant | LOW | c.1691-7T>C | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 14/47 | chr2 | 127588385 | |||||||
chr2:127588588 | C | A | 1 | a0001c0004t0001g0246 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.1854+33C>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 15/47 | chr2 | 127588588 | |||||||
chr2:127588653 | A | C | 254 | a0001c0002t0001g0027 a0001c0002t0001g0032 a0001c0002t0001g0034 others(251): Show |
263 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(260): Show |
intron_variant | MODIFIER | c.1854+98A>C | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 15/47 | chr2 | 127588653 | |||||||
chr2:127588791 | G | T | 3 | a0009c0014t0001g0148 a0009c0014t0001g0174 a0045c0065t0001g0140 |
3 | HG02486.hp2 HG02818.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.1854+236G>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 15/47 | chr2 | 127588791 | |||||||
chr2:127588877 | T | C | 1 | a0024c0070t0001g0028 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1854+322T>C | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 15/47 | chr2 | 127588877 | |||||||
chr2:127588889 | ATGGATGG others(9): Show |
A | 4 | a0001c0002t0001g0144 a0001c0005t0002g0131 a0028c0064t0002g0143 others(1): Show |
4 | HG02257.hp1 HG02280.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.1854+346_1854+361d others(18): Show |
MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 15/47 | INFO_REALIGN_3_PRIME | chr2 | 127588889 | ||||||
chr2:127589031 | A | G | 3 | a0002c0012t0001g0171 a0002c0012t0001g0173 a0014c0040t0001g0190 |
3 | NA18941.hp1 NA18959.hp1 NA19056.hp1 |
intron_variant | MODIFIER | c.1854+476A>G | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 15/47 | chr2 | 127589031 | |||||||
chr2:127589086 | G | C | 7 | a0001c0002t0001g0091 a0001c0002t0001g0092 a0001c0002t0001g0100 others(4): Show |
7 | HG00642.hp1 HG02717.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.1854+531G>C | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 15/47 | chr2 | 127589086 | |||||||
chr2:127589139 | G | A | 3 | a0007c0023t0001g0149 a0007c0024t0001g0227 a0017c0053t0001g0271 |
3 | HG02109.hp1 HG02572.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.1854+584G>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 15/47 | chr2 | 127589139 | |||||||
chr2:127589267 | A | ATGGATGG others(5): Show |
1 | a0001c0002t0001g0137 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1854+728_1854+739d others(14): Show |
MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 15/47 | INFO_REALIGN_3_PRIME | chr2 | 127589267 | ||||||
chr2:127589429 | A | G | 1 | a0044c0034t0001g0070 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1855-663A>G | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 15/47 | chr2 | 127589429 | |||||||
chr2:127589462 | G | A | 4 | a0002c0006t0001g0018 a0002c0006t0001g0019 a0002c0006t0001g0156 others(1): Show |
4 | HG00099.hp1 HG01081.hp2 HG01515.hp2 others(1): Show |
intron_variant | MODIFIER | c.1855-630G>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 15/47 | chr2 | 127589462 | |||||||
chr2:127589788 | G | A | 1 | a0001c0002t0001g0101 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1855-304G>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 15/47 | chr2 | 127589788 | |||||||
chr2:127589796 | G | A | 3 | a0001c0010t0001g0163 a0012c0022t0001g0120 a0012c0022t0001g0217 |
3 | HG01069.hp1 HG01071.hp1 HG01346.hp1 |
intron_variant | MODIFIER | c.1855-296G>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 15/47 | chr2 | 127589796 | |||||||
chr2:127589851 | G | A | 24 | a0001c0004t0001g0043 a0001c0005t0001g0049 a0001c0005t0001g0098 others(21): Show |
24 | HG01070.hp1 HG01256.hp1 HG01258.hp2 others(21): Show |
intron_variant | MODIFIER | c.1855-241G>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 15/47 | chr2 | 127589851 | |||||||
chr2:127589876 | G | A | 3 | a0001c0045t0001g0142 a0011c0016t0001g0008 a0011c0016t0001g0141 |
4 | HG02630.hp1 HG02895.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.1855-216G>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 15/47 | chr2 | 127589876 | |||||||
chr2:127590010 | G | A | 1 | a0002c0011t0002g0186 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1855-82G>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 15/47 | chr2 | 127590010 | |||||||
chr2:127590272 | G | A | 6 | a0003c0003t0001g0235 a0003c0003t0001g0263 a0003c0026t0001g0146 others(3): Show |
6 | NA18941.hp2 NA18972.hp1 NA18975.hp1 others(3): Show |
intron_variant | MODIFIER | c.1992+43G>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 16/47 | chr2 | 127590272 | |||||||
chr2:127590399 | G | T | 4 | a0009c0014t0001g0148 a0009c0014t0001g0174 a0021c0046t0003g0078 others(1): Show |
4 | HG01891.hp2 HG02486.hp2 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.1992+170G>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 16/47 | chr2 | 127590399 | |||||||
chr2:127590470 | G | A | 4 | a0001c0044t0003g0080 a0001c0045t0001g0142 a0011c0016t0001g0008 others(1): Show |
5 | HG02630.hp1 HG02809.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.1992+241G>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 16/47 | chr2 | 127590470 | |||||||
chr2:127590616 | A | C | 270 | a0001c0002t0001g0027 a0001c0002t0001g0032 a0001c0002t0001g0034 others(267): Show |
279 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(276): Show |
intron_variant | MODIFIER | c.1992+387A>C | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 16/47 | chr2 | 127590616 | |||||||
chr2:127590673 | G | A | 1 | a0044c0034t0001g0070 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1992+444G>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 16/47 | chr2 | 127590673 | |||||||
chr2:127590755 | G | A | 1 | a0007c0023t0001g0122 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1992+526G>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 16/47 | chr2 | 127590755 | |||||||
chr2:127590905 | G | A | 3 | a0001c0045t0001g0142 a0011c0016t0001g0008 a0011c0016t0001g0141 |
4 | HG02630.hp1 HG02895.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.1992+676G>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 16/47 | chr2 | 127590905 | |||||||
chr2:127591060 | G | A | 8 | a0007c0023t0001g0149 a0007c0024t0001g0227 a0008c0015t0001g0047 others(5): Show |
8 | HG01243.hp2 HG02109.hp1 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.1992+831G>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 16/47 | chr2 | 127591060 | |||||||
chr2:127591203 | A | G | 254 | a0001c0002t0001g0027 a0001c0002t0001g0032 a0001c0002t0001g0034 others(251): Show |
263 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(260): Show |
intron_variant | MODIFIER | c.1992+974A>G | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 16/47 | chr2 | 127591203 | |||||||
chr2:127591369 | C | T | 24 | a0001c0004t0001g0043 a0001c0005t0001g0049 a0001c0005t0001g0098 others(21): Show |
24 | HG01070.hp1 HG01256.hp1 HG01258.hp2 others(21): Show |
intron_variant | MODIFIER | c.1992+1140C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 16/47 | chr2 | 127591369 | |||||||
chr2:127591403 | A | G | 3 | a0007c0023t0001g0149 a0007c0024t0001g0227 a0017c0053t0001g0271 |
3 | HG02109.hp1 HG02572.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.1992+1174A>G | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 16/47 | chr2 | 127591403 | |||||||
chr2:127591608 | C | T | 1 | a0030c0052t0001g0087 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.1993-1186C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 16/47 | chr2 | 127591608 | |||||||
chr2:127592070 | C | T | 1 | a0001c0002t0001g0101 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1993-724C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 16/47 | chr2 | 127592070 | |||||||
chr2:127592237 | A | C | 1 | a0007c0023t0001g0122 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1993-557A>C | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 16/47 | chr2 | 127592237 | |||||||
chr2:127592423 | A | T | 6 | a0004c0007t0001g0162 a0004c0007t0001g0164 a0004c0007t0001g0259 others(3): Show |
6 | HG00735.hp2 HG01106.hp2 HG01175.hp2 others(3): Show |
intron_variant | MODIFIER | c.1993-371A>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 16/47 | chr2 | 127592423 | |||||||
chr2:127592431 | A | T | 3 | a0001c0010t0001g0138 a0001c0010t0001g0139 a0009c0014t0001g0104 |
3 | HG02109.hp2 HG02572.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.1993-363A>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 16/47 | chr2 | 127592431 | |||||||
chr2:127592572 | C | T | 1 | a0001c0002t0001g0027 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.1993-222C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 16/47 | chr2 | 127592572 | |||||||
chr2:127592775 | G | A | 5 | a0008c0015t0001g0047 a0008c0015t0001g0107 a0008c0015t0001g0168 others(2): Show |
5 | HG01243.hp2 HG02145.hp1 HG02280.hp1 others(2): Show |
intron_variant | MODIFIER | c.1993-19G>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 16/47 | chr2 | 127592775 | |||||||
chr2:127592976 | G | A | 152 | a0001c0002t0001g0027 a0001c0002t0001g0032 a0001c0002t0001g0034 others(149): Show |
155 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(152): Show |
intron_variant | MODIFIER | c.2145+30G>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 17/47 | chr2 | 127592976 | |||||||
chr2:127593003 | T | TG | 268 | a0001c0002t0001g0027 a0001c0002t0001g0032 a0001c0002t0001g0034 others(265): Show |
277 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(274): Show |
intron_variant | MODIFIER | c.2145+59dupG | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 17/47 | INFO_REALIGN_3_PRIME | chr2 | 127593003 | ||||||
chr2:127593034 | C | G | 2 | a0001c0002t0001g0155 a0002c0011t0002g0270 |
2 | HG01884.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.2145+88C>G | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 17/47 | chr2 | 127593034 | |||||||
chr2:127593054 | C | G | 1 | a0002c0001t0001g0200 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.2145+108C>G | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 17/47 | chr2 | 127593054 | |||||||
chr2:127593119 | C | G | 1 | a0003c0003t0001g0229 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.2145+173C>G | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 17/47 | chr2 | 127593119 | |||||||
chr2:127593169 | C | A | 184 | a0001c0002t0001g0027 a0001c0002t0001g0032 a0001c0002t0001g0034 others(181): Show |
187 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(184): Show |
intron_variant | MODIFIER | c.2145+223C>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 17/47 | chr2 | 127593169 | |||||||
chr2:127593233 | C | T | 200 | a0001c0002t0001g0027 a0001c0002t0001g0032 a0001c0002t0001g0034 others(197): Show |
204 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(201): Show |
intron_variant | MODIFIER | c.2145+287C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 17/47 | chr2 | 127593233 | |||||||
chr2:127593279 | T | C | 2 | a0001c0002t0001g0155 a0002c0011t0002g0270 |
2 | HG01884.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.2146-267T>C | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 17/47 | chr2 | 127593279 | |||||||
chr2:127593371 | T | TC | 5 | a0008c0015t0001g0047 a0008c0015t0001g0107 a0008c0015t0001g0168 others(2): Show |
5 | HG01243.hp2 HG02145.hp1 HG02280.hp1 others(2): Show |
intron_variant | MODIFIER | c.2146-172dupC | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 17/47 | INFO_REALIGN_3_PRIME | chr2 | 127593371 | ||||||
chr2:127593375 | T | A | 3 | a0001c0045t0001g0142 a0011c0016t0001g0008 a0011c0016t0001g0141 |
4 | HG02630.hp1 HG02895.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.2146-171T>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 17/47 | chr2 | 127593375 | |||||||
chr2:127593390 | C | T | 193 | a0001c0002t0001g0027 a0001c0002t0001g0032 a0001c0002t0001g0034 others(190): Show |
196 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(193): Show |
intron_variant | MODIFIER | c.2146-156C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 17/47 | chr2 | 127593390 | |||||||
chr2:127593404 | C | T | 1 | a0001c0002t0001g0269 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.2146-142C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 17/47 | chr2 | 127593404 | |||||||
chr2:127593457 | G | C | 1 | a0001c0004t0001g0057 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.2146-89G>C | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 17/47 | chr2 | 127593457 | |||||||
chr2:127593771 | T | C | 200 | a0001c0002t0001g0027 a0001c0002t0001g0032 a0001c0002t0001g0034 others(197): Show |
204 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(201): Show |
intron_variant | MODIFIER | c.2244+127T>C | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 18/47 | chr2 | 127593771 | |||||||
chr2:127593808 | C | T | 2 | a0001c0002t0001g0137 a0009c0014t0001g0136 |
2 | HG02970.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.2244+164C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 18/47 | chr2 | 127593808 | |||||||
chr2:127593868 | T | C | 1 | a0001c0044t0003g0080 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.2244+224T>C | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 18/47 | chr2 | 127593868 | |||||||
chr2:127593882 | G | T | 1 | a0001c0005t0002g0065 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.2244+238G>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 18/47 | chr2 | 127593882 | |||||||
chr2:127593929 | C | T | 4 | a0001c0002t0001g0144 a0001c0005t0002g0131 a0028c0064t0002g0143 others(1): Show |
4 | HG02257.hp1 HG02280.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.2244+285C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 18/47 | chr2 | 127593929 | |||||||
chr2:127594209 | C | T | 5 | a0008c0015t0001g0047 a0008c0015t0001g0107 a0008c0015t0001g0168 others(2): Show |
5 | HG01243.hp2 HG02145.hp1 HG02280.hp1 others(2): Show |
intron_variant | MODIFIER | c.2244+565C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 18/47 | chr2 | 127594209 | |||||||
chr2:127594280 | A | C | 2 | a0001c0002t0001g0155 a0002c0011t0002g0270 |
2 | HG01884.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.2244+636A>C | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 18/47 | chr2 | 127594280 | |||||||
chr2:127594529 | C | T | 1 | a0017c0053t0001g0271 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.2244+885C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 18/47 | chr2 | 127594529 | |||||||
chr2:127594901 | C | T | 1 | a0001c0002t0001g0137 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.2244+1257C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 18/47 | chr2 | 127594901 | |||||||
chr2:127595020 | A | G | 2 | a0001c0018t0001g0267 a0001c0018t0001g0268 |
2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.2244+1376A>G | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 18/47 | chr2 | 127595020 | |||||||
chr2:127595045 | A | T | 1 | a0001c0002t0001g0036 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.2244+1401A>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 18/47 | chr2 | 127595045 | |||||||
chr2:127595157 | G | T | 5 | a0008c0015t0001g0047 a0008c0015t0001g0107 a0008c0015t0001g0168 others(2): Show |
5 | HG01243.hp2 HG02145.hp1 HG02280.hp1 others(2): Show |
intron_variant | MODIFIER | c.2245-1305G>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 18/47 | chr2 | 127595157 | |||||||
chr2:127595288 | T | G | 193 | a0001c0002t0001g0027 a0001c0002t0001g0032 a0001c0002t0001g0034 others(190): Show |
196 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(193): Show |
intron_variant | MODIFIER | c.2245-1174T>G | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 18/47 | chr2 | 127595288 | |||||||
chr2:127595435 | A | G | 5 | a0005c0008t0001g0003 a0005c0008t0001g0152 a0005c0008t0001g0153 others(2): Show |
6 | HG02717.hp1 HG02896.hp1 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.2245-1027A>G | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 18/47 | chr2 | 127595435 | |||||||
chr2:127595454 | G | A | 1 | a0001c0002t0001g0269 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.2245-1008G>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 18/47 | chr2 | 127595454 | |||||||
chr2:127595540 | A | C | 1 | a0002c0001t0001g0112 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.2245-922A>C | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 18/47 | chr2 | 127595540 | |||||||
chr2:127595661 | A | G | 2 | a0001c0002t0001g0155 a0002c0011t0002g0270 |
2 | HG01884.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.2245-801A>G | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 18/47 | chr2 | 127595661 | |||||||
chr2:127595701 | G | T | 1 | a0001c0044t0003g0080 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.2245-761G>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 18/47 | chr2 | 127595701 | |||||||
chr2:127595908 | T | C | 1 | a0007c0023t0001g0122 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.2245-554T>C | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 18/47 | chr2 | 127595908 | |||||||
chr2:127596074 | A | G | 34 | a0001c0004t0001g0043 a0001c0005t0001g0049 a0001c0005t0001g0098 others(31): Show |
34 | HG01070.hp1 HG01256.hp1 HG01258.hp2 others(31): Show |
intron_variant | MODIFIER | c.2245-388A>G | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 18/47 | chr2 | 127596074 | |||||||
chr2:127596130 | A | T | 187 | a0001c0002t0001g0027 a0001c0002t0001g0032 a0001c0002t0001g0034 others(184): Show |
190 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(187): Show |
intron_variant | MODIFIER | c.2245-332A>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 18/47 | chr2 | 127596130 | |||||||
chr2:127596235 | A | G | 1 | a0041c0028t0001g0195 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.2245-227A>G | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 18/47 | chr2 | 127596235 | |||||||
chr2:127596338 | T | A | 1 | a0001c0002t0001g0137 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.2245-124T>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 18/47 | chr2 | 127596338 | |||||||
chr2:127596449 | T | C | 1 | a0003c0003t0001g0236 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.2245-13T>C | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 18/47 | chr2 | 127596449 | |||||||
chr2:127596560 | C | T | 1 | a0045c0065t0001g0140 | 1 | NA19043.hp1 | splice_region_variant&intron_variant | LOW | c.2339+4C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 19/47 | chr2 | 127596560 | |||||||
chr2:127596804 | G | A | 1 | a0005c0008t0001g0209 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.2339+248G>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 19/47 | chr2 | 127596804 | |||||||
chr2:127596979 | G | A | 1 | a0001c0044t0003g0080 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.2339+423G>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 19/47 | chr2 | 127596979 | |||||||
chr2:127597074 | G | A | 2 | a0001c0002t0001g0035 a0001c0002t0001g0085 |
2 | NA18964.hp2 NA18981.hp1 |
intron_variant | MODIFIER | c.2339+518G>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 19/47 | chr2 | 127597074 | |||||||
chr2:127597092 | C | T | 67 | a0001c0002t0001g0027 a0001c0002t0001g0032 a0001c0002t0001g0034 others(64): Show |
68 | HG00099.hp1 HG00323.hp2 HG00642.hp1 others(65): Show |
intron_variant | MODIFIER | c.2339+536C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 19/47 | chr2 | 127597092 | |||||||
chr2:127597135 | A | G | 1 | a0045c0065t0001g0140 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.2339+579A>G | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 19/47 | chr2 | 127597135 | |||||||
chr2:127597160 | C | T | 1 | a0001c0004t0001g0023 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.2339+604C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 19/47 | chr2 | 127597160 | |||||||
chr2:127597248 | G | C | 48 | a0001c0004t0001g0246 a0001c0005t0002g0065 a0003c0003t0001g0033 others(45): Show |
49 | HG00280.hp1 HG00323.hp1 HG00621.hp2 others(46): Show |
intron_variant | MODIFIER | c.2339+692G>C | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 19/47 | chr2 | 127597248 | |||||||
chr2:127597277 | A | G | 73 | a0001c0002t0001g0027 a0001c0002t0001g0032 a0001c0002t0001g0034 others(70): Show |
75 | HG00099.hp1 HG00323.hp2 HG00642.hp1 others(72): Show |
intron_variant | MODIFIER | c.2339+721A>G | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 19/47 | chr2 | 127597277 | |||||||
chr2:127597356 | A | C | 6 | a0001c0002t0001g0045 a0001c0002t0001g0088 a0001c0002t0001g0155 others(3): Show |
6 | HG01884.hp1 HG01884.hp2 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.2339+800A>C | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 19/47 | chr2 | 127597356 | |||||||
chr2:127597384 | G | A | 6 | a0001c0002t0001g0045 a0001c0002t0001g0088 a0001c0002t0001g0155 others(3): Show |
7 | HG01884.hp2 HG02451.hp2 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.2339+828G>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 19/47 | chr2 | 127597384 | |||||||
chr2:127597611 | A | ATATT | 67 | a0001c0002t0001g0027 a0001c0002t0001g0032 a0001c0002t0001g0034 others(64): Show |
69 | HG00099.hp1 HG00323.hp2 HG00642.hp1 others(66): Show |
intron_variant | MODIFIER | c.2339+1093_2339+109 others(8): Show |
MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 19/47 | INFO_REALIGN_3_PRIME | chr2 | 127597611 | ||||||
chr2:127597611 | A | ATATTTAT others(1): Show |
19 | a0001c0002t0001g0077 a0001c0002t0001g0083 a0001c0002t0001g0134 others(16): Show |
20 | HG01069.hp1 HG01071.hp1 HG01175.hp1 others(17): Show |
intron_variant | MODIFIER | c.2339+1089_2339+109 others(12): Show |
MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 19/47 | INFO_REALIGN_3_PRIME | chr2 | 127597611 | ||||||
chr2:127597611 | A | ATATTTAT others(5): Show |
2 | a0001c0005t0002g0131 a0007c0024t0001g0227 |
2 | HG02280.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.2339+1085_2339+109 others(16): Show |
MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 19/47 | INFO_REALIGN_3_PRIME | chr2 | 127597611 | ||||||
chr2:127597611 | ATATT | A | 51 | a0001c0017t0004g0024 a0001c0017t0004g0025 a0001c0017t0004g0075 others(48): Show |
51 | HG00280.hp1 HG00323.hp1 HG00621.hp2 others(48): Show |
intron_variant | MODIFIER | c.2339+1093_2339+109 others(8): Show |
MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 19/47 | INFO_REALIGN_3_PRIME | chr2 | 127597611 | ||||||
chr2:127597611 | ATATTTAT others(1): Show |
A | 26 | a0001c0004t0001g0043 a0001c0005t0001g0049 a0001c0005t0001g0098 others(23): Show |
26 | HG01070.hp1 HG01256.hp1 HG01258.hp2 others(23): Show |
intron_variant | MODIFIER | c.2339+1089_2339+109 others(12): Show |
MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 19/47 | INFO_REALIGN_3_PRIME | chr2 | 127597611 | ||||||
chr2:127597655 | A | G | 1 | a0001c0044t0003g0080 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.2339+1099A>G | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 19/47 | chr2 | 127597655 | |||||||
chr2:127597822 | G | A | 22 | a0001c0002t0001g0137 a0001c0005t0002g0131 a0001c0010t0001g0138 others(19): Show |
22 | HG02109.hp1 HG02109.hp2 HG02258.hp2 others(19): Show |
intron_variant | MODIFIER | c.2339+1266G>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 19/47 | chr2 | 127597822 | |||||||
chr2:127597880 | C | T | 7 | a0001c0002t0001g0225 a0002c0006t0001g0015 a0002c0006t0001g0016 others(4): Show |
7 | HG00099.hp1 HG00741.hp1 HG01069.hp2 others(4): Show |
intron_variant | MODIFIER | c.2339+1324C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 19/47 | chr2 | 127597880 | |||||||
chr2:127597962 | C | T | 4 | a0001c0017t0004g0024 a0001c0017t0004g0025 a0001c0017t0004g0075 others(1): Show |
4 | HG02258.hp2 HG02630.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.2339+1406C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 19/47 | chr2 | 127597962 | |||||||
chr2:127598005 | A | G | 6 | a0001c0005t0002g0065 a0001c0045t0001g0142 a0007c0024t0001g0227 others(3): Show |
7 | HG02572.hp1 HG02630.hp1 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.2339+1449A>G | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 19/47 | chr2 | 127598005 | |||||||
chr2:127598025 | C | T | 1 | a0001c0005t0002g0054 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.2339+1469C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 19/47 | chr2 | 127598025 | |||||||
chr2:127598186 | A | C | 1 | a0017c0053t0001g0271 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.2339+1630A>C | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 19/47 | chr2 | 127598186 | |||||||
chr2:127598207 | C | T | 105 | a0001c0004t0001g0043 a0001c0004t0001g0218 a0001c0004t0001g0246 others(102): Show |
107 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(104): Show |
intron_variant | MODIFIER | c.2339+1651C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 19/47 | chr2 | 127598207 | |||||||
chr2:127598307 | G | A | 4 | a0001c0010t0001g0163 a0012c0022t0001g0120 a0012c0022t0001g0217 others(1): Show |
4 | HG01069.hp1 HG01071.hp1 HG01346.hp1 others(1): Show |
intron_variant | MODIFIER | c.2339+1751G>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 19/47 | chr2 | 127598307 | |||||||
chr2:127598759 | C | T | 6 | a0002c0001t0001g0002 a0002c0001t0001g0181 a0002c0001t0001g0182 others(3): Show |
8 | HG01168.hp2 HG01257.hp1 HG01361.hp2 others(5): Show |
intron_variant | MODIFIER | c.2339+2203C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 19/47 | chr2 | 127598759 | |||||||
chr2:127599066 | C | T | 1 | a0002c0012t0001g0173 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.2339+2510C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 19/47 | chr2 | 127599066 | |||||||
chr2:127599392 | A | T | 2 | a0007c0023t0001g0122 a0007c0023t0001g0149 |
2 | HG02109.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.2339+2836A>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 19/47 | chr2 | 127599392 | |||||||
chr2:127599422 | C | T | 182 | a0001c0002t0001g0027 a0001c0002t0001g0032 a0001c0002t0001g0034 others(179): Show |
186 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(183): Show |
intron_variant | MODIFIER | c.2339+2866C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 19/47 | chr2 | 127599422 | |||||||
chr2:127599453 | G | T | 1 | a0001c0004t0001g0057 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.2339+2897G>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 19/47 | chr2 | 127599453 | |||||||
chr2:127599811 | C | T | 1 | a0038c0033t0001g0069 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.2339+3255C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 19/47 | chr2 | 127599811 | |||||||
chr2:127599812 | G | A | 1 | a0021c0046t0003g0078 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.2339+3256G>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 19/47 | chr2 | 127599812 | |||||||
chr2:127599952 | G | A | 2 | a0003c0003t0001g0033 a0003c0003t0001g0081 |
2 | HG00621.hp2 NA18983.hp1 |
intron_variant | MODIFIER | c.2339+3396G>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 19/47 | chr2 | 127599952 | |||||||
chr2:127599980 | T | G | 2 | a0002c0001t0001g0113 a0013c0019t0001g0178 |
2 | HG02300.hp1 HG02300.hp2 |
intron_variant | MODIFIER | c.2339+3424T>G | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 19/47 | chr2 | 127599980 | |||||||
chr2:127600072 | C | T | 198 | a0001c0002t0001g0027 a0001c0002t0001g0032 a0001c0002t0001g0034 others(195): Show |
202 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(199): Show |
intron_variant | MODIFIER | c.2339+3516C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 19/47 | chr2 | 127600072 | |||||||
chr2:127600073 | G | A | 1 | a0002c0001t0001g0176 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.2339+3517G>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 19/47 | chr2 | 127600073 | |||||||
chr2:127600121 | G | A | 46 | a0001c0004t0001g0246 a0003c0003t0001g0033 a0003c0003t0001g0081 others(43): Show |
47 | HG00280.hp1 HG00323.hp1 HG00621.hp2 others(44): Show |
intron_variant | MODIFIER | c.2339+3565G>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 19/47 | chr2 | 127600121 | |||||||
chr2:127600191 | T | C | 7 | a0008c0015t0001g0047 a0008c0015t0001g0107 a0008c0015t0001g0168 others(4): Show |
7 | HG01243.hp2 HG02145.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.2339+3635T>C | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 19/47 | chr2 | 127600191 | |||||||
chr2:127600207 | T | G | 2 | a0007c0023t0001g0122 a0007c0023t0001g0149 |
2 | HG02109.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.2339+3651T>G | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 19/47 | chr2 | 127600207 | |||||||
chr2:127600211 | C | T | 1 | a0024c0070t0001g0028 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.2339+3655C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 19/47 | chr2 | 127600211 | |||||||
chr2:127600270 | G | A | 19 | a0001c0004t0001g0218 a0004c0007t0001g0162 a0004c0007t0001g0164 others(16): Show |
19 | HG00280.hp2 HG00642.hp2 HG00735.hp2 others(16): Show |
intron_variant | MODIFIER | c.2339+3714G>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 19/47 | chr2 | 127600270 | |||||||
chr2:127600289 | C | G | 23 | a0001c0004t0001g0043 a0001c0005t0001g0049 a0001c0005t0001g0098 others(20): Show |
23 | HG01070.hp1 HG01256.hp1 HG01258.hp2 others(20): Show |
intron_variant | MODIFIER | c.2339+3733C>G | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 19/47 | chr2 | 127600289 | |||||||
chr2:127600433 | G | A | 1 | a0001c0044t0003g0080 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.2339+3877G>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 19/47 | chr2 | 127600433 | |||||||
chr2:127600475 | C | T | 5 | a0001c0045t0001g0142 a0007c0024t0001g0227 a0011c0016t0001g0008 others(2): Show |
6 | HG02572.hp1 HG02630.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.2339+3919C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 19/47 | chr2 | 127600475 | |||||||
chr2:127600538 | C | A | 19 | a0001c0004t0001g0218 a0004c0007t0001g0162 a0004c0007t0001g0164 others(16): Show |
19 | HG00280.hp2 HG00642.hp2 HG00735.hp2 others(16): Show |
intron_variant | MODIFIER | c.2339+3982C>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 19/47 | chr2 | 127600538 | |||||||
chr2:127600937 | A | G | 1 | a0004c0007t0001g0261 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.2339+4381A>G | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 19/47 | chr2 | 127600937 | |||||||
chr2:127601013 | T | G | 1 | a0002c0012t0001g0171 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.2339+4457T>G | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 19/47 | chr2 | 127601013 | |||||||
chr2:127601373 | T | C | 1 | a0034c0059t0001g0031 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.2340-4471T>C | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 19/47 | chr2 | 127601373 | |||||||
chr2:127601518 | T | C | 46 | a0001c0004t0001g0246 a0003c0003t0001g0033 a0003c0003t0001g0081 others(43): Show |
47 | HG00280.hp1 HG00323.hp1 HG00621.hp2 others(44): Show |
intron_variant | MODIFIER | c.2340-4326T>C | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 19/47 | chr2 | 127601518 | |||||||
chr2:127601846 | G | A | 3 | a0009c0014t0001g0148 a0009c0014t0001g0174 a0045c0065t0001g0140 |
3 | HG02486.hp2 HG02818.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.2340-3998G>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 19/47 | chr2 | 127601846 | |||||||
chr2:127601910 | A | G | 1 | a0003c0003t0001g0126 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.2340-3934A>G | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 19/47 | chr2 | 127601910 | |||||||
chr2:127601927 | G | A | 1 | a0021c0046t0003g0078 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.2340-3917G>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 19/47 | chr2 | 127601927 | |||||||
chr2:127602076 | T | C | 23 | a0001c0004t0001g0043 a0001c0005t0001g0049 a0001c0005t0001g0098 others(20): Show |
23 | HG01070.hp1 HG01256.hp1 HG01258.hp2 others(20): Show |
intron_variant | MODIFIER | c.2340-3768T>C | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 19/47 | chr2 | 127602076 | |||||||
chr2:127602098 | C | G | 2 | a0001c0005t0002g0131 a0002c0011t0002g0270 |
2 | HG02280.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.2340-3746C>G | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 19/47 | chr2 | 127602098 | |||||||
chr2:127602241 | T | C | 1 | a0001c0004t0001g0009 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.2340-3603T>C | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 19/47 | chr2 | 127602241 | |||||||
chr2:127602626 | A | G | 182 | a0001c0002t0001g0027 a0001c0002t0001g0032 a0001c0002t0001g0034 others(179): Show |
186 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(183): Show |
intron_variant | MODIFIER | c.2340-3218A>G | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 19/47 | chr2 | 127602626 | |||||||
chr2:127602651 | AAAAAAGA others(4): Show |
A | 6 | a0008c0015t0001g0047 a0008c0015t0001g0107 a0008c0015t0001g0168 others(3): Show |
6 | HG01243.hp2 HG02145.hp1 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.2340-3189_2340-317 others(15): Show |
MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 19/47 | INFO_REALIGN_3_PRIME | chr2 | 127602651 | ||||||
chr2:127603176 | T | A | 23 | a0001c0004t0001g0043 a0001c0005t0001g0049 a0001c0005t0001g0098 others(20): Show |
23 | HG01070.hp1 HG01256.hp1 HG01258.hp2 others(20): Show |
intron_variant | MODIFIER | c.2340-2668T>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 19/47 | chr2 | 127603176 | |||||||
chr2:127603216 | C | G | 1 | a0021c0046t0003g0078 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.2340-2628C>G | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 19/47 | chr2 | 127603216 | |||||||
chr2:127603221 | C | T | 1 | a0021c0046t0003g0078 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.2340-2623C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 19/47 | chr2 | 127603221 | |||||||
chr2:127603232 | A | G | 73 | a0001c0002t0001g0027 a0001c0002t0001g0032 a0001c0002t0001g0034 others(70): Show |
75 | HG00099.hp1 HG00323.hp2 HG00642.hp1 others(72): Show |
intron_variant | MODIFIER | c.2340-2612A>G | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 19/47 | chr2 | 127603232 | |||||||
chr2:127603781 | T | C | 1 | a0026c0035t0001g0114 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.2340-2063T>C | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 19/47 | chr2 | 127603781 | |||||||
chr2:127603805 | C | T | 45 | a0003c0003t0001g0033 a0003c0003t0001g0081 a0003c0003t0001g0109 others(42): Show |
46 | HG00280.hp1 HG00323.hp1 HG00621.hp2 others(43): Show |
intron_variant | MODIFIER | c.2340-2039C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 19/47 | chr2 | 127603805 | |||||||
chr2:127603861 | T | C | 4 | a0003c0026t0001g0146 a0003c0026t0001g0253 a0003c0069t0001g0250 others(1): Show |
4 | HG01192.hp1 NA18972.hp1 NA19060.hp1 others(1): Show |
intron_variant | MODIFIER | c.2340-1983T>C | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 19/47 | chr2 | 127603861 | |||||||
chr2:127603871 | T | C | 1 | a0024c0070t0001g0028 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.2340-1973T>C | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 19/47 | chr2 | 127603871 | |||||||
chr2:127603937 | G | T | 2 | a0003c0003t0001g0230 a0003c0003t0001g0233 |
2 | NA18950.hp2 NA18966.hp2 |
intron_variant | MODIFIER | c.2340-1907G>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 19/47 | chr2 | 127603937 | |||||||
chr2:127603942 | G | A | 1 | a0009c0014t0001g0148 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.2340-1902G>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 19/47 | chr2 | 127603942 | |||||||
chr2:127603956 | AC | A | 19 | a0003c0003t0001g0236 a0004c0007t0001g0162 a0004c0007t0001g0164 others(16): Show |
19 | HG00280.hp2 HG00642.hp2 HG00735.hp2 others(16): Show |
intron_variant | MODIFIER | c.2340-1884delC | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 19/47 | INFO_REALIGN_3_PRIME | chr2 | 127603956 | ||||||
chr2:127603990 | G | A | 73 | a0001c0005t0001g0098 a0001c0005t0002g0065 a0003c0003t0001g0033 others(70): Show |
74 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(71): Show |
intron_variant | MODIFIER | c.2340-1854G>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 19/47 | chr2 | 127603990 | |||||||
chr2:127604023 | C | T | 1 | a0001c0002t0001g0092 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.2340-1821C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 19/47 | chr2 | 127604023 | |||||||
chr2:127604048 | G | A | 2 | a0001c0005t0002g0131 a0002c0011t0002g0270 |
2 | HG02280.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.2340-1796G>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 19/47 | chr2 | 127604048 | |||||||
chr2:127604074 | A | G | 2 | a0001c0002t0001g0091 a0001c0002t0001g0092 |
2 | HG02896.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.2340-1770A>G | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 19/47 | chr2 | 127604074 | |||||||
chr2:127604132 | C | A | 75 | a0001c0005t0002g0065 a0001c0045t0001g0142 a0003c0003t0001g0033 others(72): Show |
77 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(74): Show |
intron_variant | MODIFIER | c.2340-1712C>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 19/47 | chr2 | 127604132 | |||||||
chr2:127604209 | G | A | 22 | a0001c0004t0001g0043 a0001c0005t0001g0049 a0001c0005t0001g0098 others(19): Show |
22 | HG01070.hp1 HG01256.hp1 HG01258.hp2 others(19): Show |
intron_variant | MODIFIER | c.2340-1635G>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 19/47 | chr2 | 127604209 | |||||||
chr2:127604223 | A | G | 18 | a0004c0007t0001g0162 a0004c0007t0001g0164 a0004c0007t0001g0220 others(15): Show |
18 | HG00280.hp2 HG00642.hp2 HG00735.hp2 others(15): Show |
intron_variant | MODIFIER | c.2340-1621A>G | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 19/47 | chr2 | 127604223 | |||||||
chr2:127604253 | T | G | 1 | a0017c0053t0001g0271 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.2340-1591T>G | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 19/47 | chr2 | 127604253 | |||||||
chr2:127604539 | G | A | 1 | a0009c0014t0001g0104 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.2340-1305G>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 19/47 | chr2 | 127604539 | |||||||
chr2:127604725 | C | T | 1 | a0003c0003t0001g0128 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.2340-1119C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 19/47 | chr2 | 127604725 | |||||||
chr2:127604726 | G | A | 1 | a0001c0002t0001g0137 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.2340-1118G>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 19/47 | chr2 | 127604726 | |||||||
chr2:127604789 | G | A | 1 | a0008c0063t0001g0257 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.2340-1055G>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 19/47 | chr2 | 127604789 | |||||||
chr2:127604947 | C | T | 1 | a0034c0059t0001g0031 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.2340-897C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 19/47 | chr2 | 127604947 | |||||||
chr2:127604985 | A | G | 18 | a0001c0010t0001g0138 a0001c0010t0001g0139 a0001c0010t0001g0163 others(15): Show |
18 | HG01069.hp1 HG01071.hp1 HG01346.hp1 others(15): Show |
intron_variant | MODIFIER | c.2340-859A>G | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 19/47 | chr2 | 127604985 | |||||||
chr2:127605129 | G | A | 1 | a0001c0044t0003g0080 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.2340-715G>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 19/47 | chr2 | 127605129 | |||||||
chr2:127605145 | C | T | 1 | a0021c0046t0003g0078 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.2340-699C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 19/47 | chr2 | 127605145 | |||||||
chr2:127605412 | G | A | 94 | a0001c0010t0001g0138 a0001c0010t0001g0139 a0001c0010t0001g0163 others(91): Show |
96 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(93): Show |
intron_variant | MODIFIER | c.2340-432G>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 19/47 | chr2 | 127605412 | |||||||
chr2:127605426 | T | C | 2 | a0011c0016t0001g0008 a0011c0016t0001g0141 |
3 | HG02630.hp1 HG03041.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.2340-418T>C | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 19/47 | chr2 | 127605426 | |||||||
chr2:127605551 | C | T | 78 | a0001c0002t0001g0027 a0001c0002t0001g0032 a0001c0002t0001g0034 others(75): Show |
80 | HG00099.hp1 HG00323.hp2 HG00642.hp1 others(77): Show |
intron_variant | MODIFIER | c.2340-293C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 19/47 | chr2 | 127605551 | |||||||
chr2:127606033 | G | A | 46 | a0003c0003t0001g0033 a0003c0003t0001g0081 a0003c0003t0001g0109 others(43): Show |
47 | HG00280.hp1 HG00323.hp1 HG00621.hp2 others(44): Show |
intron_variant | MODIFIER | c.2424+105G>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 20/47 | chr2 | 127606033 | |||||||
chr2:127606034 | G | A | 1 | a0001c0004t0001g0254 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.2424+106G>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 20/47 | chr2 | 127606034 | |||||||
chr2:127606073 | A | T | 26 | a0001c0005t0001g0049 a0001c0005t0001g0098 a0001c0005t0002g0044 others(23): Show |
26 | HG01070.hp1 HG01256.hp1 HG01258.hp2 others(23): Show |
intron_variant | MODIFIER | c.2424+145A>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 20/47 | chr2 | 127606073 | |||||||
chr2:127606356 | T | C | 1 | a0001c0004t0001g0232 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.2424+428T>C | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 20/47 | chr2 | 127606356 | |||||||
chr2:127606416 | G | A | 1 | a0001c0010t0001g0138 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.2424+488G>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 20/47 | chr2 | 127606416 | |||||||
chr2:127606557 | C | G | 23 | a0001c0010t0001g0138 a0001c0010t0001g0139 a0001c0010t0001g0163 others(20): Show |
23 | HG01069.hp1 HG01071.hp1 HG01346.hp1 others(20): Show |
intron_variant | MODIFIER | c.2424+629C>G | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 20/47 | chr2 | 127606557 | |||||||
chr2:127606648 | G | A | 1 | a0009c0014t0001g0104 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.2425-558G>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 20/47 | chr2 | 127606648 | |||||||
chr2:127606679 | G | A | 1 | a0045c0065t0001g0140 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.2425-527G>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 20/47 | chr2 | 127606679 | |||||||
chr2:127606696 | G | A | 2 | a0015c0066t0001g0067 a0015c0071t0001g0123 |
2 | HG01884.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.2425-510G>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 20/47 | chr2 | 127606696 | |||||||
chr2:127607082 | C | T | 2 | a0001c0002t0001g0032 a0001c0002t0001g0038 |
2 | NA18942.hp1 NA18983.hp2 |
intron_variant | MODIFIER | c.2425-124C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 20/47 | chr2 | 127607082 | |||||||
chr2:127607109 | G | A | 45 | a0003c0003t0001g0033 a0003c0003t0001g0081 a0003c0003t0001g0109 others(42): Show |
46 | HG00280.hp1 HG00323.hp1 HG00621.hp2 others(43): Show |
intron_variant | MODIFIER | c.2425-97G>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 20/47 | chr2 | 127607109 | |||||||
chr2:127607133 | T | C | 1 | a0001c0005t0002g0044 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.2425-73T>C | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 20/47 | chr2 | 127607133 | |||||||
chr2:127607147 | C | T | 2 | a0003c0003t0001g0210 a0017c0053t0001g0271 |
2 | HG01433.hp2 HG02572.hp1 |
intron_variant | MODIFIER | c.2425-59C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 20/47 | chr2 | 127607147 | |||||||
chr2:127607588 | A | G | 2 | a0003c0003t0001g0229 a0003c0003t0001g0240 |
2 | NA18959.hp2 NA18985.hp2 |
intron_variant | MODIFIER | c.2643+164A>G | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 21/47 | chr2 | 127607588 | |||||||
chr2:127607592 | C | T | 1 | a0009c0014t0001g0104 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.2643+168C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 21/47 | chr2 | 127607592 | |||||||
chr2:127607727 | G | A | 2 | a0011c0016t0001g0008 a0011c0016t0001g0141 |
3 | HG02630.hp1 HG03041.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.2643+303G>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 21/47 | chr2 | 127607727 | |||||||
chr2:127607809 | G | T | 1 | a0009c0014t0001g0104 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.2643+385G>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 21/47 | chr2 | 127607809 | |||||||
chr2:127607893 | G | A | 1 | a0006c0009t0001g0061 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.2643+469G>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 21/47 | chr2 | 127607893 | |||||||
chr2:127607925 | A | G | 2 | a0017c0072t0001g0012 a0046c0073t0001g0068 |
2 | HG02922.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.2643+501A>G | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 21/47 | chr2 | 127607925 | |||||||
chr2:127607945 | C | T | 1 | a0004c0007t0003g0223 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.2643+521C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 21/47 | chr2 | 127607945 | |||||||
chr2:127608089 | G | A | 1 | a0001c0044t0003g0080 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.2644-619G>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 21/47 | chr2 | 127608089 | |||||||
chr2:127608182 | G | T | 1 | a0009c0014t0001g0136 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.2644-526G>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 21/47 | chr2 | 127608182 | |||||||
chr2:127608339 | G | A | 22 | a0001c0010t0001g0138 a0001c0010t0001g0139 a0001c0010t0001g0163 others(19): Show |
22 | HG01069.hp1 HG01071.hp1 HG01346.hp1 others(19): Show |
intron_variant | MODIFIER | c.2644-369G>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 21/47 | chr2 | 127608339 | |||||||
chr2:127608376 | G | C | 1 | a0001c0002t0001g0137 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.2644-332G>C | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 21/47 | chr2 | 127608376 | |||||||
chr2:127608466 | C | A | 1 | a0045c0065t0001g0140 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.2644-242C>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 21/47 | chr2 | 127608466 | |||||||
chr2:127608483 | C | T | 2 | a0011c0016t0001g0008 a0011c0016t0001g0141 |
3 | HG02630.hp1 HG03041.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.2644-225C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 21/47 | chr2 | 127608483 | |||||||
chr2:127608526 | T | C | 1 | a0045c0065t0001g0140 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.2644-182T>C | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 21/47 | chr2 | 127608526 | |||||||
chr2:127608582 | T | G | 1 | a0029c0048t0001g0132 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.2644-126T>G | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 21/47 | chr2 | 127608582 | |||||||
chr2:127608697 | G | A | 24 | a0004c0007t0001g0162 a0004c0007t0001g0164 a0004c0007t0001g0220 others(21): Show |
25 | HG00280.hp2 HG00642.hp2 HG00735.hp2 others(22): Show |
intron_variant | MODIFIER | c.2644-11G>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 21/47 | chr2 | 127608697 | |||||||
chr2:127609061 | G | C | 96 | a0001c0010t0001g0138 a0001c0010t0001g0139 a0001c0010t0001g0163 others(93): Show |
98 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(95): Show |
intron_variant | MODIFIER | c.2814+183G>C | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 22/47 | chr2 | 127609061 | |||||||
chr2:127609192 | G | A | 1 | a0002c0011t0002g0207 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.2814+314G>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 22/47 | chr2 | 127609192 | |||||||
chr2:127609204 | T | C | 23 | a0001c0005t0001g0049 a0001c0005t0001g0098 a0001c0005t0002g0044 others(20): Show |
23 | HG01070.hp1 HG01256.hp1 HG01258.hp2 others(20): Show |
intron_variant | MODIFIER | c.2815-302T>C | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 22/47 | chr2 | 127609204 | |||||||
chr2:127609784 | G | A | 22 | a0004c0007t0001g0162 a0004c0007t0001g0164 a0004c0007t0001g0220 others(19): Show |
22 | HG00280.hp2 HG00642.hp2 HG00735.hp2 others(19): Show |
intron_variant | MODIFIER | c.3025-65G>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 23/47 | chr2 | 127609784 | |||||||
chr2:127610102 | C | T | 1 | a0002c0001t0001g0185 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.3192+86C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 24/47 | chr2 | 127610102 | |||||||
chr2:127610318 | A | G | 2 | a0009c0014t0001g0148 a0009c0014t0001g0174 |
2 | HG02486.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.3192+302A>G | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 24/47 | chr2 | 127610318 | |||||||
chr2:127610475 | G | A | 46 | a0003c0003t0001g0033 a0003c0003t0001g0081 a0003c0003t0001g0109 others(43): Show |
47 | HG00280.hp1 HG00323.hp1 HG00621.hp2 others(44): Show |
intron_variant | MODIFIER | c.3192+459G>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 24/47 | chr2 | 127610475 | |||||||
chr2:127610614 | C | T | 2 | a0001c0005t0002g0052 a0001c0005t0002g0095 |
2 | HG01256.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.3192+598C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 24/47 | chr2 | 127610614 | |||||||
chr2:127610660 | T | C | 96 | a0001c0010t0001g0138 a0001c0010t0001g0139 a0001c0010t0001g0163 others(93): Show |
98 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(95): Show |
intron_variant | MODIFIER | c.3192+644T>C | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 24/47 | chr2 | 127610660 | |||||||
chr2:127610750 | G | C | 1 | a0024c0070t0001g0028 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.3192+734G>C | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 24/47 | chr2 | 127610750 | |||||||
chr2:127610805 | A | G | 18 | a0004c0007t0001g0162 a0004c0007t0001g0164 a0004c0007t0001g0220 others(15): Show |
18 | HG00280.hp2 HG00642.hp2 HG00735.hp2 others(15): Show |
intron_variant | MODIFIER | c.3192+789A>G | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 24/47 | chr2 | 127610805 | |||||||
chr2:127610926 | A | G | 2 | a0002c0001t0001g0194 a0014c0031t0001g0193 |
2 | HG01081.hp1 HG01358.hp1 |
intron_variant | MODIFIER | c.3192+910A>G | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 24/47 | chr2 | 127610926 | |||||||
chr2:127611081 | G | A | 1 | a0001c0044t0003g0080 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.3192+1065G>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 24/47 | chr2 | 127611081 | |||||||
chr2:127611149 | C | T | 1 | a0004c0007t0003g0121 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.3193-1101C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 24/47 | chr2 | 127611149 | |||||||
chr2:127611203 | T | G | 2 | a0011c0016t0001g0008 a0011c0016t0001g0141 |
3 | HG02630.hp1 HG03041.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.3193-1047T>G | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 24/47 | chr2 | 127611203 | |||||||
chr2:127611300 | C | T | 2 | a0031c0074t0001g0026 a0033c0029t0001g0201 |
2 | HG03654.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.3193-950C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 24/47 | chr2 | 127611300 | |||||||
chr2:127611792 | C | T | 1 | a0029c0048t0001g0132 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.3193-458C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 24/47 | chr2 | 127611792 | |||||||
chr2:127611800 | C | T | 4 | a0009c0014t0001g0104 a0009c0014t0001g0136 a0009c0014t0001g0148 others(1): Show |
4 | HG02486.hp2 HG02572.hp2 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.3193-450C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 24/47 | chr2 | 127611800 | |||||||
chr2:127612177 | A | G | 46 | a0003c0003t0001g0033 a0003c0003t0001g0081 a0003c0003t0001g0109 others(43): Show |
47 | HG00280.hp1 HG00323.hp1 HG00621.hp2 others(44): Show |
intron_variant | MODIFIER | c.3193-73A>G | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 24/47 | chr2 | 127612177 | |||||||
chr2:127612182 | G | A | 1 | a0045c0065t0001g0140 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.3193-68G>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 24/47 | chr2 | 127612182 | |||||||
chr2:127612228 | C | T | 2 | a0001c0002t0001g0091 a0001c0002t0001g0092 |
2 | HG02896.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.3193-22C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 24/47 | chr2 | 127612228 | |||||||
chr2:127612342 | C | T | 46 | a0003c0003t0001g0033 a0003c0003t0001g0081 a0003c0003t0001g0109 others(43): Show |
47 | HG00280.hp1 HG00323.hp1 HG00621.hp2 others(44): Show |
intron_variant | MODIFIER | c.3270+15C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 25/47 | chr2 | 127612342 | |||||||
chr2:127612352 | G | A | 1 | a0001c0044t0003g0080 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.3270+25G>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 25/47 | chr2 | 127612352 | |||||||
chr2:127612625 | G | A | 48 | a0003c0003t0001g0033 a0003c0003t0001g0081 a0003c0003t0001g0109 others(45): Show |
49 | HG00280.hp1 HG00323.hp1 HG00621.hp2 others(46): Show |
intron_variant | MODIFIER | c.3398+22G>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 26/47 | chr2 | 127612625 | |||||||
chr2:127612753 | C | T | 1 | a0027c0057t0001g0079 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.3398+150C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 26/47 | chr2 | 127612753 | |||||||
chr2:127612891 | C | T | 46 | a0003c0003t0001g0033 a0003c0003t0001g0081 a0003c0003t0001g0109 others(43): Show |
47 | HG00280.hp1 HG00323.hp1 HG00621.hp2 others(44): Show |
intron_variant | MODIFIER | c.3398+288C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 26/47 | chr2 | 127612891 | |||||||
chr2:127613012 | T | C | 1 | a0003c0003t0001g0241 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.3398+409T>C | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 26/47 | chr2 | 127613012 | |||||||
chr2:127613180 | C | G | 1 | a0028c0064t0002g0143 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.3398+577C>G | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 26/47 | chr2 | 127613180 | |||||||
chr2:127613245 | T | C | 1 | a0026c0035t0001g0114 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.3398+642T>C | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 26/47 | chr2 | 127613245 | |||||||
chr2:127613281 | T | C | 46 | a0003c0003t0001g0033 a0003c0003t0001g0081 a0003c0003t0001g0109 others(43): Show |
47 | HG00280.hp1 HG00323.hp1 HG00621.hp2 others(44): Show |
intron_variant | MODIFIER | c.3398+678T>C | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 26/47 | chr2 | 127613281 | |||||||
chr2:127613583 | G | T | 2 | a0007c0023t0001g0122 a0007c0023t0001g0149 |
2 | HG02109.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.3398+980G>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 26/47 | chr2 | 127613583 | |||||||
chr2:127613678 | G | C | 1 | a0038c0033t0001g0069 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.3398+1075G>C | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 26/47 | chr2 | 127613678 | |||||||
chr2:127613890 | T | C | 1 | a0002c0006t0001g0013 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.3398+1287T>C | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 26/47 | chr2 | 127613890 | |||||||
chr2:127613961 | T | C | 1 | a0045c0065t0001g0140 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.3398+1358T>C | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 26/47 | chr2 | 127613961 | |||||||
chr2:127614104 | GCCA | G | 6 | a0001c0010t0001g0228 a0001c0010t0001g0264 a0001c0010t0001g0265 others(3): Show |
6 | HG02451.hp1 HG02622.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.3398+1506_3398+150 others(7): Show |
MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 26/47 | INFO_REALIGN_3_PRIME | chr2 | 127614104 | ||||||
chr2:127614446 | T | C | 6 | a0003c0003t0001g0235 a0003c0003t0001g0263 a0003c0026t0001g0146 others(3): Show |
6 | NA18941.hp2 NA18972.hp1 NA18975.hp1 others(3): Show |
intron_variant | MODIFIER | c.3398+1843T>C | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 26/47 | chr2 | 127614446 | |||||||
chr2:127614504 | C | G | 22 | a0004c0007t0001g0162 a0004c0007t0001g0164 a0004c0007t0001g0220 others(19): Show |
22 | HG00280.hp2 HG00642.hp2 HG00735.hp2 others(19): Show |
intron_variant | MODIFIER | c.3398+1901C>G | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 26/47 | chr2 | 127614504 | |||||||
chr2:127614533 | C | T | 4 | a0001c0002t0001g0106 a0001c0013t0001g0005 a0001c0013t0001g0166 others(1): Show |
5 | HG01243.hp1 HG02055.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.3398+1930C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 26/47 | chr2 | 127614533 | |||||||
chr2:127614562 | A | G | 2 | a0001c0058t0002g0103 a0002c0001t0001g0071 |
2 | NA18957.hp1 NA18985.hp1 |
intron_variant | MODIFIER | c.3398+1959A>G | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 26/47 | chr2 | 127614562 | |||||||
chr2:127614624 | C | T | 2 | a0003c0003t0001g0210 a0003c0003t0001g0224 |
2 | HG01123.hp2 HG01433.hp2 |
intron_variant | MODIFIER | c.3398+2021C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 26/47 | chr2 | 127614624 | |||||||
chr2:127614735 | A | G | 1 | a0045c0065t0001g0140 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.3398+2132A>G | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 26/47 | chr2 | 127614735 | |||||||
chr2:127614764 | G | A | 2 | a0011c0016t0001g0008 a0011c0016t0001g0141 |
3 | HG02630.hp1 HG03041.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.3398+2161G>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 26/47 | chr2 | 127614764 | |||||||
chr2:127614807 | A | T | 1 | a0029c0048t0001g0132 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.3398+2204A>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 26/47 | chr2 | 127614807 | |||||||
chr2:127614825 | A | G | 22 | a0001c0010t0001g0138 a0001c0010t0001g0139 a0001c0010t0001g0163 others(19): Show |
22 | HG01069.hp1 HG01071.hp1 HG01346.hp1 others(19): Show |
intron_variant | MODIFIER | c.3398+2222A>G | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 26/47 | chr2 | 127614825 | |||||||
chr2:127614855 | C | T | 1 | a0001c0005t0003g0063 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.3398+2252C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 26/47 | chr2 | 127614855 | |||||||
chr2:127614947 | T | C | 23 | a0001c0010t0001g0138 a0001c0010t0001g0139 a0001c0010t0001g0163 others(20): Show |
23 | HG01069.hp1 HG01071.hp1 HG01346.hp1 others(20): Show |
intron_variant | MODIFIER | c.3398+2344T>C | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 26/47 | chr2 | 127614947 | |||||||
chr2:127615210 | G | A | 1 | a0004c0007t0003g0223 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.3398+2607G>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 26/47 | chr2 | 127615210 | |||||||
chr2:127615281 | T | C | 129 | a0001c0002t0001g0027 a0001c0002t0001g0032 a0001c0002t0001g0034 others(126): Show |
131 | HG00099.hp1 HG00323.hp2 HG00642.hp1 others(128): Show |
intron_variant | MODIFIER | c.3398+2678T>C | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 26/47 | chr2 | 127615281 | |||||||
chr2:127615386 | G | A | 2 | a0002c0006t0001g0156 a0019c0039t0001g0017 |
2 | HG01081.hp2 HG01515.hp2 |
intron_variant | MODIFIER | c.3398+2783G>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 26/47 | chr2 | 127615386 | |||||||
chr2:127615448 | G | A | 77 | a0001c0002t0001g0027 a0001c0002t0001g0032 a0001c0002t0001g0034 others(74): Show |
79 | HG00099.hp1 HG00323.hp2 HG00642.hp1 others(76): Show |
intron_variant | MODIFIER | c.3398+2845G>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 26/47 | chr2 | 127615448 | |||||||
chr2:127615464 | C | T | 1 | a0001c0004t0001g0057 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.3398+2861C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 26/47 | chr2 | 127615464 | |||||||
chr2:127615465 | G | A | 1 | a0024c0070t0001g0028 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.3398+2862G>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 26/47 | chr2 | 127615465 | |||||||
chr2:127615470 | G | C | 1 | a0024c0070t0001g0028 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.3398+2867G>C | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 26/47 | chr2 | 127615470 | |||||||
chr2:127615744 | C | T | 1 | a0041c0028t0001g0195 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.3398+3141C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 26/47 | chr2 | 127615744 | |||||||
chr2:127615768 | A | G | 22 | a0001c0005t0001g0049 a0001c0005t0001g0098 a0001c0005t0002g0044 others(19): Show |
22 | HG01070.hp1 HG01256.hp1 HG01258.hp2 others(19): Show |
intron_variant | MODIFIER | c.3398+3165A>G | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 26/47 | chr2 | 127615768 | |||||||
chr2:127615783 | T | C | 1 | a0003c0003t0001g0239 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.3398+3180T>C | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 26/47 | chr2 | 127615783 | |||||||
chr2:127615852 | C | T | 1 | a0001c0010t0001g0163 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.3398+3249C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 26/47 | chr2 | 127615852 | |||||||
chr2:127615853 | G | A | 2 | a0002c0001t0001g0177 a0003c0003t0001g0240 |
2 | NA18985.hp2 NA18995.hp2 |
intron_variant | MODIFIER | c.3398+3250G>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 26/47 | chr2 | 127615853 | |||||||
chr2:127615987 | G | A | 51 | a0003c0003t0001g0033 a0003c0003t0001g0081 a0003c0003t0001g0109 others(48): Show |
53 | HG00280.hp1 HG00323.hp1 HG00621.hp2 others(50): Show |
intron_variant | MODIFIER | c.3398+3384G>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 26/47 | chr2 | 127615987 | |||||||
chr2:127615996 | C | G | 1 | a0005c0008t0001g0213 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.3398+3393C>G | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 26/47 | chr2 | 127615996 | |||||||
chr2:127616053 | G | A | 1 | a0024c0070t0001g0028 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.3398+3450G>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 26/47 | chr2 | 127616053 | |||||||
chr2:127616125 | G | A | 48 | a0001c0005t0001g0049 a0001c0005t0001g0098 a0001c0005t0002g0044 others(45): Show |
48 | HG00280.hp2 HG00642.hp2 HG00735.hp2 others(45): Show |
intron_variant | MODIFIER | c.3398+3522G>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 26/47 | chr2 | 127616125 | |||||||
chr2:127616359 | A | G | 2 | a0009c0014t0001g0104 a0009c0014t0001g0136 |
2 | HG02572.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.3398+3756A>G | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 26/47 | chr2 | 127616359 | |||||||
chr2:127616409 | G | A | 18 | a0004c0007t0001g0162 a0004c0007t0001g0164 a0004c0007t0001g0220 others(15): Show |
18 | HG00280.hp2 HG00642.hp2 HG00735.hp2 others(15): Show |
intron_variant | MODIFIER | c.3398+3806G>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 26/47 | chr2 | 127616409 | |||||||
chr2:127616455 | C | T | 1 | a0001c0002t0001g0137 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.3398+3852C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 26/47 | chr2 | 127616455 | |||||||
chr2:127616533 | G | A | 44 | a0001c0005t0001g0049 a0001c0005t0001g0098 a0001c0005t0002g0044 others(41): Show |
44 | HG00280.hp2 HG00642.hp2 HG00735.hp2 others(41): Show |
intron_variant | MODIFIER | c.3399-3807G>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 26/47 | chr2 | 127616533 | |||||||
chr2:127616605 | T | A | 47 | a0003c0003t0001g0033 a0003c0003t0001g0081 a0003c0003t0001g0109 others(44): Show |
48 | HG00280.hp1 HG00323.hp1 HG00621.hp2 others(45): Show |
intron_variant | MODIFIER | c.3399-3735T>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 26/47 | chr2 | 127616605 | |||||||
chr2:127616802 | C | G | 48 | a0001c0005t0001g0049 a0001c0005t0001g0098 a0001c0005t0002g0044 others(45): Show |
48 | HG00280.hp2 HG00642.hp2 HG00735.hp2 others(45): Show |
intron_variant | MODIFIER | c.3399-3538C>G | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 26/47 | chr2 | 127616802 | |||||||
chr2:127616827 | G | A | 1 | a0007c0024t0001g0227 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.3399-3513G>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 26/47 | chr2 | 127616827 | |||||||
chr2:127616862 | G | A | 2 | a0001c0010t0001g0138 a0001c0010t0001g0139 |
2 | HG02109.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.3399-3478G>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 26/47 | chr2 | 127616862 | |||||||
chr2:127616886 | A | G | 4 | a0009c0014t0001g0104 a0009c0014t0001g0136 a0009c0014t0001g0148 others(1): Show |
4 | HG02486.hp2 HG02572.hp2 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.3399-3454A>G | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 26/47 | chr2 | 127616886 | |||||||
chr2:127616962 | C | T | 48 | a0001c0005t0001g0049 a0001c0005t0001g0098 a0001c0005t0002g0044 others(45): Show |
48 | HG00280.hp2 HG00642.hp2 HG00735.hp2 others(45): Show |
intron_variant | MODIFIER | c.3399-3378C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 26/47 | chr2 | 127616962 | |||||||
chr2:127617036 | T | G | 1 | a0002c0001t0001g0110 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.3399-3304T>G | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 26/47 | chr2 | 127617036 | |||||||
chr2:127617071 | C | G | 1 | a0001c0002t0001g0133 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.3399-3269C>G | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 26/47 | chr2 | 127617071 | |||||||
chr2:127617232 | G | A | 48 | a0001c0005t0001g0049 a0001c0005t0001g0098 a0001c0005t0002g0044 others(45): Show |
48 | HG00280.hp2 HG00642.hp2 HG00735.hp2 others(45): Show |
intron_variant | MODIFIER | c.3399-3108G>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 26/47 | chr2 | 127617232 | |||||||
chr2:127617275 | C | G | 1 | a0021c0046t0003g0078 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.3399-3065C>G | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 26/47 | chr2 | 127617275 | |||||||
chr2:127617453 | A | C | 1 | a0001c0004t0001g0214 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.3399-2887A>C | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 26/47 | chr2 | 127617453 | |||||||
chr2:127617475 | ACTTGTAA others(318): Show |
A | 1 | a0001c0044t0003g0080 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.3399-2849_3399-252 others(4): Show |
MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 26/47 | INFO_REALIGN_3_PRIME | chr2 | 127617475 | ||||||
chr2:127617486 | G | T | 1 | a0021c0046t0003g0078 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.3399-2854G>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 26/47 | chr2 | 127617486 | |||||||
chr2:127617487 | G | GT | 27 | a0001c0002t0001g0036 a0001c0002t0001g0048 a0001c0002t0001g0089 others(24): Show |
27 | HG00738.hp2 HG01081.hp1 HG01981.hp2 others(24): Show |
intron_variant | MODIFIER | c.3399-2827dupT | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 26/47 | INFO_REALIGN_3_PRIME | chr2 | 127617487 | ||||||
chr2:127617487 | G | GTT | 31 | a0001c0002t0001g0027 a0001c0002t0001g0032 a0001c0002t0001g0035 others(28): Show |
32 | HG00099.hp1 HG00735.hp2 HG01099.hp1 others(29): Show |
intron_variant | MODIFIER | c.3399-2828_3399-282 others(6): Show |
MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 26/47 | INFO_REALIGN_3_PRIME | chr2 | 127617487 | ||||||
chr2:127617487 | G | GTTT | 56 | a0001c0002t0001g0034 a0001c0002t0001g0039 a0001c0002t0001g0041 others(53): Show |
56 | HG00280.hp2 HG00323.hp2 HG00733.hp2 others(53): Show |
intron_variant | MODIFIER | c.3399-2829_3399-282 others(7): Show |
MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 26/47 | INFO_REALIGN_3_PRIME | chr2 | 127617487 | ||||||
chr2:127617487 | G | GTTTT | 29 | a0001c0002t0001g0100 a0001c0002t0001g0101 a0001c0002t0001g0106 others(26): Show |
30 | HG00642.hp1 HG00642.hp2 HG00741.hp2 others(27): Show |
intron_variant | MODIFIER | c.3399-2830_3399-282 others(8): Show |
MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 26/47 | INFO_REALIGN_3_PRIME | chr2 | 127617487 | ||||||
chr2:127617487 | G | GTTTTT | 10 | a0001c0013t0001g0167 a0002c0006t0001g0004 a0004c0007t0001g0164 others(7): Show |
10 | HG00738.hp1 HG01106.hp2 HG01175.hp2 others(7): Show |
intron_variant | MODIFIER | c.3399-2831_3399-282 others(9): Show |
MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 26/47 | INFO_REALIGN_3_PRIME | chr2 | 127617487 | ||||||
chr2:127617487 | G | GTTTTTTT | 11 | a0001c0005t0002g0044 a0001c0005t0002g0050 a0001c0005t0002g0094 others(8): Show |
11 | HG01070.hp1 HG01256.hp1 HG01346.hp2 others(8): Show |
intron_variant | MODIFIER | c.3399-2833_3399-282 others(11): Show |
MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 26/47 | INFO_REALIGN_3_PRIME | chr2 | 127617487 | ||||||
chr2:127617487 | G | GTTTTTTT others(1): Show |
12 | a0001c0005t0001g0049 a0001c0005t0001g0098 a0001c0005t0002g0052 others(9): Show |
12 | HG01258.hp2 HG01516.hp1 HG02027.hp2 others(9): Show |
intron_variant | MODIFIER | c.3399-2834_3399-282 others(12): Show |
MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 26/47 | INFO_REALIGN_3_PRIME | chr2 | 127617487 | ||||||
chr2:127617487 | G | T | 1 | a0021c0046t0003g0078 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.3399-2853G>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 26/47 | chr2 | 127617487 | |||||||
chr2:127617487 | GT | G | 21 | a0003c0003t0001g0033 a0003c0003t0001g0081 a0003c0003t0001g0109 others(18): Show |
22 | HG00280.hp1 HG00323.hp1 HG00621.hp2 others(19): Show |
intron_variant | MODIFIER | c.3399-2827delT | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 26/47 | INFO_REALIGN_3_PRIME | chr2 | 127617487 | ||||||
chr2:127617487 | GTT | G | 6 | a0001c0002t0001g0269 a0003c0003t0001g0125 a0003c0003t0001g0230 others(3): Show |
6 | HG02074.hp2 HG02647.hp1 NA18747.hp2 others(3): Show |
intron_variant | MODIFIER | c.3399-2828_3399-282 others(6): Show |
MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 26/47 | INFO_REALIGN_3_PRIME | chr2 | 127617487 | ||||||
chr2:127617487 | GTTTTTTT others(6): Show |
G | 1 | a0001c0004t0001g0242 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.3399-2839_3399-282 others(17): Show |
MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 26/47 | INFO_REALIGN_3_PRIME | chr2 | 127617487 | ||||||
chr2:127617487 | GTTTTTTT others(7): Show |
G | 3 | a0001c0004t0001g0066 a0001c0004t0001g0124 a0001c0004t0001g0232 |
3 | NA18612.hp2 NA18942.hp2 NA19070.hp1 |
intron_variant | MODIFIER | c.3399-2840_3399-282 others(18): Show |
MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 26/47 | INFO_REALIGN_3_PRIME | chr2 | 127617487 | ||||||
chr2:127617503 | T | G | 1 | a0007c0025t0001g0042 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.3399-2837T>G | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 26/47 | chr2 | 127617503 | |||||||
chr2:127617519 | G | A | 8 | a0004c0007t0001g0220 a0004c0007t0001g0222 a0004c0007t0003g0007 others(5): Show |
8 | HG00280.hp2 HG00642.hp2 HG01168.hp1 others(5): Show |
intron_variant | MODIFIER | c.3399-2821G>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 26/47 | chr2 | 127617519 | |||||||
chr2:127617550 | C | CG | 9 | a0002c0006t0001g0015 a0006c0009t0001g0020 a0006c0009t0001g0037 others(6): Show |
9 | HG00323.hp2 HG00733.hp2 HG01106.hp1 others(6): Show |
intron_variant | MODIFIER | c.3399-2788dupG | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 26/47 | INFO_REALIGN_3_PRIME | chr2 | 127617550 | ||||||
chr2:127617566 | C | A | 99 | a0001c0005t0001g0049 a0001c0005t0001g0098 a0001c0005t0002g0044 others(96): Show |
101 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(98): Show |
intron_variant | MODIFIER | c.3399-2774C>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 26/47 | chr2 | 127617566 | |||||||
chr2:127617567 | A | G | 1 | a0028c0064t0002g0143 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.3399-2773A>G | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 26/47 | chr2 | 127617567 | |||||||
chr2:127617591 | T | C | 1 | a0021c0046t0003g0078 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.3399-2749T>C | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 26/47 | chr2 | 127617591 | |||||||
chr2:127617596 | A | G | 205 | a0001c0002t0001g0027 a0001c0002t0001g0032 a0001c0002t0001g0034 others(202): Show |
209 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(206): Show |
intron_variant | MODIFIER | c.3399-2744A>G | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 26/47 | chr2 | 127617596 | |||||||
chr2:127617643 | C | CT | 2 | a0011c0016t0001g0008 a0011c0016t0001g0141 |
3 | HG02630.hp1 HG03041.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.3399-2697_3399-269 others(5): Show |
MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 26/47 | chr2 | 127617643 | |||||||
chr2:127617658 | G | T | 1 | a0045c0065t0001g0140 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.3399-2682G>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 26/47 | chr2 | 127617658 | |||||||
chr2:127617659 | C | T | 6 | a0004c0007t0001g0162 a0004c0007t0001g0164 a0004c0007t0001g0259 others(3): Show |
6 | HG00735.hp2 HG01106.hp2 HG01175.hp2 others(3): Show |
intron_variant | MODIFIER | c.3399-2681C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 26/47 | chr2 | 127617659 | |||||||
chr2:127617664 | G | A | 1 | a0045c0065t0001g0140 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.3399-2676G>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 26/47 | chr2 | 127617664 | |||||||
chr2:127617692 | C | T | 51 | a0001c0005t0001g0049 a0001c0005t0001g0098 a0001c0005t0002g0044 others(48): Show |
52 | HG00280.hp2 HG00642.hp2 HG00735.hp2 others(49): Show |
intron_variant | MODIFIER | c.3399-2648C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 26/47 | chr2 | 127617692 | |||||||
chr2:127617710 | G | T | 1 | a0040c0060t0001g0055 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.3399-2630G>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 26/47 | chr2 | 127617710 | |||||||
chr2:127617748 | C | T | 1 | a0021c0046t0003g0078 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.3399-2592C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 26/47 | chr2 | 127617748 | |||||||
chr2:127617779 | G | A | 2 | a0002c0012t0001g0115 a0002c0012t0001g0191 |
2 | NA19000.hp2 NA19079.hp1 |
intron_variant | MODIFIER | c.3399-2561G>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 26/47 | chr2 | 127617779 | |||||||
chr2:127617797 | C | T | 1 | a0002c0001t0001g0175 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.3399-2543C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 26/47 | chr2 | 127617797 | |||||||
chr2:127617815 | T | A | 1 | a0001c0044t0003g0080 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.3399-2525T>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 26/47 | chr2 | 127617815 | |||||||
chr2:127617855 | G | GT | 6 | a0002c0001t0001g0185 a0003c0003t0001g0244 a0005c0008t0001g0209 others(3): Show |
6 | HG01256.hp2 HG02486.hp2 HG02683.hp1 others(3): Show |
intron_variant | MODIFIER | c.3399-2471dupT | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 26/47 | INFO_REALIGN_3_PRIME | chr2 | 127617855 | ||||||
chr2:127617855 | G | GTT | 82 | a0001c0002t0001g0036 a0001c0005t0001g0049 a0001c0005t0001g0098 others(79): Show |
82 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(79): Show |
intron_variant | MODIFIER | c.3399-2472_3399-247 others(6): Show |
MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 26/47 | INFO_REALIGN_3_PRIME | chr2 | 127617855 | ||||||
chr2:127617855 | G | GTTT | 108 | a0001c0002t0001g0027 a0001c0002t0001g0032 a0001c0002t0001g0034 others(105): Show |
111 | HG00099.hp1 HG00323.hp2 HG00642.hp1 others(108): Show |
intron_variant | MODIFIER | c.3399-2473_3399-247 others(7): Show |
MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 26/47 | INFO_REALIGN_3_PRIME | chr2 | 127617855 | ||||||
chr2:127617901 | A | G | 150 | a0001c0002t0001g0027 a0001c0002t0001g0032 a0001c0002t0001g0034 others(147): Show |
152 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(149): Show |
intron_variant | MODIFIER | c.3399-2439A>G | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 26/47 | chr2 | 127617901 | |||||||
chr2:127617967 | C | T | 48 | a0003c0003t0001g0033 a0003c0003t0001g0081 a0003c0003t0001g0109 others(45): Show |
49 | HG00280.hp1 HG00323.hp1 HG00621.hp2 others(46): Show |
intron_variant | MODIFIER | c.3399-2373C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 26/47 | chr2 | 127617967 | |||||||
chr2:127617982 | C | T | 1 | a0002c0006t0001g0156 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.3399-2358C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 26/47 | chr2 | 127617982 | |||||||
chr2:127617990 | A | G | 44 | a0001c0005t0001g0049 a0001c0005t0001g0098 a0001c0005t0002g0044 others(41): Show |
44 | HG00280.hp2 HG00642.hp2 HG00735.hp2 others(41): Show |
intron_variant | MODIFIER | c.3399-2350A>G | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 26/47 | chr2 | 127617990 | |||||||
chr2:127618095 | G | T | 53 | a0001c0005t0001g0049 a0001c0005t0001g0098 a0001c0005t0002g0044 others(50): Show |
54 | HG00280.hp2 HG00642.hp2 HG00735.hp2 others(51): Show |
intron_variant | MODIFIER | c.3399-2245G>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 26/47 | chr2 | 127618095 | |||||||
chr2:127618096 | C | G | 1 | a0001c0005t0002g0065 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.3399-2244C>G | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 26/47 | chr2 | 127618096 | |||||||
chr2:127618147 | C | T | 99 | a0001c0005t0001g0049 a0001c0005t0001g0098 a0001c0005t0002g0044 others(96): Show |
101 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(98): Show |
intron_variant | MODIFIER | c.3399-2193C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 26/47 | chr2 | 127618147 | |||||||
chr2:127618157 | C | A | 1 | a0001c0002t0001g0137 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.3399-2183C>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 26/47 | chr2 | 127618157 | |||||||
chr2:127618238 | G | A | 2 | a0017c0072t0001g0012 a0046c0073t0001g0068 |
2 | HG02922.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.3399-2102G>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 26/47 | chr2 | 127618238 | |||||||
chr2:127618246 | G | C | 48 | a0001c0005t0001g0049 a0001c0005t0001g0098 a0001c0005t0002g0044 others(45): Show |
48 | HG00280.hp2 HG00642.hp2 HG00735.hp2 others(45): Show |
intron_variant | MODIFIER | c.3399-2094G>C | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 26/47 | chr2 | 127618246 | |||||||
chr2:127618260 | G | T | 1 | a0031c0074t0001g0026 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.3399-2080G>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 26/47 | chr2 | 127618260 | |||||||
chr2:127618270 | G | A | 1 | a0001c0044t0003g0080 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.3399-2070G>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 26/47 | chr2 | 127618270 | |||||||
chr2:127618271 | T | C | 1 | a0002c0001t0001g0176 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.3399-2069T>C | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 26/47 | chr2 | 127618271 | |||||||
chr2:127618277 | T | C | 5 | a0003c0003t0001g0127 a0003c0003t0001g0129 a0003c0003t0001g0210 others(2): Show |
5 | HG01123.hp2 HG01433.hp2 HG01975.hp2 others(2): Show |
intron_variant | MODIFIER | c.3399-2063T>C | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 26/47 | chr2 | 127618277 | |||||||
chr2:127618279 | A | G | 2 | a0009c0014t0001g0104 a0009c0014t0001g0136 |
2 | HG02572.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.3399-2061A>G | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 26/47 | chr2 | 127618279 | |||||||
chr2:127618367 | C | T | 1 | a0001c0017t0004g0024 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.3399-1973C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 26/47 | chr2 | 127618367 | |||||||
chr2:127618368 | A | G | 202 | a0001c0002t0001g0027 a0001c0002t0001g0032 a0001c0002t0001g0034 others(199): Show |
206 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(203): Show |
intron_variant | MODIFIER | c.3399-1972A>G | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 26/47 | chr2 | 127618368 | |||||||
chr2:127618378 | A | G | 1 | a0045c0065t0001g0140 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.3399-1962A>G | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 26/47 | chr2 | 127618378 | |||||||
chr2:127618420 | G | A | 1 | a0001c0044t0003g0080 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.3399-1920G>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 26/47 | chr2 | 127618420 | |||||||
chr2:127618424 | C | T | 51 | a0003c0003t0001g0033 a0003c0003t0001g0081 a0003c0003t0001g0109 others(48): Show |
53 | HG00280.hp1 HG00323.hp1 HG00621.hp2 others(50): Show |
intron_variant | MODIFIER | c.3399-1916C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 26/47 | chr2 | 127618424 | |||||||
chr2:127618425 | G | A | 3 | a0001c0044t0003g0080 a0021c0046t0003g0078 a0024c0070t0001g0028 |
3 | HG01891.hp2 HG02257.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.3399-1915G>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 26/47 | chr2 | 127618425 | |||||||
chr2:127618443 | C | T | 102 | a0001c0005t0001g0049 a0001c0005t0001g0098 a0001c0005t0002g0044 others(99): Show |
104 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(101): Show |
intron_variant | MODIFIER | c.3399-1897C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 26/47 | chr2 | 127618443 | |||||||
chr2:127618460 | T | G | 47 | a0003c0003t0001g0033 a0003c0003t0001g0081 a0003c0003t0001g0109 others(44): Show |
48 | HG00280.hp1 HG00323.hp1 HG00621.hp2 others(45): Show |
intron_variant | MODIFIER | c.3399-1880T>G | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 26/47 | chr2 | 127618460 | |||||||
chr2:127618497 | T | A | 1 | a0002c0001t0001g0188 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.3399-1843T>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 26/47 | chr2 | 127618497 | |||||||
chr2:127618542 | C | T | 220 | a0001c0002t0001g0027 a0001c0002t0001g0032 a0001c0002t0001g0034 others(217): Show |
224 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(221): Show |
intron_variant | MODIFIER | c.3399-1798C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 26/47 | chr2 | 127618542 | |||||||
chr2:127618600 | T | C | 54 | a0003c0003t0001g0033 a0003c0003t0001g0081 a0003c0003t0001g0109 others(51): Show |
56 | HG00280.hp1 HG00323.hp1 HG00621.hp2 others(53): Show |
intron_variant | MODIFIER | c.3399-1740T>C | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 26/47 | chr2 | 127618600 | |||||||
chr2:127618613 | C | T | 1 | a0024c0070t0001g0028 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.3399-1727C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 26/47 | chr2 | 127618613 | |||||||
chr2:127618632 | T | C | 1 | a0045c0065t0001g0140 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.3399-1708T>C | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 26/47 | chr2 | 127618632 | |||||||
chr2:127618826 | G | A | 100 | a0001c0005t0001g0049 a0001c0005t0001g0098 a0001c0005t0002g0044 others(97): Show |
102 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(99): Show |
intron_variant | MODIFIER | c.3399-1514G>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 26/47 | chr2 | 127618826 | |||||||
chr2:127618885 | A | C | 3 | a0011c0016t0001g0008 a0011c0016t0001g0141 a0029c0048t0001g0132 |
4 | HG02630.hp1 HG03041.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.3399-1455A>C | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 26/47 | chr2 | 127618885 | |||||||
chr2:127618984 | C | T | 3 | a0011c0016t0001g0008 a0011c0016t0001g0141 a0029c0048t0001g0132 |
4 | HG02630.hp1 HG03041.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.3399-1356C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 26/47 | chr2 | 127618984 | |||||||
chr2:127619038 | G | GGTGGGCG others(11): Show |
3 | a0011c0016t0001g0008 a0011c0016t0001g0141 a0029c0048t0001g0132 |
4 | HG02630.hp1 HG03041.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.3399-1296_3399-127 others(22): Show |
MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 26/47 | INFO_REALIGN_3_PRIME | chr2 | 127619038 | ||||||
chr2:127619054 | A | ATTGTGGG others(11): Show |
5 | a0001c0010t0001g0163 a0012c0022t0001g0120 a0012c0022t0001g0217 others(2): Show |
5 | HG01069.hp1 HG01071.hp1 HG01346.hp1 others(2): Show |
intron_variant | MODIFIER | c.3399-1250_3399-123 others(22): Show |
MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 26/47 | INFO_REALIGN_3_PRIME | chr2 | 127619054 | ||||||
chr2:127619056 | TGTG | T | 47 | a0003c0003t0001g0033 a0003c0003t0001g0081 a0003c0003t0001g0109 others(44): Show |
48 | HG00280.hp1 HG00323.hp1 HG00621.hp2 others(45): Show |
intron_variant | MODIFIER | c.3399-1282_3399-128 others(7): Show |
MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 26/47 | INFO_REALIGN_3_PRIME | chr2 | 127619056 | ||||||
chr2:127619062 | G | A | 45 | a0001c0005t0001g0049 a0001c0005t0001g0098 a0001c0005t0002g0044 others(42): Show |
45 | HG00280.hp2 HG00642.hp2 HG00735.hp2 others(42): Show |
intron_variant | MODIFIER | c.3399-1278G>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 26/47 | chr2 | 127619062 | |||||||
chr2:127619138 | A | G | 3 | a0011c0016t0001g0008 a0011c0016t0001g0141 a0029c0048t0001g0132 |
4 | HG02630.hp1 HG03041.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.3399-1202A>G | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 26/47 | chr2 | 127619138 | |||||||
chr2:127619149 | G | C | 4 | a0002c0006t0001g0004 a0002c0006t0001g0158 a0002c0006t0001g0159 others(1): Show |
5 | HG00738.hp1 HG00741.hp2 HG01070.hp2 others(2): Show |
intron_variant | MODIFIER | c.3399-1191G>C | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 26/47 | chr2 | 127619149 | |||||||
chr2:127619173 | T | C | 3 | a0011c0016t0001g0008 a0011c0016t0001g0141 a0029c0048t0001g0132 |
4 | HG02630.hp1 HG03041.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.3399-1167T>C | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 26/47 | chr2 | 127619173 | |||||||
chr2:127619226 | GTGGTTGG others(11): Show |
G | 2 | a0007c0024t0001g0086 a0007c0024t0001g0227 |
2 | HG03195.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.3399-1099_3399-108 others(22): Show |
MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 26/47 | INFO_REALIGN_3_PRIME | chr2 | 127619226 | ||||||
chr2:127619230 | TTGGGTTG others(44): Show |
T | 3 | a0011c0016t0001g0008 a0011c0016t0001g0141 a0029c0048t0001g0132 |
4 | HG02630.hp1 HG03041.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.3399-1104_3399-105 others(55): Show |
MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 26/47 | INFO_REALIGN_3_PRIME | chr2 | 127619230 | ||||||
chr2:127619260 | C | T | 1 | a0001c0044t0003g0080 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.3399-1080C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 26/47 | chr2 | 127619260 | |||||||
chr2:127619279 | G | A | 6 | a0004c0007t0001g0162 a0004c0007t0001g0164 a0004c0007t0001g0259 others(3): Show |
6 | HG00735.hp2 HG01106.hp2 HG01175.hp2 others(3): Show |
intron_variant | MODIFIER | c.3399-1061G>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 26/47 | chr2 | 127619279 | |||||||
chr2:127619285 | G | A | 3 | a0011c0016t0001g0008 a0011c0016t0001g0141 a0029c0048t0001g0132 |
4 | HG02630.hp1 HG03041.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.3399-1055G>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 26/47 | chr2 | 127619285 | |||||||
chr2:127619294 | G | T | 3 | a0011c0016t0001g0008 a0011c0016t0001g0141 a0029c0048t0001g0132 |
4 | HG02630.hp1 HG03041.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.3399-1046G>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 26/47 | chr2 | 127619294 | |||||||
chr2:127619303 | G | A | 3 | a0011c0016t0001g0008 a0011c0016t0001g0141 a0029c0048t0001g0132 |
4 | HG02630.hp1 HG03041.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.3399-1037G>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 26/47 | chr2 | 127619303 | |||||||
chr2:127619336 | T | C | 3 | a0011c0016t0001g0008 a0011c0016t0001g0141 a0029c0048t0001g0132 |
4 | HG02630.hp1 HG03041.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.3399-1004T>C | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 26/47 | chr2 | 127619336 | |||||||
chr2:127619349 | C | T | 3 | a0011c0016t0001g0008 a0011c0016t0001g0141 a0029c0048t0001g0132 |
4 | HG02630.hp1 HG03041.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.3399-991C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 26/47 | chr2 | 127619349 | |||||||
chr2:127619353 | G | A | 3 | a0011c0016t0001g0008 a0011c0016t0001g0141 a0029c0048t0001g0132 |
4 | HG02630.hp1 HG03041.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.3399-987G>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 26/47 | chr2 | 127619353 | |||||||
chr2:127619361 | C | G | 6 | a0008c0015t0001g0107 a0008c0015t0001g0168 a0008c0015t0001g0169 others(3): Show |
7 | HG02145.hp1 HG02280.hp1 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.3399-979C>G | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 26/47 | chr2 | 127619361 | |||||||
chr2:127619365 | AGCTGAGT others(11): Show |
A | 3 | a0011c0016t0001g0008 a0011c0016t0001g0141 a0029c0048t0001g0132 |
4 | HG02630.hp1 HG03041.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.3399-970_3399-953d others(20): Show |
MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 26/47 | INFO_REALIGN_3_PRIME | chr2 | 127619365 | ||||||
chr2:127619383 | G | A | 1 | a0010c0020t0001g0150 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.3399-957G>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 26/47 | chr2 | 127619383 | |||||||
chr2:127619400 | T | C | 3 | a0011c0016t0001g0008 a0011c0016t0001g0141 a0029c0048t0001g0132 |
4 | HG02630.hp1 HG03041.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.3399-940T>C | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 26/47 | chr2 | 127619400 | |||||||
chr2:127619403 | A | C | 3 | a0011c0016t0001g0008 a0011c0016t0001g0141 a0029c0048t0001g0132 |
4 | HG02630.hp1 HG03041.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.3399-937A>C | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 26/47 | chr2 | 127619403 | |||||||
chr2:127619407 | A | G | 3 | a0011c0016t0001g0008 a0011c0016t0001g0141 a0029c0048t0001g0132 |
4 | HG02630.hp1 HG03041.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.3399-933A>G | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 26/47 | chr2 | 127619407 | |||||||
chr2:127619473 | C | T | 1 | a0001c0004t0001g0246 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.3399-867C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 26/47 | chr2 | 127619473 | |||||||
chr2:127619497 | C | T | 2 | a0009c0014t0001g0104 a0009c0014t0001g0136 |
2 | HG02572.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.3399-843C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 26/47 | chr2 | 127619497 | |||||||
chr2:127619679 | T | G | 3 | a0011c0016t0001g0008 a0011c0016t0001g0141 a0029c0048t0001g0132 |
4 | HG02630.hp1 HG03041.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.3399-661T>G | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 26/47 | chr2 | 127619679 | |||||||
chr2:127619857 | C | T | 3 | a0011c0016t0001g0008 a0011c0016t0001g0141 a0029c0048t0001g0132 |
4 | HG02630.hp1 HG03041.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.3399-483C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 26/47 | chr2 | 127619857 | |||||||
chr2:127619983 | G | A | 1 | a0002c0006t0001g0014 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.3399-357G>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 26/47 | chr2 | 127619983 | |||||||
chr2:127620003 | G | A | 1 | a0027c0057t0001g0079 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.3399-337G>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 26/47 | chr2 | 127620003 | |||||||
chr2:127620126 | G | A | 1 | a0001c0002t0001g0269 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.3399-214G>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 26/47 | chr2 | 127620126 | |||||||
chr2:127620213 | C | T | 1 | a0001c0002t0001g0036 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.3399-127C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 26/47 | chr2 | 127620213 | |||||||
chr2:127620216 | C | T | 3 | a0011c0016t0001g0008 a0011c0016t0001g0141 a0029c0048t0001g0132 |
4 | HG02630.hp1 HG03041.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.3399-124C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 26/47 | chr2 | 127620216 | |||||||
chr2:127620229 | C | A | 3 | a0011c0016t0001g0008 a0011c0016t0001g0141 a0029c0048t0001g0132 |
4 | HG02630.hp1 HG03041.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.3399-111C>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 26/47 | chr2 | 127620229 | |||||||
chr2:127620258 | C | G | 205 | a0001c0002t0001g0027 a0001c0002t0001g0032 a0001c0002t0001g0034 others(202): Show |
209 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(206): Show |
intron_variant | MODIFIER | c.3399-82C>G | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 26/47 | chr2 | 127620258 | |||||||
chr2:127620267 | T | C | 18 | a0004c0007t0001g0162 a0004c0007t0001g0164 a0004c0007t0001g0220 others(15): Show |
18 | HG00280.hp2 HG00642.hp2 HG00735.hp2 others(15): Show |
intron_variant | MODIFIER | c.3399-73T>C | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 26/47 | chr2 | 127620267 | |||||||
chr2:127620561 | A | C | 102 | a0001c0005t0001g0049 a0001c0005t0001g0098 a0001c0005t0002g0044 others(99): Show |
104 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(101): Show |
intron_variant | MODIFIER | c.3525+95A>C | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 27/47 | chr2 | 127620561 | |||||||
chr2:127620562 | C | T | 3 | a0001c0044t0003g0080 a0008c0015t0001g0047 a0008c0063t0001g0257 |
3 | HG01243.hp2 HG02809.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.3525+96C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 27/47 | chr2 | 127620562 | |||||||
chr2:127620619 | C | T | 1 | a0021c0046t0003g0078 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.3525+153C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 27/47 | chr2 | 127620619 | |||||||
chr2:127620623 | A | C | 3 | a0011c0016t0001g0008 a0011c0016t0001g0141 a0029c0048t0001g0132 |
4 | HG02630.hp1 HG03041.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.3525+157A>C | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 27/47 | chr2 | 127620623 | |||||||
chr2:127620680 | G | A | 1 | a0024c0070t0001g0028 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.3525+214G>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 27/47 | chr2 | 127620680 | |||||||
chr2:127620685 | G | T | 1 | a0001c0004t0001g0218 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.3525+219G>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 27/47 | chr2 | 127620685 | |||||||
chr2:127620726 | T | C | 3 | a0011c0016t0001g0008 a0011c0016t0001g0141 a0029c0048t0001g0132 |
4 | HG02630.hp1 HG03041.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.3525+260T>C | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 27/47 | chr2 | 127620726 | |||||||
chr2:127620760 | G | A | 1 | a0045c0065t0001g0140 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.3525+294G>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 27/47 | chr2 | 127620760 | |||||||
chr2:127620790 | G | T | 3 | a0001c0005t0002g0052 a0001c0005t0002g0095 a0034c0059t0001g0031 |
3 | HG01256.hp1 HG01258.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.3525+324G>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 27/47 | chr2 | 127620790 | |||||||
chr2:127620812 | C | T | 1 | a0008c0042t0001g0064 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.3525+346C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 27/47 | chr2 | 127620812 | |||||||
chr2:127620884 | C | G | 2 | a0017c0072t0001g0012 a0046c0073t0001g0068 |
2 | HG02922.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.3525+418C>G | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 27/47 | chr2 | 127620884 | |||||||
chr2:127620965 | C | T | 2 | a0007c0024t0001g0086 a0021c0046t0003g0078 |
2 | HG01891.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.3525+499C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 27/47 | chr2 | 127620965 | |||||||
chr2:127620988 | G | A | 102 | a0001c0005t0001g0049 a0001c0005t0001g0098 a0001c0005t0002g0044 others(99): Show |
104 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(101): Show |
intron_variant | MODIFIER | c.3525+522G>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 27/47 | chr2 | 127620988 | |||||||
chr2:127620998 | C | T | 3 | a0001c0005t0001g0049 a0001c0005t0002g0044 a0002c0011t0002g0108 |
3 | HG04184.hp2 NA18968.hp2 NA18975.hp2 |
intron_variant | MODIFIER | c.3525+532C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 27/47 | chr2 | 127620998 | |||||||
chr2:127621249 | T | G | 4 | a0001c0017t0004g0024 a0001c0017t0004g0025 a0001c0017t0004g0075 others(1): Show |
4 | HG02258.hp2 HG02630.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.3526-733T>G | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 27/47 | chr2 | 127621249 | |||||||
chr2:127621253 | AT | A | 146 | a0001c0002t0001g0027 a0001c0002t0001g0032 a0001c0002t0001g0034 others(143): Show |
149 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(146): Show |
intron_variant | MODIFIER | c.3526-718delT | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 27/47 | INFO_REALIGN_3_PRIME | chr2 | 127621253 | ||||||
chr2:127621259 | T | G | 1 | a0001c0044t0003g0080 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.3526-723T>G | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 27/47 | chr2 | 127621259 | |||||||
chr2:127621263 | T | TG | 4 | a0001c0005t0002g0050 a0001c0005t0002g0052 a0001c0005t0002g0095 others(1): Show |
4 | HG01256.hp1 HG01258.hp2 HG01346.hp2 others(1): Show |
intron_variant | MODIFIER | c.3526-719_3526-718i others(3): Show |
MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 27/47 | chr2 | 127621263 | |||||||
chr2:127621264 | T | G | 49 | a0001c0002t0001g0035 a0001c0002t0001g0060 a0001c0005t0001g0049 others(46): Show |
49 | HG00099.hp1 HG00280.hp2 HG00642.hp2 others(46): Show |
intron_variant | MODIFIER | c.3526-718T>G | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 27/47 | chr2 | 127621264 | |||||||
chr2:127621265 | G | T | 53 | a0001c0002t0001g0035 a0001c0002t0001g0060 a0001c0005t0001g0049 others(50): Show |
53 | HG00099.hp1 HG00280.hp2 HG00642.hp2 others(50): Show |
intron_variant | MODIFIER | c.3526-717G>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 27/47 | chr2 | 127621265 | |||||||
chr2:127621266 | T | G | 1 | a0002c0012t0001g0206 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.3526-716T>G | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 27/47 | chr2 | 127621266 | |||||||
chr2:127621267 | T | G | 2 | a0024c0070t0001g0028 a0028c0064t0002g0143 |
2 | HG02257.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.3526-715T>G | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 27/47 | chr2 | 127621267 | |||||||
chr2:127621303 | G | A | 1 | a0011c0016t0001g0141 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.3526-679G>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 27/47 | chr2 | 127621303 | |||||||
chr2:127621460 | C | T | 1 | a0001c0002t0001g0137 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.3526-522C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 27/47 | chr2 | 127621460 | |||||||
chr2:127621753 | T | C | 1 | a0001c0044t0003g0080 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.3526-229T>C | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 27/47 | chr2 | 127621753 | |||||||
chr2:127621765 | A | G | 105 | a0001c0002t0001g0027 a0001c0002t0001g0032 a0001c0002t0001g0034 others(102): Show |
107 | HG00099.hp1 HG00323.hp2 HG00642.hp1 others(104): Show |
intron_variant | MODIFIER | c.3526-217A>G | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 27/47 | chr2 | 127621765 | |||||||
chr2:127621863 | G | T | 4 | a0009c0014t0001g0104 a0009c0014t0001g0136 a0009c0014t0001g0148 others(1): Show |
4 | HG02486.hp2 HG02572.hp2 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.3526-119G>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 27/47 | chr2 | 127621863 | |||||||
chr2:127621907 | G | A | 18 | a0001c0002t0001g0027 a0001c0002t0001g0032 a0001c0002t0001g0034 others(15): Show |
18 | HG01099.hp1 HG01943.hp1 HG01952.hp2 others(15): Show |
intron_variant | MODIFIER | c.3526-75G>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 27/47 | chr2 | 127621907 | |||||||
chr2:127622144 | C | T | 3 | a0011c0016t0001g0008 a0011c0016t0001g0141 a0029c0048t0001g0132 |
4 | HG02630.hp1 HG03041.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.3645+43C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 28/47 | chr2 | 127622144 | |||||||
chr2:127622231 | A | G | 1 | a0045c0065t0001g0140 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.3645+130A>G | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 28/47 | chr2 | 127622231 | |||||||
chr2:127622261 | T | C | 1 | a0024c0070t0001g0028 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.3645+160T>C | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 28/47 | chr2 | 127622261 | |||||||
chr2:127622274 | C | T | 1 | a0001c0044t0003g0080 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.3645+173C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 28/47 | chr2 | 127622274 | |||||||
chr2:127622375 | G | A | 4 | a0001c0017t0004g0024 a0001c0017t0004g0025 a0001c0017t0004g0075 others(1): Show |
4 | HG02258.hp2 HG02630.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.3645+274G>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 28/47 | chr2 | 127622375 | |||||||
chr2:127622376 | C | G | 5 | a0001c0010t0001g0163 a0012c0022t0001g0120 a0012c0022t0001g0217 others(2): Show |
5 | HG01069.hp1 HG01071.hp1 HG01346.hp1 others(2): Show |
intron_variant | MODIFIER | c.3645+275C>G | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 28/47 | chr2 | 127622376 | |||||||
chr2:127622416 | G | C | 46 | a0003c0003t0001g0033 a0003c0003t0001g0081 a0003c0003t0001g0109 others(43): Show |
47 | HG00280.hp1 HG00323.hp1 HG00621.hp2 others(44): Show |
intron_variant | MODIFIER | c.3645+315G>C | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 28/47 | chr2 | 127622416 | |||||||
chr2:127622524 | G | A | 1 | a0030c0052t0001g0087 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.3645+423G>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 28/47 | chr2 | 127622524 | |||||||
chr2:127622526 | T | C | 1 | a0027c0057t0001g0079 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.3645+425T>C | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 28/47 | chr2 | 127622526 | |||||||
chr2:127622622 | C | T | 1 | a0001c0002t0001g0137 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.3645+521C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 28/47 | chr2 | 127622622 | |||||||
chr2:127622646 | G | A | 2 | a0002c0001t0001g0184 a0016c0027t0001g0226 |
2 | HG01891.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.3645+545G>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 28/47 | chr2 | 127622646 | |||||||
chr2:127622712 | C | G | 2 | a0007c0023t0001g0122 a0007c0023t0001g0149 |
2 | HG02109.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.3646-490C>G | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 28/47 | chr2 | 127622712 | |||||||
chr2:127622737 | C | T | 1 | a0021c0046t0003g0078 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.3646-465C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 28/47 | chr2 | 127622737 | |||||||
chr2:127622959 | C | T | 1 | a0002c0001t0006g0180 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.3646-243C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 28/47 | chr2 | 127622959 | |||||||
chr2:127623104 | C | T | 1 | a0021c0046t0003g0078 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.3646-98C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 28/47 | chr2 | 127623104 | |||||||
chr2:127623397 | C | T | 8 | a0001c0010t0001g0138 a0001c0010t0001g0139 a0001c0010t0001g0228 others(5): Show |
8 | HG02109.hp2 HG02451.hp1 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.3819+22C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 29/47 | chr2 | 127623397 | |||||||
chr2:127623509 | C | T | 1 | a0001c0010t0001g0264 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.3819+134C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 29/47 | chr2 | 127623509 | |||||||
chr2:127623579 | G | A | 98 | a0001c0005t0001g0049 a0001c0005t0001g0098 a0001c0005t0002g0044 others(95): Show |
99 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(96): Show |
intron_variant | MODIFIER | c.3819+204G>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 29/47 | chr2 | 127623579 | |||||||
chr2:127623636 | A | C | 2 | a0002c0006t0001g0015 a0002c0006t0001g0016 |
2 | HG00741.hp1 HG03239.hp2 |
intron_variant | MODIFIER | c.3819+261A>C | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 29/47 | chr2 | 127623636 | |||||||
chr2:127623752 | A | G | 1 | a0001c0044t0003g0080 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.3820-341A>G | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 29/47 | chr2 | 127623752 | |||||||
chr2:127623753 | C | A | 1 | a0001c0044t0003g0080 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.3820-340C>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 29/47 | chr2 | 127623753 | |||||||
chr2:127623803 | T | TCAGA | 3 | a0011c0016t0001g0008 a0011c0016t0001g0141 a0029c0048t0001g0132 |
4 | HG02630.hp1 HG03041.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.3820-288_3820-287i others(6): Show |
MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 29/47 | INFO_REALIGN_3_PRIME | chr2 | 127623803 | ||||||
chr2:127623810 | C | G | 2 | a0007c0023t0001g0122 a0007c0023t0001g0149 |
2 | HG02109.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.3820-283C>G | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 29/47 | chr2 | 127623810 | |||||||
chr2:127623810 | C | T | 1 | a0001c0005t0002g0131 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.3820-283C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 29/47 | chr2 | 127623810 | |||||||
chr2:127623828 | C | T | 3 | a0011c0016t0001g0008 a0011c0016t0001g0141 a0029c0048t0001g0132 |
4 | HG02630.hp1 HG03041.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.3820-265C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 29/47 | chr2 | 127623828 | |||||||
chr2:127623969 | C | T | 3 | a0011c0016t0001g0008 a0011c0016t0001g0141 a0029c0048t0001g0132 |
4 | HG02630.hp1 HG03041.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.3820-124C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 29/47 | chr2 | 127623969 | |||||||
chr2:127624019 | C | T | 46 | a0003c0003t0001g0033 a0003c0003t0001g0081 a0003c0003t0001g0109 others(43): Show |
47 | HG00280.hp1 HG00323.hp1 HG00621.hp2 others(44): Show |
intron_variant | MODIFIER | c.3820-74C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 29/47 | chr2 | 127624019 | |||||||
chr2:127624020 | G | A | 4 | a0001c0017t0004g0024 a0001c0017t0004g0025 a0001c0017t0004g0075 others(1): Show |
4 | HG02258.hp2 HG02630.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.3820-73G>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 29/47 | chr2 | 127624020 | |||||||
chr2:127624414 | A | C | 4 | a0002c0001t0001g0006 a0002c0001t0001g0177 a0002c0001t0001g0185 others(1): Show |
4 | HG02135.hp2 NA18964.hp1 NA18966.hp1 others(1): Show |
intron_variant | MODIFIER | c.4047+94A>C | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 30/47 | chr2 | 127624414 | |||||||
chr2:127624519 | C | T | 1 | a0004c0007t0001g0162 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.4047+199C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 30/47 | chr2 | 127624519 | |||||||
chr2:127624569 | C | T | 3 | a0001c0018t0001g0266 a0001c0018t0001g0267 a0001c0018t0001g0268 |
3 | HG02622.hp1 HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.4047+249C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 30/47 | chr2 | 127624569 | |||||||
chr2:127624607 | C | T | 3 | a0011c0016t0001g0008 a0011c0016t0001g0141 a0029c0048t0001g0132 |
4 | HG02630.hp1 HG03041.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.4047+287C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 30/47 | chr2 | 127624607 | |||||||
chr2:127624761 | G | A | 1 | a0002c0011t0002g0187 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.4047+441G>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 30/47 | chr2 | 127624761 | |||||||
chr2:127624862 | G | A | 3 | a0011c0016t0001g0008 a0011c0016t0001g0141 a0029c0048t0001g0132 |
4 | HG02630.hp1 HG03041.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.4048-506G>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 30/47 | chr2 | 127624862 | |||||||
chr2:127624898 | A | G | 2 | a0007c0023t0001g0122 a0007c0023t0001g0149 |
2 | HG02109.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.4048-470A>G | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 30/47 | chr2 | 127624898 | |||||||
chr2:127624914 | C | T | 1 | a0009c0014t0001g0148 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.4048-454C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 30/47 | chr2 | 127624914 | |||||||
chr2:127625079 | G | A | 1 | a0002c0006t0001g0015 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.4048-289G>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 30/47 | chr2 | 127625079 | |||||||
chr2:127625082 | G | A | 26 | a0001c0005t0001g0049 a0001c0005t0001g0098 a0001c0005t0002g0044 others(23): Show |
26 | HG01070.hp1 HG01256.hp1 HG01258.hp2 others(23): Show |
intron_variant | MODIFIER | c.4048-286G>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 30/47 | chr2 | 127625082 | |||||||
chr2:127625086 | C | T | 3 | a0017c0053t0001g0271 a0017c0072t0001g0012 a0046c0073t0001g0068 |
3 | HG02572.hp1 HG02922.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.4048-282C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 30/47 | chr2 | 127625086 | |||||||
chr2:127625103 | C | G | 26 | a0001c0005t0001g0049 a0001c0005t0001g0098 a0001c0005t0002g0044 others(23): Show |
26 | HG01070.hp1 HG01256.hp1 HG01258.hp2 others(23): Show |
intron_variant | MODIFIER | c.4048-265C>G | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 30/47 | chr2 | 127625103 | |||||||
chr2:127625230 | G | A | 1 | a0001c0002t0001g0137 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.4048-138G>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 30/47 | chr2 | 127625230 | |||||||
chr2:127625262 | T | C | 22 | a0001c0005t0001g0049 a0001c0005t0001g0098 a0001c0005t0002g0044 others(19): Show |
22 | HG01070.hp1 HG01256.hp1 HG01258.hp2 others(19): Show |
intron_variant | MODIFIER | c.4048-106T>C | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 30/47 | chr2 | 127625262 | |||||||
chr2:127625267 | T | C | 51 | a0003c0003t0001g0033 a0003c0003t0001g0081 a0003c0003t0001g0109 others(48): Show |
53 | HG00280.hp1 HG00323.hp1 HG00621.hp2 others(50): Show |
intron_variant | MODIFIER | c.4048-101T>C | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 30/47 | chr2 | 127625267 | |||||||
chr2:127625284 | C | T | 208 | a0001c0002t0001g0027 a0001c0002t0001g0032 a0001c0002t0001g0034 others(205): Show |
212 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(209): Show |
intron_variant | MODIFIER | c.4048-84C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 30/47 | chr2 | 127625284 | |||||||
chr2:127625599 | T | C | 19 | a0004c0007t0001g0162 a0004c0007t0001g0164 a0004c0007t0001g0220 others(16): Show |
19 | HG00280.hp2 HG00642.hp2 HG00735.hp2 others(16): Show |
intron_variant | MODIFIER | c.4215+64T>C | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 31/47 | chr2 | 127625599 | |||||||
chr2:127625791 | T | C | 47 | a0001c0002t0001g0262 a0001c0005t0001g0049 a0001c0005t0001g0098 others(44): Show |
47 | HG00280.hp2 HG00642.hp2 HG00735.hp2 others(44): Show |
intron_variant | MODIFIER | c.4215+256T>C | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 31/47 | chr2 | 127625791 | |||||||
chr2:127625795 | C | T | 1 | a0003c0003t0001g0248 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.4215+260C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 31/47 | chr2 | 127625795 | |||||||
chr2:127625871 | C | A | 2 | a0001c0005t0002g0131 a0002c0011t0002g0270 |
2 | HG02280.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.4215+336C>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 31/47 | chr2 | 127625871 | |||||||
chr2:127625936 | C | T | 2 | a0011c0016t0001g0008 a0011c0016t0001g0141 |
3 | HG02630.hp1 HG03041.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.4215+401C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 31/47 | chr2 | 127625936 | |||||||
chr2:127626004 | T | C | 2 | a0011c0016t0001g0008 a0011c0016t0001g0141 |
3 | HG02630.hp1 HG03041.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.4215+469T>C | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 31/47 | chr2 | 127626004 | |||||||
chr2:127626069 | A | T | 5 | a0001c0010t0001g0163 a0012c0022t0001g0120 a0012c0022t0001g0217 others(2): Show |
5 | HG01069.hp1 HG01071.hp1 HG01346.hp1 others(2): Show |
intron_variant | MODIFIER | c.4215+534A>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 31/47 | chr2 | 127626069 | |||||||
chr2:127626243 | A | G | 2 | a0007c0024t0001g0086 a0007c0024t0001g0227 |
2 | HG03195.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.4215+708A>G | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 31/47 | chr2 | 127626243 | |||||||
chr2:127626280 | G | A | 2 | a0011c0016t0001g0008 a0011c0016t0001g0141 |
3 | HG02630.hp1 HG03041.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.4216-695G>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 31/47 | chr2 | 127626280 | |||||||
chr2:127626305 | C | T | 1 | a0002c0006t0001g0014 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.4216-670C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 31/47 | chr2 | 127626305 | |||||||
chr2:127626402 | GC | G | 4 | a0009c0014t0001g0104 a0009c0014t0001g0136 a0009c0014t0001g0148 others(1): Show |
4 | HG02486.hp2 HG02572.hp2 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.4216-569delC | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 31/47 | INFO_REALIGN_3_PRIME | chr2 | 127626402 | ||||||
chr2:127626405 | C | T | 4 | a0009c0014t0001g0104 a0009c0014t0001g0136 a0009c0014t0001g0148 others(1): Show |
4 | HG02486.hp2 HG02572.hp2 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.4216-570C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 31/47 | chr2 | 127626405 | |||||||
chr2:127626406 | C | A | 4 | a0009c0014t0001g0104 a0009c0014t0001g0136 a0009c0014t0001g0148 others(1): Show |
4 | HG02486.hp2 HG02572.hp2 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.4216-569C>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 31/47 | chr2 | 127626406 | |||||||
chr2:127626440 | C | T | 2 | a0011c0016t0001g0008 a0011c0016t0001g0141 |
3 | HG02630.hp1 HG03041.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.4216-535C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 31/47 | chr2 | 127626440 | |||||||
chr2:127626574 | A | C | 1 | a0021c0046t0003g0078 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.4216-401A>C | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 31/47 | chr2 | 127626574 | |||||||
chr2:127626639 | C | T | 23 | a0002c0006t0001g0018 a0002c0006t0001g0019 a0002c0006t0001g0156 others(20): Show |
23 | HG00099.hp1 HG00280.hp2 HG00642.hp2 others(20): Show |
intron_variant | MODIFIER | c.4216-336C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 31/47 | chr2 | 127626639 | |||||||
chr2:127626651 | C | T | 26 | a0001c0005t0001g0049 a0001c0005t0001g0098 a0001c0005t0002g0044 others(23): Show |
26 | HG01070.hp1 HG01256.hp1 HG01258.hp2 others(23): Show |
intron_variant | MODIFIER | c.4216-324C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 31/47 | chr2 | 127626651 | |||||||
chr2:127626719 | C | T | 1 | a0008c0063t0001g0257 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.4216-256C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 31/47 | chr2 | 127626719 | |||||||
chr2:127626734 | G | A | 1 | a0002c0006t0001g0159 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.4216-241G>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 31/47 | chr2 | 127626734 | |||||||
chr2:127626765 | C | T | 1 | a0002c0001t0001g0183 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.4216-210C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 31/47 | chr2 | 127626765 | |||||||
chr2:127626799 | A | C | 1 | a0002c0001t0001g0183 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.4216-176A>C | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 31/47 | chr2 | 127626799 | |||||||
chr2:127627139 | C | G | 1 | a0003c0003t0001g0033 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.4334-45C>G | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 32/47 | chr2 | 127627139 | |||||||
chr2:127627169 | G | A | 22 | a0001c0010t0001g0138 a0001c0010t0001g0139 a0001c0010t0001g0163 others(19): Show |
22 | HG01069.hp1 HG01071.hp1 HG01346.hp1 others(19): Show |
intron_variant | MODIFIER | c.4334-15G>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 32/47 | chr2 | 127627169 | |||||||
chr2:127627392 | G | A | 2 | a0011c0016t0001g0008 a0011c0016t0001g0141 |
3 | HG02630.hp1 HG03041.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.4460+82G>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 33/47 | chr2 | 127627392 | |||||||
chr2:127627617 | C | T | 1 | a0047c0032t0001g0172 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.4460+307C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 33/47 | chr2 | 127627617 | |||||||
chr2:127627649 | C | G | 100 | a0001c0005t0001g0049 a0001c0005t0001g0098 a0001c0005t0002g0044 others(97): Show |
101 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(98): Show |
intron_variant | MODIFIER | c.4460+339C>G | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 33/47 | chr2 | 127627649 | |||||||
chr2:127627653 | G | A | 1 | a0003c0003t0001g0129 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.4460+343G>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 33/47 | chr2 | 127627653 | |||||||
chr2:127627669 | T | C | 51 | a0001c0005t0001g0049 a0001c0005t0001g0098 a0001c0005t0002g0044 others(48): Show |
51 | HG00099.hp1 HG00280.hp2 HG00642.hp2 others(48): Show |
intron_variant | MODIFIER | c.4460+359T>C | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 33/47 | chr2 | 127627669 | |||||||
chr2:127627756 | C | CCCATGGG others(3): Show |
1 | a0001c0002t0001g0106 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.4460+453_4460+462d others(12): Show |
MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 33/47 | INFO_REALIGN_3_PRIME | chr2 | 127627756 | ||||||
chr2:127627765 | C | A | 4 | a0001c0004t0001g0254 a0002c0001t0001g0002 a0002c0001t0001g0181 others(1): Show |
6 | HG01168.hp2 HG01257.hp1 HG01361.hp2 others(3): Show |
intron_variant | MODIFIER | c.4460+455C>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 33/47 | chr2 | 127627765 | |||||||
chr2:127627811 | G | A | 1 | a0001c0005t0003g0063 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.4460+501G>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 33/47 | chr2 | 127627811 | |||||||
chr2:127627892 | G | A | 1 | a0042c0030t0001g0202 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.4461-480G>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 33/47 | chr2 | 127627892 | |||||||
chr2:127628024 | C | T | 2 | a0001c0002t0001g0035 a0001c0002t0001g0085 |
2 | NA18964.hp2 NA18981.hp1 |
intron_variant | MODIFIER | c.4461-348C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 33/47 | chr2 | 127628024 | |||||||
chr2:127628177 | C | T | 2 | a0007c0023t0001g0122 a0007c0023t0001g0149 |
2 | HG02109.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.4461-195C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 33/47 | chr2 | 127628177 | |||||||
chr2:127628247 | T | C | 2 | a0011c0016t0001g0008 a0011c0016t0001g0141 |
3 | HG02630.hp1 HG03041.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.4461-125T>C | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 33/47 | chr2 | 127628247 | |||||||
chr2:127628358 | T | C | 2 | a0011c0016t0001g0008 a0011c0016t0001g0141 |
3 | HG02630.hp1 HG03041.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.4461-14T>C | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 33/47 | chr2 | 127628358 | |||||||
chr2:127628545 | TGGGTG | T | 206 | a0001c0002t0001g0027 a0001c0002t0001g0032 a0001c0002t0001g0034 others(203): Show |
210 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(207): Show |
intron_variant | MODIFIER | c.4624+39_4624+43del others(5): Show |
MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 34/47 | INFO_REALIGN_3_PRIME | chr2 | 127628545 | ||||||
chr2:127628545 | TGGGTGGG others(3): Show |
T | 2 | a0001c0002t0001g0133 a0002c0001t0001g0181 |
2 | HG01361.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.4624+34_4624+43del others(10): Show |
MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 34/47 | INFO_REALIGN_3_PRIME | chr2 | 127628545 | ||||||
chr2:127628545 | TGGGTGGG others(13): Show |
T | 1 | a0001c0044t0003g0080 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.4624+24_4624+43del others(20): Show |
MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 34/47 | INFO_REALIGN_3_PRIME | chr2 | 127628545 | ||||||
chr2:127628563 | G | T | 2 | a0009c0014t0001g0148 a0009c0014t0001g0174 |
2 | HG02486.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.4624+28G>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 34/47 | chr2 | 127628563 | |||||||
chr2:127628632 | G | A | 1 | a0008c0015t0001g0168 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.4624+97G>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 34/47 | chr2 | 127628632 | |||||||
chr2:127628675 | G | A | 77 | a0001c0002t0001g0027 a0001c0002t0001g0032 a0001c0002t0001g0034 others(74): Show |
79 | HG00323.hp2 HG00642.hp1 HG00733.hp2 others(76): Show |
intron_variant | MODIFIER | c.4624+140G>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 34/47 | chr2 | 127628675 | |||||||
chr2:127628711 | C | T | 1 | a0042c0030t0001g0202 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.4624+176C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 34/47 | chr2 | 127628711 | |||||||
chr2:127628734 | G | A | 1 | a0001c0044t0003g0080 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.4624+199G>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 34/47 | chr2 | 127628734 | |||||||
chr2:127628789 | G | T | 21 | a0001c0005t0001g0049 a0001c0005t0001g0098 a0001c0005t0002g0044 others(18): Show |
21 | HG01070.hp1 HG01256.hp1 HG01258.hp2 others(18): Show |
intron_variant | MODIFIER | c.4624+254G>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 34/47 | chr2 | 127628789 | |||||||
chr2:127629045 | G | A | 2 | a0011c0016t0001g0008 a0011c0016t0001g0141 |
3 | HG02630.hp1 HG03041.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.4624+510G>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 34/47 | chr2 | 127629045 | |||||||
chr2:127629069 | G | C | 124 | a0001c0005t0001g0049 a0001c0005t0001g0098 a0001c0005t0002g0044 others(121): Show |
126 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(123): Show |
intron_variant | MODIFIER | c.4624+534G>C | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 34/47 | chr2 | 127629069 | |||||||
chr2:127629129 | G | A | 1 | a0001c0005t0002g0131 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.4625-516G>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 34/47 | chr2 | 127629129 | |||||||
chr2:127629235 | A | C | 1 | a0001c0002t0001g0133 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.4625-410A>C | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 34/47 | chr2 | 127629235 | |||||||
chr2:127629415 | G | A | 3 | a0001c0018t0001g0266 a0001c0018t0001g0267 a0001c0018t0001g0268 |
3 | HG02622.hp1 HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.4625-230G>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 34/47 | chr2 | 127629415 | |||||||
chr2:127629614 | C | T | 1 | a0001c0005t0003g0063 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.4625-31C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 34/47 | chr2 | 127629614 | |||||||
chr2:127629864 | C | T | 1 | a0003c0003t0001g0210 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.4806+38C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 35/47 | chr2 | 127629864 | |||||||
chr2:127629958 | C | T | 1 | a0002c0011t0002g0270 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.4806+132C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 35/47 | chr2 | 127629958 | |||||||
chr2:127630068 | T | G | 1 | a0004c0007t0003g0010 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.4806+242T>G | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 35/47 | chr2 | 127630068 | |||||||
chr2:127630082 | C | A | 1 | a0002c0001t0001g0112 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.4806+256C>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 35/47 | chr2 | 127630082 | |||||||
chr2:127630105 | C | G | 2 | a0007c0023t0001g0122 a0007c0023t0001g0149 |
2 | HG02109.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.4806+279C>G | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 35/47 | chr2 | 127630105 | |||||||
chr2:127630144 | G | A | 22 | a0001c0010t0001g0138 a0001c0010t0001g0139 a0001c0010t0001g0163 others(19): Show |
22 | HG01069.hp1 HG01071.hp1 HG01346.hp1 others(19): Show |
intron_variant | MODIFIER | c.4806+318G>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 35/47 | chr2 | 127630144 | |||||||
chr2:127630168 | A | T | 46 | a0003c0003t0001g0033 a0003c0003t0001g0081 a0003c0003t0001g0109 others(43): Show |
47 | HG00280.hp1 HG00323.hp1 HG00621.hp2 others(44): Show |
intron_variant | MODIFIER | c.4806+342A>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 35/47 | chr2 | 127630168 | |||||||
chr2:127630181 | C | G | 2 | a0011c0016t0001g0008 a0011c0016t0001g0141 |
3 | HG02630.hp1 HG03041.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.4806+355C>G | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 35/47 | chr2 | 127630181 | |||||||
chr2:127630267 | TAGC | T | 4 | a0009c0014t0001g0104 a0009c0014t0001g0136 a0009c0014t0001g0148 others(1): Show |
4 | HG02486.hp2 HG02572.hp2 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.4806+445_4806+447d others(5): Show |
MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 35/47 | INFO_REALIGN_3_PRIME | chr2 | 127630267 | ||||||
chr2:127630362 | G | A | 49 | a0001c0005t0001g0049 a0001c0005t0001g0098 a0001c0005t0002g0044 others(46): Show |
49 | HG00099.hp1 HG00280.hp2 HG00642.hp2 others(46): Show |
intron_variant | MODIFIER | c.4807-416G>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 35/47 | chr2 | 127630362 | |||||||
chr2:127630364 | G | A | 1 | a0003c0003t0001g0247 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.4807-414G>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 35/47 | chr2 | 127630364 | |||||||
chr2:127630395 | C | T | 4 | a0009c0014t0001g0104 a0009c0014t0001g0136 a0009c0014t0001g0148 others(1): Show |
4 | HG02486.hp2 HG02572.hp2 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.4807-383C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 35/47 | chr2 | 127630395 | |||||||
chr2:127630512 | C | T | 2 | a0009c0014t0001g0148 a0009c0014t0001g0174 |
2 | HG02486.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.4807-266C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 35/47 | chr2 | 127630512 | |||||||
chr2:127630732 | C | T | 1 | a0013c0019t0001g0179 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.4807-46C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 35/47 | chr2 | 127630732 | |||||||
chr2:127630758 | C | T | 1 | a0001c0005t0002g0131 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.4807-20C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 35/47 | chr2 | 127630758 | |||||||
chr2:127630925 | C | T | 2 | a0011c0016t0001g0008 a0011c0016t0001g0141 |
3 | HG02630.hp1 HG03041.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.4937+17C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 36/47 | chr2 | 127630925 | |||||||
chr2:127630929 | G | A | 1 | a0004c0007t0003g0223 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.4937+21G>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 36/47 | chr2 | 127630929 | |||||||
chr2:127630940 | CCCCCACC others(6): Show |
C | 1 | a0002c0006t0001g0014 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.4937+42_4937+54del others(13): Show |
MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 36/47 | INFO_REALIGN_3_PRIME | chr2 | 127630940 | ||||||
chr2:127631030 | C | CCA | 5 | a0002c0001t0001g0071 a0002c0001t0001g0203 a0002c0001t0001g0204 others(2): Show |
5 | NA18947.hp1 NA18950.hp1 NA18984.hp1 others(2): Show |
intron_variant | MODIFIER | c.4937+124_4937+125d others(4): Show |
MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 36/47 | INFO_REALIGN_3_PRIME | chr2 | 127631030 | ||||||
chr2:127631091 | C | T | 1 | a0001c0044t0003g0080 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.4938-115C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 36/47 | chr2 | 127631091 | |||||||
chr2:127631093 | G | A | 2 | a0011c0016t0001g0008 a0011c0016t0001g0141 |
3 | HG02630.hp1 HG03041.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.4938-113G>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 36/47 | chr2 | 127631093 | |||||||
chr2:127631584 | T | C | 2 | a0002c0006t0001g0018 a0002c0006t0001g0019 |
2 | HG00099.hp1 HG01516.hp2 |
intron_variant | MODIFIER | c.5096-16T>C | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 37/47 | chr2 | 127631584 | |||||||
chr2:127631765 | C | G | 1 | a0002c0001t0001g0189 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.5249+12C>G | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 38/47 | chr2 | 127631765 | |||||||
chr2:127631766 | G | C | 1 | a0002c0001t0001g0189 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.5249+13G>C | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 38/47 | chr2 | 127631766 | |||||||
chr2:127631768 | C | T | 123 | a0001c0005t0001g0049 a0001c0005t0001g0098 a0001c0005t0002g0044 others(120): Show |
124 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(121): Show |
intron_variant | MODIFIER | c.5249+15C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 38/47 | chr2 | 127631768 | |||||||
chr2:127631847 | G | C | 125 | a0001c0005t0001g0049 a0001c0005t0001g0098 a0001c0005t0002g0044 others(122): Show |
127 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(124): Show |
intron_variant | MODIFIER | c.5249+94G>C | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 38/47 | chr2 | 127631847 | |||||||
chr2:127631853 | G | A | 6 | a0003c0003t0001g0125 a0003c0003t0001g0230 a0003c0003t0001g0233 others(3): Show |
6 | HG02074.hp2 HG02135.hp1 NA18747.hp2 others(3): Show |
intron_variant | MODIFIER | c.5249+100G>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 38/47 | chr2 | 127631853 | |||||||
chr2:127631902 | C | G | 4 | a0009c0014t0001g0104 a0009c0014t0001g0136 a0009c0014t0001g0148 others(1): Show |
4 | HG02486.hp2 HG02572.hp2 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.5249+149C>G | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 38/47 | chr2 | 127631902 | |||||||
chr2:127631929 | G | A | 2 | a0004c0007t0001g0220 a0004c0007t0001g0222 |
2 | HG01257.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.5249+176G>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 38/47 | chr2 | 127631929 | |||||||
chr2:127631998 | C | T | 4 | a0009c0014t0001g0104 a0009c0014t0001g0136 a0009c0014t0001g0148 others(1): Show |
4 | HG02486.hp2 HG02572.hp2 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.5249+245C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 38/47 | chr2 | 127631998 | |||||||
chr2:127632003 | C | T | 76 | a0001c0002t0001g0027 a0001c0002t0001g0032 a0001c0002t0001g0034 others(73): Show |
78 | HG00323.hp2 HG00642.hp1 HG00733.hp2 others(75): Show |
intron_variant | MODIFIER | c.5250-243C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 38/47 | chr2 | 127632003 | |||||||
chr2:127632049 | G | A | 125 | a0001c0005t0001g0049 a0001c0005t0001g0098 a0001c0005t0002g0044 others(122): Show |
127 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(124): Show |
intron_variant | MODIFIER | c.5250-197G>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 38/47 | chr2 | 127632049 | |||||||
chr2:127632075 | C | T | 70 | a0001c0010t0001g0138 a0001c0010t0001g0139 a0001c0010t0001g0163 others(67): Show |
71 | HG00280.hp1 HG00323.hp1 HG00621.hp2 others(68): Show |
intron_variant | MODIFIER | c.5250-171C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 38/47 | chr2 | 127632075 | |||||||
chr2:127632135 | C | T | 1 | a0002c0012t0001g0191 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.5250-111C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 38/47 | chr2 | 127632135 | |||||||
chr2:127632176 | C | T | 21 | a0001c0002t0001g0027 a0001c0002t0001g0032 a0001c0002t0001g0034 others(18): Show |
21 | HG01081.hp1 HG01099.hp1 HG01358.hp1 others(18): Show |
intron_variant | MODIFIER | c.5250-70C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 38/47 | chr2 | 127632176 | |||||||
chr2:127632197 | C | G | 1 | a0002c0001t0001g0183 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.5250-49C>G | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 38/47 | chr2 | 127632197 | |||||||
chr2:127632223 | G | A | 1 | a0001c0005t0003g0063 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.5250-23G>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 38/47 | chr2 | 127632223 | |||||||
chr2:127632224 | G | A | 2 | a0011c0016t0001g0008 a0011c0016t0001g0141 |
3 | HG02630.hp1 HG03041.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.5250-22G>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 38/47 | chr2 | 127632224 | |||||||
chr2:127632469 | G | A | 1 | a0001c0044t0003g0080 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.5405+68G>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 39/47 | chr2 | 127632469 | |||||||
chr2:127632611 | C | A | 1 | a0004c0007t0003g0223 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.5405+210C>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 39/47 | chr2 | 127632611 | |||||||
chr2:127632734 | AGTCCATG others(41): Show |
A | 1 | a0028c0064t0002g0143 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.5405+335_5405+382d others(50): Show |
MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 39/47 | INFO_REALIGN_3_PRIME | chr2 | 127632734 | ||||||
chr2:127632757 | G | A | 2 | a0004c0007t0001g0164 a0004c0054t0001g0165 |
2 | HG01175.hp2 HG02258.hp1 |
intron_variant | MODIFIER | c.5405+356G>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 39/47 | chr2 | 127632757 | |||||||
chr2:127632825 | G | A | 25 | a0001c0005t0001g0049 a0001c0005t0001g0098 a0001c0005t0002g0044 others(22): Show |
25 | HG01070.hp1 HG01256.hp1 HG01258.hp2 others(22): Show |
intron_variant | MODIFIER | c.5405+424G>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 39/47 | chr2 | 127632825 | |||||||
chr2:127632879 | A | G | 1 | a0001c0004t0001g0124 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.5406-379A>G | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 39/47 | chr2 | 127632879 | |||||||
chr2:127632911 | G | A | 21 | a0001c0005t0001g0049 a0001c0005t0001g0098 a0001c0005t0002g0044 others(18): Show |
21 | HG01070.hp1 HG01256.hp1 HG01258.hp2 others(18): Show |
intron_variant | MODIFIER | c.5406-347G>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 39/47 | chr2 | 127632911 | |||||||
chr2:127632913 | C | T | 1 | a0003c0003t0001g0248 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.5406-345C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 39/47 | chr2 | 127632913 | |||||||
chr2:127632939 | G | A | 1 | a0046c0073t0001g0068 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.5406-319G>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 39/47 | chr2 | 127632939 | |||||||
chr2:127632965 | C | T | 1 | a0029c0048t0001g0132 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.5406-293C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 39/47 | chr2 | 127632965 | |||||||
chr2:127633008 | G | A | 2 | a0017c0053t0001g0271 a0017c0072t0001g0012 |
2 | HG02572.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.5406-250G>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 39/47 | chr2 | 127633008 | |||||||
chr2:127633013 | C | T | 81 | a0001c0002t0001g0027 a0001c0002t0001g0032 a0001c0002t0001g0034 others(78): Show |
83 | HG00323.hp2 HG00642.hp1 HG00733.hp2 others(80): Show |
intron_variant | MODIFIER | c.5406-245C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 39/47 | chr2 | 127633013 | |||||||
chr2:127633087 | C | T | 18 | a0001c0010t0001g0138 a0001c0010t0001g0139 a0001c0010t0001g0228 others(15): Show |
18 | HG02109.hp1 HG02109.hp2 HG02258.hp2 others(15): Show |
intron_variant | MODIFIER | c.5406-171C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 39/47 | chr2 | 127633087 | |||||||
chr2:127633088 | G | A | 5 | a0004c0007t0003g0010 a0004c0007t0003g0256 a0007c0025t0001g0042 others(2): Show |
5 | HG02132.hp1 HG03654.hp1 HG03688.hp1 others(2): Show |
intron_variant | MODIFIER | c.5406-170G>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 39/47 | chr2 | 127633088 | |||||||
chr2:127633114 | A | G | 208 | a0001c0002t0001g0027 a0001c0002t0001g0032 a0001c0002t0001g0034 others(205): Show |
212 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(209): Show |
intron_variant | MODIFIER | c.5406-144A>G | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 39/47 | chr2 | 127633114 | |||||||
chr2:127633183 | G | A | 2 | a0002c0006t0001g0015 a0002c0006t0001g0016 |
2 | HG00741.hp1 HG03239.hp2 |
intron_variant | MODIFIER | c.5406-75G>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 39/47 | chr2 | 127633183 | |||||||
chr2:127633243 | C | T | 3 | a0001c0005t0002g0062 a0001c0005t0002g0102 a0001c0058t0002g0103 |
3 | NA18957.hp1 NA18986.hp1 NA19007.hp2 |
intron_variant | MODIFIER | c.5406-15C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 39/47 | chr2 | 127633243 | |||||||
chr2:127633399 | G | A | 1 | a0045c0065t0001g0140 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.5511+36G>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 40/47 | chr2 | 127633399 | |||||||
chr2:127633520 | A | G | 1 | a0002c0001t0001g0198 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.5511+157A>G | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 40/47 | chr2 | 127633520 | |||||||
chr2:127633636 | A | G | 2 | a0017c0053t0001g0271 a0017c0072t0001g0012 |
2 | HG02572.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.5511+273A>G | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 40/47 | chr2 | 127633636 | |||||||
chr2:127633687 | G | A | 2 | a0011c0016t0001g0008 a0011c0016t0001g0141 |
3 | HG02630.hp1 HG03041.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.5511+324G>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 40/47 | chr2 | 127633687 | |||||||
chr2:127633839 | AGTGGGCA others(15): Show |
A | 1 | a0001c0005t0002g0054 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.5512-336_5512-315d others(24): Show |
MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 40/47 | chr2 | 127633839 | |||||||
chr2:127634066 | T | C | 1 | a0001c0004t0001g0232 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.5512-110T>C | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 40/47 | chr2 | 127634066 | |||||||
chr2:127634148 | G | A | 1 | a0002c0006t0001g0015 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.5512-28G>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 40/47 | chr2 | 127634148 | |||||||
chr2:127634156 | C | T | 1 | a0002c0006t0001g0159 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.5512-20C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 40/47 | chr2 | 127634156 | |||||||
chr2:127634322 | C | T | 2 | a0012c0022t0001g0120 a0012c0022t0001g0217 |
2 | HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.5625+33C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 41/47 | chr2 | 127634322 | |||||||
chr2:127634374 | C | T | 3 | a0001c0010t0001g0163 a0012c0022t0001g0120 a0012c0022t0001g0217 |
3 | HG01069.hp1 HG01071.hp1 HG01346.hp1 |
intron_variant | MODIFIER | c.5625+85C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 41/47 | chr2 | 127634374 | |||||||
chr2:127634380 | G | A | 5 | a0001c0010t0001g0163 a0012c0022t0001g0120 a0012c0022t0001g0217 others(2): Show |
5 | HG01069.hp1 HG01071.hp1 HG01346.hp1 others(2): Show |
intron_variant | MODIFIER | c.5625+91G>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 41/47 | chr2 | 127634380 | |||||||
chr2:127634556 | C | T | 1 | a0001c0005t0002g0208 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.5626-40C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 41/47 | chr2 | 127634556 | |||||||
chr2:127634569 | A | G | 1 | a0027c0057t0001g0079 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.5626-27A>G | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 41/47 | chr2 | 127634569 | |||||||
chr2:127634690 | AGGCCTCT others(47): Show |
A | 3 | a0008c0015t0001g0107 a0008c0015t0001g0168 a0008c0015t0001g0169 |
3 | HG02145.hp1 HG02280.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.5713+18_5713+71del others(54): Show |
MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 42/47 | INFO_REALIGN_3_PRIME | chr2 | 127634690 | ||||||
chr2:127634731 | G | A | 2 | a0001c0005t0002g0044 a0002c0001t0001g0002 |
2 | HG02698.hp2 NA18968.hp2 |
intron_variant | MODIFIER | c.5713+48G>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 42/47 | chr2 | 127634731 | |||||||
chr2:127634745 | G | A | 1 | a0017c0072t0001g0012 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.5713+62G>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 42/47 | chr2 | 127634745 | |||||||
chr2:127634756 | G | A | 1 | a0045c0065t0001g0140 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.5713+73G>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 42/47 | chr2 | 127634756 | |||||||
chr2:127634893 | A | G | 205 | a0001c0002t0001g0027 a0001c0002t0001g0032 a0001c0002t0001g0034 others(202): Show |
209 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(206): Show |
intron_variant | MODIFIER | c.5713+210A>G | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 42/47 | chr2 | 127634893 | |||||||
chr2:127634972 | A | C | 209 | a0001c0002t0001g0027 a0001c0002t0001g0032 a0001c0002t0001g0034 others(206): Show |
213 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(210): Show |
intron_variant | MODIFIER | c.5714-148A>C | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 42/47 | chr2 | 127634972 | |||||||
chr2:127635072 | G | T | 43 | a0001c0005t0002g0044 a0001c0005t0002g0050 a0001c0005t0002g0052 others(40): Show |
44 | HG00735.hp2 HG01069.hp1 HG01071.hp1 others(41): Show |
intron_variant | MODIFIER | c.5714-48G>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 42/47 | chr2 | 127635072 | |||||||
chr2:127635113 | C | T | 9 | a0001c0002t0003g0046 a0001c0044t0003g0080 a0004c0007t0003g0007 others(6): Show |
9 | HG00280.hp2 HG00642.hp2 HG01168.hp1 others(6): Show |
splice_region_variant&intron_variant | LOW | c.5714-7C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 42/47 | chr2 | 127635113 | |||||||
chr2:127635307 | G | A | 1 | a0002c0011t0002g0207 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.5820+81G>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 43/47 | chr2 | 127635307 | |||||||
chr2:127635576 | C | T | 1 | a0001c0002t0001g0137 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.5821-146C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 43/47 | chr2 | 127635576 | |||||||
chr2:127635654 | G | A | 1 | a0001c0005t0003g0063 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.5821-68G>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 43/47 | chr2 | 127635654 | |||||||
chr2:127635686 | T | C | 209 | a0001c0002t0001g0027 a0001c0002t0001g0032 a0001c0002t0001g0034 others(206): Show |
213 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(210): Show |
intron_variant | MODIFIER | c.5821-36T>C | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 43/47 | chr2 | 127635686 | |||||||
chr2:127635714 | T | C | 108 | a0001c0005t0002g0044 a0001c0005t0002g0050 a0001c0005t0002g0052 others(105): Show |
110 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(107): Show |
splice_region_variant&intron_variant | LOW | c.5821-8T>C | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 43/47 | chr2 | 127635714 | |||||||
chr2:127635918 | G | A | 1 | a0001c0002t0001g0134 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.6006+11G>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 44/47 | chr2 | 127635918 | |||||||
chr2:127635920 | G | T | 1 | a0003c0026t0001g0253 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.6006+13G>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 44/47 | chr2 | 127635920 | |||||||
chr2:127635956 | G | A | 1 | a0001c0004t0001g0043 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.6006+49G>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 44/47 | chr2 | 127635956 | |||||||
chr2:127635979 | C | T | 2 | a0009c0014t0001g0148 a0009c0014t0001g0174 |
2 | HG02486.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.6006+72C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 44/47 | chr2 | 127635979 | |||||||
chr2:127636044 | C | G | 1 | a0001c0005t0003g0063 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.6006+137C>G | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 44/47 | chr2 | 127636044 | |||||||
chr2:127636333 | T | C | 5 | a0002c0006t0001g0018 a0002c0006t0001g0019 a0002c0006t0001g0156 others(2): Show |
5 | HG00099.hp1 HG00733.hp1 HG01081.hp2 others(2): Show |
intron_variant | MODIFIER | c.6123+9T>C | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 45/47 | chr2 | 127636333 | |||||||
chr2:127636368 | C | T | 1 | a0001c0005t0003g0063 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.6123+44C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 45/47 | chr2 | 127636368 | |||||||
chr2:127636496 | A | G | 1 | a0009c0014t0001g0136 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.6124-49A>G | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 45/47 | chr2 | 127636496 | |||||||
chr2:127636511 | G | C | 2 | a0007c0023t0001g0122 a0007c0023t0001g0149 |
2 | HG02109.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.6124-34G>C | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 45/47 | chr2 | 127636511 | |||||||
chr2:127636669 | CCAGGGAC others(5): Show |
C | 1 | a0001c0005t0002g0208 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.6207+46_6207+57del others(12): Show |
MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 46/47 | INFO_REALIGN_3_PRIME | chr2 | 127636669 | ||||||
chr2:127636682 | C | T | 1 | a0034c0059t0001g0031 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.6207+54C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 46/47 | chr2 | 127636682 | |||||||
chr2:127636720 | T | C | 1 | a0001c0005t0003g0063 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.6208-74T>C | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 46/47 | chr2 | 127636720 | |||||||
chr2:127636738 | A | T | 8 | a0006c0009t0001g0020 a0006c0009t0001g0037 a0006c0009t0001g0051 others(5): Show |
8 | HG00323.hp2 HG00733.hp2 HG01106.hp1 others(5): Show |
intron_variant | MODIFIER | c.6208-56A>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 46/47 | chr2 | 127636738 | |||||||
chr2:127636745 | G | C | 1 | a0032c0038t0002g0105 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.6208-49G>C | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 46/47 | chr2 | 127636745 | |||||||
chr2:127636750 | C | T | 2 | a0017c0053t0001g0271 a0017c0072t0001g0012 |
2 | HG02572.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.6208-44C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 46/47 | chr2 | 127636750 | |||||||
chr2:127636767 | C | T | 1 | a0001c0044t0003g0080 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.6208-27C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 46/47 | chr2 | 127636767 | |||||||
chr2:127637048 | G | A | 1 | a0024c0070t0001g0028 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.6327+135G>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 47/47 | chr2 | 127637048 | |||||||
chr2:127637111 | T | A | 2 | a0009c0014t0001g0148 a0009c0014t0001g0174 |
2 | HG02486.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.6327+198T>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 47/47 | chr2 | 127637111 | |||||||
chr2:127637183 | T | C | 132 | a0001c0002t0001g0137 a0001c0002t0003g0046 a0001c0005t0002g0044 others(129): Show |
135 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(132): Show |
intron_variant | MODIFIER | c.6328-133T>C | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 47/47 | chr2 | 127637183 | |||||||
chr2:127637300 | C | CA | 108 | a0001c0005t0002g0044 a0001c0005t0002g0050 a0001c0005t0002g0052 others(105): Show |
110 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(107): Show |
intron_variant | MODIFIER | c.6328-16_6328-15ins others(1): Show |
MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 47/47 | chr2 | 127637300 | |||||||
chr2:127637302 | C | CT | 98 | a0001c0002t0001g0027 a0001c0002t0001g0032 a0001c0002t0001g0034 others(95): Show |
100 | HG00280.hp2 HG00323.hp2 HG00642.hp1 others(97): Show |
intron_variant | MODIFIER | c.6328-14_6328-13ins others(1): Show |
MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 47/47 | chr2 | 127637302 | |||||||
chr2:127637302 | C | T | 108 | a0001c0005t0002g0044 a0001c0005t0002g0050 a0001c0005t0002g0052 others(105): Show |
110 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(107): Show |
intron_variant | MODIFIER | c.6328-14C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 47/47 | chr2 | 127637302 |