Item | Value |
---|---|
geneid | 93649 |
ensemblid | ENSG00000141052.18 |
hgncid | 16067 |
symbol | MYOCD |
name | myocardin |
refseq_nuc | NM_001146312.3 |
refseq_prot | NP_001139784.1 |
ensembl_nuc | ENST00000425538.6 |
ensembl_prot | ENSP00000401678.1 |
mane_status | MANE Select |
chr | chr17 |
start | 12665890 |
end | 12768949 |
strand | + |
ver | v1.2 |
region | chr17:12665890-12768949 |
region5000 | chr17:12660890-12773949 |
regionname0 | MYOCD_chr17_12665890_12768949 |
regionname5000 | MYOCD_chr17_12660890_12773949 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 986 | 313 | 79 | 56 | 131 | 10 | 35 | 96 | MYOCD_chr17_12660890_12773949 | MYOCD | MTLLG others(981): Show |
chr17 | 12660890 | 12773949 |
a0002 | 0/0 | 986 | 7 | 0 | 1 | 3 | 0 | 3 | 2 | MYOCD_chr17_12660890_12773949 | MYOCD | MTLLG others(981): Show |
chr17 | 12660890 | 12773949 |
a0003 | 0/0 | 986 | 4 | 4 | 0 | 0 | 0 | 0 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | MTLLG others(981): Show |
chr17 | 12660890 | 12773949 |
a0004 | 0/0 | 986 | 3 | 0 | 2 | 1 | 0 | 0 | 1 | MYOCD_chr17_12660890_12773949 | MYOCD | MTLLG others(981): Show |
chr17 | 12660890 | 12773949 |
a0005 | 0/0 | 986 | 2 | 1 | 0 | 1 | 0 | 0 | 1 | MYOCD_chr17_12660890_12773949 | MYOCD | MTLLG others(981): Show |
chr17 | 12660890 | 12773949 |
a0006 | 0/0 | 986 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | MTLLG others(981): Show |
chr17 | 12660890 | 12773949 |
a0007 | 0/0 | 986 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | MTLLG others(981): Show |
chr17 | 12660890 | 12773949 |
a0008 | 0/0 | 986 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | MTLLG others(981): Show |
chr17 | 12660890 | 12773949 |
a0009 | 0/0 | 986 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | MTLLG others(981): Show |
chr17 | 12660890 | 12773949 |
a0010 | 0/0 | 986 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | MTLLG others(981): Show |
chr17 | 12660890 | 12773949 |
a0011 | 0/0 | 986 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | MTLLG others(981): Show |
chr17 | 12660890 | 12773949 |
a0012 | 0/0 | 986 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | MTLLG others(981): Show |
chr17 | 12660890 | 12773949 |
a0013 | 0/0 | 986 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | MTLLG others(981): Show |
chr17 | 12660890 | 12773949 |
a0014 | 0/0 | 986 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | MTLLG others(981): Show |
chr17 | 12660890 | 12773949 |
a0015 | 0/0 | 986 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | MTLLG others(981): Show |
chr17 | 12660890 | 12773949 |
a0016 | 0/0 | 986 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | MTLLG others(981): Show |
chr17 | 12660890 | 12773949 |
a0017 | 0/0 | 986 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | MTLLG others(981): Show |
chr17 | 12660890 | 12773949 |
a0018 | 0/0 | 986 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | MYOCD_chr17_12660890_12773949 | MYOCD | MTLLG others(981): Show |
chr17 | 12660890 | 12773949 |
a0019 | 0/0 | 986 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | MYOCD_chr17_12660890_12773949 | MYOCD | MTLLG others(981): Show |
chr17 | 12660890 | 12773949 |
a0020 | 0/0 | 986 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | MTLLG others(981): Show |
chr17 | 12660890 | 12773949 |
a0021 | 0/0 | 986 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | MTLLG others(981): Show |
chr17 | 12660890 | 12773949 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 2958 | 249 | 56 | 45 | 106 | 7 | 33 | MYOCD_chr17_12660890_12773949 | MYOCD | ATGAC others(2953): Show |
chr17 | 12660890 | 12773949 | ||
a0001c0002 | 0/0 | 2958 | 29 | 0 | 3 | 25 | 0 | 1 | MYOCD_chr17_12660890_12773949 | MYOCD | ATGAC others(2953): Show |
chr17 | 12660890 | 12773949 | ||
a0001c0003 | 0/0 | 2958 | 15 | 15 | 0 | 0 | 0 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | ATGAC others(2953): Show |
chr17 | 12660890 | 12773949 | ||
a0001c0004 | 0/0 | 2958 | 7 | 0 | 7 | 0 | 0 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | ATGAC others(2953): Show |
chr17 | 12660890 | 12773949 | ||
a0001c0006 | 0/0 | 2958 | 5 | 5 | 0 | 0 | 0 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | ATGAC others(2953): Show |
chr17 | 12660890 | 12773949 | ||
a0001c0007 | 0/0 | 2958 | 4 | 0 | 1 | 0 | 3 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | ATGAC others(2953): Show |
chr17 | 12660890 | 12773949 | ||
a0001c0011 | 0/0 | 2958 | 2 | 2 | 0 | 0 | 0 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | ATGAC others(2953): Show |
chr17 | 12660890 | 12773949 | ||
a0001c0015 | 0/0 | 2958 | 1 | 1 | 0 | 0 | 0 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | ATGAC others(2953): Show |
chr17 | 12660890 | 12773949 | ||
a0001c0028 | 0/0 | 2958 | 1 | 0 | 0 | 0 | 0 | 1 | MYOCD_chr17_12660890_12773949 | MYOCD | ATGAC others(2953): Show |
chr17 | 12660890 | 12773949 | ||
a0002c0005 | 0/0 | 2958 | 7 | 0 | 1 | 3 | 0 | 3 | MYOCD_chr17_12660890_12773949 | MYOCD | ATGAC others(2953): Show |
chr17 | 12660890 | 12773949 | ||
a0003c0008 | 0/0 | 2958 | 4 | 4 | 0 | 0 | 0 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | ATGAC others(2953): Show |
chr17 | 12660890 | 12773949 | ||
a0004c0009 | 0/0 | 2958 | 2 | 0 | 2 | 0 | 0 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | ATGAC others(2953): Show |
chr17 | 12660890 | 12773949 | ||
a0004c0017 | 0/0 | 2958 | 1 | 0 | 0 | 1 | 0 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | ATGAC others(2953): Show |
chr17 | 12660890 | 12773949 | ||
a0005c0010 | 0/0 | 2958 | 2 | 1 | 0 | 1 | 0 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | ATGAC others(2953): Show |
chr17 | 12660890 | 12773949 | ||
a0006c0012 | 0/0 | 2958 | 2 | 2 | 0 | 0 | 0 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | ATGAC others(2953): Show |
chr17 | 12660890 | 12773949 | ||
a0007c0022 | 0/0 | 2958 | 1 | 0 | 0 | 1 | 0 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | ATGAC others(2953): Show |
chr17 | 12660890 | 12773949 | ||
a0008c0018 | 0/0 | 2958 | 1 | 0 | 1 | 0 | 0 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | ATGAC others(2953): Show |
chr17 | 12660890 | 12773949 | ||
a0009c0020 | 0/0 | 2958 | 1 | 1 | 0 | 0 | 0 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | ATGAC others(2953): Show |
chr17 | 12660890 | 12773949 | ||
a0010c0025 | 0/0 | 2958 | 1 | 0 | 0 | 1 | 0 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | ATGAC others(2953): Show |
chr17 | 12660890 | 12773949 | ||
a0011c0030 | 0/0 | 2958 | 1 | 1 | 0 | 0 | 0 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | ATGAC others(2953): Show |
chr17 | 12660890 | 12773949 | ||
a0012c0029 | 0/0 | 2958 | 1 | 1 | 0 | 0 | 0 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | ATGAC others(2953): Show |
chr17 | 12660890 | 12773949 | ||
a0013c0027 | 0/0 | 2958 | 1 | 1 | 0 | 0 | 0 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | ATGAC others(2953): Show |
chr17 | 12660890 | 12773949 | ||
a0014c0016 | 0/0 | 2958 | 1 | 1 | 0 | 0 | 0 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | ATGAC others(2953): Show |
chr17 | 12660890 | 12773949 | ||
a0015c0023 | 0/0 | 2958 | 1 | 1 | 0 | 0 | 0 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | ATGAC others(2953): Show |
chr17 | 12660890 | 12773949 | ||
a0016c0021 | 0/0 | 2958 | 1 | 0 | 0 | 0 | 0 | 1 | MYOCD_chr17_12660890_12773949 | MYOCD | ATGAC others(2953): Show |
chr17 | 12660890 | 12773949 | ||
a0017c0013 | 0/0 | 2958 | 1 | 1 | 0 | 0 | 0 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | ATGAC others(2953): Show |
chr17 | 12660890 | 12773949 | ||
a0018c0026 | 0/0 | 2958 | 1 | 0 | 0 | 1 | 0 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | ATGAC others(2953): Show |
chr17 | 12660890 | 12773949 | ||
a0019c0024 | 0/0 | 2958 | 1 | 0 | 0 | 1 | 0 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | ATGAC others(2953): Show |
chr17 | 12660890 | 12773949 | ||
a0020c0014 | 0/0 | 2958 | 1 | 1 | 0 | 0 | 0 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | ATGAC others(2953): Show |
chr17 | 12660890 | 12773949 | ||
a0021c0019 | 0/0 | 2958 | 1 | 0 | 0 | 0 | 0 | 1 | MYOCD_chr17_12660890_12773949 | MYOCD | ATGAC others(2953): Show |
chr17 | 12660890 | 12773949 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 8565 | 19 | 1 | 3 | 6 | 1 | 8 | MYOCD_chr17_12660890_12773949 | MYOCD | AATCG others(8560): Show |
chr17 | 12660890 | 12773949 |
a0001c0001t0002 | 0/0 | 8565 | 10 | 2 | 4 | 2 | 2 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | AATCG others(8560): Show |
chr17 | 12660890 | 12773949 |
a0001c0001t0003 | 0/0 | 8566 | 6 | 0 | 3 | 1 | 0 | 2 | MYOCD_chr17_12660890_12773949 | MYOCD | AATCG others(8561): Show |
chr17 | 12660890 | 12773949 |
a0001c0001t0004 | 0/0 | 8565 | 5 | 0 | 0 | 5 | 0 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | AATCG others(8560): Show |
chr17 | 12660890 | 12773949 |
a0001c0001t0005 | 0/0 | 8565 | 8 | 1 | 2 | 4 | 0 | 1 | MYOCD_chr17_12660890_12773949 | MYOCD | AATCG others(8560): Show |
chr17 | 12660890 | 12773949 |
a0001c0001t0006 | 0/0 | 8566 | 8 | 0 | 0 | 5 | 0 | 3 | MYOCD_chr17_12660890_12773949 | MYOCD | AATCG others(8561): Show |
chr17 | 12660890 | 12773949 |
a0001c0001t0007 | 0/0 | 8565 | 3 | 0 | 0 | 3 | 0 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | AATCG others(8560): Show |
chr17 | 12660890 | 12773949 |
a0001c0001t0008 | 0/0 | 8566 | 6 | 0 | 0 | 5 | 0 | 1 | MYOCD_chr17_12660890_12773949 | MYOCD | AATCG others(8561): Show |
chr17 | 12660890 | 12773949 |
a0001c0001t0009 | 0/0 | 8565 | 3 | 0 | 3 | 0 | 0 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | AATCG others(8560): Show |
chr17 | 12660890 | 12773949 |
a0001c0001t0010 | 0/0 | 8566 | 5 | 0 | 1 | 1 | 0 | 3 | MYOCD_chr17_12660890_12773949 | MYOCD | AATCG others(8561): Show |
chr17 | 12660890 | 12773949 |
a0001c0001t0011 | 0/0 | 8560 | 3 | 3 | 0 | 0 | 0 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | AATCG others(8555): Show |
chr17 | 12660890 | 12773949 |
a0001c0001t0012 | 0/0 | 8564 | 2 | 0 | 0 | 2 | 0 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | AATCG others(8559): Show |
chr17 | 12660890 | 12773949 |
a0001c0001t0013 | 1/0 | 8565 | 4 | 3 | 0 | 0 | 0 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | AATCG others(8560): Show |
chr17 | 12660890 | 12773949 |
a0001c0001t0014 | 0/0 | 8562 | 2 | 1 | 1 | 0 | 0 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | AATCG others(8557): Show |
chr17 | 12660890 | 12773949 |
a0001c0001t0015 | 0/0 | 8566 | 3 | 0 | 0 | 3 | 0 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | AATCG others(8561): Show |
chr17 | 12660890 | 12773949 |
a0001c0001t0017 | 0/0 | 8566 | 3 | 0 | 0 | 3 | 0 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | AATCG others(8561): Show |
chr17 | 12660890 | 12773949 |
a0001c0001t0018 | 0/0 | 8565 | 3 | 3 | 0 | 0 | 0 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | AATCG others(8560): Show |
chr17 | 12660890 | 12773949 |
a0001c0001t0019 | 0/0 | 8566 | 3 | 0 | 1 | 1 | 1 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | AATCG others(8561): Show |
chr17 | 12660890 | 12773949 |
a0001c0001t0021 | 0/0 | 8566 | 2 | 0 | 0 | 2 | 0 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | AATCG others(8561): Show |
chr17 | 12660890 | 12773949 |
a0001c0001t0022 | 0/0 | 8566 | 2 | 0 | 0 | 2 | 0 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | AATCG others(8561): Show |
chr17 | 12660890 | 12773949 |
a0001c0001t0023 | 0/0 | 8565 | 2 | 0 | 0 | 2 | 0 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | AATCG others(8560): Show |
chr17 | 12660890 | 12773949 |
a0001c0001t0024 | 0/0 | 8565 | 2 | 0 | 0 | 2 | 0 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | AATCG others(8560): Show |
chr17 | 12660890 | 12773949 |
a0001c0001t0025 | 0/0 | 8565 | 2 | 1 | 0 | 1 | 0 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | AATCG others(8560): Show |
chr17 | 12660890 | 12773949 |
a0001c0001t0026 | 0/0 | 8566 | 2 | 0 | 0 | 2 | 0 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | AATCG others(8561): Show |
chr17 | 12660890 | 12773949 |
a0001c0001t0027 | 0/0 | 8567 | 1 | 0 | 0 | 1 | 0 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | AATCG others(8562): Show |
chr17 | 12660890 | 12773949 |
a0001c0001t0028 | 0/0 | 8570 | 2 | 2 | 0 | 0 | 0 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | AATCG others(8565): Show |
chr17 | 12660890 | 12773949 |
a0001c0001t0029 | 0/0 | 8566 | 2 | 0 | 2 | 0 | 0 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | AATCG others(8561): Show |
chr17 | 12660890 | 12773949 |
a0001c0001t0030 | 0/0 | 8565 | 2 | 0 | 0 | 1 | 0 | 1 | MYOCD_chr17_12660890_12773949 | MYOCD | AATCG others(8560): Show |
chr17 | 12660890 | 12773949 |
a0001c0001t0032 | 0/0 | 8563 | 1 | 0 | 0 | 1 | 0 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | AATCG others(8558): Show |
chr17 | 12660890 | 12773949 |
a0001c0001t0033 | 0/0 | 8567 | 2 | 2 | 0 | 0 | 0 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | AATCG others(8562): Show |
chr17 | 12660890 | 12773949 |
a0001c0001t0034 | 0/0 | 8566 | 1 | 0 | 0 | 1 | 0 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | AATCG others(8561): Show |
chr17 | 12660890 | 12773949 |
a0001c0001t0035 | 0/0 | 8565 | 2 | 0 | 1 | 1 | 0 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | AATCG others(8560): Show |
chr17 | 12660890 | 12773949 |
a0001c0001t0036 | 0/0 | 8566 | 2 | 2 | 0 | 0 | 0 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | AATCG others(8561): Show |
chr17 | 12660890 | 12773949 |
a0001c0001t0037 | 0/0 | 8564 | 2 | 0 | 0 | 0 | 0 | 2 | MYOCD_chr17_12660890_12773949 | MYOCD | AATCG others(8559): Show |
chr17 | 12660890 | 12773949 |
a0001c0001t0038 | 0/0 | 8566 | 2 | 0 | 0 | 2 | 0 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | AATCG others(8561): Show |
chr17 | 12660890 | 12773949 |
a0001c0001t0039 | 0/0 | 8565 | 2 | 0 | 0 | 2 | 0 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | AATCG others(8560): Show |
chr17 | 12660890 | 12773949 |
a0001c0001t0040 | 0/0 | 8565 | 2 | 2 | 0 | 0 | 0 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | AATCG others(8560): Show |
chr17 | 12660890 | 12773949 |
a0001c0001t0041 | 0/0 | 8564 | 2 | 0 | 2 | 0 | 0 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | AATCG others(8559): Show |
chr17 | 12660890 | 12773949 |
a0001c0001t0042 | 0/0 | 8564 | 2 | 2 | 0 | 0 | 0 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | AATCG others(8559): Show |
chr17 | 12660890 | 12773949 |
a0001c0001t0044 | 0/0 | 8567 | 1 | 0 | 0 | 0 | 0 | 1 | MYOCD_chr17_12660890_12773949 | MYOCD | AATCG others(8562): Show |
chr17 | 12660890 | 12773949 |
a0001c0001t0045 | 0/0 | 8566 | 2 | 0 | 2 | 0 | 0 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | AATCG others(8561): Show |
chr17 | 12660890 | 12773949 |
a0001c0001t0047 | 0/0 | 8564 | 1 | 0 | 0 | 1 | 0 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | AATCG others(8559): Show |
chr17 | 12660890 | 12773949 |
a0001c0001t0048 | 0/0 | 8566 | 2 | 0 | 0 | 2 | 0 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | AATCG others(8561): Show |
chr17 | 12660890 | 12773949 |
a0001c0001t0051 | 0/0 | 8563 | 1 | 0 | 1 | 0 | 0 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | AATCG others(8558): Show |
chr17 | 12660890 | 12773949 |
a0001c0001t0052 | 0/0 | 8563 | 1 | 0 | 1 | 0 | 0 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | AATCG others(8558): Show |
chr17 | 12660890 | 12773949 |
a0001c0001t0053 | 0/0 | 8566 | 1 | 0 | 0 | 1 | 0 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | AATCG others(8561): Show |
chr17 | 12660890 | 12773949 |
a0001c0001t0054 | 0/0 | 8565 | 1 | 1 | 0 | 0 | 0 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | AATCG others(8560): Show |
chr17 | 12660890 | 12773949 |
a0001c0001t0055 | 0/0 | 8565 | 1 | 0 | 1 | 0 | 0 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | AATCG others(8560): Show |
chr17 | 12660890 | 12773949 |
a0001c0001t0056 | 0/0 | 8565 | 1 | 1 | 0 | 0 | 0 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | AATCG others(8560): Show |
chr17 | 12660890 | 12773949 |
a0001c0001t0057 | 0/0 | 8567 | 1 | 1 | 0 | 0 | 0 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | AATCG others(8562): Show |
chr17 | 12660890 | 12773949 |
a0001c0001t0058 | 0/0 | 8564 | 1 | 0 | 0 | 1 | 0 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | AATCG others(8559): Show |
chr17 | 12660890 | 12773949 |
a0001c0001t0059 | 0/0 | 8566 | 1 | 0 | 0 | 1 | 0 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | AATCG others(8561): Show |
chr17 | 12660890 | 12773949 |
a0001c0001t0060 | 0/0 | 8566 | 1 | 0 | 0 | 1 | 0 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | AATCG others(8561): Show |
chr17 | 12660890 | 12773949 |
a0001c0001t0061 | 0/0 | 8566 | 1 | 1 | 0 | 0 | 0 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | AATCG others(8561): Show |
chr17 | 12660890 | 12773949 |
a0001c0001t0063 | 0/0 | 8565 | 1 | 1 | 0 | 0 | 0 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | AATCG others(8560): Show |
chr17 | 12660890 | 12773949 |
a0001c0001t0064 | 0/0 | 8564 | 1 | 0 | 0 | 1 | 0 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | AATCG others(8559): Show |
chr17 | 12660890 | 12773949 |
a0001c0001t0065 | 0/0 | 8565 | 1 | 0 | 1 | 0 | 0 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | AATCG others(8560): Show |
chr17 | 12660890 | 12773949 |
a0001c0001t0066 | 0/0 | 8564 | 1 | 0 | 1 | 0 | 0 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | AATCG others(8559): Show |
chr17 | 12660890 | 12773949 |
a0001c0001t0067 | 0/0 | 8568 | 1 | 1 | 0 | 0 | 0 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | AATCG others(8563): Show |
chr17 | 12660890 | 12773949 |
a0001c0001t0068 | 0/0 | 8567 | 1 | 0 | 0 | 0 | 0 | 1 | MYOCD_chr17_12660890_12773949 | MYOCD | AATCG others(8562): Show |
chr17 | 12660890 | 12773949 |
a0001c0001t0070 | 0/0 | 8565 | 1 | 0 | 0 | 1 | 0 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | AATCG others(8560): Show |
chr17 | 12660890 | 12773949 |
a0001c0001t0073 | 0/0 | 8567 | 1 | 1 | 0 | 0 | 0 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | AATCG others(8562): Show |
chr17 | 12660890 | 12773949 |
a0001c0001t0074 | 0/0 | 8566 | 1 | 0 | 0 | 1 | 0 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | AATCG others(8561): Show |
chr17 | 12660890 | 12773949 |
a0001c0001t0075 | 0/0 | 8564 | 1 | 1 | 0 | 0 | 0 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | AATCG others(8559): Show |
chr17 | 12660890 | 12773949 |
a0001c0001t0076 | 0/0 | 8567 | 1 | 0 | 0 | 1 | 0 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | AATCG others(8562): Show |
chr17 | 12660890 | 12773949 |
a0001c0001t0078 | 0/0 | 8566 | 1 | 0 | 0 | 1 | 0 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | AATCG others(8561): Show |
chr17 | 12660890 | 12773949 |
a0001c0001t0079 | 0/0 | 8565 | 1 | 0 | 0 | 1 | 0 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | AATCG others(8560): Show |
chr17 | 12660890 | 12773949 |
a0001c0001t0080 | 0/0 | 8565 | 1 | 0 | 0 | 1 | 0 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | AATCG others(8560): Show |
chr17 | 12660890 | 12773949 |
a0001c0001t0081 | 0/0 | 8566 | 1 | 0 | 0 | 1 | 0 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | AATCG others(8561): Show |
chr17 | 12660890 | 12773949 |
a0001c0001t0082 | 0/0 | 8566 | 1 | 0 | 0 | 1 | 0 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | AATCG others(8561): Show |
chr17 | 12660890 | 12773949 |
a0001c0001t0083 | 0/0 | 8566 | 1 | 0 | 0 | 1 | 0 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | AATCG others(8561): Show |
chr17 | 12660890 | 12773949 |
a0001c0001t0084 | 0/0 | 8565 | 1 | 0 | 0 | 1 | 0 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | AATCG others(8560): Show |
chr17 | 12660890 | 12773949 |
a0001c0001t0086 | 0/0 | 8566 | 1 | 0 | 0 | 1 | 0 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | AATCG others(8561): Show |
chr17 | 12660890 | 12773949 |
a0001c0001t0087 | 0/0 | 8565 | 1 | 0 | 0 | 1 | 0 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | AATCG others(8560): Show |
chr17 | 12660890 | 12773949 |
a0001c0001t0088 | 0/0 | 8565 | 1 | 0 | 0 | 1 | 0 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | AATCG others(8560): Show |
chr17 | 12660890 | 12773949 |
a0001c0001t0089 | 0/0 | 8565 | 1 | 0 | 0 | 1 | 0 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | AATCG others(8560): Show |
chr17 | 12660890 | 12773949 |
a0001c0001t0090 | 0/0 | 8566 | 1 | 0 | 0 | 1 | 0 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | AATCG others(8561): Show |
chr17 | 12660890 | 12773949 |
a0001c0001t0091 | 0/0 | 8565 | 1 | 1 | 0 | 0 | 0 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | AATCG others(8560): Show |
chr17 | 12660890 | 12773949 |
a0001c0001t0092 | 0/0 | 8565 | 1 | 1 | 0 | 0 | 0 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | AATCG others(8560): Show |
chr17 | 12660890 | 12773949 |
a0001c0001t0095 | 0/0 | 8565 | 1 | 0 | 0 | 0 | 0 | 1 | MYOCD_chr17_12660890_12773949 | MYOCD | AATCG others(8560): Show |
chr17 | 12660890 | 12773949 |
a0001c0001t0096 | 0/0 | 8566 | 1 | 0 | 0 | 1 | 0 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | AATCG others(8561): Show |
chr17 | 12660890 | 12773949 |
a0001c0001t0097 | 0/0 | 8567 | 1 | 1 | 0 | 0 | 0 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | AATCG others(8562): Show |
chr17 | 12660890 | 12773949 |
a0001c0001t0098 | 0/0 | 8565 | 1 | 0 | 0 | 1 | 0 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | AATCG others(8560): Show |
chr17 | 12660890 | 12773949 |
a0001c0001t0100 | 0/0 | 8565 | 1 | 1 | 0 | 0 | 0 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | AATCG others(8560): Show |
chr17 | 12660890 | 12773949 |
a0001c0001t0103 | 0/0 | 8568 | 1 | 1 | 0 | 0 | 0 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | AATCG others(8563): Show |
chr17 | 12660890 | 12773949 |
a0001c0001t0106 | 0/0 | 8565 | 1 | 1 | 0 | 0 | 0 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | AATCG others(8560): Show |
chr17 | 12660890 | 12773949 |
a0001c0001t0107 | 0/0 | 8565 | 1 | 1 | 0 | 0 | 0 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | AATCG others(8560): Show |
chr17 | 12660890 | 12773949 |
a0001c0001t0108 | 0/0 | 8566 | 1 | 1 | 0 | 0 | 0 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | AATCG others(8561): Show |
chr17 | 12660890 | 12773949 |
a0001c0001t0113 | 0/0 | 8567 | 1 | 1 | 0 | 0 | 0 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | AATCG others(8562): Show |
chr17 | 12660890 | 12773949 |
a0001c0001t0116 | 0/0 | 8564 | 1 | 0 | 1 | 0 | 0 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | AATCG others(8559): Show |
chr17 | 12660890 | 12773949 |
a0001c0001t0117 | 0/0 | 8565 | 1 | 1 | 0 | 0 | 0 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | AATCG others(8560): Show |
chr17 | 12660890 | 12773949 |
a0001c0001t0119 | 0/0 | 8565 | 1 | 1 | 0 | 0 | 0 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | AATCG others(8560): Show |
chr17 | 12660890 | 12773949 |
a0001c0001t0120 | 0/0 | 8565 | 1 | 1 | 0 | 0 | 0 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | AATCG others(8560): Show |
chr17 | 12660890 | 12773949 |
a0001c0001t0121 | 0/0 | 8566 | 1 | 1 | 0 | 0 | 0 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | AATCG others(8561): Show |
chr17 | 12660890 | 12773949 |
a0001c0001t0122 | 0/0 | 8565 | 1 | 0 | 0 | 1 | 0 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | AATCG others(8560): Show |
chr17 | 12660890 | 12773949 |
a0001c0001t0123 | 0/0 | 8566 | 1 | 0 | 0 | 1 | 0 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | AATCG others(8561): Show |
chr17 | 12660890 | 12773949 |
a0001c0001t0125 | 0/0 | 8565 | 1 | 1 | 0 | 0 | 0 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | AATCG others(8560): Show |
chr17 | 12660890 | 12773949 |
a0001c0001t0126 | 0/0 | 8566 | 1 | 0 | 0 | 1 | 0 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | AATCG others(8561): Show |
chr17 | 12660890 | 12773949 |
a0001c0001t0127 | 0/0 | 8565 | 1 | 1 | 0 | 0 | 0 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | AATCG others(8560): Show |
chr17 | 12660890 | 12773949 |
a0001c0001t0128 | 0/0 | 8565 | 1 | 0 | 0 | 1 | 0 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | AATCG others(8560): Show |
chr17 | 12660890 | 12773949 |
a0001c0001t0130 | 0/0 | 8566 | 1 | 0 | 1 | 0 | 0 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | AATCG others(8561): Show |
chr17 | 12660890 | 12773949 |
a0001c0001t0131 | 0/0 | 8565 | 1 | 0 | 0 | 0 | 1 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | AATCG others(8560): Show |
chr17 | 12660890 | 12773949 |
a0001c0001t0132 | 0/0 | 8565 | 1 | 0 | 0 | 1 | 0 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | AATCG others(8560): Show |
chr17 | 12660890 | 12773949 |
a0001c0001t0134 | 0/0 | 8566 | 1 | 0 | 1 | 0 | 0 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | AATCG others(8561): Show |
chr17 | 12660890 | 12773949 |
a0001c0001t0135 | 0/0 | 8567 | 1 | 0 | 0 | 0 | 0 | 1 | MYOCD_chr17_12660890_12773949 | MYOCD | AATCG others(8562): Show |
chr17 | 12660890 | 12773949 |
a0001c0001t0136 | 0/0 | 8566 | 1 | 0 | 0 | 1 | 0 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | AATCG others(8561): Show |
chr17 | 12660890 | 12773949 |
a0001c0001t0137 | 0/0 | 8566 | 1 | 0 | 0 | 0 | 0 | 1 | MYOCD_chr17_12660890_12773949 | MYOCD | AATCG others(8561): Show |
chr17 | 12660890 | 12773949 |
a0001c0001t0138 | 0/0 | 8565 | 1 | 0 | 0 | 1 | 0 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | AATCG others(8560): Show |
chr17 | 12660890 | 12773949 |
a0001c0001t0139 | 0/0 | 8567 | 1 | 0 | 0 | 0 | 0 | 1 | MYOCD_chr17_12660890_12773949 | MYOCD | AATCG others(8562): Show |
chr17 | 12660890 | 12773949 |
a0001c0001t0140 | 0/0 | 8566 | 1 | 1 | 0 | 0 | 0 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | AATCG others(8561): Show |
chr17 | 12660890 | 12773949 |
a0001c0001t0141 | 0/0 | 8565 | 1 | 0 | 0 | 0 | 0 | 1 | MYOCD_chr17_12660890_12773949 | MYOCD | AATCG others(8560): Show |
chr17 | 12660890 | 12773949 |
a0001c0001t0142 | 0/1 | 8565 | 1 | 0 | 0 | 0 | 0 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | AATCG others(8560): Show |
chr17 | 12660890 | 12773949 |
a0001c0001t0143 | 0/0 | 8565 | 1 | 0 | 1 | 0 | 0 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | AATCG others(8560): Show |
chr17 | 12660890 | 12773949 |
a0001c0001t0144 | 0/0 | 8565 | 1 | 0 | 1 | 0 | 0 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | AATCG others(8560): Show |
chr17 | 12660890 | 12773949 |
a0001c0001t0146 | 0/0 | 8567 | 1 | 0 | 1 | 0 | 0 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | AATCG others(8562): Show |
chr17 | 12660890 | 12773949 |
a0001c0001t0147 | 0/0 | 8565 | 1 | 0 | 0 | 1 | 0 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | AATCG others(8560): Show |
chr17 | 12660890 | 12773949 |
a0001c0001t0148 | 0/0 | 8566 | 1 | 0 | 1 | 0 | 0 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | AATCG others(8561): Show |
chr17 | 12660890 | 12773949 |
a0001c0001t0150 | 0/0 | 8565 | 1 | 0 | 0 | 0 | 0 | 1 | MYOCD_chr17_12660890_12773949 | MYOCD | AATCG others(8560): Show |
chr17 | 12660890 | 12773949 |
a0001c0001t0151 | 0/0 | 8564 | 1 | 0 | 0 | 0 | 1 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | AATCG others(8559): Show |
chr17 | 12660890 | 12773949 |
a0001c0001t0152 | 0/0 | 8565 | 1 | 0 | 0 | 1 | 0 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | AATCG others(8560): Show |
chr17 | 12660890 | 12773949 |
a0001c0001t0153 | 0/0 | 8565 | 1 | 0 | 0 | 0 | 0 | 1 | MYOCD_chr17_12660890_12773949 | MYOCD | AATCG others(8560): Show |
chr17 | 12660890 | 12773949 |
a0001c0001t0154 | 0/0 | 8565 | 1 | 0 | 0 | 1 | 0 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | AATCG others(8560): Show |
chr17 | 12660890 | 12773949 |
a0001c0001t0155 | 0/0 | 8544 | 1 | 1 | 0 | 0 | 0 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | AATCG others(8539): Show |
chr17 | 12660890 | 12773949 |
a0001c0001t0156 | 0/0 | 8565 | 1 | 1 | 0 | 0 | 0 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | AATCG others(8560): Show |
chr17 | 12660890 | 12773949 |
a0001c0001t0157 | 0/0 | 8564 | 1 | 0 | 0 | 1 | 0 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | AATCG others(8559): Show |
chr17 | 12660890 | 12773949 |
a0001c0001t0158 | 0/0 | 8565 | 1 | 0 | 0 | 1 | 0 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | AATCG others(8560): Show |
chr17 | 12660890 | 12773949 |
a0001c0001t0159 | 0/0 | 8563 | 1 | 0 | 0 | 0 | 0 | 1 | MYOCD_chr17_12660890_12773949 | MYOCD | AATCG others(8558): Show |
chr17 | 12660890 | 12773949 |
a0001c0001t0160 | 0/0 | 8563 | 1 | 0 | 1 | 0 | 0 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | AATCG others(8558): Show |
chr17 | 12660890 | 12773949 |
a0001c0001t0161 | 0/0 | 8563 | 1 | 0 | 1 | 0 | 0 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | AATCG others(8558): Show |
chr17 | 12660890 | 12773949 |
a0001c0001t0162 | 0/0 | 8566 | 1 | 0 | 0 | 1 | 0 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | AATCG others(8561): Show |
chr17 | 12660890 | 12773949 |
a0001c0001t0163 | 0/0 | 8565 | 1 | 0 | 0 | 0 | 0 | 1 | MYOCD_chr17_12660890_12773949 | MYOCD | AATCG others(8560): Show |
chr17 | 12660890 | 12773949 |
a0001c0001t0164 | 0/0 | 8565 | 1 | 0 | 1 | 0 | 0 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | AATCG others(8560): Show |
chr17 | 12660890 | 12773949 |
a0001c0001t0165 | 0/0 | 8563 | 1 | 0 | 1 | 0 | 0 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | AATCG others(8558): Show |
chr17 | 12660890 | 12773949 |
a0001c0001t0166 | 0/0 | 8566 | 1 | 1 | 0 | 0 | 0 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | AATCG others(8561): Show |
chr17 | 12660890 | 12773949 |
a0001c0001t0167 | 0/0 | 8561 | 1 | 1 | 0 | 0 | 0 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | AATCG others(8556): Show |
chr17 | 12660890 | 12773949 |
a0001c0001t0168 | 0/0 | 8566 | 1 | 1 | 0 | 0 | 0 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | AATCG others(8561): Show |
chr17 | 12660890 | 12773949 |
a0001c0001t0169 | 0/0 | 8566 | 1 | 0 | 1 | 0 | 0 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | AATCG others(8561): Show |
chr17 | 12660890 | 12773949 |
a0001c0001t0170 | 0/0 | 8567 | 1 | 0 | 1 | 0 | 0 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | AATCG others(8562): Show |
chr17 | 12660890 | 12773949 |
a0001c0001t0171 | 0/0 | 8566 | 1 | 0 | 0 | 0 | 0 | 1 | MYOCD_chr17_12660890_12773949 | MYOCD | AATCG others(8561): Show |
chr17 | 12660890 | 12773949 |
a0001c0001t0172 | 0/0 | 8566 | 1 | 0 | 1 | 0 | 0 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | AATCG others(8561): Show |
chr17 | 12660890 | 12773949 |
a0001c0001t0173 | 0/0 | 8566 | 1 | 0 | 1 | 0 | 0 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | AATCG others(8561): Show |
chr17 | 12660890 | 12773949 |
a0001c0001t0174 | 0/0 | 8565 | 1 | 0 | 0 | 0 | 1 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | AATCG others(8560): Show |
chr17 | 12660890 | 12773949 |
a0001c0001t0179 | 0/0 | 8565 | 1 | 0 | 0 | 1 | 0 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | AATCG others(8560): Show |
chr17 | 12660890 | 12773949 |
a0001c0001t0183 | 0/0 | 8565 | 1 | 1 | 0 | 0 | 0 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | AATCG others(8560): Show |
chr17 | 12660890 | 12773949 |
a0001c0001t0184 | 0/0 | 8565 | 1 | 0 | 0 | 1 | 0 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | AATCG others(8560): Show |
chr17 | 12660890 | 12773949 |
a0001c0001t0186 | 0/0 | 8565 | 1 | 0 | 0 | 1 | 0 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | AATCG others(8560): Show |
chr17 | 12660890 | 12773949 |
a0001c0001t0188 | 0/0 | 8566 | 1 | 0 | 0 | 1 | 0 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | AATCG others(8561): Show |
chr17 | 12660890 | 12773949 |
a0001c0001t0189 | 0/0 | 8565 | 1 | 0 | 0 | 1 | 0 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | AATCG others(8560): Show |
chr17 | 12660890 | 12773949 |
a0001c0001t0195 | 0/0 | 8565 | 1 | 0 | 0 | 1 | 0 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | AATCG others(8560): Show |
chr17 | 12660890 | 12773949 |
a0001c0001t0196 | 0/0 | 8564 | 1 | 0 | 0 | 1 | 0 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | AATCG others(8559): Show |
chr17 | 12660890 | 12773949 |
a0001c0001t0201 | 0/0 | 8565 | 1 | 1 | 0 | 0 | 0 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | AATCG others(8560): Show |
chr17 | 12660890 | 12773949 |
a0001c0002t0001 | 0/0 | 8565 | 1 | 0 | 0 | 1 | 0 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | AATCG others(8560): Show |
chr17 | 12660890 | 12773949 |
a0001c0002t0002 | 0/0 | 8565 | 1 | 0 | 0 | 1 | 0 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | AATCG others(8560): Show |
chr17 | 12660890 | 12773949 |
a0001c0002t0003 | 0/0 | 8566 | 1 | 0 | 0 | 0 | 0 | 1 | MYOCD_chr17_12660890_12773949 | MYOCD | AATCG others(8561): Show |
chr17 | 12660890 | 12773949 |
a0001c0002t0004 | 0/0 | 8565 | 5 | 0 | 0 | 5 | 0 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | AATCG others(8560): Show |
chr17 | 12660890 | 12773949 |
a0001c0002t0005 | 0/0 | 8565 | 1 | 0 | 0 | 1 | 0 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | AATCG others(8560): Show |
chr17 | 12660890 | 12773949 |
a0001c0002t0006 | 0/0 | 8566 | 1 | 0 | 0 | 1 | 0 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | AATCG others(8561): Show |
chr17 | 12660890 | 12773949 |
a0001c0002t0007 | 0/0 | 8565 | 2 | 0 | 0 | 2 | 0 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | AATCG others(8560): Show |
chr17 | 12660890 | 12773949 |
a0001c0002t0009 | 0/0 | 8565 | 1 | 0 | 1 | 0 | 0 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | AATCG others(8560): Show |
chr17 | 12660890 | 12773949 |
a0001c0002t0032 | 0/0 | 8563 | 1 | 0 | 0 | 1 | 0 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | AATCG others(8558): Show |
chr17 | 12660890 | 12773949 |
a0001c0002t0047 | 0/0 | 8564 | 1 | 0 | 0 | 1 | 0 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | AATCG others(8559): Show |
chr17 | 12660890 | 12773949 |
a0001c0002t0062 | 0/0 | 8566 | 1 | 0 | 1 | 0 | 0 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | AATCG others(8561): Show |
chr17 | 12660890 | 12773949 |
a0001c0002t0069 | 0/0 | 8565 | 1 | 0 | 0 | 1 | 0 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | AATCG others(8560): Show |
chr17 | 12660890 | 12773949 |
a0001c0002t0085 | 0/0 | 8567 | 1 | 0 | 0 | 1 | 0 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | AATCG others(8562): Show |
chr17 | 12660890 | 12773949 |
a0001c0002t0124 | 0/0 | 8563 | 1 | 0 | 0 | 1 | 0 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | AATCG others(8558): Show |
chr17 | 12660890 | 12773949 |
a0001c0002t0133 | 0/0 | 8564 | 1 | 0 | 0 | 1 | 0 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | AATCG others(8559): Show |
chr17 | 12660890 | 12773949 |
a0001c0002t0149 | 0/0 | 8564 | 1 | 0 | 0 | 1 | 0 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | AATCG others(8559): Show |
chr17 | 12660890 | 12773949 |
a0001c0002t0177 | 0/0 | 8565 | 1 | 0 | 0 | 1 | 0 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | AATCG others(8560): Show |
chr17 | 12660890 | 12773949 |
a0001c0002t0178 | 0/0 | 8567 | 1 | 0 | 0 | 1 | 0 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | AATCG others(8562): Show |
chr17 | 12660890 | 12773949 |
a0001c0002t0187 | 0/0 | 8566 | 1 | 0 | 0 | 1 | 0 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | AATCG others(8561): Show |
chr17 | 12660890 | 12773949 |
a0001c0002t0190 | 0/0 | 8565 | 1 | 0 | 0 | 1 | 0 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | AATCG others(8560): Show |
chr17 | 12660890 | 12773949 |
a0001c0002t0191 | 0/0 | 8565 | 1 | 0 | 1 | 0 | 0 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | AATCG others(8560): Show |
chr17 | 12660890 | 12773949 |
a0001c0002t0192 | 0/0 | 8567 | 1 | 0 | 0 | 1 | 0 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | AATCG others(8562): Show |
chr17 | 12660890 | 12773949 |
a0001c0002t0193 | 0/0 | 8566 | 1 | 0 | 0 | 1 | 0 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | AATCG others(8561): Show |
chr17 | 12660890 | 12773949 |
a0001c0002t0198 | 0/0 | 8566 | 1 | 0 | 0 | 1 | 0 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | AATCG others(8561): Show |
chr17 | 12660890 | 12773949 |
a0001c0003t0046 | 0/0 | 8567 | 2 | 2 | 0 | 0 | 0 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | AATCG others(8562): Show |
chr17 | 12660890 | 12773949 |
a0001c0003t0049 | 0/0 | 8570 | 1 | 1 | 0 | 0 | 0 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | AATCG others(8565): Show |
chr17 | 12660890 | 12773949 |
a0001c0003t0077 | 0/0 | 8566 | 1 | 1 | 0 | 0 | 0 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | AATCG others(8561): Show |
chr17 | 12660890 | 12773949 |
a0001c0003t0105 | 0/0 | 8566 | 1 | 1 | 0 | 0 | 0 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | AATCG others(8561): Show |
chr17 | 12660890 | 12773949 |
a0001c0003t0109 | 0/0 | 8565 | 1 | 1 | 0 | 0 | 0 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | AATCG others(8560): Show |
chr17 | 12660890 | 12773949 |
a0001c0003t0112 | 0/0 | 8565 | 1 | 1 | 0 | 0 | 0 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | AATCG others(8560): Show |
chr17 | 12660890 | 12773949 |
a0001c0003t0180 | 0/0 | 8565 | 1 | 1 | 0 | 0 | 0 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | AATCG others(8560): Show |
chr17 | 12660890 | 12773949 |
a0001c0003t0181 | 0/0 | 8566 | 1 | 1 | 0 | 0 | 0 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | AATCG others(8561): Show |
chr17 | 12660890 | 12773949 |
a0001c0003t0182 | 0/0 | 8567 | 1 | 1 | 0 | 0 | 0 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | AATCG others(8562): Show |
chr17 | 12660890 | 12773949 |
a0001c0003t0202 | 0/0 | 8564 | 1 | 1 | 0 | 0 | 0 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | AATCG others(8559): Show |
chr17 | 12660890 | 12773949 |
a0001c0003t0203 | 0/0 | 8566 | 1 | 1 | 0 | 0 | 0 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | AATCG others(8561): Show |
chr17 | 12660890 | 12773949 |
a0001c0003t0204 | 0/0 | 8566 | 1 | 1 | 0 | 0 | 0 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | AATCG others(8561): Show |
chr17 | 12660890 | 12773949 |
a0001c0003t0205 | 0/0 | 8562 | 1 | 1 | 0 | 0 | 0 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | AATCG others(8557): Show |
chr17 | 12660890 | 12773949 |
a0001c0003t0206 | 0/0 | 8565 | 1 | 1 | 0 | 0 | 0 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | AATCG others(8560): Show |
chr17 | 12660890 | 12773949 |
a0001c0004t0001 | 0/0 | 8565 | 1 | 0 | 1 | 0 | 0 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | AATCG others(8560): Show |
chr17 | 12660890 | 12773949 |
a0001c0004t0002 | 0/0 | 8565 | 2 | 0 | 2 | 0 | 0 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | AATCG others(8560): Show |
chr17 | 12660890 | 12773949 |
a0001c0004t0003 | 0/0 | 8566 | 2 | 0 | 2 | 0 | 0 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | AATCG others(8561): Show |
chr17 | 12660890 | 12773949 |
a0001c0004t0005 | 0/0 | 8565 | 1 | 0 | 1 | 0 | 0 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | AATCG others(8560): Show |
chr17 | 12660890 | 12773949 |
a0001c0004t0034 | 0/0 | 8566 | 1 | 0 | 1 | 0 | 0 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | AATCG others(8561): Show |
chr17 | 12660890 | 12773949 |
a0001c0006t0016 | 0/0 | 8564 | 2 | 2 | 0 | 0 | 0 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | AATCG others(8559): Show |
chr17 | 12660890 | 12773949 |
a0001c0006t0050 | 0/0 | 8562 | 1 | 1 | 0 | 0 | 0 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | AATCG others(8557): Show |
chr17 | 12660890 | 12773949 |
a0001c0006t0093 | 0/0 | 8568 | 1 | 1 | 0 | 0 | 0 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | AATCG others(8563): Show |
chr17 | 12660890 | 12773949 |
a0001c0006t0094 | 0/0 | 8566 | 1 | 1 | 0 | 0 | 0 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | AATCG others(8561): Show |
chr17 | 12660890 | 12773949 |
a0001c0007t0001 | 0/0 | 8565 | 1 | 0 | 0 | 0 | 1 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | AATCG others(8560): Show |
chr17 | 12660890 | 12773949 |
a0001c0007t0002 | 0/0 | 8565 | 1 | 0 | 1 | 0 | 0 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | AATCG others(8560): Show |
chr17 | 12660890 | 12773949 |
a0001c0007t0043 | 0/0 | 8563 | 2 | 0 | 0 | 0 | 2 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | AATCG others(8558): Show |
chr17 | 12660890 | 12773949 |
a0001c0011t0020 | 0/0 | 8564 | 2 | 2 | 0 | 0 | 0 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | AATCG others(8559): Show |
chr17 | 12660890 | 12773949 |
a0001c0015t0001 | 0/0 | 8565 | 1 | 1 | 0 | 0 | 0 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | AATCG others(8560): Show |
chr17 | 12660890 | 12773949 |
a0001c0028t0044 | 0/0 | 8567 | 1 | 0 | 0 | 0 | 0 | 1 | MYOCD_chr17_12660890_12773949 | MYOCD | AATCG others(8562): Show |
chr17 | 12660890 | 12773949 |
a0002c0005t0002 | 0/0 | 8565 | 1 | 0 | 1 | 0 | 0 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | AATCG others(8560): Show |
chr17 | 12660890 | 12773949 |
a0002c0005t0003 | 0/0 | 8566 | 1 | 0 | 0 | 0 | 0 | 1 | MYOCD_chr17_12660890_12773949 | MYOCD | AATCG others(8561): Show |
chr17 | 12660890 | 12773949 |
a0002c0005t0012 | 0/0 | 8564 | 1 | 0 | 0 | 1 | 0 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | AATCG others(8559): Show |
chr17 | 12660890 | 12773949 |
a0002c0005t0102 | 0/0 | 8565 | 1 | 0 | 0 | 0 | 0 | 1 | MYOCD_chr17_12660890_12773949 | MYOCD | AATCG others(8560): Show |
chr17 | 12660890 | 12773949 |
a0002c0005t0129 | 0/0 | 8565 | 1 | 0 | 0 | 1 | 0 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | AATCG others(8560): Show |
chr17 | 12660890 | 12773949 |
a0002c0005t0185 | 0/0 | 8566 | 1 | 0 | 0 | 1 | 0 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | AATCG others(8561): Show |
chr17 | 12660890 | 12773949 |
a0002c0005t0199 | 0/0 | 8566 | 1 | 0 | 0 | 0 | 0 | 1 | MYOCD_chr17_12660890_12773949 | MYOCD | AATCG others(8561): Show |
chr17 | 12660890 | 12773949 |
a0003c0008t0071 | 0/0 | 8565 | 1 | 1 | 0 | 0 | 0 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | AATCG others(8560): Show |
chr17 | 12660890 | 12773949 |
a0003c0008t0072 | 0/0 | 8566 | 1 | 1 | 0 | 0 | 0 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | AATCG others(8561): Show |
chr17 | 12660890 | 12773949 |
a0003c0008t0104 | 0/0 | 8560 | 1 | 1 | 0 | 0 | 0 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | AATCG others(8555): Show |
chr17 | 12660890 | 12773949 |
a0003c0008t0111 | 0/0 | 8564 | 1 | 1 | 0 | 0 | 0 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | AATCG others(8559): Show |
chr17 | 12660890 | 12773949 |
a0004c0009t0197 | 0/0 | 8566 | 1 | 0 | 1 | 0 | 0 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | AATCG others(8561): Show |
chr17 | 12660890 | 12773949 |
a0004c0009t0200 | 0/0 | 8565 | 1 | 0 | 1 | 0 | 0 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | AATCG others(8560): Show |
chr17 | 12660890 | 12773949 |
a0004c0017t0007 | 0/0 | 8565 | 1 | 0 | 0 | 1 | 0 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | AATCG others(8560): Show |
chr17 | 12660890 | 12773949 |
a0005c0010t0099 | 0/0 | 8565 | 1 | 1 | 0 | 0 | 0 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | AATCG others(8560): Show |
chr17 | 12660890 | 12773949 |
a0005c0010t0145 | 0/0 | 8565 | 1 | 0 | 0 | 1 | 0 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | AATCG others(8560): Show |
chr17 | 12660890 | 12773949 |
a0006c0012t0031 | 0/0 | 8565 | 2 | 2 | 0 | 0 | 0 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | AATCG others(8560): Show |
chr17 | 12660890 | 12773949 |
a0007c0022t0176 | 0/0 | 8566 | 1 | 0 | 0 | 1 | 0 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | AATCG others(8561): Show |
chr17 | 12660890 | 12773949 |
a0008c0018t0016 | 0/0 | 8564 | 1 | 0 | 1 | 0 | 0 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | AATCG others(8559): Show |
chr17 | 12660890 | 12773949 |
a0009c0020t0194 | 0/0 | 8566 | 1 | 1 | 0 | 0 | 0 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | AATCG others(8561): Show |
chr17 | 12660890 | 12773949 |
a0010c0025t0003 | 0/0 | 8566 | 1 | 0 | 0 | 1 | 0 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | AATCG others(8561): Show |
chr17 | 12660890 | 12773949 |
a0011c0030t0114 | 0/0 | 8565 | 1 | 1 | 0 | 0 | 0 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | AATCG others(8560): Show |
chr17 | 12660890 | 12773949 |
a0012c0029t0115 | 0/0 | 8565 | 1 | 1 | 0 | 0 | 0 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | AATCG others(8560): Show |
chr17 | 12660890 | 12773949 |
a0013c0027t0110 | 0/0 | 8565 | 1 | 1 | 0 | 0 | 0 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | AATCG others(8560): Show |
chr17 | 12660890 | 12773949 |
a0014c0016t0118 | 0/0 | 8567 | 1 | 1 | 0 | 0 | 0 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | AATCG others(8562): Show |
chr17 | 12660890 | 12773949 |
a0015c0023t0014 | 0/0 | 8562 | 1 | 1 | 0 | 0 | 0 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | AATCG others(8557): Show |
chr17 | 12660890 | 12773949 |
a0016c0021t0175 | 0/0 | 8566 | 1 | 0 | 0 | 0 | 0 | 1 | MYOCD_chr17_12660890_12773949 | MYOCD | AATCG others(8561): Show |
chr17 | 12660890 | 12773949 |
a0017c0013t0011 | 0/0 | 8560 | 1 | 1 | 0 | 0 | 0 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | AATCG others(8555): Show |
chr17 | 12660890 | 12773949 |
a0018c0026t0027 | 0/0 | 8567 | 1 | 0 | 0 | 1 | 0 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | AATCG others(8562): Show |
chr17 | 12660890 | 12773949 |
a0019c0024t0012 | 0/0 | 8564 | 1 | 0 | 0 | 1 | 0 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | AATCG others(8559): Show |
chr17 | 12660890 | 12773949 |
a0020c0014t0101 | 0/0 | 8566 | 1 | 1 | 0 | 0 | 0 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | AATCG others(8561): Show |
chr17 | 12660890 | 12773949 |
a0021c0019t0009 | 0/0 | 8565 | 1 | 0 | 0 | 0 | 0 | 1 | MYOCD_chr17_12660890_12773949 | MYOCD | AATCG others(8560): Show |
chr17 | 12660890 | 12773949 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
a0001c0001t0001g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
a0001c0001t0001g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
a0001c0001t0001g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
a0001c0001t0001g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
a0001c0001t0001g0343 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
a0001c0001t0002g0018 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
a0001c0001t0002g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
a0001c0001t0002g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
a0001c0001t0002g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
a0001c0001t0002g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
a0001c0001t0002g0187 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
a0001c0001t0002g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
a0001c0001t0002g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
a0001c0001t0002g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
a0001c0001t0002g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
a0001c0001t0003g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
a0001c0001t0003g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
a0001c0001t0003g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
a0001c0001t0003g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
a0001c0001t0003g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
a0001c0001t0003g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
a0001c0001t0004g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
a0001c0001t0004g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
a0001c0001t0004g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
a0001c0001t0004g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
a0001c0001t0004g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
a0001c0001t0005g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
a0001c0001t0005g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
a0001c0001t0005g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
a0001c0001t0005g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
a0001c0001t0005g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
a0001c0001t0005g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
a0001c0001t0005g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
a0001c0001t0005g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
a0001c0001t0006g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
a0001c0001t0006g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
a0001c0001t0006g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
a0001c0001t0006g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
a0001c0001t0006g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
a0001c0001t0006g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
a0001c0001t0006g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
a0001c0001t0006g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
a0001c0001t0007g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
a0001c0001t0007g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
a0001c0001t0007g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
a0001c0001t0008g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
a0001c0001t0008g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
a0001c0001t0008g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
a0001c0001t0008g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
a0001c0001t0008g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
a0001c0001t0008g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
a0001c0001t0009g0326 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
a0001c0001t0009g0328 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
a0001c0001t0009g0329 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
a0001c0001t0010g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
a0001c0001t0010g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
a0001c0001t0010g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
a0001c0001t0010g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
a0001c0001t0010g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
a0001c0001t0011g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
a0001c0001t0011g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
a0001c0001t0011g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
a0001c0001t0012g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
a0001c0001t0012g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
a0001c0001t0013g0039 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
a0001c0001t0013g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
a0001c0001t0013g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
a0001c0001t0013g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
a0001c0001t0014g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
a0001c0001t0014g0338 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
a0001c0001t0015g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
a0001c0001t0015g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
a0001c0001t0015g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
a0001c0001t0017g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
a0001c0001t0017g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
a0001c0001t0017g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
a0001c0001t0018g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
a0001c0001t0018g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
a0001c0001t0018g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
a0001c0001t0019g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
a0001c0001t0019g0113 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
a0001c0001t0019g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
a0001c0001t0021g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
a0001c0001t0021g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
a0001c0001t0022g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
a0001c0001t0022g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
a0001c0001t0023g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
a0001c0001t0023g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
a0001c0001t0024g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
a0001c0001t0024g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
a0001c0001t0025g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
a0001c0001t0025g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
a0001c0001t0026g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
a0001c0001t0026g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
a0001c0001t0027g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
a0001c0001t0028g0002 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
a0001c0001t0029g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
a0001c0001t0029g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
a0001c0001t0030g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
a0001c0001t0030g0301 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
a0001c0001t0032g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
a0001c0001t0033g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
a0001c0001t0033g0333 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
a0001c0001t0034g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
a0001c0001t0035g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
a0001c0001t0035g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
a0001c0001t0036g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
a0001c0001t0036g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
a0001c0001t0037g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
a0001c0001t0037g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
a0001c0001t0038g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
a0001c0001t0038g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
a0001c0001t0039g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
a0001c0001t0039g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
a0001c0001t0040g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
a0001c0001t0040g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
a0001c0001t0041g0011 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
a0001c0001t0041g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
a0001c0001t0042g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
a0001c0001t0042g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
a0001c0001t0044g0012 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
a0001c0001t0045g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
a0001c0001t0045g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
a0001c0001t0047g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
a0001c0001t0048g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
a0001c0001t0048g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
a0001c0001t0051g0009 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
a0001c0001t0052g0008 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
a0001c0001t0053g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
a0001c0001t0054g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
a0001c0001t0055g0336 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
a0001c0001t0056g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
a0001c0001t0057g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
a0001c0001t0058g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
a0001c0001t0059g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
a0001c0001t0060g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
a0001c0001t0061g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
a0001c0001t0063g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
a0001c0001t0064g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
a0001c0001t0065g0330 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
a0001c0001t0066g0327 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
a0001c0001t0067g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
a0001c0001t0068g0324 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
a0001c0001t0070g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
a0001c0001t0073g0337 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
a0001c0001t0074g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
a0001c0001t0075g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
a0001c0001t0076g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
a0001c0001t0078g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
a0001c0001t0079g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
a0001c0001t0080g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
a0001c0001t0081g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
a0001c0001t0082g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
a0001c0001t0083g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
a0001c0001t0084g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
a0001c0001t0086g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
a0001c0001t0087g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
a0001c0001t0088g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
a0001c0001t0089g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
a0001c0001t0090g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
a0001c0001t0091g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
a0001c0001t0092g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
a0001c0001t0095g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
a0001c0001t0096g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
a0001c0001t0097g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
a0001c0001t0098g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
a0001c0001t0100g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
a0001c0001t0103g0339 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
a0001c0001t0106g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
a0001c0001t0107g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
a0001c0001t0108g0342 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
a0001c0001t0113g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
a0001c0001t0116g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
a0001c0001t0117g0340 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
a0001c0001t0119g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
a0001c0001t0120g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
a0001c0001t0121g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
a0001c0001t0122g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
a0001c0001t0123g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
a0001c0001t0125g0341 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
a0001c0001t0126g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
a0001c0001t0127g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
a0001c0001t0128g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
a0001c0001t0130g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
a0001c0001t0131g0114 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
a0001c0001t0132g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
a0001c0001t0134g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
a0001c0001t0135g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
a0001c0001t0136g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
a0001c0001t0137g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
a0001c0001t0138g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
a0001c0001t0139g0013 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
a0001c0001t0140g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
a0001c0001t0141g0015 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
a0001c0001t0142g0050 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
a0001c0001t0143g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
a0001c0001t0144g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
a0001c0001t0146g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
a0001c0001t0147g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
a0001c0001t0148g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
a0001c0001t0150g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
a0001c0001t0151g0182 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
a0001c0001t0152g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
a0001c0001t0153g0010 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
a0001c0001t0154g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
a0001c0001t0155g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
a0001c0001t0156g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
a0001c0001t0157g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
a0001c0001t0158g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
a0001c0001t0159g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
a0001c0001t0160g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
a0001c0001t0161g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
a0001c0001t0162g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
a0001c0001t0163g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
a0001c0001t0164g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
a0001c0001t0165g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
a0001c0001t0166g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
a0001c0001t0167g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
a0001c0001t0168g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
a0001c0001t0169g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
a0001c0001t0170g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
a0001c0001t0171g0014 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
a0001c0001t0172g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
a0001c0001t0173g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
a0001c0001t0174g0075 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
a0001c0001t0179g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
a0001c0001t0183g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
a0001c0001t0184g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
a0001c0001t0186g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
a0001c0001t0188g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
a0001c0001t0189g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
a0001c0001t0195g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
a0001c0001t0196g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
a0001c0001t0201g0334 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
a0001c0002t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
a0001c0002t0002g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
a0001c0002t0003g0299 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
a0001c0002t0004g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
a0001c0002t0004g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
a0001c0002t0004g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
a0001c0002t0004g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
a0001c0002t0004g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
a0001c0002t0005g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
a0001c0002t0006g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
a0001c0002t0007g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
a0001c0002t0007g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
a0001c0002t0009g0321 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
a0001c0002t0032g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
a0001c0002t0047g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
a0001c0002t0062g0322 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
a0001c0002t0069g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
a0001c0002t0085g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
a0001c0002t0124g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
a0001c0002t0133g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
a0001c0002t0149g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
a0001c0002t0177g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
a0001c0002t0178g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
a0001c0002t0187g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
a0001c0002t0190g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
a0001c0002t0191g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
a0001c0002t0192g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
a0001c0002t0193g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
a0001c0002t0198g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
a0001c0003t0046g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
a0001c0003t0046g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
a0001c0003t0049g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
a0001c0003t0077g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
a0001c0003t0105g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
a0001c0003t0109g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
a0001c0003t0112g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
a0001c0003t0180g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
a0001c0003t0181g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
a0001c0003t0182g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
a0001c0003t0202g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
a0001c0003t0203g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
a0001c0003t0204g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
a0001c0003t0205g0332 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
a0001c0003t0206g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
a0001c0004t0001g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
a0001c0004t0002g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
a0001c0004t0002g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
a0001c0004t0003g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
a0001c0004t0003g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
a0001c0004t0005g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
a0001c0004t0034g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
a0001c0006t0016g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
a0001c0006t0016g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
a0001c0006t0050g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
a0001c0006t0093g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
a0001c0006t0094g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
a0001c0007t0001g0220 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
a0001c0007t0002g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
a0001c0007t0043g0204 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
a0001c0007t0043g0205 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
a0001c0011t0020g0001 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
a0001c0015t0001g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
a0001c0028t0044g0249 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
a0002c0005t0002g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
a0002c0005t0003g0295 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
a0002c0005t0012g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
a0002c0005t0102g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
a0002c0005t0129g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
a0002c0005t0185g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
a0002c0005t0199g0296 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
a0003c0008t0071g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
a0003c0008t0072g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
a0003c0008t0104g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
a0003c0008t0111g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
a0004c0009t0197g0004 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
a0004c0009t0200g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
a0004c0017t0007g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
a0005c0010t0099g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
a0005c0010t0145g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
a0006c0012t0031g0003 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
a0007c0022t0176g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
a0008c0018t0016g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
a0009c0020t0194g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
a0010c0025t0003g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
a0011c0030t0114g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
a0012c0029t0115g0335 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
a0013c0027t0110g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
a0014c0016t0118g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
a0015c0023t0014g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
a0016c0021t0175g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
a0017c0013t0011g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
a0018c0026t0027g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
a0019c0024t0012g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
a0020c0014t0101g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
a0021c0019t0009g0331 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00280 | hp1 | a0001 | c0001 | t0131 | g0114 | EUR | FIN | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
HG00280 | hp2 | a0001 | c0001 | t0002 | g0018 | EUR | FIN | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
HG00323 | hp1 | a0001 | c0007 | t0001 | g0220 | EUR | FIN | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
HG00323 | hp2 | a0001 | c0001 | t0001 | g0207 | EUR | FIN | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
HG00408 | hp1 | a0001 | c0002 | t0198 | g0197 | EAS | CHS | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
HG00408 | hp2 | a0001 | c0002 | t0178 | g0072 | EAS | CHS | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
HG00423 | hp1 | a0001 | c0001 | t0147 | g0237 | EAS | CHS | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
HG00423 | hp2 | a0001 | c0001 | t0010 | g0074 | EAS | CHS | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
HG00544 | hp1 | a0002 | c0005 | t0185 | g0277 | EAS | CHS | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
HG00544 | hp2 | a0001 | c0001 | t0027 | g0297 | EAS | CHS | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
HG00558 | hp1 | a0001 | c0001 | t0001 | g0079 | EAS | CHS | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
HG00558 | hp2 | a0001 | c0001 | t0152 | g0120 | EAS | CHS | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
HG00597 | hp1 | a0001 | c0001 | t0004 | g0082 | EAS | CHS | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
HG00597 | hp2 | a0001 | c0001 | t0053 | g0325 | EAS | CHS | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
HG00609 | hp1 | a0001 | c0001 | t0001 | g0124 | EAS | CHS | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
HG00609 | hp2 | a0001 | c0001 | t0026 | g0289 | EAS | CHS | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
HG00621 | hp1 | a0001 | c0001 | t0007 | g0088 | EAS | CHS | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
HG00621 | hp2 | a0007 | c0022 | t0176 | g0279 | EAS | CHS | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
HG00639 | hp1 | a0001 | c0002 | t0191 | g0110 | AMR | PUR | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
HG00639 | hp2 | a0001 | c0001 | t0134 | g0215 | AMR | PUR | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
HG00642 | hp1 | a0001 | c0001 | t0065 | g0330 | AMR | PUR | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
HG00642 | hp2 | a0001 | c0001 | t0164 | g0189 | AMR | PUR | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
HG00673 | hp1 | a0001 | c0001 | t0026 | g0234 | EAS | CHS | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
HG00673 | hp2 | a0001 | c0001 | t0096 | g0109 | EAS | CHS | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
HG00733 | hp1 | a0001 | c0001 | t0144 | g0219 | AMR | PUR | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
HG00733 | hp2 | a0001 | c0001 | t0029 | g0097 | AMR | PUR | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
HG00735 | hp1 | a0001 | c0001 | t0066 | g0327 | AMR | PUR | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
HG00735 | hp2 | a0001 | c0001 | t0041 | g0011 | AMR | PUR | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
HG00738 | hp1 | a0001 | c0007 | t0002 | g0209 | AMR | PUR | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
HG00738 | hp2 | a0001 | c0002 | t0062 | g0322 | AMR | PUR | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
HG00741 | hp1 | a0001 | c0004 | t0003 | g0254 | AMR | PUR | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
HG00741 | hp2 | a0001 | c0001 | t0165 | g0198 | AMR | PUR | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
HG01081 | hp1 | a0001 | c0001 | t0003 | g0201 | AMR | PUR | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
HG01081 | hp2 | a0001 | c0001 | t0001 | g0176 | AMR | PUR | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
HG01106 | hp1 | a0001 | c0004 | t0003 | g0128 | AMR | PUR | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
HG01106 | hp2 | a0001 | c0001 | t0143 | g0186 | AMR | PUR | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
HG01109 | hp1 | a0001 | c0001 | t0170 | g0099 | AMR | PUR | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
HG01109 | hp2 | a0001 | c0001 | t0051 | g0009 | AMR | PUR | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
HG01175 | hp1 | a0008 | c0018 | t0016 | g0096 | AMR | PUR | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
HG01175 | hp2 | a0001 | c0001 | t0002 | g0090 | AMR | PUR | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
HG01192 | hp1 | a0001 | c0001 | t0055 | g0336 | AMR | PUR | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
HG01192 | hp2 | a0001 | c0001 | t0005 | g0054 | AMR | PUR | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
HG01243 | hp1 | a0001 | c0001 | t0014 | g0338 | AMR | PUR | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
HG01243 | hp2 | a0001 | c0001 | t0052 | g0008 | AMR | PUR | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
HG01255 | hp1 | a0001 | c0001 | t0146 | g0019 | AMR | CLM | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
HG01255 | hp2 | a0001 | c0001 | t0041 | g0055 | AMR | CLM | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
HG01256 | hp1 | a0001 | c0001 | t0173 | g0070 | AMR | CLM | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
HG01256 | hp2 | a0001 | c0001 | t0169 | g0263 | AMR | CLM | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
HG01257 | hp1 | a0001 | c0001 | t0130 | g0101 | AMR | CLM | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
HG01257 | hp2 | a0004 | c0009 | t0197 | g0004 | AMR | CLM | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
HG01261 | hp1 | a0001 | c0001 | t0160 | g0108 | AMR | CLM | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
HG01261 | hp2 | a0002 | c0005 | t0002 | g0185 | AMR | CLM | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
HG01346 | hp1 | a0001 | c0001 | t0009 | g0328 | AMR | CLM | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
HG01346 | hp2 | a0001 | c0001 | t0001 | g0177 | AMR | CLM | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
HG01358 | hp1 | a0001 | c0001 | t0045 | g0065 | AMR | CLM | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
HG01358 | hp2 | a0001 | c0002 | t0009 | g0321 | AMR | CLM | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
HG01361 | hp1 | a0001 | c0001 | t0002 | g0208 | AMR | CLM | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
HG01361 | hp2 | a0001 | c0001 | t0019 | g0115 | AMR | CLM | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
HG01433 | hp1 | a0001 | c0001 | t0003 | g0212 | AMR | CLM | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
HG01433 | hp2 | a0001 | c0001 | t0045 | g0066 | AMR | CLM | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
HG01496 | hp1 | a0001 | c0001 | t0001 | g0181 | AMR | CLM | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
HG01496 | hp2 | a0001 | c0004 | t0002 | g0049 | AMR | CLM | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
HG01515 | hp1 | a0001 | c0001 | t0151 | g0182 | EUR | IBS | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
HG01515 | hp2 | a0001 | c0007 | t0043 | g0205 | EUR | IBS | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
HG01517 | hp1 | a0001 | c0007 | t0043 | g0204 | EUR | IBS | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
HG01517 | hp2 | a0001 | c0001 | t0174 | g0075 | EUR | IBS | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
HG01884 | hp1 | a0001 | c0001 | t0033 | g0034 | AFR | ACB | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
HG01884 | hp2 | a0003 | c0008 | t0071 | g0305 | AFR | ACB | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
HG01891 | hp1 | a0001 | c0001 | t0067 | g0315 | AFR | ACB | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
HG01891 | hp2 | a0001 | c0001 | t0013 | g0259 | AFR | ACB | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
HG01934 | hp1 | a0001 | c0001 | t0116 | g0270 | AMR | PEL | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
HG01934 | hp2 | a0004 | c0009 | t0200 | g0076 | AMR | PEL | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
HG01952 | hp1 | a0001 | c0001 | t0009 | g0329 | AMR | PEL | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
HG01952 | hp2 | a0001 | c0001 | t0010 | g0094 | AMR | PEL | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
HG01978 | hp1 | a0001 | c0004 | t0034 | g0238 | AMR | PEL | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
HG01978 | hp2 | a0001 | c0001 | t0172 | g0043 | AMR | PEL | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
HG01981 | hp1 | a0001 | c0001 | t0161 | g0190 | AMR | PEL | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
HG01981 | hp2 | a0001 | c0004 | t0001 | g0100 | AMR | PEL | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
HG01993 | hp1 | a0001 | c0004 | t0002 | g0233 | AMR | PEL | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
HG01993 | hp2 | a0001 | c0001 | t0009 | g0326 | AMR | PEL | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
HG02004 | hp1 | a0001 | c0001 | t0035 | g0129 | AMR | PEL | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
HG02004 | hp2 | a0001 | c0001 | t0029 | g0171 | AMR | PEL | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
HG02027 | hp1 | a0001 | c0002 | t0193 | g0123 | EAS | KHV | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
HG02027 | hp2 | a0001 | c0001 | t0195 | g0284 | EAS | KHV | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
HG02055 | hp1 | a0001 | c0006 | t0094 | g0293 | AFR | ACB | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
HG02055 | hp2 | a0009 | c0020 | t0194 | g0226 | AFR | ACB | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
HG02056 | hp1 | a0001 | c0001 | t0005 | g0141 | EAS | KHV | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
HG02056 | hp2 | a0001 | c0002 | t0190 | g0290 | EAS | KHV | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
HG02074 | hp1 | a0001 | c0002 | t0187 | g0132 | EAS | KHV | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
HG02074 | hp2 | a0001 | c0002 | t0177 | g0192 | EAS | KHV | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
HG02080 | hp1 | a0001 | c0001 | t0001 | g0089 | EAS | KHV | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
HG02080 | hp2 | a0001 | c0001 | t0007 | g0163 | EAS | KHV | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
HG02129 | hp1 | a0001 | c0001 | t0128 | g0168 | EAS | KHV | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
HG02129 | hp2 | a0001 | c0001 | t0019 | g0046 | EAS | KHV | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
HG02132 | hp1 | a0001 | c0001 | t0098 | g0080 | EAS | KHV | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
HG02132 | hp2 | a0001 | c0001 | t0188 | g0302 | EAS | KHV | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
HG02135 | hp1 | a0001 | c0001 | t0060 | g0320 | EAS | KHV | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
HG02135 | hp2 | a0001 | c0001 | t0126 | g0062 | EAS | KHV | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
HG02145 | hp1 | a0001 | c0001 | t0033 | g0333 | AFR | ACB | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
HG02145 | hp2 | a0001 | c0003 | t0205 | g0332 | AFR | ACB | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
HG02155 | hp1 | a0001 | c0001 | t0087 | g0179 | EAS | CDX | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
HG02155 | hp2 | a0010 | c0025 | t0003 | g0152 | EAS | CDX | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
HG02257 | hp1 | a0001 | c0001 | t0002 | g0119 | AFR | ACB | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
HG02257 | hp2 | a0001 | c0001 | t0075 | g0266 | AFR | ACB | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
HG02258 | hp1 | a0001 | c0001 | t0127 | g0275 | AFR | ACB | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
HG02258 | hp2 | a0001 | c0001 | t0013 | g0200 | AFR | ACB | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
HG02273 | hp1 | a0001 | c0001 | t0002 | g0241 | AMR | PEL | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
HG02273 | hp2 | a0001 | c0001 | t0005 | g0095 | AMR | PEL | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
HG02280 | hp1 | a0001 | c0003 | t0112 | g0035 | AFR | ACB | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
HG02280 | hp2 | a0001 | c0001 | t0025 | g0203 | AFR | ACB | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
HG02293 | hp1 | a0001 | c0001 | t0002 | g0242 | AMR | PEL | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
HG02293 | hp2 | a0001 | c0001 | t0003 | g0093 | AMR | PEL | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
HG02300 | hp1 | a0001 | c0004 | t0005 | g0211 | AMR | PEL | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
HG02300 | hp2 | a0001 | c0001 | t0148 | g0247 | AMR | PEL | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
HG02451 | hp1 | a0011 | c0030 | t0114 | g0262 | AFR | ACB | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
HG02451 | hp2 | a0005 | c0010 | t0099 | g0265 | AFR | ACB | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
HG02523 | hp1 | a0001 | c0002 | t0001 | g0167 | EAS | KHV | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
HG02523 | hp2 | a0001 | c0002 | t0004 | g0240 | EAS | KHV | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
HG02572 | hp1 | a0001 | c0001 | t0097 | g0307 | AFR | GWD | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
HG02572 | hp2 | a0001 | c0003 | t0109 | g0306 | AFR | GWD | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
HG02602 | hp1 | a0001 | c0001 | t0006 | g0140 | SAS | PJL | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
HG02602 | hp2 | a0001 | c0001 | t0037 | g0063 | SAS | PJL | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
HG02615 | hp1 | a0001 | c0001 | t0040 | g0272 | AFR | GWD | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
HG02615 | hp2 | a0001 | c0001 | t0120 | g0308 | AFR | GWD | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
HG02622 | hp1 | a0001 | c0001 | t0103 | g0339 | AFR | GWD | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
HG02622 | hp2 | a0001 | c0001 | t0011 | g0230 | AFR | GWD | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
HG02630 | hp1 | a0001 | c0001 | t0092 | g0311 | AFR | GWD | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
HG02630 | hp2 | a0001 | c0001 | t0156 | g0269 | AFR | GWD | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
HG02647 | hp1 | a0012 | c0029 | t0115 | g0335 | AFR | GWD | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
HG02647 | hp2 | a0001 | c0001 | t0106 | g0310 | AFR | GWD | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
HG02683 | hp1 | a0001 | c0001 | t0150 | g0206 | SAS | PJL | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
HG02683 | hp2 | a0001 | c0001 | t0044 | g0012 | SAS | PJL | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
HG02698 | hp1 | a0001 | c0001 | t0010 | g0064 | SAS | PJL | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
HG02698 | hp2 | a0001 | c0001 | t0003 | g0188 | SAS | PJL | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
HG02717 | hp1 | a0001 | c0001 | t0167 | g0202 | AFR | GWD | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
HG02717 | hp2 | a0001 | c0001 | t0042 | g0071 | AFR | GWD | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
HG02723 | hp1 | a0013 | c0027 | t0110 | g0222 | AFR | GWD | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
HG02723 | hp2 | a0001 | c0001 | t0091 | g0309 | AFR | GWD | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
HG02735 | hp1 | a0001 | c0001 | t0001 | g0051 | SAS | PJL | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
HG02735 | hp2 | a0001 | c0001 | t0008 | g0173 | SAS | PJL | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
HG02738 | hp1 | a0001 | c0001 | t0141 | g0015 | SAS | PJL | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
HG02738 | hp2 | a0001 | c0001 | t0001 | g0136 | SAS | PJL | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
HG02809 | hp1 | a0001 | c0001 | t0121 | g0037 | AFR | GWD | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
HG02809 | hp2 | a0001 | c0001 | t0036 | g0036 | AFR | GWD | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
HG02818 | hp1 | a0001 | c0001 | t0014 | g0007 | AFR | GWD | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
HG02818 | hp2 | a0001 | c0006 | t0016 | g0032 | AFR | GWD | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
HG02886 | hp1 | a0001 | c0001 | t0201 | g0334 | AFR | GWD | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
HG02886 | hp2 | a0001 | c0001 | t0108 | g0342 | AFR | GWD | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
HG02896 | hp1 | a0001 | c0003 | t0046 | g0121 | AFR | GWD | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
HG02896 | hp2 | a0001 | c0011 | t0020 | g0001 | AFR | GWD | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
HG02897 | hp1 | a0001 | c0011 | t0020 | g0001 | AFR | GWD | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
HG02897 | hp2 | a0001 | c0003 | t0046 | g0122 | AFR | GWD | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
HG02922 | hp1 | a0001 | c0001 | t0061 | g0318 | AFR | ESN | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
HG02922 | hp2 | a0006 | c0012 | t0031 | g0003 | AFR | ESN | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
HG02965 | hp1 | a0006 | c0012 | t0031 | g0003 | AFR | ESN | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
HG02965 | hp2 | a0001 | c0001 | t0011 | g0229 | AFR | ESN | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
HG02976 | hp1 | a0001 | c0001 | t0113 | g0282 | AFR | ESN | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
HG02976 | hp2 | a0001 | c0001 | t0054 | g0314 | AFR | ESN | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
HG03017 | hp1 | a0001 | c0001 | t0005 | g0127 | SAS | PJL | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
HG03017 | hp2 | a0001 | c0001 | t0159 | g0184 | SAS | PJL | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
HG03041 | hp1 | a0001 | c0003 | t0182 | g0271 | AFR | GWD | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
HG03041 | hp2 | a0001 | c0001 | t0018 | g0033 | AFR | GWD | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
HG03098 | hp1 | a0014 | c0016 | t0118 | g0268 | AFR | MSL | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
HG03098 | hp2 | a0001 | c0003 | t0049 | g0134 | AFR | MSL | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
HG03130 | hp1 | a0001 | c0001 | t0125 | g0341 | AFR | ESN | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
HG03130 | hp2 | a0001 | c0001 | t0168 | g0260 | AFR | ESN | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
HG03139 | hp1 | a0001 | c0006 | t0093 | g0059 | AFR | ESN | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
HG03139 | hp2 | a0001 | c0001 | t0028 | g0002 | AFR | ESN | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
HG03209 | hp1 | a0001 | c0001 | t0100 | g0258 | AFR | MSL | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
HG03209 | hp2 | a0001 | c0003 | t0181 | g0031 | AFR | MSL | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
HG03225 | hp1 | a0001 | c0001 | t0183 | g0040 | AFR | MSL | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
HG03225 | hp2 | a0001 | c0006 | t0016 | g0231 | AFR | MSL | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
HG03239 | hp1 | a0001 | c0028 | t0044 | g0249 | SAS | PJL | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
HG03239 | hp2 | a0001 | c0001 | t0001 | g0069 | SAS | PJL | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
HG03453 | hp1 | a0015 | c0023 | t0014 | g0005 | AFR | MSL | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
HG03453 | hp2 | a0003 | c0008 | t0104 | g0021 | AFR | MSL | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
HG03486 | hp1 | a0001 | c0003 | t0203 | g0281 | AFR | MSL | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
HG03486 | hp2 | a0001 | c0001 | t0166 | g0267 | AFR | MSL | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
HG03490 | hp1 | a0001 | c0001 | t0001 | g0261 | SAS | PJL | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
HG03490 | hp2 | a0001 | c0001 | t0171 | g0014 | SAS | PJL | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
HG03491 | hp1 | a0001 | c0001 | t0037 | g0175 | SAS | PJL | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
HG03491 | hp2 | a0001 | c0001 | t0068 | g0324 | SAS | PJL | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
HG03516 | hp1 | a0001 | c0001 | t0117 | g0340 | AFR | ESN | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
HG03516 | hp2 | a0001 | c0001 | t0002 | g0112 | AFR | ESN | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
HG03540 | hp1 | a0003 | c0008 | t0072 | g0227 | AFR | GWD | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
HG03540 | hp2 | a0001 | c0003 | t0204 | g0038 | AFR | GWD | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
HG03579 | hp1 | a0001 | c0001 | t0018 | g0223 | AFR | MSL | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
HG03579 | hp2 | a0003 | c0008 | t0111 | g0303 | AFR | MSL | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
HG03688 | hp1 | a0002 | c0005 | t0102 | g0160 | SAS | STU | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
HG03688 | hp2 | a0001 | c0001 | t0001 | g0343 | SAS | STU | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
HG03704 | hp1 | a0016 | c0021 | t0175 | g0087 | SAS | PJL | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
HG03704 | hp2 | a0001 | c0001 | t0010 | g0183 | SAS | PJL | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
HG03710 | hp1 | a0001 | c0001 | t0135 | g0056 | SAS | PJL | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
HG03710 | hp2 | a0001 | c0001 | t0001 | g0155 | SAS | PJL | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
HG03831 | hp1 | a0001 | c0001 | t0139 | g0013 | SAS | BEB | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
HG03831 | hp2 | a0001 | c0001 | t0163 | g0218 | SAS | BEB | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
HG03834 | hp1 | a0001 | c0001 | t0006 | g0060 | SAS | BEB | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
HG03834 | hp2 | a0002 | c0005 | t0199 | g0296 | SAS | BEB | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
HG03927 | hp1 | a0001 | c0001 | t0003 | g0116 | SAS | BEB | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
HG03927 | hp2 | a0001 | c0002 | t0003 | g0299 | SAS | BEB | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
HG03942 | hp1 | a0001 | c0001 | t0153 | g0010 | SAS | BEB | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
HG03942 | hp2 | a0002 | c0005 | t0003 | g0295 | SAS | BEB | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
HG04115 | hp1 | a0001 | c0001 | t0030 | g0301 | SAS | STU | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
HG04115 | hp2 | a0001 | c0001 | t0001 | g0104 | SAS | STU | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
HG04184 | hp1 | a0001 | c0001 | t0001 | g0058 | SAS | BEB | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
HG04184 | hp2 | a0001 | c0001 | t0137 | g0151 | SAS | BEB | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
HG04228 | hp1 | a0001 | c0001 | t0006 | g0174 | SAS | STU | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
HG04228 | hp2 | a0001 | c0001 | t0010 | g0191 | SAS | STU | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
NA18522 | hp1 | a0001 | c0001 | t0057 | g0317 | AFR | YRI | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
NA18522 | hp2 | a0001 | c0003 | t0180 | g0304 | AFR | YRI | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
NA18612 | hp1 | a0001 | c0001 | t0004 | g0221 | EAS | CHB | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
NA18612 | hp2 | a0001 | c0001 | t0023 | g0253 | EAS | CHB | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
NA18747 | hp1 | a0001 | c0001 | t0078 | g0084 | EAS | CHB | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
NA18747 | hp2 | a0001 | c0002 | t0002 | g0239 | EAS | CHB | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
NA18906 | hp1 | a0017 | c0013 | t0011 | g0276 | AFR | YRI | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
NA18906 | hp2 | a0001 | c0003 | t0105 | g0020 | AFR | YRI | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
NA18939 | hp1 | a0001 | c0001 | t0017 | g0156 | EAS | JPT | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
NA18939 | hp2 | a0001 | c0001 | t0006 | g0067 | EAS | JPT | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
NA18941 | hp1 | a0001 | c0002 | t0085 | g0288 | EAS | JPT | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
NA18941 | hp2 | a0001 | c0001 | t0084 | g0194 | EAS | JPT | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
NA18942 | hp1 | a0001 | c0001 | t0039 | g0178 | EAS | JPT | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
NA18942 | hp2 | a0001 | c0002 | t0124 | g0170 | EAS | JPT | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
NA18944 | hp1 | a0001 | c0002 | t0004 | g0142 | EAS | JPT | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
NA18944 | hp2 | a0001 | c0001 | t0138 | g0133 | EAS | JPT | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
NA18946 | hp1 | a0001 | c0001 | t0058 | g0312 | EAS | JPT | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
NA18946 | hp2 | a0001 | c0002 | t0032 | g0145 | EAS | JPT | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
NA18947 | hp1 | a0001 | c0001 | t0008 | g0137 | EAS | JPT | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
NA18947 | hp2 | a0001 | c0001 | t0070 | g0246 | EAS | JPT | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
NA18948 | hp1 | a0001 | c0001 | t0015 | g0111 | EAS | JPT | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
NA18948 | hp2 | a0001 | c0001 | t0179 | g0135 | EAS | JPT | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
NA18949 | hp1 | a0001 | c0001 | t0162 | g0057 | EAS | JPT | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
NA18949 | hp2 | a0001 | c0001 | t0080 | g0291 | EAS | JPT | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
NA18951 | hp1 | a0001 | c0001 | t0059 | g0323 | EAS | JPT | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
NA18951 | hp2 | a0002 | c0005 | t0129 | g0193 | EAS | JPT | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
NA18953 | hp1 | a0001 | c0001 | t0003 | g0150 | EAS | JPT | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
NA18953 | hp2 | a0001 | c0001 | t0079 | g0023 | EAS | JPT | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
NA18954 | hp1 | a0001 | c0001 | t0004 | g0278 | EAS | JPT | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
NA18954 | hp2 | a0001 | c0002 | t0149 | g0162 | EAS | JPT | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
NA18956 | hp1 | a0001 | c0001 | t0038 | g0024 | EAS | JPT | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
NA18956 | hp2 | a0001 | c0001 | t0017 | g0139 | EAS | JPT | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
NA18959 | hp1 | a0001 | c0001 | t0090 | g0083 | EAS | JPT | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
NA18959 | hp2 | a0001 | c0002 | t0006 | g0287 | EAS | JPT | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
NA18960 | hp1 | a0001 | c0001 | t0015 | g0081 | EAS | JPT | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
NA18960 | hp2 | a0001 | c0001 | t0184 | g0217 | EAS | JPT | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
NA18963 | hp1 | a0001 | c0001 | t0158 | g0125 | EAS | JPT | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
NA18963 | hp2 | a0001 | c0001 | t0006 | g0250 | EAS | JPT | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
NA18964 | hp1 | a0001 | c0001 | t0035 | g0243 | EAS | JPT | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
NA18964 | hp2 | a0001 | c0002 | t0192 | g0130 | EAS | JPT | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
NA18968 | hp1 | a0001 | c0001 | t0007 | g0195 | EAS | JPT | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
NA18968 | hp2 | a0001 | c0001 | t0086 | g0092 | EAS | JPT | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
NA18970 | hp1 | a0001 | c0001 | t0032 | g0029 | EAS | JPT | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
NA18970 | hp2 | a0001 | c0001 | t0001 | g0161 | EAS | JPT | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
NA18971 | hp1 | a0001 | c0001 | t0196 | g0078 | EAS | JPT | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
NA18971 | hp2 | a0001 | c0002 | t0004 | g0248 | EAS | JPT | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
NA18974 | hp1 | a0001 | c0001 | t0039 | g0138 | EAS | JPT | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
NA18974 | hp2 | a0001 | c0001 | t0023 | g0251 | EAS | JPT | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
NA18975 | hp1 | a0001 | c0001 | t0123 | g0166 | EAS | JPT | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
NA18975 | hp2 | a0001 | c0002 | t0047 | g0300 | EAS | JPT | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
NA18977 | hp1 | a0018 | c0026 | t0027 | g0017 | EAS | JPT | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
NA18977 | hp2 | a0001 | c0001 | t0154 | g0027 | EAS | JPT | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
NA18978 | hp1 | a0001 | c0001 | t0082 | g0026 | EAS | JPT | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
NA18978 | hp2 | a0001 | c0001 | t0002 | g0157 | EAS | JPT | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
NA18979 | hp1 | a0001 | c0001 | t0021 | g0147 | EAS | JPT | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
NA18979 | hp2 | a0001 | c0002 | t0004 | g0144 | EAS | JPT | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
NA18981 | hp1 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
NA18981 | hp2 | a0001 | c0001 | t0005 | g0091 | EAS | JPT | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
NA18983 | hp1 | a0001 | c0001 | t0081 | g0228 | EAS | JPT | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
NA18983 | hp2 | a0001 | c0001 | t0006 | g0098 | EAS | JPT | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
NA18984 | hp1 | a0019 | c0024 | t0012 | g0117 | EAS | JPT | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
NA18984 | hp2 | a0001 | c0001 | t0034 | g0146 | EAS | JPT | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
NA18987 | hp1 | a0001 | c0001 | t0122 | g0102 | EAS | JPT | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
NA18987 | hp2 | a0001 | c0001 | t0012 | g0235 | EAS | JPT | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
NA18990 | hp1 | a0001 | c0001 | t0089 | g0022 | EAS | JPT | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
NA18990 | hp2 | a0004 | c0017 | t0007 | g0252 | EAS | JPT | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
NA18991 | hp1 | a0001 | c0002 | t0007 | g0048 | EAS | JPT | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
NA18991 | hp2 | a0005 | c0010 | t0145 | g0149 | EAS | JPT | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
NA18995 | hp1 | a0001 | c0001 | t0030 | g0245 | EAS | JPT | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
NA18995 | hp2 | a0001 | c0001 | t0001 | g0086 | EAS | JPT | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
NA18998 | hp1 | a0001 | c0001 | t0021 | g0061 | EAS | JPT | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
NA18998 | hp2 | a0001 | c0002 | t0005 | g0169 | EAS | JPT | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
NA18999 | hp1 | a0001 | c0001 | t0064 | g0316 | EAS | JPT | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
NA18999 | hp2 | a0001 | c0001 | t0008 | g0047 | EAS | JPT | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
NA19000 | hp1 | a0001 | c0001 | t0048 | g0158 | EAS | JPT | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
NA19000 | hp2 | a0001 | c0001 | t0008 | g0131 | EAS | JPT | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
NA19002 | hp1 | a0001 | c0001 | t0004 | g0044 | EAS | JPT | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
NA19002 | hp2 | a0001 | c0002 | t0004 | g0143 | EAS | JPT | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
NA19004 | hp1 | a0001 | c0001 | t0186 | g0214 | EAS | JPT | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
NA19004 | hp2 | a0001 | c0002 | t0069 | g0159 | EAS | JPT | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
NA19005 | hp1 | a0001 | c0001 | t0005 | g0232 | EAS | JPT | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
NA19005 | hp2 | a0001 | c0001 | t0006 | g0118 | EAS | JPT | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
NA19007 | hp1 | a0001 | c0001 | t0015 | g0107 | EAS | JPT | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
NA19007 | hp2 | a0001 | c0001 | t0024 | g0165 | EAS | JPT | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
NA19010 | hp1 | a0001 | c0001 | t0189 | g0216 | EAS | JPT | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
NA19010 | hp2 | a0001 | c0001 | t0008 | g0052 | EAS | JPT | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
NA19011 | hp1 | a0001 | c0001 | t0076 | g0106 | EAS | JPT | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
NA19011 | hp2 | a0001 | c0001 | t0157 | g0030 | EAS | JPT | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
NA19030 | hp1 | a0001 | c0001 | t0073 | g0337 | AFR | LWK | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
NA19030 | hp2 | a0001 | c0003 | t0202 | g0210 | AFR | LWK | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
NA19043 | hp1 | a0001 | c0003 | t0206 | g0294 | AFR | LWK | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
NA19043 | hp2 | a0001 | c0001 | t0063 | g0319 | AFR | LWK | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
NA19055 | hp1 | a0001 | c0001 | t0047 | g0298 | EAS | JPT | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
NA19055 | hp2 | a0001 | c0001 | t0005 | g0199 | EAS | JPT | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
NA19056 | hp1 | a0001 | c0002 | t0133 | g0264 | EAS | JPT | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
NA19056 | hp2 | a0001 | c0001 | t0024 | g0016 | EAS | JPT | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
NA19060 | hp1 | a0001 | c0001 | t0048 | g0196 | EAS | JPT | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
NA19060 | hp2 | a0001 | c0001 | t0022 | g0148 | EAS | JPT | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
NA19062 | hp1 | a0001 | c0001 | t0012 | g0126 | EAS | JPT | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
NA19062 | hp2 | a0001 | c0001 | t0038 | g0236 | EAS | JPT | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
NA19063 | hp1 | a0001 | c0002 | t0007 | g0292 | EAS | JPT | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
NA19063 | hp2 | a0001 | c0001 | t0004 | g0164 | EAS | JPT | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
NA19065 | hp1 | a0001 | c0001 | t0017 | g0153 | EAS | JPT | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
NA19065 | hp2 | a0001 | c0001 | t0022 | g0286 | EAS | JPT | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
NA19080 | hp1 | a0001 | c0001 | t0002 | g0244 | EAS | JPT | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
NA19080 | hp2 | a0001 | c0001 | t0083 | g0154 | EAS | JPT | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
NA19085 | hp1 | a0001 | c0001 | t0025 | g0045 | EAS | JPT | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
NA19085 | hp2 | a0002 | c0005 | t0012 | g0283 | EAS | JPT | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
NA19088 | hp1 | a0001 | c0001 | t0008 | g0180 | EAS | JPT | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
NA19088 | hp2 | a0001 | c0001 | t0088 | g0103 | EAS | JPT | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
NA19090 | hp1 | a0001 | c0001 | t0136 | g0053 | EAS | JPT | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
NA19090 | hp2 | a0001 | c0001 | t0006 | g0068 | EAS | JPT | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
NA19091 | hp1 | a0001 | c0001 | t0132 | g0025 | EAS | JPT | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
NA19091 | hp2 | a0001 | c0001 | t0074 | g0105 | EAS | JPT | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
NA19240 | hp1 | a0001 | c0001 | t0028 | g0002 | AFR | YRI | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
NA19240 | hp2 | a0001 | c0001 | t0119 | g0280 | AFR | YRI | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
NA20129 | hp1 | a0001 | c0015 | t0001 | g0255 | AFR | ASW | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
NA20129 | hp2 | a0020 | c0014 | t0101 | g0274 | AFR | ASW | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
NA20805 | hp1 | a0001 | c0001 | t0019 | g0113 | EUR | TSI | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
NA20805 | hp2 | a0001 | c0001 | t0002 | g0187 | EUR | TSI | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
NA20905 | hp1 | a0021 | c0019 | t0009 | g0331 | SAS | GIH | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
NA20905 | hp2 | a0001 | c0001 | t0095 | g0213 | SAS | GIH | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
HG02109 | hp1 | a0001 | c0001 | t0013 | g0273 | AFR | ACB | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
HG02109 | hp2 | a0001 | c0001 | t0036 | g0257 | AFR | ACB | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
HG02486 | hp1 | a0001 | c0001 | t0040 | g0256 | AFR | ACB | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
HG02486 | hp2 | a0001 | c0001 | t0107 | g0041 | AFR | ACB | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
HG02559 | hp1 | a0001 | c0003 | t0077 | g0285 | AFR | ACB | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
HG02559 | hp2 | a0001 | c0001 | t0011 | g0224 | AFR | ACB | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
HG03471 | hp1 | a0001 | c0001 | t0018 | g0042 | AFR | MSL | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
HG03471 | hp2 | a0001 | c0006 | t0050 | g0006 | AFR | MSL | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
HG06807 | hp1 | a0001 | c0001 | t0042 | g0225 | AFR | USA | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
HG06807 | hp2 | a0001 | c0001 | t0001 | g0077 | AFR | USA | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
NA20300 | hp1 | a0001 | c0001 | t0056 | g0313 | AFR | USA | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
NA20300 | hp2 | a0001 | c0001 | t0005 | g0085 | AFR | USA | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
NA21309 | hp1 | a0001 | c0001 | t0140 | g0073 | AFR | LWK | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
NA21309 | hp2 | a0001 | c0001 | t0155 | g0172 | AFR | LWK | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
homoSapiens | chm13v2 | a0001 | c0001 | t0142 | g0050 | REF | REF | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
homoSapiens | grch38p0 | a0001 | c0001 | t0013 | g0039 | REF | REF | MYOCD_chr17_12660890_12773949 | MYOCD | chr17 | 12660890 | 12773949 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr17:12715528 | G | T | 1 | a0011 | 1 | HG02451.hp1 | missense_variant | MODERATE | c.131G>T | p.Arg44Leu | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 3/14 | 430/8565 | 131/2961 | 44/986 | chr17 | 12715528 | |||
chr17:12717394 | G | A | 2 | a0017 a0020 |
2 | NA18906.hp1 NA20129.hp2 |
missense_variant | MODERATE | c.226G>A | p.Asp76Asn | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 4/14 | 525/8565 | 226/2961 | 76/986 | chr17 | 12717394 | |||
chr17:12736188 | C | T | 1 | a0012 | 1 | HG02647.hp1 | missense_variant | MODERATE | c.443C>T | p.Thr148Met | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 6/14 | 742/8565 | 443/2961 | 148/986 | chr17 | 12736188 | |||
chr17:12744328 | G | A | 1 | a0014 | 1 | HG03098.hp1 | missense_variant | MODERATE | c.863G>A | p.Arg288Gln | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 8/14 | 1162/8565 | 863/2961 | 288/986 | chr17 | 12744328 | |||
chr17:12744412 | T | C | 1 | a0004 | 3 | HG01257.hp2 HG01934.hp2 NA18990.hp2 |
missense_variant | MODERATE | c.947T>C | p.Leu316Pro | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 8/14 | 1246/8565 | 947/2961 | 316/986 | chr17 | 12744412 | |||
chr17:12745978 | C | T | 1 | a0013 | 1 | HG02723.hp1 | missense_variant | MODERATE | c.1031C>T | p.Thr344Ile | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 9/14 | 1330/8565 | 1031/2961 | 344/986 | chr17 | 12745978 | |||
chr17:12752621 | G | A | 1 | a0005 | 2 | HG02451.hp2 NA18991.hp2 |
missense_variant | MODERATE | c.1333G>A | p.Gly445Ser | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 10/14 | 1632/8565 | 1333/2961 | 445/986 | chr17 | 12752621 | |||
chr17:12752703 | C | T | 1 | a0018 | 1 | NA18977.hp1 | missense_variant | MODERATE | c.1415C>T | p.Pro472Leu | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 10/14 | 1714/8565 | 1415/2961 | 472/986 | chr17 | 12752703 | |||
chr17:12752735 | G | A | 2 | a0008 a0017 |
2 | HG01175.hp1 NA18906.hp1 |
missense_variant | MODERATE | c.1447G>A | p.Gly483Ser | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 10/14 | 1746/8565 | 1447/2961 | 483/986 | chr17 | 12752735 | |||
chr17:12752799 | G | A | 1 | a0021 | 1 | NA20905.hp1 | missense_variant | MODERATE | c.1511G>A | p.Gly504Asp | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 10/14 | 1810/8565 | 1511/2961 | 504/986 | chr17 | 12752799 | |||
chr17:12752973 | C | T | 1 | a0010 | 1 | HG02155.hp2 | missense_variant | MODERATE | c.1685C>T | p.Pro562Leu | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 10/14 | 1984/8565 | 1685/2961 | 562/986 | chr17 | 12752973 | |||
chr17:12753044 | C | T | 1 | a0019 | 1 | NA18984.hp1 | missense_variant | MODERATE | c.1756C>T | p.Pro586Ser | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 10/14 | 2055/8565 | 1756/2961 | 586/986 | chr17 | 12753044 | |||
chr17:12753229 | G | C | 1 | a0002 | 7 | HG00544.hp1 HG01261.hp2 HG03688.hp1 others(4): Show |
missense_variant | MODERATE | c.1941G>C | p.Gln647His | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 10/14 | 2240/8565 | 1941/2961 | 647/986 | chr17 | 12753229 | |||
chr17:12753279 | C | A | 1 | a0009 | 1 | HG02055.hp2 | missense_variant | MODERATE | c.1991C>A | p.Ser664Tyr | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 10/14 | 2290/8565 | 1991/2961 | 664/986 | chr17 | 12753279 | |||
chr17:12756429 | G | A | 1 | a0016 | 1 | HG03704.hp1 | missense_variant | MODERATE | c.2074G>A | p.Asp692Asn | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 11/14 | 2373/8565 | 2074/2961 | 692/986 | chr17 | 12756429 | |||
chr17:12758107 | A | G | 1 | a0016 | 1 | HG03704.hp1 | missense_variant | MODERATE | c.2225A>G | p.Asp742Gly | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 12/14 | 2524/8565 | 2225/2961 | 742/986 | chr17 | 12758107 | |||
chr17:12758161 | C | T | 1 | a0006 | 2 | HG02922.hp2 HG02965.hp1 |
missense_variant | MODERATE | c.2279C>T | p.Ser760Leu | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 12/14 | 2578/8565 | 2279/2961 | 760/986 | chr17 | 12758161 | |||
chr17:12758205 | G | A | 1 | a0003 | 4 | HG01884.hp2 HG03453.hp2 HG03540.hp1 others(1): Show |
missense_variant | MODERATE | c.2323G>A | p.Val775Ile | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 12/14 | 2622/8565 | 2323/2961 | 775/986 | chr17 | 12758205 | |||
chr17:12763203 | C | A | 2 | a0007 a0016 |
2 | HG00621.hp2 HG03704.hp1 |
missense_variant | MODERATE | c.2520C>A | p.Ser840Arg | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 14/14 | 2819/8565 | 2520/2961 | 840/986 | chr17 | 12763203 | |||
chr17:12763451 | G | A | 1 | a0015 | 1 | HG03453.hp1 | missense_variant | MODERATE | c.2768G>A | p.Ser923Asn | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 14/14 | 3067/8565 | 2768/2961 | 923/986 | chr17 | 12763451 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr17:12736168 | G | A | 2 | a0001c0004 a0001c0015 |
8 | HG00741.hp1 HG01106.hp1 HG01496.hp2 others(5): Show |
synonymous_variant | LOW | c.423G>A | p.Gln141Gln | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 6/14 | 722/8565 | 423/2961 | 141/986 | chr17 | 12736168 | |||
chr17:12736297 | C | T | 1 | a0001c0028 | 1 | HG03239.hp1 | synonymous_variant | LOW | c.552C>T | p.Ala184Ala | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 6/14 | 851/8565 | 552/2961 | 184/986 | chr17 | 12736297 | |||
chr17:12752434 | G | A | 1 | a0013c0027 | 1 | HG02723.hp1 | synonymous_variant | LOW | c.1146G>A | p.Gln382Gln | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 10/14 | 1445/8565 | 1146/2961 | 382/986 | chr17 | 12752434 | |||
chr17:12752794 | T | C | 3 | a0001c0002 a0004c0009 a0013c0027 |
32 | HG00408.hp1 HG00408.hp2 HG00639.hp1 others(29): Show |
synonymous_variant | LOW | c.1506T>C | p.Asn502Asn | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 10/14 | 1805/8565 | 1506/2961 | 502/986 | chr17 | 12752794 | |||
chr17:12753100 | T | C | 1 | a0001c0007 | 4 | HG00323.hp1 HG00738.hp1 HG01515.hp2 others(1): Show |
synonymous_variant | LOW | c.1812T>C | p.Ala604Ala | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 10/14 | 2111/8565 | 1812/2961 | 604/986 | chr17 | 12753100 | |||
chr17:12763086 | C | T | 1 | a0001c0011 | 2 | HG02896.hp2 HG02897.hp1 |
synonymous_variant | LOW | c.2403C>T | p.Asp801Asp | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 14/14 | 2702/8565 | 2403/2961 | 801/986 | chr17 | 12763086 | |||
chr17:12763317 | C | T | 4 | a0001c0006 a0008c0018 a0009c0020 others(1): Show |
8 | HG01175.hp1 HG02055.hp1 HG02055.hp2 others(5): Show |
synonymous_variant | LOW | c.2634C>T | p.Ser878Ser | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 14/14 | 2933/8565 | 2634/2961 | 878/986 | chr17 | 12763317 | |||
chr17:12763404 | C | G | 2 | a0001c0003 a0013c0027 |
16 | HG02145.hp2 HG02280.hp1 HG02559.hp1 others(13): Show |
synonymous_variant | LOW | c.2721C>G | p.Gly907Gly | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 14/14 | 3020/8565 | 2721/2961 | 907/986 | chr17 | 12763404 | |||
chr17:12763422 | G | A | 4 | a0001c0006 a0008c0018 a0009c0020 others(1): Show |
8 | HG01175.hp1 HG02055.hp1 HG02055.hp2 others(5): Show |
synonymous_variant | LOW | c.2739G>A | p.Gln913Gln | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 14/14 | 3038/8565 | 2739/2961 | 913/986 | chr17 | 12763422 | |||
chr17:12763584 | C | T | 1 | a0001c0015 | 1 | NA20129.hp1 | synonymous_variant | LOW | c.2901C>T | p.Phe967Phe | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 14/14 | 3200/8565 | 2901/2961 | 967/986 | chr17 | 12763584 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr17:12665995 | C | A | 1 | a0001c0003t0049 | 1 | HG03098.hp2 | 5_prime_UTR_variant | MODIFIER | c.-194C>A | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/14 | 194 | chr17 | 12665995 | ||||||
chr17:12666050 | ACTC | A | 6 | a0001c0001t0014 a0001c0001t0051 a0001c0001t0052 others(3): Show |
8 | HG01109.hp2 HG01243.hp1 HG01243.hp2 others(5): Show |
5_prime_UTR_variant | MODIFIER | c.-136_-134delCCT | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/14 | 134 | INFO_REALIGN_3_PRIME | chr17 | 12666050 | |||||
chr17:12666125 | G | A | 19 | a0001c0001t0009 a0001c0001t0053 a0001c0001t0054 others(16): Show |
21 | HG00597.hp2 HG00642.hp1 HG00735.hp1 others(18): Show |
5_prime_UTR_variant | MODIFIER | c.-64G>A | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/14 | 64 | chr17 | 12666125 | ||||||
chr17:12763659 | C | G | 7 | a0001c0001t0201 a0001c0003t0049 a0001c0003t0202 others(4): Show |
7 | HG02145.hp2 HG02886.hp1 HG03098.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*15C>G | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 14/14 | 15 | chr17 | 12763659 | ||||||
chr17:12763852 | T | C | 1 | a0001c0002t0069 | 1 | NA19004.hp2 | 3_prime_UTR_variant | MODIFIER | c.*208T>C | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 14/14 | 208 | chr17 | 12763852 | ||||||
chr17:12764019 | C | T | 37 | a0001c0001t0047 a0001c0001t0048 a0001c0001t0179 others(34): Show |
39 | HG00408.hp1 HG00408.hp2 HG00544.hp1 others(36): Show |
3_prime_UTR_variant | MODIFIER | c.*375C>T | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 14/14 | 375 | chr17 | 12764019 | ||||||
chr17:12764219 | C | A | 109 | a0001c0001t0007 a0001c0001t0008 a0001c0001t0011 others(106): Show |
133 | HG00408.hp2 HG00544.hp1 HG00544.hp2 others(130): Show |
3_prime_UTR_variant | MODIFIER | c.*575C>A | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 14/14 | 575 | chr17 | 12764219 | ||||||
chr17:12764233 | A | G | 7 | a0001c0001t0057 a0001c0001t0119 a0001c0001t0120 others(4): Show |
8 | HG02055.hp2 HG02615.hp2 HG02809.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*589A>G | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 14/14 | 589 | chr17 | 12764233 | ||||||
chr17:12764241 | G | A | 5 | a0001c0001t0021 a0001c0001t0022 a0001c0001t0070 others(2): Show |
7 | HG00621.hp2 HG03704.hp1 NA18947.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*597G>A | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 14/14 | 597 | chr17 | 12764241 | ||||||
chr17:12764265 | T | A | 53 | a0001c0001t0007 a0001c0001t0008 a0001c0001t0023 others(50): Show |
68 | HG00408.hp2 HG00544.hp2 HG00597.hp2 others(65): Show |
3_prime_UTR_variant | MODIFIER | c.*621T>A | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 14/14 | 621 | chr17 | 12764265 | ||||||
chr17:12764280 | A | T | 4 | a0001c0001t0045 a0001c0001t0172 a0001c0001t0173 others(1): Show |
5 | HG01256.hp1 HG01358.hp1 HG01433.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*636A>T | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 14/14 | 636 | chr17 | 12764280 | ||||||
chr17:12764342 | C | CT | 18 | a0001c0001t0044 a0001c0001t0045 a0001c0001t0051 others(15): Show |
19 | HG01109.hp1 HG01109.hp2 HG01243.hp2 others(16): Show |
3_prime_UTR_variant | MODIFIER | c.*704dupT | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 14/14 | 705 | INFO_REALIGN_3_PRIME | chr17 | 12764342 | |||||
chr17:12764519 | C | T | 3 | a0001c0001t0164 a0001c0001t0165 a0001c0007t0043 |
4 | HG00642.hp2 HG00741.hp2 HG01515.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*875C>T | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 14/14 | 875 | chr17 | 12764519 | ||||||
chr17:12764533 | G | A | 1 | a0001c0001t0166 | 1 | HG03486.hp2 | 3_prime_UTR_variant | MODIFIER | c.*889G>A | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 14/14 | 889 | chr17 | 12764533 | ||||||
chr17:12764617 | G | A | 31 | a0001c0001t0011 a0001c0001t0015 a0001c0001t0032 others(28): Show |
38 | HG00673.hp2 HG01175.hp1 HG01884.hp1 others(35): Show |
3_prime_UTR_variant | MODIFIER | c.*973G>A | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 14/14 | 973 | chr17 | 12764617 | ||||||
chr17:12764726 | C | T | 1 | a0001c0001t0163 | 1 | HG03831.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1082C>T | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 14/14 | 1082 | chr17 | 12764726 | ||||||
chr17:12764736 | T | G | 13 | a0001c0001t0023 a0001c0001t0024 a0001c0001t0034 others(10): Show |
15 | HG01257.hp2 HG01978.hp1 HG01978.hp2 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*1092T>G | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 14/14 | 1092 | chr17 | 12764736 | ||||||
chr17:12764742 | T | C | 7 | a0001c0001t0011 a0001c0001t0028 a0001c0001t0091 others(4): Show |
10 | HG02559.hp2 HG02622.hp2 HG02630.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*1098T>C | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 14/14 | 1098 | chr17 | 12764742 | ||||||
chr17:12764750 | C | A | 1 | a0001c0003t0049 | 1 | HG03098.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1106C>A | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 14/14 | 1106 | chr17 | 12764750 | ||||||
chr17:12764752 | T | C | 10 | a0001c0001t0011 a0001c0001t0021 a0001c0001t0028 others(7): Show |
14 | HG02559.hp2 HG02622.hp2 HG02630.hp1 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*1108T>C | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 14/14 | 1108 | chr17 | 12764752 | ||||||
chr17:12765044 | A | G | 181 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(178): Show |
253 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(250): Show |
3_prime_UTR_variant | MODIFIER | c.*1400A>G | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 14/14 | 1400 | chr17 | 12765044 | ||||||
chr17:12765098 | C | T | 1 | a0001c0001t0117 | 1 | HG03516.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1454C>T | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 14/14 | 1454 | chr17 | 12765098 | ||||||
chr17:12765131 | A | G | 4 | a0001c0001t0166 a0001c0003t0077 a0001c0003t0202 others(1): Show |
4 | HG02145.hp2 HG02559.hp1 HG03486.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1487A>G | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 14/14 | 1487 | chr17 | 12765131 | ||||||
chr17:12765147 | C | T | 11 | a0001c0001t0026 a0001c0001t0027 a0001c0001t0076 others(8): Show |
12 | HG00408.hp2 HG00544.hp2 HG00609.hp2 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*1503C>T | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 14/14 | 1503 | chr17 | 12765147 | ||||||
chr17:12765159 | T | C | 2 | a0001c0001t0103 a0001c0006t0093 |
2 | HG02622.hp1 HG03139.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1515T>C | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 14/14 | 1515 | chr17 | 12765159 | ||||||
chr17:12765186 | G | C | 1 | a0001c0001t0134 | 1 | HG00639.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1542G>C | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 14/14 | 1542 | chr17 | 12765186 | ||||||
chr17:12765295 | G | A | 3 | a0001c0001t0011 a0003c0008t0104 a0017c0013t0011 |
5 | HG02559.hp2 HG02622.hp2 HG02965.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1651G>A | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 14/14 | 1651 | chr17 | 12765295 | ||||||
chr17:12765314 | T | TA | 21 | a0001c0001t0017 a0001c0001t0026 a0001c0001t0027 others(18): Show |
24 | HG00408.hp2 HG00544.hp2 HG00609.hp2 others(21): Show |
3_prime_UTR_variant | MODIFIER | c.*1685dupA | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 14/14 | 1686 | INFO_REALIGN_3_PRIME | chr17 | 12765314 | |||||
chr17:12765314 | TA | T | 17 | a0001c0001t0041 a0001c0001t0042 a0001c0001t0052 others(14): Show |
19 | HG00735.hp1 HG00735.hp2 HG01243.hp2 others(16): Show |
3_prime_UTR_variant | MODIFIER | c.*1685delA | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 14/14 | 1685 | INFO_REALIGN_3_PRIME | chr17 | 12765314 | |||||
chr17:12765314 | TAA | T | 5 | a0001c0001t0159 a0001c0001t0160 a0001c0001t0161 others(2): Show |
6 | HG00741.hp2 HG01261.hp1 HG01515.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1684_*1685delAA | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 14/14 | 1684 | INFO_REALIGN_3_PRIME | chr17 | 12765314 | |||||
chr17:12765542 | C | CATGT | 5 | a0001c0001t0028 a0001c0001t0067 a0001c0001t0103 others(2): Show |
6 | HG01891.hp1 HG02622.hp1 HG03098.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1905_*1908dupGTAT | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 14/14 | 1909 | INFO_REALIGN_3_PRIME | chr17 | 12765542 | |||||
chr17:12765601 | C | T | 5 | a0001c0001t0028 a0001c0001t0067 a0001c0001t0103 others(2): Show |
6 | HG01891.hp1 HG02622.hp1 HG03098.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1957C>T | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 14/14 | 1957 | chr17 | 12765601 | ||||||
chr17:12765616 | C | T | 3 | a0001c0001t0011 a0003c0008t0104 a0017c0013t0011 |
5 | HG02559.hp2 HG02622.hp2 HG02965.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1972C>T | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 14/14 | 1972 | chr17 | 12765616 | ||||||
chr17:12765722 | T | C | 1 | a0001c0001t0081 | 1 | NA18983.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2078T>C | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 14/14 | 2078 | chr17 | 12765722 | ||||||
chr17:12765837 | C | G | 6 | a0001c0001t0116 a0001c0001t0159 a0001c0001t0160 others(3): Show |
7 | HG00741.hp2 HG01261.hp1 HG01515.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*2193C>G | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 14/14 | 2193 | chr17 | 12765837 | ||||||
chr17:12765911 | G | A | 2 | a0001c0003t0202 a0001c0011t0020 |
3 | HG02896.hp2 HG02897.hp1 NA19030.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2267G>A | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 14/14 | 2267 | chr17 | 12765911 | ||||||
chr17:12766081 | G | C | 3 | a0001c0001t0106 a0001c0001t0183 a0001c0003t0203 |
3 | HG02647.hp2 HG03225.hp1 HG03486.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2437G>C | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 14/14 | 2437 | chr17 | 12766081 | ||||||
chr17:12766169 | C | T | 1 | a0005c0010t0099 | 1 | HG02451.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2525C>T | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 14/14 | 2525 | chr17 | 12766169 | ||||||
chr17:12766237 | A | T | 1 | a0001c0001t0117 | 1 | HG03516.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2593A>T | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 14/14 | 2593 | chr17 | 12766237 | ||||||
chr17:12766621 | T | C | 1 | a0001c0001t0107 | 1 | HG02486.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2977T>C | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 14/14 | 2977 | chr17 | 12766621 | ||||||
chr17:12766626 | C | T | 1 | a0012c0029t0115 | 1 | HG02647.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2982C>T | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 14/14 | 2982 | chr17 | 12766626 | ||||||
chr17:12766808 | C | T | 6 | a0001c0001t0116 a0001c0001t0159 a0001c0001t0160 others(3): Show |
7 | HG00741.hp2 HG01261.hp1 HG01515.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*3164C>T | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 14/14 | 3164 | chr17 | 12766808 | ||||||
chr17:12766831 | TATCTA | T | 5 | a0001c0001t0011 a0001c0001t0167 a0001c0003t0205 others(2): Show |
7 | HG02145.hp2 HG02559.hp2 HG02622.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*3189_*3193delTCTA others(1): Show |
MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 14/14 | 3189 | INFO_REALIGN_3_PRIME | chr17 | 12766831 | |||||
chr17:12766857 | C | T | 1 | a0001c0001t0179 | 1 | NA18948.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3213C>T | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 14/14 | 3213 | chr17 | 12766857 | ||||||
chr17:12766975 | GGAGGAAG others(14): Show |
G | 1 | a0001c0001t0155 | 1 | NA21309.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3339_*3359delAAGA others(17): Show |
MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 14/14 | 3339 | INFO_REALIGN_3_PRIME | chr17 | 12766975 | |||||
chr17:12767026 | G | C | 70 | a0001c0001t0001 a0001c0001t0004 a0001c0001t0007 others(67): Show |
112 | HG00323.hp1 HG00323.hp2 HG00423.hp2 others(109): Show |
3_prime_UTR_variant | MODIFIER | c.*3382G>C | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 14/14 | 3382 | chr17 | 12767026 | ||||||
chr17:12767026 | G | T | 6 | a0001c0001t0040 a0001c0001t0107 a0001c0001t0113 others(3): Show |
7 | HG02451.hp1 HG02486.hp1 HG02486.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*3382G>T | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 14/14 | 3382 | chr17 | 12767026 | ||||||
chr17:12767140 | TTA | T | 3 | a0001c0001t0032 a0001c0002t0032 a0001c0002t0124 |
3 | NA18942.hp2 NA18946.hp2 NA18970.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3498_*3499delAT | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 14/14 | 3498 | INFO_REALIGN_3_PRIME | chr17 | 12767140 | |||||
chr17:12767155 | C | A | 1 | a0001c0001t0138 | 1 | NA18944.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3511C>A | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 14/14 | 3511 | chr17 | 12767155 | ||||||
chr17:12767294 | A | G | 1 | a0001c0001t0144 | 1 | HG00733.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3650A>G | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 14/14 | 3650 | chr17 | 12767294 | ||||||
chr17:12767304 | A | G | 2 | a0001c0003t0049 a0001c0003t0077 |
2 | HG02559.hp1 HG03098.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3660A>G | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 14/14 | 3660 | chr17 | 12767304 | ||||||
chr17:12767399 | G | C | 1 | a0005c0010t0145 | 1 | NA18991.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3755G>C | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 14/14 | 3755 | chr17 | 12767399 | ||||||
chr17:12767459 | C | G | 1 | a0001c0001t0056 | 1 | NA20300.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3815C>G | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 14/14 | 3815 | chr17 | 12767459 | ||||||
chr17:12767537 | G | A | 2 | a0001c0001t0057 a0001c0001t0113 |
2 | HG02976.hp1 NA18522.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3893G>A | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 14/14 | 3893 | chr17 | 12767537 | ||||||
chr17:12767605 | C | T | 215 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(212): Show |
320 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(317): Show |
3_prime_UTR_variant | MODIFIER | c.*3961C>T | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 14/14 | 3961 | chr17 | 12767605 | ||||||
chr17:12767609 | G | GA | 50 | a0001c0001t0003 a0001c0001t0006 a0001c0001t0008 others(47): Show |
77 | HG00408.hp1 HG00408.hp2 HG00544.hp1 others(74): Show |
3_prime_UTR_variant | MODIFIER | c.*3976dupA | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 14/14 | 3977 | INFO_REALIGN_3_PRIME | chr17 | 12767609 | |||||
chr17:12767620 | A | AG | 6 | a0001c0001t0015 a0001c0001t0038 a0001c0001t0074 others(3): Show |
9 | NA18948.hp1 NA18953.hp2 NA18956.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*3980dupG | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 14/14 | 3981 | INFO_REALIGN_3_PRIME | chr17 | 12767620 | |||||
chr17:12767620 | A | G | 17 | a0001c0001t0017 a0001c0001t0026 a0001c0001t0027 others(14): Show |
20 | HG00544.hp2 HG00609.hp2 HG00673.hp1 others(17): Show |
3_prime_UTR_variant | MODIFIER | c.*3976A>G | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 14/14 | 3976 | chr17 | 12767620 | ||||||
chr17:12767643 | G | T | 94 | a0001c0001t0001 a0001c0001t0004 a0001c0001t0005 others(91): Show |
148 | HG00323.hp1 HG00323.hp2 HG00423.hp2 others(145): Show |
3_prime_UTR_variant | MODIFIER | c.*3999G>T | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 14/14 | 3999 | chr17 | 12767643 | ||||||
chr17:12767645 | G | T | 32 | a0001c0001t0002 a0001c0001t0014 a0001c0001t0024 others(29): Show |
47 | HG00280.hp1 HG00280.hp2 HG00423.hp1 others(44): Show |
3_prime_UTR_variant | MODIFIER | c.*4001G>T | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 14/14 | 4001 | chr17 | 12767645 | ||||||
chr17:12767812 | C | G | 1 | a0001c0001t0128 | 1 | HG02129.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4168C>G | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 14/14 | 4168 | chr17 | 12767812 | ||||||
chr17:12768027 | G | A | 2 | a0001c0003t0105 a0001c0003t0181 |
2 | HG03209.hp2 NA18906.hp2 |
3_prime_UTR_variant | MODIFIER | c.*4383G>A | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 14/14 | 4383 | chr17 | 12768027 | ||||||
chr17:12768138 | G | A | 35 | a0001c0001t0017 a0001c0001t0018 a0001c0001t0026 others(32): Show |
42 | HG00423.hp1 HG00609.hp2 HG00673.hp1 others(39): Show |
3_prime_UTR_variant | MODIFIER | c.*4494G>A | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 14/14 | 4494 | chr17 | 12768138 | ||||||
chr17:12768278 | G | A | 1 | a0001c0001t0153 | 1 | HG03942.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4634G>A | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 14/14 | 4634 | chr17 | 12768278 | ||||||
chr17:12768357 | G | A | 1 | a0001c0001t0150 | 1 | HG02683.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4713G>A | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 14/14 | 4713 | chr17 | 12768357 | ||||||
chr17:12768456 | G | A | 1 | a0001c0001t0092 | 1 | HG02630.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4812G>A | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 14/14 | 4812 | chr17 | 12768456 | ||||||
chr17:12768498 | C | T | 6 | a0001c0001t0011 a0001c0001t0092 a0001c0001t0167 others(3): Show |
8 | HG02559.hp2 HG02622.hp2 HG02630.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*4854C>T | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 14/14 | 4854 | chr17 | 12768498 | ||||||
chr17:12768558 | A | G | 1 | a0001c0001t0143 | 1 | HG01106.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4914A>G | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 14/14 | 4914 | chr17 | 12768558 | ||||||
chr17:12768596 | T | A | 1 | a0001c0001t0141 | 1 | HG02738.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4952T>A | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 14/14 | 4952 | chr17 | 12768596 | ||||||
chr17:12768737 | A | G | 1 | a0013c0027t0110 | 1 | HG02723.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5093A>G | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 14/14 | 5093 | chr17 | 12768737 | ||||||
chr17:12768759 | C | G | 1 | a0001c0001t0152 | 1 | HG00558.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5115C>G | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 14/14 | 5115 | chr17 | 12768759 | ||||||
chr17:12768888 | C | CT | 38 | a0001c0001t0010 a0001c0001t0027 a0001c0001t0029 others(35): Show |
47 | HG00423.hp2 HG00544.hp2 HG00597.hp2 others(44): Show |
3_prime_UTR_variant | MODIFIER | c.*5250dupT | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 14/14 | 5251 | INFO_REALIGN_3_PRIME | chr17 | 12768888 | |||||
chr17:12768894 | TA | T | 20 | a0001c0001t0012 a0001c0001t0037 a0001c0001t0047 others(17): Show |
23 | HG01175.hp1 HG01515.hp1 HG01517.hp2 others(20): Show |
3_prime_UTR_variant | MODIFIER | c.*5265delA | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 14/14 | 5265 | INFO_REALIGN_3_PRIME | chr17 | 12768894 | |||||
chr17:12768895 | A | T | 176 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(173): Show |
271 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(268): Show |
3_prime_UTR_variant | MODIFIER | c.*5251A>T | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 14/14 | 5251 | chr17 | 12768895 | ||||||
chr17:12768896 | A | T | 56 | a0001c0001t0012 a0001c0001t0017 a0001c0001t0026 others(53): Show |
65 | HG00423.hp1 HG00609.hp2 HG00673.hp1 others(62): Show |
3_prime_UTR_variant | MODIFIER | c.*5252A>T | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 14/14 | 5252 | chr17 | 12768896 | ||||||
chr17:12768897 | A | T | 4 | a0001c0001t0042 a0001c0001t0103 a0001c0001t0106 others(1): Show |
5 | HG02622.hp1 HG02647.hp2 HG02717.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*5253A>T | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 14/14 | 5253 | chr17 | 12768897 | ||||||
chr17:12768910 | T | A | 79 | a0001c0001t0010 a0001c0001t0011 a0001c0001t0017 others(76): Show |
94 | HG00423.hp1 HG00423.hp2 HG00544.hp2 others(91): Show |
3_prime_UTR_variant | MODIFIER | c.*5266T>A | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 14/14 | 5266 | chr17 | 12768910 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr17:12666302 | C | G | 1 | a0001c0001t0001g0343 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.55+59C>G | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | chr17 | 12666302 | |||||||
chr17:12666305 | G | C | 1 | a0004c0009t0197g0004 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.55+62G>C | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | chr17 | 12666305 | |||||||
chr17:12666455 | T | C | 6 | a0001c0001t0014g0007 a0001c0001t0051g0009 a0001c0001t0052g0008 others(3): Show |
7 | HG01109.hp2 HG01243.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.55+212T>C | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | chr17 | 12666455 | |||||||
chr17:12666557 | A | G | 3 | a0001c0001t0108g0342 a0001c0001t0117g0340 a0001c0001t0125g0341 |
3 | HG02886.hp2 HG03130.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.55+314A>G | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | chr17 | 12666557 | |||||||
chr17:12666751 | C | T | 1 | a0001c0001t0103g0339 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.55+508C>T | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | chr17 | 12666751 | |||||||
chr17:12666836 | T | C | 1 | a0001c0001t0153g0010 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.55+593T>C | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | chr17 | 12666836 | |||||||
chr17:12667296 | T | G | 1 | a0001c0001t0041g0011 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.55+1053T>G | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | chr17 | 12667296 | |||||||
chr17:12667418 | C | T | 121 | a0001c0001t0001g0261 a0001c0001t0002g0241 a0001c0001t0002g0242 others(118): Show |
123 | HG00423.hp1 HG00544.hp1 HG00544.hp2 others(120): Show |
intron_variant | MODIFIER | c.55+1175C>T | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | chr17 | 12667418 | |||||||
chr17:12667481 | G | A | 4 | a0001c0001t0044g0012 a0001c0001t0139g0013 a0001c0001t0141g0015 others(1): Show |
4 | HG02683.hp2 HG02738.hp1 HG03490.hp2 others(1): Show |
intron_variant | MODIFIER | c.55+1238G>A | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | chr17 | 12667481 | |||||||
chr17:12667505 | A | C | 28 | a0001c0001t0001g0207 a0001c0001t0002g0208 a0001c0001t0003g0201 others(25): Show |
28 | HG00323.hp1 HG00323.hp2 HG00639.hp2 others(25): Show |
intron_variant | MODIFIER | c.55+1262A>C | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | chr17 | 12667505 | |||||||
chr17:12667670 | A | T | 1 | a0001c0001t0103g0339 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.55+1427A>T | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | chr17 | 12667670 | |||||||
chr17:12667749 | T | A | 55 | a0001c0001t0001g0207 a0001c0001t0002g0208 a0001c0001t0002g0241 others(52): Show |
55 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(52): Show |
intron_variant | MODIFIER | c.55+1506T>A | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | chr17 | 12667749 | |||||||
chr17:12667920 | GATATCAC others(3): Show |
G | 6 | a0001c0001t0013g0259 a0001c0001t0036g0257 a0001c0001t0040g0256 others(3): Show |
7 | HG01891.hp2 HG02109.hp2 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.55+1679_55+1688del others(10): Show |
MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr17 | 12667920 | ||||||
chr17:12667921 | A | C | 5 | a0001c0001t0044g0012 a0001c0001t0139g0013 a0001c0001t0141g0015 others(2): Show |
5 | HG02074.hp2 HG02683.hp2 HG02738.hp1 others(2): Show |
intron_variant | MODIFIER | c.55+1678A>C | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | chr17 | 12667921 | |||||||
chr17:12667930 | C | T | 1 | a0001c0001t0150g0206 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.55+1687C>T | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | chr17 | 12667930 | |||||||
chr17:12667998 | T | C | 4 | a0001c0001t0001g0261 a0001c0001t0169g0263 a0001c0002t0133g0264 others(1): Show |
4 | HG01256.hp2 HG02451.hp1 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.55+1755T>C | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | chr17 | 12667998 | |||||||
chr17:12668124 | G | A | 2 | a0001c0001t0075g0266 a0005c0010t0099g0265 |
2 | HG02257.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.55+1881G>A | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | chr17 | 12668124 | |||||||
chr17:12668236 | T | C | 2 | a0001c0001t0024g0016 a0018c0026t0027g0017 |
2 | NA18977.hp1 NA19056.hp2 |
intron_variant | MODIFIER | c.55+1993T>C | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | chr17 | 12668236 | |||||||
chr17:12668283 | A | ACT | 12 | a0001c0001t0014g0007 a0001c0001t0014g0338 a0001c0001t0033g0333 others(9): Show |
13 | HG01109.hp2 HG01192.hp1 HG01243.hp1 others(10): Show |
intron_variant | MODIFIER | c.55+2042_55+2043dup others(2): Show |
MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr17 | 12668283 | ||||||
chr17:12668419 | C | G | 1 | a0001c0003t0205g0332 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.55+2176C>G | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | chr17 | 12668419 | |||||||
chr17:12668433 | C | T | 1 | a0001c0001t0013g0200 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.55+2190C>T | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | chr17 | 12668433 | |||||||
chr17:12668448 | G | A | 105 | a0001c0001t0001g0207 a0001c0001t0002g0018 a0001c0001t0002g0208 others(102): Show |
106 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(103): Show |
intron_variant | MODIFIER | c.55+2205G>A | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | chr17 | 12668448 | |||||||
chr17:12668453 | G | T | 40 | a0001c0001t0001g0261 a0001c0001t0009g0326 a0001c0001t0009g0328 others(37): Show |
41 | HG00597.hp2 HG00642.hp1 HG00735.hp1 others(38): Show |
intron_variant | MODIFIER | c.55+2210G>T | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | chr17 | 12668453 | |||||||
chr17:12668514 | A | G | 1 | a0003c0008t0072g0227 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.55+2271A>G | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | chr17 | 12668514 | |||||||
chr17:12668780 | T | C | 3 | a0001c0001t0011g0229 a0001c0001t0011g0230 a0001c0006t0016g0231 |
3 | HG02622.hp2 HG02965.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.55+2537T>C | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | chr17 | 12668780 | |||||||
chr17:12668891 | G | T | 2 | a0001c0001t0014g0338 a0009c0020t0194g0226 |
2 | HG01243.hp1 HG02055.hp2 |
intron_variant | MODIFIER | c.55+2648G>T | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | chr17 | 12668891 | |||||||
chr17:12669048 | G | A | 2 | a0001c0001t0014g0338 a0009c0020t0194g0226 |
2 | HG01243.hp1 HG02055.hp2 |
intron_variant | MODIFIER | c.55+2805G>A | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | chr17 | 12669048 | |||||||
chr17:12669075 | G | A | 41 | a0001c0001t0001g0261 a0001c0001t0009g0326 a0001c0001t0009g0328 others(38): Show |
42 | HG00597.hp2 HG00642.hp1 HG00735.hp1 others(39): Show |
intron_variant | MODIFIER | c.55+2832G>A | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | chr17 | 12669075 | |||||||
chr17:12669170 | T | C | 1 | a0001c0001t0001g0343 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.55+2927T>C | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | chr17 | 12669170 | |||||||
chr17:12669266 | T | G | 52 | a0001c0001t0001g0207 a0001c0001t0002g0208 a0001c0001t0002g0241 others(49): Show |
52 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(49): Show |
intron_variant | MODIFIER | c.55+3023T>G | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | chr17 | 12669266 | |||||||
chr17:12669424 | CCCACCCC others(17): Show |
C | 1 | a0001c0001t0005g0199 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.55+3182_55+3205del others(24): Show |
MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | chr17 | 12669424 | |||||||
chr17:12669594 | AC | A | 3 | a0001c0001t0011g0229 a0001c0001t0011g0230 a0001c0006t0016g0231 |
3 | HG02622.hp2 HG02965.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.55+3354delC | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr17 | 12669594 | ||||||
chr17:12669623 | T | G | 1 | a0001c0001t0005g0199 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.55+3380T>G | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | chr17 | 12669623 | |||||||
chr17:12669624 | G | T | 1 | a0001c0001t0005g0199 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.55+3381G>T | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | chr17 | 12669624 | |||||||
chr17:12669625 | T | G | 1 | a0001c0001t0005g0199 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.55+3382T>G | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | chr17 | 12669625 | |||||||
chr17:12669681 | C | T | 3 | a0001c0003t0180g0304 a0003c0008t0071g0305 a0003c0008t0111g0303 |
3 | HG01884.hp2 HG03579.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.55+3438C>T | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | chr17 | 12669681 | |||||||
chr17:12669682 | G | A | 1 | a0001c0001t0058g0312 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.55+3439G>A | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | chr17 | 12669682 | |||||||
chr17:12669779 | C | T | 5 | a0001c0001t0091g0309 a0001c0001t0092g0311 a0001c0001t0097g0307 others(2): Show |
5 | HG02572.hp1 HG02615.hp2 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.55+3536C>T | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | chr17 | 12669779 | |||||||
chr17:12669981 | C | A | 1 | a0001c0001t0005g0199 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.55+3738C>A | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | chr17 | 12669981 | |||||||
chr17:12669982 | T | G | 1 | a0001c0001t0005g0199 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.55+3739T>G | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | chr17 | 12669982 | |||||||
chr17:12670026 | C | A | 1 | a0001c0001t0005g0199 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.55+3783C>A | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | chr17 | 12670026 | |||||||
chr17:12670071 | C | T | 1 | a0001c0001t0165g0198 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.55+3828C>T | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | chr17 | 12670071 | |||||||
chr17:12670079 | C | T | 45 | a0001c0001t0002g0018 a0001c0001t0004g0278 a0001c0001t0013g0259 others(42): Show |
46 | HG00280.hp2 HG00544.hp1 HG00544.hp2 others(43): Show |
intron_variant | MODIFIER | c.55+3836C>T | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | chr17 | 12670079 | |||||||
chr17:12670124 | G | A | 1 | a0001c0001t0005g0199 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.55+3881G>A | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | chr17 | 12670124 | |||||||
chr17:12670142 | G | C | 1 | a0001c0001t0005g0199 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.55+3899G>C | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | chr17 | 12670142 | |||||||
chr17:12670347 | A | G | 3 | a0001c0001t0011g0224 a0001c0001t0018g0223 a0001c0001t0042g0225 |
3 | HG02559.hp2 HG03579.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.55+4104A>G | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | chr17 | 12670347 | |||||||
chr17:12670353 | C | G | 17 | a0001c0001t0001g0261 a0001c0001t0014g0007 a0001c0001t0014g0338 others(14): Show |
18 | HG01109.hp2 HG01192.hp1 HG01243.hp1 others(15): Show |
intron_variant | MODIFIER | c.55+4110C>G | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | chr17 | 12670353 | |||||||
chr17:12670399 | G | A | 44 | a0001c0001t0002g0018 a0001c0001t0004g0278 a0001c0001t0013g0259 others(41): Show |
45 | HG00280.hp2 HG00544.hp1 HG00544.hp2 others(42): Show |
intron_variant | MODIFIER | c.55+4156G>A | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | chr17 | 12670399 | |||||||
chr17:12670515 | C | CA | 21 | a0001c0001t0009g0326 a0001c0001t0009g0328 a0001c0001t0009g0329 others(18): Show |
21 | HG00597.hp2 HG00642.hp1 HG00735.hp1 others(18): Show |
intron_variant | MODIFIER | c.55+4272_55+4273ins others(1): Show |
MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | chr17 | 12670515 | |||||||
chr17:12670517 | GAA | G | 21 | a0001c0001t0009g0326 a0001c0001t0009g0328 a0001c0001t0009g0329 others(18): Show |
21 | HG00597.hp2 HG00642.hp1 HG00735.hp1 others(18): Show |
intron_variant | MODIFIER | c.55+4275_55+4276del others(2): Show |
MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | chr17 | 12670517 | |||||||
chr17:12670560 | A | G | 1 | a0001c0001t0001g0343 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.55+4317A>G | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | chr17 | 12670560 | |||||||
chr17:12670611 | A | G | 10 | a0001c0001t0014g0007 a0001c0001t0051g0009 a0001c0001t0052g0008 others(7): Show |
11 | HG01109.hp2 HG01192.hp1 HG01243.hp2 others(8): Show |
intron_variant | MODIFIER | c.55+4368A>G | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | chr17 | 12670611 | |||||||
chr17:12670699 | T | C | 1 | a0001c0003t0109g0306 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.55+4456T>C | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | chr17 | 12670699 | |||||||
chr17:12670809 | A | G | 1 | a0001c0002t0133g0264 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.55+4566A>G | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | chr17 | 12670809 | |||||||
chr17:12670984 | C | T | 1 | a0001c0001t0108g0342 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.55+4741C>T | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | chr17 | 12670984 | |||||||
chr17:12671122 | T | A | 1 | a0001c0001t0005g0199 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.55+4879T>A | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | chr17 | 12671122 | |||||||
chr17:12671158 | A | G | 5 | a0001c0001t0007g0195 a0001c0001t0048g0196 a0001c0001t0084g0194 others(2): Show |
5 | HG00408.hp1 NA18941.hp2 NA18951.hp2 others(2): Show |
intron_variant | MODIFIER | c.55+4915A>G | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | chr17 | 12671158 | |||||||
chr17:12671184 | A | G | 226 | a0001c0001t0001g0136 a0001c0001t0001g0155 a0001c0001t0001g0161 others(223): Show |
228 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(225): Show |
intron_variant | MODIFIER | c.55+4941A>G | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | chr17 | 12671184 | |||||||
chr17:12671429 | A | C | 27 | a0001c0001t0001g0207 a0001c0001t0002g0208 a0001c0001t0003g0201 others(24): Show |
27 | HG00323.hp1 HG00323.hp2 HG00639.hp2 others(24): Show |
intron_variant | MODIFIER | c.55+5186A>C | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | chr17 | 12671429 | |||||||
chr17:12671433 | G | T | 2 | a0001c0001t0008g0131 a0001c0001t0073g0337 |
2 | NA19000.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.55+5190G>T | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | chr17 | 12671433 | |||||||
chr17:12671465 | T | A | 2 | a0001c0001t0054g0314 a0001c0001t0056g0313 |
2 | HG02976.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.55+5222T>A | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | chr17 | 12671465 | |||||||
chr17:12671547 | C | T | 44 | a0001c0001t0002g0018 a0001c0001t0004g0278 a0001c0001t0013g0259 others(41): Show |
45 | HG00280.hp2 HG00544.hp1 HG00544.hp2 others(42): Show |
intron_variant | MODIFIER | c.55+5304C>T | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | chr17 | 12671547 | |||||||
chr17:12671565 | A | G | 1 | a0001c0002t0192g0130 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.55+5322A>G | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | chr17 | 12671565 | |||||||
chr17:12671673 | C | CA | 5 | a0001c0001t0091g0309 a0001c0001t0092g0311 a0001c0001t0097g0307 others(2): Show |
5 | HG02572.hp1 HG02615.hp2 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.55+5431dupA | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr17 | 12671673 | ||||||
chr17:12671720 | A | G | 1 | a0001c0003t0105g0020 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.55+5477A>G | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | chr17 | 12671720 | |||||||
chr17:12671735 | C | T | 2 | a0001c0001t0035g0129 a0001c0002t0177g0192 |
2 | HG02004.hp1 HG02074.hp2 |
intron_variant | MODIFIER | c.55+5492C>T | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | chr17 | 12671735 | |||||||
chr17:12671833 | A | G | 1 | a0001c0001t0010g0191 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.55+5590A>G | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | chr17 | 12671833 | |||||||
chr17:12672010 | C | T | 3 | a0001c0001t0139g0013 a0001c0001t0141g0015 a0001c0001t0171g0014 |
3 | HG02738.hp1 HG03490.hp2 HG03831.hp1 |
intron_variant | MODIFIER | c.55+5767C>T | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | chr17 | 12672010 | |||||||
chr17:12672057 | G | T | 44 | a0001c0001t0002g0018 a0001c0001t0004g0278 a0001c0001t0013g0259 others(41): Show |
45 | HG00280.hp2 HG00544.hp1 HG00544.hp2 others(42): Show |
intron_variant | MODIFIER | c.55+5814G>T | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | chr17 | 12672057 | |||||||
chr17:12672098 | C | A | 1 | a0001c0001t0067g0315 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.55+5855C>A | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | chr17 | 12672098 | |||||||
chr17:12672162 | G | T | 1 | a0001c0001t0161g0190 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.55+5919G>T | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | chr17 | 12672162 | |||||||
chr17:12672189 | T | C | 10 | a0001c0001t0014g0007 a0001c0001t0051g0009 a0001c0001t0052g0008 others(7): Show |
11 | HG01109.hp2 HG01192.hp1 HG01243.hp2 others(8): Show |
intron_variant | MODIFIER | c.55+5946T>C | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | chr17 | 12672189 | |||||||
chr17:12672309 | G | T | 1 | a0001c0001t0067g0315 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.55+6066G>T | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | chr17 | 12672309 | |||||||
chr17:12672380 | G | A | 44 | a0001c0001t0002g0018 a0001c0001t0004g0278 a0001c0001t0013g0259 others(41): Show |
45 | HG00280.hp2 HG00544.hp1 HG00544.hp2 others(42): Show |
intron_variant | MODIFIER | c.55+6137G>A | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | chr17 | 12672380 | |||||||
chr17:12672424 | A | G | 1 | a0001c0001t0001g0343 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.55+6181A>G | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | chr17 | 12672424 | |||||||
chr17:12672441 | G | GT | 41 | a0001c0001t0001g0161 a0001c0001t0001g0176 a0001c0001t0001g0177 others(38): Show |
41 | HG00408.hp1 HG00642.hp2 HG00735.hp2 others(38): Show |
intron_variant | MODIFIER | c.55+6199dupT | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr17 | 12672441 | ||||||
chr17:12672465 | G | T | 48 | a0001c0001t0002g0018 a0001c0001t0004g0278 a0001c0001t0011g0229 others(45): Show |
49 | HG00280.hp2 HG00544.hp1 HG00544.hp2 others(46): Show |
intron_variant | MODIFIER | c.55+6222G>T | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | chr17 | 12672465 | |||||||
chr17:12672533 | T | C | 10 | a0001c0001t0014g0007 a0001c0001t0051g0009 a0001c0001t0052g0008 others(7): Show |
11 | HG01109.hp2 HG01192.hp1 HG01243.hp2 others(8): Show |
intron_variant | MODIFIER | c.55+6290T>C | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | chr17 | 12672533 | |||||||
chr17:12672860 | G | C | 1 | a0001c0001t0201g0334 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.55+6617G>C | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | chr17 | 12672860 | |||||||
chr17:12672922 | T | C | 2 | a0001c0001t0014g0338 a0001c0001t0033g0333 |
2 | HG01243.hp1 HG02145.hp1 |
intron_variant | MODIFIER | c.55+6679T>C | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | chr17 | 12672922 | |||||||
chr17:12672954 | A | G | 27 | a0001c0001t0001g0207 a0001c0001t0002g0208 a0001c0001t0003g0201 others(24): Show |
27 | HG00323.hp1 HG00323.hp2 HG00639.hp2 others(24): Show |
intron_variant | MODIFIER | c.55+6711A>G | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | chr17 | 12672954 | |||||||
chr17:12673018 | T | C | 1 | a0001c0003t0205g0332 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.55+6775T>C | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | chr17 | 12673018 | |||||||
chr17:12673035 | G | A | 1 | a0001c0001t0001g0261 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.55+6792G>A | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | chr17 | 12673035 | |||||||
chr17:12673367 | T | C | 2 | a0001c0001t0041g0011 a0001c0001t0044g0012 |
2 | HG00735.hp2 HG02683.hp2 |
intron_variant | MODIFIER | c.55+7124T>C | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | chr17 | 12673367 | |||||||
chr17:12673387 | C | T | 22 | a0001c0001t0009g0326 a0001c0001t0009g0328 a0001c0001t0009g0329 others(19): Show |
22 | HG00597.hp2 HG00642.hp1 HG00735.hp1 others(19): Show |
intron_variant | MODIFIER | c.55+7144C>T | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | chr17 | 12673387 | |||||||
chr17:12673394 | A | G | 4 | a0001c0001t0001g0343 a0001c0001t0011g0229 a0001c0001t0011g0230 others(1): Show |
4 | HG02622.hp2 HG02965.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.55+7151A>G | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | chr17 | 12673394 | |||||||
chr17:12673766 | G | C | 3 | a0001c0001t0011g0229 a0001c0001t0011g0230 a0001c0006t0016g0231 |
3 | HG02622.hp2 HG02965.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.55+7523G>C | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | chr17 | 12673766 | |||||||
chr17:12673832 | T | C | 1 | a0001c0001t0103g0339 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.55+7589T>C | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | chr17 | 12673832 | |||||||
chr17:12673974 | T | C | 3 | a0001c0001t0011g0229 a0001c0001t0011g0230 a0001c0006t0016g0231 |
3 | HG02622.hp2 HG02965.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.55+7731T>C | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | chr17 | 12673974 | |||||||
chr17:12673998 | G | A | 1 | a0001c0001t0103g0339 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.55+7755G>A | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | chr17 | 12673998 | |||||||
chr17:12674016 | CA | C | 10 | a0001c0001t0001g0181 a0001c0001t0002g0187 a0001c0001t0003g0188 others(7): Show |
10 | HG00642.hp2 HG00741.hp2 HG01106.hp2 others(7): Show |
intron_variant | MODIFIER | c.55+7774delA | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | chr17 | 12674016 | |||||||
chr17:12674148 | C | T | 1 | a0001c0001t0103g0339 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.55+7905C>T | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | chr17 | 12674148 | |||||||
chr17:12674176 | G | T | 1 | a0001c0001t0103g0339 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.55+7933G>T | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | chr17 | 12674176 | |||||||
chr17:12674347 | C | T | 2 | a0001c0001t0001g0261 a0001c0001t0169g0263 |
2 | HG01256.hp2 HG03490.hp1 |
intron_variant | MODIFIER | c.55+8104C>T | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | chr17 | 12674347 | |||||||
chr17:12674511 | A | C | 1 | a0001c0001t0001g0343 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.55+8268A>C | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | chr17 | 12674511 | |||||||
chr17:12674584 | G | A | 6 | a0001c0001t0038g0024 a0001c0001t0079g0023 a0001c0001t0082g0026 others(3): Show |
6 | HG03453.hp2 NA18953.hp2 NA18956.hp1 others(3): Show |
intron_variant | MODIFIER | c.55+8341G>A | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | chr17 | 12674584 | |||||||
chr17:12674640 | C | T | 3 | a0001c0001t0011g0229 a0001c0001t0011g0230 a0001c0006t0016g0231 |
3 | HG02622.hp2 HG02965.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.55+8397C>T | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | chr17 | 12674640 | |||||||
chr17:12674653 | A | C | 3 | a0001c0001t0011g0229 a0001c0001t0011g0230 a0001c0006t0016g0231 |
3 | HG02622.hp2 HG02965.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.55+8410A>C | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | chr17 | 12674653 | |||||||
chr17:12674662 | C | T | 3 | a0001c0001t0011g0229 a0001c0001t0011g0230 a0001c0006t0016g0231 |
3 | HG02622.hp2 HG02965.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.55+8419C>T | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | chr17 | 12674662 | |||||||
chr17:12674749 | C | T | 22 | a0001c0001t0009g0326 a0001c0001t0009g0328 a0001c0001t0009g0329 others(19): Show |
22 | HG00597.hp2 HG00642.hp1 HG00735.hp1 others(19): Show |
intron_variant | MODIFIER | c.55+8506C>T | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | chr17 | 12674749 | |||||||
chr17:12674804 | G | A | 225 | a0001c0001t0001g0028 a0001c0001t0001g0136 a0001c0001t0001g0155 others(222): Show |
227 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(224): Show |
intron_variant | MODIFIER | c.55+8561G>A | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | chr17 | 12674804 | |||||||
chr17:12675183 | T | G | 24 | a0001c0001t0002g0241 a0001c0001t0002g0242 a0001c0001t0002g0244 others(21): Show |
24 | HG00423.hp1 HG00673.hp1 HG00741.hp1 others(21): Show |
intron_variant | MODIFIER | c.55+8940T>G | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | chr17 | 12675183 | |||||||
chr17:12675300 | G | C | 1 | a0001c0001t0103g0339 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.55+9057G>C | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | chr17 | 12675300 | |||||||
chr17:12675337 | A | G | 1 | a0001c0004t0003g0128 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.55+9094A>G | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | chr17 | 12675337 | |||||||
chr17:12675347 | C | T | 46 | a0001c0001t0001g0028 a0001c0001t0002g0018 a0001c0001t0004g0278 others(43): Show |
47 | HG00280.hp2 HG00544.hp1 HG00544.hp2 others(44): Show |
intron_variant | MODIFIER | c.55+9104C>T | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | chr17 | 12675347 | |||||||
chr17:12675480 | T | C | 1 | a0001c0001t0003g0201 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.55+9237T>C | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | chr17 | 12675480 | |||||||
chr17:12675499 | C | T | 1 | a0001c0001t0005g0127 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.55+9256C>T | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | chr17 | 12675499 | |||||||
chr17:12675503 | G | A | 1 | a0001c0001t0032g0029 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.55+9260G>A | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | chr17 | 12675503 | |||||||
chr17:12675635 | G | C | 1 | a0001c0001t0157g0030 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.55+9392G>C | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | chr17 | 12675635 | |||||||
chr17:12675715 | T | C | 58 | a0001c0001t0001g0028 a0001c0001t0001g0343 a0001c0001t0002g0018 others(55): Show |
59 | HG00280.hp2 HG00544.hp1 HG00544.hp2 others(56): Show |
intron_variant | MODIFIER | c.55+9472T>C | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | chr17 | 12675715 | |||||||
chr17:12675716 | G | A | 2 | a0001c0001t0002g0018 a0001c0001t0146g0019 |
2 | HG00280.hp2 HG01255.hp1 |
intron_variant | MODIFIER | c.55+9473G>A | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | chr17 | 12675716 | |||||||
chr17:12675791 | G | A | 46 | a0001c0001t0002g0018 a0001c0001t0004g0278 a0001c0001t0013g0259 others(43): Show |
47 | HG00280.hp2 HG00544.hp1 HG00544.hp2 others(44): Show |
intron_variant | MODIFIER | c.55+9548G>A | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | chr17 | 12675791 | |||||||
chr17:12675815 | C | T | 6 | a0001c0001t0009g0326 a0001c0001t0009g0328 a0001c0001t0009g0329 others(3): Show |
6 | HG00642.hp1 HG00735.hp1 HG01346.hp1 others(3): Show |
intron_variant | MODIFIER | c.55+9572C>T | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | chr17 | 12675815 | |||||||
chr17:12675883 | A | G | 54 | a0001c0001t0001g0028 a0001c0001t0001g0343 a0001c0001t0002g0018 others(51): Show |
55 | HG00280.hp2 HG00544.hp1 HG00544.hp2 others(52): Show |
intron_variant | MODIFIER | c.55+9640A>G | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | chr17 | 12675883 | |||||||
chr17:12675901 | A | G | 1 | a0001c0001t0164g0189 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.55+9658A>G | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | chr17 | 12675901 | |||||||
chr17:12676045 | C | A | 3 | a0001c0001t0011g0224 a0001c0001t0018g0223 a0001c0001t0042g0225 |
3 | HG02559.hp2 HG03579.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.55+9802C>A | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | chr17 | 12676045 | |||||||
chr17:12676052 | A | G | 1 | a0001c0001t0156g0269 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.55+9809A>G | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | chr17 | 12676052 | |||||||
chr17:12676237 | G | A | 2 | a0001c0001t0001g0161 a0001c0002t0149g0162 |
2 | NA18954.hp2 NA18970.hp2 |
intron_variant | MODIFIER | c.55+9994G>A | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | chr17 | 12676237 | |||||||
chr17:12676239 | G | A | 47 | a0001c0001t0001g0028 a0001c0001t0002g0018 a0001c0001t0004g0278 others(44): Show |
48 | HG00280.hp2 HG00544.hp1 HG00544.hp2 others(45): Show |
intron_variant | MODIFIER | c.55+9996G>A | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | chr17 | 12676239 | |||||||
chr17:12676243 | A | ACG | 5 | a0001c0001t0001g0181 a0001c0001t0004g0164 a0001c0001t0024g0165 others(2): Show |
5 | HG01496.hp1 NA18944.hp2 NA18975.hp1 others(2): Show |
intron_variant | MODIFIER | c.55+10002_55+10003d others(4): Show |
MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr17 | 12676243 | ||||||
chr17:12676245 | G | GCA | 3 | a0001c0001t0036g0036 a0001c0001t0121g0037 a0001c0003t0112g0035 |
3 | HG02280.hp1 HG02809.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.55+10049_55+10050d others(4): Show |
MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr17 | 12676245 | ||||||
chr17:12676245 | G | GCACA | 5 | a0001c0001t0005g0199 a0001c0001t0018g0033 a0001c0001t0033g0034 others(2): Show |
5 | HG01884.hp1 HG02818.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.55+10047_55+10050d others(6): Show |
MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr17 | 12676245 | ||||||
chr17:12676245 | GCA | G | 39 | a0001c0001t0001g0051 a0001c0001t0001g0136 a0001c0001t0001g0161 others(36): Show |
39 | HG00642.hp2 HG01496.hp2 HG01978.hp2 others(36): Show |
intron_variant | MODIFIER | c.55+10049_55+10050d others(4): Show |
MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr17 | 12676245 | ||||||
chr17:12676245 | GCACA | G | 106 | a0001c0001t0001g0058 a0001c0001t0001g0069 a0001c0001t0001g0077 others(103): Show |
106 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(103): Show |
intron_variant | MODIFIER | c.55+10047_55+10050d others(6): Show |
MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr17 | 12676245 | ||||||
chr17:12676245 | GCACACA | G | 43 | a0001c0001t0001g0155 a0001c0001t0002g0112 a0001c0001t0002g0157 others(40): Show |
43 | HG00280.hp1 HG00639.hp1 HG00639.hp2 others(40): Show |
intron_variant | MODIFIER | c.55+10045_55+10050d others(8): Show |
MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr17 | 12676245 | ||||||
chr17:12676245 | GCACACAC others(1): Show |
G | 27 | a0001c0001t0001g0124 a0001c0001t0001g0176 a0001c0001t0001g0177 others(24): Show |
27 | HG00323.hp1 HG00558.hp2 HG00609.hp1 others(24): Show |
intron_variant | MODIFIER | c.55+10043_55+10050d others(10): Show |
MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr17 | 12676245 | ||||||
chr17:12676245 | GCACACAC others(3): Show |
G | 42 | a0001c0001t0002g0241 a0001c0001t0002g0242 a0001c0001t0002g0244 others(39): Show |
43 | HG00423.hp1 HG00642.hp1 HG00673.hp1 others(40): Show |
intron_variant | MODIFIER | c.55+10041_55+10050d others(12): Show |
MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr17 | 12676245 | ||||||
chr17:12676245 | GCACACAC others(5): Show |
G | 5 | a0001c0001t0042g0225 a0001c0001t0051g0009 a0001c0001t0053g0325 others(2): Show |
5 | HG00597.hp2 HG01109.hp2 HG02257.hp2 others(2): Show |
intron_variant | MODIFIER | c.55+10039_55+10050d others(14): Show |
MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr17 | 12676245 | ||||||
chr17:12676245 | GCACACAC others(21): Show |
G | 52 | a0001c0001t0001g0028 a0001c0001t0001g0343 a0001c0001t0002g0018 others(49): Show |
53 | HG00280.hp2 HG00544.hp1 HG00544.hp2 others(50): Show |
intron_variant | MODIFIER | c.55+10023_55+10050d others(30): Show |
MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr17 | 12676245 | ||||||
chr17:12676246 | CACACACA others(20): Show |
C | 1 | a0001c0001t0154g0027 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.55+10004_55+10030d others(29): Show |
MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | chr17 | 12676246 | |||||||
chr17:12676247 | A | G | 2 | a0001c0001t0007g0163 a0001c0002t0187g0132 |
2 | HG02074.hp1 HG02080.hp2 |
intron_variant | MODIFIER | c.55+10004A>G | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | chr17 | 12676247 | |||||||
chr17:12676249 | A | G | 24 | a0001c0001t0001g0136 a0001c0001t0001g0161 a0001c0001t0005g0141 others(21): Show |
24 | HG00642.hp2 HG02056.hp1 HG02129.hp1 others(21): Show |
intron_variant | MODIFIER | c.55+10006A>G | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | chr17 | 12676249 | |||||||
chr17:12676251 | A | G | 18 | a0001c0001t0003g0150 a0001c0001t0007g0195 a0001c0001t0010g0183 others(15): Show |
18 | HG00408.hp1 HG00735.hp2 HG01261.hp2 others(15): Show |
intron_variant | MODIFIER | c.55+10008A>G | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | chr17 | 12676251 | |||||||
chr17:12676253 | A | G | 14 | a0001c0001t0001g0155 a0001c0001t0002g0157 a0001c0001t0006g0174 others(11): Show |
14 | HG00741.hp2 HG01106.hp2 HG01981.hp1 others(11): Show |
intron_variant | MODIFIER | c.55+10010A>G | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | chr17 | 12676253 | |||||||
chr17:12676255 | A | G | 5 | a0001c0001t0001g0176 a0001c0001t0001g0177 a0001c0001t0002g0187 others(2): Show |
5 | HG01081.hp2 HG01346.hp2 HG02698.hp2 others(2): Show |
intron_variant | MODIFIER | c.55+10012A>G | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | chr17 | 12676255 | |||||||
chr17:12676273 | A | C | 1 | a0001c0001t0082g0026 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.55+10030A>C | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | chr17 | 12676273 | |||||||
chr17:12676275 | A | G | 1 | a0002c0005t0102g0160 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.55+10032A>G | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | chr17 | 12676275 | |||||||
chr17:12676291 | A | G | 1 | a0001c0001t0060g0320 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.55+10048A>G | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | chr17 | 12676291 | |||||||
chr17:12676292 | C | G | 1 | a0001c0001t0005g0054 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.55+10049C>G | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | chr17 | 12676292 | |||||||
chr17:12676323 | A | G | 24 | a0001c0001t0002g0241 a0001c0001t0002g0242 a0001c0001t0002g0244 others(21): Show |
24 | HG00423.hp1 HG00673.hp1 HG00741.hp1 others(21): Show |
intron_variant | MODIFIER | c.55+10080A>G | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | chr17 | 12676323 | |||||||
chr17:12676357 | C | A | 6 | a0001c0001t0075g0266 a0001c0001t0108g0342 a0001c0001t0156g0269 others(3): Show |
6 | HG02257.hp2 HG02451.hp2 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.55+10114C>A | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | chr17 | 12676357 | |||||||
chr17:12676380 | A | G | 47 | a0001c0001t0001g0261 a0001c0001t0009g0326 a0001c0001t0009g0328 others(44): Show |
48 | HG00597.hp2 HG00642.hp1 HG00735.hp1 others(45): Show |
intron_variant | MODIFIER | c.55+10137A>G | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | chr17 | 12676380 | |||||||
chr17:12676502 | T | A | 49 | a0001c0001t0001g0028 a0001c0001t0002g0018 a0001c0001t0004g0278 others(46): Show |
50 | HG00280.hp2 HG00544.hp1 HG00544.hp2 others(47): Show |
intron_variant | MODIFIER | c.55+10259T>A | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | chr17 | 12676502 | |||||||
chr17:12676548 | C | CT | 52 | a0001c0001t0001g0028 a0001c0001t0002g0018 a0001c0001t0004g0278 others(49): Show |
53 | HG00280.hp2 HG00544.hp1 HG00544.hp2 others(50): Show |
intron_variant | MODIFIER | c.55+10314dupT | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr17 | 12676548 | ||||||
chr17:12676620 | G | A | 1 | a0001c0001t0005g0232 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.55+10377G>A | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | chr17 | 12676620 | |||||||
chr17:12676632 | C | T | 2 | a0001c0001t0015g0107 a0001c0001t0136g0053 |
2 | NA19007.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.55+10389C>T | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | chr17 | 12676632 | |||||||
chr17:12676693 | A | C | 52 | a0001c0001t0001g0028 a0001c0001t0002g0018 a0001c0001t0004g0278 others(49): Show |
53 | HG00280.hp2 HG00544.hp1 HG00544.hp2 others(50): Show |
intron_variant | MODIFIER | c.55+10450A>C | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | chr17 | 12676693 | |||||||
chr17:12677127 | T | C | 24 | a0001c0001t0002g0241 a0001c0001t0002g0242 a0001c0001t0002g0244 others(21): Show |
24 | HG00423.hp1 HG00673.hp1 HG00741.hp1 others(21): Show |
intron_variant | MODIFIER | c.55+10884T>C | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | chr17 | 12677127 | |||||||
chr17:12677415 | TA | T | 24 | a0001c0001t0002g0241 a0001c0001t0002g0242 a0001c0001t0002g0244 others(21): Show |
24 | HG00423.hp1 HG00673.hp1 HG00741.hp1 others(21): Show |
intron_variant | MODIFIER | c.55+11181delA | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr17 | 12677415 | ||||||
chr17:12677416 | A | T | 41 | a0001c0001t0001g0261 a0001c0001t0009g0326 a0001c0001t0009g0328 others(38): Show |
42 | HG00597.hp2 HG00642.hp1 HG00735.hp1 others(39): Show |
intron_variant | MODIFIER | c.55+11173A>T | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | chr17 | 12677416 | |||||||
chr17:12677426 | T | A | 225 | a0001c0001t0001g0028 a0001c0001t0001g0136 a0001c0001t0001g0155 others(222): Show |
227 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(224): Show |
intron_variant | MODIFIER | c.55+11183T>A | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | chr17 | 12677426 | |||||||
chr17:12677453 | C | T | 1 | a0001c0001t0188g0302 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.55+11210C>T | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | chr17 | 12677453 | |||||||
chr17:12677469 | T | C | 57 | a0001c0001t0001g0028 a0001c0001t0002g0018 a0001c0001t0004g0278 others(54): Show |
58 | HG00280.hp2 HG00544.hp1 HG00544.hp2 others(55): Show |
intron_variant | MODIFIER | c.55+11226T>C | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | chr17 | 12677469 | |||||||
chr17:12677494 | C | T | 13 | a0001c0001t0014g0007 a0001c0001t0014g0338 a0001c0001t0033g0333 others(10): Show |
14 | HG01109.hp2 HG01192.hp1 HG01243.hp1 others(11): Show |
intron_variant | MODIFIER | c.55+11251C>T | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | chr17 | 12677494 | |||||||
chr17:12677540 | A | G | 57 | a0001c0001t0001g0028 a0001c0001t0002g0018 a0001c0001t0004g0278 others(54): Show |
58 | HG00280.hp2 HG00544.hp1 HG00544.hp2 others(55): Show |
intron_variant | MODIFIER | c.55+11297A>G | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | chr17 | 12677540 | |||||||
chr17:12677569 | G | A | 1 | a0001c0001t0139g0013 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.55+11326G>A | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | chr17 | 12677569 | |||||||
chr17:12677702 | ACT | A | 20 | a0001c0001t0009g0326 a0001c0001t0009g0328 a0001c0001t0009g0329 others(17): Show |
20 | HG00597.hp2 HG00642.hp1 HG00735.hp1 others(17): Show |
intron_variant | MODIFIER | c.55+11462_55+11463d others(4): Show |
MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr17 | 12677702 | ||||||
chr17:12677829 | T | C | 1 | a0001c0001t0002g0119 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.55+11586T>C | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | chr17 | 12677829 | |||||||
chr17:12677839 | C | T | 1 | a0001c0001t0095g0213 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.55+11596C>T | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | chr17 | 12677839 | |||||||
chr17:12677858 | A | T | 3 | a0001c0001t0008g0052 a0001c0001t0074g0105 a0001c0001t0076g0106 |
3 | NA19010.hp2 NA19011.hp1 NA19091.hp2 |
intron_variant | MODIFIER | c.55+11615A>T | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | chr17 | 12677858 | |||||||
chr17:12677859 | T | A | 3 | a0001c0001t0008g0052 a0001c0001t0074g0105 a0001c0001t0076g0106 |
3 | NA19010.hp2 NA19011.hp1 NA19091.hp2 |
intron_variant | MODIFIER | c.55+11616T>A | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | chr17 | 12677859 | |||||||
chr17:12677882 | T | C | 3 | a0001c0001t0011g0229 a0001c0001t0011g0230 a0001c0006t0016g0231 |
3 | HG02622.hp2 HG02965.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.55+11639T>C | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | chr17 | 12677882 | |||||||
chr17:12677896 | G | GT | 31 | a0001c0001t0001g0051 a0001c0001t0001g0104 a0001c0001t0002g0157 others(28): Show |
31 | HG00597.hp2 HG00642.hp1 HG00735.hp1 others(28): Show |
intron_variant | MODIFIER | c.55+11668dupT | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr17 | 12677896 | ||||||
chr17:12677896 | GT | G | 47 | a0001c0001t0001g0028 a0001c0001t0002g0018 a0001c0001t0004g0278 others(44): Show |
48 | HG00280.hp2 HG00544.hp1 HG00544.hp2 others(45): Show |
intron_variant | MODIFIER | c.55+11668delT | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr17 | 12677896 | ||||||
chr17:12677896 | GTT | G | 6 | a0001c0001t0013g0259 a0001c0001t0036g0257 a0001c0001t0040g0256 others(3): Show |
7 | HG01891.hp2 HG02109.hp2 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.55+11667_55+11668d others(4): Show |
MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr17 | 12677896 | ||||||
chr17:12677992 | T | C | 56 | a0001c0001t0001g0028 a0001c0001t0002g0018 a0001c0001t0004g0278 others(53): Show |
57 | HG00280.hp2 HG00544.hp1 HG00544.hp2 others(54): Show |
intron_variant | MODIFIER | c.55+11749T>C | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | chr17 | 12677992 | |||||||
chr17:12678037 | C | T | 3 | a0001c0001t0011g0229 a0001c0001t0011g0230 a0001c0006t0016g0231 |
3 | HG02622.hp2 HG02965.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.55+11794C>T | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | chr17 | 12678037 | |||||||
chr17:12678091 | C | T | 9 | a0001c0001t0014g0007 a0001c0001t0051g0009 a0001c0001t0052g0008 others(6): Show |
10 | HG01109.hp2 HG01192.hp1 HG01243.hp2 others(7): Show |
intron_variant | MODIFIER | c.55+11848C>T | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | chr17 | 12678091 | |||||||
chr17:12678221 | G | A | 3 | a0001c0001t0108g0342 a0001c0001t0117g0340 a0001c0001t0125g0341 |
3 | HG02886.hp2 HG03130.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.55+11978G>A | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | chr17 | 12678221 | |||||||
chr17:12678313 | C | CA | 61 | a0001c0001t0001g0207 a0001c0001t0001g0261 a0001c0001t0002g0208 others(58): Show |
61 | HG00323.hp1 HG00323.hp2 HG00597.hp2 others(58): Show |
intron_variant | MODIFIER | c.55+12082dupA | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr17 | 12678313 | ||||||
chr17:12678313 | C | CAA | 29 | a0001c0001t0001g0343 a0001c0001t0002g0241 a0001c0001t0002g0242 others(26): Show |
29 | HG00423.hp1 HG00673.hp1 HG00741.hp1 others(26): Show |
intron_variant | MODIFIER | c.55+12081_55+12082d others(4): Show |
MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr17 | 12678313 | ||||||
chr17:12678313 | CA | C | 118 | a0001c0001t0001g0028 a0001c0001t0001g0136 a0001c0001t0001g0155 others(115): Show |
119 | HG00280.hp2 HG00408.hp1 HG00544.hp1 others(116): Show |
intron_variant | MODIFIER | c.55+12082delA | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr17 | 12678313 | ||||||
chr17:12678328 | G | T | 55 | a0001c0001t0001g0028 a0001c0001t0002g0018 a0001c0001t0004g0278 others(52): Show |
56 | HG00280.hp2 HG00544.hp1 HG00544.hp2 others(53): Show |
intron_variant | MODIFIER | c.55+12085G>T | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | chr17 | 12678328 | |||||||
chr17:12678362 | A | C | 3 | a0001c0001t0018g0042 a0001c0001t0033g0034 a0001c0001t0121g0037 |
3 | HG01884.hp1 HG02809.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.55+12119A>C | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | chr17 | 12678362 | |||||||
chr17:12678536 | AAG | A | 3 | a0001c0001t0011g0229 a0001c0001t0011g0230 a0001c0006t0016g0231 |
3 | HG02622.hp2 HG02965.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.55+12309_55+12310d others(4): Show |
MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr17 | 12678536 | ||||||
chr17:12678560 | A | G | 3 | a0001c0001t0011g0229 a0001c0001t0011g0230 a0001c0006t0016g0231 |
3 | HG02622.hp2 HG02965.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.55+12317A>G | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | chr17 | 12678560 | |||||||
chr17:12678589 | C | G | 1 | a0001c0001t0008g0131 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.55+12346C>G | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | chr17 | 12678589 | |||||||
chr17:12678612 | T | C | 1 | a0001c0001t0108g0342 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.55+12369T>C | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | chr17 | 12678612 | |||||||
chr17:12678691 | A | C | 5 | a0001c0001t0021g0147 a0001c0001t0022g0148 a0001c0001t0030g0301 others(2): Show |
5 | HG02683.hp2 HG02886.hp1 HG04115.hp1 others(2): Show |
intron_variant | MODIFIER | c.55+12448A>C | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | chr17 | 12678691 | |||||||
chr17:12678735 | A | G | 156 | a0001c0001t0001g0028 a0001c0001t0001g0207 a0001c0001t0001g0261 others(153): Show |
158 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(155): Show |
intron_variant | MODIFIER | c.55+12492A>G | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | chr17 | 12678735 | |||||||
chr17:12678789 | G | A | 2 | a0001c0001t0005g0054 a0003c0008t0104g0021 |
2 | HG01192.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.55+12546G>A | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | chr17 | 12678789 | |||||||
chr17:12678871 | A | AT | 73 | a0001c0001t0001g0207 a0001c0001t0001g0261 a0001c0001t0002g0208 others(70): Show |
74 | HG00323.hp1 HG00323.hp2 HG00597.hp2 others(71): Show |
intron_variant | MODIFIER | c.55+12635dupT | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr17 | 12678871 | ||||||
chr17:12678910 | G | A | 3 | a0001c0001t0011g0229 a0001c0001t0011g0230 a0001c0006t0016g0231 |
3 | HG02622.hp2 HG02965.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.55+12667G>A | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | chr17 | 12678910 | |||||||
chr17:12678933 | G | A | 4 | a0001c0001t0014g0338 a0001c0001t0033g0333 a0001c0003t0109g0306 others(1): Show |
4 | HG01243.hp1 HG02055.hp2 HG02145.hp1 others(1): Show |
intron_variant | MODIFIER | c.55+12690G>A | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | chr17 | 12678933 | |||||||
chr17:12678950 | A | G | 55 | a0001c0001t0001g0028 a0001c0001t0002g0018 a0001c0001t0004g0278 others(52): Show |
56 | HG00280.hp2 HG00544.hp1 HG00544.hp2 others(53): Show |
intron_variant | MODIFIER | c.55+12707A>G | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | chr17 | 12678950 | |||||||
chr17:12678977 | A | G | 54 | a0001c0001t0001g0028 a0001c0001t0002g0018 a0001c0001t0004g0278 others(51): Show |
55 | HG00280.hp2 HG00544.hp1 HG00544.hp2 others(52): Show |
intron_variant | MODIFIER | c.55+12734A>G | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | chr17 | 12678977 | |||||||
chr17:12679074 | C | T | 1 | a0001c0004t0003g0254 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.55+12831C>T | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | chr17 | 12679074 | |||||||
chr17:12679213 | A | T | 83 | a0001c0001t0001g0028 a0001c0001t0001g0343 a0001c0001t0002g0018 others(80): Show |
84 | HG00280.hp2 HG00423.hp1 HG00544.hp1 others(81): Show |
intron_variant | MODIFIER | c.55+12970A>T | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | chr17 | 12679213 | |||||||
chr17:12679275 | A | G | 1 | a0001c0001t0001g0343 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.55+13032A>G | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | chr17 | 12679275 | |||||||
chr17:12679279 | G | A | 1 | a0001c0001t0116g0270 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.55+13036G>A | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | chr17 | 12679279 | |||||||
chr17:12679376 | T | G | 2 | a0001c0001t0002g0119 a0001c0001t0152g0120 |
2 | HG00558.hp2 HG02257.hp1 |
intron_variant | MODIFIER | c.55+13133T>G | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | chr17 | 12679376 | |||||||
chr17:12679378 | C | T | 1 | a0001c0001t0161g0190 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.55+13135C>T | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | chr17 | 12679378 | |||||||
chr17:12679470 | T | G | 96 | a0001c0001t0001g0207 a0001c0001t0001g0261 a0001c0001t0001g0343 others(93): Show |
97 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(94): Show |
intron_variant | MODIFIER | c.55+13227T>G | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | chr17 | 12679470 | |||||||
chr17:12679555 | T | C | 55 | a0001c0001t0001g0028 a0001c0001t0002g0018 a0001c0001t0004g0278 others(52): Show |
56 | HG00280.hp2 HG00544.hp1 HG00544.hp2 others(53): Show |
intron_variant | MODIFIER | c.55+13312T>C | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | chr17 | 12679555 | |||||||
chr17:12679701 | A | T | 3 | a0001c0001t0139g0013 a0001c0001t0141g0015 a0001c0001t0171g0014 |
3 | HG02738.hp1 HG03490.hp2 HG03831.hp1 |
intron_variant | MODIFIER | c.55+13458A>T | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | chr17 | 12679701 | |||||||
chr17:12679974 | T | G | 1 | a0001c0003t0204g0038 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.55+13731T>G | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | chr17 | 12679974 | |||||||
chr17:12680187 | AC | A | 3 | a0001c0001t0011g0229 a0001c0001t0011g0230 a0001c0006t0016g0231 |
3 | HG02622.hp2 HG02965.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.55+13947delC | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr17 | 12680187 | ||||||
chr17:12680227 | T | C | 4 | a0001c0001t0001g0343 a0001c0001t0011g0229 a0001c0001t0011g0230 others(1): Show |
4 | HG02622.hp2 HG02965.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.55+13984T>C | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | chr17 | 12680227 | |||||||
chr17:12680290 | A | G | 1 | a0001c0001t0030g0301 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.55+14047A>G | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | chr17 | 12680290 | |||||||
chr17:12680337 | A | G | 3 | a0001c0001t0011g0229 a0001c0001t0011g0230 a0001c0006t0016g0231 |
3 | HG02622.hp2 HG02965.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.55+14094A>G | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | chr17 | 12680337 | |||||||
chr17:12680354 | C | T | 3 | a0001c0001t0091g0309 a0001c0001t0092g0311 a0001c0001t0106g0310 |
3 | HG02630.hp1 HG02647.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.55+14111C>T | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | chr17 | 12680354 | |||||||
chr17:12680355 | T | G | 43 | a0001c0001t0001g0261 a0001c0001t0009g0326 a0001c0001t0009g0328 others(40): Show |
44 | HG00597.hp2 HG00642.hp1 HG00735.hp1 others(41): Show |
intron_variant | MODIFIER | c.55+14112T>G | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | chr17 | 12680355 | |||||||
chr17:12680385 | C | T | 1 | a0001c0001t0034g0146 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.55+14142C>T | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | chr17 | 12680385 | |||||||
chr17:12680388 | G | T | 1 | a0001c0001t0146g0019 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.55+14145G>T | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | chr17 | 12680388 | |||||||
chr17:12680554 | A | G | 58 | a0001c0001t0001g0028 a0001c0001t0002g0018 a0001c0001t0004g0278 others(55): Show |
59 | HG00280.hp2 HG00544.hp1 HG00544.hp2 others(56): Show |
intron_variant | MODIFIER | c.55+14311A>G | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | chr17 | 12680554 | |||||||
chr17:12680557 | T | A | 3 | a0001c0001t0011g0229 a0001c0001t0011g0230 a0001c0006t0016g0231 |
3 | HG02622.hp2 HG02965.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.55+14314T>A | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | chr17 | 12680557 | |||||||
chr17:12680581 | A | G | 49 | a0001c0001t0001g0028 a0001c0001t0002g0018 a0001c0001t0004g0278 others(46): Show |
50 | HG00280.hp2 HG00544.hp1 HG00544.hp2 others(47): Show |
intron_variant | MODIFIER | c.55+14338A>G | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | chr17 | 12680581 | |||||||
chr17:12680588 | T | A | 2 | a0001c0001t0040g0272 a0001c0003t0182g0271 |
2 | HG02615.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.55+14345T>A | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | chr17 | 12680588 | |||||||
chr17:12680707 | C | T | 2 | a0001c0001t0014g0338 a0001c0001t0033g0333 |
2 | HG01243.hp1 HG02145.hp1 |
intron_variant | MODIFIER | c.55+14464C>T | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | chr17 | 12680707 | |||||||
chr17:12680755 | G | A | 1 | a0001c0001t0041g0055 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.55+14512G>A | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | chr17 | 12680755 | |||||||
chr17:12680888 | G | A | 4 | a0001c0001t0003g0150 a0001c0001t0138g0133 a0001c0001t0179g0135 others(1): Show |
4 | HG02074.hp1 NA18944.hp2 NA18948.hp2 others(1): Show |
intron_variant | MODIFIER | c.55+14645G>A | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | chr17 | 12680888 | |||||||
chr17:12680924 | C | G | 1 | a0001c0007t0001g0220 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.55+14681C>G | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | chr17 | 12680924 | |||||||
chr17:12680937 | C | G | 2 | a0001c0001t0117g0340 a0001c0001t0125g0341 |
2 | HG03130.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.55+14694C>G | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | chr17 | 12680937 | |||||||
chr17:12680961 | G | A | 3 | a0001c0001t0011g0229 a0001c0001t0011g0230 a0001c0006t0016g0231 |
3 | HG02622.hp2 HG02965.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.55+14718G>A | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | chr17 | 12680961 | |||||||
chr17:12680983 | C | G | 3 | a0001c0001t0108g0342 a0001c0001t0117g0340 a0001c0001t0125g0341 |
3 | HG02886.hp2 HG03130.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.55+14740C>G | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | chr17 | 12680983 | |||||||
chr17:12681010 | T | C | 3 | a0001c0001t0108g0342 a0001c0001t0117g0340 a0001c0001t0125g0341 |
3 | HG02886.hp2 HG03130.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.55+14767T>C | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | chr17 | 12681010 | |||||||
chr17:12681068 | T | A | 56 | a0001c0001t0001g0028 a0001c0001t0002g0018 a0001c0001t0004g0278 others(53): Show |
57 | HG00280.hp2 HG00544.hp1 HG00544.hp2 others(54): Show |
intron_variant | MODIFIER | c.55+14825T>A | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | chr17 | 12681068 | |||||||
chr17:12681271 | G | A | 3 | a0001c0001t0013g0273 a0001c0001t0127g0275 a0020c0014t0101g0274 |
3 | HG02109.hp1 HG02258.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.55+15028G>A | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | chr17 | 12681271 | |||||||
chr17:12681338 | A | G | 1 | a0004c0009t0197g0004 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.55+15095A>G | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | chr17 | 12681338 | |||||||
chr17:12681377 | G | C | 25 | a0001c0001t0001g0207 a0001c0001t0002g0208 a0001c0001t0003g0201 others(22): Show |
25 | HG00323.hp1 HG00323.hp2 HG00639.hp2 others(22): Show |
intron_variant | MODIFIER | c.55+15134G>C | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | chr17 | 12681377 | |||||||
chr17:12681534 | T | C | 2 | a0001c0002t0009g0321 a0001c0002t0062g0322 |
2 | HG00738.hp2 HG01358.hp2 |
intron_variant | MODIFIER | c.55+15291T>C | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | chr17 | 12681534 | |||||||
chr17:12681835 | G | A | 25 | a0001c0001t0001g0207 a0001c0001t0002g0208 a0001c0001t0003g0201 others(22): Show |
25 | HG00323.hp1 HG00323.hp2 HG00639.hp2 others(22): Show |
intron_variant | MODIFIER | c.55+15592G>A | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | chr17 | 12681835 | |||||||
chr17:12681991 | C | T | 1 | a0001c0001t0103g0339 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.55+15748C>T | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | chr17 | 12681991 | |||||||
chr17:12682075 | C | T | 1 | a0001c0003t0049g0134 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.55+15832C>T | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | chr17 | 12682075 | |||||||
chr17:12682109 | A | G | 1 | a0001c0001t0009g0329 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.55+15866A>G | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | chr17 | 12682109 | |||||||
chr17:12682135 | C | T | 1 | a0001c0001t0088g0103 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.55+15892C>T | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | chr17 | 12682135 | |||||||
chr17:12682141 | C | T | 1 | a0001c0001t0005g0199 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.55+15898C>T | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | chr17 | 12682141 | |||||||
chr17:12682142 | G | A | 62 | a0001c0001t0001g0261 a0001c0001t0002g0241 a0001c0001t0002g0242 others(59): Show |
63 | HG00423.hp1 HG00597.hp2 HG00642.hp1 others(60): Show |
intron_variant | MODIFIER | c.55+15899G>A | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | chr17 | 12682142 | |||||||
chr17:12682216 | C | T | 25 | a0001c0001t0001g0207 a0001c0001t0002g0208 a0001c0001t0003g0201 others(22): Show |
25 | HG00323.hp1 HG00323.hp2 HG00639.hp2 others(22): Show |
intron_variant | MODIFIER | c.55+15973C>T | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | chr17 | 12682216 | |||||||
chr17:12682251 | A | G | 61 | a0001c0001t0001g0028 a0001c0001t0002g0018 a0001c0001t0004g0278 others(58): Show |
62 | HG00280.hp2 HG00544.hp1 HG00544.hp2 others(59): Show |
intron_variant | MODIFIER | c.55+16008A>G | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | chr17 | 12682251 | |||||||
chr17:12682328 | A | G | 1 | a0001c0003t0109g0306 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.55+16085A>G | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | chr17 | 12682328 | |||||||
chr17:12682533 | G | A | 1 | a0001c0001t0135g0056 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.55+16290G>A | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | chr17 | 12682533 | |||||||
chr17:12682549 | A | G | 61 | a0001c0001t0001g0028 a0001c0001t0002g0018 a0001c0001t0004g0278 others(58): Show |
62 | HG00280.hp2 HG00544.hp1 HG00544.hp2 others(59): Show |
intron_variant | MODIFIER | c.55+16306A>G | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | chr17 | 12682549 | |||||||
chr17:12682673 | A | G | 59 | a0001c0001t0001g0028 a0001c0001t0002g0018 a0001c0001t0004g0278 others(56): Show |
60 | HG00280.hp2 HG00544.hp1 HG00544.hp2 others(57): Show |
intron_variant | MODIFIER | c.55+16430A>G | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | chr17 | 12682673 | |||||||
chr17:12682969 | CTT | C | 25 | a0001c0001t0001g0207 a0001c0001t0002g0208 a0001c0001t0003g0201 others(22): Show |
25 | HG00323.hp1 HG00323.hp2 HG00639.hp2 others(22): Show |
intron_variant | MODIFIER | c.55+16727_55+16728d others(4): Show |
MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | chr17 | 12682969 | |||||||
chr17:12682972 | A | T | 59 | a0001c0001t0001g0028 a0001c0001t0002g0018 a0001c0001t0004g0278 others(56): Show |
60 | HG00280.hp2 HG00544.hp1 HG00544.hp2 others(57): Show |
intron_variant | MODIFIER | c.55+16729A>T | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | chr17 | 12682972 | |||||||
chr17:12683015 | C | A | 156 | a0001c0001t0001g0028 a0001c0001t0001g0207 a0001c0001t0001g0261 others(153): Show |
158 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(155): Show |
intron_variant | MODIFIER | c.55+16772C>A | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | chr17 | 12683015 | |||||||
chr17:12683279 | A | G | 25 | a0001c0001t0001g0343 a0001c0001t0002g0241 a0001c0001t0002g0242 others(22): Show |
25 | HG00423.hp1 HG00673.hp1 HG00741.hp1 others(22): Show |
intron_variant | MODIFIER | c.55+17036A>G | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | chr17 | 12683279 | |||||||
chr17:12683481 | G | C | 156 | a0001c0001t0001g0028 a0001c0001t0001g0207 a0001c0001t0001g0261 others(153): Show |
158 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(155): Show |
intron_variant | MODIFIER | c.55+17238G>C | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | chr17 | 12683481 | |||||||
chr17:12683508 | C | G | 1 | a0001c0003t0205g0332 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.55+17265C>G | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | chr17 | 12683508 | |||||||
chr17:12683519 | G | A | 1 | a0001c0001t0001g0161 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.55+17276G>A | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | chr17 | 12683519 | |||||||
chr17:12683605 | T | C | 5 | a0001c0001t0067g0315 a0001c0001t0091g0309 a0001c0001t0092g0311 others(2): Show |
5 | HG01891.hp1 HG02622.hp1 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.55+17362T>C | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | chr17 | 12683605 | |||||||
chr17:12683964 | A | G | 1 | a0001c0001t0122g0102 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.55+17721A>G | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | chr17 | 12683964 | |||||||
chr17:12684001 | C | T | 3 | a0001c0001t0011g0229 a0001c0001t0011g0230 a0001c0006t0016g0231 |
3 | HG02622.hp2 HG02965.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.55+17758C>T | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | chr17 | 12684001 | |||||||
chr17:12684155 | C | T | 1 | a0019c0024t0012g0117 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.55+17912C>T | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | chr17 | 12684155 | |||||||
chr17:12684275 | G | T | 103 | a0001c0001t0001g0028 a0001c0001t0001g0261 a0001c0001t0002g0018 others(100): Show |
105 | HG00280.hp2 HG00423.hp1 HG00544.hp1 others(102): Show |
intron_variant | MODIFIER | c.55+18032G>T | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | chr17 | 12684275 | |||||||
chr17:12684372 | A | G | 9 | a0001c0001t0001g0261 a0001c0001t0014g0338 a0001c0001t0033g0333 others(6): Show |
9 | HG01243.hp1 HG01256.hp2 HG02055.hp2 others(6): Show |
intron_variant | MODIFIER | c.55+18129A>G | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | chr17 | 12684372 | |||||||
chr17:12684497 | G | A | 82 | a0001c0001t0001g0207 a0001c0001t0001g0261 a0001c0001t0001g0343 others(79): Show |
82 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(79): Show |
intron_variant | MODIFIER | c.55+18254G>A | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | chr17 | 12684497 | |||||||
chr17:12684569 | G | A | 1 | a0001c0001t0141g0015 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.55+18326G>A | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | chr17 | 12684569 | |||||||
chr17:12684569 | G | T | 3 | a0001c0001t0108g0342 a0001c0001t0117g0340 a0001c0001t0125g0341 |
3 | HG02886.hp2 HG03130.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.55+18326G>T | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | chr17 | 12684569 | |||||||
chr17:12684587 | C | T | 1 | a0001c0001t0130g0101 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.55+18344C>T | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | chr17 | 12684587 | |||||||
chr17:12684738 | C | T | 1 | a0021c0019t0009g0331 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.55+18495C>T | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | chr17 | 12684738 | |||||||
chr17:12684845 | C | CA | 11 | a0001c0001t0001g0051 a0001c0001t0001g0058 a0001c0001t0001g0136 others(8): Show |
11 | HG01978.hp2 HG02145.hp2 HG02630.hp1 others(8): Show |
intron_variant | MODIFIER | c.55+18619dupA | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr17 | 12684845 | ||||||
chr17:12684845 | CA | C | 7 | a0001c0001t0033g0333 a0001c0001t0037g0175 a0001c0001t0108g0342 others(4): Show |
7 | HG02145.hp1 HG02886.hp2 HG03130.hp1 others(4): Show |
intron_variant | MODIFIER | c.55+18619delA | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr17 | 12684845 | ||||||
chr17:12684895 | C | T | 2 | a0001c0001t0097g0307 a0001c0001t0120g0308 |
2 | HG02572.hp1 HG02615.hp2 |
intron_variant | MODIFIER | c.55+18652C>T | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | chr17 | 12684895 | |||||||
chr17:12684989 | G | C | 28 | a0001c0001t0001g0343 a0001c0001t0002g0241 a0001c0001t0002g0242 others(25): Show |
28 | HG00423.hp1 HG00673.hp1 HG00741.hp1 others(25): Show |
intron_variant | MODIFIER | c.55+18746G>C | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | chr17 | 12684989 | |||||||
chr17:12685061 | C | T | 1 | a0001c0001t0067g0315 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.55+18818C>T | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | chr17 | 12685061 | |||||||
chr17:12685066 | CAGGTGGA others(7): Show |
C | 3 | a0001c0001t0013g0273 a0001c0001t0127g0275 a0020c0014t0101g0274 |
3 | HG02109.hp1 HG02258.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.55+18828_55+18841d others(16): Show |
MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr17 | 12685066 | ||||||
chr17:12685199 | C | G | 1 | a0001c0002t0005g0169 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.55+18956C>G | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | chr17 | 12685199 | |||||||
chr17:12685284 | C | A | 1 | a0001c0001t0001g0343 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.55+19041C>A | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | chr17 | 12685284 | |||||||
chr17:12685331 | A | C | 37 | a0001c0001t0001g0261 a0001c0001t0002g0241 a0001c0001t0002g0242 others(34): Show |
38 | HG00423.hp1 HG00673.hp1 HG00741.hp1 others(35): Show |
intron_variant | MODIFIER | c.55+19088A>C | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | chr17 | 12685331 | |||||||
chr17:12685333 | A | G | 65 | a0001c0001t0001g0207 a0001c0001t0001g0343 a0001c0001t0002g0208 others(62): Show |
66 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(63): Show |
intron_variant | MODIFIER | c.55+19090A>G | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | chr17 | 12685333 | |||||||
chr17:12685343 | G | A | 1 | a0001c0001t0001g0343 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.55+19100G>A | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | chr17 | 12685343 | |||||||
chr17:12685352 | C | T | 4 | a0001c0001t0011g0224 a0001c0001t0018g0223 a0001c0001t0042g0225 others(1): Show |
4 | HG02486.hp2 HG02559.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.55+19109C>T | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | chr17 | 12685352 | |||||||
chr17:12685359 | A | G | 1 | a0001c0001t0005g0199 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.55+19116A>G | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | chr17 | 12685359 | |||||||
chr17:12685482 | T | C | 63 | a0001c0001t0001g0028 a0001c0001t0002g0018 a0001c0001t0004g0278 others(60): Show |
64 | HG00280.hp2 HG00544.hp1 HG00544.hp2 others(61): Show |
intron_variant | MODIFIER | c.55+19239T>C | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | chr17 | 12685482 | |||||||
chr17:12685498 | C | T | 1 | a0009c0020t0194g0226 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.55+19255C>T | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | chr17 | 12685498 | |||||||
chr17:12685508 | C | A | 5 | a0001c0001t0001g0261 a0001c0001t0001g0343 a0001c0001t0169g0263 others(2): Show |
5 | HG01256.hp2 HG02451.hp1 HG03490.hp1 others(2): Show |
intron_variant | MODIFIER | c.55+19265C>A | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | chr17 | 12685508 | |||||||
chr17:12685547 | G | A | 4 | a0001c0001t0001g0261 a0001c0001t0169g0263 a0001c0002t0133g0264 others(1): Show |
4 | HG01256.hp2 HG02451.hp1 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.55+19304G>A | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | chr17 | 12685547 | |||||||
chr17:12685604 | TA | T | 254 | a0001c0001t0001g0051 a0001c0001t0001g0058 a0001c0001t0001g0069 others(251): Show |
255 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(252): Show |
intron_variant | MODIFIER | c.55+19378delA | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr17 | 12685604 | ||||||
chr17:12685604 | TAA | T | 14 | a0001c0001t0001g0343 a0001c0001t0003g0116 a0001c0001t0014g0007 others(11): Show |
15 | HG01109.hp2 HG01192.hp1 HG01243.hp2 others(12): Show |
intron_variant | MODIFIER | c.55+19377_55+19378d others(4): Show |
MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr17 | 12685604 | ||||||
chr17:12685659 | A | T | 5 | a0001c0001t0001g0261 a0001c0001t0001g0343 a0001c0001t0169g0263 others(2): Show |
5 | HG01256.hp2 HG02451.hp1 HG03490.hp1 others(2): Show |
intron_variant | MODIFIER | c.55+19416A>T | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | chr17 | 12685659 | |||||||
chr17:12685814 | CT | C | 5 | a0001c0001t0001g0261 a0001c0001t0001g0343 a0001c0001t0169g0263 others(2): Show |
5 | HG01256.hp2 HG02451.hp1 HG03490.hp1 others(2): Show |
intron_variant | MODIFIER | c.56-19311delT | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr17 | 12685814 | ||||||
chr17:12685857 | A | G | 1 | a0001c0001t0001g0343 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.56-19271A>G | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | chr17 | 12685857 | |||||||
chr17:12686110 | C | T | 38 | a0001c0001t0001g0261 a0001c0001t0001g0343 a0001c0001t0002g0241 others(35): Show |
39 | HG00423.hp1 HG00673.hp1 HG00741.hp1 others(36): Show |
intron_variant | MODIFIER | c.56-19018C>T | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | chr17 | 12686110 | |||||||
chr17:12686114 | C | A | 5 | a0001c0001t0011g0224 a0001c0001t0018g0223 a0001c0001t0042g0225 others(2): Show |
5 | HG01891.hp1 HG02486.hp2 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.56-19014C>A | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | chr17 | 12686114 | |||||||
chr17:12686388 | A | G | 4 | a0001c0001t0001g0261 a0001c0001t0169g0263 a0001c0002t0133g0264 others(1): Show |
4 | HG01256.hp2 HG02451.hp1 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.56-18740A>G | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | chr17 | 12686388 | |||||||
chr17:12686527 | C | T | 9 | a0001c0001t0014g0007 a0001c0001t0051g0009 a0001c0001t0052g0008 others(6): Show |
10 | HG01109.hp2 HG01192.hp1 HG01243.hp2 others(7): Show |
intron_variant | MODIFIER | c.56-18601C>T | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | chr17 | 12686527 | |||||||
chr17:12686554 | A | T | 22 | a0001c0001t0001g0207 a0001c0001t0002g0208 a0001c0001t0003g0201 others(19): Show |
22 | HG00323.hp1 HG00323.hp2 HG00639.hp2 others(19): Show |
intron_variant | MODIFIER | c.56-18574A>T | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | chr17 | 12686554 | |||||||
chr17:12686652 | G | A | 2 | a0001c0003t0046g0121 a0001c0003t0046g0122 |
2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.56-18476G>A | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | chr17 | 12686652 | |||||||
chr17:12686744 | TAAGAA | T | 9 | a0001c0001t0014g0007 a0001c0001t0051g0009 a0001c0001t0052g0008 others(6): Show |
10 | HG01109.hp2 HG01192.hp1 HG01243.hp2 others(7): Show |
intron_variant | MODIFIER | c.56-18380_56-18376d others(7): Show |
MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr17 | 12686744 | ||||||
chr17:12686900 | C | T | 1 | a0001c0002t0005g0169 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.56-18228C>T | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | chr17 | 12686900 | |||||||
chr17:12686935 | T | C | 5 | a0001c0001t0001g0261 a0001c0001t0001g0343 a0001c0001t0169g0263 others(2): Show |
5 | HG01256.hp2 HG02451.hp1 HG03490.hp1 others(2): Show |
intron_variant | MODIFIER | c.56-18193T>C | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | chr17 | 12686935 | |||||||
chr17:12686963 | C | T | 1 | a0001c0001t0003g0212 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.56-18165C>T | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | chr17 | 12686963 | |||||||
chr17:12686964 | G | C | 5 | a0001c0001t0001g0261 a0001c0001t0001g0343 a0001c0001t0169g0263 others(2): Show |
5 | HG01256.hp2 HG02451.hp1 HG03490.hp1 others(2): Show |
intron_variant | MODIFIER | c.56-18164G>C | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | chr17 | 12686964 | |||||||
chr17:12687077 | A | C | 35 | a0001c0001t0002g0241 a0001c0001t0002g0242 a0001c0001t0002g0244 others(32): Show |
36 | HG00423.hp1 HG00673.hp1 HG00741.hp1 others(33): Show |
intron_variant | MODIFIER | c.56-18051A>C | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | chr17 | 12687077 | |||||||
chr17:12687190 | T | C | 25 | a0001c0001t0002g0241 a0001c0001t0002g0242 a0001c0001t0002g0244 others(22): Show |
25 | HG00423.hp1 HG00673.hp1 HG00741.hp1 others(22): Show |
intron_variant | MODIFIER | c.56-17938T>C | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | chr17 | 12687190 | |||||||
chr17:12687267 | C | T | 1 | a0001c0003t0105g0020 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.56-17861C>T | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | chr17 | 12687267 | |||||||
chr17:12687374 | G | C | 1 | a0001c0001t0030g0301 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.56-17754G>C | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | chr17 | 12687374 | |||||||
chr17:12687399 | G | T | 338 | a0001c0001t0001g0028 a0001c0001t0001g0051 a0001c0001t0001g0058 others(335): Show |
341 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(338): Show |
intron_variant | MODIFIER | c.56-17729G>T | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | chr17 | 12687399 | |||||||
chr17:12687404 | G | A | 34 | a0001c0001t0002g0241 a0001c0001t0002g0242 a0001c0001t0002g0244 others(31): Show |
35 | HG00423.hp1 HG00673.hp1 HG00741.hp1 others(32): Show |
intron_variant | MODIFIER | c.56-17724G>A | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | chr17 | 12687404 | |||||||
chr17:12687505 | T | A | 4 | a0001c0001t0013g0273 a0001c0001t0127g0275 a0017c0013t0011g0276 others(1): Show |
4 | HG02109.hp1 HG02258.hp1 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.56-17623T>A | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | chr17 | 12687505 | |||||||
chr17:12687618 | T | C | 6 | a0001c0001t0001g0261 a0001c0001t0001g0343 a0001c0001t0169g0263 others(3): Show |
6 | HG01256.hp2 HG02451.hp1 HG03490.hp1 others(3): Show |
intron_variant | MODIFIER | c.56-17510T>C | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | chr17 | 12687618 | |||||||
chr17:12687716 | C | G | 6 | a0001c0001t0001g0261 a0001c0001t0001g0343 a0001c0001t0169g0263 others(3): Show |
6 | HG01256.hp2 HG02451.hp1 HG03490.hp1 others(3): Show |
intron_variant | MODIFIER | c.56-17412C>G | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | chr17 | 12687716 | |||||||
chr17:12687717 | G | A | 1 | a0001c0001t0162g0057 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.56-17411G>A | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | chr17 | 12687717 | |||||||
chr17:12687868 | G | C | 1 | a0001c0004t0002g0233 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.56-17260G>C | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | chr17 | 12687868 | |||||||
chr17:12687904 | A | G | 112 | a0001c0001t0001g0028 a0001c0001t0001g0161 a0001c0001t0001g0176 others(109): Show |
113 | HG00280.hp2 HG00408.hp1 HG00544.hp2 others(110): Show |
intron_variant | MODIFIER | c.56-17224A>G | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | chr17 | 12687904 | |||||||
chr17:12688000 | C | G | 106 | a0001c0001t0001g0028 a0001c0001t0001g0343 a0001c0001t0002g0018 others(103): Show |
108 | HG00280.hp2 HG00423.hp1 HG00544.hp2 others(105): Show |
intron_variant | MODIFIER | c.56-17128C>G | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | chr17 | 12688000 | |||||||
chr17:12688126 | A | T | 13 | a0001c0001t0003g0201 a0001c0001t0004g0221 a0001c0001t0005g0091 others(10): Show |
13 | HG00639.hp2 HG01081.hp1 HG01515.hp1 others(10): Show |
intron_variant | MODIFIER | c.56-17002A>T | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | chr17 | 12688126 | |||||||
chr17:12688233 | A | T | 8 | a0001c0001t0001g0261 a0001c0001t0001g0343 a0001c0001t0011g0229 others(5): Show |
8 | HG01256.hp2 HG02055.hp2 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.56-16895A>T | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | chr17 | 12688233 | |||||||
chr17:12688443 | C | T | 3 | a0001c0001t0073g0337 a0001c0001t0103g0339 a0001c0001t0201g0334 |
3 | HG02622.hp1 HG02886.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.56-16685C>T | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | chr17 | 12688443 | |||||||
chr17:12688473 | T | C | 1 | a0001c0001t0001g0343 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.56-16655T>C | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | chr17 | 12688473 | |||||||
chr17:12688495 | T | C | 3 | a0001c0001t0001g0261 a0001c0001t0169g0263 a0009c0020t0194g0226 |
3 | HG01256.hp2 HG02055.hp2 HG03490.hp1 |
intron_variant | MODIFIER | c.56-16633T>C | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | chr17 | 12688495 | |||||||
chr17:12688496 | CCT | C | 3 | a0001c0001t0011g0229 a0001c0001t0011g0230 a0001c0006t0016g0231 |
3 | HG02622.hp2 HG02965.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.56-16631_56-16630d others(4): Show |
MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | chr17 | 12688496 | |||||||
chr17:12688528 | TCTTC | T | 4 | a0001c0001t0057g0317 a0001c0001t0061g0318 a0001c0001t0063g0319 others(1): Show |
4 | HG01934.hp1 HG02922.hp1 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.56-16586_56-16583d others(6): Show |
MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr17 | 12688528 | ||||||
chr17:12688528 | TCTTCCTT others(19): Show |
T | 98 | a0001c0001t0001g0028 a0001c0001t0002g0241 a0001c0001t0002g0242 others(95): Show |
99 | HG00423.hp1 HG00544.hp2 HG00609.hp2 others(96): Show |
intron_variant | MODIFIER | c.56-16578_56-16553d others(28): Show |
MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr17 | 12688528 | ||||||
chr17:12688532 | C | CCTTCCTT others(11): Show |
4 | a0001c0001t0011g0229 a0001c0001t0011g0230 a0001c0006t0016g0231 others(1): Show |
4 | HG02055.hp2 HG02622.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.56-16582_56-16565d others(20): Show |
MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr17 | 12688532 | ||||||
chr17:12688550 | T | TCTTCCTT others(15): Show |
1 | a0001c0001t0001g0343 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.56-16565_56-16564i others(24): Show |
MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr17 | 12688550 | ||||||
chr17:12688554 | C | CCTTCCTT others(7): Show |
2 | a0001c0001t0001g0261 a0001c0001t0169g0263 |
2 | HG01256.hp2 HG03490.hp1 |
intron_variant | MODIFIER | c.56-16565_56-16564i others(16): Show |
MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr17 | 12688554 | ||||||
chr17:12688578 | G | A | 1 | a0001c0001t0036g0036 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.56-16550G>A | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | chr17 | 12688578 | |||||||
chr17:12688678 | TCTTC | T | 13 | a0001c0001t0001g0207 a0001c0001t0002g0208 a0001c0001t0025g0203 others(10): Show |
13 | HG00323.hp1 HG00323.hp2 HG00733.hp1 others(10): Show |
intron_variant | MODIFIER | c.56-16435_56-16432d others(6): Show |
MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr17 | 12688678 | ||||||
chr17:12688910 | C | T | 34 | a0001c0001t0002g0241 a0001c0001t0002g0242 a0001c0001t0002g0244 others(31): Show |
34 | HG00423.hp1 HG00741.hp1 HG01106.hp1 others(31): Show |
intron_variant | MODIFIER | c.56-16218C>T | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | chr17 | 12688910 | |||||||
chr17:12689158 | G | T | 1 | a0001c0001t0047g0298 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.56-15970G>T | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | chr17 | 12689158 | |||||||
chr17:12689469 | T | C | 12 | a0001c0001t0014g0007 a0001c0001t0033g0333 a0001c0001t0051g0009 others(9): Show |
13 | HG01109.hp2 HG01192.hp1 HG01243.hp2 others(10): Show |
intron_variant | MODIFIER | c.56-15659T>C | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | chr17 | 12689469 | |||||||
chr17:12689540 | A | C | 108 | a0001c0001t0001g0028 a0001c0001t0001g0261 a0001c0001t0001g0343 others(105): Show |
109 | HG00423.hp1 HG00544.hp2 HG00609.hp2 others(106): Show |
intron_variant | MODIFIER | c.56-15588A>C | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | chr17 | 12689540 | |||||||
chr17:12689623 | G | A | 1 | a0001c0001t0172g0043 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.56-15505G>A | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | chr17 | 12689623 | |||||||
chr17:12689649 | T | C | 1 | a0001c0001t0018g0042 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.56-15479T>C | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | chr17 | 12689649 | |||||||
chr17:12689661 | G | A | 3 | a0001c0001t0011g0229 a0001c0001t0011g0230 a0001c0006t0016g0231 |
3 | HG02622.hp2 HG02965.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.56-15467G>A | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | chr17 | 12689661 | |||||||
chr17:12689902 | T | A | 1 | a0001c0001t0164g0189 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.56-15226T>A | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | chr17 | 12689902 | |||||||
chr17:12690200 | C | CAGCTACT others(151): Show |
1 | a0001c0001t0170g0099 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.56-14927_56-14926i others(160): Show |
MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr17 | 12690200 | ||||||
chr17:12690224 | C | A | 6 | a0001c0001t0097g0307 a0001c0001t0113g0282 a0001c0001t0119g0280 others(3): Show |
6 | HG02572.hp1 HG02615.hp2 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.56-14904C>A | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | chr17 | 12690224 | |||||||
chr17:12690273 | T | A | 1 | a0001c0001t0201g0334 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.56-14855T>A | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | chr17 | 12690273 | |||||||
chr17:12690327 | TTTC | T | 5 | a0001c0001t0009g0326 a0001c0001t0009g0329 a0001c0001t0065g0330 others(2): Show |
5 | HG00642.hp1 HG00735.hp1 HG01952.hp1 others(2): Show |
intron_variant | MODIFIER | c.56-14791_56-14789d others(5): Show |
MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr17 | 12690327 | ||||||
chr17:12690426 | A | C | 112 | a0001c0001t0001g0051 a0001c0001t0001g0176 a0001c0001t0001g0177 others(109): Show |
113 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(110): Show |
intron_variant | MODIFIER | c.56-14702A>C | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | chr17 | 12690426 | |||||||
chr17:12690453 | G | T | 48 | a0001c0001t0001g0261 a0001c0001t0001g0343 a0001c0001t0002g0241 others(45): Show |
48 | HG00423.hp1 HG00741.hp1 HG01106.hp1 others(45): Show |
intron_variant | MODIFIER | c.56-14675G>T | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | chr17 | 12690453 | |||||||
chr17:12690459 | G | A | 3 | a0001c0001t0091g0309 a0001c0001t0092g0311 a0001c0001t0106g0310 |
3 | HG02630.hp1 HG02647.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.56-14669G>A | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | chr17 | 12690459 | |||||||
chr17:12690460 | G | A | 4 | a0001c0001t0073g0337 a0001c0001t0103g0339 a0001c0001t0201g0334 others(1): Show |
4 | HG02622.hp1 HG02647.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.56-14668G>A | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | chr17 | 12690460 | |||||||
chr17:12690492 | T | C | 48 | a0001c0001t0001g0261 a0001c0001t0001g0343 a0001c0001t0002g0241 others(45): Show |
48 | HG00423.hp1 HG00741.hp1 HG01106.hp1 others(45): Show |
intron_variant | MODIFIER | c.56-14636T>C | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | chr17 | 12690492 | |||||||
chr17:12690632 | G | A | 39 | a0001c0001t0002g0241 a0001c0001t0002g0242 a0001c0001t0002g0244 others(36): Show |
39 | HG00423.hp1 HG00741.hp1 HG01106.hp1 others(36): Show |
intron_variant | MODIFIER | c.56-14496G>A | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | chr17 | 12690632 | |||||||
chr17:12690635 | T | G | 1 | a0001c0001t0001g0343 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.56-14493T>G | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | chr17 | 12690635 | |||||||
chr17:12690650 | C | T | 48 | a0001c0001t0001g0261 a0001c0001t0001g0343 a0001c0001t0002g0241 others(45): Show |
48 | HG00423.hp1 HG00741.hp1 HG01106.hp1 others(45): Show |
intron_variant | MODIFIER | c.56-14478C>T | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | chr17 | 12690650 | |||||||
chr17:12690715 | C | CTAAA | 48 | a0001c0001t0001g0261 a0001c0001t0001g0343 a0001c0001t0002g0241 others(45): Show |
48 | HG00423.hp1 HG00741.hp1 HG01106.hp1 others(45): Show |
intron_variant | MODIFIER | c.56-14411_56-14410i others(6): Show |
MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr17 | 12690715 | ||||||
chr17:12690737 | G | C | 48 | a0001c0001t0001g0261 a0001c0001t0001g0343 a0001c0001t0002g0241 others(45): Show |
48 | HG00423.hp1 HG00741.hp1 HG01106.hp1 others(45): Show |
intron_variant | MODIFIER | c.56-14391G>C | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | chr17 | 12690737 | |||||||
chr17:12690881 | A | T | 3 | a0001c0001t0091g0309 a0001c0001t0092g0311 a0001c0001t0106g0310 |
3 | HG02630.hp1 HG02647.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.56-14247A>T | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | chr17 | 12690881 | |||||||
chr17:12690907 | A | T | 175 | a0001c0001t0001g0028 a0001c0001t0001g0051 a0001c0001t0001g0176 others(172): Show |
177 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(174): Show |
intron_variant | MODIFIER | c.56-14221A>T | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | chr17 | 12690907 | |||||||
chr17:12691106 | C | T | 1 | a0001c0001t0131g0114 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.56-14022C>T | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | chr17 | 12691106 | |||||||
chr17:12691303 | G | A | 1 | a0001c0001t0033g0333 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.56-13825G>A | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | chr17 | 12691303 | |||||||
chr17:12691464 | G | A | 38 | a0001c0001t0002g0241 a0001c0001t0002g0242 a0001c0001t0002g0244 others(35): Show |
38 | HG00423.hp1 HG00741.hp1 HG01106.hp1 others(35): Show |
intron_variant | MODIFIER | c.56-13664G>A | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | chr17 | 12691464 | |||||||
chr17:12691492 | TC | T | 3 | a0001c0001t0003g0150 a0001c0001t0138g0133 a0001c0002t0187g0132 |
3 | HG02074.hp1 NA18944.hp2 NA18953.hp1 |
intron_variant | MODIFIER | c.56-13635delC | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | chr17 | 12691492 | |||||||
chr17:12691542 | A | C | 38 | a0001c0001t0002g0241 a0001c0001t0002g0242 a0001c0001t0002g0244 others(35): Show |
38 | HG00423.hp1 HG00741.hp1 HG01106.hp1 others(35): Show |
intron_variant | MODIFIER | c.56-13586A>C | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | chr17 | 12691542 | |||||||
chr17:12691638 | T | TA | 34 | a0001c0001t0002g0241 a0001c0001t0002g0242 a0001c0001t0002g0244 others(31): Show |
34 | HG00423.hp1 HG00741.hp1 HG01106.hp1 others(31): Show |
intron_variant | MODIFIER | c.56-13485dupA | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr17 | 12691638 | ||||||
chr17:12691758 | A | G | 29 | a0001c0001t0001g0051 a0001c0001t0001g0176 a0001c0001t0001g0177 others(26): Show |
29 | HG00597.hp2 HG00642.hp1 HG00735.hp1 others(26): Show |
intron_variant | MODIFIER | c.56-13370A>G | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | chr17 | 12691758 | |||||||
chr17:12691762 | A | G | 10 | a0001c0001t0001g0261 a0001c0001t0001g0343 a0001c0001t0011g0224 others(7): Show |
10 | HG01256.hp2 HG02055.hp2 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.56-13366A>G | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | chr17 | 12691762 | |||||||
chr17:12691895 | C | A | 1 | a0009c0020t0194g0226 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.56-13233C>A | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | chr17 | 12691895 | |||||||
chr17:12692008 | G | A | 38 | a0001c0001t0002g0241 a0001c0001t0002g0242 a0001c0001t0002g0244 others(35): Show |
38 | HG00423.hp1 HG00741.hp1 HG01106.hp1 others(35): Show |
intron_variant | MODIFIER | c.56-13120G>A | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | chr17 | 12692008 | |||||||
chr17:12692137 | T | C | 1 | a0001c0003t0049g0134 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.56-12991T>C | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | chr17 | 12692137 | |||||||
chr17:12692284 | T | C | 38 | a0001c0001t0002g0241 a0001c0001t0002g0242 a0001c0001t0002g0244 others(35): Show |
38 | HG00423.hp1 HG00741.hp1 HG01106.hp1 others(35): Show |
intron_variant | MODIFIER | c.56-12844T>C | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | chr17 | 12692284 | |||||||
chr17:12692500 | G | T | 4 | a0001c0001t0001g0343 a0001c0001t0011g0229 a0001c0001t0011g0230 others(1): Show |
4 | HG02622.hp2 HG02965.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.56-12628G>T | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | chr17 | 12692500 | |||||||
chr17:12692559 | G | A | 5 | a0001c0001t0001g0343 a0001c0001t0073g0337 a0001c0001t0103g0339 others(2): Show |
5 | HG02622.hp1 HG02647.hp1 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.56-12569G>A | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | chr17 | 12692559 | |||||||
chr17:12692614 | G | C | 4 | a0001c0001t0073g0337 a0001c0001t0103g0339 a0001c0001t0201g0334 others(1): Show |
4 | HG02622.hp1 HG02647.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.56-12514G>C | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | chr17 | 12692614 | |||||||
chr17:12692822 | A | G | 1 | a0001c0007t0001g0220 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.56-12306A>G | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | chr17 | 12692822 | |||||||
chr17:12692842 | A | C | 1 | a0001c0001t0005g0091 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.56-12286A>C | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | chr17 | 12692842 | |||||||
chr17:12692895 | A | G | 29 | a0001c0001t0001g0051 a0001c0001t0001g0176 a0001c0001t0001g0177 others(26): Show |
29 | HG00597.hp2 HG00642.hp1 HG00735.hp1 others(26): Show |
intron_variant | MODIFIER | c.56-12233A>G | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | chr17 | 12692895 | |||||||
chr17:12692988 | A | T | 111 | a0001c0001t0001g0051 a0001c0001t0001g0176 a0001c0001t0001g0177 others(108): Show |
112 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(109): Show |
intron_variant | MODIFIER | c.56-12140A>T | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | chr17 | 12692988 | |||||||
chr17:12693004 | A | C | 1 | a0011c0030t0114g0262 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.56-12124A>C | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | chr17 | 12693004 | |||||||
chr17:12693032 | A | G | 111 | a0001c0001t0001g0051 a0001c0001t0001g0176 a0001c0001t0001g0177 others(108): Show |
112 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(109): Show |
intron_variant | MODIFIER | c.56-12096A>G | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | chr17 | 12693032 | |||||||
chr17:12693088 | C | A | 13 | a0001c0001t0001g0207 a0001c0001t0002g0208 a0001c0001t0025g0203 others(10): Show |
13 | HG00323.hp1 HG00323.hp2 HG00733.hp1 others(10): Show |
intron_variant | MODIFIER | c.56-12040C>A | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | chr17 | 12693088 | |||||||
chr17:12693310 | C | CA | 3 | a0001c0001t0012g0235 a0001c0001t0038g0236 a0012c0029t0115g0335 |
3 | HG02647.hp1 NA18987.hp2 NA19062.hp2 |
intron_variant | MODIFIER | c.56-11815dupA | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr17 | 12693310 | ||||||
chr17:12693314 | C | A | 40 | a0001c0001t0002g0241 a0001c0001t0002g0242 a0001c0001t0002g0244 others(37): Show |
40 | HG00423.hp1 HG00741.hp1 HG01106.hp1 others(37): Show |
intron_variant | MODIFIER | c.56-11814C>A | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | chr17 | 12693314 | |||||||
chr17:12693347 | C | T | 1 | a0001c0001t0139g0013 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.56-11781C>T | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | chr17 | 12693347 | |||||||
chr17:12693368 | G | C | 31 | a0001c0001t0001g0028 a0001c0001t0022g0286 a0001c0001t0026g0289 others(28): Show |
31 | HG00544.hp2 HG00609.hp2 HG01891.hp1 others(28): Show |
intron_variant | MODIFIER | c.56-11760G>C | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | chr17 | 12693368 | |||||||
chr17:12693384 | C | T | 1 | a0001c0006t0093g0059 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.56-11744C>T | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | chr17 | 12693384 | |||||||
chr17:12693439 | G | A | 1 | a0003c0008t0072g0227 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.56-11689G>A | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | chr17 | 12693439 | |||||||
chr17:12693471 | A | G | 1 | a0001c0001t0153g0010 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.56-11657A>G | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | chr17 | 12693471 | |||||||
chr17:12693477 | G | A | 2 | a0001c0001t0001g0104 a0001c0001t0006g0060 |
2 | HG03834.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.56-11651G>A | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | chr17 | 12693477 | |||||||
chr17:12693524 | C | T | 1 | a0001c0002t0007g0048 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.56-11604C>T | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | chr17 | 12693524 | |||||||
chr17:12693525 | G | A | 1 | a0001c0001t0001g0343 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.56-11603G>A | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | chr17 | 12693525 | |||||||
chr17:12693592 | G | A | 9 | a0001c0001t0018g0033 a0001c0001t0018g0042 a0001c0001t0028g0002 others(6): Show |
10 | HG01884.hp1 HG02809.hp1 HG02809.hp2 others(7): Show |
intron_variant | MODIFIER | c.56-11536G>A | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | chr17 | 12693592 | |||||||
chr17:12693623 | TAGAATAA others(5): Show |
T | 3 | a0001c0001t0011g0224 a0001c0001t0018g0223 a0001c0001t0042g0225 |
3 | HG02559.hp2 HG03579.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.56-11503_56-11492d others(14): Show |
MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr17 | 12693623 | ||||||
chr17:12693623 | TAGAATAA others(10): Show |
T | 6 | a0001c0001t0001g0261 a0001c0001t0001g0343 a0001c0001t0011g0229 others(3): Show |
6 | HG02055.hp2 HG02622.hp2 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.56-11503_56-11487d others(19): Show |
MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr17 | 12693623 | ||||||
chr17:12693625 | G | GAATAA | 30 | a0001c0001t0001g0028 a0001c0001t0009g0326 a0001c0001t0009g0329 others(27): Show |
30 | HG00323.hp1 HG00544.hp2 HG00642.hp1 others(27): Show |
intron_variant | MODIFIER | c.56-11447_56-11443d others(7): Show |
MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr17 | 12693625 | ||||||
chr17:12693625 | G | GAATAAAA others(3): Show |
9 | a0001c0001t0001g0176 a0001c0001t0053g0325 a0001c0001t0054g0314 others(6): Show |
9 | HG00597.hp2 HG01081.hp2 HG02896.hp1 others(6): Show |
intron_variant | MODIFIER | c.56-11452_56-11443d others(12): Show |
MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr17 | 12693625 | ||||||
chr17:12693625 | G | GAATAAAA others(8): Show |
5 | a0001c0001t0001g0177 a0001c0001t0064g0316 a0001c0001t0125g0341 others(2): Show |
5 | HG00738.hp2 HG01346.hp2 HG01358.hp2 others(2): Show |
intron_variant | MODIFIER | c.56-11457_56-11443d others(17): Show |
MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr17 | 12693625 | ||||||
chr17:12693625 | G | GAATAAAA others(18): Show |
1 | a0001c0001t0001g0051 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.56-11467_56-11443d others(27): Show |
MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr17 | 12693625 | ||||||
chr17:12693625 | G | GAATAAAA others(33): Show |
1 | a0001c0001t0019g0115 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.56-11482_56-11443d others(42): Show |
MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr17 | 12693625 | ||||||
chr17:12693625 | GAATAA | G | 138 | a0001c0001t0001g0058 a0001c0001t0001g0069 a0001c0001t0001g0079 others(135): Show |
139 | HG00280.hp1 HG00280.hp2 HG00423.hp2 others(136): Show |
intron_variant | MODIFIER | c.56-11447_56-11443d others(7): Show |
MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr17 | 12693625 | ||||||
chr17:12693625 | GAATAAAA others(3): Show |
G | 27 | a0001c0001t0001g0124 a0001c0001t0001g0207 a0001c0001t0003g0201 others(24): Show |
27 | HG00323.hp2 HG00408.hp1 HG00609.hp1 others(24): Show |
intron_variant | MODIFIER | c.56-11452_56-11443d others(12): Show |
MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr17 | 12693625 | ||||||
chr17:12693625 | GAATAAAA others(8): Show |
G | 4 | a0001c0001t0091g0309 a0001c0001t0092g0311 a0001c0001t0106g0310 others(1): Show |
4 | HG02630.hp1 HG02647.hp2 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.56-11457_56-11443d others(17): Show |
MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr17 | 12693625 | ||||||
chr17:12693625 | GAATAAAA others(13): Show |
G | 38 | a0001c0001t0002g0241 a0001c0001t0002g0242 a0001c0001t0002g0244 others(35): Show |
38 | HG00423.hp1 HG00741.hp1 HG01106.hp1 others(35): Show |
intron_variant | MODIFIER | c.56-11462_56-11443d others(22): Show |
MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr17 | 12693625 | ||||||
chr17:12693677 | A | G | 10 | a0001c0001t0001g0261 a0001c0001t0001g0343 a0001c0001t0011g0224 others(7): Show |
10 | HG01256.hp2 HG02055.hp2 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.56-11451A>G | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | chr17 | 12693677 | |||||||
chr17:12693683 | T | C | 1 | a0001c0001t0001g0343 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.56-11445T>C | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | chr17 | 12693683 | |||||||
chr17:12693926 | G | C | 7 | a0001c0001t0008g0137 a0001c0001t0017g0139 a0001c0001t0021g0147 others(4): Show |
7 | NA18942.hp2 NA18947.hp1 NA18956.hp2 others(4): Show |
intron_variant | MODIFIER | c.56-11202G>C | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | chr17 | 12693926 | |||||||
chr17:12693958 | T | C | 1 | a0001c0001t0003g0116 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.56-11170T>C | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | chr17 | 12693958 | |||||||
chr17:12693963 | A | T | 1 | a0001c0001t0044g0012 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.56-11165A>T | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | chr17 | 12693963 | |||||||
chr17:12694155 | A | C | 1 | a0001c0001t0128g0168 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.56-10973A>C | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | chr17 | 12694155 | |||||||
chr17:12694309 | G | A | 38 | a0001c0001t0002g0241 a0001c0001t0002g0242 a0001c0001t0002g0244 others(35): Show |
38 | HG00423.hp1 HG00741.hp1 HG01106.hp1 others(35): Show |
intron_variant | MODIFIER | c.56-10819G>A | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | chr17 | 12694309 | |||||||
chr17:12694315 | T | C | 48 | a0001c0001t0001g0261 a0001c0001t0001g0343 a0001c0001t0002g0241 others(45): Show |
48 | HG00423.hp1 HG00741.hp1 HG01106.hp1 others(45): Show |
intron_variant | MODIFIER | c.56-10813T>C | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | chr17 | 12694315 | |||||||
chr17:12694372 | G | C | 48 | a0001c0001t0001g0261 a0001c0001t0001g0343 a0001c0001t0002g0241 others(45): Show |
48 | HG00423.hp1 HG00741.hp1 HG01106.hp1 others(45): Show |
intron_variant | MODIFIER | c.56-10756G>C | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | chr17 | 12694372 | |||||||
chr17:12694531 | G | C | 1 | a0009c0020t0194g0226 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.56-10597G>C | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | chr17 | 12694531 | |||||||
chr17:12694547 | G | C | 38 | a0001c0001t0002g0241 a0001c0001t0002g0242 a0001c0001t0002g0244 others(35): Show |
38 | HG00423.hp1 HG00741.hp1 HG01106.hp1 others(35): Show |
intron_variant | MODIFIER | c.56-10581G>C | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | chr17 | 12694547 | |||||||
chr17:12694749 | T | C | 38 | a0001c0001t0001g0207 a0001c0001t0002g0208 a0001c0001t0003g0201 others(35): Show |
39 | HG00323.hp1 HG00323.hp2 HG00639.hp2 others(36): Show |
intron_variant | MODIFIER | c.56-10379T>C | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | chr17 | 12694749 | |||||||
chr17:12694772 | G | A | 1 | a0001c0001t0001g0343 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.56-10356G>A | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | chr17 | 12694772 | |||||||
chr17:12694881 | C | CA | 48 | a0001c0001t0001g0051 a0001c0001t0001g0176 a0001c0001t0001g0177 others(45): Show |
48 | HG00597.hp2 HG00621.hp2 HG00639.hp2 others(45): Show |
intron_variant | MODIFIER | c.56-10225dupA | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr17 | 12694881 | ||||||
chr17:12694881 | C | CAA | 24 | a0001c0001t0001g0207 a0001c0001t0002g0208 a0001c0001t0014g0007 others(21): Show |
25 | HG00323.hp1 HG00323.hp2 HG00733.hp1 others(22): Show |
intron_variant | MODIFIER | c.56-10226_56-10225d others(4): Show |
MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr17 | 12694881 | ||||||
chr17:12694881 | CA | C | 6 | a0001c0001t0006g0098 a0001c0001t0036g0036 a0001c0001t0048g0158 others(3): Show |
6 | HG01261.hp2 HG02809.hp2 NA18946.hp2 others(3): Show |
intron_variant | MODIFIER | c.56-10225delA | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr17 | 12694881 | ||||||
chr17:12694881 | CAAAAAAA | C | 38 | a0001c0001t0002g0241 a0001c0001t0002g0242 a0001c0001t0002g0244 others(35): Show |
38 | HG00423.hp1 HG00741.hp1 HG01106.hp1 others(35): Show |
intron_variant | MODIFIER | c.56-10231_56-10225d others(9): Show |
MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr17 | 12694881 | ||||||
chr17:12694881 | CAAAAAAA others(1): Show |
C | 10 | a0001c0001t0001g0261 a0001c0001t0001g0343 a0001c0001t0011g0224 others(7): Show |
10 | HG01256.hp2 HG02055.hp2 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.56-10232_56-10225d others(10): Show |
MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr17 | 12694881 | ||||||
chr17:12695084 | C | G | 1 | a0001c0001t0014g0338 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.56-10044C>G | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | chr17 | 12695084 | |||||||
chr17:12695328 | A | G | 1 | a0002c0005t0199g0296 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.56-9800A>G | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | chr17 | 12695328 | |||||||
chr17:12695391 | A | G | 1 | a0001c0001t0018g0033 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.56-9737A>G | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | chr17 | 12695391 | |||||||
chr17:12695472 | G | C | 31 | a0001c0001t0001g0028 a0001c0001t0022g0286 a0001c0001t0026g0289 others(28): Show |
31 | HG00544.hp2 HG00609.hp2 HG01891.hp1 others(28): Show |
intron_variant | MODIFIER | c.56-9656G>C | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | chr17 | 12695472 | |||||||
chr17:12695685 | A | C | 71 | a0001c0001t0001g0051 a0001c0001t0001g0176 a0001c0001t0001g0177 others(68): Show |
71 | HG00423.hp1 HG00597.hp2 HG00642.hp1 others(68): Show |
intron_variant | MODIFIER | c.56-9443A>C | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | chr17 | 12695685 | |||||||
chr17:12695692 | T | G | 1 | a0003c0008t0111g0303 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.56-9436T>G | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | chr17 | 12695692 | |||||||
chr17:12695756 | A | G | 38 | a0001c0001t0001g0343 a0001c0001t0002g0241 a0001c0001t0002g0242 others(35): Show |
38 | HG00423.hp1 HG00741.hp1 HG01106.hp1 others(35): Show |
intron_variant | MODIFIER | c.56-9372A>G | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | chr17 | 12695756 | |||||||
chr17:12695829 | T | G | 34 | a0001c0001t0002g0241 a0001c0001t0002g0242 a0001c0001t0002g0244 others(31): Show |
34 | HG00423.hp1 HG00741.hp1 HG01106.hp1 others(31): Show |
intron_variant | MODIFIER | c.56-9299T>G | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | chr17 | 12695829 | |||||||
chr17:12695947 | A | G | 3 | a0001c0001t0011g0224 a0001c0001t0018g0223 a0001c0001t0042g0225 |
3 | HG02559.hp2 HG03579.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.56-9181A>G | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | chr17 | 12695947 | |||||||
chr17:12695970 | C | T | 1 | a0001c0001t0168g0260 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.56-9158C>T | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | chr17 | 12695970 | |||||||
chr17:12696008 | A | G | 1 | a0001c0003t0205g0332 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.56-9120A>G | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | chr17 | 12696008 | |||||||
chr17:12696048 | T | TTTG | 7 | a0001c0001t0001g0261 a0001c0001t0091g0309 a0001c0001t0092g0311 others(4): Show |
7 | HG00423.hp1 HG01256.hp2 HG02055.hp2 others(4): Show |
intron_variant | MODIFIER | c.56-9056_56-9054dup others(3): Show |
MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr17 | 12696048 | ||||||
chr17:12696048 | T | TTTGTTG | 3 | a0001c0001t0011g0224 a0001c0001t0018g0223 a0001c0001t0042g0225 |
3 | HG02559.hp2 HG03579.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.56-9059_56-9054dup others(6): Show |
MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr17 | 12696048 | ||||||
chr17:12696088 | C | T | 2 | a0001c0001t0167g0202 a0003c0008t0072g0227 |
2 | HG02717.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.56-9040C>T | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | chr17 | 12696088 | |||||||
chr17:12696128 | C | G | 13 | a0001c0001t0001g0207 a0001c0001t0002g0208 a0001c0001t0025g0203 others(10): Show |
13 | HG00323.hp1 HG00323.hp2 HG00733.hp1 others(10): Show |
intron_variant | MODIFIER | c.56-9000C>G | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | chr17 | 12696128 | |||||||
chr17:12696150 | ATTTT | A | 27 | a0001c0001t0001g0051 a0001c0001t0001g0176 a0001c0001t0001g0177 others(24): Show |
27 | HG00597.hp2 HG00642.hp1 HG00735.hp1 others(24): Show |
intron_variant | MODIFIER | c.56-8972_56-8969del others(4): Show |
MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr17 | 12696150 | ||||||
chr17:12696180 | A | G | 12 | a0001c0001t0014g0007 a0001c0001t0033g0333 a0001c0001t0051g0009 others(9): Show |
13 | HG01109.hp2 HG01192.hp1 HG01243.hp2 others(10): Show |
intron_variant | MODIFIER | c.56-8948A>G | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | chr17 | 12696180 | |||||||
chr17:12696188 | G | A | 13 | a0001c0001t0001g0207 a0001c0001t0002g0208 a0001c0001t0025g0203 others(10): Show |
13 | HG00323.hp1 HG00323.hp2 HG00733.hp1 others(10): Show |
intron_variant | MODIFIER | c.56-8940G>A | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | chr17 | 12696188 | |||||||
chr17:12696224 | C | T | 1 | a0003c0008t0071g0305 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.56-8904C>T | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | chr17 | 12696224 | |||||||
chr17:12696229 | C | T | 1 | a0001c0001t0163g0218 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.56-8899C>T | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | chr17 | 12696229 | |||||||
chr17:12696272 | C | T | 13 | a0001c0001t0001g0207 a0001c0001t0002g0208 a0001c0001t0025g0203 others(10): Show |
13 | HG00323.hp1 HG00323.hp2 HG00733.hp1 others(10): Show |
intron_variant | MODIFIER | c.56-8856C>T | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | chr17 | 12696272 | |||||||
chr17:12696321 | G | A | 6 | a0001c0002t0004g0142 a0001c0002t0004g0143 a0001c0002t0004g0144 others(3): Show |
6 | NA18944.hp1 NA18946.hp2 NA18979.hp2 others(3): Show |
intron_variant | MODIFIER | c.56-8807G>A | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | chr17 | 12696321 | |||||||
chr17:12696477 | AT | A | 27 | a0001c0001t0001g0051 a0001c0001t0001g0176 a0001c0001t0001g0177 others(24): Show |
27 | HG00597.hp2 HG00642.hp1 HG00735.hp1 others(24): Show |
intron_variant | MODIFIER | c.56-8647delT | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr17 | 12696477 | ||||||
chr17:12696711 | G | T | 64 | a0001c0001t0001g0058 a0001c0001t0001g0079 a0001c0001t0001g0086 others(61): Show |
64 | HG00280.hp2 HG00558.hp1 HG00597.hp1 others(61): Show |
intron_variant | MODIFIER | c.56-8417G>T | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | chr17 | 12696711 | |||||||
chr17:12696763 | T | C | 29 | a0001c0001t0001g0051 a0001c0001t0001g0176 a0001c0001t0001g0177 others(26): Show |
29 | HG00597.hp2 HG00642.hp1 HG00735.hp1 others(26): Show |
intron_variant | MODIFIER | c.56-8365T>C | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | chr17 | 12696763 | |||||||
chr17:12696778 | C | T | 1 | a0001c0002t0149g0162 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.56-8350C>T | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | chr17 | 12696778 | |||||||
chr17:12696908 | G | A | 1 | a0001c0001t0033g0333 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.56-8220G>A | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | chr17 | 12696908 | |||||||
chr17:12696957 | G | A | 1 | a0001c0001t0001g0343 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.56-8171G>A | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | chr17 | 12696957 | |||||||
chr17:12696984 | A | G | 111 | a0001c0001t0001g0051 a0001c0001t0001g0176 a0001c0001t0001g0177 others(108): Show |
112 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(109): Show |
intron_variant | MODIFIER | c.56-8144A>G | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | chr17 | 12696984 | |||||||
chr17:12697009 | G | T | 60 | a0001c0001t0001g0028 a0001c0001t0013g0259 a0001c0001t0013g0273 others(57): Show |
61 | HG00544.hp2 HG00609.hp2 HG01243.hp1 others(58): Show |
intron_variant | MODIFIER | c.56-8119G>T | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | chr17 | 12697009 | |||||||
chr17:12697064 | T | C | 4 | a0001c0001t0053g0325 a0001c0001t0058g0312 a0001c0001t0059g0323 others(1): Show |
4 | HG00597.hp2 NA18946.hp1 NA18951.hp1 others(1): Show |
intron_variant | MODIFIER | c.56-8064T>C | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | chr17 | 12697064 | |||||||
chr17:12697251 | CA | C | 3 | a0001c0001t0011g0229 a0001c0001t0011g0230 a0001c0006t0016g0231 |
3 | HG02622.hp2 HG02965.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.56-7875delA | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr17 | 12697251 | ||||||
chr17:12697333 | G | T | 9 | a0001c0001t0003g0201 a0001c0001t0004g0221 a0001c0001t0005g0091 others(6): Show |
9 | HG00639.hp2 HG01081.hp1 HG02300.hp1 others(6): Show |
intron_variant | MODIFIER | c.56-7795G>T | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | chr17 | 12697333 | |||||||
chr17:12697335 | G | GTA | 15 | a0001c0001t0006g0098 a0001c0001t0007g0195 a0001c0001t0008g0180 others(12): Show |
15 | HG00408.hp1 HG00621.hp2 HG01109.hp1 others(12): Show |
intron_variant | MODIFIER | c.56-7769_56-7768dup others(2): Show |
MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr17 | 12697335 | ||||||
chr17:12697335 | G | GTATA | 14 | a0001c0001t0001g0161 a0001c0001t0004g0164 a0001c0001t0006g0174 others(11): Show |
14 | HG00735.hp2 HG01952.hp1 HG02129.hp1 others(11): Show |
intron_variant | MODIFIER | c.56-7771_56-7768dup others(4): Show |
MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr17 | 12697335 | ||||||
chr17:12697335 | G | GTATATAT others(5): Show |
1 | a0001c0001t0070g0246 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.56-7779_56-7768dup others(12): Show |
MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr17 | 12697335 | ||||||
chr17:12697335 | GTA | G | 9 | a0001c0001t0001g0058 a0001c0001t0001g0155 a0001c0001t0002g0090 others(6): Show |
9 | HG01175.hp2 HG02809.hp1 HG03710.hp2 others(6): Show |
intron_variant | MODIFIER | c.56-7769_56-7768del others(2): Show |
MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr17 | 12697335 | ||||||
chr17:12697348 | TATATATA others(4): Show |
T | 1 | a0009c0020t0194g0226 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.56-7779_56-7769del others(11): Show |
MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | chr17 | 12697348 | |||||||
chr17:12697353 | ATATATAT others(4): Show |
A | 3 | a0001c0001t0011g0224 a0001c0001t0018g0223 a0001c0001t0042g0225 |
3 | HG02559.hp2 HG03579.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.56-7773_56-7763del others(11): Show |
MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr17 | 12697353 | ||||||
chr17:12697353 | ATATATAT others(5): Show |
A | 2 | a0001c0001t0073g0337 a0001c0001t0201g0334 |
2 | HG02886.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.56-7773_56-7762del others(12): Show |
MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr17 | 12697353 | ||||||
chr17:12697353 | ATATATAT others(6): Show |
A | 1 | a0001c0001t0023g0253 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.56-7773_56-7761del others(13): Show |
MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr17 | 12697353 | ||||||
chr17:12697355 | ATATATTT others(5): Show |
A | 2 | a0001c0001t0103g0339 a0012c0029t0115g0335 |
2 | HG02622.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.56-7771_56-7760del others(12): Show |
MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr17 | 12697355 | ||||||
chr17:12697357 | ATATT | A | 20 | a0001c0001t0036g0257 a0001c0001t0040g0256 a0001c0001t0040g0272 others(17): Show |
20 | HG01255.hp1 HG01884.hp2 HG02055.hp1 others(17): Show |
intron_variant | MODIFIER | c.56-7769_56-7766del others(4): Show |
MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr17 | 12697357 | ||||||
chr17:12697357 | ATATTT | A | 8 | a0001c0001t0003g0201 a0001c0001t0013g0259 a0001c0001t0134g0215 others(5): Show |
9 | HG00639.hp2 HG01081.hp1 HG01891.hp2 others(6): Show |
intron_variant | MODIFIER | c.56-7769_56-7765del others(5): Show |
MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr17 | 12697357 | ||||||
chr17:12697357 | ATATTTT | A | 6 | a0001c0001t0004g0221 a0001c0001t0005g0091 a0001c0001t0163g0218 others(3): Show |
6 | HG03831.hp2 NA18612.hp1 NA18960.hp2 others(3): Show |
intron_variant | MODIFIER | c.56-7769_56-7764del others(6): Show |
MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr17 | 12697357 | ||||||
chr17:12697359 | A | AT | 9 | a0001c0001t0002g0208 a0001c0001t0025g0203 a0001c0001t0095g0213 others(6): Show |
9 | HG00280.hp1 HG00738.hp1 HG01361.hp1 others(6): Show |
intron_variant | MODIFIER | c.56-7748dupT | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr17 | 12697359 | ||||||
chr17:12697359 | A | ATATATAT others(23): Show |
1 | a0001c0006t0016g0231 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.56-7768_56-7767ins others(30): Show |
MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr17 | 12697359 | ||||||
chr17:12697359 | A | ATATATAT others(19): Show |
2 | a0001c0001t0011g0229 a0001c0001t0011g0230 |
2 | HG02622.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.56-7768_56-7767ins others(26): Show |
MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr17 | 12697359 | ||||||
chr17:12697359 | AT | A | 16 | a0001c0001t0001g0079 a0001c0001t0002g0157 a0001c0001t0006g0068 others(13): Show |
16 | HG00558.hp1 HG00639.hp1 HG01255.hp2 others(13): Show |
intron_variant | MODIFIER | c.56-7748delT | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr17 | 12697359 | ||||||
chr17:12697359 | ATT | A | 83 | a0001c0001t0001g0086 a0001c0001t0001g0089 a0001c0001t0001g0124 others(80): Show |
85 | HG00280.hp2 HG00597.hp1 HG00609.hp1 others(82): Show |
intron_variant | MODIFIER | c.56-7749_56-7748del others(2): Show |
MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr17 | 12697359 | ||||||
chr17:12697359 | ATTT | A | 12 | a0001c0001t0004g0278 a0001c0001t0005g0199 a0001c0001t0006g0118 others(9): Show |
12 | HG02109.hp1 HG02630.hp1 HG02723.hp2 others(9): Show |
intron_variant | MODIFIER | c.56-7750_56-7748del others(3): Show |
MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr17 | 12697359 | ||||||
chr17:12697359 | ATTTT | A | 43 | a0001c0001t0001g0028 a0001c0001t0001g0051 a0001c0001t0001g0176 others(40): Show |
43 | HG00597.hp2 HG00609.hp2 HG00642.hp1 others(40): Show |
intron_variant | MODIFIER | c.56-7751_56-7748del others(4): Show |
MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr17 | 12697359 | ||||||
chr17:12697360 | T | TA | 8 | a0001c0001t0009g0328 a0001c0001t0010g0064 a0001c0001t0037g0063 others(5): Show |
8 | HG01346.hp1 HG01358.hp1 HG02602.hp2 others(5): Show |
intron_variant | MODIFIER | c.56-7768_56-7767ins others(1): Show |
MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | chr17 | 12697360 | |||||||
chr17:12697360 | T | TATA | 6 | a0001c0001t0001g0181 a0001c0001t0003g0188 a0001c0001t0010g0183 others(3): Show |
6 | HG00733.hp1 HG01496.hp1 HG02698.hp2 others(3): Show |
intron_variant | MODIFIER | c.56-7768_56-7767ins others(3): Show |
MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | chr17 | 12697360 | |||||||
chr17:12697360 | T | TATATATA others(2): Show |
6 | a0001c0001t0003g0093 a0001c0001t0006g0250 a0001c0001t0010g0094 others(3): Show |
6 | HG01261.hp2 HG01496.hp2 HG01952.hp2 others(3): Show |
intron_variant | MODIFIER | c.56-7768_56-7767ins others(9): Show |
MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | chr17 | 12697360 | |||||||
chr17:12697360 | T | TATATATA others(4): Show |
5 | a0001c0001t0005g0095 a0001c0001t0147g0237 a0001c0002t0004g0248 others(2): Show |
5 | HG00423.hp1 HG02273.hp2 HG03239.hp1 others(2): Show |
intron_variant | MODIFIER | c.56-7768_56-7767ins others(11): Show |
MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | chr17 | 12697360 | |||||||
chr17:12697360 | T | TATATATA others(6): Show |
1 | a0001c0001t0005g0232 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.56-7768_56-7767ins others(13): Show |
MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | chr17 | 12697360 | |||||||
chr17:12697360 | T | TATATATA others(8): Show |
7 | a0001c0001t0002g0244 a0001c0001t0012g0235 a0001c0001t0030g0245 others(4): Show |
7 | HG01106.hp1 NA18964.hp1 NA18987.hp2 others(4): Show |
intron_variant | MODIFIER | c.56-7768_56-7767ins others(15): Show |
MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | chr17 | 12697360 | |||||||
chr17:12697360 | T | TATATATA others(10): Show |
3 | a0001c0001t0148g0247 a0001c0002t0004g0240 a0001c0004t0001g0100 |
3 | HG01981.hp2 HG02300.hp2 HG02523.hp2 |
intron_variant | MODIFIER | c.56-7768_56-7767ins others(17): Show |
MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | chr17 | 12697360 | |||||||
chr17:12697360 | T | TATATATA others(12): Show |
3 | a0001c0001t0002g0241 a0001c0001t0039g0178 a0001c0002t0002g0239 |
3 | HG02273.hp1 NA18747.hp2 NA18942.hp1 |
intron_variant | MODIFIER | c.56-7768_56-7767ins others(19): Show |
MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | chr17 | 12697360 | |||||||
chr17:12697360 | T | TATATATA others(14): Show |
4 | a0001c0001t0002g0242 a0001c0001t0074g0105 a0001c0001t0076g0106 others(1): Show |
4 | HG01993.hp1 HG02293.hp1 NA19011.hp1 others(1): Show |
intron_variant | MODIFIER | c.56-7768_56-7767ins others(21): Show |
MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | chr17 | 12697360 | |||||||
chr17:12697360 | T | TATATATA others(16): Show |
1 | a0001c0004t0003g0254 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.56-7768_56-7767ins others(23): Show |
MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | chr17 | 12697360 | |||||||
chr17:12697360 | T | TATATATA others(20): Show |
2 | a0001c0001t0008g0052 a0001c0001t0086g0092 |
2 | NA18968.hp2 NA19010.hp2 |
intron_variant | MODIFIER | c.56-7768_56-7767ins others(27): Show |
MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | chr17 | 12697360 | |||||||
chr17:12697360 | T | TATATATA others(22): Show |
1 | a0001c0004t0034g0238 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.56-7768_56-7767ins others(29): Show |
MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | chr17 | 12697360 | |||||||
chr17:12697361 | T | A | 46 | a0001c0001t0001g0136 a0001c0001t0001g0161 a0001c0001t0004g0044 others(43): Show |
46 | HG00323.hp1 HG00408.hp1 HG00621.hp2 others(43): Show |
intron_variant | MODIFIER | c.56-7767T>A | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | chr17 | 12697361 | |||||||
chr17:12697362 | T | A | 47 | a0001c0001t0001g0079 a0001c0001t0001g0181 a0001c0001t0002g0241 others(44): Show |
47 | HG00423.hp1 HG00558.hp1 HG00741.hp1 others(44): Show |
intron_variant | MODIFIER | c.56-7766T>A | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | chr17 | 12697362 | |||||||
chr17:12697363 | T | A | 58 | a0001c0001t0001g0161 a0001c0001t0003g0116 a0001c0001t0004g0164 others(55): Show |
59 | HG00621.hp2 HG00735.hp2 HG00738.hp2 others(56): Show |
intron_variant | MODIFIER | c.56-7765T>A | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | chr17 | 12697363 | |||||||
chr17:12697364 | T | A | 41 | a0001c0001t0001g0181 a0001c0001t0002g0241 a0001c0001t0002g0242 others(38): Show |
41 | HG00423.hp1 HG00741.hp1 HG01106.hp1 others(38): Show |
intron_variant | MODIFIER | c.56-7764T>A | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | chr17 | 12697364 | |||||||
chr17:12697365 | T | A | 47 | a0001c0001t0001g0051 a0001c0001t0001g0176 a0001c0001t0001g0177 others(44): Show |
48 | HG00597.hp2 HG00642.hp1 HG00735.hp1 others(45): Show |
intron_variant | MODIFIER | c.56-7763T>A | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | chr17 | 12697365 | |||||||
chr17:12697366 | T | A | 21 | a0001c0001t0002g0241 a0001c0001t0002g0244 a0001c0001t0008g0052 others(18): Show |
21 | HG00741.hp1 HG01978.hp1 HG01981.hp2 others(18): Show |
intron_variant | MODIFIER | c.56-7762T>A | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | chr17 | 12697366 | |||||||
chr17:12697367 | T | A | 35 | a0001c0001t0001g0051 a0001c0001t0001g0176 a0001c0001t0001g0177 others(32): Show |
36 | HG00597.hp2 HG00642.hp1 HG00735.hp1 others(33): Show |
intron_variant | MODIFIER | c.56-7761T>A | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | chr17 | 12697367 | |||||||
chr17:12697368 | T | A | 4 | a0001c0001t0039g0178 a0001c0002t0002g0239 a0001c0002t0004g0240 others(1): Show |
4 | HG01978.hp1 HG02523.hp2 NA18747.hp2 others(1): Show |
intron_variant | MODIFIER | c.56-7760T>A | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | chr17 | 12697368 | |||||||
chr17:12697369 | T | A | 8 | a0001c0001t0001g0176 a0001c0001t0001g0177 a0001c0001t0009g0326 others(5): Show |
8 | HG00642.hp1 HG00735.hp1 HG01081.hp2 others(5): Show |
intron_variant | MODIFIER | c.56-7759T>A | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | chr17 | 12697369 | |||||||
chr17:12697371 | T | A | 2 | a0001c0001t0001g0176 a0001c0001t0001g0177 |
2 | HG01081.hp2 HG01346.hp2 |
intron_variant | MODIFIER | c.56-7757T>A | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | chr17 | 12697371 | |||||||
chr17:12697386 | G | A | 3 | a0001c0001t0011g0229 a0001c0001t0011g0230 a0001c0006t0016g0231 |
3 | HG02622.hp2 HG02965.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.56-7742G>A | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | chr17 | 12697386 | |||||||
chr17:12697389 | G | T | 60 | a0001c0001t0001g0028 a0001c0001t0013g0259 a0001c0001t0013g0273 others(57): Show |
61 | HG00544.hp2 HG00609.hp2 HG01243.hp1 others(58): Show |
intron_variant | MODIFIER | c.56-7739G>T | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | chr17 | 12697389 | |||||||
chr17:12697393 | C | T | 2 | a0001c0001t0002g0119 a0001c0001t0141g0015 |
2 | HG02257.hp1 HG02738.hp1 |
intron_variant | MODIFIER | c.56-7735C>T | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | chr17 | 12697393 | |||||||
chr17:12697398 | T | G | 4 | a0001c0001t0073g0337 a0001c0001t0103g0339 a0001c0001t0201g0334 others(1): Show |
4 | HG02622.hp1 HG02647.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.56-7730T>G | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | chr17 | 12697398 | |||||||
chr17:12697424 | G | A | 34 | a0001c0001t0002g0241 a0001c0001t0002g0242 a0001c0001t0002g0244 others(31): Show |
34 | HG00423.hp1 HG00741.hp1 HG01106.hp1 others(31): Show |
intron_variant | MODIFIER | c.56-7704G>A | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | chr17 | 12697424 | |||||||
chr17:12697566 | G | A | 1 | a0001c0001t0019g0115 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.56-7562G>A | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | chr17 | 12697566 | |||||||
chr17:12697653 | A | G | 7 | a0001c0001t0001g0261 a0001c0001t0011g0224 a0001c0001t0018g0223 others(4): Show |
7 | HG01256.hp2 HG02055.hp2 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.56-7475A>G | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | chr17 | 12697653 | |||||||
chr17:12697783 | G | T | 7 | a0001c0001t0001g0261 a0001c0001t0011g0224 a0001c0001t0018g0223 others(4): Show |
7 | HG01256.hp2 HG02055.hp2 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.56-7345G>T | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | chr17 | 12697783 | |||||||
chr17:12697918 | T | G | 7 | a0001c0001t0001g0261 a0001c0001t0011g0224 a0001c0001t0018g0223 others(4): Show |
7 | HG01256.hp2 HG02055.hp2 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.56-7210T>G | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | chr17 | 12697918 | |||||||
chr17:12697967 | G | A | 4 | a0001c0001t0073g0337 a0001c0001t0103g0339 a0001c0001t0201g0334 others(1): Show |
4 | HG02622.hp1 HG02647.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.56-7161G>A | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | chr17 | 12697967 | |||||||
chr17:12697997 | C | G | 51 | a0001c0001t0001g0207 a0001c0001t0001g0343 a0001c0001t0002g0208 others(48): Show |
51 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(48): Show |
intron_variant | MODIFIER | c.56-7131C>G | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | chr17 | 12697997 | |||||||
chr17:12698053 | T | C | 1 | a0001c0003t0202g0210 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.56-7075T>C | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | chr17 | 12698053 | |||||||
chr17:12698057 | G | T | 13 | a0001c0001t0001g0207 a0001c0001t0002g0208 a0001c0001t0025g0203 others(10): Show |
13 | HG00323.hp1 HG00323.hp2 HG00733.hp1 others(10): Show |
intron_variant | MODIFIER | c.56-7071G>T | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | chr17 | 12698057 | |||||||
chr17:12698431 | T | C | 34 | a0001c0001t0002g0241 a0001c0001t0002g0242 a0001c0001t0002g0244 others(31): Show |
34 | HG00423.hp1 HG00741.hp1 HG01106.hp1 others(31): Show |
intron_variant | MODIFIER | c.56-6697T>C | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | chr17 | 12698431 | |||||||
chr17:12698612 | A | G | 1 | a0001c0001t0164g0189 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.56-6516A>G | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | chr17 | 12698612 | |||||||
chr17:12698729 | C | CT | 23 | a0001c0001t0001g0181 a0001c0001t0004g0164 a0001c0001t0006g0098 others(20): Show |
23 | HG00735.hp2 HG00738.hp1 HG01346.hp1 others(20): Show |
intron_variant | MODIFIER | c.56-6370dupT | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr17 | 12698729 | ||||||
chr17:12698729 | C | CTT | 12 | a0001c0001t0001g0161 a0001c0001t0007g0163 a0001c0001t0029g0171 others(9): Show |
12 | HG00408.hp1 HG00621.hp2 HG01109.hp1 others(9): Show |
intron_variant | MODIFIER | c.56-6371_56-6370dup others(2): Show |
MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr17 | 12698729 | ||||||
chr17:12698729 | CT | C | 126 | a0001c0001t0001g0058 a0001c0001t0001g0069 a0001c0001t0001g0086 others(123): Show |
128 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(125): Show |
intron_variant | MODIFIER | c.56-6370delT | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr17 | 12698729 | ||||||
chr17:12698729 | CTT | C | 67 | a0001c0001t0001g0028 a0001c0001t0001g0051 a0001c0001t0001g0079 others(64): Show |
67 | HG00558.hp1 HG00597.hp2 HG00639.hp2 others(64): Show |
intron_variant | MODIFIER | c.56-6371_56-6370del others(2): Show |
MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr17 | 12698729 | ||||||
chr17:12698729 | CTTT | C | 31 | a0001c0001t0001g0261 a0001c0001t0004g0221 a0001c0001t0005g0091 others(28): Show |
31 | HG00544.hp2 HG00609.hp2 HG01256.hp2 others(28): Show |
intron_variant | MODIFIER | c.56-6372_56-6370del others(3): Show |
MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr17 | 12698729 | ||||||
chr17:12698729 | CTTTTTTT others(1): Show |
C | 34 | a0001c0001t0002g0241 a0001c0001t0002g0242 a0001c0001t0002g0244 others(31): Show |
34 | HG00423.hp1 HG00741.hp1 HG01106.hp1 others(31): Show |
intron_variant | MODIFIER | c.56-6377_56-6370del others(8): Show |
MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr17 | 12698729 | ||||||
chr17:12698802 | GC | G | 11 | a0001c0001t0013g0273 a0001c0001t0033g0333 a0001c0001t0055g0336 others(8): Show |
11 | HG01192.hp1 HG02109.hp1 HG02145.hp1 others(8): Show |
intron_variant | MODIFIER | c.56-6325delC | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | chr17 | 12698802 | |||||||
chr17:12698819 | T | G | 5 | a0001c0001t0006g0067 a0001c0001t0017g0153 a0001c0001t0048g0158 others(2): Show |
5 | NA18939.hp2 NA18978.hp1 NA19000.hp1 others(2): Show |
intron_variant | MODIFIER | c.56-6309T>G | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | chr17 | 12698819 | |||||||
chr17:12698834 | C | T | 1 | a0001c0003t0203g0281 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.56-6294C>T | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | chr17 | 12698834 | |||||||
chr17:12698899 | C | T | 1 | a0001c0001t0005g0127 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.56-6229C>T | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | chr17 | 12698899 | |||||||
chr17:12698963 | C | T | 4 | a0001c0001t0011g0224 a0001c0001t0011g0229 a0001c0001t0011g0230 others(1): Show |
4 | HG02559.hp2 HG02622.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.56-6165C>T | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | chr17 | 12698963 | |||||||
chr17:12698988 | C | T | 1 | a0001c0001t0146g0019 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.56-6140C>T | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | chr17 | 12698988 | |||||||
chr17:12698994 | G | A | 34 | a0001c0001t0002g0241 a0001c0001t0002g0242 a0001c0001t0002g0244 others(31): Show |
34 | HG00423.hp1 HG00741.hp1 HG01106.hp1 others(31): Show |
intron_variant | MODIFIER | c.56-6134G>A | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | chr17 | 12698994 | |||||||
chr17:12699021 | C | A | 133 | a0001c0001t0001g0028 a0001c0001t0001g0051 a0001c0001t0001g0155 others(130): Show |
136 | HG00544.hp2 HG00597.hp2 HG00609.hp2 others(133): Show |
intron_variant | MODIFIER | c.56-6107C>A | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | chr17 | 12699021 | |||||||
chr17:12699090 | C | A | 1 | a0001c0001t0073g0337 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.56-6038C>A | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | chr17 | 12699090 | |||||||
chr17:12699312 | A | G | 113 | a0001c0001t0001g0058 a0001c0001t0001g0069 a0001c0001t0001g0077 others(110): Show |
113 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(110): Show |
intron_variant | MODIFIER | c.56-5816A>G | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | chr17 | 12699312 | |||||||
chr17:12699424 | T | G | 2 | a0001c0001t0117g0340 a0001c0001t0125g0341 |
2 | HG03130.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.56-5704T>G | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | chr17 | 12699424 | |||||||
chr17:12699425 | T | C | 2 | a0001c0001t0117g0340 a0001c0001t0125g0341 |
2 | HG03130.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.56-5703T>C | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | chr17 | 12699425 | |||||||
chr17:12699469 | G | A | 1 | a0001c0001t0001g0343 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.56-5659G>A | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | chr17 | 12699469 | |||||||
chr17:12699544 | C | A | 3 | a0001c0001t0008g0052 a0001c0001t0074g0105 a0001c0001t0076g0106 |
3 | NA19010.hp2 NA19011.hp1 NA19091.hp2 |
intron_variant | MODIFIER | c.56-5584C>A | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | chr17 | 12699544 | |||||||
chr17:12699892 | C | A | 24 | a0001c0001t0001g0051 a0001c0001t0001g0176 a0001c0001t0001g0177 others(21): Show |
24 | HG00597.hp2 HG00642.hp1 HG00735.hp1 others(21): Show |
intron_variant | MODIFIER | c.56-5236C>A | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | chr17 | 12699892 | |||||||
chr17:12699892 | CT | C | 87 | a0001c0001t0001g0069 a0001c0001t0001g0104 a0001c0001t0001g0136 others(84): Show |
87 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(84): Show |
intron_variant | MODIFIER | c.56-5223delT | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr17 | 12699892 | ||||||
chr17:12699905 | T | A | 2 | a0001c0001t0010g0074 a0001c0001t0045g0065 |
2 | HG00423.hp2 HG01358.hp1 |
intron_variant | MODIFIER | c.56-5223T>A | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | chr17 | 12699905 | |||||||
chr17:12699906 | A | C | 2 | a0001c0001t0010g0074 a0001c0001t0045g0065 |
2 | HG00423.hp2 HG01358.hp1 |
intron_variant | MODIFIER | c.56-5222A>C | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | chr17 | 12699906 | |||||||
chr17:12699906 | A | T | 2 | a0001c0001t0100g0258 a0001c0001t0168g0260 |
2 | HG03130.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.56-5222A>T | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | chr17 | 12699906 | |||||||
chr17:12699907 | C | A | 2 | a0001c0001t0100g0258 a0001c0001t0168g0260 |
2 | HG03130.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.56-5221C>A | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | chr17 | 12699907 | |||||||
chr17:12699908 | C | T | 2 | a0001c0001t0010g0074 a0001c0001t0045g0065 |
2 | HG00423.hp2 HG01358.hp1 |
intron_variant | MODIFIER | c.56-5220C>T | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | chr17 | 12699908 | |||||||
chr17:12699908 | CT | C | 214 | a0001c0001t0001g0028 a0001c0001t0001g0051 a0001c0001t0001g0161 others(211): Show |
217 | HG00408.hp1 HG00423.hp1 HG00597.hp2 others(214): Show |
intron_variant | MODIFIER | c.56-5202delT | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr17 | 12699908 | ||||||
chr17:12699909 | T | C | 2 | a0001c0001t0100g0258 a0001c0001t0168g0260 |
2 | HG03130.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.56-5219T>C | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | chr17 | 12699909 | |||||||
chr17:12699978 | C | T | 1 | a0001c0001t0001g0207 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.56-5150C>T | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | chr17 | 12699978 | |||||||
chr17:12700053 | C | T | 3 | a0001c0001t0091g0309 a0001c0001t0092g0311 a0001c0001t0106g0310 |
3 | HG02630.hp1 HG02647.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.56-5075C>T | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | chr17 | 12700053 | |||||||
chr17:12700066 | G | C | 24 | a0001c0001t0001g0051 a0001c0001t0001g0176 a0001c0001t0001g0177 others(21): Show |
24 | HG00597.hp2 HG00642.hp1 HG00735.hp1 others(21): Show |
intron_variant | MODIFIER | c.56-5062G>C | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | chr17 | 12700066 | |||||||
chr17:12700099 | C | T | 54 | a0001c0001t0001g0161 a0001c0001t0001g0181 a0001c0001t0003g0188 others(51): Show |
54 | HG00408.hp1 HG00621.hp2 HG00639.hp2 others(51): Show |
intron_variant | MODIFIER | c.56-5029C>T | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | chr17 | 12700099 | |||||||
chr17:12700144 | C | T | 50 | a0001c0001t0001g0028 a0001c0001t0001g0051 a0001c0001t0001g0176 others(47): Show |
50 | HG00544.hp2 HG00597.hp2 HG00609.hp2 others(47): Show |
intron_variant | MODIFIER | c.56-4984C>T | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | chr17 | 12700144 | |||||||
chr17:12700145 | G | A | 1 | a0017c0013t0011g0276 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.56-4983G>A | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | chr17 | 12700145 | |||||||
chr17:12700196 | A | G | 1 | a0001c0001t0014g0338 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.56-4932A>G | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | chr17 | 12700196 | |||||||
chr17:12700199 | A | G | 2 | a0001c0001t0001g0079 a0001c0001t0098g0080 |
2 | HG00558.hp1 HG02132.hp1 |
intron_variant | MODIFIER | c.56-4929A>G | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | chr17 | 12700199 | |||||||
chr17:12700200 | C | T | 1 | a0001c0001t0140g0073 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.56-4928C>T | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | chr17 | 12700200 | |||||||
chr17:12700287 | C | T | 2 | a0001c0001t0006g0060 a0001c0001t0037g0063 |
2 | HG02602.hp2 HG03834.hp1 |
intron_variant | MODIFIER | c.56-4841C>T | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | chr17 | 12700287 | |||||||
chr17:12700332 | G | A | 1 | a0001c0003t0046g0121 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.56-4796G>A | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | chr17 | 12700332 | |||||||
chr17:12700360 | G | GAAAGAGT others(5): Show |
1 | a0001c0002t0062g0322 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.56-4765_56-4754dup others(12): Show |
MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr17 | 12700360 | ||||||
chr17:12700399 | A | AT | 41 | a0001c0001t0001g0086 a0001c0001t0001g0136 a0001c0001t0002g0119 others(38): Show |
41 | HG00408.hp2 HG00621.hp1 HG00639.hp1 others(38): Show |
intron_variant | MODIFIER | c.56-4700dupT | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr17 | 12700399 | ||||||
chr17:12700399 | A | ATT | 23 | a0001c0001t0005g0232 a0001c0001t0006g0250 a0001c0001t0008g0131 others(20): Show |
23 | HG00423.hp1 HG01106.hp1 HG01496.hp2 others(20): Show |
intron_variant | MODIFIER | c.56-4701_56-4700dup others(2): Show |
MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr17 | 12700399 | ||||||
chr17:12700399 | A | ATTT | 46 | a0001c0001t0001g0161 a0001c0001t0001g0181 a0001c0001t0003g0188 others(43): Show |
47 | HG00408.hp1 HG00621.hp2 HG00639.hp2 others(44): Show |
intron_variant | MODIFIER | c.56-4702_56-4700dup others(3): Show |
MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr17 | 12700399 | ||||||
chr17:12700399 | A | ATTTT | 14 | a0001c0001t0006g0174 a0001c0001t0007g0195 a0001c0001t0008g0173 others(11): Show |
14 | HG00735.hp2 HG01192.hp1 HG01891.hp2 others(11): Show |
intron_variant | MODIFIER | c.56-4703_56-4700dup others(4): Show |
MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr17 | 12700399 | ||||||
chr17:12700399 | A | ATTTTT | 9 | a0001c0001t0014g0007 a0001c0001t0051g0009 a0001c0001t0151g0182 others(6): Show |
10 | HG01109.hp2 HG01515.hp1 HG02818.hp1 others(7): Show |
intron_variant | MODIFIER | c.56-4704_56-4700dup others(5): Show |
MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr17 | 12700399 | ||||||
chr17:12700399 | A | ATTTTTT | 20 | a0001c0001t0022g0286 a0001c0001t0026g0289 a0001c0001t0047g0298 others(17): Show |
20 | HG00609.hp2 HG01243.hp2 HG01255.hp1 others(17): Show |
intron_variant | MODIFIER | c.56-4705_56-4700dup others(6): Show |
MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr17 | 12700399 | ||||||
chr17:12700399 | A | ATTTTTTT | 22 | a0001c0001t0001g0028 a0001c0001t0001g0261 a0001c0001t0027g0297 others(19): Show |
22 | HG00544.hp2 HG01891.hp1 HG02055.hp1 others(19): Show |
intron_variant | MODIFIER | c.56-4706_56-4700dup others(7): Show |
MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr17 | 12700399 | ||||||
chr17:12700399 | A | ATTTTTTT others(1): Show |
9 | a0001c0001t0001g0343 a0001c0001t0014g0338 a0001c0001t0028g0002 others(6): Show |
10 | HG01243.hp1 HG01256.hp2 HG01884.hp2 others(7): Show |
intron_variant | MODIFIER | c.56-4707_56-4700dup others(8): Show |
MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr17 | 12700399 | ||||||
chr17:12700399 | A | ATTTTTTT others(2): Show |
9 | a0001c0001t0001g0155 a0001c0001t0017g0153 a0001c0001t0039g0138 others(6): Show |
9 | HG02451.hp2 HG02723.hp2 HG02896.hp1 others(6): Show |
intron_variant | MODIFIER | c.56-4708_56-4700dup others(9): Show |
MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr17 | 12700399 | ||||||
chr17:12700399 | A | ATTTTTTT others(3): Show |
24 | a0001c0001t0001g0176 a0001c0001t0003g0150 a0001c0001t0009g0326 others(21): Show |
24 | HG00642.hp1 HG01081.hp2 HG01993.hp2 others(21): Show |
intron_variant | MODIFIER | c.56-4709_56-4700dup others(10): Show |
MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr17 | 12700399 | ||||||
chr17:12700399 | A | ATTTTTTT others(4): Show |
17 | a0001c0001t0001g0177 a0001c0001t0005g0141 a0001c0001t0006g0067 others(14): Show |
17 | HG00597.hp2 HG00735.hp1 HG01346.hp2 others(14): Show |
intron_variant | MODIFIER | c.56-4710_56-4700dup others(11): Show |
MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr17 | 12700399 | ||||||
chr17:12700399 | A | ATTTTTTT others(5): Show |
6 | a0001c0001t0001g0051 a0001c0001t0034g0146 a0001c0001t0060g0320 others(3): Show |
6 | HG02135.hp1 HG02257.hp2 HG02735.hp1 others(3): Show |
intron_variant | MODIFIER | c.56-4711_56-4700dup others(12): Show |
MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr17 | 12700399 | ||||||
chr17:12700399 | A | ATTTTTTT others(6): Show |
3 | a0001c0001t0018g0223 a0001c0001t0019g0115 a0001c0001t0153g0010 |
3 | HG01361.hp2 HG03579.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.56-4712_56-4700dup others(13): Show |
MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr17 | 12700399 | ||||||
chr17:12700399 | A | ATTTTTTT others(8): Show |
1 | a0001c0002t0062g0322 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.56-4714_56-4700dup others(15): Show |
MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr17 | 12700399 | ||||||
chr17:12700399 | ATTTTTTT others(5): Show |
A | 1 | a0020c0014t0101g0274 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.56-4711_56-4700del others(12): Show |
MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr17 | 12700399 | ||||||
chr17:12700474 | C | T | 27 | a0001c0001t0001g0155 a0001c0001t0003g0150 a0001c0001t0005g0141 others(24): Show |
27 | HG02056.hp1 HG02074.hp1 HG02155.hp2 others(24): Show |
intron_variant | MODIFIER | c.56-4654C>T | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | chr17 | 12700474 | |||||||
chr17:12700474 | CG | C | 6 | a0001c0001t0001g0261 a0001c0001t0040g0272 a0001c0001t0068g0324 others(3): Show |
6 | HG01256.hp2 HG02615.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.56-4653delG | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | chr17 | 12700474 | |||||||
chr17:12700559 | A | G | 34 | a0001c0001t0001g0343 a0001c0001t0002g0241 a0001c0001t0002g0242 others(31): Show |
34 | HG00423.hp1 HG00741.hp1 HG01106.hp1 others(31): Show |
intron_variant | MODIFIER | c.56-4569A>G | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | chr17 | 12700559 | |||||||
chr17:12700576 | GCTAATTT others(159): Show |
G | 2 | a0001c0001t0040g0256 a0001c0006t0094g0293 |
2 | HG02055.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.56-4548_56-4383del | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr17 | 12700576 | ||||||
chr17:12700649 | C | T | 27 | a0001c0001t0001g0155 a0001c0001t0003g0150 a0001c0001t0005g0141 others(24): Show |
27 | HG02056.hp1 HG02074.hp1 HG02155.hp2 others(24): Show |
intron_variant | MODIFIER | c.56-4479C>T | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | chr17 | 12700649 | |||||||
chr17:12700660 | C | T | 34 | a0001c0001t0002g0241 a0001c0001t0002g0242 a0001c0001t0002g0244 others(31): Show |
34 | HG00423.hp1 HG00741.hp1 HG01106.hp1 others(31): Show |
intron_variant | MODIFIER | c.56-4468C>T | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | chr17 | 12700660 | |||||||
chr17:12700674 | A | G | 1 | a0011c0030t0114g0262 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.56-4454A>G | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | chr17 | 12700674 | |||||||
chr17:12700729 | C | T | 24 | a0001c0001t0001g0051 a0001c0001t0001g0176 a0001c0001t0001g0177 others(21): Show |
24 | HG00597.hp2 HG00642.hp1 HG00735.hp1 others(21): Show |
intron_variant | MODIFIER | c.56-4399C>T | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | chr17 | 12700729 | |||||||
chr17:12700745 | A | C | 58 | a0001c0001t0001g0161 a0001c0001t0001g0181 a0001c0001t0003g0188 others(55): Show |
58 | HG00408.hp1 HG00621.hp2 HG00639.hp2 others(55): Show |
intron_variant | MODIFIER | c.56-4383A>C | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | chr17 | 12700745 | |||||||
chr17:12700880 | C | T | 132 | a0001c0001t0001g0028 a0001c0001t0001g0051 a0001c0001t0001g0155 others(129): Show |
135 | HG00544.hp2 HG00597.hp2 HG00609.hp2 others(132): Show |
intron_variant | MODIFIER | c.56-4248C>T | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | chr17 | 12700880 | |||||||
chr17:12700995 | T | G | 58 | a0001c0001t0001g0161 a0001c0001t0001g0181 a0001c0001t0003g0188 others(55): Show |
58 | HG00408.hp1 HG00621.hp2 HG00639.hp2 others(55): Show |
intron_variant | MODIFIER | c.56-4133T>G | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | chr17 | 12700995 | |||||||
chr17:12701014 | C | T | 1 | a0001c0001t0007g0088 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.56-4114C>T | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | chr17 | 12701014 | |||||||
chr17:12701327 | G | A | 1 | a0001c0003t0049g0134 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.56-3801G>A | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | chr17 | 12701327 | |||||||
chr17:12701360 | C | T | 1 | a0001c0001t0001g0343 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.56-3768C>T | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | chr17 | 12701360 | |||||||
chr17:12701561 | T | G | 1 | a0001c0001t0070g0246 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.56-3567T>G | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | chr17 | 12701561 | |||||||
chr17:12701742 | A | G | 1 | a0001c0001t0067g0315 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.56-3386A>G | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | chr17 | 12701742 | |||||||
chr17:12701747 | G | A | 188 | a0001c0001t0001g0028 a0001c0001t0001g0051 a0001c0001t0001g0155 others(185): Show |
191 | HG00408.hp1 HG00544.hp2 HG00597.hp2 others(188): Show |
intron_variant | MODIFIER | c.56-3381G>A | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | chr17 | 12701747 | |||||||
chr17:12701821 | A | C | 137 | a0001c0001t0001g0028 a0001c0001t0001g0051 a0001c0001t0001g0155 others(134): Show |
140 | HG00544.hp2 HG00597.hp2 HG00609.hp2 others(137): Show |
intron_variant | MODIFIER | c.56-3307A>C | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | chr17 | 12701821 | |||||||
chr17:12701920 | T | C | 1 | a0001c0001t0001g0343 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.56-3208T>C | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | chr17 | 12701920 | |||||||
chr17:12701972 | T | C | 57 | a0001c0001t0001g0161 a0001c0001t0001g0181 a0001c0001t0003g0188 others(54): Show |
57 | HG00408.hp1 HG00621.hp2 HG00639.hp2 others(54): Show |
intron_variant | MODIFIER | c.56-3156T>C | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | chr17 | 12701972 | |||||||
chr17:12702114 | G | C | 28 | a0001c0001t0001g0155 a0001c0001t0003g0150 a0001c0001t0005g0141 others(25): Show |
28 | HG02056.hp1 HG02074.hp1 HG02155.hp2 others(25): Show |
intron_variant | MODIFIER | c.56-3014G>C | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | chr17 | 12702114 | |||||||
chr17:12702349 | A | G | 1 | a0002c0005t0012g0283 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.56-2779A>G | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | chr17 | 12702349 | |||||||
chr17:12702394 | C | T | 191 | a0001c0001t0001g0028 a0001c0001t0001g0051 a0001c0001t0001g0155 others(188): Show |
194 | HG00408.hp1 HG00544.hp2 HG00597.hp2 others(191): Show |
intron_variant | MODIFIER | c.56-2734C>T | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | chr17 | 12702394 | |||||||
chr17:12702433 | T | G | 190 | a0001c0001t0001g0028 a0001c0001t0001g0051 a0001c0001t0001g0155 others(187): Show |
193 | HG00408.hp1 HG00544.hp2 HG00597.hp2 others(190): Show |
intron_variant | MODIFIER | c.56-2695T>G | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | chr17 | 12702433 | |||||||
chr17:12702504 | C | T | 1 | a0001c0001t0001g0343 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.56-2624C>T | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | chr17 | 12702504 | |||||||
chr17:12702620 | A | G | 34 | a0001c0001t0002g0241 a0001c0001t0002g0242 a0001c0001t0002g0244 others(31): Show |
34 | HG00423.hp1 HG00741.hp1 HG01106.hp1 others(31): Show |
intron_variant | MODIFIER | c.56-2508A>G | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | chr17 | 12702620 | |||||||
chr17:12702684 | GT | G | 340 | a0001c0001t0001g0028 a0001c0001t0001g0051 a0001c0001t0001g0058 others(337): Show |
343 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(340): Show |
intron_variant | MODIFIER | c.56-2436delT | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr17 | 12702684 | ||||||
chr17:12702769 | T | C | 4 | a0001c0001t0011g0224 a0001c0001t0011g0229 a0001c0001t0011g0230 others(1): Show |
4 | HG02559.hp2 HG02622.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.56-2359T>C | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | chr17 | 12702769 | |||||||
chr17:12702782 | G | A | 1 | a0001c0001t0001g0343 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.56-2346G>A | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | chr17 | 12702782 | |||||||
chr17:12702853 | T | C | 191 | a0001c0001t0001g0028 a0001c0001t0001g0051 a0001c0001t0001g0155 others(188): Show |
194 | HG00408.hp1 HG00544.hp2 HG00597.hp2 others(191): Show |
intron_variant | MODIFIER | c.56-2275T>C | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | chr17 | 12702853 | |||||||
chr17:12702864 | C | T | 190 | a0001c0001t0001g0028 a0001c0001t0001g0051 a0001c0001t0001g0155 others(187): Show |
193 | HG00408.hp1 HG00544.hp2 HG00597.hp2 others(190): Show |
intron_variant | MODIFIER | c.56-2264C>T | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | chr17 | 12702864 | |||||||
chr17:12703117 | A | G | 190 | a0001c0001t0001g0028 a0001c0001t0001g0051 a0001c0001t0001g0155 others(187): Show |
193 | HG00408.hp1 HG00544.hp2 HG00597.hp2 others(190): Show |
intron_variant | MODIFIER | c.56-2011A>G | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | chr17 | 12703117 | |||||||
chr17:12703270 | A | C | 1 | a0001c0001t0008g0052 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.56-1858A>C | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | chr17 | 12703270 | |||||||
chr17:12703283 | C | T | 1 | a0001c0001t0001g0343 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.56-1845C>T | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | chr17 | 12703283 | |||||||
chr17:12703359 | C | T | 190 | a0001c0001t0001g0028 a0001c0001t0001g0051 a0001c0001t0001g0155 others(187): Show |
193 | HG00408.hp1 HG00544.hp2 HG00597.hp2 others(190): Show |
intron_variant | MODIFIER | c.56-1769C>T | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | chr17 | 12703359 | |||||||
chr17:12703428 | AT | A | 4 | a0001c0001t0036g0257 a0001c0001t0075g0266 a0005c0010t0099g0265 others(1): Show |
4 | HG02109.hp2 HG02257.hp2 HG02451.hp2 others(1): Show |
intron_variant | MODIFIER | c.56-1697delT | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr17 | 12703428 | ||||||
chr17:12703509 | A | G | 57 | a0001c0001t0001g0161 a0001c0001t0001g0181 a0001c0001t0003g0188 others(54): Show |
57 | HG00408.hp1 HG00621.hp2 HG00639.hp2 others(54): Show |
intron_variant | MODIFIER | c.56-1619A>G | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | chr17 | 12703509 | |||||||
chr17:12703571 | T | C | 1 | a0001c0001t0018g0033 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.56-1557T>C | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | chr17 | 12703571 | |||||||
chr17:12703748 | C | T | 1 | a0001c0001t0008g0180 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.56-1380C>T | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | chr17 | 12703748 | |||||||
chr17:12703751 | A | AT | 36 | a0001c0001t0002g0241 a0001c0001t0002g0242 a0001c0001t0002g0244 others(33): Show |
36 | HG00423.hp1 HG00733.hp1 HG00733.hp2 others(33): Show |
intron_variant | MODIFIER | c.56-1368dupT | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr17 | 12703751 | ||||||
chr17:12704205 | T | C | 1 | a0001c0001t0001g0343 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.56-923T>C | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | chr17 | 12704205 | |||||||
chr17:12704272 | T | A | 2 | a0001c0001t0013g0259 a0006c0012t0031g0003 |
3 | HG01891.hp2 HG02922.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.56-856T>A | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | chr17 | 12704272 | |||||||
chr17:12704426 | G | A | 14 | a0001c0001t0013g0259 a0001c0001t0013g0273 a0001c0001t0018g0033 others(11): Show |
15 | HG01192.hp1 HG01891.hp2 HG02109.hp1 others(12): Show |
intron_variant | MODIFIER | c.56-702G>A | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | chr17 | 12704426 | |||||||
chr17:12704624 | T | C | 1 | a0003c0008t0111g0303 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.56-504T>C | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | chr17 | 12704624 | |||||||
chr17:12704692 | G | C | 222 | a0001c0001t0001g0028 a0001c0001t0001g0051 a0001c0001t0001g0155 others(219): Show |
225 | HG00408.hp1 HG00423.hp1 HG00544.hp2 others(222): Show |
intron_variant | MODIFIER | c.56-436G>C | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | chr17 | 12704692 | |||||||
chr17:12704864 | G | A | 2 | a0001c0001t0002g0241 a0001c0001t0002g0242 |
2 | HG02273.hp1 HG02293.hp1 |
intron_variant | MODIFIER | c.56-264G>A | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | chr17 | 12704864 | |||||||
chr17:12704886 | C | T | 1 | a0001c0001t0001g0343 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.56-242C>T | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | chr17 | 12704886 | |||||||
chr17:12704954 | T | C | 26 | a0001c0001t0001g0051 a0001c0001t0001g0176 a0001c0001t0001g0177 others(23): Show |
26 | HG00597.hp2 HG00642.hp1 HG00735.hp1 others(23): Show |
intron_variant | MODIFIER | c.56-174T>C | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 1/13 | chr17 | 12704954 | |||||||
chr17:12705424 | G | A | 1 | a0001c0001t0001g0058 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.121+231G>A | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 2/13 | chr17 | 12705424 | |||||||
chr17:12705452 | T | C | 34 | a0001c0001t0002g0241 a0001c0001t0002g0242 a0001c0001t0002g0244 others(31): Show |
34 | HG00423.hp1 HG00741.hp1 HG01106.hp1 others(31): Show |
intron_variant | MODIFIER | c.121+259T>C | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 2/13 | chr17 | 12705452 | |||||||
chr17:12705623 | G | A | 1 | a0001c0001t0026g0234 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.121+430G>A | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 2/13 | chr17 | 12705623 | |||||||
chr17:12705635 | C | T | 3 | a0001c0001t0091g0309 a0001c0001t0092g0311 a0001c0001t0106g0310 |
3 | HG02630.hp1 HG02647.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.121+442C>T | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 2/13 | chr17 | 12705635 | |||||||
chr17:12705660 | T | C | 51 | a0001c0001t0001g0161 a0001c0001t0001g0181 a0001c0001t0003g0188 others(48): Show |
51 | HG00408.hp1 HG00639.hp2 HG00735.hp2 others(48): Show |
intron_variant | MODIFIER | c.121+467T>C | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 2/13 | chr17 | 12705660 | |||||||
chr17:12705688 | A | G | 2 | a0001c0001t0002g0187 a0001c0001t0143g0186 |
2 | HG01106.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.121+495A>G | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 2/13 | chr17 | 12705688 | |||||||
chr17:12705718 | T | C | 1 | a0001c0001t0164g0189 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.121+525T>C | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 2/13 | chr17 | 12705718 | |||||||
chr17:12705802 | A | T | 51 | a0001c0001t0001g0161 a0001c0001t0001g0181 a0001c0001t0003g0188 others(48): Show |
51 | HG00408.hp1 HG00639.hp2 HG00735.hp2 others(48): Show |
intron_variant | MODIFIER | c.121+609A>T | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 2/13 | chr17 | 12705802 | |||||||
chr17:12705835 | A | T | 51 | a0001c0001t0001g0161 a0001c0001t0001g0181 a0001c0001t0003g0188 others(48): Show |
51 | HG00408.hp1 HG00639.hp2 HG00735.hp2 others(48): Show |
intron_variant | MODIFIER | c.121+642A>T | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 2/13 | chr17 | 12705835 | |||||||
chr17:12705836 | T | G | 1 | a0011c0030t0114g0262 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.121+643T>G | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 2/13 | chr17 | 12705836 | |||||||
chr17:12705911 | A | C | 24 | a0001c0001t0001g0155 a0001c0001t0003g0150 a0001c0001t0006g0067 others(21): Show |
24 | HG02074.hp1 HG02602.hp1 HG03491.hp1 others(21): Show |
intron_variant | MODIFIER | c.121+718A>C | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 2/13 | chr17 | 12705911 | |||||||
chr17:12705921 | G | A | 51 | a0001c0001t0001g0161 a0001c0001t0001g0181 a0001c0001t0003g0188 others(48): Show |
51 | HG00408.hp1 HG00639.hp2 HG00735.hp2 others(48): Show |
intron_variant | MODIFIER | c.121+728G>A | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 2/13 | chr17 | 12705921 | |||||||
chr17:12705944 | T | C | 1 | a0011c0030t0114g0262 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.121+751T>C | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 2/13 | chr17 | 12705944 | |||||||
chr17:12705964 | C | T | 34 | a0001c0001t0002g0241 a0001c0001t0002g0242 a0001c0001t0002g0244 others(31): Show |
34 | HG00423.hp1 HG00741.hp1 HG01106.hp1 others(31): Show |
intron_variant | MODIFIER | c.121+771C>T | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 2/13 | chr17 | 12705964 | |||||||
chr17:12706021 | G | C | 1 | a0001c0001t0029g0171 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.121+828G>C | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 2/13 | chr17 | 12706021 | |||||||
chr17:12706069 | T | C | 5 | a0001c0001t0008g0137 a0001c0001t0017g0139 a0001c0001t0039g0138 others(2): Show |
5 | NA18942.hp2 NA18947.hp1 NA18956.hp2 others(2): Show |
intron_variant | MODIFIER | c.121+876T>C | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 2/13 | chr17 | 12706069 | |||||||
chr17:12706080 | T | C | 1 | a0001c0001t0067g0315 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.121+887T>C | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 2/13 | chr17 | 12706080 | |||||||
chr17:12706154 | T | C | 34 | a0001c0001t0002g0241 a0001c0001t0002g0242 a0001c0001t0002g0244 others(31): Show |
34 | HG00423.hp1 HG00741.hp1 HG01106.hp1 others(31): Show |
intron_variant | MODIFIER | c.121+961T>C | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 2/13 | chr17 | 12706154 | |||||||
chr17:12706159 | T | C | 1 | a0012c0029t0115g0335 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.121+966T>C | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 2/13 | chr17 | 12706159 | |||||||
chr17:12706280 | T | C | 226 | a0001c0001t0001g0028 a0001c0001t0001g0051 a0001c0001t0001g0079 others(223): Show |
229 | HG00408.hp1 HG00423.hp1 HG00544.hp2 others(226): Show |
intron_variant | MODIFIER | c.121+1087T>C | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 2/13 | chr17 | 12706280 | |||||||
chr17:12706314 | A | G | 1 | a0011c0030t0114g0262 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.121+1121A>G | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 2/13 | chr17 | 12706314 | |||||||
chr17:12706466 | G | A | 1 | a0001c0001t0001g0343 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.121+1273G>A | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 2/13 | chr17 | 12706466 | |||||||
chr17:12706809 | A | G | 1 | a0001c0001t0130g0101 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.121+1616A>G | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 2/13 | chr17 | 12706809 | |||||||
chr17:12706963 | G | T | 1 | a0001c0001t0015g0111 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.121+1770G>T | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 2/13 | chr17 | 12706963 | |||||||
chr17:12707027 | C | G | 192 | a0001c0001t0001g0028 a0001c0001t0001g0155 a0001c0001t0001g0161 others(189): Show |
195 | HG00408.hp1 HG00423.hp1 HG00544.hp2 others(192): Show |
intron_variant | MODIFIER | c.121+1834C>G | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 2/13 | chr17 | 12707027 | |||||||
chr17:12707029 | G | T | 93 | a0001c0001t0001g0028 a0001c0001t0001g0155 a0001c0001t0001g0261 others(90): Show |
95 | HG00544.hp2 HG00609.hp2 HG01109.hp2 others(92): Show |
intron_variant | MODIFIER | c.121+1836G>T | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 2/13 | chr17 | 12707029 | |||||||
chr17:12707085 | G | A | 1 | a0001c0001t0151g0182 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.121+1892G>A | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 2/13 | chr17 | 12707085 | |||||||
chr17:12707248 | G | A | 51 | a0001c0001t0001g0161 a0001c0001t0001g0181 a0001c0001t0003g0188 others(48): Show |
51 | HG00408.hp1 HG00639.hp2 HG00735.hp2 others(48): Show |
intron_variant | MODIFIER | c.121+2055G>A | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 2/13 | chr17 | 12707248 | |||||||
chr17:12707359 | C | A | 13 | a0001c0001t0013g0259 a0001c0001t0013g0273 a0001c0001t0018g0033 others(10): Show |
14 | HG01192.hp1 HG01891.hp2 HG02109.hp1 others(11): Show |
intron_variant | MODIFIER | c.121+2166C>A | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 2/13 | chr17 | 12707359 | |||||||
chr17:12707401 | C | T | 1 | a0002c0005t0185g0277 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.121+2208C>T | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 2/13 | chr17 | 12707401 | |||||||
chr17:12707515 | C | G | 34 | a0001c0001t0002g0241 a0001c0001t0002g0242 a0001c0001t0002g0244 others(31): Show |
34 | HG00423.hp1 HG00741.hp1 HG01106.hp1 others(31): Show |
intron_variant | MODIFIER | c.121+2322C>G | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 2/13 | chr17 | 12707515 | |||||||
chr17:12707529 | A | C | 217 | a0001c0001t0001g0028 a0001c0001t0001g0051 a0001c0001t0001g0155 others(214): Show |
220 | HG00408.hp1 HG00423.hp1 HG00544.hp2 others(217): Show |
intron_variant | MODIFIER | c.121+2336A>C | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 2/13 | chr17 | 12707529 | |||||||
chr17:12707544 | A | C | 1 | a0011c0030t0114g0262 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.121+2351A>C | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 2/13 | chr17 | 12707544 | |||||||
chr17:12707549 | C | CA | 34 | a0001c0001t0002g0241 a0001c0001t0002g0242 a0001c0001t0002g0244 others(31): Show |
34 | HG00423.hp1 HG00741.hp1 HG01106.hp1 others(31): Show |
intron_variant | MODIFIER | c.121+2364dupA | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr17 | 12707549 | ||||||
chr17:12707588 | C | T | 2 | a0001c0001t0117g0340 a0001c0001t0125g0341 |
2 | HG03130.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.121+2395C>T | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 2/13 | chr17 | 12707588 | |||||||
chr17:12707606 | C | T | 156 | a0001c0001t0001g0028 a0001c0001t0001g0155 a0001c0001t0001g0161 others(153): Show |
159 | HG00408.hp1 HG00544.hp2 HG00609.hp2 others(156): Show |
intron_variant | MODIFIER | c.121+2413C>T | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 2/13 | chr17 | 12707606 | |||||||
chr17:12707617 | G | A | 141 | a0001c0001t0001g0028 a0001c0001t0001g0155 a0001c0001t0001g0261 others(138): Show |
144 | HG00423.hp1 HG00544.hp2 HG00609.hp2 others(141): Show |
intron_variant | MODIFIER | c.121+2424G>A | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 2/13 | chr17 | 12707617 | |||||||
chr17:12707691 | G | A | 51 | a0001c0001t0001g0161 a0001c0001t0001g0181 a0001c0001t0003g0188 others(48): Show |
51 | HG00408.hp1 HG00639.hp2 HG00735.hp2 others(48): Show |
intron_variant | MODIFIER | c.121+2498G>A | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 2/13 | chr17 | 12707691 | |||||||
chr17:12707693 | A | T | 51 | a0001c0001t0001g0161 a0001c0001t0001g0181 a0001c0001t0003g0188 others(48): Show |
51 | HG00408.hp1 HG00639.hp2 HG00735.hp2 others(48): Show |
intron_variant | MODIFIER | c.121+2500A>T | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 2/13 | chr17 | 12707693 | |||||||
chr17:12707745 | T | A | 25 | a0001c0001t0001g0051 a0001c0001t0001g0176 a0001c0001t0001g0177 others(22): Show |
25 | HG00597.hp2 HG00642.hp1 HG00735.hp1 others(22): Show |
intron_variant | MODIFIER | c.121+2552T>A | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 2/13 | chr17 | 12707745 | |||||||
chr17:12707912 | G | A | 1 | a0003c0008t0071g0305 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.121+2719G>A | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 2/13 | chr17 | 12707912 | |||||||
chr17:12707937 | G | A | 217 | a0001c0001t0001g0028 a0001c0001t0001g0051 a0001c0001t0001g0155 others(214): Show |
220 | HG00408.hp1 HG00423.hp1 HG00544.hp2 others(217): Show |
intron_variant | MODIFIER | c.121+2744G>A | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 2/13 | chr17 | 12707937 | |||||||
chr17:12707955 | A | ATG | 36 | a0001c0001t0001g0069 a0001c0001t0001g0077 a0001c0001t0001g0104 others(33): Show |
36 | HG00280.hp1 HG00408.hp2 HG00423.hp2 others(33): Show |
intron_variant | MODIFIER | c.121+2776_121+2777d others(4): Show |
MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr17 | 12707955 | ||||||
chr17:12707955 | A | G | 51 | a0001c0001t0001g0161 a0001c0001t0001g0181 a0001c0001t0003g0188 others(48): Show |
51 | HG00408.hp1 HG00639.hp2 HG00735.hp2 others(48): Show |
intron_variant | MODIFIER | c.121+2762A>G | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 2/13 | chr17 | 12707955 | |||||||
chr17:12707992 | C | A | 192 | a0001c0001t0001g0028 a0001c0001t0001g0155 a0001c0001t0001g0161 others(189): Show |
195 | HG00408.hp1 HG00423.hp1 HG00544.hp2 others(192): Show |
intron_variant | MODIFIER | c.121+2799C>A | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 2/13 | chr17 | 12707992 | |||||||
chr17:12708026 | A | C | 192 | a0001c0001t0001g0028 a0001c0001t0001g0155 a0001c0001t0001g0161 others(189): Show |
195 | HG00408.hp1 HG00423.hp1 HG00544.hp2 others(192): Show |
intron_variant | MODIFIER | c.121+2833A>C | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 2/13 | chr17 | 12708026 | |||||||
chr17:12708092 | C | T | 1 | a0012c0029t0115g0335 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.121+2899C>T | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 2/13 | chr17 | 12708092 | |||||||
chr17:12708129 | G | A | 217 | a0001c0001t0001g0028 a0001c0001t0001g0051 a0001c0001t0001g0155 others(214): Show |
220 | HG00408.hp1 HG00423.hp1 HG00544.hp2 others(217): Show |
intron_variant | MODIFIER | c.121+2936G>A | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 2/13 | chr17 | 12708129 | |||||||
chr17:12708166 | A | G | 217 | a0001c0001t0001g0028 a0001c0001t0001g0051 a0001c0001t0001g0155 others(214): Show |
220 | HG00408.hp1 HG00423.hp1 HG00544.hp2 others(217): Show |
intron_variant | MODIFIER | c.121+2973A>G | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 2/13 | chr17 | 12708166 | |||||||
chr17:12708370 | T | G | 1 | a0001c0003t0049g0134 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.121+3177T>G | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 2/13 | chr17 | 12708370 | |||||||
chr17:12708548 | A | G | 1 | a0020c0014t0101g0274 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.121+3355A>G | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 2/13 | chr17 | 12708548 | |||||||
chr17:12708626 | C | T | 1 | a0001c0001t0201g0334 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.121+3433C>T | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 2/13 | chr17 | 12708626 | |||||||
chr17:12708627 | G | A | 2 | a0001c0001t0116g0270 a0001c0006t0016g0231 |
2 | HG01934.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.121+3434G>A | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 2/13 | chr17 | 12708627 | |||||||
chr17:12708682 | C | T | 1 | a0001c0001t0060g0320 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.121+3489C>T | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 2/13 | chr17 | 12708682 | |||||||
chr17:12708962 | C | A | 218 | a0001c0001t0001g0028 a0001c0001t0001g0051 a0001c0001t0001g0155 others(215): Show |
221 | HG00408.hp1 HG00423.hp1 HG00544.hp2 others(218): Show |
intron_variant | MODIFIER | c.121+3769C>A | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 2/13 | chr17 | 12708962 | |||||||
chr17:12709016 | G | A | 1 | a0001c0001t0106g0310 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.121+3823G>A | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 2/13 | chr17 | 12709016 | |||||||
chr17:12709043 | T | C | 191 | a0001c0001t0001g0028 a0001c0001t0001g0155 a0001c0001t0001g0161 others(188): Show |
194 | HG00408.hp1 HG00423.hp1 HG00544.hp2 others(191): Show |
intron_variant | MODIFIER | c.121+3850T>C | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 2/13 | chr17 | 12709043 | |||||||
chr17:12709136 | T | C | 1 | a0017c0013t0011g0276 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.121+3943T>C | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 2/13 | chr17 | 12709136 | |||||||
chr17:12709232 | T | A | 139 | a0001c0001t0001g0028 a0001c0001t0001g0155 a0001c0001t0001g0261 others(136): Show |
142 | HG00423.hp1 HG00544.hp2 HG00609.hp2 others(139): Show |
intron_variant | MODIFIER | c.121+4039T>A | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 2/13 | chr17 | 12709232 | |||||||
chr17:12709246 | G | T | 5 | a0001c0001t0003g0212 a0001c0001t0005g0085 a0001c0001t0035g0129 others(2): Show |
5 | HG01433.hp1 HG02004.hp1 HG02027.hp1 others(2): Show |
intron_variant | MODIFIER | c.121+4053G>T | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 2/13 | chr17 | 12709246 | |||||||
chr17:12709315 | C | T | 25 | a0001c0001t0001g0051 a0001c0001t0001g0176 a0001c0001t0001g0177 others(22): Show |
25 | HG00597.hp2 HG00642.hp1 HG00735.hp1 others(22): Show |
intron_variant | MODIFIER | c.121+4122C>T | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 2/13 | chr17 | 12709315 | |||||||
chr17:12709381 | A | C | 1 | a0001c0001t0001g0343 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.121+4188A>C | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 2/13 | chr17 | 12709381 | |||||||
chr17:12709419 | C | A | 12 | a0001c0001t0013g0259 a0001c0001t0013g0273 a0001c0001t0018g0033 others(9): Show |
13 | HG01192.hp1 HG01891.hp2 HG02109.hp1 others(10): Show |
intron_variant | MODIFIER | c.121+4226C>A | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 2/13 | chr17 | 12709419 | |||||||
chr17:12709501 | A | T | 24 | a0001c0001t0001g0155 a0001c0001t0003g0150 a0001c0001t0006g0067 others(21): Show |
24 | HG02074.hp1 HG02602.hp1 HG03491.hp1 others(21): Show |
intron_variant | MODIFIER | c.121+4308A>T | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 2/13 | chr17 | 12709501 | |||||||
chr17:12709568 | GTC | G | 8 | a0001c0001t0011g0224 a0001c0001t0011g0229 a0001c0001t0011g0230 others(5): Show |
9 | HG01109.hp2 HG01243.hp2 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.121+4380_121+4381d others(4): Show |
MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr17 | 12709568 | ||||||
chr17:12709614 | T | C | 25 | a0001c0001t0001g0051 a0001c0001t0001g0176 a0001c0001t0001g0177 others(22): Show |
25 | HG00597.hp2 HG00642.hp1 HG00735.hp1 others(22): Show |
intron_variant | MODIFIER | c.121+4421T>C | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 2/13 | chr17 | 12709614 | |||||||
chr17:12709718 | C | T | 51 | a0001c0001t0001g0028 a0001c0001t0001g0261 a0001c0001t0014g0338 others(48): Show |
52 | HG00544.hp2 HG00609.hp2 HG01243.hp1 others(49): Show |
intron_variant | MODIFIER | c.121+4525C>T | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 2/13 | chr17 | 12709718 | |||||||
chr17:12709746 | A | G | 276 | a0001c0001t0001g0028 a0001c0001t0001g0051 a0001c0001t0001g0069 others(273): Show |
279 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(276): Show |
intron_variant | MODIFIER | c.121+4553A>G | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 2/13 | chr17 | 12709746 | |||||||
chr17:12709863 | C | T | 51 | a0001c0001t0001g0161 a0001c0001t0001g0181 a0001c0001t0003g0188 others(48): Show |
51 | HG00408.hp1 HG00639.hp2 HG00735.hp2 others(48): Show |
intron_variant | MODIFIER | c.121+4670C>T | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 2/13 | chr17 | 12709863 | |||||||
chr17:12709869 | T | C | 51 | a0001c0001t0001g0161 a0001c0001t0001g0181 a0001c0001t0003g0188 others(48): Show |
51 | HG00408.hp1 HG00639.hp2 HG00735.hp2 others(48): Show |
intron_variant | MODIFIER | c.121+4676T>C | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 2/13 | chr17 | 12709869 | |||||||
chr17:12710020 | G | A | 51 | a0001c0001t0001g0161 a0001c0001t0001g0181 a0001c0001t0003g0188 others(48): Show |
51 | HG00408.hp1 HG00639.hp2 HG00735.hp2 others(48): Show |
intron_variant | MODIFIER | c.121+4827G>A | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 2/13 | chr17 | 12710020 | |||||||
chr17:12710305 | A | G | 2 | a0001c0001t0144g0219 a0001c0007t0001g0220 |
2 | HG00323.hp1 HG00733.hp1 |
intron_variant | MODIFIER | c.121+5112A>G | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 2/13 | chr17 | 12710305 | |||||||
chr17:12710331 | C | T | 1 | a0001c0001t0162g0057 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.121+5138C>T | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 2/13 | chr17 | 12710331 | |||||||
chr17:12710396 | A | G | 4 | a0001c0001t0036g0257 a0001c0001t0075g0266 a0005c0010t0099g0265 others(1): Show |
4 | HG02109.hp2 HG02257.hp2 HG02451.hp2 others(1): Show |
intron_variant | MODIFIER | c.122-5123A>G | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 2/13 | chr17 | 12710396 | |||||||
chr17:12710417 | C | T | 26 | a0001c0001t0001g0155 a0001c0001t0003g0150 a0001c0001t0006g0067 others(23): Show |
26 | HG02074.hp1 HG02602.hp1 HG03098.hp2 others(23): Show |
intron_variant | MODIFIER | c.122-5102C>T | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 2/13 | chr17 | 12710417 | |||||||
chr17:12710482 | A | AT | 51 | a0001c0001t0001g0161 a0001c0001t0001g0181 a0001c0001t0003g0188 others(48): Show |
51 | HG00408.hp1 HG00639.hp2 HG00735.hp2 others(48): Show |
intron_variant | MODIFIER | c.122-5029dupT | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr17 | 12710482 | ||||||
chr17:12710523 | T | G | 1 | a0001c0001t0172g0043 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.122-4996T>G | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 2/13 | chr17 | 12710523 | |||||||
chr17:12710670 | A | G | 1 | a0011c0030t0114g0262 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.122-4849A>G | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 2/13 | chr17 | 12710670 | |||||||
chr17:12710707 | C | A | 3 | a0001c0001t0006g0174 a0001c0001t0008g0173 a0001c0001t0161g0190 |
3 | HG01981.hp1 HG02735.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.122-4812C>A | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 2/13 | chr17 | 12710707 | |||||||
chr17:12710742 | G | A | 12 | a0001c0001t0013g0259 a0001c0001t0013g0273 a0001c0001t0018g0033 others(9): Show |
13 | HG01192.hp1 HG01891.hp2 HG02109.hp1 others(10): Show |
intron_variant | MODIFIER | c.122-4777G>A | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 2/13 | chr17 | 12710742 | |||||||
chr17:12710926 | C | A | 51 | a0001c0001t0001g0161 a0001c0001t0001g0181 a0001c0001t0003g0188 others(48): Show |
51 | HG00408.hp1 HG00639.hp2 HG00735.hp2 others(48): Show |
intron_variant | MODIFIER | c.122-4593C>A | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 2/13 | chr17 | 12710926 | |||||||
chr17:12711584 | G | A | 133 | a0001c0001t0001g0028 a0001c0001t0001g0155 a0001c0001t0001g0261 others(130): Show |
135 | HG00423.hp1 HG00544.hp2 HG00609.hp2 others(132): Show |
intron_variant | MODIFIER | c.122-3935G>A | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 2/13 | chr17 | 12711584 | |||||||
chr17:12711625 | A | G | 1 | a0001c0001t0003g0212 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.122-3894A>G | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 2/13 | chr17 | 12711625 | |||||||
chr17:12711630 | T | C | 47 | a0001c0001t0001g0051 a0001c0001t0001g0176 a0001c0001t0001g0177 others(44): Show |
49 | HG00597.hp2 HG00642.hp1 HG00735.hp1 others(46): Show |
intron_variant | MODIFIER | c.122-3889T>C | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 2/13 | chr17 | 12711630 | |||||||
chr17:12711686 | A | G | 1 | a0012c0029t0115g0335 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.122-3833A>G | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 2/13 | chr17 | 12711686 | |||||||
chr17:12711716 | A | G | 33 | a0001c0001t0001g0051 a0001c0001t0001g0176 a0001c0001t0001g0177 others(30): Show |
34 | HG00597.hp2 HG00642.hp1 HG00735.hp1 others(31): Show |
intron_variant | MODIFIER | c.122-3803A>G | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 2/13 | chr17 | 12711716 | |||||||
chr17:12711909 | T | C | 3 | a0001c0001t0010g0191 a0001c0001t0137g0151 a0001c0001t0141g0015 |
3 | HG02738.hp1 HG04184.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.122-3610T>C | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 2/13 | chr17 | 12711909 | |||||||
chr17:12711914 | T | C | 35 | a0001c0001t0001g0343 a0001c0001t0002g0241 a0001c0001t0002g0242 others(32): Show |
35 | HG00423.hp1 HG00741.hp1 HG01106.hp1 others(32): Show |
intron_variant | MODIFIER | c.122-3605T>C | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 2/13 | chr17 | 12711914 | |||||||
chr17:12711924 | C | CT | 59 | a0001c0001t0001g0161 a0001c0001t0001g0181 a0001c0001t0003g0188 others(56): Show |
59 | HG00408.hp1 HG00544.hp1 HG00639.hp2 others(56): Show |
intron_variant | MODIFIER | c.122-3578dupT | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr17 | 12711924 | ||||||
chr17:12711924 | CT | C | 48 | a0001c0001t0001g0051 a0001c0001t0001g0176 a0001c0001t0001g0177 others(45): Show |
50 | HG00597.hp2 HG00642.hp1 HG00735.hp1 others(47): Show |
intron_variant | MODIFIER | c.122-3578delT | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr17 | 12711924 | ||||||
chr17:12711985 | G | A | 1 | a0001c0002t0085g0288 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.122-3534G>A | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 2/13 | chr17 | 12711985 | |||||||
chr17:12712055 | G | A | 9 | a0001c0001t0011g0224 a0001c0001t0011g0229 a0001c0001t0011g0230 others(6): Show |
10 | HG01109.hp2 HG01243.hp2 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.122-3464G>A | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 2/13 | chr17 | 12712055 | |||||||
chr17:12712113 | A | G | 169 | a0001c0001t0001g0028 a0001c0001t0001g0051 a0001c0001t0001g0155 others(166): Show |
172 | HG00423.hp1 HG00544.hp2 HG00597.hp2 others(169): Show |
intron_variant | MODIFIER | c.122-3406A>G | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 2/13 | chr17 | 12712113 | |||||||
chr17:12712141 | G | T | 1 | a0012c0029t0115g0335 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.122-3378G>T | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 2/13 | chr17 | 12712141 | |||||||
chr17:12712233 | C | T | 1 | a0001c0001t0001g0343 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.122-3286C>T | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 2/13 | chr17 | 12712233 | |||||||
chr17:12712292 | C | T | 3 | a0001c0001t0051g0009 a0001c0001t0052g0008 a0001c0011t0020g0001 |
4 | HG01109.hp2 HG01243.hp2 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.122-3227C>T | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 2/13 | chr17 | 12712292 | |||||||
chr17:12712391 | C | A | 13 | a0001c0001t0013g0259 a0001c0001t0013g0273 a0001c0001t0018g0033 others(10): Show |
14 | HG01192.hp1 HG01891.hp2 HG02109.hp1 others(11): Show |
intron_variant | MODIFIER | c.122-3128C>A | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 2/13 | chr17 | 12712391 | |||||||
chr17:12712535 | G | T | 1 | a0001c0001t0018g0223 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.122-2984G>T | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 2/13 | chr17 | 12712535 | |||||||
chr17:12712642 | G | A | 13 | a0001c0001t0013g0259 a0001c0001t0013g0273 a0001c0001t0018g0033 others(10): Show |
14 | HG01192.hp1 HG01891.hp2 HG02109.hp1 others(11): Show |
intron_variant | MODIFIER | c.122-2877G>A | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 2/13 | chr17 | 12712642 | |||||||
chr17:12712654 | G | T | 51 | a0001c0001t0001g0161 a0001c0001t0001g0181 a0001c0001t0003g0188 others(48): Show |
51 | HG00408.hp1 HG00639.hp2 HG00735.hp2 others(48): Show |
intron_variant | MODIFIER | c.122-2865G>T | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 2/13 | chr17 | 12712654 | |||||||
chr17:12712736 | T | C | 13 | a0001c0001t0013g0259 a0001c0001t0013g0273 a0001c0001t0018g0033 others(10): Show |
14 | HG01192.hp1 HG01891.hp2 HG02109.hp1 others(11): Show |
intron_variant | MODIFIER | c.122-2783T>C | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 2/13 | chr17 | 12712736 | |||||||
chr17:12712766 | T | G | 1 | a0001c0001t0108g0342 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.122-2753T>G | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 2/13 | chr17 | 12712766 | |||||||
chr17:12712790 | C | CT | 33 | a0001c0001t0001g0051 a0001c0001t0001g0176 a0001c0001t0001g0177 others(30): Show |
34 | HG00597.hp2 HG00642.hp1 HG00735.hp1 others(31): Show |
intron_variant | MODIFIER | c.122-2723dupT | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr17 | 12712790 | ||||||
chr17:12712796 | T | A | 51 | a0001c0001t0001g0028 a0001c0001t0001g0261 a0001c0001t0014g0338 others(48): Show |
52 | HG00544.hp2 HG00609.hp2 HG01243.hp1 others(49): Show |
intron_variant | MODIFIER | c.122-2723T>A | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 2/13 | chr17 | 12712796 | |||||||
chr17:12712914 | A | G | 4 | a0001c0001t0003g0150 a0001c0001t0138g0133 a0001c0001t0179g0135 others(1): Show |
4 | HG02074.hp1 NA18944.hp2 NA18948.hp2 others(1): Show |
intron_variant | MODIFIER | c.122-2605A>G | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 2/13 | chr17 | 12712914 | |||||||
chr17:12713374 | C | T | 13 | a0001c0001t0013g0259 a0001c0001t0013g0273 a0001c0001t0018g0033 others(10): Show |
14 | HG01192.hp1 HG01891.hp2 HG02109.hp1 others(11): Show |
intron_variant | MODIFIER | c.122-2145C>T | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 2/13 | chr17 | 12713374 | |||||||
chr17:12713617 | A | G | 1 | a0001c0001t0125g0341 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.122-1902A>G | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 2/13 | chr17 | 12713617 | |||||||
chr17:12713711 | G | A | 2 | a0001c0002t0007g0048 a0001c0002t0069g0159 |
2 | NA18991.hp1 NA19004.hp2 |
intron_variant | MODIFIER | c.122-1808G>A | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 2/13 | chr17 | 12713711 | |||||||
chr17:12713886 | G | T | 4 | a0001c0001t0036g0257 a0001c0001t0075g0266 a0005c0010t0099g0265 others(1): Show |
4 | HG02109.hp2 HG02257.hp2 HG02451.hp2 others(1): Show |
intron_variant | MODIFIER | c.122-1633G>T | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 2/13 | chr17 | 12713886 | |||||||
chr17:12713965 | A | G | 33 | a0001c0001t0001g0051 a0001c0001t0001g0176 a0001c0001t0001g0177 others(30): Show |
34 | HG00597.hp2 HG00642.hp1 HG00735.hp1 others(31): Show |
intron_variant | MODIFIER | c.122-1554A>G | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 2/13 | chr17 | 12713965 | |||||||
chr17:12713991 | G | A | 5 | a0001c0001t0011g0224 a0001c0001t0011g0229 a0001c0001t0011g0230 others(2): Show |
5 | HG02559.hp2 HG02622.hp2 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.122-1528G>A | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 2/13 | chr17 | 12713991 | |||||||
chr17:12714323 | G | GCA | 38 | a0001c0001t0001g0155 a0001c0001t0001g0261 a0001c0001t0001g0343 others(35): Show |
38 | HG00741.hp1 HG01106.hp1 HG01496.hp2 others(35): Show |
intron_variant | MODIFIER | c.122-1158_122-1157d others(4): Show |
MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr17 | 12714323 | ||||||
chr17:12714323 | G | GCACA | 49 | a0001c0001t0001g0104 a0001c0001t0001g0176 a0001c0001t0001g0177 others(46): Show |
50 | HG00544.hp1 HG00597.hp2 HG00642.hp1 others(47): Show |
intron_variant | MODIFIER | c.122-1160_122-1157d others(6): Show |
MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr17 | 12714323 | ||||||
chr17:12714323 | G | GCACACA | 65 | a0001c0001t0001g0069 a0001c0001t0001g0136 a0001c0001t0002g0187 others(62): Show |
66 | HG00423.hp1 HG00423.hp2 HG00558.hp2 others(63): Show |
intron_variant | MODIFIER | c.122-1162_122-1157d others(8): Show |
MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr17 | 12714323 | ||||||
chr17:12714323 | G | GCACACAC others(1): Show |
19 | a0001c0001t0004g0044 a0001c0001t0005g0091 a0001c0001t0008g0173 others(16): Show |
19 | HG00280.hp1 HG00673.hp1 HG01358.hp2 others(16): Show |
intron_variant | MODIFIER | c.122-1164_122-1157d others(10): Show |
MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr17 | 12714323 | ||||||
chr17:12714323 | G | GCACACAC others(3): Show |
29 | a0001c0001t0001g0181 a0001c0001t0001g0207 a0001c0001t0002g0090 others(26): Show |
29 | HG00323.hp2 HG00621.hp1 HG00639.hp1 others(26): Show |
intron_variant | MODIFIER | c.122-1166_122-1157d others(12): Show |
MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr17 | 12714323 | ||||||
chr17:12714323 | G | GCACACAC others(5): Show |
25 | a0001c0001t0001g0051 a0001c0001t0001g0077 a0001c0001t0001g0124 others(22): Show |
25 | HG00609.hp1 HG00673.hp2 HG00735.hp2 others(22): Show |
intron_variant | MODIFIER | c.122-1168_122-1157d others(14): Show |
MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr17 | 12714323 | ||||||
chr17:12714323 | G | GCACACAC others(7): Show |
26 | a0001c0001t0001g0058 a0001c0001t0001g0079 a0001c0001t0001g0086 others(23): Show |
26 | HG00323.hp1 HG00558.hp1 HG01361.hp1 others(23): Show |
intron_variant | MODIFIER | c.122-1170_122-1157d others(16): Show |
MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr17 | 12714323 | ||||||
chr17:12714323 | G | GCACACAC others(9): Show |
10 | a0001c0001t0002g0112 a0001c0001t0006g0098 a0001c0001t0007g0195 others(7): Show |
10 | HG01981.hp1 HG02027.hp1 HG02135.hp2 others(7): Show |
intron_variant | MODIFIER | c.122-1172_122-1157d others(18): Show |
MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr17 | 12714323 | ||||||
chr17:12714323 | G | GCACACAC others(11): Show |
10 | a0001c0001t0001g0089 a0001c0001t0004g0082 a0001c0001t0007g0163 others(7): Show |
10 | HG00408.hp1 HG00597.hp1 HG02080.hp1 others(7): Show |
intron_variant | MODIFIER | c.122-1174_122-1157d others(20): Show |
MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr17 | 12714323 | ||||||
chr17:12714323 | G | GCACACAC others(13): Show |
1 | a0001c0001t0172g0043 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.122-1176_122-1157d others(22): Show |
MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr17 | 12714323 | ||||||
chr17:12714323 | G | GCACACAC others(19): Show |
1 | a0001c0001t0019g0115 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.122-1182_122-1157d others(28): Show |
MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr17 | 12714323 | ||||||
chr17:12714323 | GCACA | G | 3 | a0001c0001t0002g0018 a0001c0001t0002g0119 a0001c0001t0130g0101 |
3 | HG00280.hp2 HG01257.hp1 HG02257.hp1 |
intron_variant | MODIFIER | c.122-1160_122-1157d others(6): Show |
MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr17 | 12714323 | ||||||
chr17:12714323 | GCACACAC others(5): Show |
G | 1 | a0018c0026t0027g0017 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.122-1168_122-1157d others(14): Show |
MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr17 | 12714323 | ||||||
chr17:12714361 | A | ACACACAC others(5): Show |
1 | a0001c0001t0001g0161 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.122-1157_122-1156i others(14): Show |
MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr17 | 12714361 | ||||||
chr17:12714362 | C | CACACACA others(6): Show |
1 | a0001c0001t0162g0057 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.122-1157_122-1156i others(15): Show |
MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 2/13 | chr17 | 12714362 | |||||||
chr17:12714362 | C | CACACACA others(10): Show |
1 | a0001c0001t0084g0194 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.122-1157_122-1156i others(19): Show |
MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 2/13 | chr17 | 12714362 | |||||||
chr17:12714384 | A | G | 168 | a0001c0001t0001g0058 a0001c0001t0001g0069 a0001c0001t0001g0077 others(165): Show |
168 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(165): Show |
intron_variant | MODIFIER | c.122-1135A>G | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 2/13 | chr17 | 12714384 | |||||||
chr17:12714418 | C | A | 1 | a0001c0001t0090g0083 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.122-1101C>A | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 2/13 | chr17 | 12714418 | |||||||
chr17:12714511 | G | GA | 13 | a0001c0001t0013g0259 a0001c0001t0013g0273 a0001c0001t0018g0033 others(10): Show |
14 | HG01192.hp1 HG01891.hp2 HG02109.hp1 others(11): Show |
intron_variant | MODIFIER | c.122-1000dupA | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr17 | 12714511 | ||||||
chr17:12714749 | A | G | 238 | a0001c0001t0001g0051 a0001c0001t0001g0058 a0001c0001t0001g0069 others(235): Show |
239 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(236): Show |
intron_variant | MODIFIER | c.122-770A>G | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 2/13 | chr17 | 12714749 | |||||||
chr17:12714787 | T | C | 2 | a0001c0001t0097g0307 a0001c0001t0120g0308 |
2 | HG02572.hp1 HG02615.hp2 |
intron_variant | MODIFIER | c.122-732T>C | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 2/13 | chr17 | 12714787 | |||||||
chr17:12715017 | A | G | 15 | a0001c0001t0001g0261 a0001c0001t0011g0224 a0001c0001t0011g0229 others(12): Show |
16 | HG01109.hp2 HG01243.hp2 HG01256.hp2 others(13): Show |
intron_variant | MODIFIER | c.122-502A>G | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 2/13 | chr17 | 12715017 | |||||||
chr17:12715063 | C | A | 14 | a0001c0001t0001g0261 a0001c0001t0011g0224 a0001c0001t0011g0229 others(11): Show |
15 | HG01109.hp2 HG01243.hp2 HG01256.hp2 others(12): Show |
intron_variant | MODIFIER | c.122-456C>A | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 2/13 | chr17 | 12715063 | |||||||
chr17:12715120 | A | G | 237 | a0001c0001t0001g0051 a0001c0001t0001g0058 a0001c0001t0001g0069 others(234): Show |
239 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(236): Show |
intron_variant | MODIFIER | c.122-399A>G | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 2/13 | chr17 | 12715120 | |||||||
chr17:12715244 | C | A | 4 | a0001c0001t0036g0257 a0001c0001t0075g0266 a0005c0010t0099g0265 others(1): Show |
4 | HG02109.hp2 HG02257.hp2 HG02451.hp2 others(1): Show |
intron_variant | MODIFIER | c.122-275C>A | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 2/13 | chr17 | 12715244 | |||||||
chr17:12715310 | C | CCT | 240 | a0001c0001t0001g0051 a0001c0001t0001g0058 a0001c0001t0001g0069 others(237): Show |
242 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(239): Show |
intron_variant | MODIFIER | c.122-209_122-208ins others(2): Show |
MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 2/13 | chr17 | 12715310 | |||||||
chr17:12715363 | G | C | 57 | a0001c0001t0001g0051 a0001c0001t0001g0155 a0001c0001t0001g0176 others(54): Show |
57 | HG00642.hp1 HG00735.hp1 HG00738.hp2 others(54): Show |
intron_variant | MODIFIER | c.122-156G>C | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 2/13 | chr17 | 12715363 | |||||||
chr17:12715389 | T | C | 2 | a0017c0013t0011g0276 a0020c0014t0101g0274 |
2 | NA18906.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.122-130T>C | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 2/13 | chr17 | 12715389 | |||||||
chr17:12715695 | G | A | 1 | a0001c0004t0002g0233 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.177+121G>A | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 3/13 | chr17 | 12715695 | |||||||
chr17:12715727 | A | T | 1 | a0001c0001t0008g0173 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.177+153A>T | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 3/13 | chr17 | 12715727 | |||||||
chr17:12715748 | G | A | 38 | a0001c0001t0001g0343 a0001c0001t0002g0241 a0001c0001t0002g0242 others(35): Show |
38 | HG00423.hp1 HG00741.hp1 HG01106.hp1 others(35): Show |
intron_variant | MODIFIER | c.177+174G>A | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 3/13 | chr17 | 12715748 | |||||||
chr17:12715791 | T | A | 1 | a0017c0013t0011g0276 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.177+217T>A | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 3/13 | chr17 | 12715791 | |||||||
chr17:12715801 | C | G | 1 | a0001c0001t0019g0046 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.177+227C>G | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 3/13 | chr17 | 12715801 | |||||||
chr17:12715956 | G | A | 1 | a0011c0030t0114g0262 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.177+382G>A | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 3/13 | chr17 | 12715956 | |||||||
chr17:12716162 | G | A | 2 | a0001c0001t0040g0272 a0013c0027t0110g0222 |
2 | HG02615.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.177+588G>A | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 3/13 | chr17 | 12716162 | |||||||
chr17:12716306 | A | G | 177 | a0001c0001t0001g0058 a0001c0001t0001g0069 a0001c0001t0001g0077 others(174): Show |
179 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(176): Show |
intron_variant | MODIFIER | c.177+732A>G | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 3/13 | chr17 | 12716306 | |||||||
chr17:12716315 | A | T | 1 | a0001c0001t0127g0275 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.177+741A>T | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 3/13 | chr17 | 12716315 | |||||||
chr17:12716363 | CAG | C | 119 | a0001c0001t0001g0058 a0001c0001t0001g0069 a0001c0001t0001g0077 others(116): Show |
119 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(116): Show |
intron_variant | MODIFIER | c.177+790_177+791del others(2): Show |
MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 3/13 | chr17 | 12716363 | |||||||
chr17:12716386 | T | C | 38 | a0001c0001t0001g0343 a0001c0001t0002g0241 a0001c0001t0002g0242 others(35): Show |
38 | HG00423.hp1 HG00741.hp1 HG01106.hp1 others(35): Show |
intron_variant | MODIFIER | c.177+812T>C | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 3/13 | chr17 | 12716386 | |||||||
chr17:12716477 | C | T | 139 | a0001c0001t0001g0058 a0001c0001t0001g0069 a0001c0001t0001g0077 others(136): Show |
141 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(138): Show |
intron_variant | MODIFIER | c.178-869C>T | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 3/13 | chr17 | 12716477 | |||||||
chr17:12716525 | A | G | 272 | a0001c0001t0001g0028 a0001c0001t0001g0051 a0001c0001t0001g0058 others(269): Show |
275 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(272): Show |
intron_variant | MODIFIER | c.178-821A>G | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 3/13 | chr17 | 12716525 | |||||||
chr17:12716599 | C | T | 119 | a0001c0001t0001g0058 a0001c0001t0001g0069 a0001c0001t0001g0077 others(116): Show |
119 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(116): Show |
intron_variant | MODIFIER | c.178-747C>T | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 3/13 | chr17 | 12716599 | |||||||
chr17:12716844 | G | T | 229 | a0001c0001t0001g0028 a0001c0001t0001g0051 a0001c0001t0001g0058 others(226): Show |
232 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(229): Show |
intron_variant | MODIFIER | c.178-502G>T | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 3/13 | chr17 | 12716844 | |||||||
chr17:12716977 | T | C | 272 | a0001c0001t0001g0028 a0001c0001t0001g0051 a0001c0001t0001g0058 others(269): Show |
275 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(272): Show |
intron_variant | MODIFIER | c.178-369T>C | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 3/13 | chr17 | 12716977 | |||||||
chr17:12716985 | CA | C | 27 | a0001c0001t0001g0161 a0001c0001t0004g0164 a0001c0001t0005g0091 others(24): Show |
27 | HG01109.hp1 HG01346.hp1 HG02055.hp2 others(24): Show |
intron_variant | MODIFIER | c.178-326delA | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr17 | 12716985 | ||||||
chr17:12716985 | CAA | C | 9 | a0001c0001t0100g0258 a0001c0001t0135g0056 a0001c0001t0151g0182 others(6): Show |
9 | HG00639.hp1 HG01515.hp1 HG03139.hp1 others(6): Show |
intron_variant | MODIFIER | c.178-327_178-326del others(2): Show |
MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr17 | 12716985 | ||||||
chr17:12716985 | CAAAAAAA others(1): Show |
C | 23 | a0001c0001t0001g0176 a0001c0001t0001g0177 a0001c0001t0005g0141 others(20): Show |
24 | HG01081.hp2 HG01192.hp1 HG01346.hp2 others(21): Show |
intron_variant | MODIFIER | c.178-333_178-326del others(8): Show |
MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr17 | 12716985 | ||||||
chr17:12716985 | CAAAAAAA others(2): Show |
C | 72 | a0001c0001t0001g0028 a0001c0001t0001g0051 a0001c0001t0001g0155 others(69): Show |
73 | HG00544.hp2 HG00609.hp2 HG00642.hp1 others(70): Show |
intron_variant | MODIFIER | c.178-334_178-326del others(9): Show |
MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr17 | 12716985 | ||||||
chr17:12716985 | CAAAAAAA others(3): Show |
C | 13 | a0001c0001t0008g0137 a0001c0001t0011g0224 a0001c0001t0011g0229 others(10): Show |
13 | HG02451.hp1 HG02559.hp2 HG02622.hp2 others(10): Show |
intron_variant | MODIFIER | c.178-335_178-326del others(10): Show |
MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr17 | 12716985 | ||||||
chr17:12716985 | CAAAAAAA others(4): Show |
C | 1 | a0001c0001t0014g0007 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.178-336_178-326del others(11): Show |
MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr17 | 12716985 | ||||||
chr17:12716985 | CAAAAAAA others(6): Show |
C | 2 | a0001c0001t0004g0044 a0001c0001t0038g0236 |
2 | NA19002.hp1 NA19062.hp2 |
intron_variant | MODIFIER | c.178-338_178-326del others(13): Show |
MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr17 | 12716985 | ||||||
chr17:12716985 | CAAAAAAA others(7): Show |
C | 36 | a0001c0001t0001g0343 a0001c0001t0002g0241 a0001c0001t0002g0242 others(33): Show |
36 | HG00423.hp1 HG00741.hp1 HG01106.hp1 others(33): Show |
intron_variant | MODIFIER | c.178-339_178-326del others(14): Show |
MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr17 | 12716985 | ||||||
chr17:12716985 | CAAAAAAA others(8): Show |
C | 3 | a0001c0001t0001g0261 a0001c0001t0068g0324 a0001c0001t0169g0263 |
3 | HG01256.hp2 HG03490.hp1 HG03491.hp2 |
intron_variant | MODIFIER | c.178-340_178-326del others(15): Show |
MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr17 | 12716985 | ||||||
chr17:12716985 | CAAAAAAA others(9): Show |
C | 3 | a0001c0001t0091g0309 a0001c0001t0092g0311 a0001c0001t0106g0310 |
3 | HG02630.hp1 HG02647.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.178-341_178-326del others(16): Show |
MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr17 | 12716985 | ||||||
chr17:12716985 | CAAAAAAA others(13): Show |
C | 2 | a0017c0013t0011g0276 a0020c0014t0101g0274 |
2 | NA18906.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.178-345_178-326del others(20): Show |
MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr17 | 12716985 | ||||||
chr17:12716985 | CAAAAAAA others(14): Show |
C | 1 | a0001c0001t0032g0029 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.178-346_178-326del others(21): Show |
MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr17 | 12716985 | ||||||
chr17:12716985 | CAAAAAAA others(15): Show |
C | 117 | a0001c0001t0001g0058 a0001c0001t0001g0069 a0001c0001t0001g0077 others(114): Show |
117 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(114): Show |
intron_variant | MODIFIER | c.178-347_178-326del others(22): Show |
MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr17 | 12716985 | ||||||
chr17:12716985 | CAAAAAAA others(16): Show |
C | 1 | a0001c0001t0005g0199 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.178-348_178-326del others(23): Show |
MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr17 | 12716985 | ||||||
chr17:12717230 | C | T | 1 | a0001c0004t0003g0128 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.178-116C>T | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 3/13 | chr17 | 12717230 | |||||||
chr17:12717444 | A | G | 229 | a0001c0001t0001g0028 a0001c0001t0001g0051 a0001c0001t0001g0058 others(226): Show |
232 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(229): Show |
intron_variant | MODIFIER | c.253+23A>G | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 4/13 | chr17 | 12717444 | |||||||
chr17:12717467 | G | A | 1 | a0011c0030t0114g0262 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.253+46G>A | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 4/13 | chr17 | 12717467 | |||||||
chr17:12717580 | G | A | 267 | a0001c0001t0001g0028 a0001c0001t0001g0051 a0001c0001t0001g0058 others(264): Show |
270 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(267): Show |
intron_variant | MODIFIER | c.253+159G>A | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 4/13 | chr17 | 12717580 | |||||||
chr17:12717636 | C | G | 1 | a0001c0003t0203g0281 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.253+215C>G | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 4/13 | chr17 | 12717636 | |||||||
chr17:12717804 | A | G | 37 | a0001c0001t0002g0241 a0001c0001t0002g0242 a0001c0001t0002g0244 others(34): Show |
37 | HG00423.hp1 HG00741.hp1 HG01106.hp1 others(34): Show |
intron_variant | MODIFIER | c.253+383A>G | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 4/13 | chr17 | 12717804 | |||||||
chr17:12717811 | G | A | 5 | a0001c0001t0001g0161 a0001c0001t0007g0163 a0001c0002t0005g0169 others(2): Show |
5 | HG02080.hp2 NA18954.hp2 NA18970.hp2 others(2): Show |
intron_variant | MODIFIER | c.253+390G>A | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 4/13 | chr17 | 12717811 | |||||||
chr17:12717998 | T | G | 15 | a0001c0001t0013g0259 a0001c0001t0013g0273 a0001c0001t0018g0033 others(12): Show |
17 | HG01109.hp2 HG01192.hp1 HG01243.hp2 others(14): Show |
intron_variant | MODIFIER | c.253+577T>G | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 4/13 | chr17 | 12717998 | |||||||
chr17:12718002 | G | A | 2 | a0017c0013t0011g0276 a0020c0014t0101g0274 |
2 | NA18906.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.253+581G>A | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 4/13 | chr17 | 12718002 | |||||||
chr17:12718037 | G | A | 38 | a0001c0001t0001g0343 a0001c0001t0002g0241 a0001c0001t0002g0242 others(35): Show |
38 | HG00423.hp1 HG00741.hp1 HG01106.hp1 others(35): Show |
intron_variant | MODIFIER | c.253+616G>A | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 4/13 | chr17 | 12718037 | |||||||
chr17:12718218 | A | G | 15 | a0001c0001t0013g0259 a0001c0001t0013g0273 a0001c0001t0018g0033 others(12): Show |
17 | HG01109.hp2 HG01192.hp1 HG01243.hp2 others(14): Show |
intron_variant | MODIFIER | c.253+797A>G | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 4/13 | chr17 | 12718218 | |||||||
chr17:12718369 | T | C | 1 | a0001c0001t0042g0071 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.253+948T>C | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 4/13 | chr17 | 12718369 | |||||||
chr17:12718465 | A | C | 214 | a0001c0001t0001g0028 a0001c0001t0001g0051 a0001c0001t0001g0058 others(211): Show |
215 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(212): Show |
intron_variant | MODIFIER | c.253+1044A>C | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 4/13 | chr17 | 12718465 | |||||||
chr17:12718492 | C | T | 1 | a0001c0001t0001g0343 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.253+1071C>T | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 4/13 | chr17 | 12718492 | |||||||
chr17:12718522 | G | A | 1 | a0001c0001t0090g0083 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.253+1101G>A | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 4/13 | chr17 | 12718522 | |||||||
chr17:12718619 | C | T | 1 | a0001c0001t0128g0168 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.253+1198C>T | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 4/13 | chr17 | 12718619 | |||||||
chr17:12718649 | A | C | 5 | a0001c0001t0011g0224 a0001c0001t0011g0229 a0001c0001t0011g0230 others(2): Show |
5 | HG02559.hp2 HG02622.hp2 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.253+1228A>C | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 4/13 | chr17 | 12718649 | |||||||
chr17:12718689 | G | A | 37 | a0001c0001t0002g0241 a0001c0001t0002g0242 a0001c0001t0002g0244 others(34): Show |
37 | HG00423.hp1 HG00741.hp1 HG01106.hp1 others(34): Show |
intron_variant | MODIFIER | c.253+1268G>A | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 4/13 | chr17 | 12718689 | |||||||
chr17:12718706 | G | A | 1 | a0001c0001t0152g0120 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.253+1285G>A | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 4/13 | chr17 | 12718706 | |||||||
chr17:12718709 | A | G | 37 | a0001c0001t0002g0241 a0001c0001t0002g0242 a0001c0001t0002g0244 others(34): Show |
37 | HG00423.hp1 HG00741.hp1 HG01106.hp1 others(34): Show |
intron_variant | MODIFIER | c.253+1288A>G | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 4/13 | chr17 | 12718709 | |||||||
chr17:12718741 | C | CAG | 43 | a0001c0001t0001g0343 a0001c0001t0002g0241 a0001c0001t0002g0242 others(40): Show |
43 | HG00423.hp1 HG00741.hp1 HG01106.hp1 others(40): Show |
intron_variant | MODIFIER | c.253+1322_253+1323d others(4): Show |
MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr17 | 12718741 | ||||||
chr17:12718764 | G | A | 37 | a0001c0001t0002g0241 a0001c0001t0002g0242 a0001c0001t0002g0244 others(34): Show |
37 | HG00423.hp1 HG00741.hp1 HG01106.hp1 others(34): Show |
intron_variant | MODIFIER | c.253+1343G>A | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 4/13 | chr17 | 12718764 | |||||||
chr17:12718896 | G | A | 5 | a0001c0001t0011g0224 a0001c0001t0011g0229 a0001c0001t0011g0230 others(2): Show |
5 | HG02559.hp2 HG02622.hp2 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.253+1475G>A | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 4/13 | chr17 | 12718896 | |||||||
chr17:12718998 | AC | A | 4 | a0001c0001t0014g0338 a0001c0003t0180g0304 a0003c0008t0071g0305 others(1): Show |
4 | HG01243.hp1 HG01884.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.253+1581delC | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr17 | 12718998 | ||||||
chr17:12719138 | G | A | 40 | a0001c0001t0002g0018 a0001c0001t0002g0119 a0001c0001t0002g0241 others(37): Show |
40 | HG00280.hp2 HG00423.hp1 HG00741.hp1 others(37): Show |
intron_variant | MODIFIER | c.253+1717G>A | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 4/13 | chr17 | 12719138 | |||||||
chr17:12719171 | T | C | 7 | a0001c0001t0013g0259 a0001c0001t0013g0273 a0001c0001t0018g0033 others(4): Show |
8 | HG01192.hp1 HG01891.hp2 HG02109.hp1 others(5): Show |
intron_variant | MODIFIER | c.253+1750T>C | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 4/13 | chr17 | 12719171 | |||||||
chr17:12719174 | C | CA | 46 | a0001c0001t0001g0028 a0001c0001t0001g0177 a0001c0001t0002g0244 others(43): Show |
46 | HG00423.hp1 HG00597.hp2 HG00741.hp1 others(43): Show |
intron_variant | MODIFIER | c.253+1783dupA | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr17 | 12719174 | ||||||
chr17:12719174 | C | CAA | 7 | a0001c0001t0033g0333 a0001c0001t0040g0256 a0001c0001t0092g0311 others(4): Show |
8 | HG01358.hp2 HG02145.hp1 HG02451.hp1 others(5): Show |
intron_variant | MODIFIER | c.253+1782_253+1783d others(4): Show |
MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr17 | 12719174 | ||||||
chr17:12719174 | C | CAAAAAAA others(3): Show |
20 | a0001c0001t0001g0161 a0001c0001t0003g0188 a0001c0001t0004g0164 others(17): Show |
20 | HG01109.hp1 HG01346.hp1 HG02004.hp2 others(17): Show |
intron_variant | MODIFIER | c.253+1774_253+1783d others(12): Show |
MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr17 | 12719174 | ||||||
chr17:12719174 | C | CAAAAAAA others(4): Show |
16 | a0001c0001t0014g0007 a0001c0001t0041g0011 a0001c0001t0048g0196 others(13): Show |
16 | HG00408.hp1 HG00735.hp2 HG01515.hp1 others(13): Show |
intron_variant | MODIFIER | c.253+1773_253+1783d others(13): Show |
MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr17 | 12719174 | ||||||
chr17:12719174 | C | CAAAAAAA others(5): Show |
8 | a0001c0001t0003g0201 a0001c0001t0134g0215 a0001c0001t0135g0056 others(5): Show |
8 | HG00639.hp2 HG00738.hp1 HG01081.hp1 others(5): Show |
intron_variant | MODIFIER | c.253+1772_253+1783d others(14): Show |
MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr17 | 12719174 | ||||||
chr17:12719174 | C | CAAAAAAA others(6): Show |
4 | a0001c0001t0001g0181 a0001c0001t0004g0221 a0001c0001t0186g0214 others(1): Show |
4 | HG01261.hp2 HG01496.hp1 NA18612.hp1 others(1): Show |
intron_variant | MODIFIER | c.253+1771_253+1783d others(15): Show |
MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr17 | 12719174 | ||||||
chr17:12719174 | C | CAAAAAAA others(7): Show |
2 | a0001c0001t0010g0183 a0001c0001t0159g0184 |
2 | HG03017.hp2 HG03704.hp2 |
intron_variant | MODIFIER | c.253+1770_253+1783d others(16): Show |
MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr17 | 12719174 | ||||||
chr17:12719174 | C | CAAAAAAA others(8): Show |
1 | a0001c0001t0007g0195 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.253+1769_253+1783d others(17): Show |
MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr17 | 12719174 | ||||||
chr17:12719174 | C | CAAAAAAA others(10): Show |
1 | a0001c0002t0191g0110 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.253+1767_253+1783d others(19): Show |
MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr17 | 12719174 | ||||||
chr17:12719174 | C | CAAAAAAA others(11): Show |
1 | a0001c0001t0005g0091 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.253+1766_253+1783d others(20): Show |
MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr17 | 12719174 | ||||||
chr17:12719174 | CA | C | 60 | a0001c0001t0001g0079 a0001c0001t0001g0086 a0001c0001t0001g0089 others(57): Show |
60 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(57): Show |
intron_variant | MODIFIER | c.253+1783delA | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr17 | 12719174 | ||||||
chr17:12719174 | CAA | C | 9 | a0001c0001t0002g0119 a0001c0001t0003g0212 a0001c0001t0005g0127 others(6): Show |
9 | HG01433.hp1 HG01515.hp2 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.253+1782_253+1783d others(4): Show |
MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr17 | 12719174 | ||||||
chr17:12719174 | CAAAAAAA others(3): Show |
C | 2 | a0001c0001t0045g0066 a0018c0026t0027g0017 |
2 | HG01433.hp2 NA18977.hp1 |
intron_variant | MODIFIER | c.253+1774_253+1783d others(12): Show |
MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr17 | 12719174 | ||||||
chr17:12719174 | CAAAAAAA others(4): Show |
C | 29 | a0001c0001t0001g0069 a0001c0001t0001g0077 a0001c0001t0001g0104 others(26): Show |
29 | HG00280.hp1 HG00408.hp2 HG00423.hp2 others(26): Show |
intron_variant | MODIFIER | c.253+1773_253+1783d others(13): Show |
MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr17 | 12719174 | ||||||
chr17:12719174 | CAAAAAAA others(5): Show |
C | 1 | a0001c0001t0173g0070 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.253+1772_253+1783d others(14): Show |
MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr17 | 12719174 | ||||||
chr17:12719627 | C | T | 1 | a0007c0022t0176g0279 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.253+2206C>T | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 4/13 | chr17 | 12719627 | |||||||
chr17:12719698 | C | CA | 38 | a0001c0001t0001g0181 a0001c0001t0010g0183 a0001c0001t0013g0259 others(35): Show |
41 | HG00639.hp1 HG00738.hp1 HG00738.hp2 others(38): Show |
intron_variant | MODIFIER | c.253+2296dupA | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr17 | 12719698 | ||||||
chr17:12719698 | C | CAA | 146 | a0001c0001t0001g0058 a0001c0001t0001g0069 a0001c0001t0001g0077 others(143): Show |
146 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(143): Show |
intron_variant | MODIFIER | c.253+2295_253+2296d others(4): Show |
MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr17 | 12719698 | ||||||
chr17:12719698 | C | CAAA | 23 | a0001c0001t0001g0079 a0001c0001t0007g0163 a0001c0001t0010g0074 others(20): Show |
23 | HG00423.hp2 HG00558.hp1 HG00735.hp2 others(20): Show |
intron_variant | MODIFIER | c.253+2294_253+2296d others(5): Show |
MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr17 | 12719698 | ||||||
chr17:12719743 | T | A | 121 | a0001c0001t0001g0058 a0001c0001t0001g0069 a0001c0001t0001g0077 others(118): Show |
121 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(118): Show |
intron_variant | MODIFIER | c.253+2322T>A | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 4/13 | chr17 | 12719743 | |||||||
chr17:12719867 | C | CA | 118 | a0001c0001t0001g0058 a0001c0001t0001g0077 a0001c0001t0001g0079 others(115): Show |
118 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(115): Show |
intron_variant | MODIFIER | c.253+2467dupA | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr17 | 12719867 | ||||||
chr17:12719867 | C | CAA | 11 | a0001c0001t0002g0090 a0001c0001t0002g0157 a0001c0001t0005g0199 others(8): Show |
11 | HG01175.hp2 HG02055.hp1 HG02155.hp1 others(8): Show |
intron_variant | MODIFIER | c.253+2466_253+2467d others(4): Show |
MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr17 | 12719867 | ||||||
chr17:12719867 | CA | C | 21 | a0001c0001t0001g0261 a0001c0001t0008g0173 a0001c0001t0013g0259 others(18): Show |
23 | HG01109.hp2 HG01192.hp1 HG01243.hp2 others(20): Show |
intron_variant | MODIFIER | c.253+2467delA | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr17 | 12719867 | ||||||
chr17:12719889 | T | A | 1 | a0001c0003t0203g0281 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.253+2468T>A | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 4/13 | chr17 | 12719889 | |||||||
chr17:12719996 | G | C | 1 | a0001c0001t0001g0343 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.253+2575G>C | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 4/13 | chr17 | 12719996 | |||||||
chr17:12720161 | G | A | 1 | a0001c0003t0205g0332 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.254-2686G>A | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 4/13 | chr17 | 12720161 | |||||||
chr17:12720212 | A | G | 1 | a0001c0001t0001g0343 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.254-2635A>G | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 4/13 | chr17 | 12720212 | |||||||
chr17:12720333 | G | T | 15 | a0001c0001t0001g0155 a0001c0001t0006g0140 a0001c0001t0017g0153 others(12): Show |
15 | HG01934.hp1 HG02602.hp1 HG03225.hp2 others(12): Show |
intron_variant | MODIFIER | c.254-2514G>T | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 4/13 | chr17 | 12720333 | |||||||
chr17:12720397 | T | C | 1 | a0001c0001t0060g0320 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.254-2450T>C | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 4/13 | chr17 | 12720397 | |||||||
chr17:12720761 | C | T | 6 | a0001c0001t0013g0259 a0001c0001t0013g0273 a0001c0001t0018g0033 others(3): Show |
7 | HG01192.hp1 HG01891.hp2 HG02109.hp1 others(4): Show |
intron_variant | MODIFIER | c.254-2086C>T | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 4/13 | chr17 | 12720761 | |||||||
chr17:12720788 | C | T | 1 | a0001c0001t0002g0090 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.254-2059C>T | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 4/13 | chr17 | 12720788 | |||||||
chr17:12720794 | G | A | 1 | a0001c0001t0002g0018 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.254-2053G>A | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 4/13 | chr17 | 12720794 | |||||||
chr17:12720839 | A | G | 37 | a0001c0001t0001g0343 a0001c0001t0002g0241 a0001c0001t0002g0242 others(34): Show |
38 | HG00423.hp1 HG00741.hp1 HG01106.hp1 others(35): Show |
intron_variant | MODIFIER | c.254-2008A>G | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 4/13 | chr17 | 12720839 | |||||||
chr17:12720914 | C | T | 3 | a0001c0001t0001g0261 a0001c0001t0068g0324 a0001c0001t0169g0263 |
3 | HG01256.hp2 HG03490.hp1 HG03491.hp2 |
intron_variant | MODIFIER | c.254-1933C>T | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 4/13 | chr17 | 12720914 | |||||||
chr17:12721021 | T | TA | 31 | a0001c0001t0001g0104 a0001c0001t0001g0136 a0001c0001t0001g0261 others(28): Show |
31 | HG01109.hp2 HG01256.hp2 HG01981.hp1 others(28): Show |
intron_variant | MODIFIER | c.254-1804dupA | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr17 | 12721021 | ||||||
chr17:12721021 | T | TAA | 32 | a0001c0001t0002g0241 a0001c0001t0002g0242 a0001c0001t0003g0093 others(29): Show |
32 | HG00423.hp1 HG00741.hp1 HG01106.hp1 others(29): Show |
intron_variant | MODIFIER | c.254-1805_254-1804d others(4): Show |
MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr17 | 12721021 | ||||||
chr17:12721021 | TA | T | 9 | a0001c0001t0001g0343 a0001c0001t0003g0201 a0001c0001t0004g0221 others(6): Show |
9 | HG01081.hp1 HG01515.hp2 HG01934.hp1 others(6): Show |
intron_variant | MODIFIER | c.254-1804delA | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr17 | 12721021 | ||||||
chr17:12721080 | A | AT | 6 | a0001c0001t0027g0297 a0001c0001t0195g0284 a0001c0002t0190g0290 others(3): Show |
6 | HG00544.hp2 HG02027.hp2 HG02056.hp2 others(3): Show |
intron_variant | MODIFIER | c.254-1758dupT | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr17 | 12721080 | ||||||
chr17:12721284 | G | A | 1 | a0001c0001t0155g0172 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.254-1563G>A | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 4/13 | chr17 | 12721284 | |||||||
chr17:12721532 | TAAGCC | T | 7 | a0001c0001t0005g0091 a0001c0001t0044g0012 a0001c0001t0139g0013 others(4): Show |
7 | HG00639.hp1 HG01515.hp1 HG02683.hp2 others(4): Show |
intron_variant | MODIFIER | c.254-1311_254-1307d others(7): Show |
MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr17 | 12721532 | ||||||
chr17:12722250 | A | G | 32 | a0001c0001t0002g0241 a0001c0001t0002g0242 a0001c0001t0003g0093 others(29): Show |
32 | HG00423.hp1 HG00741.hp1 HG01106.hp1 others(29): Show |
intron_variant | MODIFIER | c.254-597A>G | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 4/13 | chr17 | 12722250 | |||||||
chr17:12722261 | C | T | 32 | a0001c0001t0002g0241 a0001c0001t0002g0242 a0001c0001t0003g0093 others(29): Show |
32 | HG00423.hp1 HG00741.hp1 HG01106.hp1 others(29): Show |
intron_variant | MODIFIER | c.254-586C>T | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 4/13 | chr17 | 12722261 | |||||||
chr17:12722609 | G | A | 46 | a0001c0001t0001g0261 a0001c0001t0001g0343 a0001c0001t0002g0241 others(43): Show |
46 | HG00423.hp1 HG00741.hp1 HG01106.hp1 others(43): Show |
intron_variant | MODIFIER | c.254-238G>A | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 4/13 | chr17 | 12722609 | |||||||
chr17:12722788 | A | G | 1 | a0001c0001t0147g0237 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.254-59A>G | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 4/13 | chr17 | 12722788 | |||||||
chr17:12723077 | A | G | 1 | a0001c0001t0001g0343 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.415+69A>G | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 5/13 | chr17 | 12723077 | |||||||
chr17:12723278 | C | T | 1 | a0001c0001t0006g0174 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.415+270C>T | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 5/13 | chr17 | 12723278 | |||||||
chr17:12723297 | C | T | 2 | a0001c0001t0001g0176 a0001c0001t0001g0177 |
2 | HG01081.hp2 HG01346.hp2 |
intron_variant | MODIFIER | c.415+289C>T | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 5/13 | chr17 | 12723297 | |||||||
chr17:12723453 | A | G | 1 | a0012c0029t0115g0335 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.415+445A>G | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 5/13 | chr17 | 12723453 | |||||||
chr17:12723464 | C | A | 32 | a0001c0001t0002g0241 a0001c0001t0002g0242 a0001c0001t0003g0093 others(29): Show |
32 | HG00423.hp1 HG00741.hp1 HG01106.hp1 others(29): Show |
intron_variant | MODIFIER | c.415+456C>A | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 5/13 | chr17 | 12723464 | |||||||
chr17:12723853 | G | T | 33 | a0001c0001t0001g0343 a0001c0001t0002g0241 a0001c0001t0002g0242 others(30): Show |
33 | HG00423.hp1 HG00741.hp1 HG01106.hp1 others(30): Show |
intron_variant | MODIFIER | c.415+845G>T | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 5/13 | chr17 | 12723853 | |||||||
chr17:12723881 | G | A | 1 | a0001c0001t0201g0334 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.415+873G>A | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 5/13 | chr17 | 12723881 | |||||||
chr17:12723920 | A | G | 1 | a0001c0003t0204g0038 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.415+912A>G | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 5/13 | chr17 | 12723920 | |||||||
chr17:12724102 | G | A | 4 | a0001c0001t0036g0257 a0001c0001t0075g0266 a0005c0010t0099g0265 others(1): Show |
4 | HG02109.hp2 HG02257.hp2 HG02451.hp2 others(1): Show |
intron_variant | MODIFIER | c.415+1094G>A | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 5/13 | chr17 | 12724102 | |||||||
chr17:12724179 | A | G | 1 | a0001c0001t0098g0080 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.415+1171A>G | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 5/13 | chr17 | 12724179 | |||||||
chr17:12724394 | G | T | 1 | a0001c0001t0096g0109 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.415+1386G>T | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 5/13 | chr17 | 12724394 | |||||||
chr17:12724423 | T | A | 1 | a0001c0001t0096g0109 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.415+1415T>A | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 5/13 | chr17 | 12724423 | |||||||
chr17:12724492 | T | A | 1 | a0001c0003t0049g0134 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.415+1484T>A | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 5/13 | chr17 | 12724492 | |||||||
chr17:12724541 | A | C | 1 | a0001c0001t0125g0341 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.415+1533A>C | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 5/13 | chr17 | 12724541 | |||||||
chr17:12724554 | A | G | 5 | a0001c0001t0011g0224 a0001c0001t0011g0229 a0001c0001t0011g0230 others(2): Show |
5 | HG02559.hp2 HG02622.hp2 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.415+1546A>G | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 5/13 | chr17 | 12724554 | |||||||
chr17:12724963 | G | T | 1 | a0001c0003t0077g0285 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.415+1955G>T | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 5/13 | chr17 | 12724963 | |||||||
chr17:12725108 | C | T | 1 | a0001c0001t0005g0199 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.415+2100C>T | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 5/13 | chr17 | 12725108 | |||||||
chr17:12725169 | C | T | 46 | a0001c0001t0001g0343 a0001c0001t0002g0241 a0001c0001t0002g0242 others(43): Show |
47 | HG00423.hp1 HG00741.hp1 HG01106.hp1 others(44): Show |
intron_variant | MODIFIER | c.415+2161C>T | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 5/13 | chr17 | 12725169 | |||||||
chr17:12725243 | T | C | 3 | a0001c0001t0001g0261 a0001c0001t0068g0324 a0001c0001t0169g0263 |
3 | HG01256.hp2 HG03490.hp1 HG03491.hp2 |
intron_variant | MODIFIER | c.415+2235T>C | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 5/13 | chr17 | 12725243 | |||||||
chr17:12725368 | T | C | 32 | a0001c0001t0002g0241 a0001c0001t0002g0242 a0001c0001t0003g0093 others(29): Show |
32 | HG00423.hp1 HG00741.hp1 HG01106.hp1 others(29): Show |
intron_variant | MODIFIER | c.415+2360T>C | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 5/13 | chr17 | 12725368 | |||||||
chr17:12725413 | T | C | 10 | a0001c0001t0002g0241 a0001c0001t0002g0242 a0001c0001t0148g0247 others(7): Show |
10 | HG00741.hp1 HG01106.hp1 HG01978.hp1 others(7): Show |
intron_variant | MODIFIER | c.415+2405T>C | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 5/13 | chr17 | 12725413 | |||||||
chr17:12725533 | A | G | 1 | a0001c0001t0001g0343 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.415+2525A>G | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 5/13 | chr17 | 12725533 | |||||||
chr17:12725590 | A | G | 1 | a0011c0030t0114g0262 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.415+2582A>G | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 5/13 | chr17 | 12725590 | |||||||
chr17:12725602 | T | A | 32 | a0001c0001t0002g0241 a0001c0001t0002g0242 a0001c0001t0003g0093 others(29): Show |
32 | HG00423.hp1 HG00741.hp1 HG01106.hp1 others(29): Show |
intron_variant | MODIFIER | c.415+2594T>A | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 5/13 | chr17 | 12725602 | |||||||
chr17:12725635 | T | C | 1 | a0001c0001t0066g0327 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.415+2627T>C | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 5/13 | chr17 | 12725635 | |||||||
chr17:12725716 | G | A | 32 | a0001c0001t0002g0241 a0001c0001t0002g0242 a0001c0001t0003g0093 others(29): Show |
32 | HG00423.hp1 HG00741.hp1 HG01106.hp1 others(29): Show |
intron_variant | MODIFIER | c.415+2708G>A | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 5/13 | chr17 | 12725716 | |||||||
chr17:12725766 | G | A | 1 | a0001c0001t0156g0269 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.415+2758G>A | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 5/13 | chr17 | 12725766 | |||||||
chr17:12725868 | G | T | 10 | a0001c0001t0011g0224 a0001c0001t0011g0229 a0001c0001t0011g0230 others(7): Show |
10 | HG02145.hp2 HG02559.hp2 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.415+2860G>T | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 5/13 | chr17 | 12725868 | |||||||
chr17:12725923 | A | G | 1 | a0002c0005t0102g0160 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.415+2915A>G | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 5/13 | chr17 | 12725923 | |||||||
chr17:12726047 | A | G | 1 | a0001c0001t0169g0263 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.415+3039A>G | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 5/13 | chr17 | 12726047 | |||||||
chr17:12726679 | A | ATGT | 33 | a0001c0001t0001g0343 a0001c0001t0002g0241 a0001c0001t0002g0242 others(30): Show |
33 | HG00423.hp1 HG00741.hp1 HG01106.hp1 others(30): Show |
intron_variant | MODIFIER | c.415+3676_415+3678d others(5): Show |
MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr17 | 12726679 | ||||||
chr17:12726832 | A | G | 1 | a0001c0001t0001g0343 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.415+3824A>G | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 5/13 | chr17 | 12726832 | |||||||
chr17:12727010 | G | A | 1 | a0001c0001t0001g0343 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.415+4002G>A | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 5/13 | chr17 | 12727010 | |||||||
chr17:12727132 | G | A | 1 | a0001c0003t0180g0304 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.415+4124G>A | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 5/13 | chr17 | 12727132 | |||||||
chr17:12727322 | T | C | 1 | a0001c0001t0002g0018 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.415+4314T>C | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 5/13 | chr17 | 12727322 | |||||||
chr17:12727565 | T | C | 1 | a0001c0003t0205g0332 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.415+4557T>C | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 5/13 | chr17 | 12727565 | |||||||
chr17:12727952 | A | G | 8 | a0001c0001t0011g0224 a0001c0001t0011g0229 a0001c0001t0011g0230 others(5): Show |
8 | HG02559.hp2 HG02622.hp2 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.415+4944A>G | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 5/13 | chr17 | 12727952 | |||||||
chr17:12728041 | G | A | 1 | a0001c0001t0004g0221 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.415+5033G>A | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 5/13 | chr17 | 12728041 | |||||||
chr17:12728091 | T | C | 1 | a0001c0001t0156g0269 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.415+5083T>C | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 5/13 | chr17 | 12728091 | |||||||
chr17:12728172 | G | A | 5 | a0001c0001t0001g0261 a0001c0001t0068g0324 a0001c0001t0156g0269 others(2): Show |
5 | HG01256.hp2 HG02630.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.415+5164G>A | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 5/13 | chr17 | 12728172 | |||||||
chr17:12728234 | A | T | 1 | a0001c0001t0036g0257 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.415+5226A>T | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 5/13 | chr17 | 12728234 | |||||||
chr17:12728272 | C | T | 1 | a0001c0001t0141g0015 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.415+5264C>T | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 5/13 | chr17 | 12728272 | |||||||
chr17:12728502 | A | T | 28 | a0001c0001t0001g0028 a0001c0001t0002g0244 a0001c0001t0006g0098 others(25): Show |
28 | HG00408.hp1 HG00544.hp2 HG00609.hp2 others(25): Show |
intron_variant | MODIFIER | c.415+5494A>T | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 5/13 | chr17 | 12728502 | |||||||
chr17:12728510 | G | A | 10 | a0001c0001t0011g0224 a0001c0001t0011g0229 a0001c0001t0011g0230 others(7): Show |
10 | HG02559.hp2 HG02622.hp2 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.415+5502G>A | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 5/13 | chr17 | 12728510 | |||||||
chr17:12728668 | G | T | 1 | a0001c0001t0156g0269 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.415+5660G>T | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 5/13 | chr17 | 12728668 | |||||||
chr17:12728768 | C | T | 1 | a0001c0003t0112g0035 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.415+5760C>T | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 5/13 | chr17 | 12728768 | |||||||
chr17:12728769 | G | A | 1 | a0001c0001t0001g0177 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.415+5761G>A | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 5/13 | chr17 | 12728769 | |||||||
chr17:12728800 | C | T | 1 | a0001c0002t0004g0248 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.415+5792C>T | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 5/13 | chr17 | 12728800 | |||||||
chr17:12728807 | T | A | 1 | a0001c0001t0080g0291 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.415+5799T>A | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 5/13 | chr17 | 12728807 | |||||||
chr17:12728808 | A | T | 1 | a0001c0001t0080g0291 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.415+5800A>T | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 5/13 | chr17 | 12728808 | |||||||
chr17:12728937 | T | A | 1 | a0001c0001t0001g0343 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.415+5929T>A | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 5/13 | chr17 | 12728937 | |||||||
chr17:12729252 | C | T | 1 | a0001c0001t0096g0109 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.415+6244C>T | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 5/13 | chr17 | 12729252 | |||||||
chr17:12729399 | C | T | 1 | a0001c0001t0009g0328 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.415+6391C>T | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 5/13 | chr17 | 12729399 | |||||||
chr17:12729791 | C | T | 4 | a0001c0001t0001g0261 a0001c0001t0068g0324 a0001c0001t0156g0269 others(1): Show |
4 | HG01256.hp2 HG02630.hp2 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.416-6370C>T | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 5/13 | chr17 | 12729791 | |||||||
chr17:12729817 | G | A | 1 | a0016c0021t0175g0087 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.416-6344G>A | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 5/13 | chr17 | 12729817 | |||||||
chr17:12730198 | A | G | 1 | a0001c0001t0061g0318 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.416-5963A>G | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 5/13 | chr17 | 12730198 | |||||||
chr17:12730246 | C | G | 1 | a0001c0001t0138g0133 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.416-5915C>G | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 5/13 | chr17 | 12730246 | |||||||
chr17:12730250 | A | G | 6 | a0001c0001t0001g0261 a0001c0001t0068g0324 a0001c0001t0125g0341 others(3): Show |
6 | HG01256.hp2 HG02630.hp2 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.416-5911A>G | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 5/13 | chr17 | 12730250 | |||||||
chr17:12730264 | C | T | 4 | a0001c0001t0048g0196 a0001c0001t0084g0194 a0001c0001t0126g0062 others(1): Show |
4 | HG02135.hp2 NA18941.hp2 NA18951.hp2 others(1): Show |
intron_variant | MODIFIER | c.416-5897C>T | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 5/13 | chr17 | 12730264 | |||||||
chr17:12730406 | T | C | 43 | a0001c0001t0001g0261 a0001c0001t0001g0343 a0001c0001t0002g0241 others(40): Show |
44 | HG00423.hp1 HG00741.hp1 HG01106.hp1 others(41): Show |
intron_variant | MODIFIER | c.416-5755T>C | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 5/13 | chr17 | 12730406 | |||||||
chr17:12730446 | C | CA | 11 | a0001c0001t0001g0136 a0001c0001t0030g0301 a0001c0001t0038g0024 others(8): Show |
11 | HG01175.hp1 HG01891.hp1 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.416-5698dupA | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr17 | 12730446 | ||||||
chr17:12730446 | CA | C | 42 | a0001c0001t0002g0241 a0001c0001t0002g0242 a0001c0001t0004g0044 others(39): Show |
43 | HG00423.hp1 HG00741.hp1 HG01106.hp1 others(40): Show |
intron_variant | MODIFIER | c.416-5698delA | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr17 | 12730446 | ||||||
chr17:12730573 | G | A | 1 | a0001c0001t0151g0182 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.416-5588G>A | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 5/13 | chr17 | 12730573 | |||||||
chr17:12730832 | A | G | 1 | a0001c0001t0158g0125 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.416-5329A>G | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 5/13 | chr17 | 12730832 | |||||||
chr17:12730833 | T | C | 71 | a0001c0001t0001g0343 a0001c0001t0002g0244 a0001c0001t0006g0098 others(68): Show |
73 | HG00408.hp1 HG00544.hp2 HG00609.hp2 others(70): Show |
intron_variant | MODIFIER | c.416-5328T>C | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 5/13 | chr17 | 12730833 | |||||||
chr17:12730986 | G | A | 1 | a0001c0001t0001g0343 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.416-5175G>A | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 5/13 | chr17 | 12730986 | |||||||
chr17:12731005 | C | A | 1 | a0001c0001t0001g0343 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.416-5156C>A | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 5/13 | chr17 | 12731005 | |||||||
chr17:12731035 | C | T | 3 | a0001c0002t0002g0239 a0001c0002t0004g0240 a0001c0002t0004g0248 |
3 | HG02523.hp2 NA18747.hp2 NA18971.hp2 |
intron_variant | MODIFIER | c.416-5126C>T | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 5/13 | chr17 | 12731035 | |||||||
chr17:12731104 | C | T | 2 | a0001c0001t0001g0343 a0001c0001t0002g0090 |
2 | HG01175.hp2 HG03688.hp2 |
intron_variant | MODIFIER | c.416-5057C>T | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 5/13 | chr17 | 12731104 | |||||||
chr17:12731123 | A | G | 1 | a0001c0002t0193g0123 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.416-5038A>G | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 5/13 | chr17 | 12731123 | |||||||
chr17:12731136 | C | T | 1 | a0001c0001t0004g0278 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.416-5025C>T | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 5/13 | chr17 | 12731136 | |||||||
chr17:12731315 | T | C | 1 | a0001c0001t0107g0041 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.416-4846T>C | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 5/13 | chr17 | 12731315 | |||||||
chr17:12731376 | C | T | 4 | a0001c0001t0003g0212 a0001c0001t0005g0085 a0001c0001t0035g0129 others(1): Show |
4 | HG01433.hp1 HG02004.hp1 HG02027.hp1 others(1): Show |
intron_variant | MODIFIER | c.416-4785C>T | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 5/13 | chr17 | 12731376 | |||||||
chr17:12731474 | A | T | 23 | a0001c0001t0004g0044 a0001c0001t0008g0052 a0001c0001t0039g0178 others(20): Show |
23 | HG00741.hp1 HG01106.hp1 HG01257.hp2 others(20): Show |
intron_variant | MODIFIER | c.416-4687A>T | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 5/13 | chr17 | 12731474 | |||||||
chr17:12731563 | G | A | 1 | a0001c0001t0128g0168 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.416-4598G>A | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 5/13 | chr17 | 12731563 | |||||||
chr17:12731732 | G | A | 12 | a0001c0001t0013g0259 a0001c0001t0013g0273 a0001c0001t0018g0033 others(9): Show |
12 | HG01175.hp1 HG01192.hp1 HG01256.hp2 others(9): Show |
intron_variant | MODIFIER | c.416-4429G>A | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 5/13 | chr17 | 12731732 | |||||||
chr17:12731740 | A | T | 3 | a0001c0003t0180g0304 a0003c0008t0071g0305 a0003c0008t0111g0303 |
3 | HG01884.hp2 HG03579.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.416-4421A>T | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 5/13 | chr17 | 12731740 | |||||||
chr17:12731746 | G | A | 3 | a0001c0001t0017g0153 a0001c0001t0048g0158 a0001c0001t0082g0026 |
3 | NA18978.hp1 NA19000.hp1 NA19065.hp1 |
intron_variant | MODIFIER | c.416-4415G>A | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 5/13 | chr17 | 12731746 | |||||||
chr17:12731771 | G | C | 196 | a0001c0001t0001g0028 a0001c0001t0001g0051 a0001c0001t0001g0058 others(193): Show |
198 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(195): Show |
intron_variant | MODIFIER | c.416-4390G>C | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 5/13 | chr17 | 12731771 | |||||||
chr17:12731898 | C | G | 222 | a0001c0001t0001g0028 a0001c0001t0001g0051 a0001c0001t0001g0058 others(219): Show |
224 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(221): Show |
intron_variant | MODIFIER | c.416-4263C>G | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 5/13 | chr17 | 12731898 | |||||||
chr17:12732089 | G | A | 1 | a0001c0001t0034g0146 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.416-4072G>A | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 5/13 | chr17 | 12732089 | |||||||
chr17:12732149 | C | T | 1 | a0001c0003t0203g0281 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.416-4012C>T | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 5/13 | chr17 | 12732149 | |||||||
chr17:12732243 | G | T | 1 | a0001c0001t0018g0042 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.416-3918G>T | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 5/13 | chr17 | 12732243 | |||||||
chr17:12732332 | C | G | 2 | a0001c0006t0050g0006 a0003c0008t0104g0021 |
2 | HG03453.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.416-3829C>G | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 5/13 | chr17 | 12732332 | |||||||
chr17:12732339 | A | G | 23 | a0001c0001t0004g0044 a0001c0001t0008g0052 a0001c0001t0039g0178 others(20): Show |
23 | HG00741.hp1 HG01106.hp1 HG01257.hp2 others(20): Show |
intron_variant | MODIFIER | c.416-3822A>G | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 5/13 | chr17 | 12732339 | |||||||
chr17:12732364 | G | A | 25 | a0001c0001t0014g0338 a0001c0001t0030g0301 a0001c0001t0033g0034 others(22): Show |
25 | HG01243.hp1 HG01884.hp1 HG01884.hp2 others(22): Show |
intron_variant | MODIFIER | c.416-3797G>A | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 5/13 | chr17 | 12732364 | |||||||
chr17:12732383 | C | A | 36 | a0001c0001t0001g0155 a0001c0001t0003g0116 a0001c0001t0003g0188 others(33): Show |
38 | HG00597.hp2 HG02056.hp1 HG02451.hp1 others(35): Show |
intron_variant | MODIFIER | c.416-3778C>A | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 5/13 | chr17 | 12732383 | |||||||
chr17:12732431 | C | A | 1 | a0001c0002t0006g0287 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.416-3730C>A | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 5/13 | chr17 | 12732431 | |||||||
chr17:12732443 | G | C | 1 | a0016c0021t0175g0087 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.416-3718G>C | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 5/13 | chr17 | 12732443 | |||||||
chr17:12732464 | C | T | 2 | a0001c0001t0001g0028 a0001c0001t0154g0027 |
2 | NA18977.hp2 NA18981.hp1 |
intron_variant | MODIFIER | c.416-3697C>T | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 5/13 | chr17 | 12732464 | |||||||
chr17:12732554 | A | G | 39 | a0001c0001t0001g0261 a0001c0001t0001g0343 a0001c0001t0002g0187 others(36): Show |
39 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(36): Show |
intron_variant | MODIFIER | c.416-3607A>G | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 5/13 | chr17 | 12732554 | |||||||
chr17:12732560 | T | G | 23 | a0001c0001t0004g0044 a0001c0001t0008g0052 a0001c0001t0039g0178 others(20): Show |
23 | HG00741.hp1 HG01106.hp1 HG01257.hp2 others(20): Show |
intron_variant | MODIFIER | c.416-3601T>G | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 5/13 | chr17 | 12732560 | |||||||
chr17:12732591 | C | T | 1 | a0001c0001t0005g0199 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.416-3570C>T | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 5/13 | chr17 | 12732591 | |||||||
chr17:12732665 | T | C | 339 | a0001c0001t0001g0028 a0001c0001t0001g0051 a0001c0001t0001g0058 others(336): Show |
342 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(339): Show |
intron_variant | MODIFIER | c.416-3496T>C | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 5/13 | chr17 | 12732665 | |||||||
chr17:12732830 | C | A | 1 | a0001c0003t0205g0332 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.416-3331C>A | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 5/13 | chr17 | 12732830 | |||||||
chr17:12732837 | G | C | 191 | a0001c0001t0001g0028 a0001c0001t0001g0058 a0001c0001t0001g0079 others(188): Show |
193 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(190): Show |
intron_variant | MODIFIER | c.416-3324G>C | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 5/13 | chr17 | 12732837 | |||||||
chr17:12732838 | C | A | 1 | a0001c0001t0029g0171 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.416-3323C>A | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 5/13 | chr17 | 12732838 | |||||||
chr17:12732847 | T | G | 1 | a0001c0003t0077g0285 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.416-3314T>G | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 5/13 | chr17 | 12732847 | |||||||
chr17:12733053 | A | G | 210 | a0001c0001t0001g0028 a0001c0001t0001g0058 a0001c0001t0001g0069 others(207): Show |
212 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(209): Show |
intron_variant | MODIFIER | c.416-3108A>G | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 5/13 | chr17 | 12733053 | |||||||
chr17:12733062 | G | C | 1 | a0001c0001t0004g0082 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.416-3099G>C | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 5/13 | chr17 | 12733062 | |||||||
chr17:12733078 | C | T | 7 | a0001c0001t0003g0093 a0001c0001t0005g0095 a0001c0001t0005g0232 others(4): Show |
7 | HG01952.hp2 HG02273.hp2 HG02293.hp2 others(4): Show |
intron_variant | MODIFIER | c.416-3083C>T | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 5/13 | chr17 | 12733078 | |||||||
chr17:12733161 | T | C | 4 | a0001c0001t0011g0224 a0001c0001t0011g0229 a0001c0001t0011g0230 others(1): Show |
4 | HG02559.hp2 HG02622.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.416-3000T>C | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 5/13 | chr17 | 12733161 | |||||||
chr17:12733179 | A | G | 210 | a0001c0001t0001g0028 a0001c0001t0001g0058 a0001c0001t0001g0069 others(207): Show |
212 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(209): Show |
intron_variant | MODIFIER | c.416-2982A>G | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 5/13 | chr17 | 12733179 | |||||||
chr17:12733258 | C | T | 4 | a0001c0001t0011g0224 a0001c0001t0011g0229 a0001c0001t0011g0230 others(1): Show |
4 | HG02559.hp2 HG02622.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.416-2903C>T | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 5/13 | chr17 | 12733258 | |||||||
chr17:12733290 | A | C | 1 | a0002c0005t0185g0277 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.416-2871A>C | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 5/13 | chr17 | 12733290 | |||||||
chr17:12733293 | G | C | 190 | a0001c0001t0001g0028 a0001c0001t0001g0058 a0001c0001t0001g0079 others(187): Show |
192 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(189): Show |
intron_variant | MODIFIER | c.416-2868G>C | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 5/13 | chr17 | 12733293 | |||||||
chr17:12733309 | C | CA | 26 | a0001c0001t0001g0051 a0001c0001t0001g0136 a0001c0001t0001g0176 others(23): Show |
27 | HG00642.hp1 HG00735.hp1 HG00738.hp2 others(24): Show |
intron_variant | MODIFIER | c.416-2839dupA | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr17 | 12733309 | ||||||
chr17:12733309 | C | CAAA | 89 | a0001c0001t0001g0069 a0001c0001t0001g0077 a0001c0001t0001g0155 others(86): Show |
91 | HG00423.hp2 HG00597.hp2 HG00741.hp1 others(88): Show |
intron_variant | MODIFIER | c.416-2841_416-2839d others(5): Show |
MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr17 | 12733309 | ||||||
chr17:12733309 | C | CAAAA | 112 | a0001c0001t0001g0028 a0001c0001t0001g0058 a0001c0001t0001g0079 others(109): Show |
112 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(109): Show |
intron_variant | MODIFIER | c.416-2842_416-2839d others(6): Show |
MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr17 | 12733309 | ||||||
chr17:12733309 | C | CAAAAA | 8 | a0001c0001t0004g0082 a0001c0001t0005g0199 a0001c0001t0015g0111 others(5): Show |
8 | HG00423.hp1 HG00597.hp1 HG01106.hp2 others(5): Show |
intron_variant | MODIFIER | c.416-2843_416-2839d others(7): Show |
MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr17 | 12733309 | ||||||
chr17:12733416 | C | T | 190 | a0001c0001t0001g0028 a0001c0001t0001g0058 a0001c0001t0001g0079 others(187): Show |
192 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(189): Show |
intron_variant | MODIFIER | c.416-2745C>T | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 5/13 | chr17 | 12733416 | |||||||
chr17:12733418 | T | C | 190 | a0001c0001t0001g0028 a0001c0001t0001g0058 a0001c0001t0001g0079 others(187): Show |
192 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(189): Show |
intron_variant | MODIFIER | c.416-2743T>C | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 5/13 | chr17 | 12733418 | |||||||
chr17:12733488 | G | C | 1 | a0001c0001t0037g0175 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.416-2673G>C | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 5/13 | chr17 | 12733488 | |||||||
chr17:12733605 | C | T | 26 | a0001c0001t0014g0338 a0001c0001t0030g0301 a0001c0001t0033g0034 others(23): Show |
26 | HG01243.hp1 HG01884.hp1 HG01884.hp2 others(23): Show |
intron_variant | MODIFIER | c.416-2556C>T | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 5/13 | chr17 | 12733605 | |||||||
chr17:12733606 | G | A | 5 | a0001c0001t0028g0002 a0001c0001t0117g0340 a0001c0001t0183g0040 others(2): Show |
6 | HG02572.hp2 HG03098.hp2 HG03139.hp2 others(3): Show |
intron_variant | MODIFIER | c.416-2555G>A | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 5/13 | chr17 | 12733606 | |||||||
chr17:12733865 | C | CG | 10 | a0001c0001t0006g0098 a0001c0001t0022g0286 a0001c0001t0026g0289 others(7): Show |
10 | HG00408.hp1 HG00423.hp1 HG00544.hp2 others(7): Show |
intron_variant | MODIFIER | c.416-2296_416-2295i others(3): Show |
MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 5/13 | chr17 | 12733865 | |||||||
chr17:12733874 | G | A | 191 | a0001c0001t0001g0028 a0001c0001t0001g0058 a0001c0001t0001g0077 others(188): Show |
193 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(190): Show |
intron_variant | MODIFIER | c.416-2287G>A | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 5/13 | chr17 | 12733874 | |||||||
chr17:12733881 | G | A | 191 | a0001c0001t0001g0028 a0001c0001t0001g0058 a0001c0001t0001g0077 others(188): Show |
193 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(190): Show |
intron_variant | MODIFIER | c.416-2280G>A | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 5/13 | chr17 | 12733881 | |||||||
chr17:12733885 | A | AAAG | 6 | a0001c0001t0001g0155 a0001c0001t0004g0278 a0001c0001t0037g0175 others(3): Show |
6 | HG02896.hp1 HG02897.hp2 HG03491.hp1 others(3): Show |
intron_variant | MODIFIER | c.416-2274_416-2273i others(5): Show |
MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr17 | 12733885 | ||||||
chr17:12733885 | A | AAG | 43 | a0001c0001t0001g0086 a0001c0001t0001g0089 a0001c0001t0002g0090 others(40): Show |
45 | HG00597.hp2 HG01175.hp2 HG01192.hp2 others(42): Show |
intron_variant | MODIFIER | c.416-2275_416-2274i others(4): Show |
MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr17 | 12733885 | ||||||
chr17:12733885 | A | AG | 110 | a0001c0001t0001g0028 a0001c0001t0001g0058 a0001c0001t0001g0077 others(107): Show |
110 | HG00280.hp2 HG00323.hp2 HG00544.hp1 others(107): Show |
intron_variant | MODIFIER | c.416-2276_416-2275i others(3): Show |
MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 5/13 | chr17 | 12733885 | |||||||
chr17:12733885 | A | G | 32 | a0001c0001t0004g0044 a0001c0001t0006g0098 a0001c0001t0008g0052 others(29): Show |
32 | HG00408.hp1 HG00423.hp1 HG00544.hp2 others(29): Show |
intron_variant | MODIFIER | c.416-2276A>G | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 5/13 | chr17 | 12733885 | |||||||
chr17:12734054 | T | G | 190 | a0001c0001t0001g0028 a0001c0001t0001g0058 a0001c0001t0001g0079 others(187): Show |
192 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(189): Show |
intron_variant | MODIFIER | c.416-2107T>G | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 5/13 | chr17 | 12734054 | |||||||
chr17:12734114 | T | TAGA | 210 | a0001c0001t0001g0028 a0001c0001t0001g0058 a0001c0001t0001g0069 others(207): Show |
212 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(209): Show |
intron_variant | MODIFIER | c.416-2046_416-2044d others(5): Show |
MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr17 | 12734114 | ||||||
chr17:12734120 | T | C | 37 | a0001c0001t0001g0155 a0001c0001t0003g0116 a0001c0001t0003g0188 others(34): Show |
39 | HG00597.hp2 HG02056.hp1 HG02451.hp1 others(36): Show |
intron_variant | MODIFIER | c.416-2041T>C | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 5/13 | chr17 | 12734120 | |||||||
chr17:12734285 | T | C | 193 | a0001c0001t0001g0028 a0001c0001t0001g0058 a0001c0001t0001g0077 others(190): Show |
195 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(192): Show |
intron_variant | MODIFIER | c.416-1876T>C | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 5/13 | chr17 | 12734285 | |||||||
chr17:12734379 | G | A | 23 | a0001c0001t0004g0044 a0001c0001t0008g0052 a0001c0001t0039g0178 others(20): Show |
23 | HG00741.hp1 HG01106.hp1 HG01257.hp2 others(20): Show |
intron_variant | MODIFIER | c.416-1782G>A | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 5/13 | chr17 | 12734379 | |||||||
chr17:12734409 | A | G | 210 | a0001c0001t0001g0028 a0001c0001t0001g0058 a0001c0001t0001g0069 others(207): Show |
212 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(209): Show |
intron_variant | MODIFIER | c.416-1752A>G | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 5/13 | chr17 | 12734409 | |||||||
chr17:12734411 | T | C | 1 | a0001c0003t0205g0332 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.416-1750T>C | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 5/13 | chr17 | 12734411 | |||||||
chr17:12734425 | G | C | 206 | a0001c0001t0001g0028 a0001c0001t0001g0058 a0001c0001t0001g0069 others(203): Show |
208 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(205): Show |
intron_variant | MODIFIER | c.416-1736G>C | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 5/13 | chr17 | 12734425 | |||||||
chr17:12734441 | CT | C | 4 | a0001c0001t0011g0224 a0001c0001t0011g0229 a0001c0001t0011g0230 others(1): Show |
4 | HG02559.hp2 HG02622.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.416-1719delT | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 5/13 | chr17 | 12734441 | |||||||
chr17:12734504 | C | CT | 12 | a0001c0001t0001g0104 a0001c0001t0001g0136 a0001c0001t0007g0163 others(9): Show |
12 | HG00642.hp1 HG00735.hp1 HG01175.hp1 others(9): Show |
intron_variant | MODIFIER | c.416-1633dupT | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr17 | 12734504 | ||||||
chr17:12734504 | C | CTT | 14 | a0001c0001t0011g0224 a0001c0001t0011g0229 a0001c0001t0011g0230 others(11): Show |
15 | HG02451.hp1 HG02559.hp2 HG02572.hp2 others(12): Show |
intron_variant | MODIFIER | c.416-1634_416-1633d others(4): Show |
MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr17 | 12734504 | ||||||
chr17:12734504 | C | CTTT | 28 | a0001c0001t0001g0155 a0001c0001t0003g0150 a0001c0001t0003g0188 others(25): Show |
29 | HG00597.hp2 HG02056.hp1 HG02129.hp2 others(26): Show |
intron_variant | MODIFIER | c.416-1635_416-1633d others(5): Show |
MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr17 | 12734504 | ||||||
chr17:12734504 | C | CTTTT | 123 | a0001c0001t0001g0028 a0001c0001t0001g0069 a0001c0001t0001g0077 others(120): Show |
123 | HG00280.hp2 HG00323.hp2 HG00423.hp2 others(120): Show |
intron_variant | MODIFIER | c.416-1636_416-1633d others(6): Show |
MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr17 | 12734504 | ||||||
chr17:12734504 | C | CTTTTT | 45 | a0001c0001t0001g0058 a0001c0001t0001g0089 a0001c0001t0002g0090 others(42): Show |
45 | HG00408.hp1 HG00423.hp1 HG00544.hp1 others(42): Show |
intron_variant | MODIFIER | c.416-1637_416-1633d others(7): Show |
MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr17 | 12734504 | ||||||
chr17:12734504 | CT | C | 34 | a0001c0001t0002g0187 a0001c0001t0002g0208 a0001c0001t0008g0180 others(31): Show |
34 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(31): Show |
intron_variant | MODIFIER | c.416-1633delT | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr17 | 12734504 | ||||||
chr17:12734550 | G | A | 24 | a0001c0001t0001g0155 a0001c0001t0003g0116 a0001c0001t0003g0188 others(21): Show |
25 | HG00597.hp2 HG02056.hp1 HG02602.hp2 others(22): Show |
intron_variant | MODIFIER | c.416-1611G>A | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 5/13 | chr17 | 12734550 | |||||||
chr17:12734839 | C | T | 209 | a0001c0001t0001g0028 a0001c0001t0001g0058 a0001c0001t0001g0069 others(206): Show |
211 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(208): Show |
intron_variant | MODIFIER | c.416-1322C>T | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 5/13 | chr17 | 12734839 | |||||||
chr17:12734869 | A | G | 209 | a0001c0001t0001g0028 a0001c0001t0001g0058 a0001c0001t0001g0069 others(206): Show |
211 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(208): Show |
intron_variant | MODIFIER | c.416-1292A>G | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 5/13 | chr17 | 12734869 | |||||||
chr17:12734899 | A | AC | 148 | a0001c0001t0001g0028 a0001c0001t0001g0058 a0001c0001t0001g0079 others(145): Show |
148 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(145): Show |
intron_variant | MODIFIER | c.416-1260dupC | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr17 | 12734899 | ||||||
chr17:12734900 | C | CG | 25 | a0001c0001t0001g0069 a0001c0001t0001g0077 a0001c0001t0001g0181 others(22): Show |
25 | HG00423.hp2 HG01255.hp1 HG01256.hp1 others(22): Show |
intron_variant | MODIFIER | c.416-1261_416-1260i others(3): Show |
MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 5/13 | chr17 | 12734900 | |||||||
chr17:12734957 | G | A | 1 | a0001c0002t0062g0322 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.416-1204G>A | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 5/13 | chr17 | 12734957 | |||||||
chr17:12735017 | T | C | 1 | a0001c0001t0006g0174 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.416-1144T>C | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 5/13 | chr17 | 12735017 | |||||||
chr17:12735161 | C | T | 15 | a0001c0001t0004g0044 a0001c0001t0008g0052 a0001c0001t0039g0178 others(12): Show |
15 | HG00741.hp1 HG01106.hp1 HG01496.hp2 others(12): Show |
intron_variant | MODIFIER | c.416-1000C>T | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 5/13 | chr17 | 12735161 | |||||||
chr17:12735182 | A | G | 1 | a0011c0030t0114g0262 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.416-979A>G | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 5/13 | chr17 | 12735182 | |||||||
chr17:12735341 | A | AACGTAAG others(4): Show |
206 | a0001c0001t0001g0028 a0001c0001t0001g0058 a0001c0001t0001g0069 others(203): Show |
208 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(205): Show |
intron_variant | MODIFIER | c.416-819_416-818ins others(11): Show |
MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr17 | 12735341 | ||||||
chr17:12735343 | T | C | 1 | a0001c0001t0007g0088 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.416-818T>C | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 5/13 | chr17 | 12735343 | |||||||
chr17:12735344 | G | A | 206 | a0001c0001t0001g0028 a0001c0001t0001g0058 a0001c0001t0001g0069 others(203): Show |
208 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(205): Show |
intron_variant | MODIFIER | c.416-817G>A | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 5/13 | chr17 | 12735344 | |||||||
chr17:12735344 | G | GTAAGGGA others(4): Show |
1 | a0001c0001t0019g0046 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.416-812_416-811ins others(11): Show |
MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr17 | 12735344 | ||||||
chr17:12735345 | T | TAAGGGAC others(4): Show |
1 | a0001c0001t0007g0088 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.416-812_416-811ins others(11): Show |
MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr17 | 12735345 | ||||||
chr17:12735432 | A | G | 208 | a0001c0001t0001g0028 a0001c0001t0001g0058 a0001c0001t0001g0069 others(205): Show |
210 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(207): Show |
intron_variant | MODIFIER | c.416-729A>G | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 5/13 | chr17 | 12735432 | |||||||
chr17:12735474 | A | G | 1 | a0003c0008t0072g0227 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.416-687A>G | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 5/13 | chr17 | 12735474 | |||||||
chr17:12735977 | T | C | 226 | a0001c0001t0001g0028 a0001c0001t0001g0058 a0001c0001t0001g0077 others(223): Show |
227 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(224): Show |
intron_variant | MODIFIER | c.416-184T>C | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 5/13 | chr17 | 12735977 | |||||||
chr17:12736088 | A | G | 2 | a0001c0002t0069g0159 a0005c0010t0145g0149 |
2 | NA18991.hp2 NA19004.hp2 |
intron_variant | MODIFIER | c.416-73A>G | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 5/13 | chr17 | 12736088 | |||||||
chr17:12736122 | C | T | 4 | a0001c0001t0018g0042 a0001c0001t0054g0314 a0001c0001t0056g0313 others(1): Show |
4 | HG02280.hp1 HG02976.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.416-39C>T | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 5/13 | chr17 | 12736122 | |||||||
chr17:12736453 | C | CCT | 3 | a0001c0007t0002g0209 a0001c0007t0043g0204 a0001c0007t0043g0205 |
3 | HG00738.hp1 HG01515.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.591+118_591+119dup others(2): Show |
MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr17 | 12736453 | ||||||
chr17:12736669 | A | C | 2 | a0001c0001t0146g0019 a0020c0014t0101g0274 |
2 | HG01255.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.591+333A>C | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 6/13 | chr17 | 12736669 | |||||||
chr17:12736725 | A | C | 32 | a0001c0001t0001g0155 a0001c0001t0003g0116 a0001c0001t0003g0188 others(29): Show |
33 | HG00597.hp2 HG02056.hp1 HG02451.hp1 others(30): Show |
intron_variant | MODIFIER | c.591+389A>C | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 6/13 | chr17 | 12736725 | |||||||
chr17:12736745 | G | A | 1 | a0001c0001t0159g0184 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.591+409G>A | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 6/13 | chr17 | 12736745 | |||||||
chr17:12737026 | G | A | 3 | a0001c0001t0005g0141 a0001c0001t0081g0228 a0001c0001t0123g0166 |
3 | HG02056.hp1 NA18975.hp1 NA18983.hp1 |
intron_variant | MODIFIER | c.591+690G>A | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 6/13 | chr17 | 12737026 | |||||||
chr17:12737262 | G | A | 30 | a0001c0001t0001g0155 a0001c0001t0003g0116 a0001c0001t0003g0188 others(27): Show |
31 | HG00597.hp2 HG02056.hp1 HG02451.hp1 others(28): Show |
intron_variant | MODIFIER | c.591+926G>A | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 6/13 | chr17 | 12737262 | |||||||
chr17:12737263 | GA | G | 6 | a0001c0001t0001g0069 a0001c0001t0002g0244 a0001c0001t0004g0082 others(3): Show |
6 | HG00597.hp1 HG03239.hp2 NA18964.hp1 others(3): Show |
intron_variant | MODIFIER | c.591+936delA | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr17 | 12737263 | ||||||
chr17:12737281 | A | G | 1 | a0001c0003t0205g0332 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.591+945A>G | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 6/13 | chr17 | 12737281 | |||||||
chr17:12737340 | G | A | 2 | a0001c0003t0049g0134 a0001c0003t0077g0285 |
2 | HG02559.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.591+1004G>A | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 6/13 | chr17 | 12737340 | |||||||
chr17:12737375 | C | G | 2 | a0001c0001t0022g0286 a0001c0001t0026g0289 |
2 | HG00609.hp2 NA19065.hp2 |
intron_variant | MODIFIER | c.591+1039C>G | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 6/13 | chr17 | 12737375 | |||||||
chr17:12737430 | A | G | 1 | a0001c0003t0202g0210 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.591+1094A>G | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 6/13 | chr17 | 12737430 | |||||||
chr17:12737535 | C | G | 2 | a0001c0001t0001g0261 a0001c0001t0001g0343 |
2 | HG03490.hp1 HG03688.hp2 |
intron_variant | MODIFIER | c.591+1199C>G | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 6/13 | chr17 | 12737535 | |||||||
chr17:12737564 | T | C | 22 | a0001c0001t0004g0044 a0001c0001t0008g0052 a0001c0001t0039g0178 others(19): Show |
22 | HG00741.hp1 HG01106.hp1 HG01257.hp2 others(19): Show |
intron_variant | MODIFIER | c.591+1228T>C | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 6/13 | chr17 | 12737564 | |||||||
chr17:12737567 | G | A | 2 | a0001c0001t0004g0278 a0001c0001t0038g0236 |
2 | NA18954.hp1 NA19062.hp2 |
intron_variant | MODIFIER | c.591+1231G>A | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 6/13 | chr17 | 12737567 | |||||||
chr17:12737643 | C | T | 1 | a0012c0029t0115g0335 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.591+1307C>T | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 6/13 | chr17 | 12737643 | |||||||
chr17:12737719 | C | T | 1 | a0001c0001t0039g0138 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.591+1383C>T | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 6/13 | chr17 | 12737719 | |||||||
chr17:12738015 | G | A | 179 | a0001c0001t0001g0028 a0001c0001t0001g0051 a0001c0001t0001g0058 others(176): Show |
181 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(178): Show |
intron_variant | MODIFIER | c.592-1188G>A | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 6/13 | chr17 | 12738015 | |||||||
chr17:12738141 | C | T | 22 | a0001c0001t0001g0051 a0001c0001t0001g0136 a0001c0001t0001g0176 others(19): Show |
23 | HG00642.hp1 HG00735.hp1 HG01081.hp2 others(20): Show |
intron_variant | MODIFIER | c.592-1062C>T | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 6/13 | chr17 | 12738141 | |||||||
chr17:12738308 | T | C | 7 | a0001c0001t0036g0257 a0001c0001t0073g0337 a0001c0001t0075g0266 others(4): Show |
7 | HG02109.hp2 HG02257.hp2 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.592-895T>C | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 6/13 | chr17 | 12738308 | |||||||
chr17:12738450 | C | T | 31 | a0001c0001t0001g0155 a0001c0001t0003g0116 a0001c0001t0003g0188 others(28): Show |
32 | HG00558.hp2 HG00597.hp2 HG02451.hp1 others(29): Show |
intron_variant | MODIFIER | c.592-753C>T | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 6/13 | chr17 | 12738450 | |||||||
chr17:12738451 | G | A | 2 | a0001c0001t0184g0217 a0001c0001t0186g0214 |
2 | NA18960.hp2 NA19004.hp1 |
intron_variant | MODIFIER | c.592-752G>A | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 6/13 | chr17 | 12738451 | |||||||
chr17:12738949 | TTA | T | 203 | a0001c0001t0001g0028 a0001c0001t0001g0051 a0001c0001t0001g0058 others(200): Show |
205 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(202): Show |
intron_variant | MODIFIER | c.592-242_592-241del others(2): Show |
MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr17 | 12738949 | ||||||
chr17:12738980 | CAT | C | 4 | a0001c0001t0048g0196 a0001c0001t0084g0194 a0001c0002t0177g0192 others(1): Show |
4 | HG02074.hp2 NA18941.hp2 NA18951.hp2 others(1): Show |
intron_variant | MODIFIER | c.592-221_592-220del others(2): Show |
MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr17 | 12738980 | ||||||
chr17:12738986 | C | A | 3 | a0004c0009t0197g0004 a0004c0009t0200g0076 a0004c0017t0007g0252 |
3 | HG01257.hp2 HG01934.hp2 NA18990.hp2 |
intron_variant | MODIFIER | c.592-217C>A | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 6/13 | chr17 | 12738986 | |||||||
chr17:12739022 | C | T | 2 | a0001c0001t0001g0136 a0021c0019t0009g0331 |
2 | HG02738.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.592-181C>T | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 6/13 | chr17 | 12739022 | |||||||
chr17:12739345 | C | T | 1 | a0001c0001t0091g0309 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.717+17C>T | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 7/13 | chr17 | 12739345 | |||||||
chr17:12739499 | C | A | 1 | a0001c0001t0127g0275 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.717+171C>A | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 7/13 | chr17 | 12739499 | |||||||
chr17:12739516 | C | G | 3 | a0004c0009t0197g0004 a0004c0009t0200g0076 a0004c0017t0007g0252 |
3 | HG01257.hp2 HG01934.hp2 NA18990.hp2 |
intron_variant | MODIFIER | c.717+188C>G | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 7/13 | chr17 | 12739516 | |||||||
chr17:12739533 | A | G | 3 | a0004c0009t0197g0004 a0004c0009t0200g0076 a0004c0017t0007g0252 |
3 | HG01257.hp2 HG01934.hp2 NA18990.hp2 |
intron_variant | MODIFIER | c.717+205A>G | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 7/13 | chr17 | 12739533 | |||||||
chr17:12739543 | C | T | 1 | a0004c0009t0200g0076 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.717+215C>T | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 7/13 | chr17 | 12739543 | |||||||
chr17:12739573 | T | C | 178 | a0001c0001t0001g0028 a0001c0001t0001g0058 a0001c0001t0001g0069 others(175): Show |
179 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(176): Show |
intron_variant | MODIFIER | c.717+245T>C | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 7/13 | chr17 | 12739573 | |||||||
chr17:12739584 | C | T | 12 | a0001c0001t0002g0244 a0001c0001t0004g0082 a0001c0001t0023g0253 others(9): Show |
12 | HG00597.hp1 HG02523.hp1 NA18612.hp2 others(9): Show |
intron_variant | MODIFIER | c.717+256C>T | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 7/13 | chr17 | 12739584 | |||||||
chr17:12739675 | G | A | 178 | a0001c0001t0001g0028 a0001c0001t0001g0058 a0001c0001t0001g0069 others(175): Show |
179 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(176): Show |
intron_variant | MODIFIER | c.717+347G>A | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 7/13 | chr17 | 12739675 | |||||||
chr17:12739685 | G | A | 3 | a0004c0009t0197g0004 a0004c0009t0200g0076 a0004c0017t0007g0252 |
3 | HG01257.hp2 HG01934.hp2 NA18990.hp2 |
intron_variant | MODIFIER | c.717+357G>A | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 7/13 | chr17 | 12739685 | |||||||
chr17:12739725 | C | T | 1 | a0004c0017t0007g0252 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.717+397C>T | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 7/13 | chr17 | 12739725 | |||||||
chr17:12739757 | T | G | 334 | a0001c0001t0001g0028 a0001c0001t0001g0051 a0001c0001t0001g0058 others(331): Show |
337 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(334): Show |
intron_variant | MODIFIER | c.717+429T>G | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 7/13 | chr17 | 12739757 | |||||||
chr17:12739959 | A | G | 191 | a0001c0001t0001g0028 a0001c0001t0001g0051 a0001c0001t0001g0058 others(188): Show |
193 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(190): Show |
intron_variant | MODIFIER | c.717+631A>G | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 7/13 | chr17 | 12739959 | |||||||
chr17:12739975 | G | A | 1 | a0001c0001t0002g0208 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.717+647G>A | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 7/13 | chr17 | 12739975 | |||||||
chr17:12740021 | C | T | 3 | a0004c0009t0197g0004 a0004c0009t0200g0076 a0004c0017t0007g0252 |
3 | HG01257.hp2 HG01934.hp2 NA18990.hp2 |
intron_variant | MODIFIER | c.717+693C>T | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 7/13 | chr17 | 12740021 | |||||||
chr17:12740055 | C | T | 3 | a0004c0009t0197g0004 a0004c0009t0200g0076 a0004c0017t0007g0252 |
3 | HG01257.hp2 HG01934.hp2 NA18990.hp2 |
intron_variant | MODIFIER | c.717+727C>T | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 7/13 | chr17 | 12740055 | |||||||
chr17:12740061 | G | T | 1 | a0001c0001t0100g0258 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.717+733G>T | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 7/13 | chr17 | 12740061 | |||||||
chr17:12740143 | G | T | 3 | a0004c0009t0197g0004 a0004c0009t0200g0076 a0004c0017t0007g0252 |
3 | HG01257.hp2 HG01934.hp2 NA18990.hp2 |
intron_variant | MODIFIER | c.717+815G>T | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 7/13 | chr17 | 12740143 | |||||||
chr17:12740192 | T | C | 3 | a0004c0009t0197g0004 a0004c0009t0200g0076 a0004c0017t0007g0252 |
3 | HG01257.hp2 HG01934.hp2 NA18990.hp2 |
intron_variant | MODIFIER | c.717+864T>C | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 7/13 | chr17 | 12740192 | |||||||
chr17:12740245 | G | A | 2 | a0001c0003t0049g0134 a0001c0003t0077g0285 |
2 | HG02559.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.717+917G>A | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 7/13 | chr17 | 12740245 | |||||||
chr17:12740251 | G | A | 153 | a0001c0001t0001g0028 a0001c0001t0001g0058 a0001c0001t0001g0079 others(150): Show |
154 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(151): Show |
intron_variant | MODIFIER | c.717+923G>A | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 7/13 | chr17 | 12740251 | |||||||
chr17:12740369 | C | T | 1 | a0001c0002t0001g0167 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.717+1041C>T | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 7/13 | chr17 | 12740369 | |||||||
chr17:12740393 | T | C | 3 | a0004c0009t0197g0004 a0004c0009t0200g0076 a0004c0017t0007g0252 |
3 | HG01257.hp2 HG01934.hp2 NA18990.hp2 |
intron_variant | MODIFIER | c.717+1065T>C | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 7/13 | chr17 | 12740393 | |||||||
chr17:12740824 | C | T | 2 | a0001c0001t0002g0208 a0001c0001t0160g0108 |
2 | HG01261.hp1 HG01361.hp1 |
intron_variant | MODIFIER | c.717+1496C>T | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 7/13 | chr17 | 12740824 | |||||||
chr17:12740864 | C | T | 3 | a0004c0009t0197g0004 a0004c0009t0200g0076 a0004c0017t0007g0252 |
3 | HG01257.hp2 HG01934.hp2 NA18990.hp2 |
intron_variant | MODIFIER | c.717+1536C>T | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 7/13 | chr17 | 12740864 | |||||||
chr17:12740883 | T | A | 76 | a0001c0001t0001g0104 a0001c0001t0001g0161 a0001c0001t0002g0157 others(73): Show |
76 | HG00639.hp1 HG00639.hp2 HG00673.hp1 others(73): Show |
intron_variant | MODIFIER | c.717+1555T>A | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 7/13 | chr17 | 12740883 | |||||||
chr17:12741085 | C | T | 1 | a0003c0008t0072g0227 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.717+1757C>T | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 7/13 | chr17 | 12741085 | |||||||
chr17:12741159 | C | G | 1 | a0001c0001t0148g0247 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.717+1831C>G | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 7/13 | chr17 | 12741159 | |||||||
chr17:12741394 | C | T | 1 | a0001c0001t0024g0016 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.717+2066C>T | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 7/13 | chr17 | 12741394 | |||||||
chr17:12741484 | G | A | 2 | a0017c0013t0011g0276 a0020c0014t0101g0274 |
2 | NA18906.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.717+2156G>A | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 7/13 | chr17 | 12741484 | |||||||
chr17:12741491 | T | C | 3 | a0004c0009t0197g0004 a0004c0009t0200g0076 a0004c0017t0007g0252 |
3 | HG01257.hp2 HG01934.hp2 NA18990.hp2 |
intron_variant | MODIFIER | c.717+2163T>C | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 7/13 | chr17 | 12741491 | |||||||
chr17:12741561 | T | G | 3 | a0004c0009t0197g0004 a0004c0009t0200g0076 a0004c0017t0007g0252 |
3 | HG01257.hp2 HG01934.hp2 NA18990.hp2 |
intron_variant | MODIFIER | c.717+2233T>G | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 7/13 | chr17 | 12741561 | |||||||
chr17:12741640 | G | C | 157 | a0001c0001t0001g0028 a0001c0001t0001g0058 a0001c0001t0001g0079 others(154): Show |
158 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(155): Show |
intron_variant | MODIFIER | c.717+2312G>C | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 7/13 | chr17 | 12741640 | |||||||
chr17:12741696 | C | T | 1 | a0001c0001t0047g0298 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.717+2368C>T | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 7/13 | chr17 | 12741696 | |||||||
chr17:12741705 | GTA | G | 181 | a0001c0001t0001g0028 a0001c0001t0001g0051 a0001c0001t0001g0079 others(178): Show |
183 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(180): Show |
intron_variant | MODIFIER | c.717+2388_717+2389d others(4): Show |
MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr17 | 12741705 | ||||||
chr17:12741718 | A | T | 5 | a0001c0001t0005g0091 a0001c0001t0171g0014 a0001c0002t0047g0300 others(2): Show |
5 | HG00639.hp1 HG01261.hp2 HG03490.hp2 others(2): Show |
intron_variant | MODIFIER | c.717+2390A>T | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 7/13 | chr17 | 12741718 | |||||||
chr17:12741751 | A | G | 1 | a0001c0001t0189g0216 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.717+2423A>G | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 7/13 | chr17 | 12741751 | |||||||
chr17:12741932 | A | G | 1 | a0001c0001t0010g0183 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.718-2251A>G | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 7/13 | chr17 | 12741932 | |||||||
chr17:12741975 | C | T | 3 | a0004c0009t0197g0004 a0004c0009t0200g0076 a0004c0017t0007g0252 |
3 | HG01257.hp2 HG01934.hp2 NA18990.hp2 |
intron_variant | MODIFIER | c.718-2208C>T | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 7/13 | chr17 | 12741975 | |||||||
chr17:12741977 | A | C | 4 | a0001c0007t0001g0220 a0001c0007t0002g0209 a0001c0007t0043g0204 others(1): Show |
4 | HG00323.hp1 HG00738.hp1 HG01515.hp2 others(1): Show |
intron_variant | MODIFIER | c.718-2206A>C | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 7/13 | chr17 | 12741977 | |||||||
chr17:12742017 | A | G | 1 | a0001c0001t0035g0129 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.718-2166A>G | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 7/13 | chr17 | 12742017 | |||||||
chr17:12742027 | C | G | 3 | a0004c0009t0197g0004 a0004c0009t0200g0076 a0004c0017t0007g0252 |
3 | HG01257.hp2 HG01934.hp2 NA18990.hp2 |
intron_variant | MODIFIER | c.718-2156C>G | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 7/13 | chr17 | 12742027 | |||||||
chr17:12742060 | G | C | 46 | a0001c0001t0001g0261 a0001c0001t0001g0343 a0001c0001t0002g0187 others(43): Show |
47 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(44): Show |
intron_variant | MODIFIER | c.718-2123G>C | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 7/13 | chr17 | 12742060 | |||||||
chr17:12742375 | A | G | 8 | a0001c0004t0001g0100 a0001c0004t0002g0049 a0001c0004t0002g0233 others(5): Show |
8 | HG00741.hp1 HG01106.hp1 HG01496.hp2 others(5): Show |
intron_variant | MODIFIER | c.718-1808A>G | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 7/13 | chr17 | 12742375 | |||||||
chr17:12742493 | C | G | 1 | a0001c0001t0021g0061 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.718-1690C>G | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 7/13 | chr17 | 12742493 | |||||||
chr17:12742530 | T | C | 3 | a0001c0001t0103g0339 a0001c0001t0108g0342 a0001c0003t0203g0281 |
3 | HG02622.hp1 HG02886.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.718-1653T>C | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 7/13 | chr17 | 12742530 | |||||||
chr17:12742576 | AT | A | 30 | a0001c0001t0001g0051 a0001c0001t0001g0136 a0001c0001t0001g0155 others(27): Show |
31 | HG00642.hp1 HG00735.hp1 HG01081.hp2 others(28): Show |
intron_variant | MODIFIER | c.718-1595delT | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr17 | 12742576 | ||||||
chr17:12742593 | C | T | 1 | a0001c0001t0002g0241 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.718-1590C>T | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 7/13 | chr17 | 12742593 | |||||||
chr17:12742602 | G | A | 3 | a0004c0009t0197g0004 a0004c0009t0200g0076 a0004c0017t0007g0252 |
3 | HG01257.hp2 HG01934.hp2 NA18990.hp2 |
intron_variant | MODIFIER | c.718-1581G>A | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 7/13 | chr17 | 12742602 | |||||||
chr17:12742631 | C | T | 3 | a0004c0009t0197g0004 a0004c0009t0200g0076 a0004c0017t0007g0252 |
3 | HG01257.hp2 HG01934.hp2 NA18990.hp2 |
intron_variant | MODIFIER | c.718-1552C>T | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 7/13 | chr17 | 12742631 | |||||||
chr17:12742738 | T | A | 3 | a0004c0009t0197g0004 a0004c0009t0200g0076 a0004c0017t0007g0252 |
3 | HG01257.hp2 HG01934.hp2 NA18990.hp2 |
intron_variant | MODIFIER | c.718-1445T>A | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 7/13 | chr17 | 12742738 | |||||||
chr17:12742764 | G | A | 3 | a0004c0009t0197g0004 a0004c0009t0200g0076 a0004c0017t0007g0252 |
3 | HG01257.hp2 HG01934.hp2 NA18990.hp2 |
intron_variant | MODIFIER | c.718-1419G>A | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 7/13 | chr17 | 12742764 | |||||||
chr17:12742789 | C | T | 1 | a0001c0001t0007g0163 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.718-1394C>T | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 7/13 | chr17 | 12742789 | |||||||
chr17:12742861 | C | A | 28 | a0001c0001t0001g0155 a0001c0001t0003g0116 a0001c0001t0003g0188 others(25): Show |
29 | HG00597.hp2 HG02056.hp1 HG02145.hp2 others(26): Show |
intron_variant | MODIFIER | c.718-1322C>A | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 7/13 | chr17 | 12742861 | |||||||
chr17:12742867 | C | T | 3 | a0004c0009t0197g0004 a0004c0009t0200g0076 a0004c0017t0007g0252 |
3 | HG01257.hp2 HG01934.hp2 NA18990.hp2 |
intron_variant | MODIFIER | c.718-1316C>T | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 7/13 | chr17 | 12742867 | |||||||
chr17:12742929 | A | G | 3 | a0004c0009t0197g0004 a0004c0009t0200g0076 a0004c0017t0007g0252 |
3 | HG01257.hp2 HG01934.hp2 NA18990.hp2 |
intron_variant | MODIFIER | c.718-1254A>G | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 7/13 | chr17 | 12742929 | |||||||
chr17:12743237 | C | T | 2 | a0001c0003t0181g0031 a0001c0003t0182g0271 |
2 | HG03041.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.718-946C>T | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 7/13 | chr17 | 12743237 | |||||||
chr17:12743375 | C | A | 3 | a0004c0009t0197g0004 a0004c0009t0200g0076 a0004c0017t0007g0252 |
3 | HG01257.hp2 HG01934.hp2 NA18990.hp2 |
intron_variant | MODIFIER | c.718-808C>A | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 7/13 | chr17 | 12743375 | |||||||
chr17:12743435 | G | A | 3 | a0004c0009t0197g0004 a0004c0009t0200g0076 a0004c0017t0007g0252 |
3 | HG01257.hp2 HG01934.hp2 NA18990.hp2 |
intron_variant | MODIFIER | c.718-748G>A | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 7/13 | chr17 | 12743435 | |||||||
chr17:12743486 | C | CT | 8 | a0001c0001t0002g0157 a0001c0001t0017g0156 a0001c0001t0026g0234 others(5): Show |
8 | HG00673.hp1 HG01109.hp1 HG01978.hp2 others(5): Show |
intron_variant | MODIFIER | c.718-674dupT | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr17 | 12743486 | ||||||
chr17:12743486 | CT | C | 32 | a0001c0001t0001g0051 a0001c0001t0001g0136 a0001c0001t0001g0176 others(29): Show |
33 | HG00642.hp1 HG00735.hp1 HG01081.hp2 others(30): Show |
intron_variant | MODIFIER | c.718-674delT | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr17 | 12743486 | ||||||
chr17:12743486 | CTTT | C | 43 | a0001c0001t0001g0155 a0001c0001t0003g0116 a0001c0001t0003g0188 others(40): Show |
44 | HG00597.hp2 HG01257.hp2 HG02056.hp1 others(41): Show |
intron_variant | MODIFIER | c.718-676_718-674del others(3): Show |
MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr17 | 12743486 | ||||||
chr17:12743486 | CTTTT | C | 108 | a0001c0001t0001g0028 a0001c0001t0001g0058 a0001c0001t0001g0079 others(105): Show |
108 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(105): Show |
intron_variant | MODIFIER | c.718-677_718-674del others(4): Show |
MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr17 | 12743486 | ||||||
chr17:12743588 | G | A | 1 | a0001c0001t0012g0235 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.718-595G>A | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 7/13 | chr17 | 12743588 | |||||||
chr17:12743693 | G | A | 4 | a0001c0001t0139g0013 a0004c0009t0197g0004 a0004c0009t0200g0076 others(1): Show |
4 | HG01257.hp2 HG01934.hp2 HG03831.hp1 others(1): Show |
intron_variant | MODIFIER | c.718-490G>A | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 7/13 | chr17 | 12743693 | |||||||
chr17:12743784 | C | G | 1 | a0001c0001t0017g0156 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.718-399C>G | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 7/13 | chr17 | 12743784 | |||||||
chr17:12743837 | G | A | 4 | a0001c0001t0002g0157 a0001c0001t0017g0156 a0001c0001t0079g0023 others(1): Show |
4 | NA18939.hp1 NA18953.hp2 NA18978.hp2 others(1): Show |
intron_variant | MODIFIER | c.718-346G>A | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 7/13 | chr17 | 12743837 | |||||||
chr17:12743881 | C | T | 2 | a0017c0013t0011g0276 a0020c0014t0101g0274 |
2 | NA18906.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.718-302C>T | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 7/13 | chr17 | 12743881 | |||||||
chr17:12744089 | C | T | 5 | a0001c0001t0073g0337 a0001c0001t0075g0266 a0001c0001t0201g0334 others(2): Show |
5 | HG02257.hp2 HG02451.hp2 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.718-94C>T | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 7/13 | chr17 | 12744089 | |||||||
chr17:12744091 | A | G | 16 | a0001c0001t0005g0091 a0001c0001t0018g0042 a0001c0001t0018g0223 others(13): Show |
16 | HG00639.hp1 HG01175.hp1 HG01261.hp2 others(13): Show |
intron_variant | MODIFIER | c.718-92A>G | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 7/13 | chr17 | 12744091 | |||||||
chr17:12744132 | C | A | 3 | a0004c0009t0197g0004 a0004c0009t0200g0076 a0004c0017t0007g0252 |
3 | HG01257.hp2 HG01934.hp2 NA18990.hp2 |
intron_variant | MODIFIER | c.718-51C>A | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 7/13 | chr17 | 12744132 | |||||||
chr17:12744173 | T | C | 255 | a0001c0001t0001g0028 a0001c0001t0001g0051 a0001c0001t0001g0058 others(252): Show |
258 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(255): Show |
intron_variant | MODIFIER | c.718-10T>C | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 7/13 | chr17 | 12744173 | |||||||
chr17:12744479 | G | C | 1 | a0001c0001t0135g0056 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.971+43G>C | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 8/13 | chr17 | 12744479 | |||||||
chr17:12744671 | T | C | 35 | a0001c0001t0001g0155 a0001c0001t0003g0116 a0001c0001t0003g0188 others(32): Show |
36 | HG00597.hp2 HG02056.hp1 HG02145.hp2 others(33): Show |
intron_variant | MODIFIER | c.971+235T>C | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 8/13 | chr17 | 12744671 | |||||||
chr17:12744671 | T | G | 3 | a0004c0009t0197g0004 a0004c0009t0200g0076 a0004c0017t0007g0252 |
3 | HG01257.hp2 HG01934.hp2 NA18990.hp2 |
intron_variant | MODIFIER | c.971+235T>G | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 8/13 | chr17 | 12744671 | |||||||
chr17:12744745 | A | G | 1 | a0001c0001t0014g0338 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.971+309A>G | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 8/13 | chr17 | 12744745 | |||||||
chr17:12744943 | T | C | 1 | a0001c0001t0162g0057 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.971+507T>C | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 8/13 | chr17 | 12744943 | |||||||
chr17:12744958 | G | A | 1 | a0001c0004t0034g0238 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.971+522G>A | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 8/13 | chr17 | 12744958 | |||||||
chr17:12745035 | A | G | 1 | a0001c0001t0159g0184 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.971+599A>G | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 8/13 | chr17 | 12745035 | |||||||
chr17:12745095 | A | G | 3 | a0004c0009t0197g0004 a0004c0009t0200g0076 a0004c0017t0007g0252 |
3 | HG01257.hp2 HG01934.hp2 NA18990.hp2 |
intron_variant | MODIFIER | c.971+659A>G | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 8/13 | chr17 | 12745095 | |||||||
chr17:12745127 | T | C | 3 | a0004c0009t0197g0004 a0004c0009t0200g0076 a0004c0017t0007g0252 |
3 | HG01257.hp2 HG01934.hp2 NA18990.hp2 |
intron_variant | MODIFIER | c.971+691T>C | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 8/13 | chr17 | 12745127 | |||||||
chr17:12745166 | A | G | 4 | a0001c0001t0003g0212 a0001c0001t0005g0085 a0001c0001t0035g0129 others(1): Show |
4 | HG01433.hp1 HG02004.hp1 HG02300.hp2 others(1): Show |
intron_variant | MODIFIER | c.971+730A>G | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 8/13 | chr17 | 12745166 | |||||||
chr17:12745192 | T | A | 5 | a0001c0002t0177g0192 a0001c0002t0178g0072 a0004c0009t0197g0004 others(2): Show |
5 | HG00408.hp2 HG01257.hp2 HG01934.hp2 others(2): Show |
intron_variant | MODIFIER | c.972-727T>A | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 8/13 | chr17 | 12745192 | |||||||
chr17:12746236 | A | G | 2 | a0001c0003t0181g0031 a0001c0003t0182g0271 |
2 | HG03041.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.1125+164A>G | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 9/13 | chr17 | 12746236 | |||||||
chr17:12746343 | G | A | 26 | a0001c0001t0073g0337 a0001c0001t0201g0334 a0001c0002t0001g0167 others(23): Show |
26 | HG00408.hp1 HG00408.hp2 HG00639.hp1 others(23): Show |
intron_variant | MODIFIER | c.1125+271G>A | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 9/13 | chr17 | 12746343 | |||||||
chr17:12746399 | G | A | 1 | a0001c0001t0108g0342 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1125+327G>A | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 9/13 | chr17 | 12746399 | |||||||
chr17:12746472 | A | G | 30 | a0001c0001t0001g0161 a0001c0001t0073g0337 a0001c0001t0103g0339 others(27): Show |
30 | HG00408.hp1 HG00408.hp2 HG00639.hp1 others(27): Show |
intron_variant | MODIFIER | c.1125+400A>G | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 9/13 | chr17 | 12746472 | |||||||
chr17:12746507 | G | C | 1 | a0001c0001t0159g0184 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1125+435G>C | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 9/13 | chr17 | 12746507 | |||||||
chr17:12746538 | G | A | 1 | a0013c0027t0110g0222 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1125+466G>A | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 9/13 | chr17 | 12746538 | |||||||
chr17:12746638 | T | C | 1 | a0013c0027t0110g0222 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1125+566T>C | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 9/13 | chr17 | 12746638 | |||||||
chr17:12746650 | T | G | 1 | a0001c0001t0005g0232 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.1125+578T>G | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 9/13 | chr17 | 12746650 | |||||||
chr17:12746679 | C | G | 1 | a0013c0027t0110g0222 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1125+607C>G | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 9/13 | chr17 | 12746679 | |||||||
chr17:12746681 | G | A | 37 | a0001c0001t0073g0337 a0001c0001t0106g0310 a0001c0001t0201g0334 others(34): Show |
37 | HG00408.hp1 HG00408.hp2 HG00639.hp1 others(34): Show |
intron_variant | MODIFIER | c.1125+609G>A | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 9/13 | chr17 | 12746681 | |||||||
chr17:12746694 | G | A | 6 | a0001c0001t0005g0091 a0001c0003t0206g0294 a0002c0005t0002g0185 others(3): Show |
6 | HG00544.hp1 HG01261.hp2 NA18951.hp2 others(3): Show |
intron_variant | MODIFIER | c.1125+622G>A | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 9/13 | chr17 | 12746694 | |||||||
chr17:12746721 | G | A | 3 | a0001c0001t0018g0042 a0001c0001t0018g0223 a0001c0001t0040g0272 |
3 | HG02615.hp1 HG03471.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1125+649G>A | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 9/13 | chr17 | 12746721 | |||||||
chr17:12746727 | C | CT | 7 | a0001c0001t0013g0259 a0001c0001t0029g0097 a0001c0001t0064g0316 others(4): Show |
8 | HG00733.hp2 HG01891.hp2 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.1125+674dupT | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr17 | 12746727 | ||||||
chr17:12746727 | C | CTT | 201 | a0001c0001t0001g0028 a0001c0001t0001g0058 a0001c0001t0001g0077 others(198): Show |
203 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(200): Show |
intron_variant | MODIFIER | c.1125+673_1125+674d others(4): Show |
MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr17 | 12746727 | ||||||
chr17:12746727 | C | CTTT | 51 | a0001c0001t0001g0051 a0001c0001t0001g0136 a0001c0001t0001g0176 others(48): Show |
51 | HG00408.hp2 HG00544.hp1 HG00642.hp1 others(48): Show |
intron_variant | MODIFIER | c.1125+672_1125+674d others(5): Show |
MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr17 | 12746727 | ||||||
chr17:12746765 | G | A | 4 | a0001c0003t0046g0121 a0001c0003t0046g0122 a0001c0003t0181g0031 others(1): Show |
4 | HG02896.hp1 HG02897.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.1125+693G>A | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 9/13 | chr17 | 12746765 | |||||||
chr17:12746802 | C | A | 1 | a0001c0001t0005g0085 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1125+730C>A | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 9/13 | chr17 | 12746802 | |||||||
chr17:12746911 | T | G | 1 | a0013c0027t0110g0222 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1125+839T>G | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 9/13 | chr17 | 12746911 | |||||||
chr17:12746947 | C | T | 1 | a0001c0001t0155g0172 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1125+875C>T | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 9/13 | chr17 | 12746947 | |||||||
chr17:12747026 | C | A | 2 | a0001c0001t0103g0339 a0001c0001t0108g0342 |
2 | HG02622.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.1125+954C>A | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 9/13 | chr17 | 12747026 | |||||||
chr17:12747035 | AT | A | 298 | a0001c0001t0001g0028 a0001c0001t0001g0058 a0001c0001t0001g0069 others(295): Show |
301 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(298): Show |
intron_variant | MODIFIER | c.1125+977delT | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr17 | 12747035 | ||||||
chr17:12747035 | ATT | A | 15 | a0001c0001t0005g0199 a0001c0001t0006g0098 a0001c0001t0007g0163 others(12): Show |
15 | HG00639.hp1 HG02080.hp2 HG02129.hp1 others(12): Show |
intron_variant | MODIFIER | c.1125+976_1125+977d others(4): Show |
MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr17 | 12747035 | ||||||
chr17:12747035 | ATTT | A | 15 | a0001c0001t0001g0051 a0001c0001t0001g0136 a0001c0001t0001g0176 others(12): Show |
15 | HG00642.hp1 HG01081.hp2 HG01346.hp2 others(12): Show |
intron_variant | MODIFIER | c.1125+975_1125+977d others(5): Show |
MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr17 | 12747035 | ||||||
chr17:12747093 | A | C | 1 | a0001c0001t0126g0062 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.1125+1021A>C | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 9/13 | chr17 | 12747093 | |||||||
chr17:12747371 | A | AAGAG | 257 | a0001c0001t0001g0028 a0001c0001t0001g0051 a0001c0001t0001g0058 others(254): Show |
260 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(257): Show |
intron_variant | MODIFIER | c.1125+1299_1125+130 others(8): Show |
MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 9/13 | chr17 | 12747371 | |||||||
chr17:12747441 | C | T | 1 | a0001c0003t0204g0038 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1125+1369C>T | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 9/13 | chr17 | 12747441 | |||||||
chr17:12747460 | C | T | 203 | a0001c0001t0001g0028 a0001c0001t0001g0058 a0001c0001t0001g0077 others(200): Show |
206 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(203): Show |
intron_variant | MODIFIER | c.1125+1388C>T | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 9/13 | chr17 | 12747460 | |||||||
chr17:12747537 | C | A | 255 | a0001c0001t0001g0028 a0001c0001t0001g0051 a0001c0001t0001g0058 others(252): Show |
258 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(255): Show |
intron_variant | MODIFIER | c.1125+1465C>A | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 9/13 | chr17 | 12747537 | |||||||
chr17:12747546 | G | A | 37 | a0001c0001t0073g0337 a0001c0001t0106g0310 a0001c0001t0201g0334 others(34): Show |
37 | HG00408.hp1 HG00408.hp2 HG00639.hp1 others(34): Show |
intron_variant | MODIFIER | c.1125+1474G>A | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 9/13 | chr17 | 12747546 | |||||||
chr17:12747548 | C | T | 252 | a0001c0001t0001g0028 a0001c0001t0001g0051 a0001c0001t0001g0058 others(249): Show |
255 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(252): Show |
intron_variant | MODIFIER | c.1125+1476C>T | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 9/13 | chr17 | 12747548 | |||||||
chr17:12747607 | G | A | 36 | a0001c0001t0073g0337 a0001c0001t0106g0310 a0001c0001t0201g0334 others(33): Show |
36 | HG00408.hp1 HG00408.hp2 HG00639.hp1 others(33): Show |
intron_variant | MODIFIER | c.1125+1535G>A | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 9/13 | chr17 | 12747607 | |||||||
chr17:12747867 | TA | T | 118 | a0001c0001t0001g0077 a0001c0001t0001g0104 a0001c0001t0001g0161 others(115): Show |
121 | HG00323.hp1 HG00621.hp2 HG00639.hp2 others(118): Show |
intron_variant | MODIFIER | c.1125+1809delA | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr17 | 12747867 | ||||||
chr17:12747892 | G | A | 35 | a0001c0001t0011g0224 a0001c0001t0011g0229 a0001c0001t0011g0230 others(32): Show |
35 | HG00408.hp1 HG00408.hp2 HG00639.hp1 others(32): Show |
intron_variant | MODIFIER | c.1125+1820G>A | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 9/13 | chr17 | 12747892 | |||||||
chr17:12747903 | C | T | 1 | a0005c0010t0145g0149 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.1125+1831C>T | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 9/13 | chr17 | 12747903 | |||||||
chr17:12747980 | C | T | 15 | a0001c0001t0001g0051 a0001c0001t0001g0136 a0001c0001t0001g0176 others(12): Show |
15 | HG00642.hp1 HG01081.hp2 HG01346.hp2 others(12): Show |
intron_variant | MODIFIER | c.1125+1908C>T | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 9/13 | chr17 | 12747980 | |||||||
chr17:12747999 | C | A | 1 | a0013c0027t0110g0222 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1125+1927C>A | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 9/13 | chr17 | 12747999 | |||||||
chr17:12748077 | G | A | 1 | a0013c0027t0110g0222 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1125+2005G>A | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 9/13 | chr17 | 12748077 | |||||||
chr17:12748084 | C | T | 2 | a0001c0001t0103g0339 a0001c0001t0108g0342 |
2 | HG02622.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.1125+2012C>T | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 9/13 | chr17 | 12748084 | |||||||
chr17:12748087 | G | A | 1 | a0001c0001t0154g0027 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.1125+2015G>A | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 9/13 | chr17 | 12748087 | |||||||
chr17:12748160 | CA | C | 259 | a0001c0001t0001g0028 a0001c0001t0001g0069 a0001c0001t0001g0077 others(256): Show |
261 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(258): Show |
intron_variant | MODIFIER | c.1125+2106delA | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr17 | 12748160 | ||||||
chr17:12748160 | CAA | C | 18 | a0001c0001t0001g0051 a0001c0001t0001g0176 a0001c0001t0001g0177 others(15): Show |
18 | HG00642.hp1 HG01081.hp2 HG01346.hp2 others(15): Show |
intron_variant | MODIFIER | c.1125+2105_1125+210 others(6): Show |
MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr17 | 12748160 | ||||||
chr17:12748171 | A | C | 12 | a0001c0001t0028g0002 a0001c0001t0036g0036 a0001c0001t0036g0257 others(9): Show |
13 | HG02109.hp2 HG02451.hp1 HG02647.hp1 others(10): Show |
intron_variant | MODIFIER | c.1125+2099A>C | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 9/13 | chr17 | 12748171 | |||||||
chr17:12748172 | A | C | 1 | a0001c0002t0193g0123 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.1125+2100A>C | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 9/13 | chr17 | 12748172 | |||||||
chr17:12748178 | A | C | 1 | a0001c0004t0005g0211 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.1125+2106A>C | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 9/13 | chr17 | 12748178 | |||||||
chr17:12748178 | AC | A | 3 | a0001c0001t0084g0194 a0001c0003t0049g0134 a0002c0005t0002g0185 |
3 | HG01261.hp2 HG03098.hp2 NA18941.hp2 |
intron_variant | MODIFIER | c.1125+2107delC | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 9/13 | chr17 | 12748178 | |||||||
chr17:12748179 | C | A | 1 | a0001c0004t0005g0211 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.1125+2107C>A | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 9/13 | chr17 | 12748179 | |||||||
chr17:12748206 | GAGAA | G | 9 | a0001c0001t0028g0002 a0001c0001t0057g0317 a0001c0001t0119g0280 others(6): Show |
10 | HG02451.hp1 HG02647.hp1 HG02809.hp1 others(7): Show |
intron_variant | MODIFIER | c.1125+2138_1125+214 others(8): Show |
MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr17 | 12748206 | ||||||
chr17:12748249 | TTATTGA | T | 4 | a0001c0001t0018g0042 a0001c0001t0018g0223 a0001c0001t0040g0272 others(1): Show |
4 | HG01934.hp1 HG02615.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.1125+2182_1125+218 others(10): Show |
MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr17 | 12748249 | ||||||
chr17:12748298 | A | G | 36 | a0001c0001t0073g0337 a0001c0001t0106g0310 a0001c0001t0201g0334 others(33): Show |
36 | HG00408.hp1 HG00408.hp2 HG00639.hp1 others(33): Show |
intron_variant | MODIFIER | c.1125+2226A>G | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 9/13 | chr17 | 12748298 | |||||||
chr17:12748580 | G | A | 197 | a0001c0001t0001g0028 a0001c0001t0001g0058 a0001c0001t0001g0079 others(194): Show |
200 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(197): Show |
intron_variant | MODIFIER | c.1125+2508G>A | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 9/13 | chr17 | 12748580 | |||||||
chr17:12748586 | A | G | 1 | a0001c0001t0162g0057 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.1125+2514A>G | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 9/13 | chr17 | 12748586 | |||||||
chr17:12748838 | T | A | 1 | a0001c0001t0038g0236 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.1125+2766T>A | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 9/13 | chr17 | 12748838 | |||||||
chr17:12748851 | A | G | 290 | a0001c0001t0001g0028 a0001c0001t0001g0051 a0001c0001t0001g0058 others(287): Show |
293 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(290): Show |
intron_variant | MODIFIER | c.1125+2779A>G | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 9/13 | chr17 | 12748851 | |||||||
chr17:12748896 | C | CTATAA | 36 | a0001c0001t0073g0337 a0001c0001t0106g0310 a0001c0001t0201g0334 others(33): Show |
36 | HG00408.hp1 HG00408.hp2 HG00639.hp1 others(33): Show |
intron_variant | MODIFIER | c.1125+2824_1125+282 others(9): Show |
MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 9/13 | chr17 | 12748896 | |||||||
chr17:12748932 | T | C | 2 | a0001c0001t0168g0260 a0006c0012t0031g0003 |
3 | HG02922.hp2 HG02965.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.1125+2860T>C | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 9/13 | chr17 | 12748932 | |||||||
chr17:12748945 | G | A | 1 | a0013c0027t0110g0222 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1125+2873G>A | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 9/13 | chr17 | 12748945 | |||||||
chr17:12749022 | G | A | 2 | a0001c0001t0038g0024 a0001c0001t0086g0092 |
2 | NA18956.hp1 NA18968.hp2 |
intron_variant | MODIFIER | c.1125+2950G>A | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 9/13 | chr17 | 12749022 | |||||||
chr17:12749089 | CTTCTT | C | 15 | a0001c0001t0001g0051 a0001c0001t0001g0136 a0001c0001t0001g0176 others(12): Show |
15 | HG00642.hp1 HG01081.hp2 HG01346.hp2 others(12): Show |
intron_variant | MODIFIER | c.1125+3023_1125+302 others(9): Show |
MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr17 | 12749089 | ||||||
chr17:12749124 | A | G | 9 | a0001c0001t0028g0002 a0001c0001t0057g0317 a0001c0001t0119g0280 others(6): Show |
10 | HG02451.hp1 HG02647.hp1 HG02809.hp1 others(7): Show |
intron_variant | MODIFIER | c.1125+3052A>G | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 9/13 | chr17 | 12749124 | |||||||
chr17:12749156 | A | G | 1 | a0001c0001t0088g0103 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.1125+3084A>G | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 9/13 | chr17 | 12749156 | |||||||
chr17:12749177 | A | G | 4 | a0001c0003t0046g0121 a0001c0003t0046g0122 a0001c0003t0181g0031 others(1): Show |
4 | HG02896.hp1 HG02897.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.1125+3105A>G | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 9/13 | chr17 | 12749177 | |||||||
chr17:12749218 | A | G | 31 | a0001c0002t0001g0167 a0001c0002t0002g0239 a0001c0002t0003g0299 others(28): Show |
31 | HG00408.hp1 HG00408.hp2 HG00639.hp1 others(28): Show |
intron_variant | MODIFIER | c.1125+3146A>G | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 9/13 | chr17 | 12749218 | |||||||
chr17:12749266 | C | T | 4 | a0001c0001t0002g0157 a0001c0001t0017g0156 a0001c0001t0079g0023 others(1): Show |
4 | NA18939.hp1 NA18953.hp2 NA18978.hp2 others(1): Show |
intron_variant | MODIFIER | c.1126-3148C>T | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 9/13 | chr17 | 12749266 | |||||||
chr17:12749288 | G | A | 31 | a0001c0002t0001g0167 a0001c0002t0002g0239 a0001c0002t0003g0299 others(28): Show |
31 | HG00408.hp1 HG00408.hp2 HG00639.hp1 others(28): Show |
intron_variant | MODIFIER | c.1126-3126G>A | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 9/13 | chr17 | 12749288 | |||||||
chr17:12749290 | G | A | 1 | a0001c0001t0038g0236 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.1126-3124G>A | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 9/13 | chr17 | 12749290 | |||||||
chr17:12749412 | T | C | 52 | a0001c0001t0001g0051 a0001c0001t0001g0136 a0001c0001t0001g0176 others(49): Show |
52 | HG00408.hp1 HG00408.hp2 HG00639.hp1 others(49): Show |
intron_variant | MODIFIER | c.1126-3002T>C | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 9/13 | chr17 | 12749412 | |||||||
chr17:12749534 | T | TTATA | 113 | a0001c0001t0001g0028 a0001c0001t0001g0058 a0001c0001t0001g0079 others(110): Show |
115 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(112): Show |
intron_variant | MODIFIER | c.1126-2870_1126-286 others(8): Show |
MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr17 | 12749534 | ||||||
chr17:12749534 | T | TTATATA | 84 | a0001c0001t0001g0077 a0001c0001t0001g0089 a0001c0001t0001g0104 others(81): Show |
85 | HG00323.hp1 HG00621.hp2 HG00639.hp2 others(82): Show |
intron_variant | MODIFIER | c.1126-2872_1126-286 others(10): Show |
MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr17 | 12749534 | ||||||
chr17:12749548 | G | GTATGTAT others(21): Show |
1 | a0013c0027t0110g0222 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1126-2845_1126-284 others(32): Show |
MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr17 | 12749548 | ||||||
chr17:12749605 | A | C | 1 | a0013c0027t0110g0222 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1126-2809A>C | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 9/13 | chr17 | 12749605 | |||||||
chr17:12749612 | C | CAT | 37 | a0001c0001t0073g0337 a0001c0001t0106g0310 a0001c0001t0201g0334 others(34): Show |
37 | HG00408.hp1 HG00408.hp2 HG00639.hp1 others(34): Show |
intron_variant | MODIFIER | c.1126-2801_1126-280 others(6): Show |
MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr17 | 12749612 | ||||||
chr17:12749634 | CGT | C | 37 | a0001c0001t0038g0236 a0001c0001t0073g0337 a0001c0001t0106g0310 others(34): Show |
37 | HG00408.hp1 HG00408.hp2 HG00639.hp1 others(34): Show |
intron_variant | MODIFIER | c.1126-2775_1126-277 others(6): Show |
MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr17 | 12749634 | ||||||
chr17:12749707 | G | GTGTATAT others(11): Show |
2 | a0001c0001t0005g0199 a0001c0001t0023g0253 |
2 | NA18612.hp2 NA19055.hp2 |
intron_variant | MODIFIER | c.1126-2696_1126-269 others(22): Show |
MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr17 | 12749707 | ||||||
chr17:12749707 | G | GTGTATAT others(11): Show |
166 | a0001c0001t0001g0069 a0001c0001t0001g0077 a0001c0001t0001g0104 others(163): Show |
168 | HG00280.hp1 HG00323.hp1 HG00423.hp2 others(165): Show |
intron_variant | MODIFIER | c.1126-2696_1126-269 others(22): Show |
MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr17 | 12749707 | ||||||
chr17:12749707 | G | GTGTATAT others(13): Show |
15 | a0001c0001t0001g0051 a0001c0001t0001g0136 a0001c0001t0001g0176 others(12): Show |
15 | HG00642.hp1 HG01081.hp2 HG01346.hp2 others(12): Show |
intron_variant | MODIFIER | c.1126-2696_1126-269 others(24): Show |
MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr17 | 12749707 | ||||||
chr17:12749709 | G | GTATATAT others(13): Show |
105 | a0001c0001t0001g0028 a0001c0001t0001g0058 a0001c0001t0001g0086 others(102): Show |
106 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(103): Show |
intron_variant | MODIFIER | c.1126-2696_1126-269 others(24): Show |
MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr17 | 12749709 | ||||||
chr17:12749709 | G | GTATATAT others(15): Show |
1 | a0001c0001t0001g0079 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.1126-2696_1126-269 others(26): Show |
MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr17 | 12749709 | ||||||
chr17:12749711 | A | ATATATAT others(9): Show |
2 | a0001c0003t0046g0121 a0001c0003t0046g0122 |
2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.1126-2696_1126-269 others(20): Show |
MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr17 | 12749711 | ||||||
chr17:12749715 | A | ATATACAT others(17): Show |
1 | a0013c0027t0110g0222 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1126-2696_1126-269 others(28): Show |
MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr17 | 12749715 | ||||||
chr17:12749717 | A | ACATATAT others(17): Show |
31 | a0001c0002t0001g0167 a0001c0002t0002g0239 a0001c0002t0003g0299 others(28): Show |
31 | HG00408.hp1 HG00408.hp2 HG00639.hp1 others(28): Show |
intron_variant | MODIFIER | c.1126-2697_1126-269 others(28): Show |
MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 9/13 | chr17 | 12749717 | |||||||
chr17:12749717 | A | ATACATAT others(49): Show |
1 | a0020c0014t0101g0274 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1126-2696_1126-269 others(60): Show |
MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr17 | 12749717 | ||||||
chr17:12749717 | A | ATACATAT others(13): Show |
1 | a0001c0001t0195g0284 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.1126-2696_1126-269 others(24): Show |
MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr17 | 12749717 | ||||||
chr17:12749717 | A | ATACATAT others(19): Show |
4 | a0001c0001t0073g0337 a0001c0001t0106g0310 a0001c0001t0201g0334 others(1): Show |
4 | HG02647.hp2 HG02886.hp1 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.1126-2696_1126-269 others(30): Show |
MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr17 | 12749717 | ||||||
chr17:12749739 | A | G | 1 | a0001c0003t0182g0271 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1126-2675A>G | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 9/13 | chr17 | 12749739 | |||||||
chr17:12749781 | G | A | 1 | a0013c0027t0110g0222 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1126-2633G>A | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 9/13 | chr17 | 12749781 | |||||||
chr17:12749824 | T | G | 1 | a0001c0003t0049g0134 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1126-2590T>G | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 9/13 | chr17 | 12749824 | |||||||
chr17:12749829 | A | T | 1 | a0001c0001t0038g0236 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.1126-2585A>T | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 9/13 | chr17 | 12749829 | |||||||
chr17:12749831 | TG | T | 5 | a0001c0001t0073g0337 a0001c0001t0106g0310 a0001c0001t0201g0334 others(2): Show |
5 | HG02647.hp2 HG02886.hp1 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.1126-2582delG | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 9/13 | chr17 | 12749831 | |||||||
chr17:12749896 | C | T | 2 | a0001c0001t0087g0179 a0007c0022t0176g0279 |
2 | HG00621.hp2 HG02155.hp1 |
intron_variant | MODIFIER | c.1126-2518C>T | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 9/13 | chr17 | 12749896 | |||||||
chr17:12749912 | G | T | 276 | a0001c0001t0001g0028 a0001c0001t0001g0058 a0001c0001t0001g0069 others(273): Show |
279 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(276): Show |
intron_variant | MODIFIER | c.1126-2502G>T | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 9/13 | chr17 | 12749912 | |||||||
chr17:12749923 | C | A | 239 | a0001c0001t0001g0028 a0001c0001t0001g0058 a0001c0001t0001g0079 others(236): Show |
242 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(239): Show |
intron_variant | MODIFIER | c.1126-2491C>A | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 9/13 | chr17 | 12749923 | |||||||
chr17:12749951 | G | A | 1 | a0001c0001t0160g0108 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.1126-2463G>A | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 9/13 | chr17 | 12749951 | |||||||
chr17:12750124 | A | C | 31 | a0001c0002t0001g0167 a0001c0002t0002g0239 a0001c0002t0003g0299 others(28): Show |
31 | HG00408.hp1 HG00408.hp2 HG00639.hp1 others(28): Show |
intron_variant | MODIFIER | c.1126-2290A>C | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 9/13 | chr17 | 12750124 | |||||||
chr17:12750278 | T | C | 32 | a0001c0002t0001g0167 a0001c0002t0002g0239 a0001c0002t0003g0299 others(29): Show |
32 | HG00408.hp1 HG00408.hp2 HG00639.hp1 others(29): Show |
intron_variant | MODIFIER | c.1126-2136T>C | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 9/13 | chr17 | 12750278 | |||||||
chr17:12750300 | A | G | 2 | a0001c0001t0001g0176 a0001c0001t0001g0177 |
2 | HG01081.hp2 HG01346.hp2 |
intron_variant | MODIFIER | c.1126-2114A>G | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 9/13 | chr17 | 12750300 | |||||||
chr17:12750410 | C | T | 1 | a0001c0001t0001g0069 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.1126-2004C>T | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 9/13 | chr17 | 12750410 | |||||||
chr17:12750470 | T | C | 1 | a0001c0001t0108g0342 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1126-1944T>C | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 9/13 | chr17 | 12750470 | |||||||
chr17:12750518 | G | A | 3 | a0001c0006t0016g0231 a0001c0006t0093g0059 a0011c0030t0114g0262 |
3 | HG02451.hp1 HG03139.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.1126-1896G>A | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 9/13 | chr17 | 12750518 | |||||||
chr17:12750555 | G | T | 6 | a0001c0001t0011g0224 a0001c0001t0011g0229 a0001c0001t0011g0230 others(3): Show |
6 | HG02055.hp2 HG02559.hp2 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.1126-1859G>T | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 9/13 | chr17 | 12750555 | |||||||
chr17:12750587 | G | T | 1 | a0013c0027t0110g0222 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1126-1827G>T | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 9/13 | chr17 | 12750587 | |||||||
chr17:12750684 | G | A | 1 | a0001c0001t0002g0242 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.1126-1730G>A | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 9/13 | chr17 | 12750684 | |||||||
chr17:12750734 | GTCT | G | 83 | a0001c0001t0001g0104 a0001c0001t0001g0161 a0001c0001t0003g0201 others(80): Show |
84 | HG00323.hp1 HG00621.hp2 HG00639.hp2 others(81): Show |
intron_variant | MODIFIER | c.1126-1675_1126-167 others(7): Show |
MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr17 | 12750734 | ||||||
chr17:12750822 | A | G | 82 | a0001c0001t0001g0104 a0001c0001t0001g0161 a0001c0001t0003g0201 others(79): Show |
83 | HG00323.hp1 HG00621.hp2 HG00639.hp2 others(80): Show |
intron_variant | MODIFIER | c.1126-1592A>G | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 9/13 | chr17 | 12750822 | |||||||
chr17:12750855 | G | A | 1 | a0001c0003t0112g0035 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1126-1559G>A | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 9/13 | chr17 | 12750855 | |||||||
chr17:12750866 | G | C | 26 | a0001c0002t0001g0167 a0001c0002t0002g0239 a0001c0002t0003g0299 others(23): Show |
26 | HG00408.hp1 HG00408.hp2 HG00639.hp1 others(23): Show |
intron_variant | MODIFIER | c.1126-1548G>C | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 9/13 | chr17 | 12750866 | |||||||
chr17:12750884 | T | C | 1 | a0001c0001t0140g0073 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1126-1530T>C | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 9/13 | chr17 | 12750884 | |||||||
chr17:12751171 | C | T | 3 | a0001c0001t0005g0199 a0001c0001t0023g0253 a0004c0017t0007g0252 |
3 | NA18612.hp2 NA18990.hp2 NA19055.hp2 |
intron_variant | MODIFIER | c.1126-1243C>T | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 9/13 | chr17 | 12751171 | |||||||
chr17:12751218 | C | T | 3 | a0001c0002t0001g0167 a0001c0002t0177g0192 a0001c0002t0178g0072 |
3 | HG00408.hp2 HG02074.hp2 HG02523.hp1 |
intron_variant | MODIFIER | c.1126-1196C>T | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 9/13 | chr17 | 12751218 | |||||||
chr17:12751299 | G | A | 200 | a0001c0001t0001g0028 a0001c0001t0001g0058 a0001c0001t0001g0079 others(197): Show |
203 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(200): Show |
intron_variant | MODIFIER | c.1126-1115G>A | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 9/13 | chr17 | 12751299 | |||||||
chr17:12751360 | A | G | 3 | a0001c0001t0073g0337 a0001c0001t0201g0334 a0001c0003t0204g0038 |
3 | HG02886.hp1 HG03540.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.1126-1054A>G | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 9/13 | chr17 | 12751360 | |||||||
chr17:12751640 | C | T | 47 | a0001c0001t0001g0051 a0001c0001t0001g0069 a0001c0001t0001g0136 others(44): Show |
47 | HG00280.hp1 HG00423.hp2 HG00642.hp1 others(44): Show |
intron_variant | MODIFIER | c.1126-774C>T | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 9/13 | chr17 | 12751640 | |||||||
chr17:12751700 | G | A | 3 | a0001c0001t0024g0016 a0001c0001t0024g0165 a0001c0001t0080g0291 |
3 | NA18949.hp2 NA19007.hp2 NA19056.hp2 |
intron_variant | MODIFIER | c.1126-714G>A | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 9/13 | chr17 | 12751700 | |||||||
chr17:12751764 | A | G | 142 | a0001c0001t0001g0028 a0001c0001t0001g0058 a0001c0001t0001g0079 others(139): Show |
143 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(140): Show |
intron_variant | MODIFIER | c.1126-650A>G | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 9/13 | chr17 | 12751764 | |||||||
chr17:12751886 | C | T | 1 | a0001c0001t0033g0034 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1126-528C>T | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 9/13 | chr17 | 12751886 | |||||||
chr17:12751912 | A | C | 4 | a0001c0003t0046g0121 a0001c0003t0046g0122 a0001c0003t0181g0031 others(1): Show |
4 | HG02896.hp1 HG02897.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.1126-502A>C | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 9/13 | chr17 | 12751912 | |||||||
chr17:12751949 | A | G | 6 | a0001c0001t0011g0224 a0001c0001t0011g0229 a0001c0001t0011g0230 others(3): Show |
6 | HG02055.hp2 HG02559.hp2 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.1126-465A>G | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 9/13 | chr17 | 12751949 | |||||||
chr17:12752115 | A | C | 48 | a0001c0001t0001g0051 a0001c0001t0001g0069 a0001c0001t0001g0077 others(45): Show |
48 | HG00280.hp1 HG00423.hp2 HG00642.hp1 others(45): Show |
intron_variant | MODIFIER | c.1126-299A>C | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 9/13 | chr17 | 12752115 | |||||||
chr17:12752129 | G | T | 31 | a0001c0002t0001g0167 a0001c0002t0002g0239 a0001c0002t0003g0299 others(28): Show |
31 | HG00408.hp1 HG00408.hp2 HG00639.hp1 others(28): Show |
intron_variant | MODIFIER | c.1126-285G>T | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 9/13 | chr17 | 12752129 | |||||||
chr17:12752282 | G | A | 1 | a0001c0001t0011g0230 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1126-132G>A | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 9/13 | chr17 | 12752282 | |||||||
chr17:12752360 | C | T | 1 | a0001c0001t0009g0328 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.1126-54C>T | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 9/13 | chr17 | 12752360 | |||||||
chr17:12753394 | G | A | 104 | a0001c0001t0001g0104 a0001c0001t0001g0161 a0001c0001t0003g0201 others(101): Show |
106 | HG00323.hp1 HG00621.hp2 HG00639.hp2 others(103): Show |
intron_variant | MODIFIER | c.2058+48G>A | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 10/13 | chr17 | 12753394 | |||||||
chr17:12753478 | G | T | 2 | a0001c0001t0002g0187 a0001c0001t0066g0327 |
2 | HG00735.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.2058+132G>T | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 10/13 | chr17 | 12753478 | |||||||
chr17:12753497 | C | A | 110 | a0001c0001t0001g0028 a0001c0001t0001g0058 a0001c0001t0001g0079 others(107): Show |
111 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(108): Show |
intron_variant | MODIFIER | c.2058+151C>A | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 10/13 | chr17 | 12753497 | |||||||
chr17:12753498 | C | T | 186 | a0001c0001t0001g0051 a0001c0001t0001g0069 a0001c0001t0001g0077 others(183): Show |
188 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(185): Show |
intron_variant | MODIFIER | c.2058+152C>T | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 10/13 | chr17 | 12753498 | |||||||
chr17:12753528 | A | T | 1 | a0001c0001t0179g0135 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.2058+182A>T | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 10/13 | chr17 | 12753528 | |||||||
chr17:12753599 | G | A | 2 | a0001c0001t0033g0034 a0001c0003t0105g0020 |
2 | HG01884.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.2058+253G>A | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 10/13 | chr17 | 12753599 | |||||||
chr17:12753680 | G | C | 105 | a0001c0001t0001g0104 a0001c0001t0001g0161 a0001c0001t0003g0201 others(102): Show |
107 | HG00323.hp1 HG00621.hp2 HG00639.hp2 others(104): Show |
intron_variant | MODIFIER | c.2058+334G>C | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 10/13 | chr17 | 12753680 | |||||||
chr17:12753834 | T | A | 32 | a0001c0001t0048g0196 a0001c0001t0195g0284 a0001c0002t0001g0167 others(29): Show |
32 | HG00408.hp1 HG00408.hp2 HG00639.hp1 others(29): Show |
intron_variant | MODIFIER | c.2058+488T>A | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 10/13 | chr17 | 12753834 | |||||||
chr17:12753852 | C | A | 1 | a0001c0003t0202g0210 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.2058+506C>A | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 10/13 | chr17 | 12753852 | |||||||
chr17:12754061 | G | GGTGT | 29 | a0001c0001t0003g0201 a0001c0001t0065g0330 a0001c0001t0195g0284 others(26): Show |
29 | HG00408.hp2 HG00639.hp1 HG00642.hp1 others(26): Show |
intron_variant | MODIFIER | c.2058+726_2058+729d others(6): Show |
MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr17 | 12754061 | ||||||
chr17:12754061 | G | GGTGTGT | 13 | a0001c0001t0001g0176 a0001c0001t0001g0177 a0001c0001t0005g0085 others(10): Show |
13 | HG01081.hp2 HG01346.hp2 HG01358.hp1 others(10): Show |
intron_variant | MODIFIER | c.2058+724_2058+729d others(8): Show |
MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr17 | 12754061 | ||||||
chr17:12754061 | G | GGTGTGTG others(1): Show |
11 | a0001c0001t0001g0051 a0001c0001t0001g0136 a0001c0001t0007g0163 others(8): Show |
11 | HG01109.hp1 HG01175.hp1 HG01952.hp1 others(8): Show |
intron_variant | MODIFIER | c.2058+722_2058+729d others(10): Show |
MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr17 | 12754061 | ||||||
chr17:12754061 | G | GGTGTGTG others(3): Show |
19 | a0001c0001t0002g0018 a0001c0001t0002g0187 a0001c0001t0002g0208 others(16): Show |
19 | HG00280.hp2 HG00423.hp2 HG00733.hp1 others(16): Show |
intron_variant | MODIFIER | c.2058+720_2058+729d others(12): Show |
MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr17 | 12754061 | ||||||
chr17:12754061 | G | GGTGTGTG others(5): Show |
1 | a0001c0001t0131g0114 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.2058+718_2058+729d others(14): Show |
MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr17 | 12754061 | ||||||
chr17:12754061 | G | GGTGTGTG others(9): Show |
1 | a0001c0001t0161g0190 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.2058+729_2058+730i others(18): Show |
MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr17 | 12754061 | ||||||
chr17:12754074 | GTA | G | 117 | a0001c0001t0001g0104 a0001c0001t0001g0155 a0001c0001t0001g0161 others(114): Show |
119 | HG00323.hp1 HG00597.hp2 HG00621.hp2 others(116): Show |
intron_variant | MODIFIER | c.2058+730_2058+731d others(4): Show |
MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr17 | 12754074 | ||||||
chr17:12754076 | A | G | 77 | a0001c0001t0001g0051 a0001c0001t0001g0136 a0001c0001t0001g0176 others(74): Show |
77 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(74): Show |
intron_variant | MODIFIER | c.2058+730A>G | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 10/13 | chr17 | 12754076 | |||||||
chr17:12754076 | ATG | A | 20 | a0001c0001t0026g0234 a0001c0001t0030g0301 a0001c0001t0054g0314 others(17): Show |
20 | HG00544.hp1 HG00673.hp1 HG00741.hp2 others(17): Show |
intron_variant | MODIFIER | c.2058+748_2058+749d others(4): Show |
MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr17 | 12754076 | ||||||
chr17:12754080 | G | A | 117 | a0001c0001t0001g0104 a0001c0001t0001g0155 a0001c0001t0001g0161 others(114): Show |
119 | HG00323.hp1 HG00597.hp2 HG00621.hp2 others(116): Show |
intron_variant | MODIFIER | c.2058+734G>A | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 10/13 | chr17 | 12754080 | |||||||
chr17:12754197 | C | T | 1 | a0003c0008t0104g0021 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.2058+851C>T | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 10/13 | chr17 | 12754197 | |||||||
chr17:12754198 | G | A | 30 | a0001c0001t0048g0196 a0001c0001t0195g0284 a0001c0002t0001g0167 others(27): Show |
30 | HG00408.hp1 HG00408.hp2 HG00639.hp1 others(27): Show |
intron_variant | MODIFIER | c.2058+852G>A | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 10/13 | chr17 | 12754198 | |||||||
chr17:12754207 | C | T | 6 | a0001c0001t0001g0028 a0001c0001t0001g0089 a0001c0001t0006g0068 others(3): Show |
6 | HG00609.hp2 HG02080.hp1 NA18964.hp1 others(3): Show |
intron_variant | MODIFIER | c.2058+861C>T | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 10/13 | chr17 | 12754207 | |||||||
chr17:12754256 | C | G | 1 | a0012c0029t0115g0335 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.2058+910C>G | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 10/13 | chr17 | 12754256 | |||||||
chr17:12754278 | AT | A | 8 | a0001c0001t0028g0002 a0001c0001t0057g0317 a0001c0001t0061g0318 others(5): Show |
9 | HG02647.hp1 HG02809.hp1 HG02922.hp1 others(6): Show |
intron_variant | MODIFIER | c.2058+937delT | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr17 | 12754278 | ||||||
chr17:12754309 | G | A | 1 | a0001c0001t0151g0182 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.2058+963G>A | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 10/13 | chr17 | 12754309 | |||||||
chr17:12754338 | G | A | 1 | a0001c0001t0146g0019 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.2058+992G>A | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 10/13 | chr17 | 12754338 | |||||||
chr17:12754382 | G | A | 4 | a0001c0001t0040g0256 a0001c0003t0181g0031 a0001c0003t0182g0271 others(1): Show |
4 | HG02055.hp1 HG02486.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.2058+1036G>A | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 10/13 | chr17 | 12754382 | |||||||
chr17:12754392 | A | G | 10 | a0001c0001t0002g0157 a0001c0001t0006g0067 a0001c0001t0017g0156 others(7): Show |
10 | HG02055.hp1 HG02486.hp1 HG03041.hp1 others(7): Show |
intron_variant | MODIFIER | c.2058+1046A>G | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 10/13 | chr17 | 12754392 | |||||||
chr17:12754393 | T | C | 6 | a0001c0001t0002g0157 a0001c0001t0006g0067 a0001c0001t0017g0156 others(3): Show |
6 | NA18939.hp1 NA18939.hp2 NA18953.hp2 others(3): Show |
intron_variant | MODIFIER | c.2058+1047T>C | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 10/13 | chr17 | 12754393 | |||||||
chr17:12754398 | A | G | 4 | a0001c0001t0040g0256 a0001c0003t0181g0031 a0001c0003t0182g0271 others(1): Show |
4 | HG02055.hp1 HG02486.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.2058+1052A>G | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 10/13 | chr17 | 12754398 | |||||||
chr17:12754527 | G | A | 174 | a0001c0001t0001g0028 a0001c0001t0001g0051 a0001c0001t0001g0058 others(171): Show |
174 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(171): Show |
intron_variant | MODIFIER | c.2058+1181G>A | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 10/13 | chr17 | 12754527 | |||||||
chr17:12754623 | A | G | 1 | a0001c0001t0010g0191 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.2058+1277A>G | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 10/13 | chr17 | 12754623 | |||||||
chr17:12754651 | G | A | 86 | a0001c0001t0001g0028 a0001c0001t0001g0058 a0001c0001t0001g0069 others(83): Show |
86 | HG00280.hp1 HG00323.hp2 HG00423.hp1 others(83): Show |
intron_variant | MODIFIER | c.2058+1305G>A | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 10/13 | chr17 | 12754651 | |||||||
chr17:12754706 | G | A | 226 | a0001c0001t0001g0028 a0001c0001t0001g0051 a0001c0001t0001g0058 others(223): Show |
227 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(224): Show |
intron_variant | MODIFIER | c.2058+1360G>A | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 10/13 | chr17 | 12754706 | |||||||
chr17:12754750 | T | G | 3 | a0001c0001t0155g0172 a0001c0003t0206g0294 a0009c0020t0194g0226 |
3 | HG02055.hp2 NA19043.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.2058+1404T>G | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 10/13 | chr17 | 12754750 | |||||||
chr17:12754784 | T | C | 259 | a0001c0001t0001g0028 a0001c0001t0001g0051 a0001c0001t0001g0058 others(256): Show |
261 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(258): Show |
intron_variant | MODIFIER | c.2058+1438T>C | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 10/13 | chr17 | 12754784 | |||||||
chr17:12754989 | G | T | 2 | a0001c0003t0181g0031 a0001c0003t0182g0271 |
2 | HG03041.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.2059-1425G>T | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 10/13 | chr17 | 12754989 | |||||||
chr17:12755053 | A | G | 100 | a0001c0001t0001g0104 a0001c0001t0001g0155 a0001c0001t0003g0116 others(97): Show |
101 | HG00597.hp2 HG00621.hp2 HG00733.hp2 others(98): Show |
intron_variant | MODIFIER | c.2059-1361A>G | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 10/13 | chr17 | 12755053 | |||||||
chr17:12755108 | GTGGGAGA others(4): Show |
G | 1 | a0001c0001t0039g0138 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.2059-1305_2059-129 others(15): Show |
MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 10/13 | chr17 | 12755108 | |||||||
chr17:12755259 | C | T | 262 | a0001c0001t0001g0028 a0001c0001t0001g0051 a0001c0001t0001g0058 others(259): Show |
264 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(261): Show |
intron_variant | MODIFIER | c.2059-1155C>T | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 10/13 | chr17 | 12755259 | |||||||
chr17:12755336 | C | T | 1 | a0001c0002t0001g0167 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.2059-1078C>T | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 10/13 | chr17 | 12755336 | |||||||
chr17:12755337 | G | A | 4 | a0001c0001t0134g0215 a0001c0001t0184g0217 a0001c0001t0186g0214 others(1): Show |
4 | HG00639.hp2 NA18960.hp2 NA19004.hp1 others(1): Show |
intron_variant | MODIFIER | c.2059-1077G>A | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 10/13 | chr17 | 12755337 | |||||||
chr17:12755380 | G | A | 1 | a0001c0001t0004g0164 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.2059-1034G>A | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 10/13 | chr17 | 12755380 | |||||||
chr17:12755409 | G | C | 1 | a0001c0001t0001g0089 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.2059-1005G>C | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 10/13 | chr17 | 12755409 | |||||||
chr17:12755561 | T | G | 1 | a0001c0001t0017g0139 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.2059-853T>G | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 10/13 | chr17 | 12755561 | |||||||
chr17:12755667 | A | G | 1 | a0016c0021t0175g0087 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.2059-747A>G | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 10/13 | chr17 | 12755667 | |||||||
chr17:12755679 | C | T | 1 | a0001c0001t0146g0019 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.2059-735C>T | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 10/13 | chr17 | 12755679 | |||||||
chr17:12755683 | C | T | 1 | a0001c0001t0106g0310 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.2059-731C>T | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 10/13 | chr17 | 12755683 | |||||||
chr17:12755732 | C | T | 2 | a0001c0001t0005g0232 a0001c0001t0023g0251 |
2 | NA18974.hp2 NA19005.hp1 |
intron_variant | MODIFIER | c.2059-682C>T | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 10/13 | chr17 | 12755732 | |||||||
chr17:12755743 | G | A | 7 | a0001c0001t0018g0042 a0001c0001t0018g0223 a0001c0001t0040g0272 others(4): Show |
7 | HG02615.hp1 HG02896.hp1 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.2059-671G>A | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 10/13 | chr17 | 12755743 | |||||||
chr17:12755744 | C | T | 8 | a0001c0001t0057g0317 a0001c0001t0119g0280 a0001c0001t0121g0037 others(5): Show |
9 | HG02451.hp1 HG02809.hp1 HG02922.hp2 others(6): Show |
intron_variant | MODIFIER | c.2059-670C>T | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 10/13 | chr17 | 12755744 | |||||||
chr17:12755772 | T | C | 65 | a0001c0001t0001g0058 a0001c0001t0001g0069 a0001c0001t0001g0077 others(62): Show |
65 | HG00280.hp1 HG00323.hp2 HG00423.hp1 others(62): Show |
intron_variant | MODIFIER | c.2059-642T>C | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 10/13 | chr17 | 12755772 | |||||||
chr17:12755779 | A | G | 96 | a0001c0001t0001g0028 a0001c0001t0001g0058 a0001c0001t0001g0069 others(93): Show |
96 | HG00280.hp1 HG00323.hp2 HG00423.hp1 others(93): Show |
intron_variant | MODIFIER | c.2059-635A>G | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 10/13 | chr17 | 12755779 | |||||||
chr17:12755846 | C | T | 7 | a0001c0001t0018g0042 a0001c0001t0018g0223 a0001c0001t0040g0272 others(4): Show |
7 | HG02615.hp1 HG02896.hp1 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.2059-568C>T | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 10/13 | chr17 | 12755846 | |||||||
chr17:12755850 | C | T | 7 | a0001c0001t0018g0042 a0001c0001t0018g0223 a0001c0001t0040g0272 others(4): Show |
7 | HG02615.hp1 HG02896.hp1 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.2059-564C>T | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 10/13 | chr17 | 12755850 | |||||||
chr17:12755867 | G | A | 1 | a0001c0001t0073g0337 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.2059-547G>A | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 10/13 | chr17 | 12755867 | |||||||
chr17:12755977 | G | T | 87 | a0001c0001t0001g0028 a0001c0001t0001g0058 a0001c0001t0001g0069 others(84): Show |
87 | HG00280.hp1 HG00323.hp2 HG00423.hp1 others(84): Show |
intron_variant | MODIFIER | c.2059-437G>T | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 10/13 | chr17 | 12755977 | |||||||
chr17:12756180 | TC | T | 3 | a0001c0001t0106g0310 a0001c0003t0105g0020 a0013c0027t0110g0222 |
3 | HG02647.hp2 HG02723.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.2059-232delC | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr17 | 12756180 | ||||||
chr17:12756182 | C | T | 87 | a0001c0001t0001g0028 a0001c0001t0001g0058 a0001c0001t0001g0069 others(84): Show |
87 | HG00280.hp1 HG00323.hp2 HG00423.hp1 others(84): Show |
intron_variant | MODIFIER | c.2059-232C>T | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 10/13 | chr17 | 12756182 | |||||||
chr17:12756576 | G | A | 2 | a0001c0001t0034g0146 a0001c0001t0059g0323 |
2 | NA18951.hp1 NA18984.hp2 |
intron_variant | MODIFIER | c.2202+19G>A | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 11/13 | chr17 | 12756576 | |||||||
chr17:12756695 | C | CA | 11 | a0001c0001t0006g0067 a0001c0001t0006g0250 a0001c0001t0008g0052 others(8): Show |
11 | HG00323.hp1 HG01175.hp1 HG01981.hp1 others(8): Show |
intron_variant | MODIFIER | c.2202+157dupA | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr17 | 12756695 | ||||||
chr17:12756695 | C | CAAAAAAA others(3): Show |
2 | a0001c0001t0073g0337 a0001c0003t0202g0210 |
2 | NA19030.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.2202+148_2202+157d others(12): Show |
MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr17 | 12756695 | ||||||
chr17:12756695 | C | CAAAAAAA others(4): Show |
4 | a0001c0001t0001g0069 a0001c0001t0015g0081 a0001c0001t0165g0198 others(1): Show |
4 | HG00741.hp2 HG01261.hp2 HG03239.hp2 others(1): Show |
intron_variant | MODIFIER | c.2202+147_2202+157d others(13): Show |
MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr17 | 12756695 | ||||||
chr17:12756695 | C | CAAAAAAA others(5): Show |
46 | a0001c0001t0001g0058 a0001c0001t0001g0079 a0001c0001t0001g0086 others(43): Show |
46 | HG00280.hp1 HG00323.hp2 HG00423.hp1 others(43): Show |
intron_variant | MODIFIER | c.2202+146_2202+157d others(14): Show |
MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr17 | 12756695 | ||||||
chr17:12756695 | C | CAAAAAAA others(6): Show |
14 | a0001c0001t0001g0089 a0001c0001t0001g0136 a0001c0001t0002g0112 others(11): Show |
14 | HG00558.hp2 HG01106.hp2 HG02080.hp1 others(11): Show |
intron_variant | MODIFIER | c.2202+145_2202+157d others(15): Show |
MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr17 | 12756695 | ||||||
chr17:12756695 | CA | C | 62 | a0001c0001t0001g0051 a0001c0001t0001g0077 a0001c0001t0001g0176 others(59): Show |
64 | HG00280.hp2 HG00423.hp2 HG00639.hp1 others(61): Show |
intron_variant | MODIFIER | c.2202+157delA | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr17 | 12756695 | ||||||
chr17:12756760 | A | T | 3 | a0001c0001t0155g0172 a0001c0003t0206g0294 a0009c0020t0194g0226 |
3 | HG02055.hp2 NA19043.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.2202+203A>T | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 11/13 | chr17 | 12756760 | |||||||
chr17:12756765 | T | C | 1 | a0001c0001t0028g0002 | 2 | HG03139.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.2202+208T>C | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 11/13 | chr17 | 12756765 | |||||||
chr17:12756789 | G | A | 74 | a0001c0001t0001g0058 a0001c0001t0001g0069 a0001c0001t0001g0079 others(71): Show |
74 | HG00280.hp1 HG00323.hp2 HG00423.hp1 others(71): Show |
intron_variant | MODIFIER | c.2202+232G>A | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 11/13 | chr17 | 12756789 | |||||||
chr17:12756797 | G | A | 3 | a0001c0001t0106g0310 a0001c0003t0105g0020 a0013c0027t0110g0222 |
3 | HG02647.hp2 HG02723.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.2202+240G>A | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 11/13 | chr17 | 12756797 | |||||||
chr17:12757525 | C | T | 1 | a0005c0010t0145g0149 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.2203-560C>T | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 11/13 | chr17 | 12757525 | |||||||
chr17:12757557 | C | T | 72 | a0001c0001t0001g0058 a0001c0001t0001g0069 a0001c0001t0001g0079 others(69): Show |
72 | HG00280.hp1 HG00323.hp2 HG00423.hp1 others(69): Show |
intron_variant | MODIFIER | c.2203-528C>T | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 11/13 | chr17 | 12757557 | |||||||
chr17:12757590 | A | T | 1 | a0001c0001t0001g0343 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.2203-495A>T | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 11/13 | chr17 | 12757590 | |||||||
chr17:12757595 | C | G | 33 | a0001c0001t0006g0098 a0001c0001t0027g0297 a0001c0001t0048g0196 others(30): Show |
33 | HG00408.hp1 HG00408.hp2 HG00544.hp2 others(30): Show |
intron_variant | MODIFIER | c.2203-490C>G | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 11/13 | chr17 | 12757595 | |||||||
chr17:12757599 | C | T | 1 | a0001c0001t0019g0113 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.2203-486C>T | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 11/13 | chr17 | 12757599 | |||||||
chr17:12757644 | A | G | 55 | a0001c0001t0001g0051 a0001c0001t0001g0077 a0001c0001t0001g0176 others(52): Show |
55 | HG00280.hp2 HG00423.hp2 HG00642.hp1 others(52): Show |
intron_variant | MODIFIER | c.2203-441A>G | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 11/13 | chr17 | 12757644 | |||||||
chr17:12757813 | T | C | 1 | a0001c0001t0087g0179 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.2203-272T>C | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 11/13 | chr17 | 12757813 | |||||||
chr17:12757895 | C | T | 1 | a0001c0001t0170g0099 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.2203-190C>T | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 11/13 | chr17 | 12757895 | |||||||
chr17:12758234 | T | C | 1 | a0001c0002t0198g0197 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.2331+21T>C | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 12/13 | chr17 | 12758234 | |||||||
chr17:12758274 | G | C | 4 | a0001c0001t0106g0310 a0001c0003t0105g0020 a0001c0003t0109g0306 others(1): Show |
4 | HG02572.hp2 HG02647.hp2 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.2331+61G>C | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 12/13 | chr17 | 12758274 | |||||||
chr17:12758291 | C | T | 1 | a0001c0001t0001g0124 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.2331+78C>T | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 12/13 | chr17 | 12758291 | |||||||
chr17:12758292 | G | A | 1 | a0001c0001t0002g0157 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.2331+79G>A | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 12/13 | chr17 | 12758292 | |||||||
chr17:12758332 | A | G | 1 | a0001c0001t0060g0320 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.2331+119A>G | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 12/13 | chr17 | 12758332 | |||||||
chr17:12758504 | G | T | 1 | a0001c0001t0116g0270 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.2331+291G>T | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 12/13 | chr17 | 12758504 | |||||||
chr17:12758537 | C | A | 3 | a0001c0001t0155g0172 a0001c0003t0206g0294 a0009c0020t0194g0226 |
3 | HG02055.hp2 NA19043.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.2331+324C>A | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 12/13 | chr17 | 12758537 | |||||||
chr17:12758603 | T | G | 1 | a0001c0001t0039g0138 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.2331+390T>G | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 12/13 | chr17 | 12758603 | |||||||
chr17:12758627 | G | C | 1 | a0001c0001t0039g0138 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.2331+414G>C | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 12/13 | chr17 | 12758627 | |||||||
chr17:12758628 | C | T | 1 | a0001c0001t0039g0138 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.2331+415C>T | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 12/13 | chr17 | 12758628 | |||||||
chr17:12758631 | T | A | 1 | a0001c0001t0039g0138 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.2331+418T>A | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 12/13 | chr17 | 12758631 | |||||||
chr17:12758984 | G | C | 1 | a0001c0001t0005g0232 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.2331+771G>C | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 12/13 | chr17 | 12758984 | |||||||
chr17:12758997 | G | A | 4 | a0001c0001t0091g0309 a0001c0001t0092g0311 a0001c0001t0107g0041 others(1): Show |
4 | HG02486.hp2 HG02630.hp1 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.2331+784G>A | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 12/13 | chr17 | 12758997 | |||||||
chr17:12759066 | A | G | 1 | a0016c0021t0175g0087 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.2331+853A>G | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 12/13 | chr17 | 12759066 | |||||||
chr17:12759298 | G | C | 1 | a0001c0003t0049g0134 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.2331+1085G>C | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 12/13 | chr17 | 12759298 | |||||||
chr17:12759328 | C | T | 38 | a0001c0001t0001g0051 a0001c0001t0001g0176 a0001c0001t0001g0177 others(35): Show |
38 | HG00280.hp2 HG00423.hp2 HG00642.hp1 others(35): Show |
intron_variant | MODIFIER | c.2331+1115C>T | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 12/13 | chr17 | 12759328 | |||||||
chr17:12759533 | T | C | 1 | a0016c0021t0175g0087 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.2332-1117T>C | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 12/13 | chr17 | 12759533 | |||||||
chr17:12760138 | A | G | 44 | a0001c0001t0001g0051 a0001c0001t0001g0077 a0001c0001t0001g0176 others(41): Show |
44 | HG00280.hp2 HG00423.hp2 HG00642.hp1 others(41): Show |
intron_variant | MODIFIER | c.2332-512A>G | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 12/13 | chr17 | 12760138 | |||||||
chr17:12760225 | G | A | 2 | a0001c0001t0038g0024 a0001c0001t0086g0092 |
2 | NA18956.hp1 NA18968.hp2 |
intron_variant | MODIFIER | c.2332-425G>A | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 12/13 | chr17 | 12760225 | |||||||
chr17:12760260 | A | C | 71 | a0001c0001t0001g0058 a0001c0001t0001g0069 a0001c0001t0001g0079 others(68): Show |
71 | HG00280.hp1 HG00323.hp2 HG00423.hp1 others(68): Show |
intron_variant | MODIFIER | c.2332-390A>C | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 12/13 | chr17 | 12760260 | |||||||
chr17:12760379 | G | A | 129 | a0001c0001t0001g0058 a0001c0001t0001g0069 a0001c0001t0001g0079 others(126): Show |
129 | HG00280.hp1 HG00323.hp2 HG00423.hp1 others(126): Show |
intron_variant | MODIFIER | c.2332-271G>A | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 12/13 | chr17 | 12760379 | |||||||
chr17:12760384 | C | T | 1 | a0011c0030t0114g0262 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.2332-266C>T | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 12/13 | chr17 | 12760384 | |||||||
chr17:12760385 | G | A | 1 | a0001c0001t0002g0208 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.2332-265G>A | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 12/13 | chr17 | 12760385 | |||||||
chr17:12760404 | G | T | 65 | a0001c0001t0001g0058 a0001c0001t0001g0069 a0001c0001t0001g0079 others(62): Show |
65 | HG00280.hp1 HG00323.hp2 HG00423.hp1 others(62): Show |
intron_variant | MODIFIER | c.2332-246G>T | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 12/13 | chr17 | 12760404 | |||||||
chr17:12760435 | G | T | 1 | a0001c0001t0039g0138 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.2332-215G>T | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 12/13 | chr17 | 12760435 | |||||||
chr17:12760436 | G | A | 1 | a0001c0001t0172g0043 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.2332-214G>A | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 12/13 | chr17 | 12760436 | |||||||
chr17:12760524 | C | T | 3 | a0001c0001t0073g0337 a0001c0001t0103g0339 a0001c0001t0108g0342 |
3 | HG02622.hp1 HG02886.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.2332-126C>T | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 12/13 | chr17 | 12760524 | |||||||
chr17:12760806 | G | T | 1 | a0001c0001t0006g0140 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.2389+99G>T | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 13/13 | chr17 | 12760806 | |||||||
chr17:12760853 | C | T | 30 | a0001c0001t0006g0098 a0001c0001t0027g0297 a0001c0001t0048g0196 others(27): Show |
30 | HG00408.hp1 HG00408.hp2 HG00544.hp2 others(27): Show |
intron_variant | MODIFIER | c.2389+146C>T | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 13/13 | chr17 | 12760853 | |||||||
chr17:12760854 | G | A | 1 | a0001c0001t0019g0113 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.2389+147G>A | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 13/13 | chr17 | 12760854 | |||||||
chr17:12760860 | T | C | 73 | a0001c0001t0001g0058 a0001c0001t0001g0069 a0001c0001t0001g0077 others(70): Show |
73 | HG00280.hp1 HG00323.hp2 HG00423.hp1 others(70): Show |
intron_variant | MODIFIER | c.2389+153T>C | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 13/13 | chr17 | 12760860 | |||||||
chr17:12760876 | A | G | 2 | a0001c0001t0034g0146 a0001c0001t0059g0323 |
2 | NA18951.hp1 NA18984.hp2 |
intron_variant | MODIFIER | c.2389+169A>G | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 13/13 | chr17 | 12760876 | |||||||
chr17:12760942 | A | T | 3 | a0001c0001t0018g0042 a0001c0001t0018g0223 a0001c0001t0040g0272 |
3 | HG02615.hp1 HG03471.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.2389+235A>T | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 13/13 | chr17 | 12760942 | |||||||
chr17:12760999 | CTTCT | C | 71 | a0001c0001t0001g0058 a0001c0001t0001g0069 a0001c0001t0001g0079 others(68): Show |
71 | HG00280.hp1 HG00323.hp2 HG00423.hp1 others(68): Show |
intron_variant | MODIFIER | c.2389+297_2389+300d others(6): Show |
MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 13/13 | INFO_REALIGN_3_PRIME | chr17 | 12760999 | ||||||
chr17:12761030 | A | G | 71 | a0001c0001t0001g0058 a0001c0001t0001g0069 a0001c0001t0001g0079 others(68): Show |
71 | HG00280.hp1 HG00323.hp2 HG00423.hp1 others(68): Show |
intron_variant | MODIFIER | c.2389+323A>G | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 13/13 | chr17 | 12761030 | |||||||
chr17:12761083 | C | G | 30 | a0001c0001t0006g0098 a0001c0001t0027g0297 a0001c0001t0048g0196 others(27): Show |
30 | HG00408.hp1 HG00408.hp2 HG00544.hp2 others(27): Show |
intron_variant | MODIFIER | c.2389+376C>G | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 13/13 | chr17 | 12761083 | |||||||
chr17:12761105 | A | C | 4 | a0001c0001t0134g0215 a0001c0001t0184g0217 a0001c0001t0186g0214 others(1): Show |
4 | HG00639.hp2 NA18960.hp2 NA19004.hp1 others(1): Show |
intron_variant | MODIFIER | c.2389+398A>C | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 13/13 | chr17 | 12761105 | |||||||
chr17:12761231 | G | A | 6 | a0001c0001t0011g0224 a0001c0001t0011g0229 a0001c0001t0011g0230 others(3): Show |
6 | HG02145.hp2 HG02559.hp1 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.2389+524G>A | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 13/13 | chr17 | 12761231 | |||||||
chr17:12761406 | TA | T | 71 | a0001c0001t0001g0058 a0001c0001t0001g0069 a0001c0001t0001g0079 others(68): Show |
71 | HG00280.hp1 HG00323.hp2 HG00423.hp1 others(68): Show |
intron_variant | MODIFIER | c.2389+700delA | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 13/13 | chr17 | 12761406 | |||||||
chr17:12761408 | T | G | 71 | a0001c0001t0001g0058 a0001c0001t0001g0069 a0001c0001t0001g0079 others(68): Show |
71 | HG00280.hp1 HG00323.hp2 HG00423.hp1 others(68): Show |
intron_variant | MODIFIER | c.2389+701T>G | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 13/13 | chr17 | 12761408 | |||||||
chr17:12761409 | G | C | 71 | a0001c0001t0001g0058 a0001c0001t0001g0069 a0001c0001t0001g0079 others(68): Show |
71 | HG00280.hp1 HG00323.hp2 HG00423.hp1 others(68): Show |
intron_variant | MODIFIER | c.2389+702G>C | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 13/13 | chr17 | 12761409 | |||||||
chr17:12761449 | G | A | 1 | a0001c0001t0005g0091 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.2389+742G>A | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 13/13 | chr17 | 12761449 | |||||||
chr17:12761490 | C | T | 1 | a0001c0001t0001g0077 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.2389+783C>T | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 13/13 | chr17 | 12761490 | |||||||
chr17:12761528 | A | C | 1 | a0016c0021t0175g0087 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.2389+821A>C | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 13/13 | chr17 | 12761528 | |||||||
chr17:12761590 | T | TAC | 47 | a0001c0001t0001g0028 a0001c0001t0001g0161 a0001c0001t0002g0018 others(44): Show |
48 | HG00280.hp2 HG00323.hp1 HG00642.hp1 others(45): Show |
intron_variant | MODIFIER | c.2389+929_2389+930d others(4): Show |
MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 13/13 | INFO_REALIGN_3_PRIME | chr17 | 12761590 | ||||||
chr17:12761590 | T | TACAC | 45 | a0001c0001t0001g0051 a0001c0001t0001g0176 a0001c0001t0001g0177 others(42): Show |
47 | HG00423.hp2 HG00544.hp1 HG00642.hp2 others(44): Show |
intron_variant | MODIFIER | c.2389+927_2389+930d others(6): Show |
MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 13/13 | INFO_REALIGN_3_PRIME | chr17 | 12761590 | ||||||
chr17:12761590 | T | TACACAC | 23 | a0001c0001t0002g0119 a0001c0001t0005g0085 a0001c0001t0006g0067 others(20): Show |
23 | HG00639.hp1 HG01255.hp1 HG01433.hp2 others(20): Show |
intron_variant | MODIFIER | c.2389+925_2389+930d others(8): Show |
MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 13/13 | INFO_REALIGN_3_PRIME | chr17 | 12761590 | ||||||
chr17:12761590 | T | TACACACA others(1): Show |
7 | a0001c0001t0006g0098 a0001c0001t0037g0175 a0001c0001t0048g0158 others(4): Show |
7 | HG00408.hp1 HG02132.hp2 HG03491.hp1 others(4): Show |
intron_variant | MODIFIER | c.2389+923_2389+930d others(10): Show |
MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 13/13 | INFO_REALIGN_3_PRIME | chr17 | 12761590 | ||||||
chr17:12761590 | T | TACACACA others(3): Show |
4 | a0001c0001t0002g0157 a0001c0001t0139g0013 a0001c0002t0047g0300 others(1): Show |
4 | HG02074.hp2 HG03831.hp1 NA18975.hp2 others(1): Show |
intron_variant | MODIFIER | c.2389+921_2389+930d others(12): Show |
MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 13/13 | INFO_REALIGN_3_PRIME | chr17 | 12761590 | ||||||
chr17:12761590 | T | TACACACA others(5): Show |
1 | a0001c0002t0062g0322 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.2389+919_2389+930d others(14): Show |
MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 13/13 | INFO_REALIGN_3_PRIME | chr17 | 12761590 | ||||||
chr17:12761590 | T | TACACACA others(7): Show |
4 | a0001c0001t0005g0232 a0001c0001t0132g0025 a0001c0002t0009g0321 others(1): Show |
4 | HG01358.hp2 HG01934.hp2 NA19005.hp1 others(1): Show |
intron_variant | MODIFIER | c.2389+917_2389+930d others(16): Show |
MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 13/13 | INFO_REALIGN_3_PRIME | chr17 | 12761590 | ||||||
chr17:12761590 | T | TACACACA others(11): Show |
1 | a0001c0002t0178g0072 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.2389+913_2389+930d others(20): Show |
MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 13/13 | INFO_REALIGN_3_PRIME | chr17 | 12761590 | ||||||
chr17:12761590 | TAC | T | 8 | a0001c0001t0011g0224 a0001c0001t0011g0229 a0001c0001t0011g0230 others(5): Show |
8 | HG01891.hp1 HG02559.hp2 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.2389+929_2389+930d others(4): Show |
MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 13/13 | INFO_REALIGN_3_PRIME | chr17 | 12761590 | ||||||
chr17:12761590 | TACACACA others(1): Show |
T | 22 | a0001c0001t0001g0155 a0001c0001t0004g0278 a0001c0001t0005g0141 others(19): Show |
22 | HG01106.hp1 HG02056.hp1 HG02129.hp2 others(19): Show |
intron_variant | MODIFIER | c.2389+923_2389+930d others(10): Show |
MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 13/13 | INFO_REALIGN_3_PRIME | chr17 | 12761590 | ||||||
chr17:12761590 | TACACACA others(3): Show |
T | 143 | a0001c0001t0001g0058 a0001c0001t0001g0069 a0001c0001t0001g0077 others(140): Show |
143 | HG00280.hp1 HG00323.hp2 HG00558.hp1 others(140): Show |
intron_variant | MODIFIER | c.2389+921_2389+930d others(12): Show |
MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 13/13 | INFO_REALIGN_3_PRIME | chr17 | 12761590 | ||||||
chr17:12761590 | TACACACA others(5): Show |
T | 15 | a0001c0001t0001g0086 a0001c0001t0001g0181 a0001c0001t0002g0244 others(12): Show |
15 | HG00423.hp1 HG00544.hp2 HG00735.hp2 others(12): Show |
intron_variant | MODIFIER | c.2389+919_2389+930d others(14): Show |
MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 13/13 | INFO_REALIGN_3_PRIME | chr17 | 12761590 | ||||||
chr17:12761590 | TACACACA others(7): Show |
T | 1 | a0001c0001t0003g0201 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.2389+917_2389+930d others(16): Show |
MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 13/13 | INFO_REALIGN_3_PRIME | chr17 | 12761590 | ||||||
chr17:12761709 | C | T | 1 | a0005c0010t0099g0265 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.2389+1002C>T | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 13/13 | chr17 | 12761709 | |||||||
chr17:12761769 | G | A | 1 | a0001c0001t0019g0115 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.2389+1062G>A | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 13/13 | chr17 | 12761769 | |||||||
chr17:12761814 | G | A | 10 | a0001c0001t0028g0002 a0001c0001t0057g0317 a0001c0001t0119g0280 others(7): Show |
12 | HG02055.hp1 HG02451.hp1 HG02809.hp1 others(9): Show |
intron_variant | MODIFIER | c.2389+1107G>A | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 13/13 | chr17 | 12761814 | |||||||
chr17:12761967 | G | A | 1 | a0001c0003t0205g0332 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.2390-1106G>A | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 13/13 | chr17 | 12761967 | |||||||
chr17:12762156 | G | T | 10 | a0001c0001t0001g0181 a0001c0001t0002g0157 a0001c0001t0006g0067 others(7): Show |
10 | HG01109.hp1 HG01496.hp1 HG03704.hp2 others(7): Show |
intron_variant | MODIFIER | c.2390-917G>T | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 13/13 | chr17 | 12762156 | |||||||
chr17:12762361 | G | A | 1 | a0010c0025t0003g0152 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.2390-712G>A | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 13/13 | chr17 | 12762361 | |||||||
chr17:12762447 | C | T | 1 | a0001c0001t0161g0190 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.2390-626C>T | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 13/13 | chr17 | 12762447 | |||||||
chr17:12762535 | CTG | C | 123 | a0001c0001t0001g0051 a0001c0001t0001g0176 a0001c0001t0001g0177 others(120): Show |
125 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(122): Show |
intron_variant | MODIFIER | c.2390-535_2390-534d others(4): Show |
MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 13/13 | INFO_REALIGN_3_PRIME | chr17 | 12762535 | ||||||
chr17:12762585 | G | A | 1 | a0001c0003t0202g0210 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.2390-488G>A | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 13/13 | chr17 | 12762585 | |||||||
chr17:12762631 | G | A | 2 | a0001c0001t0097g0307 a0005c0010t0099g0265 |
2 | HG02451.hp2 HG02572.hp1 |
intron_variant | MODIFIER | c.2390-442G>A | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 13/13 | chr17 | 12762631 | |||||||
chr17:12762642 | A | C | 1 | a0001c0001t0007g0195 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.2390-431A>C | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 13/13 | chr17 | 12762642 | |||||||
chr17:12762697 | A | T | 75 | a0001c0001t0001g0051 a0001c0001t0001g0176 a0001c0001t0001g0177 others(72): Show |
76 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(73): Show |
intron_variant | MODIFIER | c.2390-376A>T | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 13/13 | chr17 | 12762697 | |||||||
chr17:12762706 | G | C | 1 | a0001c0001t0012g0235 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.2390-367G>C | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 13/13 | chr17 | 12762706 | |||||||
chr17:12762711 | G | T | 1 | a0001c0001t0001g0079 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.2390-362G>T | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 13/13 | chr17 | 12762711 | |||||||
chr17:12762793 | G | T | 1 | a0001c0001t0012g0235 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.2390-280G>T | MYOCD | ENSG00000141052.18 | transcript | ENST00000425538.6 | protein_coding | 13/13 | chr17 | 12762793 |