Item | Value |
---|---|
geneid | 3910 |
ensemblid | ENSG00000112769.20 |
hgncid | 6484 |
symbol | LAMA4 |
name | laminin subunit alpha 4 |
refseq_nuc | NM_001105206.3 |
refseq_prot | NP_001098676.2 |
ensembl_nuc | ENST00000230538.12 |
ensembl_prot | ENSP00000230538.7 |
mane_status | MANE Select |
chr | chr6 |
start | 112107931 |
end | 112254567 |
strand | - |
ver | v1.2 |
region | chr6:112107931-112254567 |
region5000 | chr6:112102931-112259567 |
regionname0 | LAMA4_chr6_112107931_112254567 |
regionname5000 | LAMA4_chr6_112102931_112259567 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 0/1 | 1823 | 135 | 30 | 24 | 61 | 4 | 15 | 43 | LAMA4_chr6_112102931_112259567 | LAMA4 | MALSS others(1818): Show |
chr6 | 112102931 | 112259567 |
a0002 | 0/0 | 1823 | 46 | 10 | 10 | 18 | 2 | 6 | 14 | LAMA4_chr6_112102931_112259567 | LAMA4 | MALSS others(1818): Show |
chr6 | 112102931 | 112259567 |
a0003 | 0/0 | 1823 | 40 | 10 | 6 | 19 | 2 | 3 | 14 | LAMA4_chr6_112102931_112259567 | LAMA4 | MALSS others(1818): Show |
chr6 | 112102931 | 112259567 |
a0004 | 0/0 | 1823 | 27 | 8 | 5 | 12 | 1 | 1 | 9 | LAMA4_chr6_112102931_112259567 | LAMA4 | MALSS others(1818): Show |
chr6 | 112102931 | 112259567 |
a0005 | 1/0 | 1823 | 15 | 5 | 4 | 3 | 1 | 1 | 2 | LAMA4_chr6_112102931_112259567 | LAMA4 | MALSS others(1818): Show |
chr6 | 112102931 | 112259567 |
a0006 | 0/0 | 1823 | 12 | 0 | 0 | 11 | 0 | 1 | 9 | LAMA4_chr6_112102931_112259567 | LAMA4 | MALSS others(1818): Show |
chr6 | 112102931 | 112259567 |
a0007 | 0/0 | 1823 | 10 | 3 | 2 | 5 | 0 | 0 | 5 | LAMA4_chr6_112102931_112259567 | LAMA4 | MALSS others(1818): Show |
chr6 | 112102931 | 112259567 |
a0008 | 0/0 | 1823 | 6 | 5 | 0 | 0 | 0 | 1 | 0 | LAMA4_chr6_112102931_112259567 | LAMA4 | MALSS others(1818): Show |
chr6 | 112102931 | 112259567 |
a0009 | 0/0 | 1823 | 4 | 4 | 0 | 0 | 0 | 0 | 0 | LAMA4_chr6_112102931_112259567 | LAMA4 | MALSS others(1818): Show |
chr6 | 112102931 | 112259567 |
a0010 | 0/0 | 1823 | 2 | 0 | 1 | 0 | 0 | 1 | 0 | LAMA4_chr6_112102931_112259567 | LAMA4 | MALSS others(1818): Show |
chr6 | 112102931 | 112259567 |
a0011 | 0/0 | 1823 | 2 | 1 | 1 | 0 | 0 | 0 | 0 | LAMA4_chr6_112102931_112259567 | LAMA4 | MALSS others(1818): Show |
chr6 | 112102931 | 112259567 |
a0012 | 0/0 | 1823 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | LAMA4_chr6_112102931_112259567 | LAMA4 | MALSS others(1818): Show |
chr6 | 112102931 | 112259567 |
a0013 | 0/0 | 1823 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | LAMA4_chr6_112102931_112259567 | LAMA4 | MALSS others(1818): Show |
chr6 | 112102931 | 112259567 |
a0014 | 0/0 | 1823 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | LAMA4_chr6_112102931_112259567 | LAMA4 | MALSS others(1818): Show |
chr6 | 112102931 | 112259567 |
a0015 | 0/0 | 1823 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | LAMA4_chr6_112102931_112259567 | LAMA4 | MALSS others(1818): Show |
chr6 | 112102931 | 112259567 |
a0016 | 0/0 | 1823 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | LAMA4_chr6_112102931_112259567 | LAMA4 | MALSS others(1818): Show |
chr6 | 112102931 | 112259567 |
a0017 | 0/0 | 1823 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | LAMA4_chr6_112102931_112259567 | LAMA4 | MALSS others(1818): Show |
chr6 | 112102931 | 112259567 |
a0018 | 0/0 | 1823 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | LAMA4_chr6_112102931_112259567 | LAMA4 | MALSS others(1818): Show |
chr6 | 112102931 | 112259567 |
a0019 | 0/0 | 1823 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | LAMA4_chr6_112102931_112259567 | LAMA4 | MALSS others(1818): Show |
chr6 | 112102931 | 112259567 |
a0020 | 0/0 | 1823 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | LAMA4_chr6_112102931_112259567 | LAMA4 | MALSS others(1818): Show |
chr6 | 112102931 | 112259567 |
a0021 | 0/0 | 1823 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | LAMA4_chr6_112102931_112259567 | LAMA4 | MALSS others(1818): Show |
chr6 | 112102931 | 112259567 |
a0022 | 0/0 | 1823 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | LAMA4_chr6_112102931_112259567 | LAMA4 | MALSS others(1818): Show |
chr6 | 112102931 | 112259567 |
a0023 | 0/0 | 1823 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | LAMA4_chr6_112102931_112259567 | LAMA4 | MALSS others(1818): Show |
chr6 | 112102931 | 112259567 |
a0024 | 0/0 | 1823 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | LAMA4_chr6_112102931_112259567 | LAMA4 | MALSS others(1818): Show |
chr6 | 112102931 | 112259567 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 0/0 | 5469 | 46 | 1 | 14 | 24 | 2 | 5 | LAMA4_chr6_112102931_112259567 | LAMA4 | ATGGC others(5464): Show |
chr6 | 112102931 | 112259567 | ||
a0001c0002 | 0/1 | 5469 | 32 | 8 | 7 | 10 | 0 | 6 | LAMA4_chr6_112102931_112259567 | LAMA4 | ATGGC others(5464): Show |
chr6 | 112102931 | 112259567 | ||
a0001c0005 | 0/0 | 5469 | 19 | 0 | 2 | 14 | 0 | 3 | LAMA4_chr6_112102931_112259567 | LAMA4 | ATGGC others(5464): Show |
chr6 | 112102931 | 112259567 | ||
a0001c0009 | 0/0 | 5469 | 11 | 0 | 1 | 8 | 1 | 1 | LAMA4_chr6_112102931_112259567 | LAMA4 | ATGGC others(5464): Show |
chr6 | 112102931 | 112259567 | ||
a0001c0011 | 0/0 | 5469 | 10 | 10 | 0 | 0 | 0 | 0 | LAMA4_chr6_112102931_112259567 | LAMA4 | ATGGC others(5464): Show |
chr6 | 112102931 | 112259567 | ||
a0001c0016 | 0/0 | 5469 | 4 | 1 | 0 | 3 | 0 | 0 | LAMA4_chr6_112102931_112259567 | LAMA4 | ATGGC others(5464): Show |
chr6 | 112102931 | 112259567 | ||
a0001c0020 | 0/0 | 5469 | 3 | 3 | 0 | 0 | 0 | 0 | LAMA4_chr6_112102931_112259567 | LAMA4 | ATGGC others(5464): Show |
chr6 | 112102931 | 112259567 | ||
a0001c0022 | 0/0 | 5469 | 2 | 0 | 0 | 1 | 1 | 0 | LAMA4_chr6_112102931_112259567 | LAMA4 | ATGGC others(5464): Show |
chr6 | 112102931 | 112259567 | ||
a0001c0023 | 0/0 | 5469 | 2 | 2 | 0 | 0 | 0 | 0 | LAMA4_chr6_112102931_112259567 | LAMA4 | ATGGC others(5464): Show |
chr6 | 112102931 | 112259567 | ||
a0001c0034 | 0/0 | 5469 | 1 | 0 | 0 | 1 | 0 | 0 | LAMA4_chr6_112102931_112259567 | LAMA4 | ATGGC others(5464): Show |
chr6 | 112102931 | 112259567 | ||
a0001c0037 | 0/0 | 5469 | 1 | 1 | 0 | 0 | 0 | 0 | LAMA4_chr6_112102931_112259567 | LAMA4 | ATGGC others(5464): Show |
chr6 | 112102931 | 112259567 | ||
a0001c0050 | 0/0 | 5469 | 1 | 1 | 0 | 0 | 0 | 0 | LAMA4_chr6_112102931_112259567 | LAMA4 | ATGGC others(5464): Show |
chr6 | 112102931 | 112259567 | ||
a0001c0051 | 0/0 | 5469 | 1 | 1 | 0 | 0 | 0 | 0 | LAMA4_chr6_112102931_112259567 | LAMA4 | ATGGC others(5464): Show |
chr6 | 112102931 | 112259567 | ||
a0001c0052 | 0/0 | 5469 | 1 | 1 | 0 | 0 | 0 | 0 | LAMA4_chr6_112102931_112259567 | LAMA4 | ATGGC others(5464): Show |
chr6 | 112102931 | 112259567 | ||
a0001c0054 | 0/0 | 5469 | 1 | 1 | 0 | 0 | 0 | 0 | LAMA4_chr6_112102931_112259567 | LAMA4 | ATGGC others(5464): Show |
chr6 | 112102931 | 112259567 | ||
a0002c0003 | 0/0 | 5469 | 23 | 4 | 5 | 6 | 2 | 6 | LAMA4_chr6_112102931_112259567 | LAMA4 | ATGGC others(5464): Show |
chr6 | 112102931 | 112259567 | ||
a0002c0006 | 0/0 | 5469 | 19 | 6 | 3 | 10 | 0 | 0 | LAMA4_chr6_112102931_112259567 | LAMA4 | ATGGC others(5464): Show |
chr6 | 112102931 | 112259567 | ||
a0002c0024 | 0/0 | 5469 | 2 | 0 | 1 | 1 | 0 | 0 | LAMA4_chr6_112102931_112259567 | LAMA4 | ATGGC others(5464): Show |
chr6 | 112102931 | 112259567 | ||
a0002c0048 | 0/0 | 5469 | 1 | 0 | 0 | 1 | 0 | 0 | LAMA4_chr6_112102931_112259567 | LAMA4 | ATGGC others(5464): Show |
chr6 | 112102931 | 112259567 | ||
a0002c0055 | 0/0 | 5469 | 1 | 0 | 1 | 0 | 0 | 0 | LAMA4_chr6_112102931_112259567 | LAMA4 | ATGGC others(5464): Show |
chr6 | 112102931 | 112259567 | ||
a0003c0004 | 0/0 | 5469 | 23 | 5 | 2 | 12 | 1 | 3 | LAMA4_chr6_112102931_112259567 | LAMA4 | ATGGC others(5464): Show |
chr6 | 112102931 | 112259567 | ||
a0003c0013 | 0/0 | 5469 | 8 | 0 | 2 | 5 | 1 | 0 | LAMA4_chr6_112102931_112259567 | LAMA4 | ATGGC others(5464): Show |
chr6 | 112102931 | 112259567 | ||
a0003c0018 | 0/0 | 5469 | 3 | 1 | 0 | 2 | 0 | 0 | LAMA4_chr6_112102931_112259567 | LAMA4 | ATGGC others(5464): Show |
chr6 | 112102931 | 112259567 | ||
a0003c0025 | 0/0 | 5469 | 2 | 2 | 0 | 0 | 0 | 0 | LAMA4_chr6_112102931_112259567 | LAMA4 | ATGGC others(5464): Show |
chr6 | 112102931 | 112259567 | ||
a0003c0043 | 0/0 | 5469 | 1 | 0 | 1 | 0 | 0 | 0 | LAMA4_chr6_112102931_112259567 | LAMA4 | ATGGC others(5464): Show |
chr6 | 112102931 | 112259567 | ||
a0003c0058 | 0/0 | 5469 | 1 | 1 | 0 | 0 | 0 | 0 | LAMA4_chr6_112102931_112259567 | LAMA4 | ATGGC others(5464): Show |
chr6 | 112102931 | 112259567 | ||
a0003c0059 | 0/0 | 5469 | 1 | 1 | 0 | 0 | 0 | 0 | LAMA4_chr6_112102931_112259567 | LAMA4 | ATGGC others(5464): Show |
chr6 | 112102931 | 112259567 | ||
a0003c0061 | 0/0 | 5469 | 1 | 0 | 1 | 0 | 0 | 0 | LAMA4_chr6_112102931_112259567 | LAMA4 | ATGGC others(5464): Show |
chr6 | 112102931 | 112259567 | ||
a0004c0007 | 0/0 | 5469 | 14 | 6 | 0 | 7 | 0 | 1 | LAMA4_chr6_112102931_112259567 | LAMA4 | ATGGC others(5464): Show |
chr6 | 112102931 | 112259567 | ||
a0004c0010 | 0/0 | 5469 | 10 | 1 | 3 | 5 | 1 | 0 | LAMA4_chr6_112102931_112259567 | LAMA4 | ATGGC others(5464): Show |
chr6 | 112102931 | 112259567 | ||
a0004c0026 | 0/0 | 5469 | 2 | 0 | 2 | 0 | 0 | 0 | LAMA4_chr6_112102931_112259567 | LAMA4 | ATGGC others(5464): Show |
chr6 | 112102931 | 112259567 | ||
a0004c0057 | 0/0 | 5469 | 1 | 1 | 0 | 0 | 0 | 0 | LAMA4_chr6_112102931_112259567 | LAMA4 | ATGGC others(5464): Show |
chr6 | 112102931 | 112259567 | ||
a0005c0008 | 1/0 | 5469 | 13 | 3 | 4 | 3 | 1 | 1 | LAMA4_chr6_112102931_112259567 | LAMA4 | ATGGC others(5464): Show |
chr6 | 112102931 | 112259567 | ||
a0005c0044 | 0/0 | 5469 | 1 | 1 | 0 | 0 | 0 | 0 | LAMA4_chr6_112102931_112259567 | LAMA4 | ATGGC others(5464): Show |
chr6 | 112102931 | 112259567 | ||
a0005c0045 | 0/0 | 5469 | 1 | 1 | 0 | 0 | 0 | 0 | LAMA4_chr6_112102931_112259567 | LAMA4 | ATGGC others(5464): Show |
chr6 | 112102931 | 112259567 | ||
a0006c0012 | 0/0 | 5469 | 9 | 0 | 0 | 8 | 0 | 1 | LAMA4_chr6_112102931_112259567 | LAMA4 | ATGGC others(5464): Show |
chr6 | 112102931 | 112259567 | ||
a0006c0027 | 0/0 | 5469 | 2 | 0 | 0 | 2 | 0 | 0 | LAMA4_chr6_112102931_112259567 | LAMA4 | ATGGC others(5464): Show |
chr6 | 112102931 | 112259567 | ||
a0006c0047 | 0/0 | 5469 | 1 | 0 | 0 | 1 | 0 | 0 | LAMA4_chr6_112102931_112259567 | LAMA4 | ATGGC others(5464): Show |
chr6 | 112102931 | 112259567 | ||
a0007c0014 | 0/0 | 5469 | 6 | 2 | 2 | 2 | 0 | 0 | LAMA4_chr6_112102931_112259567 | LAMA4 | ATGGC others(5464): Show |
chr6 | 112102931 | 112259567 | ||
a0007c0019 | 0/0 | 5469 | 3 | 0 | 0 | 3 | 0 | 0 | LAMA4_chr6_112102931_112259567 | LAMA4 | ATGGC others(5464): Show |
chr6 | 112102931 | 112259567 | ||
a0007c0060 | 0/0 | 5469 | 1 | 1 | 0 | 0 | 0 | 0 | LAMA4_chr6_112102931_112259567 | LAMA4 | ATGGC others(5464): Show |
chr6 | 112102931 | 112259567 | ||
a0008c0015 | 0/0 | 5469 | 5 | 4 | 0 | 0 | 0 | 1 | LAMA4_chr6_112102931_112259567 | LAMA4 | ATGGC others(5464): Show |
chr6 | 112102931 | 112259567 | ||
a0008c0031 | 0/0 | 5469 | 1 | 1 | 0 | 0 | 0 | 0 | LAMA4_chr6_112102931_112259567 | LAMA4 | ATGGC others(5464): Show |
chr6 | 112102931 | 112259567 | ||
a0009c0017 | 0/0 | 5469 | 3 | 3 | 0 | 0 | 0 | 0 | LAMA4_chr6_112102931_112259567 | LAMA4 | ATGGC others(5464): Show |
chr6 | 112102931 | 112259567 | ||
a0009c0053 | 0/0 | 5469 | 1 | 1 | 0 | 0 | 0 | 0 | LAMA4_chr6_112102931_112259567 | LAMA4 | ATGGC others(5464): Show |
chr6 | 112102931 | 112259567 | ||
a0010c0029 | 0/0 | 5469 | 2 | 0 | 1 | 0 | 0 | 1 | LAMA4_chr6_112102931_112259567 | LAMA4 | ATGGC others(5464): Show |
chr6 | 112102931 | 112259567 | ||
a0011c0028 | 0/0 | 5469 | 2 | 1 | 1 | 0 | 0 | 0 | LAMA4_chr6_112102931_112259567 | LAMA4 | ATGGC others(5464): Show |
chr6 | 112102931 | 112259567 | ||
a0012c0021 | 0/0 | 5469 | 2 | 0 | 0 | 2 | 0 | 0 | LAMA4_chr6_112102931_112259567 | LAMA4 | ATGGC others(5464): Show |
chr6 | 112102931 | 112259567 | ||
a0013c0038 | 0/0 | 5469 | 1 | 0 | 0 | 1 | 0 | 0 | LAMA4_chr6_112102931_112259567 | LAMA4 | ATGGC others(5464): Show |
chr6 | 112102931 | 112259567 | ||
a0013c0039 | 0/0 | 5469 | 1 | 0 | 0 | 1 | 0 | 0 | LAMA4_chr6_112102931_112259567 | LAMA4 | ATGGC others(5464): Show |
chr6 | 112102931 | 112259567 | ||
a0014c0040 | 0/0 | 5469 | 1 | 0 | 0 | 1 | 0 | 0 | LAMA4_chr6_112102931_112259567 | LAMA4 | ATGGC others(5464): Show |
chr6 | 112102931 | 112259567 | ||
a0015c0049 | 0/0 | 5469 | 1 | 0 | 1 | 0 | 0 | 0 | LAMA4_chr6_112102931_112259567 | LAMA4 | ATGGC others(5464): Show |
chr6 | 112102931 | 112259567 | ||
a0016c0042 | 0/0 | 5469 | 1 | 0 | 0 | 1 | 0 | 0 | LAMA4_chr6_112102931_112259567 | LAMA4 | ATGGC others(5464): Show |
chr6 | 112102931 | 112259567 | ||
a0017c0046 | 0/0 | 5469 | 1 | 0 | 0 | 0 | 0 | 1 | LAMA4_chr6_112102931_112259567 | LAMA4 | ATGGC others(5464): Show |
chr6 | 112102931 | 112259567 | ||
a0018c0030 | 0/0 | 5469 | 1 | 1 | 0 | 0 | 0 | 0 | LAMA4_chr6_112102931_112259567 | LAMA4 | ATGGC others(5464): Show |
chr6 | 112102931 | 112259567 | ||
a0019c0036 | 0/0 | 5469 | 1 | 0 | 0 | 0 | 0 | 1 | LAMA4_chr6_112102931_112259567 | LAMA4 | ATGGC others(5464): Show |
chr6 | 112102931 | 112259567 | ||
a0020c0056 | 0/0 | 5469 | 1 | 0 | 0 | 0 | 0 | 1 | LAMA4_chr6_112102931_112259567 | LAMA4 | ATGGC others(5464): Show |
chr6 | 112102931 | 112259567 | ||
a0021c0033 | 0/0 | 5469 | 1 | 0 | 0 | 1 | 0 | 0 | LAMA4_chr6_112102931_112259567 | LAMA4 | ATGGC others(5464): Show |
chr6 | 112102931 | 112259567 | ||
a0022c0032 | 0/0 | 5469 | 1 | 1 | 0 | 0 | 0 | 0 | LAMA4_chr6_112102931_112259567 | LAMA4 | ATGGC others(5464): Show |
chr6 | 112102931 | 112259567 | ||
a0023c0035 | 0/0 | 5469 | 1 | 0 | 0 | 1 | 0 | 0 | LAMA4_chr6_112102931_112259567 | LAMA4 | ATGGC others(5464): Show |
chr6 | 112102931 | 112259567 | ||
a0024c0041 | 0/0 | 5469 | 1 | 0 | 0 | 1 | 0 | 0 | LAMA4_chr6_112102931_112259567 | LAMA4 | ATGGC others(5464): Show |
chr6 | 112102931 | 112259567 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 7228 | 45 | 1 | 14 | 24 | 1 | 5 | LAMA4_chr6_112102931_112259567 | LAMA4 | GAGAA others(7223): Show |
chr6 | 112102931 | 112259567 |
a0001c0001t0011 | 0/0 | 7228 | 1 | 0 | 0 | 0 | 1 | 0 | LAMA4_chr6_112102931_112259567 | LAMA4 | GAGAA others(7223): Show |
chr6 | 112102931 | 112259567 |
a0001c0002t0001 | 0/1 | 7228 | 32 | 8 | 7 | 10 | 0 | 6 | LAMA4_chr6_112102931_112259567 | LAMA4 | GAGAA others(7223): Show |
chr6 | 112102931 | 112259567 |
a0001c0005t0001 | 0/0 | 7228 | 19 | 0 | 2 | 14 | 0 | 3 | LAMA4_chr6_112102931_112259567 | LAMA4 | GAGAA others(7223): Show |
chr6 | 112102931 | 112259567 |
a0001c0009t0001 | 0/0 | 7228 | 10 | 0 | 1 | 8 | 0 | 1 | LAMA4_chr6_112102931_112259567 | LAMA4 | GAGAA others(7223): Show |
chr6 | 112102931 | 112259567 |
a0001c0009t0009 | 0/0 | 7228 | 1 | 0 | 0 | 0 | 1 | 0 | LAMA4_chr6_112102931_112259567 | LAMA4 | GAGAA others(7223): Show |
chr6 | 112102931 | 112259567 |
a0001c0011t0003 | 0/0 | 7228 | 10 | 10 | 0 | 0 | 0 | 0 | LAMA4_chr6_112102931_112259567 | LAMA4 | GAGAA others(7223): Show |
chr6 | 112102931 | 112259567 |
a0001c0016t0001 | 0/0 | 7228 | 2 | 1 | 0 | 1 | 0 | 0 | LAMA4_chr6_112102931_112259567 | LAMA4 | GAGAA others(7223): Show |
chr6 | 112102931 | 112259567 |
a0001c0016t0002 | 0/0 | 7228 | 1 | 0 | 0 | 1 | 0 | 0 | LAMA4_chr6_112102931_112259567 | LAMA4 | GAGAA others(7223): Show |
chr6 | 112102931 | 112259567 |
a0001c0016t0010 | 0/0 | 7228 | 1 | 0 | 0 | 1 | 0 | 0 | LAMA4_chr6_112102931_112259567 | LAMA4 | GAGAA others(7223): Show |
chr6 | 112102931 | 112259567 |
a0001c0020t0005 | 0/0 | 7228 | 3 | 3 | 0 | 0 | 0 | 0 | LAMA4_chr6_112102931_112259567 | LAMA4 | GAGAA others(7223): Show |
chr6 | 112102931 | 112259567 |
a0001c0022t0002 | 0/0 | 7228 | 2 | 0 | 0 | 1 | 1 | 0 | LAMA4_chr6_112102931_112259567 | LAMA4 | GAGAA others(7223): Show |
chr6 | 112102931 | 112259567 |
a0001c0023t0003 | 0/0 | 7228 | 2 | 2 | 0 | 0 | 0 | 0 | LAMA4_chr6_112102931_112259567 | LAMA4 | GAGAA others(7223): Show |
chr6 | 112102931 | 112259567 |
a0001c0034t0001 | 0/0 | 7228 | 1 | 0 | 0 | 1 | 0 | 0 | LAMA4_chr6_112102931_112259567 | LAMA4 | GAGAA others(7223): Show |
chr6 | 112102931 | 112259567 |
a0001c0037t0003 | 0/0 | 7228 | 1 | 1 | 0 | 0 | 0 | 0 | LAMA4_chr6_112102931_112259567 | LAMA4 | GAGAA others(7223): Show |
chr6 | 112102931 | 112259567 |
a0001c0050t0001 | 0/0 | 7228 | 1 | 1 | 0 | 0 | 0 | 0 | LAMA4_chr6_112102931_112259567 | LAMA4 | GAGAA others(7223): Show |
chr6 | 112102931 | 112259567 |
a0001c0051t0003 | 0/0 | 7228 | 1 | 1 | 0 | 0 | 0 | 0 | LAMA4_chr6_112102931_112259567 | LAMA4 | GAGAA others(7223): Show |
chr6 | 112102931 | 112259567 |
a0001c0052t0002 | 0/0 | 7228 | 1 | 1 | 0 | 0 | 0 | 0 | LAMA4_chr6_112102931_112259567 | LAMA4 | GAGAA others(7223): Show |
chr6 | 112102931 | 112259567 |
a0001c0054t0001 | 0/0 | 7228 | 1 | 1 | 0 | 0 | 0 | 0 | LAMA4_chr6_112102931_112259567 | LAMA4 | GAGAA others(7223): Show |
chr6 | 112102931 | 112259567 |
a0002c0003t0001 | 0/0 | 7228 | 1 | 1 | 0 | 0 | 0 | 0 | LAMA4_chr6_112102931_112259567 | LAMA4 | GAGAA others(7223): Show |
chr6 | 112102931 | 112259567 |
a0002c0003t0002 | 0/0 | 7228 | 20 | 1 | 5 | 6 | 2 | 6 | LAMA4_chr6_112102931_112259567 | LAMA4 | GAGAA others(7223): Show |
chr6 | 112102931 | 112259567 |
a0002c0003t0006 | 0/0 | 7228 | 2 | 2 | 0 | 0 | 0 | 0 | LAMA4_chr6_112102931_112259567 | LAMA4 | GAGAA others(7223): Show |
chr6 | 112102931 | 112259567 |
a0002c0006t0002 | 0/0 | 7228 | 19 | 6 | 3 | 10 | 0 | 0 | LAMA4_chr6_112102931_112259567 | LAMA4 | GAGAA others(7223): Show |
chr6 | 112102931 | 112259567 |
a0002c0024t0001 | 0/0 | 7228 | 2 | 0 | 1 | 1 | 0 | 0 | LAMA4_chr6_112102931_112259567 | LAMA4 | GAGAA others(7223): Show |
chr6 | 112102931 | 112259567 |
a0002c0048t0002 | 0/0 | 7228 | 1 | 0 | 0 | 1 | 0 | 0 | LAMA4_chr6_112102931_112259567 | LAMA4 | GAGAA others(7223): Show |
chr6 | 112102931 | 112259567 |
a0002c0055t0001 | 0/0 | 7228 | 1 | 0 | 1 | 0 | 0 | 0 | LAMA4_chr6_112102931_112259567 | LAMA4 | GAGAA others(7223): Show |
chr6 | 112102931 | 112259567 |
a0003c0004t0001 | 0/0 | 7228 | 22 | 5 | 2 | 12 | 1 | 2 | LAMA4_chr6_112102931_112259567 | LAMA4 | GAGAA others(7223): Show |
chr6 | 112102931 | 112259567 |
a0003c0004t0008 | 0/0 | 7228 | 1 | 0 | 0 | 0 | 0 | 1 | LAMA4_chr6_112102931_112259567 | LAMA4 | GAGAA others(7223): Show |
chr6 | 112102931 | 112259567 |
a0003c0013t0001 | 0/0 | 7228 | 8 | 0 | 2 | 5 | 1 | 0 | LAMA4_chr6_112102931_112259567 | LAMA4 | GAGAA others(7223): Show |
chr6 | 112102931 | 112259567 |
a0003c0018t0001 | 0/0 | 7228 | 2 | 0 | 0 | 2 | 0 | 0 | LAMA4_chr6_112102931_112259567 | LAMA4 | GAGAA others(7223): Show |
chr6 | 112102931 | 112259567 |
a0003c0018t0002 | 0/0 | 7228 | 1 | 1 | 0 | 0 | 0 | 0 | LAMA4_chr6_112102931_112259567 | LAMA4 | GAGAA others(7223): Show |
chr6 | 112102931 | 112259567 |
a0003c0025t0001 | 0/0 | 7228 | 2 | 2 | 0 | 0 | 0 | 0 | LAMA4_chr6_112102931_112259567 | LAMA4 | GAGAA others(7223): Show |
chr6 | 112102931 | 112259567 |
a0003c0043t0001 | 0/0 | 7228 | 1 | 0 | 1 | 0 | 0 | 0 | LAMA4_chr6_112102931_112259567 | LAMA4 | GAGAA others(7223): Show |
chr6 | 112102931 | 112259567 |
a0003c0058t0001 | 0/0 | 7228 | 1 | 1 | 0 | 0 | 0 | 0 | LAMA4_chr6_112102931_112259567 | LAMA4 | GAGAA others(7223): Show |
chr6 | 112102931 | 112259567 |
a0003c0059t0001 | 0/0 | 7228 | 1 | 1 | 0 | 0 | 0 | 0 | LAMA4_chr6_112102931_112259567 | LAMA4 | GAGAA others(7223): Show |
chr6 | 112102931 | 112259567 |
a0003c0061t0001 | 0/0 | 7228 | 1 | 0 | 1 | 0 | 0 | 0 | LAMA4_chr6_112102931_112259567 | LAMA4 | GAGAA others(7223): Show |
chr6 | 112102931 | 112259567 |
a0004c0007t0001 | 0/0 | 7228 | 13 | 6 | 0 | 6 | 0 | 1 | LAMA4_chr6_112102931_112259567 | LAMA4 | GAGAA others(7223): Show |
chr6 | 112102931 | 112259567 |
a0004c0007t0014 | 0/0 | 7228 | 1 | 0 | 0 | 1 | 0 | 0 | LAMA4_chr6_112102931_112259567 | LAMA4 | GAGAA others(7223): Show |
chr6 | 112102931 | 112259567 |
a0004c0010t0001 | 0/0 | 7228 | 6 | 1 | 1 | 4 | 0 | 0 | LAMA4_chr6_112102931_112259567 | LAMA4 | GAGAA others(7223): Show |
chr6 | 112102931 | 112259567 |
a0004c0010t0004 | 0/0 | 7228 | 3 | 0 | 2 | 0 | 1 | 0 | LAMA4_chr6_112102931_112259567 | LAMA4 | GAGAA others(7223): Show |
chr6 | 112102931 | 112259567 |
a0004c0010t0012 | 0/0 | 7228 | 1 | 0 | 0 | 1 | 0 | 0 | LAMA4_chr6_112102931_112259567 | LAMA4 | GAGAA others(7223): Show |
chr6 | 112102931 | 112259567 |
a0004c0026t0001 | 0/0 | 7228 | 2 | 0 | 2 | 0 | 0 | 0 | LAMA4_chr6_112102931_112259567 | LAMA4 | GAGAA others(7223): Show |
chr6 | 112102931 | 112259567 |
a0004c0057t0003 | 0/0 | 7228 | 1 | 1 | 0 | 0 | 0 | 0 | LAMA4_chr6_112102931_112259567 | LAMA4 | GAGAA others(7223): Show |
chr6 | 112102931 | 112259567 |
a0005c0008t0001 | 1/0 | 7228 | 9 | 2 | 2 | 3 | 0 | 1 | LAMA4_chr6_112102931_112259567 | LAMA4 | GAGAA others(7223): Show |
chr6 | 112102931 | 112259567 |
a0005c0008t0004 | 0/0 | 7228 | 4 | 1 | 2 | 0 | 1 | 0 | LAMA4_chr6_112102931_112259567 | LAMA4 | GAGAA others(7223): Show |
chr6 | 112102931 | 112259567 |
a0005c0044t0001 | 0/0 | 7228 | 1 | 1 | 0 | 0 | 0 | 0 | LAMA4_chr6_112102931_112259567 | LAMA4 | GAGAA others(7223): Show |
chr6 | 112102931 | 112259567 |
a0005c0045t0007 | 0/0 | 7228 | 1 | 1 | 0 | 0 | 0 | 0 | LAMA4_chr6_112102931_112259567 | LAMA4 | GAGAA others(7223): Show |
chr6 | 112102931 | 112259567 |
a0006c0012t0002 | 0/0 | 7228 | 9 | 0 | 0 | 8 | 0 | 1 | LAMA4_chr6_112102931_112259567 | LAMA4 | GAGAA others(7223): Show |
chr6 | 112102931 | 112259567 |
a0006c0027t0002 | 0/0 | 7228 | 2 | 0 | 0 | 2 | 0 | 0 | LAMA4_chr6_112102931_112259567 | LAMA4 | GAGAA others(7223): Show |
chr6 | 112102931 | 112259567 |
a0006c0047t0002 | 0/0 | 7228 | 1 | 0 | 0 | 1 | 0 | 0 | LAMA4_chr6_112102931_112259567 | LAMA4 | GAGAA others(7223): Show |
chr6 | 112102931 | 112259567 |
a0007c0014t0002 | 0/0 | 7228 | 6 | 2 | 2 | 2 | 0 | 0 | LAMA4_chr6_112102931_112259567 | LAMA4 | GAGAA others(7223): Show |
chr6 | 112102931 | 112259567 |
a0007c0019t0001 | 0/0 | 7228 | 3 | 0 | 0 | 3 | 0 | 0 | LAMA4_chr6_112102931_112259567 | LAMA4 | GAGAA others(7223): Show |
chr6 | 112102931 | 112259567 |
a0007c0060t0002 | 0/0 | 7228 | 1 | 1 | 0 | 0 | 0 | 0 | LAMA4_chr6_112102931_112259567 | LAMA4 | GAGAA others(7223): Show |
chr6 | 112102931 | 112259567 |
a0008c0015t0001 | 0/0 | 7228 | 5 | 4 | 0 | 0 | 0 | 1 | LAMA4_chr6_112102931_112259567 | LAMA4 | GAGAA others(7223): Show |
chr6 | 112102931 | 112259567 |
a0008c0031t0001 | 0/0 | 7228 | 1 | 1 | 0 | 0 | 0 | 0 | LAMA4_chr6_112102931_112259567 | LAMA4 | GAGAA others(7223): Show |
chr6 | 112102931 | 112259567 |
a0009c0017t0002 | 0/0 | 7228 | 3 | 3 | 0 | 0 | 0 | 0 | LAMA4_chr6_112102931_112259567 | LAMA4 | GAGAA others(7223): Show |
chr6 | 112102931 | 112259567 |
a0009c0053t0002 | 0/0 | 7228 | 1 | 1 | 0 | 0 | 0 | 0 | LAMA4_chr6_112102931_112259567 | LAMA4 | GAGAA others(7223): Show |
chr6 | 112102931 | 112259567 |
a0010c0029t0001 | 0/0 | 7228 | 2 | 0 | 1 | 0 | 0 | 1 | LAMA4_chr6_112102931_112259567 | LAMA4 | GAGAA others(7223): Show |
chr6 | 112102931 | 112259567 |
a0011c0028t0002 | 0/0 | 7228 | 2 | 1 | 1 | 0 | 0 | 0 | LAMA4_chr6_112102931_112259567 | LAMA4 | GAGAA others(7223): Show |
chr6 | 112102931 | 112259567 |
a0012c0021t0001 | 0/0 | 7228 | 2 | 0 | 0 | 2 | 0 | 0 | LAMA4_chr6_112102931_112259567 | LAMA4 | GAGAA others(7223): Show |
chr6 | 112102931 | 112259567 |
a0013c0038t0002 | 0/0 | 7228 | 1 | 0 | 0 | 1 | 0 | 0 | LAMA4_chr6_112102931_112259567 | LAMA4 | GAGAA others(7223): Show |
chr6 | 112102931 | 112259567 |
a0013c0039t0001 | 0/0 | 7228 | 1 | 0 | 0 | 1 | 0 | 0 | LAMA4_chr6_112102931_112259567 | LAMA4 | GAGAA others(7223): Show |
chr6 | 112102931 | 112259567 |
a0014c0040t0002 | 0/0 | 7228 | 1 | 0 | 0 | 1 | 0 | 0 | LAMA4_chr6_112102931_112259567 | LAMA4 | GAGAA others(7223): Show |
chr6 | 112102931 | 112259567 |
a0015c0049t0002 | 0/0 | 7228 | 1 | 0 | 1 | 0 | 0 | 0 | LAMA4_chr6_112102931_112259567 | LAMA4 | GAGAA others(7223): Show |
chr6 | 112102931 | 112259567 |
a0016c0042t0001 | 0/0 | 7228 | 1 | 0 | 0 | 1 | 0 | 0 | LAMA4_chr6_112102931_112259567 | LAMA4 | GAGAA others(7223): Show |
chr6 | 112102931 | 112259567 |
a0017c0046t0002 | 0/0 | 7228 | 1 | 0 | 0 | 0 | 0 | 1 | LAMA4_chr6_112102931_112259567 | LAMA4 | GAGAA others(7223): Show |
chr6 | 112102931 | 112259567 |
a0018c0030t0001 | 0/0 | 7228 | 1 | 1 | 0 | 0 | 0 | 0 | LAMA4_chr6_112102931_112259567 | LAMA4 | GAGAA others(7223): Show |
chr6 | 112102931 | 112259567 |
a0019c0036t0001 | 0/0 | 7228 | 1 | 0 | 0 | 0 | 0 | 1 | LAMA4_chr6_112102931_112259567 | LAMA4 | GAGAA others(7223): Show |
chr6 | 112102931 | 112259567 |
a0020c0056t0001 | 0/0 | 7228 | 1 | 0 | 0 | 0 | 0 | 1 | LAMA4_chr6_112102931_112259567 | LAMA4 | GAGAA others(7223): Show |
chr6 | 112102931 | 112259567 |
a0021c0033t0013 | 0/0 | 7228 | 1 | 0 | 0 | 1 | 0 | 0 | LAMA4_chr6_112102931_112259567 | LAMA4 | GAGAA others(7223): Show |
chr6 | 112102931 | 112259567 |
a0022c0032t0001 | 0/0 | 7228 | 1 | 1 | 0 | 0 | 0 | 0 | LAMA4_chr6_112102931_112259567 | LAMA4 | GAGAA others(7223): Show |
chr6 | 112102931 | 112259567 |
a0023c0035t0001 | 0/0 | 7228 | 1 | 0 | 0 | 1 | 0 | 0 | LAMA4_chr6_112102931_112259567 | LAMA4 | GAGAA others(7223): Show |
chr6 | 112102931 | 112259567 |
a0024c0041t0001 | 0/0 | 7228 | 1 | 0 | 0 | 1 | 0 | 0 | LAMA4_chr6_112102931_112259567 | LAMA4 | GAGAA others(7223): Show |
chr6 | 112102931 | 112259567 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
a0001c0001t0001g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
a0001c0001t0001g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
a0001c0001t0001g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
a0001c0001t0001g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
a0001c0001t0001g0027 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
a0001c0001t0001g0033 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
a0001c0001t0001g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
a0001c0001t0001g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
a0001c0001t0001g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
a0001c0001t0001g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
a0001c0001t0001g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
a0001c0001t0001g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
a0001c0001t0001g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
a0001c0001t0001g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
a0001c0001t0001g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
a0001c0001t0001g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
a0001c0001t0001g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
a0001c0001t0001g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
a0001c0001t0001g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
a0001c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
a0001c0001t0001g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
a0001c0001t0001g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
a0001c0001t0001g0285 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
a0001c0001t0011g0229 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
a0001c0002t0001g0005 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
a0001c0002t0001g0006 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
a0001c0002t0001g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
a0001c0002t0001g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
a0001c0002t0001g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
a0001c0002t0001g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
a0001c0002t0001g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
a0001c0002t0001g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
a0001c0002t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
a0001c0002t0001g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
a0001c0002t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
a0001c0002t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
a0001c0002t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
a0001c0002t0001g0148 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
a0001c0002t0001g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
a0001c0002t0001g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
a0001c0002t0001g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
a0001c0002t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
a0001c0002t0001g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
a0001c0002t0001g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
a0001c0002t0001g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
a0001c0002t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
a0001c0002t0001g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
a0001c0002t0001g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
a0001c0002t0001g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
a0001c0002t0001g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
a0001c0002t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
a0001c0002t0001g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
a0001c0002t0001g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
a0001c0002t0001g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
a0001c0002t0001g0309 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
a0001c0002t0001g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
a0001c0005t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
a0001c0005t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
a0001c0005t0001g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
a0001c0005t0001g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
a0001c0005t0001g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
a0001c0005t0001g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
a0001c0005t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
a0001c0005t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
a0001c0005t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
a0001c0005t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
a0001c0005t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
a0001c0005t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
a0001c0005t0001g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
a0001c0005t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
a0001c0005t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
a0001c0005t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
a0001c0005t0001g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
a0001c0005t0001g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
a0001c0005t0001g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
a0001c0009t0001g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
a0001c0009t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
a0001c0009t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
a0001c0009t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
a0001c0009t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
a0001c0009t0001g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
a0001c0009t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
a0001c0009t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
a0001c0009t0001g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
a0001c0009t0001g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
a0001c0009t0009g0078 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
a0001c0011t0003g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
a0001c0011t0003g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
a0001c0011t0003g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
a0001c0011t0003g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
a0001c0011t0003g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
a0001c0011t0003g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
a0001c0011t0003g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
a0001c0011t0003g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
a0001c0011t0003g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
a0001c0011t0003g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
a0001c0016t0001g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
a0001c0016t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
a0001c0016t0002g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
a0001c0016t0010g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
a0001c0020t0005g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
a0001c0020t0005g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
a0001c0020t0005g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
a0001c0022t0002g0012 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
a0001c0022t0002g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
a0001c0023t0003g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
a0001c0023t0003g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
a0001c0034t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
a0001c0037t0003g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
a0001c0050t0001g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
a0001c0051t0003g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
a0001c0052t0002g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
a0001c0054t0001g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
a0002c0003t0001g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
a0002c0003t0002g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
a0002c0003t0002g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
a0002c0003t0002g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
a0002c0003t0002g0077 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
a0002c0003t0002g0079 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
a0002c0003t0002g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
a0002c0003t0002g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
a0002c0003t0002g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
a0002c0003t0002g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
a0002c0003t0002g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
a0002c0003t0002g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
a0002c0003t0002g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
a0002c0003t0002g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
a0002c0003t0002g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
a0002c0003t0002g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
a0002c0003t0002g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
a0002c0003t0002g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
a0002c0003t0002g0290 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
a0002c0003t0002g0304 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
a0002c0003t0002g0305 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
a0002c0003t0006g0001 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
a0002c0003t0006g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
a0002c0006t0002g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
a0002c0006t0002g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
a0002c0006t0002g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
a0002c0006t0002g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
a0002c0006t0002g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
a0002c0006t0002g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
a0002c0006t0002g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
a0002c0006t0002g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
a0002c0006t0002g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
a0002c0006t0002g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
a0002c0006t0002g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
a0002c0006t0002g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
a0002c0006t0002g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
a0002c0006t0002g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
a0002c0006t0002g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
a0002c0006t0002g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
a0002c0006t0002g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
a0002c0006t0002g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
a0002c0006t0002g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
a0002c0024t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
a0002c0024t0001g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
a0002c0048t0002g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
a0002c0055t0001g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
a0003c0004t0001g0018 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
a0003c0004t0001g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
a0003c0004t0001g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
a0003c0004t0001g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
a0003c0004t0001g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
a0003c0004t0001g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
a0003c0004t0001g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
a0003c0004t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
a0003c0004t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
a0003c0004t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
a0003c0004t0001g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
a0003c0004t0001g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
a0003c0004t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
a0003c0004t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
a0003c0004t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
a0003c0004t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
a0003c0004t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
a0003c0004t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
a0003c0004t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
a0003c0004t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
a0003c0004t0001g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
a0003c0004t0001g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
a0003c0004t0008g0273 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
a0003c0013t0001g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
a0003c0013t0001g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
a0003c0013t0001g0023 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
a0003c0013t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
a0003c0013t0001g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
a0003c0013t0001g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
a0003c0013t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
a0003c0013t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
a0003c0018t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
a0003c0018t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
a0003c0018t0002g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
a0003c0025t0001g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
a0003c0025t0001g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
a0003c0043t0001g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
a0003c0058t0001g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
a0003c0059t0001g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
a0003c0061t0001g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
a0004c0007t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
a0004c0007t0001g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
a0004c0007t0001g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
a0004c0007t0001g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
a0004c0007t0001g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
a0004c0007t0001g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
a0004c0007t0001g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
a0004c0007t0001g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
a0004c0007t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
a0004c0007t0001g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
a0004c0007t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
a0004c0007t0001g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
a0004c0007t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
a0004c0007t0014g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
a0004c0010t0001g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
a0004c0010t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
a0004c0010t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
a0004c0010t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
a0004c0010t0001g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
a0004c0010t0001g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
a0004c0010t0004g0128 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
a0004c0010t0004g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
a0004c0010t0004g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
a0004c0010t0012g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
a0004c0026t0001g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
a0004c0026t0001g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
a0004c0057t0003g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
a0005c0008t0001g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
a0005c0008t0001g0031 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
a0005c0008t0001g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
a0005c0008t0001g0153 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
a0005c0008t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
a0005c0008t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
a0005c0008t0001g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
a0005c0008t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
a0005c0008t0001g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
a0005c0008t0004g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
a0005c0008t0004g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
a0005c0008t0004g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
a0005c0008t0004g0297 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
a0005c0044t0001g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
a0005c0045t0007g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
a0006c0012t0002g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
a0006c0012t0002g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
a0006c0012t0002g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
a0006c0012t0002g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
a0006c0012t0002g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
a0006c0012t0002g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
a0006c0012t0002g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
a0006c0012t0002g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
a0006c0012t0002g0271 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
a0006c0027t0002g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
a0006c0027t0002g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
a0006c0047t0002g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
a0007c0014t0002g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
a0007c0014t0002g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
a0007c0014t0002g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
a0007c0014t0002g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
a0007c0014t0002g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
a0007c0014t0002g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
a0007c0019t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
a0007c0019t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
a0007c0019t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
a0007c0060t0002g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
a0008c0015t0001g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
a0008c0015t0001g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
a0008c0015t0001g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
a0008c0015t0001g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
a0008c0015t0001g0274 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
a0008c0031t0001g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
a0009c0017t0002g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
a0009c0017t0002g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
a0009c0017t0002g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
a0009c0053t0002g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
a0010c0029t0001g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
a0010c0029t0001g0034 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
a0011c0028t0002g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
a0011c0028t0002g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
a0012c0021t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
a0012c0021t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
a0013c0038t0002g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
a0013c0039t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
a0014c0040t0002g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
a0015c0049t0002g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
a0016c0042t0001g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
a0017c0046t0002g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
a0018c0030t0001g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
a0019c0036t0001g0282 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
a0020c0056t0001g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
a0021c0033t0013g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
a0022c0032t0001g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
a0023c0035t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
a0024c0041t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0004 | c0010 | t0004 | g0128 | EUR | GBR | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
HG00099 | hp2 | a0002 | c0003 | t0002 | g0077 | EUR | GBR | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
HG00280 | hp1 | a0002 | c0003 | t0002 | g0079 | EUR | FIN | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
HG00280 | hp2 | a0001 | c0001 | t0001 | g0136 | EUR | FIN | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
HG00323 | hp1 | a0003 | c0013 | t0001 | g0023 | EUR | FIN | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
HG00323 | hp2 | a0001 | c0009 | t0009 | g0078 | EUR | FIN | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
HG00408 | hp1 | a0001 | c0001 | t0001 | g0237 | EAS | CHS | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
HG00408 | hp2 | a0001 | c0002 | t0001 | g0279 | EAS | CHS | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
HG00597 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | CHS | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
HG00597 | hp2 | a0003 | c0004 | t0001 | g0291 | EAS | CHS | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
HG00621 | hp1 | a0001 | c0002 | t0001 | g0289 | EAS | CHS | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
HG00621 | hp2 | a0005 | c0008 | t0001 | g0231 | EAS | CHS | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
HG00639 | hp1 | a0001 | c0005 | t0001 | g0092 | AMR | PUR | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
HG00639 | hp2 | a0001 | c0001 | t0001 | g0121 | AMR | PUR | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
HG00642 | hp1 | a0002 | c0003 | t0002 | g0102 | AMR | PUR | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
HG00642 | hp2 | a0005 | c0008 | t0001 | g0026 | AMR | PUR | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
HG00673 | hp1 | a0001 | c0001 | t0001 | g0042 | EAS | CHS | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
HG00673 | hp2 | a0014 | c0040 | t0002 | g0098 | EAS | CHS | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
HG00733 | hp1 | a0003 | c0004 | t0001 | g0024 | AMR | PUR | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
HG00733 | hp2 | a0002 | c0003 | t0002 | g0100 | AMR | PUR | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
HG00741 | hp1 | a0001 | c0002 | t0001 | g0254 | AMR | PUR | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
HG00741 | hp2 | a0001 | c0002 | t0001 | g0096 | AMR | PUR | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
HG01071 | hp1 | a0002 | c0024 | t0001 | g0172 | AMR | PUR | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
HG01071 | hp2 | a0003 | c0013 | t0001 | g0216 | AMR | PUR | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
HG01074 | hp1 | a0003 | c0043 | t0001 | g0036 | AMR | PUR | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
HG01074 | hp2 | a0001 | c0001 | t0001 | g0051 | AMR | PUR | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
HG01081 | hp1 | a0010 | c0029 | t0001 | g0025 | AMR | PUR | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
HG01081 | hp2 | a0001 | c0002 | t0001 | g0076 | AMR | PUR | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
HG01106 | hp1 | a0003 | c0004 | t0001 | g0030 | AMR | PUR | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
HG01106 | hp2 | a0001 | c0005 | t0001 | g0230 | AMR | PUR | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
HG01167 | hp1 | a0004 | c0026 | t0001 | g0067 | AMR | PUR | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
HG01167 | hp2 | a0002 | c0006 | t0002 | g0088 | AMR | PUR | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
HG01168 | hp1 | a0004 | c0010 | t0004 | g0129 | AMR | PUR | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
HG01168 | hp2 | a0001 | c0002 | t0001 | g0005 | AMR | PUR | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
HG01169 | hp1 | a0004 | c0026 | t0001 | g0068 | AMR | PUR | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
HG01169 | hp2 | a0001 | c0002 | t0001 | g0006 | AMR | PUR | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
HG01175 | hp1 | a0007 | c0014 | t0002 | g0292 | AMR | PUR | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
HG01175 | hp2 | a0005 | c0008 | t0004 | g0040 | AMR | PUR | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
HG01243 | hp1 | a0011 | c0028 | t0002 | g0159 | AMR | PUR | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
HG01243 | hp2 | a0001 | c0001 | t0001 | g0055 | AMR | PUR | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
HG01255 | hp1 | a0001 | c0001 | t0001 | g0053 | AMR | CLM | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
HG01255 | hp2 | a0002 | c0003 | t0002 | g0099 | AMR | CLM | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
HG01256 | hp1 | a0001 | c0002 | t0001 | g0215 | AMR | CLM | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
HG01256 | hp2 | a0002 | c0003 | t0002 | g0221 | AMR | CLM | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
HG01258 | hp1 | a0002 | c0003 | t0002 | g0054 | AMR | CLM | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
HG01258 | hp2 | a0001 | c0001 | t0001 | g0220 | AMR | CLM | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
HG01261 | hp1 | a0001 | c0001 | t0001 | g0014 | AMR | CLM | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
HG01261 | hp2 | a0007 | c0014 | t0002 | g0041 | AMR | CLM | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
HG01358 | hp1 | a0005 | c0008 | t0004 | g0245 | AMR | CLM | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
HG01358 | hp2 | a0001 | c0001 | t0001 | g0050 | AMR | CLM | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
HG01361 | hp1 | a0004 | c0010 | t0004 | g0272 | AMR | CLM | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
HG01361 | hp2 | a0001 | c0001 | t0001 | g0256 | AMR | CLM | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
HG01433 | hp1 | a0001 | c0002 | t0001 | g0087 | AMR | CLM | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
HG01433 | hp2 | a0004 | c0010 | t0001 | g0208 | AMR | CLM | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
HG01496 | hp1 | a0001 | c0001 | t0001 | g0116 | AMR | CLM | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
HG01496 | hp2 | a0001 | c0001 | t0001 | g0115 | AMR | CLM | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
HG01515 | hp1 | a0003 | c0004 | t0001 | g0018 | EUR | IBS | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
HG01515 | hp2 | a0001 | c0001 | t0011 | g0229 | EUR | IBS | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
HG01891 | hp1 | a0001 | c0051 | t0003 | g0314 | AFR | ACB | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
HG01891 | hp2 | a0001 | c0020 | t0005 | g0046 | AFR | ACB | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
HG01934 | hp1 | a0001 | c0009 | t0001 | g0134 | AMR | PEL | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
HG01934 | hp2 | a0002 | c0006 | t0002 | g0108 | AMR | PEL | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
HG01978 | hp1 | a0001 | c0001 | t0001 | g0052 | AMR | PEL | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
HG01978 | hp2 | a0002 | c0006 | t0002 | g0064 | AMR | PEL | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
HG01981 | hp1 | a0003 | c0013 | t0001 | g0145 | AMR | PEL | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
HG01981 | hp2 | a0015 | c0049 | t0002 | g0200 | AMR | PEL | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
HG02004 | hp1 | a0001 | c0001 | t0001 | g0283 | AMR | PEL | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
HG02004 | hp2 | a0001 | c0001 | t0001 | g0228 | AMR | PEL | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
HG02015 | hp1 | a0001 | c0005 | t0001 | g0263 | EAS | KHV | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
HG02015 | hp2 | a0002 | c0006 | t0002 | g0193 | EAS | KHV | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
HG02027 | hp1 | a0006 | c0012 | t0002 | g0150 | EAS | KHV | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
HG02027 | hp2 | a0003 | c0004 | t0001 | g0234 | EAS | KHV | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
HG02040 | hp1 | a0001 | c0001 | t0001 | g0204 | EAS | KHV | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
HG02040 | hp2 | a0001 | c0001 | t0001 | g0223 | EAS | KHV | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
HG02055 | hp1 | a0001 | c0011 | t0003 | g0009 | AFR | ACB | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
HG02055 | hp2 | a0001 | c0002 | t0001 | g0047 | AFR | ACB | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
HG02071 | hp1 | a0001 | c0009 | t0001 | g0082 | EAS | KHV | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
HG02071 | hp2 | a0003 | c0004 | t0001 | g0238 | EAS | KHV | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
HG02074 | hp1 | a0006 | c0012 | t0002 | g0175 | EAS | KHV | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
HG02074 | hp2 | a0004 | c0007 | t0001 | g0276 | EAS | KHV | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
HG02080 | hp1 | a0002 | c0024 | t0001 | g0147 | EAS | KHV | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
HG02080 | hp2 | a0002 | c0006 | t0002 | g0133 | EAS | KHV | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
HG02083 | hp1 | a0002 | c0003 | t0002 | g0182 | EAS | KHV | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
HG02083 | hp2 | a0001 | c0002 | t0001 | g0258 | EAS | KHV | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
HG02129 | hp1 | a0004 | c0010 | t0001 | g0284 | EAS | KHV | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
HG02129 | hp2 | a0001 | c0001 | t0001 | g0138 | EAS | KHV | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
HG02132 | hp1 | a0001 | c0002 | t0001 | g0278 | EAS | KHV | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
HG02132 | hp2 | a0001 | c0001 | t0001 | g0202 | EAS | KHV | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
HG02145 | hp1 | a0002 | c0003 | t0002 | g0206 | AFR | ACB | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
HG02145 | hp2 | a0004 | c0007 | t0001 | g0162 | AFR | ACB | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
HG02155 | hp1 | a0001 | c0009 | t0001 | g0203 | EAS | CDX | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
HG02155 | hp2 | a0003 | c0004 | t0001 | g0225 | EAS | CDX | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
HG02165 | hp1 | a0001 | c0001 | t0001 | g0149 | EAS | CDX | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
HG02165 | hp2 | a0003 | c0013 | t0001 | g0010 | EAS | CDX | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
HG02257 | hp1 | a0001 | c0011 | t0003 | g0298 | AFR | ACB | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
HG02257 | hp2 | a0007 | c0014 | t0002 | g0019 | AFR | ACB | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
HG02258 | hp1 | a0004 | c0010 | t0001 | g0013 | AFR | ACB | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
HG02258 | hp2 | a0003 | c0004 | t0001 | g0029 | AFR | ACB | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
HG02280 | hp1 | a0005 | c0008 | t0001 | g0262 | AFR | ACB | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
HG02280 | hp2 | a0003 | c0059 | t0001 | g0259 | AFR | ACB | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
HG02300 | hp1 | a0002 | c0055 | t0001 | g0093 | AMR | PEL | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
HG02300 | hp2 | a0001 | c0001 | t0001 | g0214 | AMR | PEL | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
HG02523 | hp1 | a0001 | c0022 | t0002 | g0146 | EAS | KHV | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
HG02523 | hp2 | a0016 | c0042 | t0001 | g0296 | EAS | KHV | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
HG02572 | hp1 | a0001 | c0011 | t0003 | g0155 | AFR | GWD | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
HG02572 | hp2 | a0004 | c0007 | t0001 | g0201 | AFR | GWD | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
HG02615 | hp1 | a0003 | c0004 | t0001 | g0022 | AFR | GWD | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
HG02615 | hp2 | a0001 | c0011 | t0003 | g0255 | AFR | GWD | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
HG02622 | hp1 | a0011 | c0028 | t0002 | g0154 | AFR | GWD | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
HG02622 | hp2 | a0002 | c0006 | t0002 | g0251 | AFR | GWD | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
HG02630 | hp1 | a0001 | c0011 | t0003 | g0062 | AFR | GWD | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
HG02630 | hp2 | a0003 | c0004 | t0001 | g0028 | AFR | GWD | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
HG02647 | hp1 | a0001 | c0016 | t0001 | g0048 | AFR | GWD | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
HG02647 | hp2 | a0009 | c0053 | t0002 | g0178 | AFR | GWD | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
HG02698 | hp1 | a0001 | c0001 | t0001 | g0033 | SAS | PJL | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
HG02698 | hp2 | a0017 | c0046 | t0002 | g0233 | SAS | PJL | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
HG02717 | hp1 | a0018 | c0030 | t0001 | g0004 | AFR | GWD | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
HG02717 | hp2 | a0002 | c0003 | t0001 | g0171 | AFR | GWD | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
HG02738 | hp1 | a0010 | c0029 | t0001 | g0034 | SAS | PJL | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
HG02738 | hp2 | a0002 | c0003 | t0002 | g0290 | SAS | PJL | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
HG02809 | hp1 | a0007 | c0060 | t0002 | g0260 | AFR | GWD | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
HG02809 | hp2 | a0002 | c0003 | t0006 | g0001 | AFR | GWD | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
HG02818 | hp1 | a0002 | c0003 | t0006 | g0002 | AFR | GWD | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
HG02818 | hp2 | a0008 | c0015 | t0001 | g0058 | AFR | GWD | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
HG02886 | hp1 | a0003 | c0025 | t0001 | g0086 | AFR | GWD | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
HG02886 | hp2 | a0001 | c0023 | t0003 | g0306 | AFR | GWD | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
HG02895 | hp1 | a0001 | c0020 | t0005 | g0169 | AFR | GWD | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
HG02895 | hp2 | a0009 | c0017 | t0002 | g0021 | AFR | GWD | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
HG02897 | hp1 | a0001 | c0002 | t0001 | g0311 | AFR | GWD | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
HG02897 | hp2 | a0001 | c0020 | t0005 | g0168 | AFR | GWD | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
HG02922 | hp1 | a0001 | c0011 | t0003 | g0236 | AFR | ESN | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
HG02922 | hp2 | a0001 | c0002 | t0001 | g0253 | AFR | ESN | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
HG02970 | hp1 | a0009 | c0017 | t0002 | g0308 | AFR | ESN | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
HG02970 | hp2 | a0004 | c0007 | t0001 | g0156 | AFR | ESN | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
HG02976 | hp1 | a0001 | c0052 | t0002 | g0295 | AFR | ESN | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
HG02976 | hp2 | a0002 | c0006 | t0002 | g0249 | AFR | ESN | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
HG03017 | hp1 | a0001 | c0005 | t0001 | g0101 | SAS | PJL | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
HG03017 | hp2 | a0002 | c0003 | t0002 | g0198 | SAS | PJL | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
HG03130 | hp1 | a0003 | c0004 | t0001 | g0035 | AFR | ESN | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
HG03130 | hp2 | a0001 | c0054 | t0001 | g0301 | AFR | ESN | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
HG03139 | hp1 | a0008 | c0031 | t0001 | g0056 | AFR | ESN | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
HG03139 | hp2 | a0001 | c0050 | t0001 | g0310 | AFR | ESN | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
HG03195 | hp1 | a0001 | c0037 | t0003 | g0003 | AFR | ESN | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
HG03195 | hp2 | a0001 | c0023 | t0003 | g0302 | AFR | ESN | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
HG03209 | hp1 | a0008 | c0015 | t0001 | g0057 | AFR | MSL | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
HG03209 | hp2 | a0005 | c0008 | t0004 | g0244 | AFR | MSL | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
HG03225 | hp1 | a0001 | c0011 | t0003 | g0313 | AFR | MSL | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
HG03225 | hp2 | a0001 | c0002 | t0001 | g0020 | AFR | MSL | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
HG03453 | hp1 | a0001 | c0001 | t0001 | g0167 | AFR | MSL | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
HG03453 | hp2 | a0002 | c0006 | t0002 | g0199 | AFR | MSL | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
HG03486 | hp1 | a0001 | c0002 | t0001 | g0192 | AFR | MSL | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
HG03486 | hp2 | a0003 | c0025 | t0001 | g0113 | AFR | MSL | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
HG03491 | hp1 | a0001 | c0005 | t0001 | g0063 | SAS | PJL | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
HG03491 | hp2 | a0001 | c0001 | t0001 | g0285 | SAS | PJL | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
HG03492 | hp1 | a0002 | c0003 | t0002 | g0163 | SAS | PJL | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
HG03492 | hp2 | a0001 | c0005 | t0001 | g0091 | SAS | PJL | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
HG03540 | hp1 | a0003 | c0004 | t0001 | g0312 | AFR | GWD | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
HG03540 | hp2 | a0002 | c0006 | t0002 | g0170 | AFR | GWD | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
HG03654 | hp1 | a0002 | c0003 | t0002 | g0305 | SAS | PJL | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
HG03654 | hp2 | a0001 | c0009 | t0001 | g0049 | SAS | PJL | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
HG03669 | hp1 | a0001 | c0002 | t0001 | g0188 | SAS | PJL | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
HG03669 | hp2 | a0003 | c0004 | t0008 | g0273 | SAS | PJL | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
HG03688 | hp1 | a0004 | c0007 | t0001 | g0189 | SAS | STU | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
HG03688 | hp2 | a0003 | c0004 | t0001 | g0141 | SAS | STU | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
HG03831 | hp1 | a0019 | c0036 | t0001 | g0282 | SAS | BEB | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
HG03831 | hp2 | a0002 | c0003 | t0002 | g0105 | SAS | BEB | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
HG03834 | hp1 | a0005 | c0008 | t0001 | g0031 | SAS | BEB | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
HG03834 | hp2 | a0006 | c0012 | t0002 | g0271 | SAS | BEB | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
HG03927 | hp1 | a0001 | c0001 | t0001 | g0219 | SAS | BEB | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
HG03927 | hp2 | a0020 | c0056 | t0001 | g0122 | SAS | BEB | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
HG03942 | hp1 | a0001 | c0002 | t0001 | g0164 | SAS | BEB | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
HG03942 | hp2 | a0001 | c0002 | t0001 | g0309 | SAS | BEB | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
HG04115 | hp1 | a0001 | c0001 | t0001 | g0027 | SAS | STU | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
HG04115 | hp2 | a0001 | c0002 | t0001 | g0213 | SAS | STU | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
HG04184 | hp1 | a0001 | c0002 | t0001 | g0165 | SAS | BEB | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
HG04184 | hp2 | a0003 | c0004 | t0001 | g0176 | SAS | BEB | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
HG04199 | hp1 | a0001 | c0002 | t0001 | g0107 | SAS | STU | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
HG04199 | hp2 | a0002 | c0003 | t0002 | g0304 | SAS | STU | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
HG04204 | hp1 | a0008 | c0015 | t0001 | g0274 | SAS | STU | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
HG04204 | hp2 | a0001 | c0001 | t0001 | g0227 | SAS | STU | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
NA18612 | hp1 | a0021 | c0033 | t0013 | g0124 | EAS | CHB | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
NA18612 | hp2 | a0001 | c0001 | t0001 | g0187 | EAS | CHB | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
NA18747 | hp1 | a0004 | c0007 | t0001 | g0277 | EAS | CHB | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
NA18747 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | CHB | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
NA18906 | hp1 | a0002 | c0006 | t0002 | g0303 | AFR | YRI | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
NA18906 | hp2 | a0022 | c0032 | t0001 | g0060 | AFR | YRI | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
NA18940 | hp1 | a0007 | c0014 | t0002 | g0119 | EAS | JPT | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
NA18940 | hp2 | a0001 | c0001 | t0001 | g0186 | EAS | JPT | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
NA18942 | hp1 | a0003 | c0013 | t0001 | g0065 | EAS | JPT | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
NA18942 | hp2 | a0002 | c0003 | t0002 | g0066 | EAS | JPT | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
NA18943 | hp1 | a0001 | c0005 | t0001 | g0139 | EAS | JPT | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
NA18943 | hp2 | a0002 | c0006 | t0002 | g0190 | EAS | JPT | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
NA18946 | hp1 | a0001 | c0005 | t0001 | g0235 | EAS | JPT | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
NA18946 | hp2 | a0003 | c0013 | t0001 | g0217 | EAS | JPT | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
NA18947 | hp1 | a0004 | c0010 | t0001 | g0166 | EAS | JPT | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
NA18947 | hp2 | a0001 | c0005 | t0001 | g0044 | EAS | JPT | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
NA18948 | hp1 | a0012 | c0021 | t0001 | g0144 | EAS | JPT | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
NA18948 | hp2 | a0001 | c0001 | t0001 | g0246 | EAS | JPT | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
NA18952 | hp1 | a0003 | c0004 | t0001 | g0240 | EAS | JPT | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
NA18952 | hp2 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
NA18954 | hp1 | a0012 | c0021 | t0001 | g0083 | EAS | JPT | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
NA18954 | hp2 | a0001 | c0001 | t0001 | g0224 | EAS | JPT | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
NA18960 | hp1 | a0003 | c0004 | t0001 | g0081 | EAS | JPT | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
NA18960 | hp2 | a0006 | c0012 | t0002 | g0194 | EAS | JPT | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
NA18961 | hp1 | a0001 | c0002 | t0001 | g0097 | EAS | JPT | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
NA18961 | hp2 | a0001 | c0005 | t0001 | g0275 | EAS | JPT | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
NA18963 | hp1 | a0003 | c0018 | t0001 | g0126 | EAS | JPT | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
NA18963 | hp2 | a0002 | c0006 | t0002 | g0104 | EAS | JPT | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
NA18964 | hp1 | a0006 | c0012 | t0002 | g0106 | EAS | JPT | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
NA18964 | hp2 | a0003 | c0004 | t0001 | g0114 | EAS | JPT | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
NA18966 | hp1 | a0003 | c0004 | t0001 | g0239 | EAS | JPT | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
NA18966 | hp2 | a0006 | c0027 | t0002 | g0140 | EAS | JPT | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
NA18968 | hp1 | a0003 | c0013 | t0001 | g0232 | EAS | JPT | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
NA18968 | hp2 | a0006 | c0012 | t0002 | g0075 | EAS | JPT | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
NA18970 | hp1 | a0001 | c0001 | t0001 | g0069 | EAS | JPT | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
NA18970 | hp2 | a0002 | c0003 | t0002 | g0071 | EAS | JPT | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
NA18971 | hp1 | a0004 | c0007 | t0014 | g0300 | EAS | JPT | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
NA18971 | hp2 | a0004 | c0010 | t0001 | g0152 | EAS | JPT | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
NA18973 | hp1 | a0001 | c0016 | t0001 | g0151 | EAS | JPT | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
NA18973 | hp2 | a0003 | c0013 | t0001 | g0011 | EAS | JPT | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
NA18975 | hp1 | a0001 | c0001 | t0001 | g0257 | EAS | JPT | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
NA18975 | hp2 | a0001 | c0002 | t0001 | g0191 | EAS | JPT | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
NA18977 | hp1 | a0003 | c0004 | t0001 | g0226 | EAS | JPT | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
NA18977 | hp2 | a0004 | c0007 | t0001 | g0267 | EAS | JPT | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
NA18979 | hp1 | a0002 | c0006 | t0002 | g0264 | EAS | JPT | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
NA18979 | hp2 | a0001 | c0002 | t0001 | g0212 | EAS | JPT | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
NA18980 | hp1 | a0002 | c0006 | t0002 | g0265 | EAS | JPT | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
NA18980 | hp2 | a0001 | c0034 | t0001 | g0132 | EAS | JPT | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
NA18985 | hp1 | a0003 | c0018 | t0001 | g0089 | EAS | JPT | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
NA18985 | hp2 | a0002 | c0006 | t0002 | g0142 | EAS | JPT | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
NA18988 | hp1 | a0001 | c0002 | t0001 | g0109 | EAS | JPT | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
NA18988 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
NA18992 | hp1 | a0001 | c0005 | t0001 | g0118 | EAS | JPT | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
NA18992 | hp2 | a0013 | c0039 | t0001 | g0196 | EAS | JPT | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
NA18998 | hp1 | a0007 | c0019 | t0001 | g0085 | EAS | JPT | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
NA18998 | hp2 | a0001 | c0009 | t0001 | g0288 | EAS | JPT | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
NA18999 | hp1 | a0001 | c0009 | t0001 | g0094 | EAS | JPT | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
NA18999 | hp2 | a0002 | c0003 | t0002 | g0270 | EAS | JPT | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
NA19000 | hp1 | a0001 | c0005 | t0001 | g0207 | EAS | JPT | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
NA19000 | hp2 | a0002 | c0006 | t0002 | g0294 | EAS | JPT | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
NA19002 | hp1 | a0001 | c0005 | t0001 | g0286 | EAS | JPT | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
NA19002 | hp2 | a0006 | c0012 | t0002 | g0179 | EAS | JPT | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
NA19005 | hp1 | a0003 | c0004 | t0001 | g0125 | EAS | JPT | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
NA19005 | hp2 | a0004 | c0007 | t0001 | g0269 | EAS | JPT | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
NA19006 | hp1 | a0003 | c0004 | t0001 | g0180 | EAS | JPT | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
NA19006 | hp2 | a0006 | c0012 | t0002 | g0218 | EAS | JPT | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
NA19009 | hp1 | a0023 | c0035 | t0001 | g0185 | EAS | JPT | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
NA19009 | hp2 | a0007 | c0019 | t0001 | g0135 | EAS | JPT | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
NA19010 | hp1 | a0001 | c0001 | t0001 | g0222 | EAS | JPT | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
NA19010 | hp2 | a0006 | c0027 | t0002 | g0130 | EAS | JPT | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
NA19012 | hp1 | a0002 | c0003 | t0002 | g0181 | EAS | JPT | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
NA19012 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
NA19030 | hp1 | a0003 | c0058 | t0001 | g0210 | AFR | LWK | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
NA19030 | hp2 | a0004 | c0007 | t0001 | g0211 | AFR | LWK | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
NA19043 | hp1 | a0008 | c0015 | t0001 | g0061 | AFR | LWK | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
NA19043 | hp2 | a0007 | c0014 | t0002 | g0250 | AFR | LWK | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
NA19055 | hp1 | a0001 | c0016 | t0010 | g0209 | EAS | JPT | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
NA19055 | hp2 | a0005 | c0008 | t0001 | g0174 | EAS | JPT | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
NA19056 | hp1 | a0001 | c0001 | t0001 | g0070 | EAS | JPT | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
NA19056 | hp2 | a0001 | c0005 | t0001 | g0123 | EAS | JPT | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
NA19058 | hp1 | a0001 | c0009 | t0001 | g0073 | EAS | JPT | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
NA19058 | hp2 | a0007 | c0019 | t0001 | g0127 | EAS | JPT | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
NA19060 | hp1 | a0001 | c0005 | t0001 | g0137 | EAS | JPT | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
NA19060 | hp2 | a0001 | c0001 | t0001 | g0072 | EAS | JPT | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
NA19062 | hp1 | a0001 | c0005 | t0001 | g0247 | EAS | JPT | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
NA19062 | hp2 | a0004 | c0010 | t0001 | g0080 | EAS | JPT | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
NA19064 | hp1 | a0005 | c0008 | t0001 | g0248 | EAS | JPT | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
NA19064 | hp2 | a0006 | c0012 | t0002 | g0195 | EAS | JPT | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
NA19066 | hp1 | a0002 | c0006 | t0002 | g0173 | EAS | JPT | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
NA19066 | hp2 | a0001 | c0005 | t0001 | g0103 | EAS | JPT | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
NA19068 | hp1 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
NA19068 | hp2 | a0004 | c0007 | t0001 | g0117 | EAS | JPT | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
NA19070 | hp1 | a0001 | c0009 | t0001 | g0112 | EAS | JPT | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
NA19070 | hp2 | a0001 | c0016 | t0002 | g0268 | EAS | JPT | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
NA19077 | hp1 | a0001 | c0001 | t0001 | g0281 | EAS | JPT | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
NA19077 | hp2 | a0004 | c0007 | t0001 | g0266 | EAS | JPT | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
NA19079 | hp1 | a0001 | c0005 | t0001 | g0280 | EAS | JPT | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
NA19079 | hp2 | a0002 | c0006 | t0002 | g0084 | EAS | JPT | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
NA19084 | hp1 | a0002 | c0003 | t0002 | g0131 | EAS | JPT | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
NA19084 | hp2 | a0001 | c0009 | t0001 | g0287 | EAS | JPT | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
NA19085 | hp1 | a0001 | c0001 | t0001 | g0074 | EAS | JPT | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
NA19085 | hp2 | a0002 | c0048 | t0002 | g0143 | EAS | JPT | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
NA19086 | hp1 | a0001 | c0005 | t0001 | g0043 | EAS | JPT | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
NA19086 | hp2 | a0024 | c0041 | t0001 | g0183 | EAS | JPT | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
NA19087 | hp1 | a0001 | c0002 | t0001 | g0111 | EAS | JPT | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
NA19087 | hp2 | a0001 | c0009 | t0001 | g0252 | EAS | JPT | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
NA19088 | hp1 | a0003 | c0004 | t0001 | g0242 | EAS | JPT | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
NA19088 | hp2 | a0013 | c0038 | t0002 | g0184 | EAS | JPT | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
NA19090 | hp1 | a0004 | c0010 | t0012 | g0177 | EAS | JPT | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
NA19090 | hp2 | a0006 | c0047 | t0002 | g0120 | EAS | JPT | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
NA20129 | hp1 | a0005 | c0045 | t0007 | g0039 | AFR | ASW | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
NA20129 | hp2 | a0009 | c0017 | t0002 | g0307 | AFR | ASW | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
NA20805 | hp1 | a0005 | c0008 | t0004 | g0297 | EUR | TSI | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
NA20805 | hp2 | a0001 | c0022 | t0002 | g0012 | EUR | TSI | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
HG01123 | hp1 | a0003 | c0061 | t0001 | g0299 | AMR | CLM | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
HG01123 | hp2 | a0005 | c0008 | t0001 | g0241 | AMR | CLM | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
HG02109 | hp1 | a0004 | c0007 | t0001 | g0160 | AFR | ACB | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
HG02109 | hp2 | a0001 | c0011 | t0003 | g0293 | AFR | ACB | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
HG02486 | hp1 | a0005 | c0008 | t0001 | g0032 | AFR | ACB | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
HG02486 | hp2 | a0008 | c0015 | t0001 | g0059 | AFR | ACB | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
HG02559 | hp1 | a0004 | c0007 | t0001 | g0157 | AFR | ACB | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
HG02559 | hp2 | a0001 | c0002 | t0001 | g0045 | AFR | ACB | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
HG03471 | hp1 | a0001 | c0011 | t0003 | g0158 | AFR | MSL | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
HG03471 | hp2 | a0003 | c0018 | t0002 | g0038 | AFR | MSL | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
HG06807 | hp1 | a0005 | c0044 | t0001 | g0261 | AFR | USA | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
HG06807 | hp2 | a0002 | c0006 | t0002 | g0037 | AFR | USA | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
NA18955 | hp1 | a0001 | c0002 | t0001 | g0110 | EAS | JPT | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
NA18955 | hp2 | a0007 | c0014 | t0002 | g0243 | EAS | JPT | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
NA20300 | hp1 | a0001 | c0002 | t0001 | g0197 | AFR | USA | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
NA20300 | hp2 | a0004 | c0057 | t0003 | g0017 | AFR | USA | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
NA21309 | hp1 | a0001 | c0002 | t0001 | g0205 | AFR | LWK | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
NA21309 | hp2 | a0001 | c0011 | t0003 | g0161 | AFR | LWK | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
homoSapiens | chm13v2 | a0001 | c0002 | t0001 | g0148 | REF | REF | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
homoSapiens | grch38p0 | a0005 | c0008 | t0001 | g0153 | REF | REF | LAMA4_chr6_112102931_112259567 | LAMA4 | chr6 | 112102931 | 112259567 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr6:112109466 | C | T | 2 | a0006 a0014 |
13 | HG00673.hp2 HG02027.hp1 HG02074.hp1 others(10): Show |
missense_variant | MODERATE | c.5443G>A | p.Val1815Ile | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 39/39 | 5693/7228 | 5443/5472 | 1815/1823 | chr6 | 112109466 | |||
chr6:112120302 | T | C | 1 | a0009 | 4 | HG02647.hp2 HG02895.hp2 HG02970.hp1 others(1): Show |
missense_variant | MODERATE | c.4646A>G | p.Asn1549Ser | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 33/39 | 4896/7228 | 4646/5472 | 1549/1823 | chr6 | 112120302 | |||
chr6:112130993 | C | T | 1 | a0013 | 2 | NA18992.hp2 NA19088.hp2 |
missense_variant | MODERATE | c.3943G>A | p.Val1315Ile | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 29/39 | 4193/7228 | 3943/5472 | 1315/1823 | chr6 | 112130993 | |||
chr6:112136181 | G | C | 5 | a0002 a0006 a0007 others(2): Show |
70 | HG00099.hp2 HG00280.hp1 HG00642.hp1 others(67): Show |
missense_variant | MODERATE | c.3356C>G | p.Pro1119Arg | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 25/39 | 3606/7228 | 3356/5472 | 1119/1823 | chr6 | 112136181 | |||
chr6:112136188 | C | T | 18 | a0001 a0002 a0003 others(15): Show |
265 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(262): Show |
missense_variant | MODERATE | c.3349G>A | p.Gly1117Ser | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 25/39 | 3599/7228 | 3349/5472 | 1117/1823 | chr6 | 112136188 | |||
chr6:112139163 | C | T | 1 | a0017 | 1 | HG02698.hp2 | missense_variant | MODERATE | c.3239G>A | p.Arg1080Gln | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 24/39 | 3489/7228 | 3239/5472 | 1080/1823 | chr6 | 112139163 | |||
chr6:112139227 | C | T | 1 | a0019 | 1 | HG03831.hp1 | missense_variant | MODERATE | c.3175G>A | p.Val1059Met | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 24/39 | 3425/7228 | 3175/5472 | 1059/1823 | chr6 | 112139227 | |||
chr6:112139236 | C | T | 1 | a0015 | 1 | HG01981.hp2 | missense_variant | MODERATE | c.3166G>A | p.Gly1056Ser | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 24/39 | 3416/7228 | 3166/5472 | 1056/1823 | chr6 | 112139236 | |||
chr6:112141361 | T | C | 1 | a0011 | 2 | HG01243.hp1 HG02622.hp1 |
missense_variant | MODERATE | c.2810A>G | p.Glu937Gly | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 21/39 | 3060/7228 | 2810/5472 | 937/1823 | chr6 | 112141361 | |||
chr6:112150530 | T | A | 1 | a0024 | 1 | NA19086.hp2 | missense_variant | MODERATE | c.2154A>T | p.Gln718His | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 17/39 | 2404/7228 | 2154/5472 | 718/1823 | chr6 | 112150530 | |||
chr6:112154908 | C | A | 1 | a0020 | 1 | HG03927.hp2 | missense_variant | MODERATE | c.1999G>T | p.Asp667Tyr | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 16/39 | 2249/7228 | 1999/5472 | 667/1823 | chr6 | 112154908 | |||
chr6:112158778 | T | C | 1 | a0016 | 1 | HG02523.hp2 | missense_variant | MODERATE | c.1771A>G | p.Ile591Val | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 14/39 | 2021/7228 | 1771/5472 | 591/1823 | chr6 | 112158778 | |||
chr6:112172670 | A | G | 17 | a0001 a0002 a0004 others(14): Show |
243 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(240): Show |
missense_variant | MODERATE | c.1492T>C | p.Tyr498His | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 12/39 | 1742/7228 | 1492/5472 | 498/1823 | chr6 | 112172670 | |||
chr6:112172687 | A | T | 1 | a0023 | 1 | NA19009.hp1 | missense_variant | MODERATE | c.1475T>A | p.Leu492His | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 12/39 | 1725/7228 | 1475/5472 | 492/1823 | chr6 | 112172687 | |||
chr6:112187553 | G | C | 1 | a0017 | 1 | HG02698.hp2 | missense_variant | MODERATE | c.863C>G | p.Ala288Gly | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 8/39 | 1113/7228 | 863/5472 | 288/1823 | chr6 | 112187553 | |||
chr6:112191713 | C | T | 2 | a0012 a0021 |
3 | NA18612.hp1 NA18948.hp1 NA18954.hp1 |
missense_variant | MODERATE | c.641G>A | p.Arg214His | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 6/39 | 891/7228 | 641/5472 | 214/1823 | chr6 | 112191713 | |||
chr6:112201651 | G | A | 1 | a0010 | 2 | HG01081.hp1 HG02738.hp1 |
missense_variant | MODERATE | c.460C>T | p.Arg154Trp | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 5/39 | 710/7228 | 460/5472 | 154/1823 | chr6 | 112201651 | |||
chr6:112216385 | C | T | 2 | a0008 a0022 |
7 | HG02486.hp2 HG02818.hp2 HG03139.hp1 others(4): Show |
missense_variant | MODERATE | c.280G>A | p.Gly94Ser | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 3/39 | 530/7228 | 280/5472 | 94/1823 | chr6 | 112216385 | |||
chr6:112254066 | C | T | 1 | a0018 | 1 | HG02717.hp1 | missense_variant | MODERATE | c.85G>A | p.Asp29Asn | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 2/39 | 335/7228 | 85/5472 | 29/1823 | chr6 | 112254066 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr6:112114709 | A | T | 28 | a0001c0016 a0001c0020 a0001c0022 others(25): Show |
94 | HG00099.hp2 HG00280.hp1 HG00642.hp1 others(91): Show |
synonymous_variant | LOW | c.5160T>A | p.Val1720Val | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 37/39 | 5410/7228 | 5160/5472 | 1720/1823 | chr6 | 112114709 | |||
chr6:112115959 | A | T | 1 | a0005c0044 | 1 | HG06807.hp1 | synonymous_variant | LOW | c.5016T>A | p.Ile1672Ile | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 36/39 | 5266/7228 | 5016/5472 | 1672/1823 | chr6 | 112115959 | |||
chr6:112119261 | G | A | 8 | a0001c0011 a0001c0023 a0001c0051 others(5): Show |
20 | HG01243.hp1 HG01891.hp1 HG02055.hp1 others(17): Show |
synonymous_variant | LOW | c.4716C>T | p.Leu1572Leu | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 34/39 | 4966/7228 | 4716/5472 | 1572/1823 | chr6 | 112119261 | |||
chr6:112119299 | G | T | 1 | a0001c0051 | 1 | HG01891.hp1 | synonymous_variant | LOW | c.4678C>A | p.Arg1560Arg | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 34/39 | 4928/7228 | 4678/5472 | 1560/1823 | chr6 | 112119299 | |||
chr6:112122175 | T | G | 1 | a0001c0037 | 1 | HG03195.hp1 | synonymous_variant | LOW | c.4314A>C | p.Ser1438Ser | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 32/39 | 4564/7228 | 4314/5472 | 1438/1823 | chr6 | 112122175 | |||
chr6:112129036 | A | G | 3 | a0001c0050 a0001c0054 a0003c0025 |
4 | HG02886.hp1 HG03130.hp2 HG03139.hp2 others(1): Show |
synonymous_variant | LOW | c.4173T>C | p.Tyr1391Tyr | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 31/39 | 4423/7228 | 4173/5472 | 1391/1823 | chr6 | 112129036 | |||
chr6:112129944 | G | A | 2 | a0001c0054 a0003c0025 |
3 | HG02886.hp1 HG03130.hp2 HG03486.hp2 |
synonymous_variant | LOW | c.4065C>T | p.Phe1355Phe | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 30/39 | 4315/7228 | 4065/5472 | 1355/1823 | chr6 | 112129944 | |||
chr6:112148260 | C | T | 1 | a0001c0020 | 3 | HG01891.hp2 HG02895.hp1 HG02897.hp2 |
synonymous_variant | LOW | c.2250G>A | p.Gln750Gln | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 18/39 | 2500/7228 | 2250/5472 | 750/1823 | chr6 | 112148260 | |||
chr6:112158839 | A | G | 9 | a0001c0005 a0001c0009 a0001c0034 others(6): Show |
45 | HG00323.hp1 HG00323.hp2 HG00639.hp1 others(42): Show |
synonymous_variant | LOW | c.1710T>C | p.Ser570Ser | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 14/39 | 1960/7228 | 1710/5472 | 570/1823 | chr6 | 112158839 | |||
chr6:112172728 | C | G | 1 | a0001c0034 | 1 | NA18980.hp2 | synonymous_variant | LOW | c.1434G>C | p.Leu478Leu | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 12/39 | 1684/7228 | 1434/5472 | 478/1823 | chr6 | 112172728 | |||
chr6:112187528 | G | A | 1 | a0004c0057 | 1 | NA20300.hp2 | synonymous_variant | LOW | c.888C>T | p.Ser296Ser | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 8/39 | 1138/7228 | 888/5472 | 296/1823 | chr6 | 112187528 | |||
chr6:112191703 | G | A | 21 | a0001c0002 a0001c0005 a0001c0011 others(18): Show |
117 | HG00408.hp2 HG00621.hp1 HG00639.hp1 others(114): Show |
synonymous_variant | LOW | c.651C>T | p.Thr217Thr | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 6/39 | 901/7228 | 651/5472 | 217/1823 | chr6 | 112191703 | |||
chr6:112191823 | G | A | 4 | a0003c0058 a0003c0059 a0007c0060 others(1): Show |
4 | HG02280.hp2 HG02809.hp1 NA18906.hp2 others(1): Show |
synonymous_variant | LOW | c.531C>T | p.Pro177Pro | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 6/39 | 781/7228 | 531/5472 | 177/1823 | chr6 | 112191823 | |||
chr6:112254061 | G | A | 1 | a0003c0061 | 1 | HG01123.hp1 | synonymous_variant | LOW | c.90C>T | p.Asn30Asn | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 2/39 | 340/7228 | 90/5472 | 30/1823 | chr6 | 112254061 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr6:112108141 | T | C | 1 | a0001c0020t0005 | 3 | HG01891.hp2 HG02895.hp1 HG02897.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1296A>G | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 39/39 | 1296 | chr6 | 112108141 | ||||||
chr6:112108159 | C | G | 1 | a0001c0020t0005 | 3 | HG01891.hp2 HG02895.hp1 HG02897.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1278G>C | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 39/39 | 1278 | chr6 | 112108159 | ||||||
chr6:112108205 | A | G | 1 | a0004c0010t0012 | 1 | NA19090.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1232T>C | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 39/39 | 1232 | chr6 | 112108205 | ||||||
chr6:112108289 | A | T | 1 | a0001c0001t0011 | 1 | HG01515.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1148T>A | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 39/39 | 1148 | chr6 | 112108289 | ||||||
chr6:112108295 | A | G | 1 | a0001c0016t0010 | 1 | NA19055.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1142T>C | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 39/39 | 1142 | chr6 | 112108295 | ||||||
chr6:112108388 | A | C | 1 | a0001c0009t0009 | 1 | HG00323.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1049T>G | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 39/39 | 1049 | chr6 | 112108388 | ||||||
chr6:112108508 | C | T | 2 | a0004c0010t0004 a0005c0008t0004 |
7 | HG00099.hp1 HG01168.hp1 HG01175.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*929G>A | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 39/39 | 929 | chr6 | 112108508 | ||||||
chr6:112108522 | C | T | 1 | a0003c0004t0008 | 1 | HG03669.hp2 | 3_prime_UTR_variant | MODIFIER | c.*915G>A | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 39/39 | 915 | chr6 | 112108522 | ||||||
chr6:112108584 | T | A | 22 | a0001c0016t0002 a0001c0020t0005 a0001c0022t0002 others(19): Show |
80 | HG00099.hp2 HG00280.hp1 HG00642.hp1 others(77): Show |
3_prime_UTR_variant | MODIFIER | c.*853A>T | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 39/39 | 853 | chr6 | 112108584 | ||||||
chr6:112108590 | C | T | 27 | a0001c0011t0003 a0001c0016t0002 a0001c0020t0005 others(24): Show |
95 | HG00099.hp2 HG00280.hp1 HG00642.hp1 others(92): Show |
3_prime_UTR_variant | MODIFIER | c.*847G>A | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 39/39 | 847 | chr6 | 112108590 | ||||||
chr6:112108596 | T | A | 1 | a0001c0020t0005 | 3 | HG01891.hp2 HG02895.hp1 HG02897.hp2 |
3_prime_UTR_variant | MODIFIER | c.*841A>T | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 39/39 | 841 | chr6 | 112108596 | ||||||
chr6:112108637 | A | G | 1 | a0005c0045t0007 | 1 | NA20129.hp1 | 3_prime_UTR_variant | MODIFIER | c.*800T>C | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 39/39 | 800 | chr6 | 112108637 | ||||||
chr6:112108709 | T | A | 22 | a0001c0016t0002 a0001c0020t0005 a0001c0022t0002 others(19): Show |
80 | HG00099.hp2 HG00280.hp1 HG00642.hp1 others(77): Show |
3_prime_UTR_variant | MODIFIER | c.*728A>T | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 39/39 | 728 | chr6 | 112108709 | ||||||
chr6:112108824 | G | T | 27 | a0001c0011t0003 a0001c0016t0002 a0001c0020t0005 others(24): Show |
95 | HG00099.hp2 HG00280.hp1 HG00642.hp1 others(92): Show |
3_prime_UTR_variant | MODIFIER | c.*613C>A | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 39/39 | 613 | chr6 | 112108824 | ||||||
chr6:112108934 | T | C | 1 | a0021c0033t0013 | 1 | NA18612.hp1 | 3_prime_UTR_variant | MODIFIER | c.*503A>G | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 39/39 | 503 | chr6 | 112108934 | ||||||
chr6:112108977 | A | G | 22 | a0001c0016t0002 a0001c0020t0005 a0001c0022t0002 others(19): Show |
80 | HG00099.hp2 HG00280.hp1 HG00642.hp1 others(77): Show |
3_prime_UTR_variant | MODIFIER | c.*460T>C | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 39/39 | 460 | chr6 | 112108977 | ||||||
chr6:112254241 | T | C | 1 | a0004c0007t0014 | 1 | NA18971.hp1 | 5_prime_UTR_variant | MODIFIER | c.-91A>G | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 2/39 | 91 | chr6 | 112254241 | ||||||
chr6:112254525 | G | T | 1 | a0002c0003t0006 | 2 | HG02809.hp2 HG02818.hp1 |
5_prime_UTR_variant | MODIFIER | c.-208C>A | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 1/39 | 375 | chr6 | 112254525 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr6:112109644 | CTTCCTGG others(156): Show |
C | 14 | a0001c0011t0003g0009 a0001c0011t0003g0062 a0001c0011t0003g0155 others(11): Show |
14 | HG01891.hp1 HG02055.hp1 HG02109.hp2 others(11): Show |
intron_variant | MODIFIER | c.5327-225_5327-63de others(1): Show |
LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 38/38 | chr6 | 112109644 | |||||||
chr6:112109683 | T | C | 83 | a0001c0016t0002g0268 a0001c0020t0005g0046 a0001c0020t0005g0168 others(80): Show |
83 | HG00099.hp2 HG00280.hp1 HG00642.hp1 others(80): Show |
intron_variant | MODIFIER | c.5327-101A>G | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 38/38 | chr6 | 112109683 | |||||||
chr6:112109760 | A | G | 2 | a0003c0025t0001g0086 a0003c0025t0001g0113 |
2 | HG02886.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.5327-178T>C | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 38/38 | chr6 | 112109760 | |||||||
chr6:112109883 | G | T | 2 | a0003c0025t0001g0086 a0003c0025t0001g0113 |
2 | HG02886.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.5327-301C>A | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 38/38 | chr6 | 112109883 | |||||||
chr6:112110037 | C | T | 1 | a0003c0004t0008g0273 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.5327-455G>A | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 38/38 | chr6 | 112110037 | |||||||
chr6:112110080 | C | T | 49 | a0001c0001t0001g0116 a0001c0001t0001g0283 a0001c0005t0001g0235 others(46): Show |
49 | HG00099.hp1 HG00621.hp2 HG01071.hp1 others(46): Show |
intron_variant | MODIFIER | c.5327-498G>A | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 38/38 | chr6 | 112110080 | |||||||
chr6:112110202 | C | CTCTTA | 76 | a0001c0016t0002g0268 a0001c0020t0005g0046 a0001c0020t0005g0168 others(73): Show |
76 | HG00099.hp2 HG00280.hp1 HG00642.hp1 others(73): Show |
intron_variant | MODIFIER | c.5327-625_5327-621d others(7): Show |
LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 38/38 | chr6 | 112110202 | |||||||
chr6:112110345 | T | G | 3 | a0002c0006t0002g0303 a0007c0014t0002g0250 a0007c0060t0002g0260 |
3 | HG02809.hp1 NA18906.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.5327-763A>C | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 38/38 | chr6 | 112110345 | |||||||
chr6:112110460 | G | T | 11 | a0001c0011t0003g0062 a0001c0011t0003g0155 a0001c0011t0003g0158 others(8): Show |
11 | HG01891.hp1 HG02257.hp1 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.5327-878C>A | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 38/38 | chr6 | 112110460 | |||||||
chr6:112110533 | C | T | 11 | a0001c0011t0003g0062 a0001c0011t0003g0155 a0001c0011t0003g0158 others(8): Show |
11 | HG01891.hp1 HG02257.hp1 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.5327-951G>A | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 38/38 | chr6 | 112110533 | |||||||
chr6:112110572 | T | C | 15 | a0001c0011t0003g0009 a0001c0011t0003g0062 a0001c0011t0003g0155 others(12): Show |
15 | HG01891.hp1 HG02055.hp1 HG02109.hp2 others(12): Show |
intron_variant | MODIFIER | c.5327-990A>G | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 38/38 | chr6 | 112110572 | |||||||
chr6:112110678 | C | T | 3 | a0001c0005t0001g0043 a0001c0005t0001g0044 a0001c0005t0001g0275 |
3 | NA18947.hp2 NA18961.hp2 NA19086.hp1 |
intron_variant | MODIFIER | c.5327-1096G>A | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 38/38 | chr6 | 112110678 | |||||||
chr6:112110854 | A | G | 15 | a0001c0011t0003g0009 a0001c0011t0003g0062 a0001c0011t0003g0155 others(12): Show |
15 | HG01891.hp1 HG02055.hp1 HG02109.hp2 others(12): Show |
intron_variant | MODIFIER | c.5327-1272T>C | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 38/38 | chr6 | 112110854 | |||||||
chr6:112110905 | G | T | 2 | a0001c0054t0001g0301 a0008c0031t0001g0056 |
2 | HG03130.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.5327-1323C>A | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 38/38 | chr6 | 112110905 | |||||||
chr6:112110932 | A | C | 80 | a0001c0016t0002g0268 a0001c0020t0005g0046 a0001c0020t0005g0168 others(77): Show |
80 | HG00099.hp2 HG00280.hp1 HG00642.hp1 others(77): Show |
intron_variant | MODIFIER | c.5327-1350T>G | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 38/38 | chr6 | 112110932 | |||||||
chr6:112110999 | T | A | 1 | a0001c0037t0003g0003 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.5327-1417A>T | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 38/38 | chr6 | 112110999 | |||||||
chr6:112111042 | A | G | 1 | a0001c0002t0001g0205 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.5327-1460T>C | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 38/38 | chr6 | 112111042 | |||||||
chr6:112111099 | G | A | 2 | a0001c0001t0001g0115 a0001c0001t0001g0220 |
2 | HG01258.hp2 HG01496.hp2 |
intron_variant | MODIFIER | c.5327-1517C>T | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 38/38 | chr6 | 112111099 | |||||||
chr6:112111150 | G | A | 1 | a0001c0001t0001g0095 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.5327-1568C>T | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 38/38 | chr6 | 112111150 | |||||||
chr6:112111249 | G | A | 72 | a0001c0016t0002g0268 a0001c0020t0005g0046 a0001c0020t0005g0168 others(69): Show |
72 | HG00099.hp2 HG00280.hp1 HG00642.hp1 others(69): Show |
intron_variant | MODIFIER | c.5327-1667C>T | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 38/38 | chr6 | 112111249 | |||||||
chr6:112111278 | A | G | 1 | a0004c0010t0004g0272 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.5327-1696T>C | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 38/38 | chr6 | 112111278 | |||||||
chr6:112111416 | A | T | 15 | a0001c0011t0003g0009 a0001c0011t0003g0062 a0001c0011t0003g0155 others(12): Show |
15 | HG01891.hp1 HG02055.hp1 HG02109.hp2 others(12): Show |
intron_variant | MODIFIER | c.5327-1834T>A | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 38/38 | chr6 | 112111416 | |||||||
chr6:112111705 | G | A | 1 | a0001c0005t0001g0043 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.5327-2123C>T | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 38/38 | chr6 | 112111705 | |||||||
chr6:112111712 | C | T | 1 | a0001c0001t0001g0072 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.5327-2130G>A | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 38/38 | chr6 | 112111712 | |||||||
chr6:112111947 | C | T | 11 | a0001c0011t0003g0062 a0001c0011t0003g0155 a0001c0011t0003g0158 others(8): Show |
11 | HG01891.hp1 HG02257.hp1 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.5326+2129G>A | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 38/38 | chr6 | 112111947 | |||||||
chr6:112111949 | T | C | 15 | a0001c0011t0003g0009 a0001c0011t0003g0062 a0001c0011t0003g0155 others(12): Show |
15 | HG01891.hp1 HG02055.hp1 HG02109.hp2 others(12): Show |
intron_variant | MODIFIER | c.5326+2127A>G | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 38/38 | chr6 | 112111949 | |||||||
chr6:112111973 | T | TA | 4 | a0002c0003t0002g0077 a0002c0003t0002g0079 a0002c0003t0002g0290 others(1): Show |
4 | HG00099.hp2 HG00280.hp1 HG02257.hp2 others(1): Show |
intron_variant | MODIFIER | c.5326+2102dupT | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 38/38 | chr6 | 112111973 | |||||||
chr6:112112127 | A | G | 1 | a0002c0006t0002g0193 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.5326+1949T>C | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 38/38 | chr6 | 112112127 | |||||||
chr6:112112255 | A | C | 1 | a0003c0013t0001g0145 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.5326+1821T>G | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 38/38 | chr6 | 112112255 | |||||||
chr6:112112281 | G | C | 1 | a0003c0058t0001g0210 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.5326+1795C>G | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 38/38 | chr6 | 112112281 | |||||||
chr6:112112363 | C | T | 1 | a0003c0018t0002g0038 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.5326+1713G>A | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 38/38 | chr6 | 112112363 | |||||||
chr6:112112405 | G | A | 2 | a0001c0001t0001g0007 a0001c0001t0001g0138 |
2 | HG00597.hp1 HG02129.hp2 |
intron_variant | MODIFIER | c.5326+1671C>T | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 38/38 | chr6 | 112112405 | |||||||
chr6:112112461 | T | C | 80 | a0001c0016t0002g0268 a0001c0020t0005g0046 a0001c0020t0005g0168 others(77): Show |
80 | HG00099.hp2 HG00280.hp1 HG00642.hp1 others(77): Show |
intron_variant | MODIFIER | c.5326+1615A>G | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 38/38 | chr6 | 112112461 | |||||||
chr6:112112473 | G | C | 1 | a0002c0003t0006g0002 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.5326+1603C>G | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 38/38 | chr6 | 112112473 | |||||||
chr6:112112643 | G | A | 1 | a0001c0037t0003g0003 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.5326+1433C>T | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 38/38 | chr6 | 112112643 | |||||||
chr6:112112662 | A | AAGG | 95 | a0001c0011t0003g0009 a0001c0011t0003g0062 a0001c0011t0003g0155 others(92): Show |
95 | HG00099.hp2 HG00280.hp1 HG00642.hp1 others(92): Show |
intron_variant | MODIFIER | c.5326+1411_5326+141 others(7): Show |
LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 38/38 | chr6 | 112112662 | |||||||
chr6:112112699 | T | C | 80 | a0001c0016t0002g0268 a0001c0020t0005g0046 a0001c0020t0005g0168 others(77): Show |
80 | HG00099.hp2 HG00280.hp1 HG00642.hp1 others(77): Show |
intron_variant | MODIFIER | c.5326+1377A>G | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 38/38 | chr6 | 112112699 | |||||||
chr6:112112709 | C | A | 80 | a0001c0016t0002g0268 a0001c0020t0005g0046 a0001c0020t0005g0168 others(77): Show |
80 | HG00099.hp2 HG00280.hp1 HG00642.hp1 others(77): Show |
intron_variant | MODIFIER | c.5326+1367G>T | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 38/38 | chr6 | 112112709 | |||||||
chr6:112112717 | T | C | 95 | a0001c0011t0003g0009 a0001c0011t0003g0062 a0001c0011t0003g0155 others(92): Show |
95 | HG00099.hp2 HG00280.hp1 HG00642.hp1 others(92): Show |
intron_variant | MODIFIER | c.5326+1359A>G | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 38/38 | chr6 | 112112717 | |||||||
chr6:112112758 | A | G | 2 | a0003c0018t0001g0089 a0003c0018t0001g0126 |
2 | NA18963.hp1 NA18985.hp1 |
intron_variant | MODIFIER | c.5326+1318T>C | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 38/38 | chr6 | 112112758 | |||||||
chr6:112112770 | T | G | 80 | a0001c0016t0002g0268 a0001c0020t0005g0046 a0001c0020t0005g0168 others(77): Show |
80 | HG00099.hp2 HG00280.hp1 HG00642.hp1 others(77): Show |
intron_variant | MODIFIER | c.5326+1306A>C | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 38/38 | chr6 | 112112770 | |||||||
chr6:112112956 | T | G | 83 | a0001c0011t0003g0009 a0001c0011t0003g0293 a0001c0016t0002g0268 others(80): Show |
83 | HG00099.hp2 HG00280.hp1 HG00642.hp1 others(80): Show |
intron_variant | MODIFIER | c.5326+1120A>C | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 38/38 | chr6 | 112112956 | |||||||
chr6:112113302 | T | C | 49 | a0001c0001t0001g0116 a0001c0001t0001g0283 a0001c0005t0001g0235 others(46): Show |
49 | HG00099.hp1 HG00621.hp2 HG01071.hp1 others(46): Show |
intron_variant | MODIFIER | c.5326+774A>G | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 38/38 | chr6 | 112113302 | |||||||
chr6:112113363 | T | G | 80 | a0001c0016t0002g0268 a0001c0020t0005g0046 a0001c0020t0005g0168 others(77): Show |
80 | HG00099.hp2 HG00280.hp1 HG00642.hp1 others(77): Show |
intron_variant | MODIFIER | c.5326+713A>C | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 38/38 | chr6 | 112113363 | |||||||
chr6:112113403 | G | C | 1 | a0001c0002t0001g0087 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.5326+673C>G | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 38/38 | chr6 | 112113403 | |||||||
chr6:112113598 | G | A | 1 | a0017c0046t0002g0233 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.5326+478C>T | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 38/38 | chr6 | 112113598 | |||||||
chr6:112113613 | A | G | 1 | a0001c0037t0003g0003 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.5326+463T>C | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 38/38 | chr6 | 112113613 | |||||||
chr6:112113737 | A | C | 1 | a0003c0013t0001g0011 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.5326+339T>G | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 38/38 | chr6 | 112113737 | |||||||
chr6:112113842 | G | A | 2 | a0001c0011t0003g0009 a0001c0011t0003g0293 |
2 | HG02055.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.5326+234C>T | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 38/38 | chr6 | 112113842 | |||||||
chr6:112113882 | A | G | 1 | a0001c0001t0001g0223 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.5326+194T>C | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 38/38 | chr6 | 112113882 | |||||||
chr6:112113976 | A | G | 1 | a0001c0001t0011g0229 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.5326+100T>C | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 38/38 | chr6 | 112113976 | |||||||
chr6:112114061 | T | G | 80 | a0001c0016t0002g0268 a0001c0020t0005g0046 a0001c0020t0005g0168 others(77): Show |
80 | HG00099.hp2 HG00280.hp1 HG00642.hp1 others(77): Show |
intron_variant | MODIFIER | c.5326+15A>C | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 38/38 | chr6 | 112114061 | |||||||
chr6:112114070 | A | C | 80 | a0001c0016t0002g0268 a0001c0020t0005g0046 a0001c0020t0005g0168 others(77): Show |
80 | HG00099.hp2 HG00280.hp1 HG00642.hp1 others(77): Show |
splice_region_variant&intron_variant | LOW | c.5326+6T>G | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 38/38 | chr6 | 112114070 | |||||||
chr6:112114209 | C | G | 1 | a0003c0018t0002g0038 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.5207-14G>C | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 37/38 | chr6 | 112114209 | |||||||
chr6:112114241 | G | GAAT | 80 | a0001c0016t0002g0268 a0001c0020t0005g0046 a0001c0020t0005g0168 others(77): Show |
80 | HG00099.hp2 HG00280.hp1 HG00642.hp1 others(77): Show |
intron_variant | MODIFIER | c.5207-49_5207-47dup others(3): Show |
LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 37/38 | chr6 | 112114241 | |||||||
chr6:112114329 | A | T | 1 | a0003c0018t0002g0038 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.5207-134T>A | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 37/38 | chr6 | 112114329 | |||||||
chr6:112114479 | G | A | 146 | a0001c0001t0001g0186 a0001c0005t0001g0103 a0001c0005t0001g0118 others(143): Show |
146 | HG00099.hp2 HG00280.hp1 HG00642.hp1 others(143): Show |
intron_variant | MODIFIER | c.5206+184C>T | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 37/38 | chr6 | 112114479 | |||||||
chr6:112114555 | T | C | 2 | a0001c0011t0003g0009 a0001c0011t0003g0293 |
2 | HG02055.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.5206+108A>G | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 37/38 | chr6 | 112114555 | |||||||
chr6:112114593 | G | C | 84 | a0001c0001t0001g0186 a0001c0016t0002g0268 a0001c0016t0010g0209 others(81): Show |
84 | HG00099.hp2 HG00280.hp1 HG00597.hp2 others(81): Show |
intron_variant | MODIFIER | c.5206+70C>G | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 37/38 | chr6 | 112114593 | |||||||
chr6:112114604 | G | T | 76 | a0001c0001t0001g0186 a0001c0016t0002g0268 a0001c0016t0010g0209 others(73): Show |
76 | HG00099.hp2 HG00280.hp1 HG00642.hp1 others(73): Show |
intron_variant | MODIFIER | c.5206+59C>A | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 37/38 | chr6 | 112114604 | |||||||
chr6:112114865 | CAT | C | 4 | a0009c0017t0002g0021 a0009c0017t0002g0307 a0009c0017t0002g0308 others(1): Show |
4 | HG02647.hp2 HG02895.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.5113-111_5113-110d others(4): Show |
LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 36/38 | chr6 | 112114865 | |||||||
chr6:112114893 | G | A | 5 | a0001c0002t0001g0076 a0001c0002t0001g0164 a0001c0002t0001g0165 others(2): Show |
5 | HG01081.hp2 HG03927.hp2 HG03942.hp1 others(2): Show |
intron_variant | MODIFIER | c.5113-137C>T | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 36/38 | chr6 | 112114893 | |||||||
chr6:112114922 | C | T | 15 | a0001c0011t0003g0009 a0001c0011t0003g0062 a0001c0011t0003g0155 others(12): Show |
15 | HG01891.hp1 HG02055.hp1 HG02109.hp2 others(12): Show |
intron_variant | MODIFIER | c.5113-166G>A | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 36/38 | chr6 | 112114922 | |||||||
chr6:112114995 | G | T | 134 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0014 others(131): Show |
134 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(131): Show |
intron_variant | MODIFIER | c.5113-239C>A | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 36/38 | chr6 | 112114995 | |||||||
chr6:112115311 | CTGTTA | C | 15 | a0001c0011t0003g0009 a0001c0011t0003g0062 a0001c0011t0003g0155 others(12): Show |
15 | HG01891.hp1 HG02055.hp1 HG02109.hp2 others(12): Show |
intron_variant | MODIFIER | c.5112+547_5112+551d others(7): Show |
LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 36/38 | chr6 | 112115311 | |||||||
chr6:112115402 | A | C | 1 | a0008c0031t0001g0056 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.5112+461T>G | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 36/38 | chr6 | 112115402 | |||||||
chr6:112115415 | C | T | 15 | a0001c0011t0003g0009 a0001c0011t0003g0062 a0001c0011t0003g0155 others(12): Show |
15 | HG01891.hp1 HG02055.hp1 HG02109.hp2 others(12): Show |
intron_variant | MODIFIER | c.5112+448G>A | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 36/38 | chr6 | 112115415 | |||||||
chr6:112115618 | G | A | 168 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0014 others(165): Show |
168 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(165): Show |
intron_variant | MODIFIER | c.5112+245C>T | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 36/38 | chr6 | 112115618 | |||||||
chr6:112115648 | G | C | 8 | a0001c0001t0001g0237 a0001c0002t0001g0107 a0001c0002t0001g0191 others(5): Show |
8 | HG00408.hp1 HG02071.hp2 HG02132.hp1 others(5): Show |
intron_variant | MODIFIER | c.5112+215C>G | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 36/38 | chr6 | 112115648 | |||||||
chr6:112115672 | T | C | 1 | a0001c0001t0001g0227 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.5112+191A>G | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 36/38 | chr6 | 112115672 | |||||||
chr6:112115741 | G | C | 1 | a0003c0018t0002g0038 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.5112+122C>G | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 36/38 | chr6 | 112115741 | |||||||
chr6:112116129 | C | T | 4 | a0009c0017t0002g0021 a0009c0017t0002g0307 a0009c0017t0002g0308 others(1): Show |
4 | HG02647.hp2 HG02895.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.4982-136G>A | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 35/38 | chr6 | 112116129 | |||||||
chr6:112116136 | A | G | 1 | a0003c0018t0002g0038 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.4982-143T>C | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 35/38 | chr6 | 112116136 | |||||||
chr6:112116268 | C | G | 3 | a0001c0020t0005g0046 a0001c0020t0005g0168 a0001c0020t0005g0169 |
3 | HG01891.hp2 HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.4982-275G>C | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 35/38 | chr6 | 112116268 | |||||||
chr6:112116320 | C | G | 1 | a0003c0018t0002g0038 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.4982-327G>C | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 35/38 | chr6 | 112116320 | |||||||
chr6:112116383 | G | C | 46 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0015 others(43): Show |
46 | HG00408.hp2 HG00597.hp1 HG00621.hp1 others(43): Show |
intron_variant | MODIFIER | c.4982-390C>G | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 35/38 | chr6 | 112116383 | |||||||
chr6:112116439 | C | G | 68 | a0001c0022t0002g0012 a0002c0003t0001g0171 a0002c0003t0002g0054 others(65): Show |
68 | HG00099.hp2 HG00280.hp1 HG00642.hp1 others(65): Show |
intron_variant | MODIFIER | c.4982-446G>C | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 35/38 | chr6 | 112116439 | |||||||
chr6:112116495 | C | T | 1 | a0003c0018t0002g0038 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.4982-502G>A | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 35/38 | chr6 | 112116495 | |||||||
chr6:112116520 | C | T | 16 | a0001c0011t0003g0009 a0001c0011t0003g0062 a0001c0011t0003g0155 others(13): Show |
16 | HG01891.hp1 HG02055.hp1 HG02109.hp2 others(13): Show |
intron_variant | MODIFIER | c.4982-527G>A | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 35/38 | chr6 | 112116520 | |||||||
chr6:112116572 | T | C | 244 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0014 others(241): Show |
244 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(241): Show |
intron_variant | MODIFIER | c.4982-579A>G | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 35/38 | chr6 | 112116572 | |||||||
chr6:112116902 | G | A | 4 | a0009c0017t0002g0021 a0009c0017t0002g0307 a0009c0017t0002g0308 others(1): Show |
4 | HG02647.hp2 HG02895.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.4981+837C>T | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 35/38 | chr6 | 112116902 | |||||||
chr6:112116989 | A | T | 17 | a0001c0011t0003g0009 a0001c0011t0003g0062 a0001c0011t0003g0155 others(14): Show |
17 | HG01891.hp1 HG02055.hp1 HG02109.hp2 others(14): Show |
intron_variant | MODIFIER | c.4981+750T>A | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 35/38 | chr6 | 112116989 | |||||||
chr6:112117093 | G | A | 3 | a0001c0052t0002g0295 a0011c0028t0002g0154 a0011c0028t0002g0159 |
3 | HG01243.hp1 HG02622.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.4981+646C>T | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 35/38 | chr6 | 112117093 | |||||||
chr6:112117126 | C | A | 17 | a0001c0011t0003g0009 a0001c0011t0003g0062 a0001c0011t0003g0155 others(14): Show |
17 | HG01243.hp1 HG01891.hp1 HG02055.hp1 others(14): Show |
intron_variant | MODIFIER | c.4981+613G>T | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 35/38 | chr6 | 112117126 | |||||||
chr6:112117243 | T | C | 265 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0014 others(262): Show |
265 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(262): Show |
intron_variant | MODIFIER | c.4981+496A>G | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 35/38 | chr6 | 112117243 | |||||||
chr6:112117599 | G | A | 1 | a0001c0001t0001g0219 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.4981+140C>T | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 35/38 | chr6 | 112117599 | |||||||
chr6:112117625 | T | C | 1 | a0001c0050t0001g0310 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.4981+114A>G | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 35/38 | chr6 | 112117625 | |||||||
chr6:112117701 | C | A | 1 | a0003c0013t0001g0011 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.4981+38G>T | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 35/38 | chr6 | 112117701 | |||||||
chr6:112117709 | GA | G | 89 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0015 others(86): Show |
89 | HG00323.hp1 HG00323.hp2 HG00408.hp2 others(86): Show |
intron_variant | MODIFIER | c.4981+29delT | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 35/38 | chr6 | 112117709 | |||||||
chr6:112117939 | A | T | 1 | a0009c0053t0002g0178 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.4822-41T>A | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 34/38 | chr6 | 112117939 | |||||||
chr6:112118046 | G | T | 1 | a0001c0050t0001g0310 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.4822-148C>A | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 34/38 | chr6 | 112118046 | |||||||
chr6:112118054 | C | G | 17 | a0001c0011t0003g0009 a0001c0011t0003g0062 a0001c0011t0003g0155 others(14): Show |
17 | HG01243.hp1 HG01891.hp1 HG02055.hp1 others(14): Show |
intron_variant | MODIFIER | c.4822-156G>C | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 34/38 | chr6 | 112118054 | |||||||
chr6:112118090 | T | C | 3 | a0001c0054t0001g0301 a0003c0025t0001g0086 a0003c0025t0001g0113 |
3 | HG02886.hp1 HG03130.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.4822-192A>G | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 34/38 | chr6 | 112118090 | |||||||
chr6:112118129 | T | C | 3 | a0001c0020t0005g0046 a0001c0020t0005g0168 a0001c0020t0005g0169 |
3 | HG01891.hp2 HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.4822-231A>G | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 34/38 | chr6 | 112118129 | |||||||
chr6:112118216 | A | C | 1 | a0003c0018t0002g0038 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.4822-318T>G | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 34/38 | chr6 | 112118216 | |||||||
chr6:112118302 | T | G | 1 | a0001c0037t0003g0003 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.4822-404A>C | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 34/38 | chr6 | 112118302 | |||||||
chr6:112118672 | G | T | 1 | a0002c0003t0002g0198 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.4821+484C>A | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 34/38 | chr6 | 112118672 | |||||||
chr6:112118721 | A | ATG | 160 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0014 others(157): Show |
160 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(157): Show |
intron_variant | MODIFIER | c.4821+433_4821+434d others(4): Show |
LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 34/38 | chr6 | 112118721 | |||||||
chr6:112118721 | A | ATGTG | 39 | a0001c0002t0001g0188 a0001c0005t0001g0103 a0001c0005t0001g0118 others(36): Show |
39 | HG01891.hp2 HG01934.hp1 HG01981.hp1 others(36): Show |
intron_variant | MODIFIER | c.4821+431_4821+434d others(6): Show |
LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 34/38 | chr6 | 112118721 | |||||||
chr6:112118721 | A | G | 1 | a0003c0018t0002g0038 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.4821+435T>C | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 34/38 | chr6 | 112118721 | |||||||
chr6:112118721 | ATG | A | 36 | a0001c0001t0001g0055 a0001c0011t0003g0009 a0001c0011t0003g0062 others(33): Show |
36 | HG00099.hp2 HG00280.hp1 HG01243.hp2 others(33): Show |
intron_variant | MODIFIER | c.4821+433_4821+434d others(4): Show |
LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 34/38 | chr6 | 112118721 | |||||||
chr6:112118723 | G | A | 1 | a0001c0054t0001g0301 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.4821+433C>T | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 34/38 | chr6 | 112118723 | |||||||
chr6:112118858 | T | C | 1 | a0003c0018t0002g0038 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.4821+298A>G | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 34/38 | chr6 | 112118858 | |||||||
chr6:112118904 | A | G | 1 | a0001c0037t0003g0003 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.4821+252T>C | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 34/38 | chr6 | 112118904 | |||||||
chr6:112118911 | T | C | 17 | a0001c0011t0003g0009 a0001c0011t0003g0062 a0001c0011t0003g0155 others(14): Show |
17 | HG01243.hp1 HG01891.hp1 HG02055.hp1 others(14): Show |
intron_variant | MODIFIER | c.4821+245A>G | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 34/38 | chr6 | 112118911 | |||||||
chr6:112118937 | G | C | 20 | a0001c0011t0003g0009 a0001c0011t0003g0062 a0001c0011t0003g0155 others(17): Show |
20 | HG01243.hp1 HG01891.hp1 HG02055.hp1 others(17): Show |
intron_variant | MODIFIER | c.4821+219C>G | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 34/38 | chr6 | 112118937 | |||||||
chr6:112118996 | G | T | 20 | a0001c0011t0003g0009 a0001c0011t0003g0062 a0001c0011t0003g0155 others(17): Show |
20 | HG01243.hp1 HG01891.hp1 HG02055.hp1 others(17): Show |
intron_variant | MODIFIER | c.4821+160C>A | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 34/38 | chr6 | 112118996 | |||||||
chr6:112119119 | A | C | 3 | a0001c0054t0001g0301 a0003c0025t0001g0086 a0003c0025t0001g0113 |
3 | HG02886.hp1 HG03130.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.4821+37T>G | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 34/38 | chr6 | 112119119 | |||||||
chr6:112119127 | A | G | 1 | a0007c0019t0001g0127 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.4821+29T>C | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 34/38 | chr6 | 112119127 | |||||||
chr6:112119438 | AAATGGCC others(9): Show |
A | 1 | a0001c0050t0001g0310 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.4666-143_4666-128d others(18): Show |
LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 33/38 | chr6 | 112119438 | |||||||
chr6:112119588 | C | T | 20 | a0001c0011t0003g0009 a0001c0011t0003g0062 a0001c0011t0003g0155 others(17): Show |
20 | HG01243.hp1 HG01891.hp1 HG02055.hp1 others(17): Show |
intron_variant | MODIFIER | c.4666-277G>A | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 33/38 | chr6 | 112119588 | |||||||
chr6:112119727 | T | C | 2 | a0001c0002t0001g0192 a0001c0002t0001g0253 |
2 | HG02922.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.4666-416A>G | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 33/38 | chr6 | 112119727 | |||||||
chr6:112119768 | C | A | 1 | a0004c0057t0003g0017 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.4666-457G>T | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 33/38 | chr6 | 112119768 | |||||||
chr6:112119779 | C | G | 3 | a0001c0054t0001g0301 a0003c0025t0001g0086 a0003c0025t0001g0113 |
3 | HG02886.hp1 HG03130.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.4666-468G>C | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 33/38 | chr6 | 112119779 | |||||||
chr6:112119805 | G | C | 20 | a0001c0011t0003g0009 a0001c0011t0003g0062 a0001c0011t0003g0155 others(17): Show |
20 | HG01243.hp1 HG01891.hp1 HG02055.hp1 others(17): Show |
intron_variant | MODIFIER | c.4665+478C>G | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 33/38 | chr6 | 112119805 | |||||||
chr6:112119931 | C | A | 265 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0014 others(262): Show |
265 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(262): Show |
intron_variant | MODIFIER | c.4665+352G>T | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 33/38 | chr6 | 112119931 | |||||||
chr6:112119970 | A | G | 20 | a0001c0011t0003g0009 a0001c0011t0003g0062 a0001c0011t0003g0155 others(17): Show |
20 | HG01243.hp1 HG01891.hp1 HG02055.hp1 others(17): Show |
intron_variant | MODIFIER | c.4665+313T>C | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 33/38 | chr6 | 112119970 | |||||||
chr6:112120096 | G | A | 2 | a0001c0011t0003g0009 a0001c0011t0003g0236 |
2 | HG02055.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.4665+187C>T | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 33/38 | chr6 | 112120096 | |||||||
chr6:112120132 | T | G | 1 | a0003c0018t0002g0038 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.4665+151A>C | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 33/38 | chr6 | 112120132 | |||||||
chr6:112120149 | T | A | 1 | a0003c0004t0001g0022 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.4665+134A>T | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 33/38 | chr6 | 112120149 | |||||||
chr6:112120275 | C | A | 1 | a0001c0011t0003g0009 | 1 | HG02055.hp1 | splice_region_variant&intron_variant | LOW | c.4665+8G>T | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 33/38 | chr6 | 112120275 | |||||||
chr6:112120546 | A | G | 1 | a0007c0014t0002g0292 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.4476-74T>C | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 32/38 | chr6 | 112120546 | |||||||
chr6:112120551 | GT | G | 17 | a0001c0011t0003g0009 a0001c0011t0003g0062 a0001c0011t0003g0155 others(14): Show |
17 | HG01243.hp1 HG01891.hp1 HG02055.hp1 others(14): Show |
intron_variant | MODIFIER | c.4476-80delA | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 32/38 | chr6 | 112120551 | |||||||
chr6:112120590 | A | G | 1 | a0005c0008t0001g0032 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.4476-118T>C | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 32/38 | chr6 | 112120590 | |||||||
chr6:112120625 | A | G | 20 | a0001c0011t0003g0009 a0001c0011t0003g0062 a0001c0011t0003g0155 others(17): Show |
20 | HG01243.hp1 HG01891.hp1 HG02055.hp1 others(17): Show |
intron_variant | MODIFIER | c.4476-153T>C | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 32/38 | chr6 | 112120625 | |||||||
chr6:112120944 | C | T | 89 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0015 others(86): Show |
89 | HG00323.hp1 HG00323.hp2 HG00408.hp2 others(86): Show |
intron_variant | MODIFIER | c.4476-472G>A | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 32/38 | chr6 | 112120944 | |||||||
chr6:112120945 | G | A | 20 | a0001c0011t0003g0009 a0001c0011t0003g0062 a0001c0011t0003g0155 others(17): Show |
20 | HG01243.hp1 HG01891.hp1 HG02055.hp1 others(17): Show |
intron_variant | MODIFIER | c.4476-473C>T | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 32/38 | chr6 | 112120945 | |||||||
chr6:112121057 | G | A | 2 | a0001c0001t0001g0115 a0001c0001t0001g0220 |
2 | HG01258.hp2 HG01496.hp2 |
intron_variant | MODIFIER | c.4476-585C>T | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 32/38 | chr6 | 112121057 | |||||||
chr6:112121077 | C | CA | 6 | a0002c0003t0002g0077 a0002c0003t0002g0079 a0002c0003t0002g0290 others(3): Show |
6 | HG00099.hp2 HG00280.hp1 HG01934.hp2 others(3): Show |
intron_variant | MODIFIER | c.4476-606dupT | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 32/38 | chr6 | 112121077 | |||||||
chr6:112121139 | C | G | 1 | a0003c0004t0001g0125 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.4476-667G>C | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 32/38 | chr6 | 112121139 | |||||||
chr6:112121177 | C | T | 1 | a0001c0050t0001g0310 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.4476-705G>A | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 32/38 | chr6 | 112121177 | |||||||
chr6:112121185 | A | G | 13 | a0004c0007t0001g0266 a0004c0007t0001g0267 a0004c0007t0001g0269 others(10): Show |
13 | HG02074.hp2 HG02129.hp1 HG02523.hp2 others(10): Show |
intron_variant | MODIFIER | c.4476-713T>C | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 32/38 | chr6 | 112121185 | |||||||
chr6:112121233 | C | T | 20 | a0001c0011t0003g0009 a0001c0011t0003g0062 a0001c0011t0003g0155 others(17): Show |
20 | HG01243.hp1 HG01891.hp1 HG02055.hp1 others(17): Show |
intron_variant | MODIFIER | c.4476-761G>A | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 32/38 | chr6 | 112121233 | |||||||
chr6:112121258 | C | T | 20 | a0001c0011t0003g0009 a0001c0011t0003g0062 a0001c0011t0003g0155 others(17): Show |
20 | HG01243.hp1 HG01891.hp1 HG02055.hp1 others(17): Show |
intron_variant | MODIFIER | c.4475+756G>A | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 32/38 | chr6 | 112121258 | |||||||
chr6:112121259 | G | A | 1 | a0003c0018t0002g0038 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.4475+755C>T | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 32/38 | chr6 | 112121259 | |||||||
chr6:112121289 | T | A | 1 | a0003c0004t0001g0180 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.4475+725A>T | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 32/38 | chr6 | 112121289 | |||||||
chr6:112121393 | G | A | 1 | a0005c0044t0001g0261 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.4475+621C>T | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 32/38 | chr6 | 112121393 | |||||||
chr6:112121442 | C | T | 1 | a0003c0013t0001g0011 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.4475+572G>A | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 32/38 | chr6 | 112121442 | |||||||
chr6:112121466 | T | C | 1 | a0003c0018t0002g0038 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.4475+548A>G | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 32/38 | chr6 | 112121466 | |||||||
chr6:112121551 | T | C | 1 | a0002c0003t0002g0198 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.4475+463A>G | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 32/38 | chr6 | 112121551 | |||||||
chr6:112121564 | C | T | 20 | a0001c0011t0003g0009 a0001c0011t0003g0062 a0001c0011t0003g0155 others(17): Show |
20 | HG01243.hp1 HG01891.hp1 HG02055.hp1 others(17): Show |
intron_variant | MODIFIER | c.4475+450G>A | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 32/38 | chr6 | 112121564 | |||||||
chr6:112121584 | G | A | 3 | a0001c0052t0002g0295 a0011c0028t0002g0154 a0011c0028t0002g0159 |
3 | HG01243.hp1 HG02622.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.4475+430C>T | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 32/38 | chr6 | 112121584 | |||||||
chr6:112121622 | T | C | 3 | a0001c0054t0001g0301 a0003c0025t0001g0086 a0003c0025t0001g0113 |
3 | HG02886.hp1 HG03130.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.4475+392A>G | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 32/38 | chr6 | 112121622 | |||||||
chr6:112121635 | T | C | 1 | a0001c0001t0001g0008 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.4475+379A>G | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 32/38 | chr6 | 112121635 | |||||||
chr6:112121679 | G | T | 20 | a0001c0011t0003g0009 a0001c0011t0003g0062 a0001c0011t0003g0155 others(17): Show |
20 | HG01243.hp1 HG01891.hp1 HG02055.hp1 others(17): Show |
intron_variant | MODIFIER | c.4475+335C>A | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 32/38 | chr6 | 112121679 | |||||||
chr6:112121800 | T | A | 1 | a0003c0004t0001g0180 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.4475+214A>T | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 32/38 | chr6 | 112121800 | |||||||
chr6:112121889 | G | A | 20 | a0001c0011t0003g0009 a0001c0011t0003g0062 a0001c0011t0003g0155 others(17): Show |
20 | HG01243.hp1 HG01891.hp1 HG02055.hp1 others(17): Show |
intron_variant | MODIFIER | c.4475+125C>T | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 32/38 | chr6 | 112121889 | |||||||
chr6:112121931 | G | A | 269 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0014 others(266): Show |
269 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(266): Show |
intron_variant | MODIFIER | c.4475+83C>T | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 32/38 | chr6 | 112121931 | |||||||
chr6:112121940 | C | A | 3 | a0001c0054t0001g0301 a0003c0025t0001g0086 a0003c0025t0001g0113 |
3 | HG02886.hp1 HG03130.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.4475+74G>T | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 32/38 | chr6 | 112121940 | |||||||
chr6:112121953 | C | G | 1 | a0003c0018t0002g0038 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.4475+61G>C | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 32/38 | chr6 | 112121953 | |||||||
chr6:112122513 | C | A | 20 | a0001c0011t0003g0009 a0001c0011t0003g0062 a0001c0011t0003g0155 others(17): Show |
20 | HG01243.hp1 HG01891.hp1 HG02055.hp1 others(17): Show |
intron_variant | MODIFIER | c.4288-312G>T | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 31/38 | chr6 | 112122513 | |||||||
chr6:112122569 | C | T | 20 | a0001c0011t0003g0009 a0001c0011t0003g0062 a0001c0011t0003g0155 others(17): Show |
20 | HG01243.hp1 HG01891.hp1 HG02055.hp1 others(17): Show |
intron_variant | MODIFIER | c.4288-368G>A | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 31/38 | chr6 | 112122569 | |||||||
chr6:112122670 | G | A | 20 | a0001c0011t0003g0009 a0001c0011t0003g0062 a0001c0011t0003g0155 others(17): Show |
20 | HG01243.hp1 HG01891.hp1 HG02055.hp1 others(17): Show |
intron_variant | MODIFIER | c.4288-469C>T | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 31/38 | chr6 | 112122670 | |||||||
chr6:112122821 | A | G | 1 | a0007c0014t0002g0292 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.4288-620T>C | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 31/38 | chr6 | 112122821 | |||||||
chr6:112122824 | T | A | 1 | a0004c0057t0003g0017 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.4288-623A>T | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 31/38 | chr6 | 112122824 | |||||||
chr6:112122847 | G | A | 20 | a0001c0011t0003g0009 a0001c0011t0003g0062 a0001c0011t0003g0155 others(17): Show |
20 | HG01243.hp1 HG01891.hp1 HG02055.hp1 others(17): Show |
intron_variant | MODIFIER | c.4288-646C>T | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 31/38 | chr6 | 112122847 | |||||||
chr6:112122954 | G | C | 8 | a0001c0001t0001g0050 a0001c0001t0001g0051 a0001c0001t0001g0052 others(5): Show |
8 | HG00639.hp2 HG00741.hp2 HG01074.hp2 others(5): Show |
intron_variant | MODIFIER | c.4288-753C>G | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 31/38 | chr6 | 112122954 | |||||||
chr6:112123065 | T | C | 1 | a0005c0008t0004g0297 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.4288-864A>G | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 31/38 | chr6 | 112123065 | |||||||
chr6:112123136 | C | T | 17 | a0001c0011t0003g0009 a0001c0011t0003g0062 a0001c0011t0003g0155 others(14): Show |
17 | HG01243.hp1 HG01891.hp1 HG02055.hp1 others(14): Show |
intron_variant | MODIFIER | c.4288-935G>A | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 31/38 | chr6 | 112123136 | |||||||
chr6:112123177 | C | T | 1 | a0001c0011t0003g0009 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.4288-976G>A | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 31/38 | chr6 | 112123177 | |||||||
chr6:112123222 | T | A | 1 | a0001c0005t0001g0139 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.4288-1021A>T | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 31/38 | chr6 | 112123222 | |||||||
chr6:112123402 | A | G | 1 | a0003c0018t0002g0038 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.4288-1201T>C | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 31/38 | chr6 | 112123402 | |||||||
chr6:112123541 | G | A | 1 | a0001c0037t0003g0003 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.4288-1340C>T | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 31/38 | chr6 | 112123541 | |||||||
chr6:112123549 | GACAAAAT others(7): Show |
G | 1 | a0001c0002t0001g0165 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.4288-1362_4288-134 others(18): Show |
LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 31/38 | chr6 | 112123549 | |||||||
chr6:112123588 | A | T | 3 | a0001c0052t0002g0295 a0011c0028t0002g0154 a0011c0028t0002g0159 |
3 | HG01243.hp1 HG02622.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.4288-1387T>A | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 31/38 | chr6 | 112123588 | |||||||
chr6:112123903 | C | T | 68 | a0001c0022t0002g0012 a0002c0003t0001g0171 a0002c0003t0002g0054 others(65): Show |
68 | HG00099.hp2 HG00280.hp1 HG00642.hp1 others(65): Show |
intron_variant | MODIFIER | c.4288-1702G>A | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 31/38 | chr6 | 112123903 | |||||||
chr6:112124055 | C | A | 68 | a0001c0022t0002g0012 a0002c0003t0001g0171 a0002c0003t0002g0054 others(65): Show |
68 | HG00099.hp2 HG00280.hp1 HG00642.hp1 others(65): Show |
intron_variant | MODIFIER | c.4288-1854G>T | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 31/38 | chr6 | 112124055 | |||||||
chr6:112124411 | G | A | 13 | a0001c0011t0003g0009 a0001c0011t0003g0062 a0001c0011t0003g0155 others(10): Show |
13 | HG01891.hp1 HG02055.hp1 HG02109.hp2 others(10): Show |
intron_variant | MODIFIER | c.4288-2210C>T | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 31/38 | chr6 | 112124411 | |||||||
chr6:112124423 | A | C | 1 | a0003c0061t0001g0299 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.4288-2222T>G | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 31/38 | chr6 | 112124423 | |||||||
chr6:112124584 | C | T | 1 | a0001c0037t0003g0003 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.4288-2383G>A | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 31/38 | chr6 | 112124584 | |||||||
chr6:112124759 | C | CT | 69 | a0001c0001t0001g0014 a0001c0022t0002g0012 a0002c0003t0001g0171 others(66): Show |
69 | HG00099.hp2 HG00280.hp1 HG00642.hp1 others(66): Show |
intron_variant | MODIFIER | c.4288-2559dupA | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 31/38 | chr6 | 112124759 | |||||||
chr6:112124759 | CTT | C | 17 | a0001c0011t0003g0009 a0001c0011t0003g0062 a0001c0011t0003g0155 others(14): Show |
17 | HG01243.hp1 HG01891.hp1 HG02055.hp1 others(14): Show |
intron_variant | MODIFIER | c.4288-2560_4288-255 others(6): Show |
LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 31/38 | chr6 | 112124759 | |||||||
chr6:112124780 | C | T | 1 | a0005c0008t0001g0231 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.4288-2579G>A | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 31/38 | chr6 | 112124780 | |||||||
chr6:112124791 | T | G | 1 | a0001c0001t0001g0285 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.4288-2590A>C | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 31/38 | chr6 | 112124791 | |||||||
chr6:112124859 | C | T | 3 | a0001c0054t0001g0301 a0003c0025t0001g0086 a0003c0025t0001g0113 |
3 | HG02886.hp1 HG03130.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.4288-2658G>A | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 31/38 | chr6 | 112124859 | |||||||
chr6:112124913 | T | G | 24 | a0001c0001t0001g0033 a0001c0001t0001g0050 a0001c0001t0001g0051 others(21): Show |
24 | HG00639.hp2 HG00733.hp1 HG00741.hp2 others(21): Show |
intron_variant | MODIFIER | c.4288-2712A>C | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 31/38 | chr6 | 112124913 | |||||||
chr6:112124936 | T | C | 5 | a0002c0006t0002g0104 a0002c0006t0002g0173 a0002c0006t0002g0190 others(2): Show |
5 | HG02015.hp2 HG03471.hp2 NA18943.hp2 others(2): Show |
intron_variant | MODIFIER | c.4288-2735A>G | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 31/38 | chr6 | 112124936 | |||||||
chr6:112125007 | G | A | 1 | a0001c0022t0002g0012 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.4288-2806C>T | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 31/38 | chr6 | 112125007 | |||||||
chr6:112125232 | CT | C | 11 | a0001c0011t0003g0062 a0001c0011t0003g0155 a0001c0011t0003g0158 others(8): Show |
11 | HG01891.hp1 HG02109.hp2 HG02257.hp1 others(8): Show |
intron_variant | MODIFIER | c.4288-3032delA | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 31/38 | chr6 | 112125232 | |||||||
chr6:112125352 | G | C | 308 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0014 others(305): Show |
308 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(305): Show |
intron_variant | MODIFIER | c.4288-3151C>G | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 31/38 | chr6 | 112125352 | |||||||
chr6:112125364 | C | T | 13 | a0001c0011t0003g0009 a0001c0011t0003g0062 a0001c0011t0003g0155 others(10): Show |
13 | HG01891.hp1 HG02055.hp1 HG02109.hp2 others(10): Show |
intron_variant | MODIFIER | c.4288-3163G>A | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 31/38 | chr6 | 112125364 | |||||||
chr6:112125674 | C | T | 167 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0014 others(164): Show |
167 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(164): Show |
intron_variant | MODIFIER | c.4287+3248G>A | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 31/38 | chr6 | 112125674 | |||||||
chr6:112125804 | G | T | 1 | a0003c0013t0001g0216 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.4287+3118C>A | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 31/38 | chr6 | 112125804 | |||||||
chr6:112126215 | T | C | 3 | a0001c0054t0001g0301 a0003c0025t0001g0086 a0003c0025t0001g0113 |
3 | HG02886.hp1 HG03130.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.4287+2707A>G | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 31/38 | chr6 | 112126215 | |||||||
chr6:112126254 | C | T | 3 | a0001c0052t0002g0295 a0011c0028t0002g0154 a0011c0028t0002g0159 |
3 | HG01243.hp1 HG02622.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.4287+2668G>A | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 31/38 | chr6 | 112126254 | |||||||
chr6:112126395 | A | G | 1 | a0004c0057t0003g0017 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.4287+2527T>C | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 31/38 | chr6 | 112126395 | |||||||
chr6:112126396 | C | T | 3 | a0001c0054t0001g0301 a0003c0025t0001g0086 a0003c0025t0001g0113 |
3 | HG02886.hp1 HG03130.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.4287+2526G>A | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 31/38 | chr6 | 112126396 | |||||||
chr6:112126464 | C | T | 1 | a0012c0021t0001g0144 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.4287+2458G>A | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 31/38 | chr6 | 112126464 | |||||||
chr6:112126799 | T | G | 1 | a0001c0054t0001g0301 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.4287+2123A>C | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 31/38 | chr6 | 112126799 | |||||||
chr6:112126851 | T | C | 4 | a0009c0017t0002g0021 a0009c0017t0002g0307 a0009c0017t0002g0308 others(1): Show |
4 | HG02647.hp2 HG02895.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.4287+2071A>G | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 31/38 | chr6 | 112126851 | |||||||
chr6:112126995 | T | C | 6 | a0001c0001t0001g0015 a0001c0001t0001g0072 a0001c0001t0001g0186 others(3): Show |
6 | HG00621.hp1 NA18940.hp2 NA18961.hp1 others(3): Show |
intron_variant | MODIFIER | c.4287+1927A>G | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 31/38 | chr6 | 112126995 | |||||||
chr6:112127053 | A | G | 1 | a0002c0006t0002g0037 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.4287+1869T>C | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 31/38 | chr6 | 112127053 | |||||||
chr6:112127086 | C | G | 1 | a0008c0015t0001g0061 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.4287+1836G>C | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 31/38 | chr6 | 112127086 | |||||||
chr6:112127118 | T | C | 1 | a0001c0034t0001g0132 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.4287+1804A>G | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 31/38 | chr6 | 112127118 | |||||||
chr6:112127280 | A | G | 3 | a0001c0054t0001g0301 a0003c0025t0001g0086 a0003c0025t0001g0113 |
3 | HG02886.hp1 HG03130.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.4287+1642T>C | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 31/38 | chr6 | 112127280 | |||||||
chr6:112127452 | A | G | 71 | a0001c0020t0005g0046 a0001c0020t0005g0168 a0001c0020t0005g0169 others(68): Show |
71 | HG00099.hp2 HG00280.hp1 HG00642.hp1 others(68): Show |
intron_variant | MODIFIER | c.4287+1470T>C | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 31/38 | chr6 | 112127452 | |||||||
chr6:112127518 | A | G | 1 | a0001c0050t0001g0310 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.4287+1404T>C | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 31/38 | chr6 | 112127518 | |||||||
chr6:112127556 | G | C | 1 | a0001c0009t0001g0049 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.4287+1366C>G | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 31/38 | chr6 | 112127556 | |||||||
chr6:112127631 | C | A | 1 | a0001c0001t0001g0051 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.4287+1291G>T | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 31/38 | chr6 | 112127631 | |||||||
chr6:112127634 | T | C | 4 | a0009c0017t0002g0021 a0009c0017t0002g0307 a0009c0017t0002g0308 others(1): Show |
4 | HG02647.hp2 HG02895.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.4287+1288A>G | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 31/38 | chr6 | 112127634 | |||||||
chr6:112127665 | T | C | 1 | a0001c0037t0003g0003 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.4287+1257A>G | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 31/38 | chr6 | 112127665 | |||||||
chr6:112127688 | G | A | 13 | a0001c0011t0003g0009 a0001c0011t0003g0062 a0001c0011t0003g0155 others(10): Show |
13 | HG01891.hp1 HG02055.hp1 HG02109.hp2 others(10): Show |
intron_variant | MODIFIER | c.4287+1234C>T | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 31/38 | chr6 | 112127688 | |||||||
chr6:112127808 | C | T | 3 | a0001c0054t0001g0301 a0003c0025t0001g0086 a0003c0025t0001g0113 |
3 | HG02886.hp1 HG03130.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.4287+1114G>A | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 31/38 | chr6 | 112127808 | |||||||
chr6:112128111 | T | C | 1 | a0001c0001t0001g0219 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.4287+811A>G | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 31/38 | chr6 | 112128111 | |||||||
chr6:112128279 | T | C | 1 | a0001c0050t0001g0310 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.4287+643A>G | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 31/38 | chr6 | 112128279 | |||||||
chr6:112128632 | C | G | 1 | a0001c0050t0001g0310 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.4287+290G>C | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 31/38 | chr6 | 112128632 | |||||||
chr6:112128658 | A | G | 1 | a0001c0051t0003g0314 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.4287+264T>C | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 31/38 | chr6 | 112128658 | |||||||
chr6:112128711 | C | T | 21 | a0001c0011t0003g0009 a0001c0011t0003g0062 a0001c0011t0003g0155 others(18): Show |
21 | HG01243.hp1 HG01891.hp1 HG02055.hp1 others(18): Show |
intron_variant | MODIFIER | c.4287+211G>A | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 31/38 | chr6 | 112128711 | |||||||
chr6:112128721 | A | G | 1 | a0001c0002t0001g0096 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.4287+201T>C | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 31/38 | chr6 | 112128721 | |||||||
chr6:112128819 | G | A | 1 | a0001c0011t0003g0009 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.4287+103C>T | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 31/38 | chr6 | 112128819 | |||||||
chr6:112128863 | A | G | 1 | a0001c0050t0001g0310 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.4287+59T>C | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 31/38 | chr6 | 112128863 | |||||||
chr6:112128907 | G | A | 3 | a0001c0054t0001g0301 a0003c0025t0001g0086 a0003c0025t0001g0113 |
3 | HG02886.hp1 HG03130.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.4287+15C>T | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 31/38 | chr6 | 112128907 | |||||||
chr6:112129128 | C | T | 1 | a0001c0052t0002g0295 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.4134-53G>A | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 30/38 | chr6 | 112129128 | |||||||
chr6:112129149 | G | C | 265 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0014 others(262): Show |
265 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(262): Show |
intron_variant | MODIFIER | c.4134-74C>G | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 30/38 | chr6 | 112129149 | |||||||
chr6:112129172 | GTGTGTGT others(9): Show |
G | 70 | a0001c0020t0005g0046 a0001c0020t0005g0168 a0001c0020t0005g0169 others(67): Show |
70 | HG00099.hp2 HG00280.hp1 HG00642.hp1 others(67): Show |
intron_variant | MODIFIER | c.4134-113_4134-98de others(17): Show |
LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 30/38 | chr6 | 112129172 | |||||||
chr6:112129174 | GTGTGTGT others(7): Show |
G | 1 | a0015c0049t0002g0200 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.4134-113_4134-100d others(16): Show |
LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 30/38 | chr6 | 112129174 | |||||||
chr6:112129318 | T | C | 167 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0014 others(164): Show |
167 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(164): Show |
intron_variant | MODIFIER | c.4134-243A>G | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 30/38 | chr6 | 112129318 | |||||||
chr6:112129472 | G | C | 265 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0014 others(262): Show |
265 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(262): Show |
intron_variant | MODIFIER | c.4134-397C>G | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 30/38 | chr6 | 112129472 | |||||||
chr6:112129529 | G | C | 1 | a0003c0025t0001g0113 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.4133+347C>G | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 30/38 | chr6 | 112129529 | |||||||
chr6:112129607 | C | T | 1 | a0001c0054t0001g0301 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.4133+269G>A | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 30/38 | chr6 | 112129607 | |||||||
chr6:112129682 | G | C | 1 | a0002c0006t0002g0199 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.4133+194C>G | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 30/38 | chr6 | 112129682 | |||||||
chr6:112129730 | G | A | 1 | a0004c0010t0001g0152 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.4133+146C>T | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 30/38 | chr6 | 112129730 | |||||||
chr6:112129843 | C | A | 1 | a0011c0028t0002g0159 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.4133+33G>T | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 30/38 | chr6 | 112129843 | |||||||
chr6:112130165 | G | T | 3 | a0003c0004t0008g0273 a0010c0029t0001g0025 a0010c0029t0001g0034 |
3 | HG01081.hp1 HG02738.hp1 HG03669.hp2 |
intron_variant | MODIFIER | c.3969-125C>A | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 29/38 | chr6 | 112130165 | |||||||
chr6:112130183 | T | C | 1 | a0008c0031t0001g0056 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.3969-143A>G | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 29/38 | chr6 | 112130183 | |||||||
chr6:112130298 | T | TTGTG | 3 | a0001c0011t0003g0255 a0001c0011t0003g0293 a0004c0057t0003g0017 |
3 | HG02109.hp2 HG02615.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.3969-259_3969-258i others(6): Show |
LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 29/38 | chr6 | 112130298 | |||||||
chr6:112130298 | T | TTGTGTG | 8 | a0001c0011t0003g0062 a0001c0011t0003g0155 a0001c0011t0003g0158 others(5): Show |
8 | HG01891.hp1 HG02257.hp1 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.3969-259_3969-258i others(8): Show |
LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 29/38 | chr6 | 112130298 | |||||||
chr6:112130298 | T | TTGTGTGT others(3): Show |
1 | a0001c0011t0003g0009 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.3969-259_3969-258i others(12): Show |
LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 29/38 | chr6 | 112130298 | |||||||
chr6:112130298 | T | TTGTGTGT others(7): Show |
1 | a0011c0028t0002g0159 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.3969-259_3969-258i others(16): Show |
LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 29/38 | chr6 | 112130298 | |||||||
chr6:112130298 | T | TTGTGTGT others(13): Show |
1 | a0011c0028t0002g0154 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.3969-259_3969-258i others(22): Show |
LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 29/38 | chr6 | 112130298 | |||||||
chr6:112130298 | T | TTGTGTGT others(17): Show |
1 | a0001c0052t0002g0295 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.3969-259_3969-258i others(26): Show |
LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 29/38 | chr6 | 112130298 | |||||||
chr6:112130300 | T | G | 20 | a0001c0001t0001g0027 a0001c0011t0003g0009 a0001c0011t0003g0062 others(17): Show |
20 | HG01243.hp1 HG01891.hp1 HG02055.hp1 others(17): Show |
intron_variant | MODIFIER | c.3969-260A>C | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 29/38 | chr6 | 112130300 | |||||||
chr6:112130300 | T | TTG | 15 | a0001c0001t0001g0050 a0001c0002t0001g0279 a0001c0009t0001g0094 others(12): Show |
15 | HG00408.hp2 HG00733.hp1 HG01358.hp2 others(12): Show |
intron_variant | MODIFIER | c.3969-262_3969-261d others(4): Show |
LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 29/38 | chr6 | 112130300 | |||||||
chr6:112130300 | T | TTGTG | 54 | a0001c0001t0001g0042 a0001c0022t0002g0012 a0002c0003t0001g0171 others(51): Show |
54 | HG00099.hp2 HG00280.hp1 HG00673.hp1 others(51): Show |
intron_variant | MODIFIER | c.3969-264_3969-261d others(6): Show |
LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 29/38 | chr6 | 112130300 | |||||||
chr6:112130300 | T | TTGTGTG | 7 | a0002c0006t0002g0108 a0002c0006t0002g0190 a0002c0006t0002g0193 others(4): Show |
7 | HG01175.hp1 HG01934.hp2 HG02015.hp2 others(4): Show |
intron_variant | MODIFIER | c.3969-266_3969-261d others(8): Show |
LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 29/38 | chr6 | 112130300 | |||||||
chr6:112130300 | T | TTGTGTGT others(1): Show |
4 | a0001c0050t0001g0310 a0002c0003t0002g0290 a0003c0018t0002g0038 others(1): Show |
4 | HG02257.hp2 HG02738.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.3969-268_3969-261d others(10): Show |
LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 29/38 | chr6 | 112130300 | |||||||
chr6:112130300 | T | TTGTGTGT others(5): Show |
1 | a0001c0054t0001g0301 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.3969-272_3969-261d others(14): Show |
LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 29/38 | chr6 | 112130300 | |||||||
chr6:112130300 | TTG | T | 8 | a0004c0007t0001g0157 a0004c0007t0001g0160 a0004c0007t0001g0162 others(5): Show |
8 | HG00621.hp2 HG02109.hp1 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.3969-262_3969-261d others(4): Show |
LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 29/38 | chr6 | 112130300 | |||||||
chr6:112130300 | TTGTGTG | T | 3 | a0001c0020t0005g0046 a0001c0020t0005g0168 a0001c0020t0005g0169 |
3 | HG01891.hp2 HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.3969-266_3969-261d others(8): Show |
LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 29/38 | chr6 | 112130300 | |||||||
chr6:112130300 | TTGTGTGT others(3): Show |
T | 4 | a0009c0017t0002g0021 a0009c0017t0002g0307 a0009c0017t0002g0308 others(1): Show |
4 | HG02647.hp2 HG02895.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.3969-270_3969-261d others(12): Show |
LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 29/38 | chr6 | 112130300 | |||||||
chr6:112130302 | G | T | 1 | a0003c0004t0001g0226 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.3969-262C>A | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 29/38 | chr6 | 112130302 | |||||||
chr6:112130352 | A | T | 3 | a0001c0054t0001g0301 a0003c0025t0001g0086 a0003c0025t0001g0113 |
3 | HG02886.hp1 HG03130.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.3969-312T>A | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 29/38 | chr6 | 112130352 | |||||||
chr6:112130399 | G | A | 1 | a0002c0003t0002g0102 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.3969-359C>T | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 29/38 | chr6 | 112130399 | |||||||
chr6:112130576 | C | T | 167 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0014 others(164): Show |
167 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(164): Show |
intron_variant | MODIFIER | c.3968+392G>A | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 29/38 | chr6 | 112130576 | |||||||
chr6:112130729 | C | A | 3 | a0001c0020t0005g0046 a0001c0020t0005g0168 a0001c0020t0005g0169 |
3 | HG01891.hp2 HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.3968+239G>T | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 29/38 | chr6 | 112130729 | |||||||
chr6:112130779 | T | C | 3 | a0001c0020t0005g0046 a0001c0020t0005g0168 a0001c0020t0005g0169 |
3 | HG01891.hp2 HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.3968+189A>G | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 29/38 | chr6 | 112130779 | |||||||
chr6:112131359 | G | A | 4 | a0001c0050t0001g0310 a0001c0054t0001g0301 a0003c0025t0001g0086 others(1): Show |
4 | HG02886.hp1 HG03130.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.3835-258C>T | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 28/38 | chr6 | 112131359 | |||||||
chr6:112131396 | C | G | 1 | a0003c0018t0002g0038 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.3835-295G>C | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 28/38 | chr6 | 112131396 | |||||||
chr6:112131569 | G | A | 2 | a0003c0025t0001g0086 a0003c0025t0001g0113 |
2 | HG02886.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.3835-468C>T | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 28/38 | chr6 | 112131569 | |||||||
chr6:112131588 | A | G | 4 | a0001c0050t0001g0310 a0001c0054t0001g0301 a0003c0025t0001g0086 others(1): Show |
4 | HG02886.hp1 HG03130.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.3835-487T>C | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 28/38 | chr6 | 112131588 | |||||||
chr6:112131600 | G | A | 3 | a0001c0052t0002g0295 a0011c0028t0002g0154 a0011c0028t0002g0159 |
3 | HG01243.hp1 HG02622.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.3835-499C>T | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 28/38 | chr6 | 112131600 | |||||||
chr6:112131600 | G | T | 4 | a0001c0050t0001g0310 a0001c0054t0001g0301 a0003c0025t0001g0086 others(1): Show |
4 | HG02886.hp1 HG03130.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.3835-499C>A | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 28/38 | chr6 | 112131600 | |||||||
chr6:112131605 | A | G | 1 | a0002c0003t0002g0131 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.3835-504T>C | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 28/38 | chr6 | 112131605 | |||||||
chr6:112131660 | A | G | 3 | a0001c0020t0005g0046 a0001c0020t0005g0168 a0001c0020t0005g0169 |
3 | HG01891.hp2 HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.3835-559T>C | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 28/38 | chr6 | 112131660 | |||||||
chr6:112131717 | GTTTGGGT others(19): Show |
G | 4 | a0004c0007t0001g0266 a0004c0007t0001g0267 a0004c0007t0014g0300 others(1): Show |
4 | NA18947.hp1 NA18971.hp1 NA18977.hp2 others(1): Show |
intron_variant | MODIFIER | c.3835-642_3835-617d others(28): Show |
LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 28/38 | chr6 | 112131717 | |||||||
chr6:112131913 | C | A | 1 | a0004c0007t0001g0266 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.3835-812G>T | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 28/38 | chr6 | 112131913 | |||||||
chr6:112131921 | C | T | 171 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0014 others(168): Show |
171 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(168): Show |
intron_variant | MODIFIER | c.3835-820G>A | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 28/38 | chr6 | 112131921 | |||||||
chr6:112131961 | G | A | 1 | a0002c0003t0006g0001 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.3834+792C>T | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 28/38 | chr6 | 112131961 | |||||||
chr6:112131980 | T | C | 3 | a0001c0054t0001g0301 a0003c0025t0001g0086 a0003c0025t0001g0113 |
3 | HG02886.hp1 HG03130.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.3834+773A>G | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 28/38 | chr6 | 112131980 | |||||||
chr6:112132078 | G | T | 1 | a0001c0037t0003g0003 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.3834+675C>A | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 28/38 | chr6 | 112132078 | |||||||
chr6:112132154 | T | G | 3 | a0001c0052t0002g0295 a0011c0028t0002g0154 a0011c0028t0002g0159 |
3 | HG01243.hp1 HG02622.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.3834+599A>C | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 28/38 | chr6 | 112132154 | |||||||
chr6:112132671 | T | C | 1 | a0003c0004t0001g0114 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.3834+82A>G | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 28/38 | chr6 | 112132671 | |||||||
chr6:112132983 | A | G | 57 | a0001c0001t0001g0014 a0001c0001t0001g0033 a0001c0001t0001g0050 others(54): Show |
57 | HG00280.hp2 HG00597.hp2 HG00639.hp2 others(54): Show |
intron_variant | MODIFIER | c.3697-93T>C | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 27/38 | chr6 | 112132983 | |||||||
chr6:112132996 | T | C | 1 | a0003c0018t0002g0038 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.3697-106A>G | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 27/38 | chr6 | 112132996 | |||||||
chr6:112133043 | T | C | 62 | a0001c0001t0001g0014 a0001c0001t0001g0033 a0001c0001t0001g0050 others(59): Show |
62 | HG00280.hp2 HG00597.hp2 HG00639.hp2 others(59): Show |
intron_variant | MODIFIER | c.3697-153A>G | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 27/38 | chr6 | 112133043 | |||||||
chr6:112133240 | G | A | 11 | a0001c0011t0003g0062 a0001c0011t0003g0155 a0001c0011t0003g0158 others(8): Show |
11 | HG01891.hp1 HG02109.hp2 HG02257.hp1 others(8): Show |
intron_variant | MODIFIER | c.3696+109C>T | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 27/38 | chr6 | 112133240 | |||||||
chr6:112133789 | C | T | 1 | a0010c0029t0001g0025 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.3558-302G>A | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 26/38 | chr6 | 112133789 | |||||||
chr6:112133790 | G | A | 1 | a0011c0028t0002g0159 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.3558-303C>T | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 26/38 | chr6 | 112133790 | |||||||
chr6:112133807 | A | G | 1 | a0003c0004t0001g0125 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.3558-320T>C | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 26/38 | chr6 | 112133807 | |||||||
chr6:112133818 | C | T | 1 | a0004c0057t0003g0017 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.3558-331G>A | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 26/38 | chr6 | 112133818 | |||||||
chr6:112133927 | T | C | 1 | a0004c0007t0001g0276 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.3558-440A>G | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 26/38 | chr6 | 112133927 | |||||||
chr6:112133967 | C | T | 57 | a0001c0001t0001g0014 a0001c0001t0001g0033 a0001c0001t0001g0050 others(54): Show |
57 | HG00280.hp2 HG00597.hp2 HG00639.hp2 others(54): Show |
intron_variant | MODIFIER | c.3558-480G>A | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 26/38 | chr6 | 112133967 | |||||||
chr6:112133968 | G | A | 1 | a0001c0001t0001g0074 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.3558-481C>T | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 26/38 | chr6 | 112133968 | |||||||
chr6:112134025 | A | G | 57 | a0001c0001t0001g0014 a0001c0001t0001g0033 a0001c0001t0001g0050 others(54): Show |
57 | HG00280.hp2 HG00597.hp2 HG00639.hp2 others(54): Show |
intron_variant | MODIFIER | c.3557+442T>C | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 26/38 | chr6 | 112134025 | |||||||
chr6:112134328 | C | T | 2 | a0001c0001t0001g0115 a0001c0001t0001g0220 |
2 | HG01258.hp2 HG01496.hp2 |
intron_variant | MODIFIER | c.3557+139G>A | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 26/38 | chr6 | 112134328 | |||||||
chr6:112134335 | G | A | 1 | a0001c0050t0001g0310 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.3557+132C>T | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 26/38 | chr6 | 112134335 | |||||||
chr6:112134711 | C | T | 1 | a0002c0003t0006g0001 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.3415-102G>A | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 25/38 | chr6 | 112134711 | |||||||
chr6:112134921 | CAGGT | C | 206 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0015 others(203): Show |
206 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(203): Show |
intron_variant | MODIFIER | c.3415-316_3415-313d others(6): Show |
LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 25/38 | chr6 | 112134921 | |||||||
chr6:112134941 | T | C | 5 | a0003c0018t0002g0038 a0009c0017t0002g0021 a0009c0017t0002g0307 others(2): Show |
5 | HG02647.hp2 HG02895.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.3415-332A>G | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 25/38 | chr6 | 112134941 | |||||||
chr6:112134946 | T | A | 1 | a0004c0057t0003g0017 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.3415-337A>T | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 25/38 | chr6 | 112134946 | |||||||
chr6:112134947 | A | T | 206 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0015 others(203): Show |
206 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(203): Show |
intron_variant | MODIFIER | c.3415-338T>A | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 25/38 | chr6 | 112134947 | |||||||
chr6:112134948 | A | T | 182 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0015 others(179): Show |
182 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(179): Show |
intron_variant | MODIFIER | c.3415-339T>A | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 25/38 | chr6 | 112134948 | |||||||
chr6:112134954 | C | A | 1 | a0004c0057t0003g0017 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.3415-345G>T | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 25/38 | chr6 | 112134954 | |||||||
chr6:112134993 | C | G | 113 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0015 others(110): Show |
113 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(110): Show |
intron_variant | MODIFIER | c.3415-384G>C | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 25/38 | chr6 | 112134993 | |||||||
chr6:112135108 | G | GGT | 85 | a0001c0011t0003g0009 a0001c0011t0003g0062 a0001c0011t0003g0155 others(82): Show |
85 | HG00099.hp2 HG00280.hp1 HG00642.hp1 others(82): Show |
intron_variant | MODIFIER | c.3415-501_3415-500d others(4): Show |
LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 25/38 | chr6 | 112135108 | |||||||
chr6:112135191 | A | G | 1 | a0002c0006t0002g0037 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.3415-582T>C | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 25/38 | chr6 | 112135191 | |||||||
chr6:112135490 | T | A | 1 | a0001c0034t0001g0132 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.3414+633A>T | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 25/38 | chr6 | 112135490 | |||||||
chr6:112135580 | T | C | 83 | a0001c0011t0003g0009 a0001c0011t0003g0062 a0001c0011t0003g0155 others(80): Show |
83 | HG00099.hp2 HG00280.hp1 HG00642.hp1 others(80): Show |
intron_variant | MODIFIER | c.3414+543A>G | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 25/38 | chr6 | 112135580 | |||||||
chr6:112135602 | T | C | 2 | a0003c0025t0001g0086 a0003c0025t0001g0113 |
2 | HG02886.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.3414+521A>G | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 25/38 | chr6 | 112135602 | |||||||
chr6:112135634 | G | A | 1 | a0002c0003t0006g0001 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.3414+489C>T | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 25/38 | chr6 | 112135634 | |||||||
chr6:112135800 | C | T | 42 | a0001c0001t0001g0116 a0001c0001t0011g0229 a0001c0005t0001g0043 others(39): Show |
42 | HG00323.hp1 HG00323.hp2 HG00639.hp1 others(39): Show |
intron_variant | MODIFIER | c.3414+323G>A | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 25/38 | chr6 | 112135800 | |||||||
chr6:112135815 | T | C | 1 | a0001c0011t0003g0009 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.3414+308A>G | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 25/38 | chr6 | 112135815 | |||||||
chr6:112135836 | C | T | 2 | a0002c0006t0002g0104 a0002c0006t0002g0173 |
2 | NA18963.hp2 NA19066.hp1 |
intron_variant | MODIFIER | c.3414+287G>A | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 25/38 | chr6 | 112135836 | |||||||
chr6:112135865 | C | G | 3 | a0001c0020t0005g0046 a0001c0020t0005g0168 a0001c0020t0005g0169 |
3 | HG01891.hp2 HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.3414+258G>C | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 25/38 | chr6 | 112135865 | |||||||
chr6:112135943 | A | T | 266 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0014 others(263): Show |
266 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(263): Show |
intron_variant | MODIFIER | c.3414+180T>A | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 25/38 | chr6 | 112135943 | |||||||
chr6:112135954 | T | C | 266 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0014 others(263): Show |
266 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(263): Show |
intron_variant | MODIFIER | c.3414+169A>G | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 25/38 | chr6 | 112135954 | |||||||
chr6:112135958 | T | A | 1 | a0001c0001t0001g0246 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.3414+165A>T | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 25/38 | chr6 | 112135958 | |||||||
chr6:112136269 | G | A | 266 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0014 others(263): Show |
266 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(263): Show |
intron_variant | MODIFIER | c.3283-15C>T | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 24/38 | chr6 | 112136269 | |||||||
chr6:112136691 | C | CA | 14 | a0001c0001t0001g0223 a0001c0002t0001g0047 a0001c0002t0001g0111 others(11): Show |
14 | HG02040.hp2 HG02055.hp2 HG02647.hp2 others(11): Show |
intron_variant | MODIFIER | c.3283-438dupT | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 24/38 | chr6 | 112136691 | |||||||
chr6:112136691 | C | CAA | 77 | a0001c0011t0003g0009 a0001c0011t0003g0062 a0001c0011t0003g0155 others(74): Show |
77 | HG00099.hp2 HG00280.hp1 HG00642.hp1 others(74): Show |
intron_variant | MODIFIER | c.3283-439_3283-438d others(4): Show |
LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 24/38 | chr6 | 112136691 | |||||||
chr6:112136691 | CA | C | 88 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0015 others(85): Show |
88 | HG00323.hp1 HG00323.hp2 HG00408.hp2 others(85): Show |
intron_variant | MODIFIER | c.3283-438delT | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 24/38 | chr6 | 112136691 | |||||||
chr6:112136824 | A | G | 88 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0015 others(85): Show |
88 | HG00323.hp1 HG00323.hp2 HG00408.hp2 others(85): Show |
intron_variant | MODIFIER | c.3283-570T>C | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 24/38 | chr6 | 112136824 | |||||||
chr6:112136981 | A | G | 11 | a0001c0011t0003g0062 a0001c0011t0003g0155 a0001c0011t0003g0158 others(8): Show |
11 | HG01891.hp1 HG02109.hp2 HG02257.hp1 others(8): Show |
intron_variant | MODIFIER | c.3283-727T>C | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 24/38 | chr6 | 112136981 | |||||||
chr6:112137065 | T | C | 1 | a0004c0057t0003g0017 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.3283-811A>G | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 24/38 | chr6 | 112137065 | |||||||
chr6:112137175 | T | G | 266 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0014 others(263): Show |
266 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(263): Show |
intron_variant | MODIFIER | c.3283-921A>C | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 24/38 | chr6 | 112137175 | |||||||
chr6:112137311 | C | T | 2 | a0001c0011t0003g0236 a0001c0052t0002g0295 |
2 | HG02922.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.3283-1057G>A | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 24/38 | chr6 | 112137311 | |||||||
chr6:112137404 | T | C | 82 | a0001c0011t0003g0009 a0001c0011t0003g0062 a0001c0011t0003g0155 others(79): Show |
82 | HG00099.hp2 HG00280.hp1 HG00642.hp1 others(79): Show |
intron_variant | MODIFIER | c.3283-1150A>G | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 24/38 | chr6 | 112137404 | |||||||
chr6:112137562 | A | G | 311 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0014 others(308): Show |
311 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(308): Show |
intron_variant | MODIFIER | c.3283-1308T>C | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 24/38 | chr6 | 112137562 | |||||||
chr6:112137853 | ATGTC | A | 3 | a0001c0009t0001g0094 a0001c0009t0001g0252 a0023c0035t0001g0185 |
3 | NA18999.hp1 NA19009.hp1 NA19087.hp2 |
intron_variant | MODIFIER | c.3282+1263_3282+126 others(8): Show |
LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 24/38 | chr6 | 112137853 | |||||||
chr6:112137975 | C | T | 1 | a0001c0054t0001g0301 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.3282+1145G>A | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 24/38 | chr6 | 112137975 | |||||||
chr6:112138348 | T | C | 180 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0014 others(177): Show |
180 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(177): Show |
intron_variant | MODIFIER | c.3282+772A>G | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 24/38 | chr6 | 112138348 | |||||||
chr6:112138439 | T | C | 1 | a0005c0008t0001g0231 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.3282+681A>G | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 24/38 | chr6 | 112138439 | |||||||
chr6:112138551 | C | T | 4 | a0002c0003t0002g0071 a0002c0003t0002g0105 a0002c0048t0002g0143 others(1): Show |
4 | HG03831.hp2 NA18940.hp1 NA18970.hp2 others(1): Show |
intron_variant | MODIFIER | c.3282+569G>A | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 24/38 | chr6 | 112138551 | |||||||
chr6:112138608 | TTTA | T | 113 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0015 others(110): Show |
113 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(110): Show |
intron_variant | MODIFIER | c.3282+509_3282+511d others(5): Show |
LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 24/38 | chr6 | 112138608 | |||||||
chr6:112138673 | T | A | 1 | a0001c0011t0003g0293 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.3282+447A>T | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 24/38 | chr6 | 112138673 | |||||||
chr6:112139309 | C | T | 2 | a0001c0005t0001g0235 a0003c0013t0001g0232 |
2 | NA18946.hp1 NA18968.hp1 |
intron_variant | MODIFIER | c.3111-18G>A | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 23/38 | chr6 | 112139309 | |||||||
chr6:112139339 | G | A | 104 | a0001c0011t0003g0009 a0001c0011t0003g0062 a0001c0011t0003g0155 others(101): Show |
104 | HG00099.hp2 HG00280.hp1 HG00642.hp1 others(101): Show |
intron_variant | MODIFIER | c.3111-48C>T | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 23/38 | chr6 | 112139339 | |||||||
chr6:112139446 | G | A | 113 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0015 others(110): Show |
113 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(110): Show |
intron_variant | MODIFIER | c.3111-155C>T | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 23/38 | chr6 | 112139446 | |||||||
chr6:112139461 | G | C | 3 | a0001c0020t0005g0046 a0001c0020t0005g0168 a0001c0020t0005g0169 |
3 | HG01891.hp2 HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.3111-170C>G | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 23/38 | chr6 | 112139461 | |||||||
chr6:112139636 | T | G | 2 | a0003c0025t0001g0086 a0003c0025t0001g0113 |
2 | HG02886.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.3110+116A>C | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 23/38 | chr6 | 112139636 | |||||||
chr6:112139659 | A | C | 1 | a0005c0008t0001g0174 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.3110+93T>G | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 23/38 | chr6 | 112139659 | |||||||
chr6:112140014 | G | A | 3 | a0001c0020t0005g0046 a0001c0020t0005g0168 a0001c0020t0005g0169 |
3 | HG01891.hp2 HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.2977-129C>T | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 22/38 | chr6 | 112140014 | |||||||
chr6:112140041 | T | C | 1 | a0008c0031t0001g0056 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.2977-156A>G | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 22/38 | chr6 | 112140041 | |||||||
chr6:112140344 | T | C | 24 | a0001c0002t0001g0076 a0001c0002t0001g0197 a0003c0018t0002g0038 others(21): Show |
24 | HG01081.hp2 HG02074.hp2 HG02129.hp1 others(21): Show |
intron_variant | MODIFIER | c.2976+416A>G | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 22/38 | chr6 | 112140344 | |||||||
chr6:112140540 | G | C | 4 | a0001c0020t0005g0046 a0001c0020t0005g0168 a0001c0020t0005g0169 others(1): Show |
4 | HG01891.hp2 HG02895.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.2976+220C>G | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 22/38 | chr6 | 112140540 | |||||||
chr6:112141151 | CT | C | 18 | a0001c0022t0002g0146 a0002c0003t0002g0181 a0004c0007t0001g0201 others(15): Show |
18 | HG02074.hp2 HG02129.hp1 HG02280.hp1 others(15): Show |
intron_variant | MODIFIER | c.2813+206delA | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 21/38 | chr6 | 112141151 | |||||||
chr6:112141240 | A | G | 1 | a0021c0033t0013g0124 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.2813+118T>C | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 21/38 | chr6 | 112141240 | |||||||
chr6:112141268 | A | G | 1 | a0004c0057t0003g0017 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.2813+90T>C | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 21/38 | chr6 | 112141268 | |||||||
chr6:112141288 | G | A | 17 | a0001c0022t0002g0146 a0004c0007t0001g0201 a0004c0007t0001g0211 others(14): Show |
17 | HG02074.hp2 HG02129.hp1 HG02280.hp1 others(14): Show |
intron_variant | MODIFIER | c.2813+70C>T | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 21/38 | chr6 | 112141288 | |||||||
chr6:112141656 | T | G | 18 | a0001c0022t0002g0146 a0004c0007t0001g0201 a0004c0007t0001g0211 others(15): Show |
18 | HG02074.hp2 HG02129.hp1 HG02280.hp1 others(15): Show |
intron_variant | MODIFIER | c.2668-153A>C | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 20/38 | chr6 | 112141656 | |||||||
chr6:112141680 | G | A | 86 | a0001c0011t0003g0009 a0001c0011t0003g0062 a0001c0011t0003g0155 others(83): Show |
86 | HG00099.hp2 HG00280.hp1 HG00642.hp1 others(83): Show |
intron_variant | MODIFIER | c.2668-177C>T | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 20/38 | chr6 | 112141680 | |||||||
chr6:112141874 | T | C | 165 | a0001c0001t0001g0033 a0001c0001t0001g0050 a0001c0001t0001g0051 others(162): Show |
165 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(162): Show |
intron_variant | MODIFIER | c.2667+245A>G | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 20/38 | chr6 | 112141874 | |||||||
chr6:112141946 | G | T | 1 | a0001c0011t0003g0009 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.2667+173C>A | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 20/38 | chr6 | 112141946 | |||||||
chr6:112141962 | T | A | 1 | a0001c0001t0001g0281 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.2667+157A>T | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 20/38 | chr6 | 112141962 | |||||||
chr6:112142001 | T | C | 2 | a0003c0025t0001g0086 a0003c0025t0001g0113 |
2 | HG02886.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.2667+118A>G | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 20/38 | chr6 | 112142001 | |||||||
chr6:112142353 | G | A | 1 | a0018c0030t0001g0004 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.2494-61C>T | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 19/38 | chr6 | 112142353 | |||||||
chr6:112142381 | A | C | 1 | a0004c0057t0003g0017 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.2494-89T>G | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 19/38 | chr6 | 112142381 | |||||||
chr6:112142491 | G | A | 86 | a0001c0011t0003g0009 a0001c0011t0003g0062 a0001c0011t0003g0155 others(83): Show |
86 | HG00099.hp2 HG00280.hp1 HG00642.hp1 others(83): Show |
intron_variant | MODIFIER | c.2494-199C>T | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 19/38 | chr6 | 112142491 | |||||||
chr6:112142492 | C | CA | 80 | a0001c0011t0003g0009 a0001c0011t0003g0062 a0001c0011t0003g0155 others(77): Show |
80 | HG00099.hp2 HG00280.hp1 HG00642.hp1 others(77): Show |
intron_variant | MODIFIER | c.2494-201dupT | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 19/38 | chr6 | 112142492 | |||||||
chr6:112142690 | G | C | 3 | a0001c0020t0005g0046 a0001c0020t0005g0168 a0001c0020t0005g0169 |
3 | HG01891.hp2 HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.2494-398C>G | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 19/38 | chr6 | 112142690 | |||||||
chr6:112142722 | C | T | 2 | a0001c0002t0001g0076 a0001c0002t0001g0197 |
2 | HG01081.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.2494-430G>A | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 19/38 | chr6 | 112142722 | |||||||
chr6:112142962 | T | C | 17 | a0001c0022t0002g0146 a0004c0007t0001g0201 a0004c0007t0001g0211 others(14): Show |
17 | HG02074.hp2 HG02129.hp1 HG02280.hp1 others(14): Show |
intron_variant | MODIFIER | c.2494-670A>G | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 19/38 | chr6 | 112142962 | |||||||
chr6:112142982 | G | T | 3 | a0002c0003t0002g0099 a0002c0003t0002g0100 a0007c0014t0002g0041 |
3 | HG00733.hp2 HG01255.hp2 HG01261.hp2 |
intron_variant | MODIFIER | c.2494-690C>A | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 19/38 | chr6 | 112142982 | |||||||
chr6:112142988 | T | C | 11 | a0001c0011t0003g0062 a0001c0011t0003g0155 a0001c0011t0003g0158 others(8): Show |
11 | HG01891.hp1 HG02109.hp2 HG02257.hp1 others(8): Show |
intron_variant | MODIFIER | c.2494-696A>G | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 19/38 | chr6 | 112142988 | |||||||
chr6:112143008 | C | T | 1 | a0006c0027t0002g0140 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.2494-716G>A | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 19/38 | chr6 | 112143008 | |||||||
chr6:112143122 | A | G | 1 | a0002c0003t0002g0077 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.2494-830T>C | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 19/38 | chr6 | 112143122 | |||||||
chr6:112143176 | T | C | 86 | a0001c0011t0003g0009 a0001c0011t0003g0062 a0001c0011t0003g0155 others(83): Show |
86 | HG00099.hp2 HG00280.hp1 HG00642.hp1 others(83): Show |
intron_variant | MODIFIER | c.2494-884A>G | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 19/38 | chr6 | 112143176 | |||||||
chr6:112143284 | C | CT | 13 | a0001c0001t0001g0007 a0001c0002t0001g0111 a0001c0020t0005g0046 others(10): Show |
13 | HG00597.hp1 HG01123.hp2 HG01891.hp2 others(10): Show |
intron_variant | MODIFIER | c.2494-993dupA | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 19/38 | chr6 | 112143284 | |||||||
chr6:112143284 | C | CTTT | 17 | a0001c0022t0002g0146 a0004c0007t0001g0201 a0004c0007t0001g0211 others(14): Show |
17 | HG02129.hp1 HG02280.hp1 HG02523.hp1 others(14): Show |
intron_variant | MODIFIER | c.2494-995_2494-993d others(5): Show |
LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 19/38 | chr6 | 112143284 | |||||||
chr6:112143284 | CT | C | 79 | a0001c0001t0011g0229 a0001c0009t0001g0252 a0001c0011t0003g0009 others(76): Show |
79 | HG00099.hp2 HG00280.hp1 HG00642.hp1 others(76): Show |
intron_variant | MODIFIER | c.2494-993delA | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 19/38 | chr6 | 112143284 | |||||||
chr6:112143284 | CTT | C | 6 | a0003c0018t0002g0038 a0008c0015t0001g0058 a0009c0017t0002g0021 others(3): Show |
6 | HG02647.hp2 HG02818.hp2 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.2494-994_2494-993d others(4): Show |
LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 19/38 | chr6 | 112143284 | |||||||
chr6:112143333 | G | A | 1 | a0001c0050t0001g0310 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.2494-1041C>T | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 19/38 | chr6 | 112143333 | |||||||
chr6:112143372 | T | C | 87 | a0001c0011t0003g0009 a0001c0011t0003g0062 a0001c0011t0003g0155 others(84): Show |
87 | HG00099.hp2 HG00280.hp1 HG00642.hp1 others(84): Show |
intron_variant | MODIFIER | c.2494-1080A>G | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 19/38 | chr6 | 112143372 | |||||||
chr6:112143433 | C | T | 1 | a0010c0029t0001g0034 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.2494-1141G>A | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 19/38 | chr6 | 112143433 | |||||||
chr6:112143441 | C | T | 2 | a0001c0011t0003g0009 a0003c0004t0001g0176 |
2 | HG02055.hp1 HG04184.hp2 |
intron_variant | MODIFIER | c.2494-1149G>A | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 19/38 | chr6 | 112143441 | |||||||
chr6:112143579 | C | T | 1 | a0008c0031t0001g0056 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.2493+1215G>A | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 19/38 | chr6 | 112143579 | |||||||
chr6:112143610 | C | A | 165 | a0001c0001t0001g0033 a0001c0001t0001g0050 a0001c0001t0001g0051 others(162): Show |
165 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(162): Show |
intron_variant | MODIFIER | c.2493+1184G>T | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 19/38 | chr6 | 112143610 | |||||||
chr6:112143669 | G | A | 86 | a0001c0011t0003g0009 a0001c0011t0003g0062 a0001c0011t0003g0155 others(83): Show |
86 | HG00099.hp2 HG00280.hp1 HG00642.hp1 others(83): Show |
intron_variant | MODIFIER | c.2493+1125C>T | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 19/38 | chr6 | 112143669 | |||||||
chr6:112143860 | A | C | 1 | a0001c0037t0003g0003 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.2493+934T>G | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 19/38 | chr6 | 112143860 | |||||||
chr6:112143916 | G | A | 1 | a0001c0001t0001g0228 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.2493+878C>T | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 19/38 | chr6 | 112143916 | |||||||
chr6:112144036 | C | T | 1 | a0004c0057t0003g0017 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.2493+758G>A | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 19/38 | chr6 | 112144036 | |||||||
chr6:112144037 | G | A | 1 | a0005c0044t0001g0261 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.2493+757C>T | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 19/38 | chr6 | 112144037 | |||||||
chr6:112144352 | C | A | 1 | a0001c0037t0003g0003 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.2493+442G>T | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 19/38 | chr6 | 112144352 | |||||||
chr6:112144580 | T | C | 2 | a0003c0025t0001g0086 a0003c0025t0001g0113 |
2 | HG02886.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.2493+214A>G | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 19/38 | chr6 | 112144580 | |||||||
chr6:112144747 | G | T | 1 | a0004c0057t0003g0017 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.2493+47C>A | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 19/38 | chr6 | 112144747 | |||||||
chr6:112144759 | C | T | 1 | a0004c0057t0003g0017 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.2493+35G>A | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 19/38 | chr6 | 112144759 | |||||||
chr6:112144761 | G | A | 3 | a0004c0007t0001g0211 a0005c0008t0001g0262 a0005c0044t0001g0261 |
3 | HG02280.hp1 HG06807.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.2493+33C>T | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 19/38 | chr6 | 112144761 | |||||||
chr6:112144779 | C | A | 1 | a0001c0037t0003g0003 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.2493+15G>T | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 19/38 | chr6 | 112144779 | |||||||
chr6:112145042 | A | AT | 17 | a0001c0022t0002g0146 a0004c0007t0001g0201 a0004c0007t0001g0211 others(14): Show |
17 | HG02074.hp2 HG02129.hp1 HG02280.hp1 others(14): Show |
intron_variant | MODIFIER | c.2354-110dupA | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 18/38 | chr6 | 112145042 | |||||||
chr6:112145134 | C | T | 1 | a0004c0057t0003g0017 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.2354-201G>A | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 18/38 | chr6 | 112145134 | |||||||
chr6:112145256 | T | C | 6 | a0003c0018t0002g0038 a0008c0015t0001g0058 a0009c0017t0002g0021 others(3): Show |
6 | HG02647.hp2 HG02818.hp2 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.2354-323A>G | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 18/38 | chr6 | 112145256 | |||||||
chr6:112145278 | G | A | 1 | a0002c0003t0002g0105 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.2354-345C>T | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 18/38 | chr6 | 112145278 | |||||||
chr6:112145334 | G | T | 1 | a0001c0002t0001g0311 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.2354-401C>A | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 18/38 | chr6 | 112145334 | |||||||
chr6:112145383 | C | T | 1 | a0004c0057t0003g0017 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.2354-450G>A | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 18/38 | chr6 | 112145383 | |||||||
chr6:112145424 | T | C | 1 | a0001c0011t0003g0236 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.2354-491A>G | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 18/38 | chr6 | 112145424 | |||||||
chr6:112145448 | G | A | 3 | a0001c0020t0005g0046 a0001c0020t0005g0168 a0001c0020t0005g0169 |
3 | HG01891.hp2 HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.2354-515C>T | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 18/38 | chr6 | 112145448 | |||||||
chr6:112145454 | A | G | 104 | a0001c0011t0003g0009 a0001c0011t0003g0062 a0001c0011t0003g0155 others(101): Show |
104 | HG00099.hp2 HG00280.hp1 HG00642.hp1 others(101): Show |
intron_variant | MODIFIER | c.2354-521T>C | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 18/38 | chr6 | 112145454 | |||||||
chr6:112145504 | C | T | 1 | a0011c0028t0002g0159 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.2354-571G>A | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 18/38 | chr6 | 112145504 | |||||||
chr6:112145603 | T | C | 104 | a0001c0011t0003g0009 a0001c0011t0003g0062 a0001c0011t0003g0155 others(101): Show |
104 | HG00099.hp2 HG00280.hp1 HG00642.hp1 others(101): Show |
intron_variant | MODIFIER | c.2354-670A>G | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 18/38 | chr6 | 112145603 | |||||||
chr6:112145740 | T | C | 104 | a0001c0011t0003g0009 a0001c0011t0003g0062 a0001c0011t0003g0155 others(101): Show |
104 | HG00099.hp2 HG00280.hp1 HG00642.hp1 others(101): Show |
intron_variant | MODIFIER | c.2354-807A>G | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 18/38 | chr6 | 112145740 | |||||||
chr6:112145898 | G | A | 2 | a0001c0002t0001g0164 a0001c0002t0001g0165 |
2 | HG03942.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.2354-965C>T | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 18/38 | chr6 | 112145898 | |||||||
chr6:112146163 | G | A | 42 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0015 others(39): Show |
42 | HG00408.hp2 HG00597.hp1 HG00621.hp1 others(39): Show |
intron_variant | MODIFIER | c.2354-1230C>T | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 18/38 | chr6 | 112146163 | |||||||
chr6:112146196 | G | A | 1 | a0001c0001t0001g0027 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.2354-1263C>T | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 18/38 | chr6 | 112146196 | |||||||
chr6:112146244 | C | G | 2 | a0002c0003t0002g0102 a0002c0024t0001g0172 |
2 | HG00642.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.2354-1311G>C | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 18/38 | chr6 | 112146244 | |||||||
chr6:112146289 | C | CA | 11 | a0001c0001t0001g0014 a0001c0001t0001g0256 a0001c0002t0001g0205 others(8): Show |
11 | HG00642.hp2 HG01168.hp1 HG01175.hp2 others(8): Show |
intron_variant | MODIFIER | c.2354-1357dupT | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 18/38 | chr6 | 112146289 | |||||||
chr6:112146410 | C | T | 1 | a0001c0002t0001g0020 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.2354-1477G>A | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 18/38 | chr6 | 112146410 | |||||||
chr6:112146615 | A | AG | 53 | a0001c0001t0001g0033 a0001c0001t0001g0050 a0001c0001t0001g0051 others(50): Show |
53 | HG00280.hp2 HG00408.hp1 HG00597.hp2 others(50): Show |
intron_variant | MODIFIER | c.2353+1541dupC | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 18/38 | chr6 | 112146615 | |||||||
chr6:112146759 | T | C | 104 | a0001c0011t0003g0009 a0001c0011t0003g0062 a0001c0011t0003g0155 others(101): Show |
104 | HG00099.hp2 HG00280.hp1 HG00642.hp1 others(101): Show |
intron_variant | MODIFIER | c.2353+1398A>G | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 18/38 | chr6 | 112146759 | |||||||
chr6:112146902 | C | T | 1 | a0002c0003t0002g0181 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.2353+1255G>A | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 18/38 | chr6 | 112146902 | |||||||
chr6:112146955 | C | T | 16 | a0001c0001t0001g0116 a0001c0001t0011g0229 a0001c0005t0001g0043 others(13): Show |
16 | HG00323.hp1 HG00323.hp2 HG00639.hp1 others(13): Show |
intron_variant | MODIFIER | c.2353+1202G>A | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 18/38 | chr6 | 112146955 | |||||||
chr6:112146978 | C | A | 1 | a0004c0057t0003g0017 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.2353+1179G>T | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 18/38 | chr6 | 112146978 | |||||||
chr6:112147092 | T | C | 4 | a0001c0001t0001g0070 a0001c0001t0001g0074 a0003c0018t0001g0089 others(1): Show |
4 | NA18963.hp1 NA18985.hp1 NA19056.hp1 others(1): Show |
intron_variant | MODIFIER | c.2353+1065A>G | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 18/38 | chr6 | 112147092 | |||||||
chr6:112147117 | T | C | 1 | a0006c0012t0002g0075 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.2353+1040A>G | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 18/38 | chr6 | 112147117 | |||||||
chr6:112147153 | A | G | 1 | a0002c0006t0002g0265 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.2353+1004T>C | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 18/38 | chr6 | 112147153 | |||||||
chr6:112147398 | A | T | 1 | a0001c0009t0001g0203 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.2353+759T>A | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 18/38 | chr6 | 112147398 | |||||||
chr6:112147443 | T | A | 104 | a0001c0011t0003g0009 a0001c0011t0003g0062 a0001c0011t0003g0155 others(101): Show |
104 | HG00099.hp2 HG00280.hp1 HG00642.hp1 others(101): Show |
intron_variant | MODIFIER | c.2353+714A>T | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 18/38 | chr6 | 112147443 | |||||||
chr6:112147705 | A | G | 104 | a0001c0011t0003g0009 a0001c0011t0003g0062 a0001c0011t0003g0155 others(101): Show |
104 | HG00099.hp2 HG00280.hp1 HG00642.hp1 others(101): Show |
intron_variant | MODIFIER | c.2353+452T>C | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 18/38 | chr6 | 112147705 | |||||||
chr6:112147762 | C | A | 1 | a0001c0050t0001g0310 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.2353+395G>T | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 18/38 | chr6 | 112147762 | |||||||
chr6:112147808 | G | A | 104 | a0001c0011t0003g0009 a0001c0011t0003g0062 a0001c0011t0003g0155 others(101): Show |
104 | HG00099.hp2 HG00280.hp1 HG00642.hp1 others(101): Show |
intron_variant | MODIFIER | c.2353+349C>T | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 18/38 | chr6 | 112147808 | |||||||
chr6:112147837 | C | T | 1 | a0004c0007t0001g0117 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.2353+320G>A | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 18/38 | chr6 | 112147837 | |||||||
chr6:112147948 | G | A | 2 | a0002c0003t0002g0163 a0002c0003t0002g0305 |
2 | HG03492.hp1 HG03654.hp1 |
intron_variant | MODIFIER | c.2353+209C>T | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 18/38 | chr6 | 112147948 | |||||||
chr6:112147977 | T | C | 103 | a0001c0011t0003g0009 a0001c0011t0003g0062 a0001c0011t0003g0155 others(100): Show |
103 | HG00099.hp2 HG00280.hp1 HG00642.hp1 others(100): Show |
intron_variant | MODIFIER | c.2353+180A>G | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 18/38 | chr6 | 112147977 | |||||||
chr6:112148125 | T | G | 1 | a0004c0057t0003g0017 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.2353+32A>C | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 18/38 | chr6 | 112148125 | |||||||
chr6:112148364 | T | G | 10 | a0001c0001t0001g0015 a0001c0001t0001g0070 a0001c0001t0001g0072 others(7): Show |
10 | HG00621.hp1 NA18940.hp2 NA18961.hp1 others(7): Show |
intron_variant | MODIFIER | c.2174-28A>C | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 17/38 | chr6 | 112148364 | |||||||
chr6:112148374 | A | G | 1 | a0001c0001t0001g0072 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.2174-38T>C | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 17/38 | chr6 | 112148374 | |||||||
chr6:112148405 | C | T | 1 | a0020c0056t0001g0122 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.2174-69G>A | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 17/38 | chr6 | 112148405 | |||||||
chr6:112148516 | T | A | 11 | a0001c0011t0003g0062 a0001c0011t0003g0155 a0001c0011t0003g0158 others(8): Show |
11 | HG01891.hp1 HG02109.hp2 HG02257.hp1 others(8): Show |
intron_variant | MODIFIER | c.2174-180A>T | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 17/38 | chr6 | 112148516 | |||||||
chr6:112148707 | AT | A | 166 | a0001c0001t0001g0033 a0001c0001t0001g0050 a0001c0001t0001g0051 others(163): Show |
166 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(163): Show |
intron_variant | MODIFIER | c.2174-372delA | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 17/38 | chr6 | 112148707 | |||||||
chr6:112148717 | T | C | 2 | a0001c0001t0001g0237 a0003c0004t0001g0125 |
2 | HG00408.hp1 NA19005.hp1 |
intron_variant | MODIFIER | c.2174-381A>G | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 17/38 | chr6 | 112148717 | |||||||
chr6:112148970 | G | A | 104 | a0001c0011t0003g0009 a0001c0011t0003g0062 a0001c0011t0003g0155 others(101): Show |
104 | HG00099.hp2 HG00280.hp1 HG00642.hp1 others(101): Show |
intron_variant | MODIFIER | c.2174-634C>T | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 17/38 | chr6 | 112148970 | |||||||
chr6:112149003 | A | C | 104 | a0001c0011t0003g0009 a0001c0011t0003g0062 a0001c0011t0003g0155 others(101): Show |
104 | HG00099.hp2 HG00280.hp1 HG00642.hp1 others(101): Show |
intron_variant | MODIFIER | c.2174-667T>G | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 17/38 | chr6 | 112149003 | |||||||
chr6:112149033 | C | G | 1 | a0004c0010t0004g0128 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.2174-697G>C | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 17/38 | chr6 | 112149033 | |||||||
chr6:112149088 | C | T | 1 | a0004c0007t0001g0276 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.2174-752G>A | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 17/38 | chr6 | 112149088 | |||||||
chr6:112149118 | T | A | 1 | a0001c0054t0001g0301 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.2174-782A>T | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 17/38 | chr6 | 112149118 | |||||||
chr6:112149134 | T | A | 1 | a0004c0010t0001g0208 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.2174-798A>T | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 17/38 | chr6 | 112149134 | |||||||
chr6:112149150 | TAATA | T | 103 | a0001c0011t0003g0009 a0001c0011t0003g0062 a0001c0011t0003g0155 others(100): Show |
103 | HG00099.hp2 HG00280.hp1 HG00642.hp1 others(100): Show |
intron_variant | MODIFIER | c.2174-818_2174-815d others(6): Show |
LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 17/38 | chr6 | 112149150 | |||||||
chr6:112149502 | G | A | 104 | a0001c0011t0003g0009 a0001c0011t0003g0062 a0001c0011t0003g0155 others(101): Show |
104 | HG00099.hp2 HG00280.hp1 HG00642.hp1 others(101): Show |
intron_variant | MODIFIER | c.2173+1009C>T | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 17/38 | chr6 | 112149502 | |||||||
chr6:112149689 | G | A | 17 | a0001c0022t0002g0146 a0004c0007t0001g0201 a0004c0007t0001g0211 others(14): Show |
17 | HG02074.hp2 HG02129.hp1 HG02280.hp1 others(14): Show |
intron_variant | MODIFIER | c.2173+822C>T | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 17/38 | chr6 | 112149689 | |||||||
chr6:112149713 | G | A | 1 | a0008c0015t0001g0057 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.2173+798C>T | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 17/38 | chr6 | 112149713 | |||||||
chr6:112149916 | G | T | 103 | a0001c0011t0003g0009 a0001c0011t0003g0062 a0001c0011t0003g0155 others(100): Show |
103 | HG00099.hp2 HG00280.hp1 HG00642.hp1 others(100): Show |
intron_variant | MODIFIER | c.2173+595C>A | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 17/38 | chr6 | 112149916 | |||||||
chr6:112149988 | G | T | 1 | a0008c0031t0001g0056 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.2173+523C>A | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 17/38 | chr6 | 112149988 | |||||||
chr6:112150017 | T | C | 1 | a0001c0050t0001g0310 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.2173+494A>G | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 17/38 | chr6 | 112150017 | |||||||
chr6:112150202 | G | GAC | 44 | a0001c0001t0001g0167 a0001c0001t0001g0227 a0001c0001t0011g0229 others(41): Show |
44 | HG00741.hp1 HG01243.hp1 HG01261.hp2 others(41): Show |
intron_variant | MODIFIER | c.2173+307_2173+308d others(4): Show |
LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 17/38 | chr6 | 112150202 | |||||||
chr6:112150202 | G | GACAC | 33 | a0001c0002t0001g0045 a0001c0002t0001g0164 a0001c0002t0001g0165 others(30): Show |
33 | HG00642.hp1 HG01071.hp1 HG01167.hp2 others(30): Show |
intron_variant | MODIFIER | c.2173+305_2173+308d others(6): Show |
LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 17/38 | chr6 | 112150202 | |||||||
chr6:112150202 | G | GACACAC | 8 | a0001c0002t0001g0278 a0002c0003t0002g0099 a0002c0003t0002g0163 others(5): Show |
8 | HG01175.hp1 HG01255.hp2 HG01981.hp2 others(5): Show |
intron_variant | MODIFIER | c.2173+303_2173+308d others(8): Show |
LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 17/38 | chr6 | 112150202 | |||||||
chr6:112150202 | G | GACACACA others(1): Show |
5 | a0002c0003t0002g0077 a0002c0003t0002g0079 a0002c0003t0002g0100 others(2): Show |
5 | HG00099.hp2 HG00280.hp1 HG00733.hp2 others(2): Show |
intron_variant | MODIFIER | c.2173+301_2173+308d others(10): Show |
LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 17/38 | chr6 | 112150202 | |||||||
chr6:112150202 | G | GACACACA others(3): Show |
1 | a0002c0003t0002g0290 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.2173+299_2173+308d others(12): Show |
LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 17/38 | chr6 | 112150202 | |||||||
chr6:112150202 | GAC | G | 9 | a0001c0005t0001g0118 a0001c0005t0001g0280 a0001c0009t0001g0112 others(6): Show |
9 | HG00099.hp1 HG02280.hp2 NA18952.hp1 others(6): Show |
intron_variant | MODIFIER | c.2173+307_2173+308d others(4): Show |
LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 17/38 | chr6 | 112150202 | |||||||
chr6:112150202 | GACAC | G | 5 | a0001c0005t0001g0101 a0001c0005t0001g0103 a0001c0005t0001g0230 others(2): Show |
5 | HG01106.hp2 HG01433.hp2 HG01515.hp1 others(2): Show |
intron_variant | MODIFIER | c.2173+305_2173+308d others(6): Show |
LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 17/38 | chr6 | 112150202 | |||||||
chr6:112150202 | GACACAC | G | 51 | a0001c0001t0001g0033 a0001c0001t0001g0050 a0001c0001t0001g0051 others(48): Show |
51 | HG00280.hp2 HG00408.hp1 HG00597.hp2 others(48): Show |
intron_variant | MODIFIER | c.2173+303_2173+308d others(8): Show |
LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 17/38 | chr6 | 112150202 | |||||||
chr6:112150224 | CACACACA others(5): Show |
C | 3 | a0001c0011t0003g0313 a0001c0023t0003g0302 a0001c0051t0003g0314 |
3 | HG01891.hp1 HG03195.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.2173+275_2173+286d others(14): Show |
LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 17/38 | chr6 | 112150224 | |||||||
chr6:112150226 | CACACACA others(3): Show |
C | 1 | a0001c0011t0003g0298 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.2173+275_2173+284d others(12): Show |
LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 17/38 | chr6 | 112150226 | |||||||
chr6:112150228 | CACACACA others(1): Show |
C | 6 | a0003c0018t0002g0038 a0008c0015t0001g0058 a0009c0017t0002g0021 others(3): Show |
6 | HG02647.hp2 HG02818.hp2 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.2173+275_2173+282d others(10): Show |
LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 17/38 | chr6 | 112150228 | |||||||
chr6:112150232 | CACAG | C | 5 | a0001c0011t0003g0062 a0001c0011t0003g0155 a0001c0011t0003g0158 others(2): Show |
5 | HG02572.hp1 HG02630.hp1 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.2173+275_2173+278d others(6): Show |
LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 17/38 | chr6 | 112150232 | |||||||
chr6:112150234 | CAG | C | 3 | a0001c0011t0003g0255 a0005c0008t0001g0248 a0006c0012t0002g0150 |
3 | HG02027.hp1 HG02615.hp2 NA19064.hp1 |
intron_variant | MODIFIER | c.2173+275_2173+276d others(4): Show |
LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 17/38 | chr6 | 112150234 | |||||||
chr6:112150236 | G | C | 84 | a0001c0011t0003g0293 a0001c0022t0002g0146 a0001c0037t0003g0003 others(81): Show |
84 | HG00099.hp2 HG00280.hp1 HG00642.hp1 others(81): Show |
intron_variant | MODIFIER | c.2173+275C>G | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 17/38 | chr6 | 112150236 | |||||||
chr6:112150260 | G | C | 6 | a0002c0003t0002g0054 a0002c0003t0002g0099 a0002c0003t0002g0100 others(3): Show |
6 | HG00733.hp2 HG01255.hp2 HG01256.hp2 others(3): Show |
intron_variant | MODIFIER | c.2173+251C>G | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 17/38 | chr6 | 112150260 | |||||||
chr6:112150419 | GACAA | G | 106 | a0001c0001t0001g0116 a0001c0001t0011g0229 a0001c0011t0003g0009 others(103): Show |
106 | HG00099.hp2 HG00280.hp1 HG00642.hp1 others(103): Show |
intron_variant | MODIFIER | c.2173+88_2173+91del others(4): Show |
LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 17/38 | chr6 | 112150419 | |||||||
chr6:112150425 | C | A | 17 | a0001c0022t0002g0146 a0004c0007t0001g0201 a0004c0007t0001g0211 others(14): Show |
17 | HG02074.hp2 HG02129.hp1 HG02280.hp1 others(14): Show |
intron_variant | MODIFIER | c.2173+86G>T | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 17/38 | chr6 | 112150425 | |||||||
chr6:112150486 | G | C | 106 | a0001c0001t0001g0116 a0001c0001t0011g0229 a0001c0011t0003g0009 others(103): Show |
106 | HG00099.hp2 HG00280.hp1 HG00642.hp1 others(103): Show |
intron_variant | MODIFIER | c.2173+25C>G | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 17/38 | chr6 | 112150486 | |||||||
chr6:112150696 | A | C | 1 | a0003c0061t0001g0299 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.2057-69T>G | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 16/38 | chr6 | 112150696 | |||||||
chr6:112150756 | T | C | 13 | a0001c0001t0001g0050 a0001c0001t0001g0051 a0001c0001t0001g0052 others(10): Show |
13 | HG00639.hp2 HG00741.hp2 HG01074.hp2 others(10): Show |
intron_variant | MODIFIER | c.2057-129A>G | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 16/38 | chr6 | 112150756 | |||||||
chr6:112150803 | A | G | 106 | a0001c0001t0001g0116 a0001c0001t0011g0229 a0001c0011t0003g0009 others(103): Show |
106 | HG00099.hp2 HG00280.hp1 HG00642.hp1 others(103): Show |
intron_variant | MODIFIER | c.2057-176T>C | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 16/38 | chr6 | 112150803 | |||||||
chr6:112150822 | G | T | 1 | a0007c0014t0002g0292 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.2057-195C>A | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 16/38 | chr6 | 112150822 | |||||||
chr6:112150837 | A | G | 2 | a0003c0025t0001g0086 a0003c0025t0001g0113 |
2 | HG02886.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.2057-210T>C | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 16/38 | chr6 | 112150837 | |||||||
chr6:112150893 | A | G | 3 | a0001c0020t0005g0046 a0001c0020t0005g0168 a0001c0020t0005g0169 |
3 | HG01891.hp2 HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.2057-266T>C | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 16/38 | chr6 | 112150893 | |||||||
chr6:112150930 | C | A | 41 | a0001c0005t0001g0043 a0001c0005t0001g0044 a0001c0005t0001g0063 others(38): Show |
41 | HG00323.hp1 HG00323.hp2 HG00639.hp1 others(38): Show |
intron_variant | MODIFIER | c.2057-303G>T | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 16/38 | chr6 | 112150930 | |||||||
chr6:112150950 | C | T | 2 | a0002c0003t0002g0163 a0002c0003t0002g0305 |
2 | HG03492.hp1 HG03654.hp1 |
intron_variant | MODIFIER | c.2057-323G>A | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 16/38 | chr6 | 112150950 | |||||||
chr6:112151081 | CAA | C | 106 | a0001c0001t0001g0116 a0001c0001t0011g0229 a0001c0011t0003g0009 others(103): Show |
106 | HG00099.hp2 HG00280.hp1 HG00642.hp1 others(103): Show |
intron_variant | MODIFIER | c.2057-456_2057-455d others(4): Show |
LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 16/38 | chr6 | 112151081 | |||||||
chr6:112151124 | AG | A | 52 | a0001c0001t0001g0033 a0001c0001t0001g0050 a0001c0001t0001g0051 others(49): Show |
52 | HG00280.hp2 HG00408.hp1 HG00597.hp2 others(49): Show |
intron_variant | MODIFIER | c.2057-498delC | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 16/38 | chr6 | 112151124 | |||||||
chr6:112151163 | C | T | 105 | a0001c0001t0001g0116 a0001c0001t0011g0229 a0001c0011t0003g0009 others(102): Show |
105 | HG00099.hp2 HG00280.hp1 HG00642.hp1 others(102): Show |
intron_variant | MODIFIER | c.2057-536G>A | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 16/38 | chr6 | 112151163 | |||||||
chr6:112151372 | A | C | 1 | a0024c0041t0001g0183 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.2057-745T>G | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 16/38 | chr6 | 112151372 | |||||||
chr6:112151660 | C | G | 1 | a0003c0013t0001g0010 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.2057-1033G>C | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 16/38 | chr6 | 112151660 | |||||||
chr6:112151684 | T | C | 107 | a0001c0001t0001g0116 a0001c0001t0011g0229 a0001c0002t0001g0254 others(104): Show |
107 | HG00099.hp2 HG00280.hp1 HG00642.hp1 others(104): Show |
intron_variant | MODIFIER | c.2057-1057A>G | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 16/38 | chr6 | 112151684 | |||||||
chr6:112151938 | A | C | 2 | a0001c0002t0001g0076 a0001c0002t0001g0197 |
2 | HG01081.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.2057-1311T>G | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 16/38 | chr6 | 112151938 | |||||||
chr6:112152073 | G | A | 1 | a0004c0057t0003g0017 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.2057-1446C>T | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 16/38 | chr6 | 112152073 | |||||||
chr6:112152132 | T | G | 12 | a0001c0011t0003g0009 a0001c0011t0003g0062 a0001c0011t0003g0155 others(9): Show |
12 | HG01891.hp1 HG02055.hp1 HG02109.hp2 others(9): Show |
intron_variant | MODIFIER | c.2057-1505A>C | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 16/38 | chr6 | 112152132 | |||||||
chr6:112152394 | A | G | 1 | a0004c0007t0001g0189 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.2057-1767T>C | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 16/38 | chr6 | 112152394 | |||||||
chr6:112152449 | C | T | 69 | a0001c0001t0001g0116 a0001c0001t0011g0229 a0002c0003t0001g0171 others(66): Show |
69 | HG00099.hp2 HG00280.hp1 HG00642.hp1 others(66): Show |
intron_variant | MODIFIER | c.2057-1822G>A | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 16/38 | chr6 | 112152449 | |||||||
chr6:112152488 | G | A | 1 | a0001c0005t0001g0286 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.2057-1861C>T | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 16/38 | chr6 | 112152488 | |||||||
chr6:112152640 | C | T | 12 | a0001c0011t0003g0009 a0001c0011t0003g0062 a0001c0011t0003g0155 others(9): Show |
12 | HG01891.hp1 HG02055.hp1 HG02109.hp2 others(9): Show |
intron_variant | MODIFIER | c.2057-2013G>A | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 16/38 | chr6 | 112152640 | |||||||
chr6:112152713 | C | G | 1 | a0005c0008t0001g0241 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.2057-2086G>C | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 16/38 | chr6 | 112152713 | |||||||
chr6:112152722 | G | A | 3 | a0002c0006t0002g0303 a0007c0014t0002g0250 a0007c0060t0002g0260 |
3 | HG02809.hp1 NA18906.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.2057-2095C>T | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 16/38 | chr6 | 112152722 | |||||||
chr6:112152806 | T | G | 6 | a0003c0018t0002g0038 a0008c0015t0001g0058 a0009c0017t0002g0021 others(3): Show |
6 | HG02647.hp2 HG02818.hp2 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.2056+2045A>C | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 16/38 | chr6 | 112152806 | |||||||
chr6:112153165 | A | G | 107 | a0001c0001t0001g0033 a0001c0001t0001g0116 a0001c0001t0011g0229 others(104): Show |
107 | HG00099.hp2 HG00280.hp1 HG00642.hp1 others(104): Show |
intron_variant | MODIFIER | c.2056+1686T>C | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 16/38 | chr6 | 112153165 | |||||||
chr6:112153253 | A | AG | 6 | a0002c0003t0002g0054 a0002c0003t0002g0099 a0002c0003t0002g0100 others(3): Show |
6 | HG00733.hp2 HG01255.hp2 HG01256.hp2 others(3): Show |
intron_variant | MODIFIER | c.2056+1597dupC | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 16/38 | chr6 | 112153253 | |||||||
chr6:112153305 | G | A | 10 | a0001c0011t0003g0062 a0001c0011t0003g0155 a0001c0011t0003g0158 others(7): Show |
10 | HG01891.hp1 HG02109.hp2 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.2056+1546C>T | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 16/38 | chr6 | 112153305 | |||||||
chr6:112153415 | A | T | 1 | a0001c0011t0003g0293 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.2056+1436T>A | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 16/38 | chr6 | 112153415 | |||||||
chr6:112153506 | G | A | 18 | a0001c0011t0003g0298 a0001c0022t0002g0146 a0004c0007t0001g0201 others(15): Show |
18 | HG02074.hp2 HG02129.hp1 HG02257.hp1 others(15): Show |
intron_variant | MODIFIER | c.2056+1345C>T | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 16/38 | chr6 | 112153506 | |||||||
chr6:112153509 | A | G | 1 | a0001c0011t0003g0293 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.2056+1342T>C | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 16/38 | chr6 | 112153509 | |||||||
chr6:112153653 | A | G | 53 | a0001c0001t0001g0050 a0001c0001t0001g0051 a0001c0001t0001g0052 others(50): Show |
53 | HG00280.hp2 HG00408.hp1 HG00597.hp2 others(50): Show |
intron_variant | MODIFIER | c.2056+1198T>C | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 16/38 | chr6 | 112153653 | |||||||
chr6:112153893 | A | ATAGT | 107 | a0001c0001t0001g0033 a0001c0001t0001g0116 a0001c0001t0011g0229 others(104): Show |
107 | HG00099.hp2 HG00280.hp1 HG00642.hp1 others(104): Show |
intron_variant | MODIFIER | c.2056+957_2056+958i others(6): Show |
LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 16/38 | chr6 | 112153893 | |||||||
chr6:112154110 | G | A | 107 | a0001c0001t0001g0033 a0001c0001t0001g0116 a0001c0001t0011g0229 others(104): Show |
107 | HG00099.hp2 HG00280.hp1 HG00642.hp1 others(104): Show |
intron_variant | MODIFIER | c.2056+741C>T | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 16/38 | chr6 | 112154110 | |||||||
chr6:112154254 | G | A | 1 | a0001c0002t0001g0097 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.2056+597C>T | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 16/38 | chr6 | 112154254 | |||||||
chr6:112154357 | C | CA | 12 | a0001c0011t0003g0009 a0001c0011t0003g0062 a0001c0011t0003g0155 others(9): Show |
12 | HG01891.hp1 HG02055.hp1 HG02109.hp2 others(9): Show |
intron_variant | MODIFIER | c.2056+493dupT | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 16/38 | chr6 | 112154357 | |||||||
chr6:112154357 | C | CAA | 84 | a0001c0001t0001g0033 a0001c0001t0001g0116 a0001c0001t0011g0229 others(81): Show |
84 | HG00099.hp2 HG00280.hp1 HG00642.hp1 others(81): Show |
intron_variant | MODIFIER | c.2056+492_2056+493d others(4): Show |
LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 16/38 | chr6 | 112154357 | |||||||
chr6:112154357 | CA | C | 190 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0014 others(187): Show |
190 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(187): Show |
intron_variant | MODIFIER | c.2056+493delT | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 16/38 | chr6 | 112154357 | |||||||
chr6:112154357 | CAA | C | 7 | a0001c0002t0001g0076 a0001c0002t0001g0197 a0001c0020t0005g0046 others(4): Show |
7 | HG01081.hp2 HG01891.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.2056+492_2056+493d others(4): Show |
LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 16/38 | chr6 | 112154357 | |||||||
chr6:112154404 | G | A | 4 | a0004c0007t0001g0156 a0004c0007t0001g0157 a0004c0007t0001g0160 others(1): Show |
4 | HG02109.hp1 HG02145.hp2 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.2056+447C>T | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 16/38 | chr6 | 112154404 | |||||||
chr6:112154441 | G | A | 70 | a0001c0001t0001g0033 a0001c0001t0001g0116 a0001c0001t0011g0229 others(67): Show |
70 | HG00099.hp2 HG00280.hp1 HG00642.hp1 others(67): Show |
intron_variant | MODIFIER | c.2056+410C>T | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 16/38 | chr6 | 112154441 | |||||||
chr6:112154448 | C | T | 1 | a0004c0057t0003g0017 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.2056+403G>A | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 16/38 | chr6 | 112154448 | |||||||
chr6:112154538 | AT | A | 107 | a0001c0001t0001g0033 a0001c0001t0001g0116 a0001c0001t0011g0229 others(104): Show |
107 | HG00099.hp2 HG00280.hp1 HG00642.hp1 others(104): Show |
intron_variant | MODIFIER | c.2056+312delA | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 16/38 | chr6 | 112154538 | |||||||
chr6:112154655 | C | T | 81 | a0001c0001t0001g0033 a0001c0001t0001g0116 a0001c0001t0011g0229 others(78): Show |
81 | HG00099.hp2 HG00280.hp1 HG00642.hp1 others(78): Show |
intron_variant | MODIFIER | c.2056+196G>A | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 16/38 | chr6 | 112154655 | |||||||
chr6:112154656 | A | AT | 94 | a0001c0001t0001g0033 a0001c0001t0001g0116 a0001c0001t0011g0229 others(91): Show |
94 | HG00099.hp2 HG00280.hp1 HG00642.hp1 others(91): Show |
intron_variant | MODIFIER | c.2056+194dupA | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 16/38 | chr6 | 112154656 | |||||||
chr6:112154656 | A | ATT | 11 | a0001c0011t0003g0009 a0001c0011t0003g0062 a0001c0011t0003g0155 others(8): Show |
11 | HG01891.hp1 HG02055.hp1 HG02109.hp2 others(8): Show |
intron_variant | MODIFIER | c.2056+193_2056+194d others(4): Show |
LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 16/38 | chr6 | 112154656 | |||||||
chr6:112154656 | AT | A | 22 | a0001c0001t0001g0136 a0001c0001t0001g0187 a0001c0001t0001g0237 others(19): Show |
22 | HG00280.hp2 HG00408.hp1 HG00597.hp2 others(19): Show |
intron_variant | MODIFIER | c.2056+194delA | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 16/38 | chr6 | 112154656 | |||||||
chr6:112154682 | G | A | 2 | a0008c0031t0001g0056 a0011c0028t0002g0159 |
2 | HG01243.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.2056+169C>T | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 16/38 | chr6 | 112154682 | |||||||
chr6:112154781 | C | T | 18 | a0001c0011t0003g0298 a0001c0022t0002g0146 a0004c0007t0001g0201 others(15): Show |
18 | HG02074.hp2 HG02129.hp1 HG02257.hp1 others(15): Show |
intron_variant | MODIFIER | c.2056+70G>A | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 16/38 | chr6 | 112154781 | |||||||
chr6:112154811 | C | A | 18 | a0001c0011t0003g0298 a0001c0022t0002g0146 a0004c0007t0001g0201 others(15): Show |
18 | HG02074.hp2 HG02129.hp1 HG02257.hp1 others(15): Show |
intron_variant | MODIFIER | c.2056+40G>T | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 16/38 | chr6 | 112154811 | |||||||
chr6:112154982 | C | G | 1 | a0001c0011t0003g0236 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1960-35G>C | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 15/38 | chr6 | 112154982 | |||||||
chr6:112155008 | T | C | 107 | a0001c0001t0001g0033 a0001c0001t0001g0116 a0001c0001t0011g0229 others(104): Show |
107 | HG00099.hp2 HG00280.hp1 HG00642.hp1 others(104): Show |
intron_variant | MODIFIER | c.1960-61A>G | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 15/38 | chr6 | 112155008 | |||||||
chr6:112155306 | A | G | 1 | a0001c0002t0001g0191 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.1959+259T>C | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 15/38 | chr6 | 112155306 | |||||||
chr6:112155493 | A | G | 1 | a0004c0057t0003g0017 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1959+72T>C | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 15/38 | chr6 | 112155493 | |||||||
chr6:112155497 | G | A | 1 | a0001c0050t0001g0310 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1959+68C>T | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 15/38 | chr6 | 112155497 | |||||||
chr6:112155875 | C | T | 1 | a0001c0050t0001g0310 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1818-169G>A | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 14/38 | chr6 | 112155875 | |||||||
chr6:112155937 | G | C | 81 | a0001c0001t0001g0033 a0001c0001t0001g0116 a0001c0001t0011g0229 others(78): Show |
81 | HG00099.hp2 HG00280.hp1 HG00642.hp1 others(78): Show |
intron_variant | MODIFIER | c.1818-231C>G | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 14/38 | chr6 | 112155937 | |||||||
chr6:112156081 | T | A | 18 | a0001c0011t0003g0298 a0001c0022t0002g0146 a0004c0007t0001g0201 others(15): Show |
18 | HG02074.hp2 HG02129.hp1 HG02257.hp1 others(15): Show |
intron_variant | MODIFIER | c.1818-375A>T | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 14/38 | chr6 | 112156081 | |||||||
chr6:112156082 | A | G | 18 | a0001c0011t0003g0298 a0001c0022t0002g0146 a0004c0007t0001g0201 others(15): Show |
18 | HG02074.hp2 HG02129.hp1 HG02257.hp1 others(15): Show |
intron_variant | MODIFIER | c.1818-376T>C | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 14/38 | chr6 | 112156082 | |||||||
chr6:112156090 | C | T | 1 | a0001c0001t0001g0136 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.1818-384G>A | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 14/38 | chr6 | 112156090 | |||||||
chr6:112156136 | T | C | 7 | a0003c0018t0002g0038 a0007c0060t0002g0260 a0008c0015t0001g0058 others(4): Show |
7 | HG02647.hp2 HG02809.hp1 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.1818-430A>G | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 14/38 | chr6 | 112156136 | |||||||
chr6:112156170 | T | C | 25 | a0001c0011t0003g0298 a0001c0022t0002g0146 a0003c0018t0002g0038 others(22): Show |
25 | HG02074.hp2 HG02129.hp1 HG02257.hp1 others(22): Show |
intron_variant | MODIFIER | c.1818-464A>G | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 14/38 | chr6 | 112156170 | |||||||
chr6:112156256 | G | C | 107 | a0001c0001t0001g0033 a0001c0001t0001g0116 a0001c0001t0011g0229 others(104): Show |
107 | HG00099.hp2 HG00280.hp1 HG00642.hp1 others(104): Show |
intron_variant | MODIFIER | c.1818-550C>G | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 14/38 | chr6 | 112156256 | |||||||
chr6:112156276 | C | T | 1 | a0002c0003t0002g0182 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.1818-570G>A | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 14/38 | chr6 | 112156276 | |||||||
chr6:112156426 | G | A | 107 | a0001c0001t0001g0033 a0001c0001t0001g0116 a0001c0001t0011g0229 others(104): Show |
107 | HG00099.hp2 HG00280.hp1 HG00642.hp1 others(104): Show |
intron_variant | MODIFIER | c.1818-720C>T | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 14/38 | chr6 | 112156426 | |||||||
chr6:112156460 | G | A | 1 | a0004c0010t0001g0013 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1818-754C>T | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 14/38 | chr6 | 112156460 | |||||||
chr6:112156926 | A | AT | 108 | a0001c0001t0001g0033 a0001c0001t0001g0116 a0001c0001t0011g0229 others(105): Show |
108 | HG00099.hp2 HG00280.hp1 HG00642.hp1 others(105): Show |
intron_variant | MODIFIER | c.1818-1221dupA | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 14/38 | chr6 | 112156926 | |||||||
chr6:112156942 | G | T | 83 | a0001c0001t0001g0033 a0001c0001t0001g0116 a0001c0001t0011g0229 others(80): Show |
83 | HG00099.hp2 HG00280.hp1 HG00642.hp1 others(80): Show |
intron_variant | MODIFIER | c.1818-1236C>A | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 14/38 | chr6 | 112156942 | |||||||
chr6:112156992 | T | C | 1 | a0001c0054t0001g0301 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1818-1286A>G | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 14/38 | chr6 | 112156992 | |||||||
chr6:112157153 | G | A | 2 | a0003c0018t0002g0038 a0007c0060t0002g0260 |
2 | HG02809.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.1818-1447C>T | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 14/38 | chr6 | 112157153 | |||||||
chr6:112157302 | C | A | 1 | a0001c0002t0001g0311 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.1817+1430G>T | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 14/38 | chr6 | 112157302 | |||||||
chr6:112157321 | A | AT | 108 | a0001c0001t0001g0033 a0001c0001t0001g0116 a0001c0001t0011g0229 others(105): Show |
108 | HG00099.hp2 HG00280.hp1 HG00642.hp1 others(105): Show |
intron_variant | MODIFIER | c.1817+1410dupA | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 14/38 | chr6 | 112157321 | |||||||
chr6:112157414 | C | T | 1 | a0002c0006t0002g0104 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.1817+1318G>A | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 14/38 | chr6 | 112157414 | |||||||
chr6:112157418 | C | A | 5 | a0001c0011t0003g0236 a0001c0020t0005g0046 a0001c0020t0005g0168 others(2): Show |
5 | HG01891.hp2 HG02895.hp1 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.1817+1314G>T | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 14/38 | chr6 | 112157418 | |||||||
chr6:112157419 | A | C | 1 | a0004c0057t0003g0017 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1817+1313T>G | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 14/38 | chr6 | 112157419 | |||||||
chr6:112157444 | C | T | 1 | a0008c0031t0001g0056 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1817+1288G>A | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 14/38 | chr6 | 112157444 | |||||||
chr6:112157535 | A | G | 110 | a0001c0001t0001g0033 a0001c0001t0001g0116 a0001c0001t0011g0229 others(107): Show |
110 | HG00099.hp2 HG00280.hp1 HG00642.hp1 others(107): Show |
intron_variant | MODIFIER | c.1817+1197T>C | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 14/38 | chr6 | 112157535 | |||||||
chr6:112157595 | C | T | 83 | a0001c0001t0001g0033 a0001c0001t0001g0116 a0001c0001t0011g0229 others(80): Show |
83 | HG00099.hp2 HG00280.hp1 HG00642.hp1 others(80): Show |
intron_variant | MODIFIER | c.1817+1137G>A | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 14/38 | chr6 | 112157595 | |||||||
chr6:112157712 | A | C | 2 | a0001c0002t0001g0076 a0001c0002t0001g0197 |
2 | HG01081.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.1817+1020T>G | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 14/38 | chr6 | 112157712 | |||||||
chr6:112157746 | G | A | 1 | a0008c0031t0001g0056 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1817+986C>T | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 14/38 | chr6 | 112157746 | |||||||
chr6:112157763 | T | C | 1 | a0003c0018t0002g0038 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1817+969A>G | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 14/38 | chr6 | 112157763 | |||||||
chr6:112157790 | T | C | 1 | a0008c0031t0001g0056 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1817+942A>G | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 14/38 | chr6 | 112157790 | |||||||
chr6:112157839 | T | C | 277 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0015 others(274): Show |
277 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(274): Show |
intron_variant | MODIFIER | c.1817+893A>G | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 14/38 | chr6 | 112157839 | |||||||
chr6:112157860 | C | A | 1 | a0001c0001t0001g0227 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1817+872G>T | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 14/38 | chr6 | 112157860 | |||||||
chr6:112157860 | C | T | 1 | a0007c0014t0002g0019 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1817+872G>A | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 14/38 | chr6 | 112157860 | |||||||
chr6:112157892 | C | G | 1 | a0001c0002t0001g0107 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1817+840G>C | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 14/38 | chr6 | 112157892 | |||||||
chr6:112158086 | T | G | 1 | a0001c0002t0001g0279 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.1817+646A>C | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 14/38 | chr6 | 112158086 | |||||||
chr6:112158166 | C | G | 6 | a0004c0010t0004g0129 a0005c0008t0001g0026 a0005c0008t0004g0040 others(3): Show |
6 | HG00642.hp2 HG01168.hp1 HG01175.hp2 others(3): Show |
intron_variant | MODIFIER | c.1817+566G>C | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 14/38 | chr6 | 112158166 | |||||||
chr6:112158372 | T | C | 7 | a0003c0018t0002g0038 a0007c0060t0002g0260 a0008c0015t0001g0058 others(4): Show |
7 | HG02647.hp2 HG02809.hp1 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.1817+360A>G | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 14/38 | chr6 | 112158372 | |||||||
chr6:112158540 | A | ACAAC | 80 | a0001c0001t0001g0116 a0001c0001t0011g0229 a0001c0002t0001g0192 others(77): Show |
80 | HG00099.hp2 HG00280.hp1 HG00642.hp1 others(77): Show |
intron_variant | MODIFIER | c.1817+188_1817+191d others(6): Show |
LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 14/38 | chr6 | 112158540 | |||||||
chr6:112158582 | A | G | 1 | a0002c0003t0006g0001 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1817+150T>C | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 14/38 | chr6 | 112158582 | |||||||
chr6:112158621 | C | T | 1 | a0005c0045t0007g0039 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1817+111G>A | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 14/38 | chr6 | 112158621 | |||||||
chr6:112158690 | C | T | 5 | a0001c0002t0001g0076 a0001c0002t0001g0197 a0001c0054t0001g0301 others(2): Show |
5 | HG01081.hp2 HG01243.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.1817+42G>A | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 14/38 | chr6 | 112158690 | |||||||
chr6:112159132 | TA | T | 82 | a0001c0001t0001g0116 a0001c0001t0011g0229 a0001c0002t0001g0192 others(79): Show |
82 | HG00099.hp2 HG00280.hp1 HG00642.hp1 others(79): Show |
intron_variant | MODIFIER | c.1669-253delT | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 13/38 | chr6 | 112159132 | |||||||
chr6:112159164 | CAT | C | 19 | a0001c0001t0001g0136 a0001c0001t0001g0187 a0001c0001t0001g0237 others(16): Show |
19 | HG00280.hp2 HG00408.hp1 HG00597.hp2 others(16): Show |
intron_variant | MODIFIER | c.1669-286_1669-285d others(4): Show |
LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 13/38 | chr6 | 112159164 | |||||||
chr6:112159215 | T | C | 5 | a0001c0002t0001g0076 a0001c0002t0001g0197 a0001c0054t0001g0301 others(2): Show |
5 | HG01081.hp2 HG01243.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.1669-335A>G | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 13/38 | chr6 | 112159215 | |||||||
chr6:112159259 | C | T | 7 | a0003c0018t0002g0038 a0007c0060t0002g0260 a0008c0015t0001g0058 others(4): Show |
7 | HG02647.hp2 HG02809.hp1 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.1669-379G>A | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 13/38 | chr6 | 112159259 | |||||||
chr6:112159321 | A | T | 82 | a0001c0001t0001g0116 a0001c0001t0011g0229 a0001c0002t0001g0192 others(79): Show |
82 | HG00099.hp2 HG00280.hp1 HG00642.hp1 others(79): Show |
intron_variant | MODIFIER | c.1669-441T>A | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 13/38 | chr6 | 112159321 | |||||||
chr6:112159328 | G | GTTAAC | 168 | a0001c0001t0001g0033 a0001c0001t0001g0050 a0001c0001t0001g0051 others(165): Show |
168 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(165): Show |
intron_variant | MODIFIER | c.1669-449_1669-448i others(7): Show |
LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 13/38 | chr6 | 112159328 | |||||||
chr6:112159490 | G | A | 22 | a0001c0011t0003g0298 a0001c0022t0002g0146 a0003c0018t0002g0038 others(19): Show |
22 | HG02074.hp2 HG02129.hp1 HG02257.hp1 others(19): Show |
intron_variant | MODIFIER | c.1669-610C>T | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 13/38 | chr6 | 112159490 | |||||||
chr6:112159497 | T | C | 84 | a0001c0001t0001g0116 a0001c0001t0011g0229 a0001c0002t0001g0076 others(81): Show |
84 | HG00099.hp2 HG00280.hp1 HG00642.hp1 others(81): Show |
intron_variant | MODIFIER | c.1669-617A>G | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 13/38 | chr6 | 112159497 | |||||||
chr6:112159498 | G | A | 84 | a0001c0001t0001g0116 a0001c0001t0011g0229 a0001c0002t0001g0076 others(81): Show |
84 | HG00099.hp2 HG00280.hp1 HG00642.hp1 others(81): Show |
intron_variant | MODIFIER | c.1669-618C>T | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 13/38 | chr6 | 112159498 | |||||||
chr6:112159558 | CAA | C | 3 | a0002c0003t0002g0066 a0002c0024t0001g0147 a0004c0057t0003g0017 |
3 | HG02080.hp1 NA18942.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.1669-680_1669-679d others(4): Show |
LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 13/38 | chr6 | 112159558 | |||||||
chr6:112159623 | A | T | 15 | a0001c0011t0003g0298 a0001c0022t0002g0146 a0004c0007t0001g0201 others(12): Show |
15 | HG02074.hp2 HG02129.hp1 HG02257.hp1 others(12): Show |
intron_variant | MODIFIER | c.1669-743T>A | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 13/38 | chr6 | 112159623 | |||||||
chr6:112159726 | C | T | 1 | a0003c0004t0001g0028 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1669-846G>A | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 13/38 | chr6 | 112159726 | |||||||
chr6:112160035 | A | C | 15 | a0001c0002t0001g0076 a0001c0002t0001g0192 a0001c0002t0001g0197 others(12): Show |
15 | HG01081.hp2 HG01891.hp1 HG02055.hp1 others(12): Show |
intron_variant | MODIFIER | c.1669-1155T>G | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 13/38 | chr6 | 112160035 | |||||||
chr6:112160246 | C | A | 2 | a0003c0018t0002g0038 a0007c0060t0002g0260 |
2 | HG02809.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.1669-1366G>T | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 13/38 | chr6 | 112160246 | |||||||
chr6:112160443 | AAAAC | A | 73 | a0001c0001t0001g0116 a0001c0001t0011g0229 a0001c0002t0001g0076 others(70): Show |
73 | HG00099.hp2 HG00280.hp1 HG00642.hp1 others(70): Show |
intron_variant | MODIFIER | c.1669-1567_1669-156 others(8): Show |
LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 13/38 | chr6 | 112160443 | |||||||
chr6:112160443 | AAAACAAA others(1): Show |
A | 21 | a0001c0011t0003g0298 a0001c0022t0002g0146 a0003c0018t0002g0038 others(18): Show |
21 | HG02074.hp2 HG02129.hp1 HG02257.hp1 others(18): Show |
intron_variant | MODIFIER | c.1669-1571_1669-156 others(12): Show |
LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 13/38 | chr6 | 112160443 | |||||||
chr6:112160459 | C | T | 1 | a0002c0003t0002g0198 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1669-1579G>A | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 13/38 | chr6 | 112160459 | |||||||
chr6:112160735 | C | T | 1 | a0001c0011t0003g0009 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1669-1855G>A | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 13/38 | chr6 | 112160735 | |||||||
chr6:112160748 | A | G | 49 | a0001c0001t0001g0167 a0001c0002t0001g0020 a0001c0002t0001g0045 others(46): Show |
49 | HG00741.hp1 HG01081.hp2 HG02055.hp1 others(46): Show |
intron_variant | MODIFIER | c.1669-1868T>C | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 13/38 | chr6 | 112160748 | |||||||
chr6:112160861 | A | C | 1 | a0001c0011t0003g0313 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1669-1981T>G | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 13/38 | chr6 | 112160861 | |||||||
chr6:112160907 | T | C | 3 | a0001c0011t0003g0236 a0001c0052t0002g0295 a0004c0057t0003g0017 |
3 | HG02922.hp1 HG02976.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.1669-2027A>G | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 13/38 | chr6 | 112160907 | |||||||
chr6:112160907 | T | G | 17 | a0001c0002t0001g0278 a0001c0011t0003g0298 a0001c0022t0002g0146 others(14): Show |
17 | HG02074.hp2 HG02129.hp1 HG02132.hp1 others(14): Show |
intron_variant | MODIFIER | c.1669-2027A>C | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 13/38 | chr6 | 112160907 | |||||||
chr6:112160945 | T | C | 1 | a0011c0028t0002g0154 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1669-2065A>G | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 13/38 | chr6 | 112160945 | |||||||
chr6:112160958 | G | A | 1 | a0001c0001t0001g0050 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.1669-2078C>T | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 13/38 | chr6 | 112160958 | |||||||
chr6:112161061 | T | A | 2 | a0008c0031t0001g0056 a0011c0028t0002g0159 |
2 | HG01243.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.1669-2181A>T | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 13/38 | chr6 | 112161061 | |||||||
chr6:112161119 | C | T | 13 | a0001c0001t0001g0167 a0001c0002t0001g0047 a0001c0002t0001g0107 others(10): Show |
13 | HG00280.hp1 HG01256.hp2 HG01258.hp1 others(10): Show |
intron_variant | MODIFIER | c.1669-2239G>A | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 13/38 | chr6 | 112161119 | |||||||
chr6:112161190 | C | T | 1 | a0001c0002t0001g0213 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.1669-2310G>A | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 13/38 | chr6 | 112161190 | |||||||
chr6:112161235 | T | C | 1 | a0001c0001t0001g0285 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.1669-2355A>G | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 13/38 | chr6 | 112161235 | |||||||
chr6:112161308 | A | G | 4 | a0001c0002t0001g0254 a0002c0006t0002g0170 a0002c0006t0002g0249 others(1): Show |
4 | HG00741.hp1 HG02622.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.1669-2428T>C | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 13/38 | chr6 | 112161308 | |||||||
chr6:112161524 | A | G | 1 | a0002c0006t0002g0133 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.1669-2644T>C | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 13/38 | chr6 | 112161524 | |||||||
chr6:112161546 | T | C | 1 | a0002c0003t0002g0305 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1669-2666A>G | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 13/38 | chr6 | 112161546 | |||||||
chr6:112161745 | T | C | 1 | a0002c0003t0002g0071 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.1669-2865A>G | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 13/38 | chr6 | 112161745 | |||||||
chr6:112161989 | A | C | 1 | a0008c0015t0001g0061 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1669-3109T>G | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 13/38 | chr6 | 112161989 | |||||||
chr6:112162033 | G | A | 204 | a0001c0001t0001g0007 a0001c0001t0001g0014 a0001c0001t0001g0027 others(201): Show |
204 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(201): Show |
intron_variant | MODIFIER | c.1668+3127C>T | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 13/38 | chr6 | 112162033 | |||||||
chr6:112162070 | A | T | 1 | a0003c0004t0001g0291 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.1668+3090T>A | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 13/38 | chr6 | 112162070 | |||||||
chr6:112162084 | T | C | 1 | a0004c0010t0001g0284 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.1668+3076A>G | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 13/38 | chr6 | 112162084 | |||||||
chr6:112162191 | CCTG | C | 14 | a0001c0002t0001g0192 a0001c0011t0003g0062 a0001c0011t0003g0155 others(11): Show |
14 | HG02109.hp1 HG02109.hp2 HG02145.hp2 others(11): Show |
intron_variant | MODIFIER | c.1668+2966_1668+296 others(7): Show |
LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 13/38 | chr6 | 112162191 | |||||||
chr6:112162209 | G | A | 204 | a0001c0001t0001g0007 a0001c0001t0001g0014 a0001c0001t0001g0027 others(201): Show |
204 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(201): Show |
intron_variant | MODIFIER | c.1668+2951C>T | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 13/38 | chr6 | 112162209 | |||||||
chr6:112162467 | C | T | 193 | a0001c0001t0001g0007 a0001c0001t0001g0027 a0001c0001t0001g0033 others(190): Show |
193 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(190): Show |
intron_variant | MODIFIER | c.1668+2693G>A | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 13/38 | chr6 | 112162467 | |||||||
chr6:112162616 | G | A | 7 | a0001c0002t0001g0076 a0001c0002t0001g0197 a0001c0050t0001g0310 others(4): Show |
7 | HG01081.hp2 HG02886.hp1 HG02976.hp1 others(4): Show |
intron_variant | MODIFIER | c.1668+2544C>T | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 13/38 | chr6 | 112162616 | |||||||
chr6:112162642 | T | G | 1 | a0001c0050t0001g0310 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1668+2518A>C | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 13/38 | chr6 | 112162642 | |||||||
chr6:112162713 | G | A | 203 | a0001c0001t0001g0007 a0001c0001t0001g0014 a0001c0001t0001g0027 others(200): Show |
203 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(200): Show |
intron_variant | MODIFIER | c.1668+2447C>T | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 13/38 | chr6 | 112162713 | |||||||
chr6:112162715 | C | A | 1 | a0004c0007t0001g0189 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.1668+2445G>T | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 13/38 | chr6 | 112162715 | |||||||
chr6:112162965 | C | CT | 23 | a0001c0001t0001g0007 a0001c0001t0001g0116 a0001c0001t0001g0222 others(20): Show |
23 | HG00597.hp1 HG00621.hp1 HG01496.hp1 others(20): Show |
intron_variant | MODIFIER | c.1668+2194dupA | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 13/38 | chr6 | 112162965 | |||||||
chr6:112162965 | C | CTTTTTTT others(7): Show |
1 | a0002c0006t0002g0303 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1668+2181_1668+219 others(18): Show |
LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 13/38 | chr6 | 112162965 | |||||||
chr6:112162965 | C | CTTTTTTT others(8): Show |
4 | a0001c0011t0003g0009 a0002c0006t0002g0037 a0002c0006t0002g0199 others(1): Show |
4 | HG01981.hp2 HG02055.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.1668+2180_1668+219 others(19): Show |
LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 13/38 | chr6 | 112162965 | |||||||
chr6:112162965 | CT | C | 78 | a0001c0001t0001g0008 a0001c0001t0001g0015 a0001c0001t0001g0016 others(75): Show |
78 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(75): Show |
intron_variant | MODIFIER | c.1668+2194delA | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 13/38 | chr6 | 112162965 | |||||||
chr6:112162965 | CTT | C | 13 | a0001c0016t0002g0268 a0001c0023t0003g0306 a0001c0037t0003g0003 others(10): Show |
13 | HG02647.hp2 HG02818.hp2 HG02886.hp2 others(10): Show |
intron_variant | MODIFIER | c.1668+2193_1668+219 others(6): Show |
LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 13/38 | chr6 | 112162965 | |||||||
chr6:112162965 | CTTTTTTT others(1): Show |
C | 14 | a0001c0002t0001g0192 a0001c0011t0003g0062 a0001c0011t0003g0155 others(11): Show |
14 | HG02109.hp1 HG02109.hp2 HG02145.hp2 others(11): Show |
intron_variant | MODIFIER | c.1668+2187_1668+219 others(12): Show |
LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 13/38 | chr6 | 112162965 | |||||||
chr6:112163034 | C | T | 1 | a0001c0002t0001g0047 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1668+2126G>A | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 13/38 | chr6 | 112163034 | |||||||
chr6:112163149 | A | T | 189 | a0001c0001t0001g0007 a0001c0001t0001g0027 a0001c0001t0001g0033 others(186): Show |
189 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(186): Show |
intron_variant | MODIFIER | c.1668+2011T>A | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 13/38 | chr6 | 112163149 | |||||||
chr6:112163150 | T | A | 2 | a0001c0011t0003g0236 a0004c0007t0001g0157 |
2 | HG02559.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.1668+2010A>T | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 13/38 | chr6 | 112163150 | |||||||
chr6:112163167 | A | AG | 206 | a0001c0001t0001g0007 a0001c0001t0001g0014 a0001c0001t0001g0027 others(203): Show |
206 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(203): Show |
intron_variant | MODIFIER | c.1668+1992dupC | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 13/38 | chr6 | 112163167 | |||||||
chr6:112163227 | C | T | 1 | a0001c0002t0001g0191 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.1668+1933G>A | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 13/38 | chr6 | 112163227 | |||||||
chr6:112163326 | TAAAAAAA others(24): Show |
T | 3 | a0007c0060t0002g0260 a0008c0031t0001g0056 a0022c0032t0001g0060 |
3 | HG02809.hp1 HG03139.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1668+1803_1668+183 others(35): Show |
LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 13/38 | chr6 | 112163326 | |||||||
chr6:112163470 | G | T | 1 | a0011c0028t0002g0159 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1668+1690C>A | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 13/38 | chr6 | 112163470 | |||||||
chr6:112163641 | G | C | 1 | a0001c0005t0001g0137 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.1668+1519C>G | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 13/38 | chr6 | 112163641 | |||||||
chr6:112163820 | A | G | 1 | a0001c0011t0003g0255 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1668+1340T>C | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 13/38 | chr6 | 112163820 | |||||||
chr6:112163964 | G | A | 96 | a0001c0001t0001g0007 a0001c0001t0001g0027 a0001c0001t0001g0033 others(93): Show |
96 | HG00280.hp2 HG00597.hp1 HG00642.hp1 others(93): Show |
intron_variant | MODIFIER | c.1668+1196C>T | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 13/38 | chr6 | 112163964 | |||||||
chr6:112164596 | C | A | 220 | a0001c0001t0001g0007 a0001c0001t0001g0014 a0001c0001t0001g0027 others(217): Show |
220 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(217): Show |
intron_variant | MODIFIER | c.1668+564G>T | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 13/38 | chr6 | 112164596 | |||||||
chr6:112164672 | A | G | 16 | a0001c0002t0001g0020 a0001c0011t0003g0009 a0001c0020t0005g0168 others(13): Show |
16 | HG01167.hp1 HG01169.hp1 HG01981.hp2 others(13): Show |
intron_variant | MODIFIER | c.1668+488T>C | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 13/38 | chr6 | 112164672 | |||||||
chr6:112165005 | T | A | 4 | a0001c0002t0001g0076 a0001c0002t0001g0197 a0004c0007t0001g0201 others(1): Show |
4 | HG01081.hp2 HG01243.hp1 HG02572.hp2 others(1): Show |
intron_variant | MODIFIER | c.1668+155A>T | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 13/38 | chr6 | 112165005 | |||||||
chr6:112165010 | G | A | 2 | a0001c0020t0005g0168 a0001c0020t0005g0169 |
2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.1668+150C>T | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 13/38 | chr6 | 112165010 | |||||||
chr6:112165314 | T | C | 2 | a0003c0025t0001g0086 a0003c0025t0001g0113 |
2 | HG02886.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.1552-38A>G | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 12/38 | chr6 | 112165314 | |||||||
chr6:112165376 | A | G | 1 | a0001c0001t0001g0053 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.1552-100T>C | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 12/38 | chr6 | 112165376 | |||||||
chr6:112165441 | G | T | 1 | a0024c0041t0001g0183 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.1552-165C>A | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 12/38 | chr6 | 112165441 | |||||||
chr6:112165545 | C | T | 3 | a0001c0020t0005g0168 a0001c0020t0005g0169 a0001c0054t0001g0301 |
3 | HG02895.hp1 HG02897.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.1552-269G>A | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 12/38 | chr6 | 112165545 | |||||||
chr6:112165869 | C | A | 1 | a0004c0007t0001g0201 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1552-593G>T | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 12/38 | chr6 | 112165869 | |||||||
chr6:112166114 | G | A | 5 | a0001c0002t0001g0020 a0001c0050t0001g0310 a0004c0026t0001g0067 others(2): Show |
5 | HG01167.hp1 HG01169.hp1 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.1552-838C>T | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 12/38 | chr6 | 112166114 | |||||||
chr6:112166307 | C | T | 1 | a0003c0058t0001g0210 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1552-1031G>A | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 12/38 | chr6 | 112166307 | |||||||
chr6:112166359 | C | G | 1 | a0007c0014t0002g0119 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.1552-1083G>C | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 12/38 | chr6 | 112166359 | |||||||
chr6:112166466 | G | T | 2 | a0001c0016t0002g0268 a0004c0007t0014g0300 |
2 | NA18971.hp1 NA19070.hp2 |
intron_variant | MODIFIER | c.1552-1190C>A | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 12/38 | chr6 | 112166466 | |||||||
chr6:112166516 | T | C | 4 | a0001c0002t0001g0076 a0001c0002t0001g0197 a0004c0007t0001g0201 others(1): Show |
4 | HG01081.hp2 HG01243.hp1 HG02572.hp2 others(1): Show |
intron_variant | MODIFIER | c.1552-1240A>G | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 12/38 | chr6 | 112166516 | |||||||
chr6:112166532 | T | C | 1 | a0010c0029t0001g0034 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.1552-1256A>G | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 12/38 | chr6 | 112166532 | |||||||
chr6:112166566 | C | T | 2 | a0001c0005t0001g0286 a0002c0006t0002g0294 |
2 | NA19000.hp2 NA19002.hp1 |
intron_variant | MODIFIER | c.1552-1290G>A | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 12/38 | chr6 | 112166566 | |||||||
chr6:112166627 | A | G | 3 | a0001c0020t0005g0168 a0001c0020t0005g0169 a0001c0054t0001g0301 |
3 | HG02895.hp1 HG02897.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.1552-1351T>C | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 12/38 | chr6 | 112166627 | |||||||
chr6:112166694 | T | A | 1 | a0006c0012t0002g0150 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.1552-1418A>T | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 12/38 | chr6 | 112166694 | |||||||
chr6:112166698 | G | A | 112 | a0001c0001t0001g0007 a0001c0001t0001g0014 a0001c0001t0001g0027 others(109): Show |
112 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(109): Show |
intron_variant | MODIFIER | c.1552-1422C>T | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 12/38 | chr6 | 112166698 | |||||||
chr6:112166799 | T | C | 98 | a0001c0001t0001g0007 a0001c0001t0001g0014 a0001c0001t0001g0027 others(95): Show |
98 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(95): Show |
intron_variant | MODIFIER | c.1552-1523A>G | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 12/38 | chr6 | 112166799 | |||||||
chr6:112166915 | G | A | 98 | a0001c0001t0001g0007 a0001c0001t0001g0014 a0001c0001t0001g0027 others(95): Show |
98 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(95): Show |
intron_variant | MODIFIER | c.1552-1639C>T | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 12/38 | chr6 | 112166915 | |||||||
chr6:112167028 | G | A | 1 | a0004c0010t0004g0129 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.1552-1752C>T | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 12/38 | chr6 | 112167028 | |||||||
chr6:112167042 | T | A | 109 | a0001c0001t0001g0007 a0001c0001t0001g0014 a0001c0001t0001g0027 others(106): Show |
109 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(106): Show |
intron_variant | MODIFIER | c.1552-1766A>T | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 12/38 | chr6 | 112167042 | |||||||
chr6:112167160 | T | C | 3 | a0001c0020t0005g0168 a0001c0020t0005g0169 a0001c0054t0001g0301 |
3 | HG02895.hp1 HG02897.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.1552-1884A>G | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 12/38 | chr6 | 112167160 | |||||||
chr6:112167368 | C | T | 2 | a0001c0005t0001g0043 a0001c0005t0001g0044 |
2 | NA18947.hp2 NA19086.hp1 |
intron_variant | MODIFIER | c.1552-2092G>A | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 12/38 | chr6 | 112167368 | |||||||
chr6:112167582 | G | A | 6 | a0001c0011t0003g0009 a0002c0006t0002g0037 a0002c0006t0002g0199 others(3): Show |
6 | HG01981.hp2 HG02055.hp1 HG03453.hp2 others(3): Show |
intron_variant | MODIFIER | c.1552-2306C>T | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 12/38 | chr6 | 112167582 | |||||||
chr6:112167647 | G | A | 1 | a0001c0001t0001g0186 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.1552-2371C>T | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 12/38 | chr6 | 112167647 | |||||||
chr6:112167747 | T | C | 107 | a0001c0001t0001g0007 a0001c0001t0001g0014 a0001c0001t0001g0027 others(104): Show |
107 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(104): Show |
intron_variant | MODIFIER | c.1552-2471A>G | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 12/38 | chr6 | 112167747 | |||||||
chr6:112167801 | A | T | 1 | a0003c0004t0001g0028 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1552-2525T>A | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 12/38 | chr6 | 112167801 | |||||||
chr6:112167840 | T | TCA | 19 | a0001c0001t0001g0050 a0001c0001t0001g0053 a0001c0001t0001g0219 others(16): Show |
19 | HG00741.hp1 HG01081.hp2 HG01123.hp2 others(16): Show |
intron_variant | MODIFIER | c.1552-2566_1552-256 others(6): Show |
LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 12/38 | chr6 | 112167840 | |||||||
chr6:112167840 | T | TCACA | 10 | a0001c0001t0001g0115 a0001c0001t0001g0220 a0001c0001t0001g0227 others(7): Show |
10 | HG01168.hp1 HG01168.hp2 HG01169.hp2 others(7): Show |
intron_variant | MODIFIER | c.1552-2568_1552-256 others(8): Show |
LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 12/38 | chr6 | 112167840 | |||||||
chr6:112167840 | TCA | T | 21 | a0001c0001t0001g0008 a0001c0001t0001g0095 a0001c0002t0001g0192 others(18): Show |
21 | HG00099.hp1 HG01071.hp2 HG01106.hp2 others(18): Show |
intron_variant | MODIFIER | c.1552-2566_1552-256 others(6): Show |
LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 12/38 | chr6 | 112167840 | |||||||
chr6:112167840 | TCACA | T | 43 | a0001c0001t0001g0042 a0001c0001t0001g0149 a0001c0001t0001g0187 others(40): Show |
43 | HG00621.hp2 HG00673.hp1 HG01074.hp1 others(40): Show |
intron_variant | MODIFIER | c.1552-2568_1552-256 others(8): Show |
LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 12/38 | chr6 | 112167840 | |||||||
chr6:112167840 | TCACACA | T | 34 | a0001c0002t0001g0045 a0001c0002t0001g0047 a0001c0002t0001g0109 others(31): Show |
34 | HG00323.hp1 HG00597.hp2 HG02015.hp2 others(31): Show |
intron_variant | MODIFIER | c.1552-2570_1552-256 others(10): Show |
LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 12/38 | chr6 | 112167840 | |||||||
chr6:112167840 | TCACACAC others(1): Show |
T | 25 | a0001c0001t0001g0222 a0001c0002t0001g0279 a0001c0005t0001g0044 others(22): Show |
25 | HG00408.hp2 HG02015.hp1 HG02155.hp1 others(22): Show |
intron_variant | MODIFIER | c.1552-2572_1552-256 others(12): Show |
LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 12/38 | chr6 | 112167840 | |||||||
chr6:112167840 | TCACACAC others(3): Show |
T | 42 | a0001c0001t0001g0015 a0001c0001t0001g0033 a0001c0001t0001g0204 others(39): Show |
42 | HG00642.hp2 HG01167.hp1 HG01169.hp1 others(39): Show |
intron_variant | MODIFIER | c.1552-2574_1552-256 others(14): Show |
LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 12/38 | chr6 | 112167840 | |||||||
chr6:112167840 | TCACACAC others(5): Show |
T | 73 | a0001c0001t0001g0007 a0001c0001t0001g0014 a0001c0001t0001g0027 others(70): Show |
73 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(70): Show |
intron_variant | MODIFIER | c.1552-2576_1552-256 others(16): Show |
LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 12/38 | chr6 | 112167840 | |||||||
chr6:112167840 | TCACACAC others(7): Show |
T | 8 | a0001c0002t0001g0164 a0001c0002t0001g0165 a0001c0020t0005g0046 others(5): Show |
8 | HG00099.hp2 HG01891.hp2 HG01981.hp2 others(5): Show |
intron_variant | MODIFIER | c.1552-2578_1552-256 others(18): Show |
LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 12/38 | chr6 | 112167840 | |||||||
chr6:112167840 | TCACACAC others(9): Show |
T | 4 | a0002c0003t0006g0001 a0002c0003t0006g0002 a0002c0006t0002g0303 others(1): Show |
4 | HG02809.hp2 HG02818.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.1552-2580_1552-256 others(20): Show |
LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 12/38 | chr6 | 112167840 | |||||||
chr6:112167840 | TCACACAC others(11): Show |
T | 1 | a0001c0011t0003g0009 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1552-2582_1552-256 others(22): Show |
LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 12/38 | chr6 | 112167840 | |||||||
chr6:112167840 | TCACACAC others(13): Show |
T | 1 | a0005c0008t0001g0262 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1552-2584_1552-256 others(24): Show |
LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 12/38 | chr6 | 112167840 | |||||||
chr6:112167968 | G | A | 1 | a0004c0010t0001g0284 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.1552-2692C>T | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 12/38 | chr6 | 112167968 | |||||||
chr6:112167974 | G | A | 6 | a0001c0011t0003g0009 a0002c0006t0002g0037 a0002c0006t0002g0199 others(3): Show |
6 | HG01981.hp2 HG02055.hp1 HG03453.hp2 others(3): Show |
intron_variant | MODIFIER | c.1552-2698C>T | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 12/38 | chr6 | 112167974 | |||||||
chr6:112168013 | C | A | 1 | a0008c0031t0001g0056 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1552-2737G>T | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 12/38 | chr6 | 112168013 | |||||||
chr6:112168048 | A | G | 8 | a0001c0001t0001g0050 a0001c0001t0001g0051 a0001c0001t0001g0052 others(5): Show |
8 | HG01074.hp2 HG01243.hp2 HG01255.hp1 others(5): Show |
intron_variant | MODIFIER | c.1552-2772T>C | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 12/38 | chr6 | 112168048 | |||||||
chr6:112168105 | G | A | 1 | a0001c0011t0003g0313 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1552-2829C>T | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 12/38 | chr6 | 112168105 | |||||||
chr6:112168115 | A | G | 101 | a0001c0001t0001g0007 a0001c0001t0001g0014 a0001c0001t0001g0027 others(98): Show |
101 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(98): Show |
intron_variant | MODIFIER | c.1552-2839T>C | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 12/38 | chr6 | 112168115 | |||||||
chr6:112168116 | C | T | 112 | a0001c0001t0001g0007 a0001c0001t0001g0014 a0001c0001t0001g0027 others(109): Show |
112 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(109): Show |
intron_variant | MODIFIER | c.1552-2840G>A | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 12/38 | chr6 | 112168116 | |||||||
chr6:112168152 | C | T | 1 | a0001c0002t0001g0107 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1552-2876G>A | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 12/38 | chr6 | 112168152 | |||||||
chr6:112168153 | G | A | 12 | a0001c0002t0001g0076 a0001c0002t0001g0197 a0001c0011t0003g0009 others(9): Show |
12 | HG01081.hp2 HG01243.hp1 HG01981.hp2 others(9): Show |
intron_variant | MODIFIER | c.1552-2877C>T | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 12/38 | chr6 | 112168153 | |||||||
chr6:112168193 | G | A | 1 | a0001c0005t0001g0092 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.1552-2917C>T | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 12/38 | chr6 | 112168193 | |||||||
chr6:112168197 | C | CA | 8 | a0001c0001t0001g0027 a0001c0002t0001g0254 a0003c0018t0001g0089 others(5): Show |
8 | HG00741.hp1 HG02145.hp2 HG02698.hp2 others(5): Show |
intron_variant | MODIFIER | c.1552-2922dupT | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 12/38 | chr6 | 112168197 | |||||||
chr6:112168197 | CA | C | 9 | a0001c0002t0001g0076 a0001c0002t0001g0197 a0001c0011t0003g0161 others(6): Show |
9 | HG01081.hp2 HG01243.hp1 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.1552-2922delT | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 12/38 | chr6 | 112168197 | |||||||
chr6:112168244 | A | T | 101 | a0001c0001t0001g0007 a0001c0001t0001g0014 a0001c0001t0001g0027 others(98): Show |
101 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(98): Show |
intron_variant | MODIFIER | c.1552-2968T>A | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 12/38 | chr6 | 112168244 | |||||||
chr6:112168295 | T | C | 2 | a0001c0016t0002g0268 a0004c0007t0014g0300 |
2 | NA18971.hp1 NA19070.hp2 |
intron_variant | MODIFIER | c.1552-3019A>G | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 12/38 | chr6 | 112168295 | |||||||
chr6:112168345 | C | CTT | 11 | a0001c0002t0001g0076 a0001c0002t0001g0197 a0001c0011t0003g0009 others(8): Show |
11 | HG01081.hp2 HG01243.hp1 HG01981.hp2 others(8): Show |
intron_variant | MODIFIER | c.1552-3071_1552-307 others(6): Show |
LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 12/38 | chr6 | 112168345 | |||||||
chr6:112168345 | C | CTTT | 84 | a0001c0001t0001g0014 a0001c0001t0001g0027 a0001c0001t0001g0069 others(81): Show |
84 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(81): Show |
intron_variant | MODIFIER | c.1552-3072_1552-307 others(7): Show |
LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 12/38 | chr6 | 112168345 | |||||||
chr6:112168345 | C | CTTTT | 9 | a0001c0001t0001g0007 a0001c0001t0001g0033 a0001c0001t0001g0116 others(6): Show |
9 | HG00597.hp1 HG01081.hp1 HG01433.hp2 others(6): Show |
intron_variant | MODIFIER | c.1552-3073_1552-307 others(8): Show |
LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 12/38 | chr6 | 112168345 | |||||||
chr6:112168354 | T | C | 3 | a0001c0005t0001g0101 a0001c0005t0001g0230 a0002c0006t0002g0088 |
3 | HG01106.hp2 HG01167.hp2 HG03017.hp1 |
intron_variant | MODIFIER | c.1552-3078A>G | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 12/38 | chr6 | 112168354 | |||||||
chr6:112168440 | G | T | 2 | a0002c0006t0002g0173 a0002c0006t0002g0190 |
2 | NA18943.hp2 NA19066.hp1 |
intron_variant | MODIFIER | c.1552-3164C>A | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 12/38 | chr6 | 112168440 | |||||||
chr6:112168497 | C | G | 1 | a0001c0016t0001g0048 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1552-3221G>C | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 12/38 | chr6 | 112168497 | |||||||
chr6:112168582 | G | A | 2 | a0001c0002t0001g0020 a0011c0028t0002g0154 |
2 | HG02622.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.1552-3306C>T | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 12/38 | chr6 | 112168582 | |||||||
chr6:112168846 | G | C | 3 | a0001c0020t0005g0168 a0001c0020t0005g0169 a0001c0054t0001g0301 |
3 | HG02895.hp1 HG02897.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.1552-3570C>G | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 12/38 | chr6 | 112168846 | |||||||
chr6:112168862 | G | A | 3 | a0001c0002t0001g0205 a0001c0002t0001g0253 a0001c0052t0002g0295 |
3 | HG02922.hp2 HG02976.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.1552-3586C>T | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 12/38 | chr6 | 112168862 | |||||||
chr6:112168959 | A | G | 1 | a0004c0057t0003g0017 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1551+3652T>C | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 12/38 | chr6 | 112168959 | |||||||
chr6:112169329 | A | G | 236 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0014 others(233): Show |
236 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(233): Show |
intron_variant | MODIFIER | c.1551+3282T>C | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 12/38 | chr6 | 112169329 | |||||||
chr6:112169770 | C | T | 1 | a0001c0002t0001g0188 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1551+2841G>A | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 12/38 | chr6 | 112169770 | |||||||
chr6:112170341 | C | T | 1 | a0002c0003t0002g0182 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.1551+2270G>A | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 12/38 | chr6 | 112170341 | |||||||
chr6:112170453 | T | C | 1 | a0001c0011t0003g0293 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1551+2158A>G | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 12/38 | chr6 | 112170453 | |||||||
chr6:112170907 | C | T | 2 | a0001c0002t0001g0253 a0001c0052t0002g0295 |
2 | HG02922.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.1551+1704G>A | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 12/38 | chr6 | 112170907 | |||||||
chr6:112170913 | C | T | 6 | a0001c0005t0001g0043 a0001c0005t0001g0044 a0001c0005t0001g0235 others(3): Show |
6 | NA18943.hp2 NA18946.hp1 NA18947.hp2 others(3): Show |
intron_variant | MODIFIER | c.1551+1698G>A | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 12/38 | chr6 | 112170913 | |||||||
chr6:112171124 | A | C | 1 | a0008c0031t0001g0056 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1551+1487T>G | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 12/38 | chr6 | 112171124 | |||||||
chr6:112171134 | G | A | 4 | a0005c0008t0001g0231 a0012c0021t0001g0083 a0012c0021t0001g0144 others(1): Show |
4 | HG00621.hp2 NA18612.hp1 NA18948.hp1 others(1): Show |
intron_variant | MODIFIER | c.1551+1477C>T | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 12/38 | chr6 | 112171134 | |||||||
chr6:112171215 | CT | C | 8 | a0001c0002t0001g0006 a0001c0002t0001g0076 a0001c0002t0001g0164 others(5): Show |
8 | HG01081.hp2 HG01169.hp2 HG01243.hp1 others(5): Show |
intron_variant | MODIFIER | c.1551+1395delA | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 12/38 | chr6 | 112171215 | |||||||
chr6:112171239 | G | C | 5 | a0001c0001t0001g0050 a0001c0001t0001g0052 a0001c0001t0001g0055 others(2): Show |
5 | HG01243.hp2 HG01258.hp2 HG01358.hp2 others(2): Show |
intron_variant | MODIFIER | c.1551+1372C>G | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 12/38 | chr6 | 112171239 | |||||||
chr6:112171443 | A | G | 20 | a0003c0004t0001g0081 a0003c0004t0001g0125 a0003c0004t0001g0180 others(17): Show |
20 | HG00597.hp2 HG01358.hp1 HG02071.hp2 others(17): Show |
intron_variant | MODIFIER | c.1551+1168T>C | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 12/38 | chr6 | 112171443 | |||||||
chr6:112171553 | G | A | 1 | a0002c0003t0002g0077 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.1551+1058C>T | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 12/38 | chr6 | 112171553 | |||||||
chr6:112171661 | T | A | 6 | a0001c0023t0003g0306 a0001c0037t0003g0003 a0008c0015t0001g0058 others(3): Show |
6 | HG02647.hp2 HG02818.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.1551+950A>T | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 12/38 | chr6 | 112171661 | |||||||
chr6:112171677 | CA | C | 120 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0237 others(117): Show |
120 | HG00408.hp1 HG00408.hp2 HG00621.hp1 others(117): Show |
intron_variant | MODIFIER | c.1551+933delT | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 12/38 | chr6 | 112171677 | |||||||
chr6:112171677 | CAA | C | 120 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0016 others(117): Show |
120 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(117): Show |
intron_variant | MODIFIER | c.1551+932_1551+933d others(4): Show |
LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 12/38 | chr6 | 112171677 | |||||||
chr6:112172054 | C | T | 129 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0014 others(126): Show |
129 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(126): Show |
intron_variant | MODIFIER | c.1551+557G>A | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 12/38 | chr6 | 112172054 | |||||||
chr6:112172057 | C | T | 16 | a0001c0002t0001g0192 a0001c0002t0001g0254 a0001c0011t0003g0062 others(13): Show |
16 | HG00741.hp1 HG02109.hp1 HG02109.hp2 others(13): Show |
intron_variant | MODIFIER | c.1551+554G>A | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 12/38 | chr6 | 112172057 | |||||||
chr6:112172082 | G | A | 1 | a0002c0003t0002g0079 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.1551+529C>T | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 12/38 | chr6 | 112172082 | |||||||
chr6:112172119 | T | C | 1 | a0001c0020t0005g0046 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1551+492A>G | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 12/38 | chr6 | 112172119 | |||||||
chr6:112172160 | CTT | C | 16 | a0001c0002t0001g0192 a0001c0002t0001g0254 a0001c0011t0003g0062 others(13): Show |
16 | HG00741.hp1 HG02109.hp1 HG02109.hp2 others(13): Show |
intron_variant | MODIFIER | c.1551+449_1551+450d others(4): Show |
LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 12/38 | chr6 | 112172160 | |||||||
chr6:112172332 | C | T | 2 | a0001c0011t0003g0313 a0011c0028t0002g0154 |
2 | HG02622.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.1551+279G>A | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 12/38 | chr6 | 112172332 | |||||||
chr6:112172358 | C | G | 1 | a0012c0021t0001g0144 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.1551+253G>C | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 12/38 | chr6 | 112172358 | |||||||
chr6:112172366 | A | G | 1 | a0001c0005t0001g0043 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.1551+245T>C | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 12/38 | chr6 | 112172366 | |||||||
chr6:112172981 | T | C | 1 | a0002c0006t0002g0108 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.1358-177A>G | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 11/38 | chr6 | 112172981 | |||||||
chr6:112173273 | C | T | 2 | a0001c0022t0002g0012 a0004c0010t0001g0013 |
2 | HG02258.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.1358-469G>A | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 11/38 | chr6 | 112173273 | |||||||
chr6:112173560 | T | C | 2 | a0004c0026t0001g0067 a0004c0026t0001g0068 |
2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.1358-756A>G | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 11/38 | chr6 | 112173560 | |||||||
chr6:112173843 | A | G | 2 | a0001c0001t0001g0228 a0001c0001t0011g0229 |
2 | HG01515.hp2 HG02004.hp2 |
intron_variant | MODIFIER | c.1358-1039T>C | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 11/38 | chr6 | 112173843 | |||||||
chr6:112173878 | A | G | 6 | a0001c0023t0003g0306 a0001c0037t0003g0003 a0008c0015t0001g0058 others(3): Show |
6 | HG02818.hp2 HG02886.hp2 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.1358-1074T>C | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 11/38 | chr6 | 112173878 | |||||||
chr6:112173881 | C | T | 132 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0014 others(129): Show |
132 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(129): Show |
intron_variant | MODIFIER | c.1358-1077G>A | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 11/38 | chr6 | 112173881 | |||||||
chr6:112173985 | T | C | 6 | a0001c0002t0001g0076 a0001c0002t0001g0197 a0001c0011t0003g0161 others(3): Show |
6 | HG01081.hp2 HG01243.hp1 HG02257.hp1 others(3): Show |
intron_variant | MODIFIER | c.1358-1181A>G | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 11/38 | chr6 | 112173985 | |||||||
chr6:112174053 | T | G | 6 | a0001c0022t0002g0146 a0001c0023t0003g0302 a0008c0015t0001g0057 others(3): Show |
6 | HG02486.hp2 HG02523.hp1 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.1358-1249A>C | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 11/38 | chr6 | 112174053 | |||||||
chr6:112174460 | G | A | 1 | a0001c0009t0001g0082 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.1357+853C>T | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 11/38 | chr6 | 112174460 | |||||||
chr6:112174502 | T | C | 2 | a0002c0006t0002g0264 a0002c0006t0002g0265 |
2 | NA18979.hp1 NA18980.hp1 |
intron_variant | MODIFIER | c.1357+811A>G | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 11/38 | chr6 | 112174502 | |||||||
chr6:112174786 | C | T | 81 | a0001c0001t0001g0237 a0001c0002t0001g0005 a0001c0002t0001g0006 others(78): Show |
81 | HG00408.hp1 HG00408.hp2 HG00621.hp1 others(78): Show |
intron_variant | MODIFIER | c.1357+527G>A | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 11/38 | chr6 | 112174786 | |||||||
chr6:112174869 | C | T | 81 | a0001c0001t0001g0237 a0001c0002t0001g0005 a0001c0002t0001g0006 others(78): Show |
81 | HG00408.hp1 HG00408.hp2 HG00621.hp1 others(78): Show |
intron_variant | MODIFIER | c.1357+444G>A | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 11/38 | chr6 | 112174869 | |||||||
chr6:112174948 | A | C | 1 | a0001c0001t0001g0256 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.1357+365T>G | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 11/38 | chr6 | 112174948 | |||||||
chr6:112174992 | T | A | 13 | a0001c0002t0001g0020 a0001c0011t0003g0009 a0001c0020t0005g0168 others(10): Show |
13 | HG01167.hp1 HG01169.hp1 HG01981.hp2 others(10): Show |
intron_variant | MODIFIER | c.1357+321A>T | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 11/38 | chr6 | 112174992 | |||||||
chr6:112175001 | A | T | 3 | a0001c0050t0001g0310 a0004c0026t0001g0067 a0004c0026t0001g0068 |
3 | HG01167.hp1 HG01169.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.1357+312T>A | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 11/38 | chr6 | 112175001 | |||||||
chr6:112175309 | C | A | 29 | a0001c0002t0001g0020 a0001c0002t0001g0192 a0001c0002t0001g0254 others(26): Show |
29 | HG00741.hp1 HG01167.hp1 HG01169.hp1 others(26): Show |
splice_region_variant&intron_variant | LOW | c.1357+4G>T | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 11/38 | chr6 | 112175309 | |||||||
chr6:112175488 | G | C | 16 | a0001c0002t0001g0192 a0001c0002t0001g0254 a0001c0011t0003g0062 others(13): Show |
16 | HG00741.hp1 HG02109.hp1 HG02109.hp2 others(13): Show |
splice_region_variant&intron_variant | LOW | c.1190-8C>G | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 10/38 | chr6 | 112175488 | |||||||
chr6:112175645 | G | A | 29 | a0001c0002t0001g0020 a0001c0002t0001g0192 a0001c0002t0001g0254 others(26): Show |
29 | HG00741.hp1 HG01167.hp1 HG01169.hp1 others(26): Show |
intron_variant | MODIFIER | c.1190-165C>T | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 10/38 | chr6 | 112175645 | |||||||
chr6:112175685 | C | T | 1 | a0001c0023t0003g0302 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1190-205G>A | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 10/38 | chr6 | 112175685 | |||||||
chr6:112175876 | C | T | 1 | a0006c0027t0002g0140 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.1190-396G>A | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 10/38 | chr6 | 112175876 | |||||||
chr6:112175988 | C | A | 155 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0014 others(152): Show |
155 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(152): Show |
intron_variant | MODIFIER | c.1190-508G>T | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 10/38 | chr6 | 112175988 | |||||||
chr6:112176078 | T | C | 1 | a0002c0003t0002g0182 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.1190-598A>G | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 10/38 | chr6 | 112176078 | |||||||
chr6:112176094 | G | A | 155 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0014 others(152): Show |
155 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(152): Show |
intron_variant | MODIFIER | c.1190-614C>T | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 10/38 | chr6 | 112176094 | |||||||
chr6:112176133 | C | T | 9 | a0001c0001t0001g0050 a0001c0001t0001g0051 a0001c0001t0001g0052 others(6): Show |
9 | HG00639.hp2 HG01074.hp2 HG01243.hp2 others(6): Show |
intron_variant | MODIFIER | c.1190-653G>A | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 10/38 | chr6 | 112176133 | |||||||
chr6:112176257 | G | T | 237 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0014 others(234): Show |
237 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(234): Show |
intron_variant | MODIFIER | c.1190-777C>A | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 10/38 | chr6 | 112176257 | |||||||
chr6:112176373 | C | T | 81 | a0001c0002t0001g0005 a0001c0002t0001g0006 a0001c0002t0001g0045 others(78): Show |
81 | HG00408.hp2 HG00621.hp1 HG00639.hp1 others(78): Show |
intron_variant | MODIFIER | c.1190-893G>A | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 10/38 | chr6 | 112176373 | |||||||
chr6:112176490 | A | C | 1 | a0004c0057t0003g0017 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1190-1010T>G | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 10/38 | chr6 | 112176490 | |||||||
chr6:112176918 | A | G | 1 | a0004c0007t0014g0300 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.1189+1203T>C | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 10/38 | chr6 | 112176918 | |||||||
chr6:112177021 | C | T | 81 | a0001c0001t0001g0237 a0001c0002t0001g0005 a0001c0002t0001g0006 others(78): Show |
81 | HG00408.hp1 HG00408.hp2 HG00621.hp1 others(78): Show |
intron_variant | MODIFIER | c.1189+1100G>A | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 10/38 | chr6 | 112177021 | |||||||
chr6:112177264 | T | G | 3 | a0001c0002t0001g0045 a0001c0002t0001g0047 a0001c0016t0001g0048 |
3 | HG02055.hp2 HG02559.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.1189+857A>C | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 10/38 | chr6 | 112177264 | |||||||
chr6:112177269 | C | T | 1 | a0001c0054t0001g0301 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1189+852G>A | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 10/38 | chr6 | 112177269 | |||||||
chr6:112177330 | C | T | 5 | a0001c0002t0001g0254 a0001c0011t0003g0293 a0002c0006t0002g0170 others(2): Show |
5 | HG00741.hp1 HG02109.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.1189+791G>A | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 10/38 | chr6 | 112177330 | |||||||
chr6:112177437 | A | G | 1 | a0004c0057t0003g0017 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1189+684T>C | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 10/38 | chr6 | 112177437 | |||||||
chr6:112177990 | T | G | 2 | a0001c0002t0001g0109 a0001c0002t0001g0110 |
2 | NA18955.hp1 NA18988.hp1 |
intron_variant | MODIFIER | c.1189+131A>C | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 10/38 | chr6 | 112177990 | |||||||
chr6:112178043 | G | A | 16 | a0001c0002t0001g0192 a0001c0002t0001g0254 a0001c0011t0003g0062 others(13): Show |
16 | HG00741.hp1 HG02109.hp1 HG02109.hp2 others(13): Show |
intron_variant | MODIFIER | c.1189+78C>T | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 10/38 | chr6 | 112178043 | |||||||
chr6:112178427 | A | T | 13 | a0001c0002t0001g0020 a0001c0011t0003g0009 a0001c0020t0005g0168 others(10): Show |
13 | HG01167.hp1 HG01169.hp1 HG01981.hp2 others(10): Show |
intron_variant | MODIFIER | c.1078-195T>A | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 9/38 | chr6 | 112178427 | |||||||
chr6:112178433 | T | A | 6 | a0001c0002t0001g0076 a0001c0002t0001g0197 a0001c0011t0003g0161 others(3): Show |
6 | HG01081.hp2 HG01243.hp1 HG02257.hp1 others(3): Show |
intron_variant | MODIFIER | c.1078-201A>T | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 9/38 | chr6 | 112178433 | |||||||
chr6:112178454 | G | T | 115 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0014 others(112): Show |
115 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(112): Show |
intron_variant | MODIFIER | c.1078-222C>A | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 9/38 | chr6 | 112178454 | |||||||
chr6:112178529 | G | A | 1 | a0005c0008t0004g0297 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.1078-297C>T | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 9/38 | chr6 | 112178529 | |||||||
chr6:112178575 | C | T | 2 | a0004c0026t0001g0067 a0004c0026t0001g0068 |
2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.1078-343G>A | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 9/38 | chr6 | 112178575 | |||||||
chr6:112178584 | T | C | 1 | a0001c0002t0001g0309 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.1078-352A>G | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 9/38 | chr6 | 112178584 | |||||||
chr6:112178589 | G | A | 2 | a0001c0016t0002g0268 a0004c0007t0014g0300 |
2 | NA18971.hp1 NA19070.hp2 |
intron_variant | MODIFIER | c.1078-357C>T | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 9/38 | chr6 | 112178589 | |||||||
chr6:112178672 | T | C | 143 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0014 others(140): Show |
143 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(140): Show |
intron_variant | MODIFIER | c.1078-440A>G | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 9/38 | chr6 | 112178672 | |||||||
chr6:112178675 | T | C | 116 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0014 others(113): Show |
116 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(113): Show |
intron_variant | MODIFIER | c.1078-443A>G | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 9/38 | chr6 | 112178675 | |||||||
chr6:112178756 | T | C | 80 | a0001c0002t0001g0005 a0001c0002t0001g0006 a0001c0002t0001g0045 others(77): Show |
80 | HG00408.hp2 HG00621.hp1 HG00639.hp1 others(77): Show |
intron_variant | MODIFIER | c.1078-524A>G | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 9/38 | chr6 | 112178756 | |||||||
chr6:112178808 | T | G | 2 | a0001c0011t0003g0313 a0011c0028t0002g0154 |
2 | HG02622.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.1078-576A>C | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 9/38 | chr6 | 112178808 | |||||||
chr6:112178813 | A | G | 237 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0014 others(234): Show |
237 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(234): Show |
intron_variant | MODIFIER | c.1078-581T>C | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 9/38 | chr6 | 112178813 | |||||||
chr6:112178865 | T | G | 237 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0014 others(234): Show |
237 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(234): Show |
intron_variant | MODIFIER | c.1078-633A>C | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 9/38 | chr6 | 112178865 | |||||||
chr6:112178907 | A | C | 1 | a0001c0005t0001g0207 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.1078-675T>G | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 9/38 | chr6 | 112178907 | |||||||
chr6:112179203 | T | C | 5 | a0001c0023t0003g0302 a0008c0015t0001g0057 a0008c0015t0001g0059 others(2): Show |
5 | HG02486.hp2 HG03139.hp1 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.1078-971A>G | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 9/38 | chr6 | 112179203 | |||||||
chr6:112179294 | G | T | 292 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0014 others(289): Show |
292 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(289): Show |
intron_variant | MODIFIER | c.1078-1062C>A | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 9/38 | chr6 | 112179294 | |||||||
chr6:112179448 | T | G | 127 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0014 others(124): Show |
127 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(124): Show |
intron_variant | MODIFIER | c.1078-1216A>C | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 9/38 | chr6 | 112179448 | |||||||
chr6:112179468 | C | A | 1 | a0002c0003t0002g0206 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1078-1236G>T | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 9/38 | chr6 | 112179468 | |||||||
chr6:112179488 | C | T | 1 | a0007c0014t0002g0019 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1078-1256G>A | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 9/38 | chr6 | 112179488 | |||||||
chr6:112179560 | C | T | 1 | a0001c0011t0003g0293 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1078-1328G>A | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 9/38 | chr6 | 112179560 | |||||||
chr6:112179562 | C | A | 1 | a0003c0013t0001g0011 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.1078-1330G>T | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 9/38 | chr6 | 112179562 | |||||||
chr6:112179580 | G | T | 2 | a0007c0060t0002g0260 a0022c0032t0001g0060 |
2 | HG02809.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1078-1348C>A | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 9/38 | chr6 | 112179580 | |||||||
chr6:112179640 | A | T | 3 | a0001c0009t0009g0078 a0002c0003t0002g0077 a0002c0003t0002g0079 |
3 | HG00099.hp2 HG00280.hp1 HG00323.hp2 |
intron_variant | MODIFIER | c.1078-1408T>A | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 9/38 | chr6 | 112179640 | |||||||
chr6:112179664 | C | T | 1 | a0007c0014t0002g0250 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1078-1432G>A | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 9/38 | chr6 | 112179664 | |||||||
chr6:112179958 | A | G | 16 | a0001c0002t0001g0192 a0001c0002t0001g0254 a0001c0011t0003g0062 others(13): Show |
16 | HG00741.hp1 HG02109.hp1 HG02109.hp2 others(13): Show |
intron_variant | MODIFIER | c.1078-1726T>C | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 9/38 | chr6 | 112179958 | |||||||
chr6:112179991 | T | C | 1 | a0018c0030t0001g0004 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1078-1759A>G | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 9/38 | chr6 | 112179991 | |||||||
chr6:112180179 | C | T | 142 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0014 others(139): Show |
142 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(139): Show |
intron_variant | MODIFIER | c.1078-1947G>A | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 9/38 | chr6 | 112180179 | |||||||
chr6:112180208 | A | T | 2 | a0001c0001t0001g0033 a0004c0007t0001g0189 |
2 | HG02698.hp1 HG03688.hp1 |
intron_variant | MODIFIER | c.1078-1976T>A | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 9/38 | chr6 | 112180208 | |||||||
chr6:112180266 | A | C | 142 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0014 others(139): Show |
142 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(139): Show |
intron_variant | MODIFIER | c.1078-2034T>G | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 9/38 | chr6 | 112180266 | |||||||
chr6:112180335 | T | C | 80 | a0001c0002t0001g0005 a0001c0002t0001g0006 a0001c0002t0001g0045 others(77): Show |
80 | HG00408.hp2 HG00621.hp1 HG00639.hp1 others(77): Show |
intron_variant | MODIFIER | c.1078-2103A>G | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 9/38 | chr6 | 112180335 | |||||||
chr6:112180500 | G | A | 1 | a0003c0043t0001g0036 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.1078-2268C>T | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 9/38 | chr6 | 112180500 | |||||||
chr6:112180536 | C | T | 6 | a0001c0023t0003g0306 a0001c0037t0003g0003 a0008c0015t0001g0058 others(3): Show |
6 | HG02818.hp2 HG02886.hp2 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.1078-2304G>A | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 9/38 | chr6 | 112180536 | |||||||
chr6:112180540 | T | C | 236 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0014 others(233): Show |
236 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(233): Show |
intron_variant | MODIFIER | c.1078-2308A>G | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 9/38 | chr6 | 112180540 | |||||||
chr6:112180655 | A | G | 2 | a0003c0013t0001g0010 a0003c0013t0001g0011 |
2 | HG02165.hp2 NA18973.hp2 |
intron_variant | MODIFIER | c.1078-2423T>C | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 9/38 | chr6 | 112180655 | |||||||
chr6:112180683 | G | T | 1 | a0001c0001t0001g0214 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.1078-2451C>A | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 9/38 | chr6 | 112180683 | |||||||
chr6:112180892 | C | T | 5 | a0001c0023t0003g0302 a0008c0015t0001g0057 a0008c0015t0001g0059 others(2): Show |
5 | HG02486.hp2 HG03139.hp1 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.1078-2660G>A | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 9/38 | chr6 | 112180892 | |||||||
chr6:112181079 | C | T | 7 | a0001c0002t0001g0020 a0001c0011t0003g0009 a0002c0006t0002g0037 others(4): Show |
7 | HG01981.hp2 HG02055.hp1 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.1078-2847G>A | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 9/38 | chr6 | 112181079 | |||||||
chr6:112181224 | G | A | 4 | a0001c0002t0001g0107 a0001c0022t0002g0146 a0002c0003t0002g0066 others(1): Show |
4 | HG02080.hp1 HG02523.hp1 HG04199.hp1 others(1): Show |
intron_variant | MODIFIER | c.1078-2992C>T | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 9/38 | chr6 | 112181224 | |||||||
chr6:112181506 | C | T | 1 | a0004c0057t0003g0017 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1078-3274G>A | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 9/38 | chr6 | 112181506 | |||||||
chr6:112181521 | A | G | 1 | a0001c0002t0001g0253 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1078-3289T>C | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 9/38 | chr6 | 112181521 | |||||||
chr6:112181605 | T | C | 13 | a0001c0002t0001g0020 a0001c0011t0003g0009 a0001c0020t0005g0168 others(10): Show |
13 | HG01167.hp1 HG01169.hp1 HG01981.hp2 others(10): Show |
intron_variant | MODIFIER | c.1078-3373A>G | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 9/38 | chr6 | 112181605 | |||||||
chr6:112181763 | A | G | 236 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0014 others(233): Show |
236 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(233): Show |
intron_variant | MODIFIER | c.1077+3474T>C | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 9/38 | chr6 | 112181763 | |||||||
chr6:112181787 | T | C | 142 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0014 others(139): Show |
142 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(139): Show |
intron_variant | MODIFIER | c.1077+3450A>G | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 9/38 | chr6 | 112181787 | |||||||
chr6:112181921 | G | A | 236 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0014 others(233): Show |
236 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(233): Show |
intron_variant | MODIFIER | c.1077+3316C>T | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 9/38 | chr6 | 112181921 | |||||||
chr6:112181956 | A | T | 10 | a0001c0002t0001g0020 a0001c0011t0003g0009 a0001c0020t0005g0168 others(7): Show |
10 | HG01981.hp2 HG02055.hp1 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.1077+3281T>A | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 9/38 | chr6 | 112181956 | |||||||
chr6:112182097 | A | AAAAT | 9 | a0001c0023t0003g0306 a0001c0037t0003g0003 a0003c0004t0001g0226 others(6): Show |
9 | HG02818.hp2 HG02886.hp2 HG02895.hp2 others(6): Show |
intron_variant | MODIFIER | c.1077+3136_1077+313 others(8): Show |
LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 9/38 | chr6 | 112182097 | |||||||
chr6:112182097 | A | AAAATAAA others(1): Show |
38 | a0003c0004t0001g0081 a0003c0004t0001g0125 a0003c0004t0001g0180 others(35): Show |
38 | HG00597.hp2 HG00621.hp2 HG00642.hp2 others(35): Show |
intron_variant | MODIFIER | c.1077+3132_1077+313 others(12): Show |
LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 9/38 | chr6 | 112182097 | |||||||
chr6:112182097 | A | AAAATAAA others(5): Show |
3 | a0003c0004t0001g0114 a0003c0025t0001g0113 a0003c0058t0001g0210 |
3 | HG03486.hp2 NA18964.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.1077+3128_1077+313 others(16): Show |
LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 9/38 | chr6 | 112182097 | |||||||
chr6:112182097 | AAAATAAA others(1): Show |
A | 13 | a0001c0002t0001g0020 a0001c0011t0003g0009 a0001c0020t0005g0168 others(10): Show |
13 | HG01167.hp1 HG01169.hp1 HG01981.hp2 others(10): Show |
intron_variant | MODIFIER | c.1077+3132_1077+313 others(12): Show |
LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 9/38 | chr6 | 112182097 | |||||||
chr6:112182097 | AAAATAAA others(5): Show |
A | 223 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0014 others(220): Show |
223 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(220): Show |
intron_variant | MODIFIER | c.1077+3128_1077+313 others(16): Show |
LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 9/38 | chr6 | 112182097 | |||||||
chr6:112182169 | G | T | 91 | a0001c0002t0001g0005 a0001c0002t0001g0006 a0001c0002t0001g0020 others(88): Show |
91 | HG00408.hp2 HG00621.hp1 HG00639.hp1 others(88): Show |
intron_variant | MODIFIER | c.1077+3068C>A | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 9/38 | chr6 | 112182169 | |||||||
chr6:112182233 | A | C | 1 | a0008c0015t0001g0274 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1077+3004T>G | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 9/38 | chr6 | 112182233 | |||||||
chr6:112182269 | G | A | 2 | a0003c0004t0001g0180 a0003c0004t0001g0239 |
2 | NA18966.hp1 NA19006.hp1 |
intron_variant | MODIFIER | c.1077+2968C>T | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 9/38 | chr6 | 112182269 | |||||||
chr6:112182296 | C | A | 2 | a0003c0058t0001g0210 a0003c0059t0001g0259 |
2 | HG02280.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.1077+2941G>T | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 9/38 | chr6 | 112182296 | |||||||
chr6:112182355 | C | T | 4 | a0001c0002t0001g0076 a0001c0002t0001g0197 a0004c0007t0001g0201 others(1): Show |
4 | HG01081.hp2 HG01243.hp1 HG02572.hp2 others(1): Show |
intron_variant | MODIFIER | c.1077+2882G>A | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 9/38 | chr6 | 112182355 | |||||||
chr6:112182390 | A | C | 4 | a0001c0002t0001g0076 a0001c0002t0001g0197 a0004c0007t0001g0201 others(1): Show |
4 | HG01081.hp2 HG01243.hp1 HG02572.hp2 others(1): Show |
intron_variant | MODIFIER | c.1077+2847T>G | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 9/38 | chr6 | 112182390 | |||||||
chr6:112182415 | G | A | 91 | a0001c0002t0001g0005 a0001c0002t0001g0006 a0001c0002t0001g0020 others(88): Show |
91 | HG00408.hp2 HG00621.hp1 HG00639.hp1 others(88): Show |
intron_variant | MODIFIER | c.1077+2822C>T | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 9/38 | chr6 | 112182415 | |||||||
chr6:112182450 | T | A | 1 | a0001c0016t0001g0048 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1077+2787A>T | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 9/38 | chr6 | 112182450 | |||||||
chr6:112182530 | G | A | 1 | a0002c0003t0001g0171 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1077+2707C>T | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 9/38 | chr6 | 112182530 | |||||||
chr6:112182670 | C | T | 1 | a0001c0011t0003g0155 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1077+2567G>A | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 9/38 | chr6 | 112182670 | |||||||
chr6:112182774 | C | T | 1 | a0008c0031t0001g0056 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1077+2463G>A | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 9/38 | chr6 | 112182774 | |||||||
chr6:112182778 | T | C | 82 | a0001c0001t0001g0237 a0001c0002t0001g0005 a0001c0002t0001g0006 others(79): Show |
82 | HG00408.hp1 HG00408.hp2 HG00621.hp1 others(79): Show |
intron_variant | MODIFIER | c.1077+2459A>G | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 9/38 | chr6 | 112182778 | |||||||
chr6:112182847 | C | T | 2 | a0003c0004t0001g0180 a0003c0004t0001g0239 |
2 | NA18966.hp1 NA19006.hp1 |
intron_variant | MODIFIER | c.1077+2390G>A | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 9/38 | chr6 | 112182847 | |||||||
chr6:112182907 | C | T | 1 | a0004c0057t0003g0017 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1077+2330G>A | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 9/38 | chr6 | 112182907 | |||||||
chr6:112182908 | A | G | 236 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0014 others(233): Show |
236 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(233): Show |
intron_variant | MODIFIER | c.1077+2329T>C | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 9/38 | chr6 | 112182908 | |||||||
chr6:112183038 | G | A | 8 | a0001c0001t0001g0033 a0001c0001t0001g0116 a0002c0003t0002g0163 others(5): Show |
8 | HG01081.hp1 HG01433.hp2 HG01496.hp1 others(5): Show |
intron_variant | MODIFIER | c.1077+2199C>T | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 9/38 | chr6 | 112183038 | |||||||
chr6:112183350 | C | T | 6 | a0001c0023t0003g0306 a0001c0037t0003g0003 a0008c0015t0001g0058 others(3): Show |
6 | HG02818.hp2 HG02886.hp2 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.1077+1887G>A | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 9/38 | chr6 | 112183350 | |||||||
chr6:112183428 | C | T | 81 | a0001c0002t0001g0005 a0001c0002t0001g0006 a0001c0002t0001g0045 others(78): Show |
81 | HG00408.hp2 HG00621.hp1 HG00639.hp1 others(78): Show |
intron_variant | MODIFIER | c.1077+1809G>A | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 9/38 | chr6 | 112183428 | |||||||
chr6:112183521 | G | T | 5 | a0001c0023t0003g0302 a0008c0015t0001g0057 a0008c0015t0001g0059 others(2): Show |
5 | HG02486.hp2 HG03139.hp1 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.1077+1716C>A | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 9/38 | chr6 | 112183521 | |||||||
chr6:112183907 | C | T | 107 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0014 others(104): Show |
107 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(104): Show |
intron_variant | MODIFIER | c.1077+1330G>A | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 9/38 | chr6 | 112183907 | |||||||
chr6:112183908 | G | A | 1 | a0001c0011t0003g0062 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1077+1329C>T | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 9/38 | chr6 | 112183908 | |||||||
chr6:112183950 | C | CA | 117 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0015 others(114): Show |
117 | HG00099.hp1 HG00099.hp2 HG00597.hp1 others(114): Show |
intron_variant | MODIFIER | c.1077+1286dupT | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 9/38 | chr6 | 112183950 | |||||||
chr6:112183950 | C | CAA | 27 | a0001c0001t0001g0014 a0001c0001t0001g0033 a0001c0001t0001g0042 others(24): Show |
27 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(24): Show |
intron_variant | MODIFIER | c.1077+1285_1077+128 others(6): Show |
LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 9/38 | chr6 | 112183950 | |||||||
chr6:112183950 | CA | C | 16 | a0001c0002t0001g0020 a0001c0011t0003g0009 a0001c0016t0010g0209 others(13): Show |
16 | HG01167.hp2 HG01981.hp2 HG02055.hp1 others(13): Show |
intron_variant | MODIFIER | c.1077+1286delT | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 9/38 | chr6 | 112183950 | |||||||
chr6:112183963 | A | G | 1 | a0003c0004t0001g0125 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.1077+1274T>C | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 9/38 | chr6 | 112183963 | |||||||
chr6:112183972 | A | G | 16 | a0001c0002t0001g0192 a0001c0002t0001g0254 a0001c0011t0003g0062 others(13): Show |
16 | HG00741.hp1 HG02109.hp1 HG02109.hp2 others(13): Show |
intron_variant | MODIFIER | c.1077+1265T>C | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 9/38 | chr6 | 112183972 | |||||||
chr6:112184138 | A | G | 1 | a0002c0024t0001g0147 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.1077+1099T>C | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 9/38 | chr6 | 112184138 | |||||||
chr6:112184223 | A | T | 81 | a0001c0001t0001g0237 a0001c0002t0001g0005 a0001c0002t0001g0006 others(78): Show |
81 | HG00408.hp1 HG00408.hp2 HG00621.hp1 others(78): Show |
intron_variant | MODIFIER | c.1077+1014T>A | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 9/38 | chr6 | 112184223 | |||||||
chr6:112184237 | T | A | 20 | a0001c0002t0001g0192 a0001c0002t0001g0254 a0001c0011t0003g0062 others(17): Show |
20 | HG00741.hp1 HG01167.hp1 HG01169.hp1 others(17): Show |
intron_variant | MODIFIER | c.1077+1000A>T | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 9/38 | chr6 | 112184237 | |||||||
chr6:112184324 | G | GA | 86 | a0001c0001t0001g0219 a0001c0001t0001g0237 a0001c0001t0001g0257 others(83): Show |
86 | HG00408.hp1 HG00408.hp2 HG00621.hp1 others(83): Show |
intron_variant | MODIFIER | c.1077+912dupT | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 9/38 | chr6 | 112184324 | |||||||
chr6:112184343 | T | C | 3 | a0005c0008t0004g0244 a0005c0008t0004g0245 a0005c0008t0004g0297 |
3 | HG01358.hp1 HG03209.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.1077+894A>G | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 9/38 | chr6 | 112184343 | |||||||
chr6:112184455 | C | A | 32 | a0001c0002t0001g0005 a0001c0002t0001g0006 a0001c0002t0001g0087 others(29): Show |
32 | HG00639.hp1 HG00741.hp2 HG01106.hp2 others(29): Show |
intron_variant | MODIFIER | c.1077+782G>T | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 9/38 | chr6 | 112184455 | |||||||
chr6:112184464 | T | C | 5 | a0001c0023t0003g0302 a0008c0015t0001g0057 a0008c0015t0001g0059 others(2): Show |
5 | HG02486.hp2 HG03139.hp1 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.1077+773A>G | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 9/38 | chr6 | 112184464 | |||||||
chr6:112184495 | G | C | 3 | a0001c0050t0001g0310 a0004c0026t0001g0067 a0004c0026t0001g0068 |
3 | HG01167.hp1 HG01169.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.1077+742C>G | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 9/38 | chr6 | 112184495 | |||||||
chr6:112184731 | C | T | 1 | a0004c0057t0003g0017 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1077+506G>A | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 9/38 | chr6 | 112184731 | |||||||
chr6:112184890 | A | C | 6 | a0001c0002t0001g0076 a0001c0002t0001g0197 a0001c0011t0003g0161 others(3): Show |
6 | HG01081.hp2 HG01243.hp1 HG02257.hp1 others(3): Show |
intron_variant | MODIFIER | c.1077+347T>G | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 9/38 | chr6 | 112184890 | |||||||
chr6:112184951 | G | A | 1 | a0003c0004t0001g0312 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1077+286C>T | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 9/38 | chr6 | 112184951 | |||||||
chr6:112185173 | G | A | 113 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0014 others(110): Show |
113 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(110): Show |
intron_variant | MODIFIER | c.1077+64C>T | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 9/38 | chr6 | 112185173 | |||||||
chr6:112185381 | G | T | 294 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0014 others(291): Show |
294 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(291): Show |
intron_variant | MODIFIER | c.967-34C>A | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 8/38 | chr6 | 112185381 | |||||||
chr6:112185494 | A | C | 2 | a0001c0001t0001g0283 a0001c0009t0001g0134 |
2 | HG01934.hp1 HG02004.hp1 |
intron_variant | MODIFIER | c.967-147T>G | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 8/38 | chr6 | 112185494 | |||||||
chr6:112185980 | G | C | 116 | a0001c0002t0001g0005 a0001c0002t0001g0006 a0001c0002t0001g0020 others(113): Show |
116 | HG00408.hp2 HG00621.hp1 HG00639.hp1 others(113): Show |
intron_variant | MODIFIER | c.967-633C>G | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 8/38 | chr6 | 112185980 | |||||||
chr6:112186005 | C | T | 116 | a0001c0002t0001g0005 a0001c0002t0001g0006 a0001c0002t0001g0020 others(113): Show |
116 | HG00408.hp2 HG00621.hp1 HG00639.hp1 others(113): Show |
intron_variant | MODIFIER | c.967-658G>A | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 8/38 | chr6 | 112186005 | |||||||
chr6:112186077 | T | C | 8 | a0001c0002t0001g0005 a0001c0002t0001g0006 a0001c0002t0001g0215 others(5): Show |
8 | HG01106.hp2 HG01167.hp2 HG01168.hp2 others(5): Show |
intron_variant | MODIFIER | c.967-730A>G | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 8/38 | chr6 | 112186077 | |||||||
chr6:112186426 | A | C | 1 | a0001c0001t0001g0149 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.966+1024T>G | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 8/38 | chr6 | 112186426 | |||||||
chr6:112186528 | A | G | 2 | a0002c0006t0002g0264 a0002c0006t0002g0265 |
2 | NA18979.hp1 NA18980.hp1 |
intron_variant | MODIFIER | c.966+922T>C | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 8/38 | chr6 | 112186528 | |||||||
chr6:112186568 | C | T | 1 | a0019c0036t0001g0282 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.966+882G>A | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 8/38 | chr6 | 112186568 | |||||||
chr6:112186596 | C | T | 1 | a0005c0008t0001g0241 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.966+854G>A | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 8/38 | chr6 | 112186596 | |||||||
chr6:112186707 | G | A | 110 | a0001c0002t0001g0005 a0001c0002t0001g0006 a0001c0002t0001g0020 others(107): Show |
110 | HG00408.hp2 HG00621.hp1 HG00639.hp1 others(107): Show |
intron_variant | MODIFIER | c.966+743C>T | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 8/38 | chr6 | 112186707 | |||||||
chr6:112186833 | C | T | 109 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0014 others(106): Show |
109 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(106): Show |
intron_variant | MODIFIER | c.966+617G>A | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 8/38 | chr6 | 112186833 | |||||||
chr6:112186853 | G | T | 3 | a0001c0005t0001g0063 a0001c0005t0001g0091 a0001c0005t0001g0092 |
3 | HG00639.hp1 HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.966+597C>A | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 8/38 | chr6 | 112186853 | |||||||
chr6:112186909 | T | C | 6 | a0001c0002t0001g0076 a0001c0002t0001g0197 a0001c0011t0003g0161 others(3): Show |
6 | HG01081.hp2 HG01243.hp1 HG02257.hp1 others(3): Show |
intron_variant | MODIFIER | c.966+541A>G | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 8/38 | chr6 | 112186909 | |||||||
chr6:112186964 | A | T | 1 | a0004c0010t0012g0177 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.966+486T>A | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 8/38 | chr6 | 112186964 | |||||||
chr6:112187089 | T | C | 198 | a0001c0001t0001g0138 a0001c0001t0001g0281 a0001c0002t0001g0005 others(195): Show |
198 | HG00323.hp1 HG00408.hp2 HG00597.hp2 others(195): Show |
intron_variant | MODIFIER | c.966+361A>G | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 8/38 | chr6 | 112187089 | |||||||
chr6:112187142 | G | A | 3 | a0001c0050t0001g0310 a0004c0026t0001g0067 a0004c0026t0001g0068 |
3 | HG01167.hp1 HG01169.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.966+308C>T | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 8/38 | chr6 | 112187142 | |||||||
chr6:112187306 | T | A | 6 | a0001c0002t0001g0076 a0001c0002t0001g0197 a0001c0011t0003g0161 others(3): Show |
6 | HG01081.hp2 HG01243.hp1 HG02257.hp1 others(3): Show |
intron_variant | MODIFIER | c.966+144A>T | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 8/38 | chr6 | 112187306 | |||||||
chr6:112187315 | T | C | 16 | a0001c0002t0001g0192 a0001c0002t0001g0254 a0001c0011t0003g0062 others(13): Show |
16 | HG00741.hp1 HG02109.hp1 HG02109.hp2 others(13): Show |
intron_variant | MODIFIER | c.966+135A>G | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 8/38 | chr6 | 112187315 | |||||||
chr6:112187637 | A | G | 6 | a0001c0002t0001g0076 a0001c0002t0001g0197 a0001c0011t0003g0161 others(3): Show |
6 | HG01081.hp2 HG01243.hp1 HG02257.hp1 others(3): Show |
intron_variant | MODIFIER | c.815-36T>C | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 7/38 | chr6 | 112187637 | |||||||
chr6:112187754 | T | G | 6 | a0001c0011t0003g0009 a0002c0006t0002g0037 a0002c0006t0002g0199 others(3): Show |
6 | HG01981.hp2 HG02055.hp1 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.815-153A>C | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 7/38 | chr6 | 112187754 | |||||||
chr6:112187918 | C | T | 1 | a0004c0057t0003g0017 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.815-317G>A | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 7/38 | chr6 | 112187918 | |||||||
chr6:112187919 | C | T | 1 | a0005c0044t0001g0261 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.815-318G>A | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 7/38 | chr6 | 112187919 | |||||||
chr6:112188200 | G | C | 1 | a0005c0008t0001g0262 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.815-599C>G | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 7/38 | chr6 | 112188200 | |||||||
chr6:112188217 | G | T | 16 | a0001c0002t0001g0192 a0001c0002t0001g0254 a0001c0011t0003g0062 others(13): Show |
16 | HG00741.hp1 HG02109.hp1 HG02109.hp2 others(13): Show |
intron_variant | MODIFIER | c.815-616C>A | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 7/38 | chr6 | 112188217 | |||||||
chr6:112188224 | G | A | 2 | a0001c0002t0001g0164 a0001c0002t0001g0165 |
2 | HG03942.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.815-623C>T | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 7/38 | chr6 | 112188224 | |||||||
chr6:112188515 | A | T | 117 | a0001c0002t0001g0005 a0001c0002t0001g0006 a0001c0002t0001g0020 others(114): Show |
117 | HG00408.hp2 HG00621.hp1 HG00639.hp1 others(114): Show |
intron_variant | MODIFIER | c.814+595T>A | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 7/38 | chr6 | 112188515 | |||||||
chr6:112188523 | G | A | 6 | a0001c0002t0001g0076 a0001c0002t0001g0197 a0001c0011t0003g0161 others(3): Show |
6 | HG01081.hp2 HG01243.hp1 HG02257.hp1 others(3): Show |
intron_variant | MODIFIER | c.814+587C>T | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 7/38 | chr6 | 112188523 | |||||||
chr6:112188529 | G | A | 6 | a0001c0002t0001g0076 a0001c0002t0001g0197 a0001c0011t0003g0161 others(3): Show |
6 | HG01081.hp2 HG01243.hp1 HG02257.hp1 others(3): Show |
intron_variant | MODIFIER | c.814+581C>T | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 7/38 | chr6 | 112188529 | |||||||
chr6:112188566 | G | C | 1 | a0003c0061t0001g0299 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.814+544C>G | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 7/38 | chr6 | 112188566 | |||||||
chr6:112188629 | G | C | 6 | a0001c0023t0003g0306 a0001c0037t0003g0003 a0008c0015t0001g0058 others(3): Show |
6 | HG02818.hp2 HG02886.hp2 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.814+481C>G | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 7/38 | chr6 | 112188629 | |||||||
chr6:112188740 | A | T | 34 | a0001c0002t0001g0005 a0001c0002t0001g0006 a0001c0002t0001g0087 others(31): Show |
34 | HG00639.hp1 HG00741.hp2 HG01106.hp2 others(31): Show |
intron_variant | MODIFIER | c.814+370T>A | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 7/38 | chr6 | 112188740 | |||||||
chr6:112188788 | C | T | 1 | a0001c0001t0001g0246 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.814+322G>A | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 7/38 | chr6 | 112188788 | |||||||
chr6:112189460 | C | A | 19 | a0001c0002t0001g0258 a0001c0002t0001g0278 a0001c0002t0001g0279 others(16): Show |
19 | HG00408.hp2 HG02074.hp2 HG02080.hp2 others(16): Show |
intron_variant | MODIFIER | c.719-255G>T | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 6/38 | chr6 | 112189460 | |||||||
chr6:112189616 | C | T | 117 | a0001c0002t0001g0005 a0001c0002t0001g0006 a0001c0002t0001g0020 others(114): Show |
117 | HG00408.hp2 HG00621.hp1 HG00639.hp1 others(114): Show |
intron_variant | MODIFIER | c.719-411G>A | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 6/38 | chr6 | 112189616 | |||||||
chr6:112189799 | A | T | 6 | a0001c0002t0001g0076 a0001c0002t0001g0197 a0001c0011t0003g0161 others(3): Show |
6 | HG01081.hp2 HG01243.hp1 HG02257.hp1 others(3): Show |
intron_variant | MODIFIER | c.719-594T>A | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 6/38 | chr6 | 112189799 | |||||||
chr6:112189814 | G | A | 111 | a0001c0002t0001g0005 a0001c0002t0001g0006 a0001c0002t0001g0020 others(108): Show |
111 | HG00408.hp2 HG00621.hp1 HG00639.hp1 others(108): Show |
intron_variant | MODIFIER | c.719-609C>T | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 6/38 | chr6 | 112189814 | |||||||
chr6:112190230 | C | A | 1 | a0001c0001t0001g0227 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.719-1025G>T | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 6/38 | chr6 | 112190230 | |||||||
chr6:112190417 | T | G | 195 | a0001c0001t0001g0237 a0001c0002t0001g0005 a0001c0002t0001g0006 others(192): Show |
195 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(192): Show |
intron_variant | MODIFIER | c.719-1212A>C | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 6/38 | chr6 | 112190417 | |||||||
chr6:112190650 | C | T | 194 | a0001c0002t0001g0005 a0001c0002t0001g0006 a0001c0002t0001g0020 others(191): Show |
194 | HG00323.hp1 HG00408.hp2 HG00597.hp2 others(191): Show |
intron_variant | MODIFIER | c.718+986G>A | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 6/38 | chr6 | 112190650 | |||||||
chr6:112190661 | A | T | 32 | a0001c0002t0001g0005 a0001c0002t0001g0006 a0001c0002t0001g0087 others(29): Show |
32 | HG00639.hp1 HG00741.hp2 HG01106.hp2 others(29): Show |
intron_variant | MODIFIER | c.718+975T>A | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 6/38 | chr6 | 112190661 | |||||||
chr6:112190871 | T | TTTCTTTC others(28): Show |
1 | a0002c0006t0002g0173 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.718+764_718+765ins others(35): Show |
LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 6/38 | chr6 | 112190871 | |||||||
chr6:112190871 | T | TTTTCTTT others(3): Show |
1 | a0001c0002t0001g0076 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.718+764_718+765ins others(10): Show |
LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 6/38 | chr6 | 112190871 | |||||||
chr6:112190871 | TTTTC | T | 3 | a0001c0009t0001g0134 a0001c0011t0003g0255 a0008c0015t0001g0274 |
3 | HG01934.hp1 HG02615.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.718+761_718+764del others(4): Show |
LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 6/38 | chr6 | 112190871 | |||||||
chr6:112190871 | TTTTCTTT others(1): Show |
T | 15 | a0001c0001t0001g0008 a0001c0001t0001g0219 a0001c0001t0001g0222 others(12): Show |
15 | HG00099.hp1 HG00621.hp2 HG01071.hp2 others(12): Show |
intron_variant | MODIFIER | c.718+757_718+764del others(8): Show |
LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 6/38 | chr6 | 112190871 | |||||||
chr6:112190871 | TTTTCTTT others(5): Show |
T | 5 | a0001c0005t0001g0091 a0001c0005t0001g0280 a0002c0003t0002g0077 others(2): Show |
5 | HG00099.hp2 HG03492.hp2 NA18954.hp1 others(2): Show |
intron_variant | MODIFIER | c.718+753_718+764del others(12): Show |
LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 6/38 | chr6 | 112190871 | |||||||
chr6:112190871 | TTTTCTTT others(13): Show |
T | 1 | a0001c0001t0001g0214 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.718+745_718+764del others(20): Show |
LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 6/38 | chr6 | 112190871 | |||||||
chr6:112190871 | TTTTCTTT others(17): Show |
T | 1 | a0017c0046t0002g0233 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.718+741_718+764del others(24): Show |
LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 6/38 | chr6 | 112190871 | |||||||
chr6:112190898 | TCTTTCTT others(42): Show |
T | 2 | a0003c0004t0001g0225 a0003c0004t0001g0234 |
2 | HG02027.hp2 HG02155.hp2 |
intron_variant | MODIFIER | c.718+689_718+737del others(49): Show |
LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 6/38 | chr6 | 112190898 | |||||||
chr6:112190902 | TCTTTCTT others(38): Show |
T | 2 | a0003c0004t0001g0114 a0003c0004t0001g0226 |
2 | NA18964.hp2 NA18977.hp1 |
intron_variant | MODIFIER | c.718+689_718+733del others(45): Show |
LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 6/38 | chr6 | 112190902 | |||||||
chr6:112190911 | CTTTCTTT others(37): Show |
C | 1 | a0001c0001t0001g0033 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.718+681_718+724del others(44): Show |
LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 6/38 | chr6 | 112190911 | |||||||
chr6:112190922 | T | TCTTTCTT others(10): Show |
1 | a0003c0013t0001g0217 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.718+697_718+713dup others(17): Show |
LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 6/38 | chr6 | 112190922 | |||||||
chr6:112190923 | CTTTCTTT others(8): Show |
C | 1 | a0008c0015t0001g0061 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.718+698_718+712del others(15): Show |
LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 6/38 | chr6 | 112190923 | |||||||
chr6:112190927 | CTTTCTTT others(8): Show |
C | 1 | a0001c0005t0001g0092 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.718+694_718+708del others(15): Show |
LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 6/38 | chr6 | 112190927 | |||||||
chr6:112190927 | CTTTCTTT others(17): Show |
C | 1 | a0004c0010t0001g0208 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.718+685_718+708del others(24): Show |
LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 6/38 | chr6 | 112190927 | |||||||
chr6:112190927 | CTTTCTTT others(21): Show |
C | 5 | a0002c0003t0002g0102 a0006c0012t0002g0175 a0006c0012t0002g0179 others(2): Show |
5 | HG00642.hp1 HG02074.hp1 NA18960.hp2 others(2): Show |
intron_variant | MODIFIER | c.718+681_718+708del others(28): Show |
LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 6/38 | chr6 | 112190927 | |||||||
chr6:112190930 | T | TC | 6 | a0001c0002t0001g0076 a0001c0002t0001g0279 a0003c0018t0002g0038 others(3): Show |
6 | HG00408.hp2 HG01081.hp2 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.718+705dupG | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 6/38 | chr6 | 112190930 | |||||||
chr6:112190930 | T | TCTTTCCT others(3): Show |
1 | a0004c0007t0001g0189 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.718+705_718+706ins others(10): Show |
LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 6/38 | chr6 | 112190930 | |||||||
chr6:112190930 | T | TCTTTCTT others(7): Show |
1 | a0001c0002t0001g0213 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.718+705_718+706ins others(14): Show |
LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 6/38 | chr6 | 112190930 | |||||||
chr6:112190930 | T | TCTTTCTT others(6): Show |
3 | a0001c0011t0003g0009 a0004c0007t0001g0266 a0004c0007t0001g0269 |
3 | HG02055.hp1 NA19005.hp2 NA19077.hp2 |
intron_variant | MODIFIER | c.718+693_718+705dup others(13): Show |
LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 6/38 | chr6 | 112190930 | |||||||
chr6:112190931 | CTTTCTTT | C | 4 | a0001c0005t0001g0207 a0004c0007t0001g0156 a0004c0007t0001g0201 others(1): Show |
4 | HG02572.hp2 HG02970.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.718+698_718+704del others(7): Show |
LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 6/38 | chr6 | 112190931 | |||||||
chr6:112190931 | CTTTCTTT others(4): Show |
C | 1 | a0003c0025t0001g0113 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.718+694_718+704del others(11): Show |
LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 6/38 | chr6 | 112190931 | |||||||
chr6:112190931 | CTTTCTTT others(13): Show |
C | 7 | a0001c0001t0001g0042 a0001c0001t0001g0116 a0001c0001t0001g0220 others(4): Show |
7 | HG00673.hp1 HG01256.hp2 HG01258.hp2 others(4): Show |
intron_variant | MODIFIER | c.718+685_718+704del others(20): Show |
LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 6/38 | chr6 | 112190931 | |||||||
chr6:112190931 | CTTTCTTT others(17): Show |
C | 4 | a0001c0001t0001g0016 a0002c0003t0002g0105 a0002c0003t0002g0304 others(1): Show |
4 | HG03831.hp2 HG04199.hp2 NA18747.hp2 others(1): Show |
intron_variant | MODIFIER | c.718+681_718+704del others(24): Show |
LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 6/38 | chr6 | 112190931 | |||||||
chr6:112190932 | T | C | 1 | a0001c0002t0001g0188 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.718+704A>G | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 6/38 | chr6 | 112190932 | |||||||
chr6:112190932 | TTTCTTTC others(9): Show |
T | 1 | a0002c0006t0002g0142 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.718+688_718+703del others(16): Show |
LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 6/38 | chr6 | 112190932 | |||||||
chr6:112190932 | TTTCTTTC others(13): Show |
T | 3 | a0001c0002t0001g0096 a0002c0006t0002g0108 a0002c0006t0002g0264 |
3 | HG00741.hp2 HG01934.hp2 NA18979.hp1 |
intron_variant | MODIFIER | c.718+684_718+703del others(20): Show |
LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 6/38 | chr6 | 112190932 | |||||||
chr6:112190934 | T | TC | 16 | a0001c0002t0001g0045 a0001c0002t0001g0197 a0001c0005t0001g0118 others(13): Show |
16 | HG00733.hp1 HG01123.hp1 HG01243.hp1 others(13): Show |
intron_variant | MODIFIER | c.718+701dupG | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 6/38 | chr6 | 112190934 | |||||||
chr6:112190934 | T | TCTTTC | 9 | a0001c0002t0001g0164 a0001c0005t0001g0286 a0002c0006t0002g0190 others(6): Show |
9 | HG01167.hp1 HG01358.hp1 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.718+697_718+701dup others(5): Show |
LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 6/38 | chr6 | 112190934 | |||||||
chr6:112190934 | T | TTCTTTCT others(3): Show |
1 | a0008c0015t0001g0057 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.718+701_718+702ins others(10): Show |
LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 6/38 | chr6 | 112190934 | |||||||
chr6:112190934 | TCTTTCTT others(6): Show |
T | 2 | a0001c0022t0002g0146 a0016c0042t0001g0296 |
2 | HG02523.hp1 HG02523.hp2 |
intron_variant | MODIFIER | c.718+689_718+701del others(13): Show |
LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 6/38 | chr6 | 112190934 | |||||||
chr6:112190935 | CTTTCTTT | C | 8 | a0001c0001t0001g0283 a0001c0009t0001g0049 a0001c0023t0003g0302 others(5): Show |
8 | HG02004.hp1 HG02486.hp1 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.718+694_718+700del others(7): Show |
LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 6/38 | chr6 | 112190935 | |||||||
chr6:112190935 | CTTTCTTT others(9): Show |
C | 7 | a0001c0001t0001g0095 a0001c0001t0001g0187 a0002c0003t0002g0163 others(4): Show |
7 | HG01081.hp1 HG01168.hp1 HG02129.hp1 others(4): Show |
intron_variant | MODIFIER | c.718+685_718+700del others(16): Show |
LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 6/38 | chr6 | 112190935 | |||||||
chr6:112190935 | CTTTCTTT others(13): Show |
C | 3 | a0001c0001t0001g0167 a0002c0003t0002g0066 a0002c0024t0001g0172 |
3 | HG01071.hp1 HG03453.hp1 NA18942.hp2 |
intron_variant | MODIFIER | c.718+681_718+700del others(20): Show |
LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 6/38 | chr6 | 112190935 | |||||||
chr6:112190935 | CTTTCTTT others(17): Show |
C | 1 | a0001c0009t0001g0203 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.718+677_718+700del others(24): Show |
LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 6/38 | chr6 | 112190935 | |||||||
chr6:112190936 | TTTCTTTC others(9): Show |
T | 4 | a0001c0002t0001g0087 a0001c0002t0001g0109 a0001c0002t0001g0110 others(1): Show |
4 | HG01433.hp1 HG02015.hp2 NA18955.hp1 others(1): Show |
intron_variant | MODIFIER | c.718+684_718+699del others(16): Show |
LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 6/38 | chr6 | 112190936 | |||||||
chr6:112190936 | TTTCTTTC others(13): Show |
T | 3 | a0001c0002t0001g0309 a0001c0005t0001g0101 a0002c0006t0002g0088 |
3 | HG01167.hp2 HG03017.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.718+680_718+699del others(20): Show |
LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 6/38 | chr6 | 112190936 | |||||||
chr6:112190937 | TTCTTTCT others(3): Show |
T | 1 | a0001c0001t0001g0186 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.718+689_718+698del others(10): Show |
LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 6/38 | chr6 | 112190937 | |||||||
chr6:112190938 | T | C | 1 | a0001c0002t0001g0188 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.718+698A>G | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 6/38 | chr6 | 112190938 | |||||||
chr6:112190938 | T | TC | 17 | a0001c0002t0001g0020 a0001c0002t0001g0205 a0001c0005t0001g0123 others(14): Show |
17 | HG01123.hp2 HG01981.hp1 HG02074.hp2 others(14): Show |
intron_variant | MODIFIER | c.718+697dupG | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 6/38 | chr6 | 112190938 | |||||||
chr6:112190938 | T | TCTTTC | 5 | a0001c0002t0001g0047 a0001c0002t0001g0278 a0004c0007t0001g0277 others(2): Show |
5 | HG02055.hp2 HG02132.hp1 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.718+693_718+697dup others(5): Show |
LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 6/38 | chr6 | 112190938 | |||||||
chr6:112190938 | TCTTTCTT others(2): Show |
T | 3 | a0001c0001t0001g0228 a0001c0009t0001g0073 a0010c0029t0001g0034 |
3 | HG02004.hp2 HG02738.hp1 NA19058.hp1 |
intron_variant | MODIFIER | c.718+689_718+697del others(9): Show |
LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 6/38 | chr6 | 112190938 | |||||||
chr6:112190939 | CTTT | C | 9 | a0001c0001t0001g0050 a0001c0001t0001g0246 a0001c0002t0001g0253 others(6): Show |
9 | HG00323.hp1 HG00323.hp2 HG01358.hp2 others(6): Show |
intron_variant | MODIFIER | c.718+694_718+696del others(3): Show |
LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 6/38 | chr6 | 112190939 | |||||||
chr6:112190939 | CTTTCTTT others(5): Show |
C | 8 | a0001c0001t0001g0285 a0001c0001t0011g0229 a0002c0003t0002g0198 others(5): Show |
8 | HG01515.hp2 HG02280.hp2 HG03017.hp2 others(5): Show |
intron_variant | MODIFIER | c.718+685_718+696del others(12): Show |
LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 6/38 | chr6 | 112190939 | |||||||
chr6:112190939 | CTTTCTTT others(9): Show |
C | 12 | a0001c0001t0001g0090 a0001c0001t0001g0138 a0001c0009t0001g0288 others(9): Show |
12 | HG00673.hp2 HG01361.hp1 HG02080.hp1 others(9): Show |
intron_variant | MODIFIER | c.718+681_718+696del others(16): Show |
LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 6/38 | chr6 | 112190939 | |||||||
chr6:112190939 | CTTTCTTT others(13): Show |
C | 2 | a0001c0001t0001g0202 a0004c0010t0012g0177 |
2 | HG02132.hp2 NA19090.hp1 |
intron_variant | MODIFIER | c.718+677_718+696del others(20): Show |
LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 6/38 | chr6 | 112190939 | |||||||
chr6:112190940 | T | C | 2 | a0001c0020t0005g0168 a0001c0020t0005g0169 |
2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.718+696A>G | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 6/38 | chr6 | 112190940 | |||||||
chr6:112190940 | TTTCTTTC others(5): Show |
T | 6 | a0001c0002t0001g0212 a0001c0005t0001g0044 a0002c0006t0002g0064 others(3): Show |
6 | HG01978.hp2 HG03927.hp2 NA18947.hp2 others(3): Show |
intron_variant | MODIFIER | c.718+684_718+695del others(12): Show |
LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 6/38 | chr6 | 112190940 | |||||||
chr6:112190940 | TTTCTTTC others(9): Show |
T | 1 | a0001c0005t0001g0230 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.718+680_718+695del others(16): Show |
LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 6/38 | chr6 | 112190940 | |||||||
chr6:112190942 | T | TC | 8 | a0001c0001t0001g0053 a0001c0001t0001g0136 a0001c0011t0003g0155 others(5): Show |
8 | HG00280.hp1 HG00280.hp2 HG00597.hp2 others(5): Show |
intron_variant | MODIFIER | c.718+693dupG | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 6/38 | chr6 | 112190942 | |||||||
chr6:112190943 | CTTTCCTT others(5): Show |
C | 13 | a0001c0001t0001g0027 a0001c0001t0001g0072 a0001c0001t0001g0074 others(10): Show |
13 | HG01361.hp2 HG02027.hp1 HG02083.hp1 others(10): Show |
intron_variant | MODIFIER | c.718+681_718+692del others(12): Show |
LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 6/38 | chr6 | 112190943 | |||||||
chr6:112190943 | CTTTCCTT others(9): Show |
C | 2 | a0001c0001t0001g0069 a0002c0003t0002g0071 |
2 | NA18970.hp1 NA18970.hp2 |
intron_variant | MODIFIER | c.718+677_718+692del others(16): Show |
LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 6/38 | chr6 | 112190943 | |||||||
chr6:112190944 | T | C | 20 | a0001c0001t0001g0055 a0001c0001t0001g0115 a0001c0001t0001g0204 others(17): Show |
20 | HG00733.hp2 HG01243.hp2 HG01258.hp1 others(17): Show |
intron_variant | MODIFIER | c.718+692A>G | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 6/38 | chr6 | 112190944 | |||||||
chr6:112190944 | T | TCTTTCTT others(6): Show |
1 | a0003c0004t0001g0028 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.718+691_718+692ins others(13): Show |
LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 6/38 | chr6 | 112190944 | |||||||
chr6:112190946 | TC | T | 60 | a0001c0001t0001g0050 a0001c0001t0001g0051 a0001c0001t0001g0052 others(57): Show |
60 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(57): Show |
intron_variant | MODIFIER | c.718+689delG | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 6/38 | chr6 | 112190946 | |||||||
chr6:112190947 | C | CCTTCCTT others(5): Show |
2 | a0001c0020t0005g0168 a0001c0020t0005g0169 |
2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.718+688_718+689ins others(12): Show |
LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 6/38 | chr6 | 112190947 | |||||||
chr6:112190947 | C | CCTTT | 3 | a0003c0004t0001g0030 a0003c0004t0001g0141 a0009c0017t0002g0307 |
3 | HG01106.hp1 HG03688.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.718+685_718+688dup others(4): Show |
LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 6/38 | chr6 | 112190947 | |||||||
chr6:112190947 | C | CCTTTCTT others(1): Show |
3 | a0001c0002t0001g0254 a0001c0002t0001g0289 a0001c0005t0001g0247 |
3 | HG00621.hp1 HG00741.hp1 NA19062.hp1 |
intron_variant | MODIFIER | c.718+681_718+688dup others(8): Show |
LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 6/38 | chr6 | 112190947 | |||||||
chr6:112190947 | C | CCTTTCTT others(5): Show |
3 | a0001c0005t0001g0275 a0001c0020t0005g0046 a0007c0060t0002g0260 |
3 | HG01891.hp2 HG02809.hp1 NA18961.hp2 |
intron_variant | MODIFIER | c.718+677_718+688dup others(12): Show |
LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 6/38 | chr6 | 112190947 | |||||||
chr6:112190947 | C | CCTTTCTT others(9): Show |
7 | a0001c0001t0001g0121 a0001c0011t0003g0293 a0001c0016t0010g0209 others(4): Show |
7 | HG00639.hp2 HG00642.hp2 HG02109.hp2 others(4): Show |
intron_variant | MODIFIER | c.718+673_718+688dup others(16): Show |
LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 6/38 | chr6 | 112190947 | |||||||
chr6:112190947 | C | CCTTTCTT others(13): Show |
3 | a0003c0004t0001g0018 a0004c0007t0014g0300 a0007c0014t0002g0292 |
3 | HG01175.hp1 HG01515.hp1 NA18971.hp1 |
intron_variant | MODIFIER | c.718+669_718+688dup others(20): Show |
LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 6/38 | chr6 | 112190947 | |||||||
chr6:112190947 | C | CTTT | 58 | a0001c0001t0001g0053 a0001c0001t0001g0136 a0001c0001t0001g0257 others(55): Show |
58 | HG00280.hp1 HG00280.hp2 HG00408.hp2 others(55): Show |
intron_variant | MODIFIER | c.718+688_718+689ins others(3): Show |
LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 6/38 | chr6 | 112190947 | |||||||
chr6:112190947 | C | CTTTCCTT others(5): Show |
2 | a0001c0011t0003g0236 a0012c0021t0001g0144 |
2 | HG02922.hp1 NA18948.hp1 |
intron_variant | MODIFIER | c.718+688_718+689ins others(12): Show |
LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 6/38 | chr6 | 112190947 | |||||||
chr6:112190947 | C | CTTTCCTT others(9): Show |
2 | a0001c0002t0001g0192 a0002c0006t0002g0133 |
2 | HG02080.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.718+688_718+689ins others(16): Show |
LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 6/38 | chr6 | 112190947 | |||||||
chr6:112190947 | C | CTTTCCTT others(13): Show |
1 | a0001c0005t0001g0235 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.718+688_718+689ins others(20): Show |
LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 6/38 | chr6 | 112190947 | |||||||
chr6:112190947 | C | CTTTCCTT others(21): Show |
1 | a0003c0004t0001g0081 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.718+688_718+689ins others(28): Show |
LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 6/38 | chr6 | 112190947 | |||||||
chr6:112190947 | C | CTTTCTTT others(9): Show |
1 | a0023c0035t0001g0185 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.718+688_718+689ins others(16): Show |
LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 6/38 | chr6 | 112190947 | |||||||
chr6:112190947 | C | CTTTCTTT others(4): Show |
4 | a0001c0001t0001g0015 a0001c0016t0001g0048 a0004c0026t0001g0068 others(1): Show |
4 | HG01169.hp1 HG02257.hp2 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.718+688_718+689ins others(11): Show |
LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 6/38 | chr6 | 112190947 | |||||||
chr6:112190947 | C | CTTTCTTT others(8): Show |
1 | a0004c0007t0001g0160 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.718+688_718+689ins others(15): Show |
LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 6/38 | chr6 | 112190947 | |||||||
chr6:112190947 | C | CTTTCTTT others(12): Show |
2 | a0001c0005t0001g0263 a0001c0050t0001g0310 |
2 | HG02015.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.718+688_718+689ins others(19): Show |
LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 6/38 | chr6 | 112190947 | |||||||
chr6:112190947 | C | CTTTCTTT others(24): Show |
1 | a0001c0002t0001g0165 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.718+688_718+689ins others(31): Show |
LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 6/38 | chr6 | 112190947 | |||||||
chr6:112190947 | C | T | 19 | a0001c0001t0001g0055 a0001c0001t0001g0115 a0001c0001t0001g0204 others(16): Show |
19 | HG00733.hp2 HG01243.hp2 HG01258.hp1 others(16): Show |
intron_variant | MODIFIER | c.718+689G>A | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 6/38 | chr6 | 112190947 | |||||||
chr6:112190947 | CCTTTCTT others(1): Show |
C | 3 | a0001c0001t0001g0007 a0001c0001t0001g0070 a0006c0012t0002g0271 |
3 | HG00597.hp1 HG03834.hp2 NA19056.hp1 |
intron_variant | MODIFIER | c.718+681_718+688del others(8): Show |
LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 6/38 | chr6 | 112190947 | |||||||
chr6:112190948 | C | T | 2 | a0001c0002t0001g0107 a0001c0011t0003g0009 |
2 | HG02055.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.718+688G>A | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 6/38 | chr6 | 112190948 | |||||||
chr6:112190951 | T | C | 2 | a0001c0011t0003g0009 a0001c0054t0001g0301 |
2 | HG02055.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.718+685A>G | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 6/38 | chr6 | 112190951 | |||||||
chr6:112190952 | C | T | 1 | a0001c0005t0001g0103 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.718+684G>A | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 6/38 | chr6 | 112190952 | |||||||
chr6:112190955 | T | TCTTTCTT others(6): Show |
2 | a0002c0006t0002g0037 a0002c0006t0002g0199 |
2 | HG03453.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.718+668_718+680dup others(13): Show |
LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 6/38 | chr6 | 112190955 | |||||||
chr6:112190955 | T | TCTTTCTT others(10): Show |
1 | a0015c0049t0002g0200 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.718+664_718+680dup others(17): Show |
LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 6/38 | chr6 | 112190955 | |||||||
chr6:112190959 | T | TC | 3 | a0001c0002t0001g0020 a0001c0020t0005g0168 a0001c0020t0005g0169 |
3 | HG02895.hp1 HG02897.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.718+676dupG | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 6/38 | chr6 | 112190959 | |||||||
chr6:112190959 | T | TCTTTCTT others(6): Show |
1 | a0001c0054t0001g0301 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.718+664_718+676dup others(13): Show |
LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 6/38 | chr6 | 112190959 | |||||||
chr6:112190985 | T | TTTCTTTC others(8): Show |
1 | a0001c0011t0003g0062 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.718+650_718+651ins others(15): Show |
LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 6/38 | chr6 | 112190985 | |||||||
chr6:112190988 | C | CTTTCTTT others(6): Show |
1 | a0001c0002t0001g0258 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.718+647_718+648ins others(13): Show |
LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 6/38 | chr6 | 112190988 | |||||||
chr6:112190988 | C | CTTTCTTT others(23): Show |
1 | a0007c0014t0002g0119 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.718+647_718+648ins others(30): Show |
LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 6/38 | chr6 | 112190988 | |||||||
chr6:112191154 | G | A | 16 | a0001c0002t0001g0192 a0001c0002t0001g0254 a0001c0011t0003g0062 others(13): Show |
16 | HG00741.hp1 HG02109.hp1 HG02109.hp2 others(13): Show |
intron_variant | MODIFIER | c.718+482C>T | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 6/38 | chr6 | 112191154 | |||||||
chr6:112191247 | G | T | 97 | a0001c0002t0001g0005 a0001c0002t0001g0006 a0001c0002t0001g0045 others(94): Show |
97 | HG00408.hp2 HG00621.hp1 HG00639.hp1 others(94): Show |
intron_variant | MODIFIER | c.718+389C>A | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 6/38 | chr6 | 112191247 | |||||||
chr6:112191291 | C | A | 117 | a0001c0002t0001g0005 a0001c0002t0001g0006 a0001c0002t0001g0020 others(114): Show |
117 | HG00408.hp2 HG00621.hp1 HG00639.hp1 others(114): Show |
intron_variant | MODIFIER | c.718+345G>T | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 6/38 | chr6 | 112191291 | |||||||
chr6:112191957 | C | T | 47 | a0001c0002t0001g0045 a0001c0002t0001g0047 a0001c0002t0001g0164 others(44): Show |
47 | HG00408.hp2 HG00621.hp1 HG01891.hp2 others(44): Show |
intron_variant | MODIFIER | c.504-107G>A | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 5/38 | chr6 | 112191957 | |||||||
chr6:112192120 | C | A | 1 | a0002c0003t0002g0305 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.504-270G>T | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 5/38 | chr6 | 112192120 | |||||||
chr6:112192382 | G | T | 77 | a0001c0023t0003g0302 a0001c0023t0003g0306 a0001c0037t0003g0003 others(74): Show |
77 | HG00323.hp1 HG00597.hp2 HG00621.hp2 others(74): Show |
intron_variant | MODIFIER | c.504-532C>A | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 5/38 | chr6 | 112192382 | |||||||
chr6:112192580 | G | T | 3 | a0001c0050t0001g0310 a0004c0026t0001g0067 a0004c0026t0001g0068 |
3 | HG01167.hp1 HG01169.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.504-730C>A | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 5/38 | chr6 | 112192580 | |||||||
chr6:112192638 | C | T | 2 | a0002c0003t0006g0001 a0002c0003t0006g0002 |
2 | HG02809.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.504-788G>A | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 5/38 | chr6 | 112192638 | |||||||
chr6:112192639 | C | A | 2 | a0002c0003t0006g0001 a0002c0003t0006g0002 |
2 | HG02809.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.504-789G>T | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 5/38 | chr6 | 112192639 | |||||||
chr6:112192685 | C | T | 1 | a0001c0011t0003g0293 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.504-835G>A | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 5/38 | chr6 | 112192685 | |||||||
chr6:112192892 | G | T | 108 | a0001c0002t0001g0005 a0001c0002t0001g0006 a0001c0002t0001g0020 others(105): Show |
108 | HG00408.hp2 HG00621.hp1 HG00639.hp1 others(105): Show |
intron_variant | MODIFIER | c.504-1042C>A | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 5/38 | chr6 | 112192892 | |||||||
chr6:112192893 | A | T | 3 | a0012c0021t0001g0083 a0012c0021t0001g0144 a0021c0033t0013g0124 |
3 | NA18612.hp1 NA18948.hp1 NA18954.hp1 |
intron_variant | MODIFIER | c.504-1043T>A | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 5/38 | chr6 | 112192893 | |||||||
chr6:112193154 | G | C | 16 | a0001c0002t0001g0192 a0001c0002t0001g0254 a0001c0011t0003g0062 others(13): Show |
16 | HG00741.hp1 HG02109.hp1 HG02109.hp2 others(13): Show |
intron_variant | MODIFIER | c.504-1304C>G | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 5/38 | chr6 | 112193154 | |||||||
chr6:112193415 | A | T | 1 | a0007c0014t0002g0119 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.504-1565T>A | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 5/38 | chr6 | 112193415 | |||||||
chr6:112193473 | T | TA | 102 | a0001c0002t0001g0005 a0001c0002t0001g0006 a0001c0002t0001g0020 others(99): Show |
102 | HG00408.hp2 HG00621.hp1 HG00639.hp1 others(99): Show |
intron_variant | MODIFIER | c.504-1624dupT | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 5/38 | chr6 | 112193473 | |||||||
chr6:112193503 | C | T | 1 | a0001c0002t0001g0191 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.504-1653G>A | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 5/38 | chr6 | 112193503 | |||||||
chr6:112193515 | C | A | 105 | a0001c0002t0001g0005 a0001c0002t0001g0006 a0001c0002t0001g0020 others(102): Show |
105 | HG00408.hp2 HG00621.hp1 HG00639.hp1 others(102): Show |
intron_variant | MODIFIER | c.504-1665G>T | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 5/38 | chr6 | 112193515 | |||||||
chr6:112193532 | G | A | 3 | a0001c0005t0001g0286 a0001c0011t0003g0313 a0002c0006t0002g0294 |
3 | HG03225.hp1 NA19000.hp2 NA19002.hp1 |
intron_variant | MODIFIER | c.504-1682C>T | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 5/38 | chr6 | 112193532 | |||||||
chr6:112193618 | C | A | 2 | a0003c0025t0001g0086 a0003c0025t0001g0113 |
2 | HG02886.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.504-1768G>T | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 5/38 | chr6 | 112193618 | |||||||
chr6:112193624 | C | G | 81 | a0001c0002t0001g0005 a0001c0002t0001g0006 a0001c0002t0001g0045 others(78): Show |
81 | HG00408.hp2 HG00621.hp1 HG00639.hp1 others(78): Show |
intron_variant | MODIFIER | c.504-1774G>C | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 5/38 | chr6 | 112193624 | |||||||
chr6:112193625 | G | A | 105 | a0001c0002t0001g0005 a0001c0002t0001g0006 a0001c0002t0001g0020 others(102): Show |
105 | HG00408.hp2 HG00621.hp1 HG00639.hp1 others(102): Show |
intron_variant | MODIFIER | c.504-1775C>T | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 5/38 | chr6 | 112193625 | |||||||
chr6:112193649 | A | G | 4 | a0008c0015t0001g0057 a0008c0015t0001g0059 a0008c0015t0001g0061 others(1): Show |
4 | HG02486.hp2 HG03139.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.504-1799T>C | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 5/38 | chr6 | 112193649 | |||||||
chr6:112193726 | C | A | 1 | a0019c0036t0001g0282 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.504-1876G>T | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 5/38 | chr6 | 112193726 | |||||||
chr6:112193775 | C | T | 1 | a0007c0014t0002g0119 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.504-1925G>A | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 5/38 | chr6 | 112193775 | |||||||
chr6:112193988 | G | T | 1 | a0004c0010t0004g0128 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.504-2138C>A | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 5/38 | chr6 | 112193988 | |||||||
chr6:112194137 | T | G | 1 | a0002c0006t0002g0199 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.504-2287A>C | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 5/38 | chr6 | 112194137 | |||||||
chr6:112194228 | A | G | 111 | a0001c0002t0001g0005 a0001c0002t0001g0006 a0001c0002t0001g0020 others(108): Show |
111 | HG00408.hp2 HG00621.hp1 HG00639.hp1 others(108): Show |
intron_variant | MODIFIER | c.504-2378T>C | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 5/38 | chr6 | 112194228 | |||||||
chr6:112194365 | C | A | 1 | a0002c0006t0002g0037 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.504-2515G>T | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 5/38 | chr6 | 112194365 | |||||||
chr6:112194366 | C | T | 4 | a0001c0001t0001g0007 a0001c0001t0001g0090 a0006c0012t0002g0106 others(1): Show |
4 | HG00597.hp1 NA18964.hp1 NA19006.hp2 others(1): Show |
intron_variant | MODIFIER | c.504-2516G>A | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 5/38 | chr6 | 112194366 | |||||||
chr6:112194499 | G | A | 104 | a0001c0002t0001g0005 a0001c0002t0001g0006 a0001c0002t0001g0020 others(101): Show |
104 | HG00408.hp2 HG00621.hp1 HG00639.hp1 others(101): Show |
intron_variant | MODIFIER | c.504-2649C>T | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 5/38 | chr6 | 112194499 | |||||||
chr6:112194565 | G | A | 3 | a0001c0001t0001g0149 a0001c0001t0001g0246 a0001c0009t0001g0082 |
3 | HG02071.hp1 HG02165.hp1 NA18948.hp2 |
intron_variant | MODIFIER | c.504-2715C>T | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 5/38 | chr6 | 112194565 | |||||||
chr6:112194583 | C | T | 1 | a0001c0001t0001g0256 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.504-2733G>A | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 5/38 | chr6 | 112194583 | |||||||
chr6:112194595 | A | T | 1 | a0005c0008t0001g0241 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.504-2745T>A | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 5/38 | chr6 | 112194595 | |||||||
chr6:112194727 | G | A | 198 | a0001c0002t0001g0005 a0001c0002t0001g0006 a0001c0002t0001g0020 others(195): Show |
198 | HG00323.hp1 HG00408.hp2 HG00597.hp2 others(195): Show |
intron_variant | MODIFIER | c.504-2877C>T | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 5/38 | chr6 | 112194727 | |||||||
chr6:112195255 | C | G | 198 | a0001c0002t0001g0005 a0001c0002t0001g0006 a0001c0002t0001g0020 others(195): Show |
198 | HG00323.hp1 HG00408.hp2 HG00597.hp2 others(195): Show |
intron_variant | MODIFIER | c.504-3405G>C | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 5/38 | chr6 | 112195255 | |||||||
chr6:112195268 | T | C | 194 | a0001c0002t0001g0005 a0001c0002t0001g0006 a0001c0002t0001g0020 others(191): Show |
194 | HG00323.hp1 HG00408.hp2 HG00597.hp2 others(191): Show |
intron_variant | MODIFIER | c.504-3418A>G | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 5/38 | chr6 | 112195268 | |||||||
chr6:112195383 | A | C | 194 | a0001c0002t0001g0005 a0001c0002t0001g0006 a0001c0002t0001g0020 others(191): Show |
194 | HG00323.hp1 HG00408.hp2 HG00597.hp2 others(191): Show |
intron_variant | MODIFIER | c.504-3533T>G | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 5/38 | chr6 | 112195383 | |||||||
chr6:112195485 | T | G | 1 | a0001c0001t0001g0227 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.504-3635A>C | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 5/38 | chr6 | 112195485 | |||||||
chr6:112195733 | A | T | 1 | a0001c0023t0003g0302 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.504-3883T>A | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 5/38 | chr6 | 112195733 | |||||||
chr6:112195833 | T | C | 194 | a0001c0002t0001g0005 a0001c0002t0001g0006 a0001c0002t0001g0020 others(191): Show |
194 | HG00323.hp1 HG00408.hp2 HG00597.hp2 others(191): Show |
intron_variant | MODIFIER | c.504-3983A>G | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 5/38 | chr6 | 112195833 | |||||||
chr6:112195854 | C | A | 194 | a0001c0002t0001g0005 a0001c0002t0001g0006 a0001c0002t0001g0020 others(191): Show |
194 | HG00323.hp1 HG00408.hp2 HG00597.hp2 others(191): Show |
intron_variant | MODIFIER | c.504-4004G>T | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 5/38 | chr6 | 112195854 | |||||||
chr6:112195938 | T | TAC | 18 | a0001c0001t0001g0027 a0001c0002t0001g0076 a0001c0002t0001g0197 others(15): Show |
18 | HG00408.hp2 HG01081.hp2 HG01243.hp1 others(15): Show |
intron_variant | MODIFIER | c.504-4090_504-4089d others(4): Show |
LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 5/38 | chr6 | 112195938 | |||||||
chr6:112195938 | T | TACAC | 67 | a0001c0023t0003g0302 a0001c0037t0003g0003 a0001c0050t0001g0310 others(64): Show |
67 | HG00323.hp1 HG00597.hp2 HG00621.hp2 others(64): Show |
intron_variant | MODIFIER | c.504-4092_504-4089d others(6): Show |
LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 5/38 | chr6 | 112195938 | |||||||
chr6:112195938 | T | TACACAC | 10 | a0001c0023t0003g0306 a0002c0003t0002g0290 a0003c0004t0001g0029 others(7): Show |
10 | HG01167.hp1 HG01169.hp1 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.504-4094_504-4089d others(8): Show |
LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 5/38 | chr6 | 112195938 | |||||||
chr6:112195938 | T | TACACACA others(1): Show |
4 | a0001c0020t0005g0168 a0001c0020t0005g0169 a0001c0054t0001g0301 others(1): Show |
4 | HG02280.hp2 HG02895.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.504-4096_504-4089d others(10): Show |
LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 5/38 | chr6 | 112195938 | |||||||
chr6:112195938 | TAC | T | 25 | a0001c0001t0001g0167 a0001c0001t0001g0220 a0001c0002t0001g0020 others(22): Show |
25 | HG00741.hp1 HG01256.hp2 HG01258.hp2 others(22): Show |
intron_variant | MODIFIER | c.504-4090_504-4089d others(4): Show |
LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 5/38 | chr6 | 112195938 | |||||||
chr6:112195980 | A | ATATAT | 192 | a0001c0002t0001g0005 a0001c0002t0001g0006 a0001c0002t0001g0020 others(189): Show |
192 | HG00323.hp1 HG00408.hp2 HG00597.hp2 others(189): Show |
intron_variant | MODIFIER | c.504-4135_504-4131d others(7): Show |
LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 5/38 | chr6 | 112195980 | |||||||
chr6:112196079 | C | A | 80 | a0001c0020t0005g0168 a0001c0020t0005g0169 a0001c0023t0003g0302 others(77): Show |
80 | HG00323.hp1 HG00597.hp2 HG00621.hp2 others(77): Show |
intron_variant | MODIFIER | c.504-4229G>T | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 5/38 | chr6 | 112196079 | |||||||
chr6:112196326 | C | G | 6 | a0001c0002t0001g0076 a0001c0002t0001g0197 a0001c0011t0003g0161 others(3): Show |
6 | HG01081.hp2 HG01243.hp1 HG02257.hp1 others(3): Show |
intron_variant | MODIFIER | c.504-4476G>C | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 5/38 | chr6 | 112196326 | |||||||
chr6:112196335 | AC | A | 105 | a0001c0002t0001g0005 a0001c0002t0001g0006 a0001c0002t0001g0020 others(102): Show |
105 | HG00408.hp2 HG00621.hp1 HG00639.hp1 others(102): Show |
intron_variant | MODIFIER | c.504-4486delG | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 5/38 | chr6 | 112196335 | |||||||
chr6:112196338 | A | G | 77 | a0001c0023t0003g0302 a0001c0023t0003g0306 a0001c0037t0003g0003 others(74): Show |
77 | HG00323.hp1 HG00597.hp2 HG00621.hp2 others(74): Show |
intron_variant | MODIFIER | c.504-4488T>C | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 5/38 | chr6 | 112196338 | |||||||
chr6:112196411 | T | C | 194 | a0001c0002t0001g0005 a0001c0002t0001g0006 a0001c0002t0001g0020 others(191): Show |
194 | HG00323.hp1 HG00408.hp2 HG00597.hp2 others(191): Show |
intron_variant | MODIFIER | c.504-4561A>G | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 5/38 | chr6 | 112196411 | |||||||
chr6:112196566 | T | G | 114 | a0001c0002t0001g0005 a0001c0002t0001g0006 a0001c0002t0001g0020 others(111): Show |
114 | HG00408.hp2 HG00621.hp1 HG00639.hp1 others(111): Show |
intron_variant | MODIFIER | c.504-4716A>C | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 5/38 | chr6 | 112196566 | |||||||
chr6:112196579 | T | C | 3 | a0001c0050t0001g0310 a0004c0026t0001g0067 a0004c0026t0001g0068 |
3 | HG01167.hp1 HG01169.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.504-4729A>G | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 5/38 | chr6 | 112196579 | |||||||
chr6:112196674 | C | T | 1 | a0003c0004t0001g0240 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.504-4824G>A | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 5/38 | chr6 | 112196674 | |||||||
chr6:112196730 | T | C | 105 | a0001c0002t0001g0005 a0001c0002t0001g0006 a0001c0002t0001g0020 others(102): Show |
105 | HG00408.hp2 HG00621.hp1 HG00639.hp1 others(102): Show |
intron_variant | MODIFIER | c.503+4878A>G | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 5/38 | chr6 | 112196730 | |||||||
chr6:112196805 | G | C | 1 | a0010c0029t0001g0025 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.503+4803C>G | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 5/38 | chr6 | 112196805 | |||||||
chr6:112196888 | A | G | 194 | a0001c0002t0001g0005 a0001c0002t0001g0006 a0001c0002t0001g0020 others(191): Show |
194 | HG00323.hp1 HG00408.hp2 HG00597.hp2 others(191): Show |
intron_variant | MODIFIER | c.503+4720T>C | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 5/38 | chr6 | 112196888 | |||||||
chr6:112196924 | T | A | 25 | a0001c0001t0001g0014 a0001c0001t0001g0033 a0001c0001t0001g0116 others(22): Show |
25 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(22): Show |
intron_variant | MODIFIER | c.503+4684A>T | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 5/38 | chr6 | 112196924 | |||||||
chr6:112196926 | C | G | 1 | a0001c0052t0002g0295 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.503+4682G>C | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 5/38 | chr6 | 112196926 | |||||||
chr6:112197345 | C | T | 3 | a0001c0050t0001g0310 a0004c0026t0001g0067 a0004c0026t0001g0068 |
3 | HG01167.hp1 HG01169.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.503+4263G>A | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 5/38 | chr6 | 112197345 | |||||||
chr6:112197425 | G | A | 1 | a0001c0011t0003g0255 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.503+4183C>T | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 5/38 | chr6 | 112197425 | |||||||
chr6:112197426 | C | T | 1 | a0001c0020t0005g0046 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.503+4182G>A | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 5/38 | chr6 | 112197426 | |||||||
chr6:112197432 | T | C | 105 | a0001c0002t0001g0005 a0001c0002t0001g0006 a0001c0002t0001g0020 others(102): Show |
105 | HG00408.hp2 HG00621.hp1 HG00639.hp1 others(102): Show |
intron_variant | MODIFIER | c.503+4176A>G | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 5/38 | chr6 | 112197432 | |||||||
chr6:112197540 | C | T | 1 | a0001c0023t0003g0302 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.503+4068G>A | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 5/38 | chr6 | 112197540 | |||||||
chr6:112197743 | C | T | 2 | a0004c0026t0001g0067 a0004c0026t0001g0068 |
2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.503+3865G>A | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 5/38 | chr6 | 112197743 | |||||||
chr6:112198143 | C | T | 1 | a0011c0028t0002g0154 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.503+3465G>A | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 5/38 | chr6 | 112198143 | |||||||
chr6:112198205 | T | C | 1 | a0004c0057t0003g0017 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.503+3403A>G | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 5/38 | chr6 | 112198205 | |||||||
chr6:112198363 | T | C | 1 | a0002c0003t0001g0171 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.503+3245A>G | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 5/38 | chr6 | 112198363 | |||||||
chr6:112198541 | G | A | 194 | a0001c0002t0001g0005 a0001c0002t0001g0006 a0001c0002t0001g0020 others(191): Show |
194 | HG00323.hp1 HG00408.hp2 HG00597.hp2 others(191): Show |
intron_variant | MODIFIER | c.503+3067C>T | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 5/38 | chr6 | 112198541 | |||||||
chr6:112198855 | C | G | 89 | a0001c0002t0001g0076 a0001c0002t0001g0197 a0001c0011t0003g0161 others(86): Show |
89 | HG00323.hp1 HG00597.hp2 HG00621.hp2 others(86): Show |
intron_variant | MODIFIER | c.503+2753G>C | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 5/38 | chr6 | 112198855 | |||||||
chr6:112198900 | A | G | 89 | a0001c0002t0001g0076 a0001c0002t0001g0197 a0001c0011t0003g0161 others(86): Show |
89 | HG00323.hp1 HG00597.hp2 HG00621.hp2 others(86): Show |
intron_variant | MODIFIER | c.503+2708T>C | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 5/38 | chr6 | 112198900 | |||||||
chr6:112198986 | C | T | 2 | a0001c0001t0001g0015 a0001c0001t0001g0257 |
2 | NA18975.hp1 NA18988.hp2 |
intron_variant | MODIFIER | c.503+2622G>A | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 5/38 | chr6 | 112198986 | |||||||
chr6:112199010 | A | G | 89 | a0001c0002t0001g0076 a0001c0002t0001g0197 a0001c0011t0003g0161 others(86): Show |
89 | HG00323.hp1 HG00597.hp2 HG00621.hp2 others(86): Show |
intron_variant | MODIFIER | c.503+2598T>C | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 5/38 | chr6 | 112199010 | |||||||
chr6:112199034 | C | T | 6 | a0001c0002t0001g0076 a0001c0002t0001g0197 a0001c0011t0003g0161 others(3): Show |
6 | HG01081.hp2 HG01243.hp1 HG02257.hp1 others(3): Show |
intron_variant | MODIFIER | c.503+2574G>A | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 5/38 | chr6 | 112199034 | |||||||
chr6:112199050 | T | C | 198 | a0001c0002t0001g0005 a0001c0002t0001g0006 a0001c0002t0001g0020 others(195): Show |
198 | HG00323.hp1 HG00408.hp2 HG00597.hp2 others(195): Show |
intron_variant | MODIFIER | c.503+2558A>G | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 5/38 | chr6 | 112199050 | |||||||
chr6:112199287 | G | T | 10 | a0001c0005t0001g0118 a0001c0005t0001g0123 a0001c0005t0001g0137 others(7): Show |
10 | NA18943.hp1 NA18992.hp1 NA19000.hp1 others(7): Show |
intron_variant | MODIFIER | c.503+2321C>A | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 5/38 | chr6 | 112199287 | |||||||
chr6:112199351 | T | C | 194 | a0001c0002t0001g0005 a0001c0002t0001g0006 a0001c0002t0001g0020 others(191): Show |
194 | HG00323.hp1 HG00408.hp2 HG00597.hp2 others(191): Show |
intron_variant | MODIFIER | c.503+2257A>G | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 5/38 | chr6 | 112199351 | |||||||
chr6:112199420 | G | GA | 36 | a0003c0004t0001g0081 a0003c0004t0001g0114 a0003c0004t0001g0125 others(33): Show |
36 | HG00597.hp2 HG00621.hp2 HG00642.hp2 others(33): Show |
intron_variant | MODIFIER | c.503+2187dupT | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 5/38 | chr6 | 112199420 | |||||||
chr6:112199518 | A | G | 7 | a0001c0002t0001g0020 a0001c0011t0003g0009 a0002c0006t0002g0037 others(4): Show |
7 | HG01981.hp2 HG02055.hp1 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.503+2090T>C | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 5/38 | chr6 | 112199518 | |||||||
chr6:112199770 | C | CT | 87 | a0001c0001t0001g0027 a0001c0002t0001g0076 a0001c0002t0001g0197 others(84): Show |
87 | HG00323.hp1 HG00597.hp2 HG00621.hp2 others(84): Show |
intron_variant | MODIFIER | c.503+1837dupA | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 5/38 | chr6 | 112199770 | |||||||
chr6:112199770 | C | CTTT | 7 | a0001c0002t0001g0020 a0001c0011t0003g0009 a0002c0006t0002g0037 others(4): Show |
7 | HG01981.hp2 HG02055.hp1 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.503+1835_503+1837d others(5): Show |
LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 5/38 | chr6 | 112199770 | |||||||
chr6:112199770 | CT | C | 99 | a0001c0001t0001g0055 a0001c0002t0001g0005 a0001c0002t0001g0006 others(96): Show |
99 | HG00408.hp2 HG00621.hp1 HG00639.hp1 others(96): Show |
intron_variant | MODIFIER | c.503+1837delA | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 5/38 | chr6 | 112199770 | |||||||
chr6:112199941 | G | A | 6 | a0001c0002t0001g0076 a0001c0002t0001g0197 a0001c0011t0003g0161 others(3): Show |
6 | HG01081.hp2 HG01243.hp1 HG02257.hp1 others(3): Show |
intron_variant | MODIFIER | c.503+1667C>T | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 5/38 | chr6 | 112199941 | |||||||
chr6:112199981 | G | A | 198 | a0001c0002t0001g0005 a0001c0002t0001g0006 a0001c0002t0001g0020 others(195): Show |
198 | HG00323.hp1 HG00408.hp2 HG00597.hp2 others(195): Show |
intron_variant | MODIFIER | c.503+1627C>T | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 5/38 | chr6 | 112199981 | |||||||
chr6:112200072 | G | C | 4 | a0001c0002t0001g0254 a0002c0006t0002g0170 a0002c0006t0002g0249 others(1): Show |
4 | HG00741.hp1 HG02622.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.503+1536C>G | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 5/38 | chr6 | 112200072 | |||||||
chr6:112200185 | A | C | 89 | a0001c0002t0001g0076 a0001c0002t0001g0197 a0001c0011t0003g0161 others(86): Show |
89 | HG00323.hp1 HG00597.hp2 HG00621.hp2 others(86): Show |
intron_variant | MODIFIER | c.503+1423T>G | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 5/38 | chr6 | 112200185 | |||||||
chr6:112200435 | A | G | 194 | a0001c0002t0001g0005 a0001c0002t0001g0006 a0001c0002t0001g0020 others(191): Show |
194 | HG00323.hp1 HG00408.hp2 HG00597.hp2 others(191): Show |
intron_variant | MODIFIER | c.503+1173T>C | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 5/38 | chr6 | 112200435 | |||||||
chr6:112200482 | C | T | 4 | a0001c0016t0002g0268 a0004c0007t0001g0266 a0004c0007t0001g0267 others(1): Show |
4 | NA18971.hp1 NA18977.hp2 NA19070.hp2 others(1): Show |
intron_variant | MODIFIER | c.503+1126G>A | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 5/38 | chr6 | 112200482 | |||||||
chr6:112200623 | G | C | 89 | a0001c0002t0001g0076 a0001c0002t0001g0197 a0001c0011t0003g0161 others(86): Show |
89 | HG00323.hp1 HG00597.hp2 HG00621.hp2 others(86): Show |
intron_variant | MODIFIER | c.503+985C>G | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 5/38 | chr6 | 112200623 | |||||||
chr6:112200754 | C | T | 15 | a0001c0002t0001g0192 a0001c0002t0001g0254 a0001c0011t0003g0062 others(12): Show |
15 | HG00741.hp1 HG02109.hp1 HG02109.hp2 others(12): Show |
intron_variant | MODIFIER | c.503+854G>A | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 5/38 | chr6 | 112200754 | |||||||
chr6:112200756 | G | A | 1 | a0001c0011t0003g0155 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.503+852C>T | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 5/38 | chr6 | 112200756 | |||||||
chr6:112200758 | C | G | 1 | a0001c0011t0003g0155 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.503+850G>C | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 5/38 | chr6 | 112200758 | |||||||
chr6:112200764 | T | C | 1 | a0001c0011t0003g0155 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.503+844A>G | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 5/38 | chr6 | 112200764 | |||||||
chr6:112200766 | A | G | 1 | a0001c0011t0003g0155 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.503+842T>C | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 5/38 | chr6 | 112200766 | |||||||
chr6:112200839 | A | G | 1 | a0001c0001t0001g0237 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.503+769T>C | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 5/38 | chr6 | 112200839 | |||||||
chr6:112200938 | G | A | 2 | a0001c0011t0003g0009 a0002c0003t0002g0290 |
2 | HG02055.hp1 HG02738.hp2 |
intron_variant | MODIFIER | c.503+670C>T | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 5/38 | chr6 | 112200938 | |||||||
chr6:112201064 | T | A | 3 | a0008c0015t0001g0057 a0008c0015t0001g0059 a0008c0015t0001g0061 |
3 | HG02486.hp2 HG03209.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.503+544A>T | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 5/38 | chr6 | 112201064 | |||||||
chr6:112201186 | T | C | 70 | a0002c0003t0002g0290 a0003c0004t0001g0018 a0003c0004t0001g0022 others(67): Show |
70 | HG00323.hp1 HG00597.hp2 HG00621.hp2 others(67): Show |
intron_variant | MODIFIER | c.503+422A>G | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 5/38 | chr6 | 112201186 | |||||||
chr6:112201327 | G | A | 12 | a0001c0001t0001g0070 a0001c0001t0001g0072 a0001c0001t0001g0074 others(9): Show |
12 | HG00673.hp2 HG02129.hp2 HG03831.hp2 others(9): Show |
intron_variant | MODIFIER | c.503+281C>T | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 5/38 | chr6 | 112201327 | |||||||
chr6:112201515 | C | A | 9 | a0001c0002t0001g0076 a0001c0002t0001g0197 a0001c0011t0003g0161 others(6): Show |
9 | HG01081.hp2 HG01243.hp1 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.503+93G>T | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 5/38 | chr6 | 112201515 | |||||||
chr6:112201537 | G | C | 4 | a0008c0015t0001g0057 a0008c0015t0001g0059 a0008c0015t0001g0061 others(1): Show |
4 | HG02486.hp2 HG03139.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.503+71C>G | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 5/38 | chr6 | 112201537 | |||||||
chr6:112201692 | A | C | 3 | a0001c0050t0001g0310 a0004c0026t0001g0067 a0004c0026t0001g0068 |
3 | HG01167.hp1 HG01169.hp1 HG03139.hp2 |
splice_region_variant&intron_variant | LOW | c.423-4T>G | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 4/38 | chr6 | 112201692 | |||||||
chr6:112201698 | G | A | 4 | a0008c0015t0001g0057 a0008c0015t0001g0059 a0008c0015t0001g0061 others(1): Show |
4 | HG02486.hp2 HG03139.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.423-10C>T | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 4/38 | chr6 | 112201698 | |||||||
chr6:112201890 | G | A | 16 | a0001c0002t0001g0192 a0001c0002t0001g0254 a0001c0011t0003g0062 others(13): Show |
16 | HG00741.hp1 HG02109.hp1 HG02109.hp2 others(13): Show |
intron_variant | MODIFIER | c.423-202C>T | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 4/38 | chr6 | 112201890 | |||||||
chr6:112202139 | T | C | 2 | a0002c0003t0006g0001 a0002c0003t0006g0002 |
2 | HG02809.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.423-451A>G | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 4/38 | chr6 | 112202139 | |||||||
chr6:112202194 | T | C | 84 | a0001c0002t0001g0020 a0001c0011t0003g0009 a0001c0023t0003g0302 others(81): Show |
84 | HG00323.hp1 HG00597.hp2 HG00621.hp2 others(81): Show |
intron_variant | MODIFIER | c.423-506A>G | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 4/38 | chr6 | 112202194 | |||||||
chr6:112202346 | C | A | 84 | a0001c0002t0001g0020 a0001c0011t0003g0009 a0001c0023t0003g0302 others(81): Show |
84 | HG00323.hp1 HG00597.hp2 HG00621.hp2 others(81): Show |
intron_variant | MODIFIER | c.423-658G>T | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 4/38 | chr6 | 112202346 | |||||||
chr6:112202408 | T | C | 84 | a0001c0002t0001g0020 a0001c0011t0003g0009 a0001c0023t0003g0302 others(81): Show |
84 | HG00323.hp1 HG00597.hp2 HG00621.hp2 others(81): Show |
intron_variant | MODIFIER | c.423-720A>G | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 4/38 | chr6 | 112202408 | |||||||
chr6:112202440 | A | G | 83 | a0001c0002t0001g0020 a0001c0011t0003g0009 a0001c0023t0003g0302 others(80): Show |
83 | HG00323.hp1 HG00597.hp2 HG00621.hp2 others(80): Show |
intron_variant | MODIFIER | c.423-752T>C | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 4/38 | chr6 | 112202440 | |||||||
chr6:112202443 | G | GTGT | 76 | a0001c0023t0003g0302 a0001c0023t0003g0306 a0001c0037t0003g0003 others(73): Show |
76 | HG00323.hp1 HG00597.hp2 HG00621.hp2 others(73): Show |
intron_variant | MODIFIER | c.423-756_423-755ins others(3): Show |
LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 4/38 | chr6 | 112202443 | |||||||
chr6:112202443 | G | GTGTGT | 7 | a0001c0002t0001g0020 a0001c0011t0003g0009 a0002c0006t0002g0037 others(4): Show |
7 | HG01981.hp2 HG02055.hp1 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.423-756_423-755ins others(5): Show |
LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 4/38 | chr6 | 112202443 | |||||||
chr6:112202443 | GGT | G | 110 | a0001c0001t0001g0227 a0001c0002t0001g0005 a0001c0002t0001g0006 others(107): Show |
110 | HG00408.hp2 HG00621.hp1 HG00639.hp1 others(107): Show |
intron_variant | MODIFIER | c.423-757_423-756del others(2): Show |
LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 4/38 | chr6 | 112202443 | |||||||
chr6:112202445 | T | G | 1 | a0003c0058t0001g0210 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.423-757A>C | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 4/38 | chr6 | 112202445 | |||||||
chr6:112202469 | T | C | 1 | a0018c0030t0001g0004 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.423-781A>G | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 4/38 | chr6 | 112202469 | |||||||
chr6:112202525 | G | T | 2 | a0001c0037t0003g0003 a0008c0015t0001g0058 |
2 | HG02818.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.423-837C>A | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 4/38 | chr6 | 112202525 | |||||||
chr6:112202649 | AT | A | 7 | a0001c0002t0001g0087 a0001c0002t0001g0096 a0001c0002t0001g0097 others(4): Show |
7 | HG00741.hp2 HG01433.hp1 HG01934.hp2 others(4): Show |
intron_variant | MODIFIER | c.423-962delA | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 4/38 | chr6 | 112202649 | |||||||
chr6:112202690 | G | T | 83 | a0001c0002t0001g0020 a0001c0023t0003g0302 a0001c0023t0003g0306 others(80): Show |
83 | HG00323.hp1 HG00597.hp2 HG00621.hp2 others(80): Show |
intron_variant | MODIFIER | c.423-1002C>A | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 4/38 | chr6 | 112202690 | |||||||
chr6:112202692 | A | T | 83 | a0001c0002t0001g0020 a0001c0023t0003g0302 a0001c0023t0003g0306 others(80): Show |
83 | HG00323.hp1 HG00597.hp2 HG00621.hp2 others(80): Show |
intron_variant | MODIFIER | c.423-1004T>A | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 4/38 | chr6 | 112202692 | |||||||
chr6:112202702 | G | A | 191 | a0001c0001t0001g0227 a0001c0002t0001g0005 a0001c0002t0001g0006 others(188): Show |
191 | HG00323.hp1 HG00408.hp2 HG00597.hp2 others(188): Show |
intron_variant | MODIFIER | c.423-1014C>T | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 4/38 | chr6 | 112202702 | |||||||
chr6:112202736 | C | T | 1 | a0015c0049t0002g0200 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.423-1048G>A | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 4/38 | chr6 | 112202736 | |||||||
chr6:112202777 | C | T | 6 | a0001c0002t0001g0076 a0001c0002t0001g0197 a0001c0011t0003g0161 others(3): Show |
6 | HG01081.hp2 HG01243.hp1 HG02257.hp1 others(3): Show |
intron_variant | MODIFIER | c.423-1089G>A | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 4/38 | chr6 | 112202777 | |||||||
chr6:112202829 | C | G | 7 | a0001c0002t0001g0076 a0001c0002t0001g0197 a0001c0011t0003g0161 others(4): Show |
7 | HG01081.hp2 HG01243.hp1 HG01891.hp1 others(4): Show |
intron_variant | MODIFIER | c.423-1141G>C | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 4/38 | chr6 | 112202829 | |||||||
chr6:112202926 | T | A | 5 | a0003c0004t0001g0022 a0003c0004t0001g0028 a0003c0004t0001g0029 others(2): Show |
5 | HG02258.hp2 HG02615.hp1 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.423-1238A>T | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 4/38 | chr6 | 112202926 | |||||||
chr6:112203065 | T | C | 117 | a0001c0001t0001g0008 a0001c0001t0001g0042 a0001c0001t0001g0050 others(114): Show |
117 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(114): Show |
intron_variant | MODIFIER | c.423-1377A>G | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 4/38 | chr6 | 112203065 | |||||||
chr6:112203305 | T | C | 231 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0015 others(228): Show |
231 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(228): Show |
intron_variant | MODIFIER | c.423-1617A>G | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 4/38 | chr6 | 112203305 | |||||||
chr6:112203463 | T | C | 1 | a0002c0003t0001g0171 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.423-1775A>G | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 4/38 | chr6 | 112203463 | |||||||
chr6:112203531 | G | T | 1 | a0001c0001t0001g0136 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.423-1843C>A | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 4/38 | chr6 | 112203531 | |||||||
chr6:112203571 | G | C | 100 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0015 others(97): Show |
100 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(97): Show |
intron_variant | MODIFIER | c.423-1883C>G | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 4/38 | chr6 | 112203571 | |||||||
chr6:112203760 | A | G | 1 | a0014c0040t0002g0098 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.423-2072T>C | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 4/38 | chr6 | 112203760 | |||||||
chr6:112203788 | A | AT | 25 | a0001c0002t0001g0020 a0001c0002t0001g0192 a0001c0002t0001g0254 others(22): Show |
25 | HG00741.hp1 HG01981.hp2 HG02109.hp1 others(22): Show |
intron_variant | MODIFIER | c.423-2101_423-2100i others(3): Show |
LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 4/38 | chr6 | 112203788 | |||||||
chr6:112203789 | C | T | 32 | a0001c0002t0001g0020 a0001c0002t0001g0076 a0001c0002t0001g0192 others(29): Show |
32 | HG00741.hp1 HG01081.hp2 HG01243.hp1 others(29): Show |
intron_variant | MODIFIER | c.423-2101G>A | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 4/38 | chr6 | 112203789 | |||||||
chr6:112203814 | T | C | 32 | a0001c0002t0001g0020 a0001c0002t0001g0076 a0001c0002t0001g0192 others(29): Show |
32 | HG00741.hp1 HG01081.hp2 HG01243.hp1 others(29): Show |
intron_variant | MODIFIER | c.423-2126A>G | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 4/38 | chr6 | 112203814 | |||||||
chr6:112203873 | A | G | 7 | a0001c0002t0001g0076 a0001c0002t0001g0197 a0001c0020t0005g0168 others(4): Show |
7 | HG01081.hp2 HG01243.hp1 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.423-2185T>C | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 4/38 | chr6 | 112203873 | |||||||
chr6:112203931 | A | G | 76 | a0001c0001t0001g0069 a0001c0001t0001g0090 a0001c0001t0001g0138 others(73): Show |
76 | HG00408.hp2 HG00621.hp1 HG00673.hp2 others(73): Show |
intron_variant | MODIFIER | c.423-2243T>C | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 4/38 | chr6 | 112203931 | |||||||
chr6:112204006 | T | A | 1 | a0004c0057t0003g0017 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.423-2318A>T | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 4/38 | chr6 | 112204006 | |||||||
chr6:112204271 | A | C | 3 | a0004c0010t0001g0080 a0004c0010t0001g0152 a0014c0040t0002g0098 |
3 | HG00673.hp2 NA18971.hp2 NA19062.hp2 |
intron_variant | MODIFIER | c.423-2583T>G | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 4/38 | chr6 | 112204271 | |||||||
chr6:112204362 | G | GT | 20 | a0001c0002t0001g0192 a0001c0002t0001g0254 a0001c0011t0003g0062 others(17): Show |
20 | HG00741.hp1 HG02109.hp1 HG02109.hp2 others(17): Show |
intron_variant | MODIFIER | c.422+2658dupA | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 4/38 | chr6 | 112204362 | |||||||
chr6:112204453 | G | A | 1 | a0001c0001t0001g0285 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.422+2568C>T | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 4/38 | chr6 | 112204453 | |||||||
chr6:112204474 | C | CA | 11 | a0001c0023t0003g0302 a0001c0023t0003g0306 a0001c0037t0003g0003 others(8): Show |
11 | HG00733.hp1 HG02145.hp2 HG02818.hp2 others(8): Show |
intron_variant | MODIFIER | c.422+2546dupT | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 4/38 | chr6 | 112204474 | |||||||
chr6:112204474 | CA | C | 111 | a0001c0001t0001g0069 a0001c0001t0001g0090 a0001c0001t0001g0095 others(108): Show |
111 | HG00408.hp2 HG00621.hp1 HG00639.hp1 others(108): Show |
intron_variant | MODIFIER | c.422+2546delT | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 4/38 | chr6 | 112204474 | |||||||
chr6:112204525 | G | T | 2 | a0001c0005t0001g0063 a0001c0005t0001g0091 |
2 | HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.422+2496C>A | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 4/38 | chr6 | 112204525 | |||||||
chr6:112204538 | CACA | C | 27 | a0001c0002t0001g0076 a0001c0002t0001g0192 a0001c0002t0001g0197 others(24): Show |
27 | HG00741.hp1 HG01081.hp2 HG01243.hp1 others(24): Show |
intron_variant | MODIFIER | c.422+2480_422+2482d others(5): Show |
LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 4/38 | chr6 | 112204538 | |||||||
chr6:112204550 | A | G | 1 | a0001c0037t0003g0003 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.422+2471T>C | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 4/38 | chr6 | 112204550 | |||||||
chr6:112204574 | A | C | 1 | a0001c0011t0003g0155 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.422+2447T>G | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 4/38 | chr6 | 112204574 | |||||||
chr6:112204657 | AC | A | 27 | a0001c0002t0001g0076 a0001c0002t0001g0192 a0001c0002t0001g0197 others(24): Show |
27 | HG00741.hp1 HG01081.hp2 HG01243.hp1 others(24): Show |
intron_variant | MODIFIER | c.422+2363delG | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 4/38 | chr6 | 112204657 | |||||||
chr6:112204709 | G | A | 37 | a0001c0001t0001g0027 a0001c0001t0001g0070 a0001c0001t0001g0072 others(34): Show |
37 | HG00642.hp1 HG01071.hp1 HG01361.hp1 others(34): Show |
intron_variant | MODIFIER | c.422+2312C>T | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 4/38 | chr6 | 112204709 | |||||||
chr6:112204813 | T | C | 27 | a0001c0002t0001g0076 a0001c0002t0001g0192 a0001c0002t0001g0197 others(24): Show |
27 | HG00741.hp1 HG01081.hp2 HG01243.hp1 others(24): Show |
intron_variant | MODIFIER | c.422+2208A>G | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 4/38 | chr6 | 112204813 | |||||||
chr6:112204821 | A | G | 27 | a0001c0002t0001g0076 a0001c0002t0001g0192 a0001c0002t0001g0197 others(24): Show |
27 | HG00741.hp1 HG01081.hp2 HG01243.hp1 others(24): Show |
intron_variant | MODIFIER | c.422+2200T>C | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 4/38 | chr6 | 112204821 | |||||||
chr6:112204824 | C | T | 30 | a0001c0001t0001g0095 a0001c0002t0001g0005 a0001c0002t0001g0006 others(27): Show |
30 | HG00639.hp1 HG00741.hp2 HG01168.hp2 others(27): Show |
intron_variant | MODIFIER | c.422+2197G>A | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 4/38 | chr6 | 112204824 | |||||||
chr6:112204830 | T | G | 27 | a0001c0002t0001g0076 a0001c0002t0001g0192 a0001c0002t0001g0197 others(24): Show |
27 | HG00741.hp1 HG01081.hp2 HG01243.hp1 others(24): Show |
intron_variant | MODIFIER | c.422+2191A>C | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 4/38 | chr6 | 112204830 | |||||||
chr6:112204877 | G | A | 27 | a0001c0002t0001g0076 a0001c0002t0001g0192 a0001c0002t0001g0197 others(24): Show |
27 | HG00741.hp1 HG01081.hp2 HG01243.hp1 others(24): Show |
intron_variant | MODIFIER | c.422+2144C>T | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 4/38 | chr6 | 112204877 | |||||||
chr6:112204890 | A | G | 27 | a0001c0002t0001g0076 a0001c0002t0001g0192 a0001c0002t0001g0197 others(24): Show |
27 | HG00741.hp1 HG01081.hp2 HG01243.hp1 others(24): Show |
intron_variant | MODIFIER | c.422+2131T>C | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 4/38 | chr6 | 112204890 | |||||||
chr6:112204900 | G | A | 34 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0015 others(31): Show |
34 | HG00099.hp1 HG00408.hp1 HG00597.hp1 others(31): Show |
intron_variant | MODIFIER | c.422+2121C>T | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 4/38 | chr6 | 112204900 | |||||||
chr6:112204930 | T | C | 27 | a0001c0002t0001g0076 a0001c0002t0001g0192 a0001c0002t0001g0197 others(24): Show |
27 | HG00741.hp1 HG01081.hp2 HG01243.hp1 others(24): Show |
intron_variant | MODIFIER | c.422+2091A>G | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 4/38 | chr6 | 112204930 | |||||||
chr6:112204987 | A | G | 1 | a0001c0005t0001g0137 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.422+2034T>C | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 4/38 | chr6 | 112204987 | |||||||
chr6:112205123 | A | C | 1 | a0001c0001t0001g0219 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.422+1898T>G | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 4/38 | chr6 | 112205123 | |||||||
chr6:112205131 | C | A | 27 | a0001c0002t0001g0076 a0001c0002t0001g0192 a0001c0002t0001g0197 others(24): Show |
27 | HG00741.hp1 HG01081.hp2 HG01243.hp1 others(24): Show |
intron_variant | MODIFIER | c.422+1890G>T | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 4/38 | chr6 | 112205131 | |||||||
chr6:112205203 | C | T | 274 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0014 others(271): Show |
274 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(271): Show |
intron_variant | MODIFIER | c.422+1818G>A | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 4/38 | chr6 | 112205203 | |||||||
chr6:112205293 | C | T | 27 | a0001c0002t0001g0076 a0001c0002t0001g0192 a0001c0002t0001g0197 others(24): Show |
27 | HG00741.hp1 HG01081.hp2 HG01243.hp1 others(24): Show |
intron_variant | MODIFIER | c.422+1728G>A | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 4/38 | chr6 | 112205293 | |||||||
chr6:112205370 | AG | A | 27 | a0001c0002t0001g0076 a0001c0002t0001g0192 a0001c0002t0001g0197 others(24): Show |
27 | HG00741.hp1 HG01081.hp2 HG01243.hp1 others(24): Show |
intron_variant | MODIFIER | c.422+1650delC | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 4/38 | chr6 | 112205370 | |||||||
chr6:112205436 | C | T | 3 | a0003c0004t0001g0018 a0005c0008t0001g0031 a0005c0008t0001g0032 |
3 | HG01515.hp1 HG02486.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.422+1585G>A | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 4/38 | chr6 | 112205436 | |||||||
chr6:112205458 | GA | G | 37 | a0001c0001t0001g0027 a0001c0001t0001g0070 a0001c0001t0001g0072 others(34): Show |
37 | HG00642.hp1 HG01071.hp1 HG01361.hp1 others(34): Show |
intron_variant | MODIFIER | c.422+1562delT | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 4/38 | chr6 | 112205458 | |||||||
chr6:112205565 | T | TA | 35 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0015 others(32): Show |
35 | HG00099.hp1 HG00408.hp1 HG00597.hp1 others(32): Show |
intron_variant | MODIFIER | c.422+1455dupT | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 4/38 | chr6 | 112205565 | |||||||
chr6:112205583 | G | A | 5 | a0001c0002t0001g0087 a0001c0002t0001g0096 a0001c0002t0001g0097 others(2): Show |
5 | HG00741.hp2 HG01433.hp1 HG01934.hp2 others(2): Show |
intron_variant | MODIFIER | c.422+1438C>T | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 4/38 | chr6 | 112205583 | |||||||
chr6:112205701 | AC | A | 27 | a0001c0002t0001g0076 a0001c0002t0001g0192 a0001c0002t0001g0197 others(24): Show |
27 | HG00741.hp1 HG01081.hp2 HG01243.hp1 others(24): Show |
intron_variant | MODIFIER | c.422+1319delG | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 4/38 | chr6 | 112205701 | |||||||
chr6:112205782 | C | T | 1 | a0005c0008t0001g0241 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.422+1239G>A | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 4/38 | chr6 | 112205782 | |||||||
chr6:112205783 | G | T | 27 | a0001c0002t0001g0076 a0001c0002t0001g0192 a0001c0002t0001g0197 others(24): Show |
27 | HG00741.hp1 HG01081.hp2 HG01243.hp1 others(24): Show |
intron_variant | MODIFIER | c.422+1238C>A | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 4/38 | chr6 | 112205783 | |||||||
chr6:112205787 | T | C | 2 | a0001c0001t0001g0015 a0001c0009t0001g0112 |
2 | NA18988.hp2 NA19070.hp1 |
intron_variant | MODIFIER | c.422+1234A>G | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 4/38 | chr6 | 112205787 | |||||||
chr6:112205787 | T | G | 27 | a0001c0002t0001g0076 a0001c0002t0001g0192 a0001c0002t0001g0197 others(24): Show |
27 | HG00741.hp1 HG01081.hp2 HG01243.hp1 others(24): Show |
intron_variant | MODIFIER | c.422+1234A>C | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 4/38 | chr6 | 112205787 | |||||||
chr6:112205885 | C | T | 7 | a0001c0002t0001g0076 a0001c0002t0001g0197 a0001c0020t0005g0168 others(4): Show |
7 | HG01081.hp2 HG01243.hp1 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.422+1136G>A | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 4/38 | chr6 | 112205885 | |||||||
chr6:112205934 | G | C | 1 | a0002c0006t0002g0303 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.422+1087C>G | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 4/38 | chr6 | 112205934 | |||||||
chr6:112205935 | G | T | 27 | a0001c0002t0001g0076 a0001c0002t0001g0192 a0001c0002t0001g0197 others(24): Show |
27 | HG00741.hp1 HG01081.hp2 HG01243.hp1 others(24): Show |
intron_variant | MODIFIER | c.422+1086C>A | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 4/38 | chr6 | 112205935 | |||||||
chr6:112206003 | CCTT | C | 5 | a0008c0015t0001g0057 a0008c0015t0001g0059 a0008c0015t0001g0061 others(2): Show |
5 | HG02486.hp2 HG03139.hp1 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.422+1015_422+1017d others(5): Show |
LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 4/38 | chr6 | 112206003 | |||||||
chr6:112206091 | G | A | 27 | a0001c0002t0001g0076 a0001c0002t0001g0192 a0001c0002t0001g0197 others(24): Show |
27 | HG00741.hp1 HG01081.hp2 HG01243.hp1 others(24): Show |
intron_variant | MODIFIER | c.422+930C>T | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 4/38 | chr6 | 112206091 | |||||||
chr6:112206106 | C | T | 27 | a0001c0002t0001g0076 a0001c0002t0001g0192 a0001c0002t0001g0197 others(24): Show |
27 | HG00741.hp1 HG01081.hp2 HG01243.hp1 others(24): Show |
intron_variant | MODIFIER | c.422+915G>A | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 4/38 | chr6 | 112206106 | |||||||
chr6:112206143 | A | C | 27 | a0001c0002t0001g0076 a0001c0002t0001g0192 a0001c0002t0001g0197 others(24): Show |
27 | HG00741.hp1 HG01081.hp2 HG01243.hp1 others(24): Show |
intron_variant | MODIFIER | c.422+878T>G | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 4/38 | chr6 | 112206143 | |||||||
chr6:112206155 | A | C | 27 | a0001c0002t0001g0076 a0001c0002t0001g0192 a0001c0002t0001g0197 others(24): Show |
27 | HG00741.hp1 HG01081.hp2 HG01243.hp1 others(24): Show |
intron_variant | MODIFIER | c.422+866T>G | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 4/38 | chr6 | 112206155 | |||||||
chr6:112206283 | T | C | 2 | a0001c0011t0003g0161 a0001c0011t0003g0298 |
2 | HG02257.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.422+738A>G | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 4/38 | chr6 | 112206283 | |||||||
chr6:112206350 | G | A | 27 | a0001c0002t0001g0076 a0001c0002t0001g0192 a0001c0002t0001g0197 others(24): Show |
27 | HG00741.hp1 HG01081.hp2 HG01243.hp1 others(24): Show |
intron_variant | MODIFIER | c.422+671C>T | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 4/38 | chr6 | 112206350 | |||||||
chr6:112206385 | C | G | 27 | a0001c0002t0001g0076 a0001c0002t0001g0192 a0001c0002t0001g0197 others(24): Show |
27 | HG00741.hp1 HG01081.hp2 HG01243.hp1 others(24): Show |
intron_variant | MODIFIER | c.422+636G>C | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 4/38 | chr6 | 112206385 | |||||||
chr6:112206429 | T | G | 27 | a0001c0002t0001g0076 a0001c0002t0001g0192 a0001c0002t0001g0197 others(24): Show |
27 | HG00741.hp1 HG01081.hp2 HG01243.hp1 others(24): Show |
intron_variant | MODIFIER | c.422+592A>C | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 4/38 | chr6 | 112206429 | |||||||
chr6:112206477 | AATGT | A | 7 | a0001c0002t0001g0076 a0001c0002t0001g0197 a0001c0020t0005g0168 others(4): Show |
7 | HG01081.hp2 HG01243.hp1 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.422+540_422+543del others(4): Show |
LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 4/38 | chr6 | 112206477 | |||||||
chr6:112206501 | A | T | 27 | a0001c0002t0001g0076 a0001c0002t0001g0192 a0001c0002t0001g0197 others(24): Show |
27 | HG00741.hp1 HG01081.hp2 HG01243.hp1 others(24): Show |
intron_variant | MODIFIER | c.422+520T>A | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 4/38 | chr6 | 112206501 | |||||||
chr6:112206506 | T | C | 27 | a0001c0002t0001g0076 a0001c0002t0001g0192 a0001c0002t0001g0197 others(24): Show |
27 | HG00741.hp1 HG01081.hp2 HG01243.hp1 others(24): Show |
intron_variant | MODIFIER | c.422+515A>G | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 4/38 | chr6 | 112206506 | |||||||
chr6:112206518 | C | T | 27 | a0001c0002t0001g0076 a0001c0002t0001g0192 a0001c0002t0001g0197 others(24): Show |
27 | HG00741.hp1 HG01081.hp2 HG01243.hp1 others(24): Show |
intron_variant | MODIFIER | c.422+503G>A | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 4/38 | chr6 | 112206518 | |||||||
chr6:112206519 | G | A | 1 | a0007c0060t0002g0260 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.422+502C>T | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 4/38 | chr6 | 112206519 | |||||||
chr6:112206571 | T | C | 27 | a0001c0002t0001g0076 a0001c0002t0001g0192 a0001c0002t0001g0197 others(24): Show |
27 | HG00741.hp1 HG01081.hp2 HG01243.hp1 others(24): Show |
intron_variant | MODIFIER | c.422+450A>G | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 4/38 | chr6 | 112206571 | |||||||
chr6:112206585 | C | T | 28 | a0001c0001t0001g0014 a0001c0001t0001g0033 a0001c0001t0001g0116 others(25): Show |
28 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(25): Show |
intron_variant | MODIFIER | c.422+436G>A | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 4/38 | chr6 | 112206585 | |||||||
chr6:112206708 | T | C | 27 | a0001c0002t0001g0076 a0001c0002t0001g0192 a0001c0002t0001g0197 others(24): Show |
27 | HG00741.hp1 HG01081.hp2 HG01243.hp1 others(24): Show |
intron_variant | MODIFIER | c.422+313A>G | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 4/38 | chr6 | 112206708 | |||||||
chr6:112206709 | G | A | 27 | a0001c0002t0001g0076 a0001c0002t0001g0192 a0001c0002t0001g0197 others(24): Show |
27 | HG00741.hp1 HG01081.hp2 HG01243.hp1 others(24): Show |
intron_variant | MODIFIER | c.422+312C>T | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 4/38 | chr6 | 112206709 | |||||||
chr6:112206804 | G | A | 1 | a0018c0030t0001g0004 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.422+217C>T | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 4/38 | chr6 | 112206804 | |||||||
chr6:112206811 | C | G | 27 | a0001c0002t0001g0076 a0001c0002t0001g0192 a0001c0002t0001g0197 others(24): Show |
27 | HG00741.hp1 HG01081.hp2 HG01243.hp1 others(24): Show |
intron_variant | MODIFIER | c.422+210G>C | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 4/38 | chr6 | 112206811 | |||||||
chr6:112206948 | A | AAAACAAA others(8): Show |
1 | a0001c0023t0003g0302 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.422+72_422+73insCG others(13): Show |
LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 4/38 | chr6 | 112206948 | |||||||
chr6:112206953 | A | AAAACAAA others(3): Show |
26 | a0001c0002t0001g0076 a0001c0002t0001g0192 a0001c0002t0001g0197 others(23): Show |
26 | HG00741.hp1 HG01081.hp2 HG01243.hp1 others(23): Show |
intron_variant | MODIFIER | c.422+67_422+68insCG others(8): Show |
LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 4/38 | chr6 | 112206953 | |||||||
chr6:112206984 | T | C | 1 | a0004c0010t0001g0013 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.422+37A>G | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 4/38 | chr6 | 112206984 | |||||||
chr6:112207249 | A | G | 27 | a0001c0002t0001g0076 a0001c0002t0001g0192 a0001c0002t0001g0197 others(24): Show |
27 | HG00741.hp1 HG01081.hp2 HG01243.hp1 others(24): Show |
intron_variant | MODIFIER | c.298-104T>C | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 3/38 | chr6 | 112207249 | |||||||
chr6:112207280 | A | G | 186 | a0001c0001t0001g0027 a0001c0001t0001g0069 a0001c0001t0001g0070 others(183): Show |
186 | HG00408.hp2 HG00621.hp1 HG00639.hp1 others(183): Show |
intron_variant | MODIFIER | c.298-135T>C | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 3/38 | chr6 | 112207280 | |||||||
chr6:112207324 | G | T | 37 | a0001c0001t0001g0027 a0001c0001t0001g0070 a0001c0001t0001g0072 others(34): Show |
37 | HG00642.hp1 HG01071.hp1 HG01361.hp1 others(34): Show |
intron_variant | MODIFIER | c.298-179C>A | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 3/38 | chr6 | 112207324 | |||||||
chr6:112207358 | T | A | 85 | a0001c0001t0001g0069 a0001c0001t0001g0090 a0001c0001t0001g0138 others(82): Show |
85 | HG00408.hp2 HG00621.hp1 HG00673.hp2 others(82): Show |
intron_variant | MODIFIER | c.298-213A>T | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 3/38 | chr6 | 112207358 | |||||||
chr6:112207392 | A | C | 20 | a0001c0002t0001g0192 a0001c0002t0001g0254 a0001c0011t0003g0062 others(17): Show |
20 | HG00741.hp1 HG02109.hp1 HG02109.hp2 others(17): Show |
intron_variant | MODIFIER | c.298-247T>G | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 3/38 | chr6 | 112207392 | |||||||
chr6:112207412 | A | G | 27 | a0001c0002t0001g0076 a0001c0002t0001g0192 a0001c0002t0001g0197 others(24): Show |
27 | HG00741.hp1 HG01081.hp2 HG01243.hp1 others(24): Show |
intron_variant | MODIFIER | c.298-267T>C | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 3/38 | chr6 | 112207412 | |||||||
chr6:112207500 | G | A | 1 | a0003c0004t0001g0291 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.298-355C>T | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 3/38 | chr6 | 112207500 | |||||||
chr6:112207518 | A | AAACCAAC others(17): Show |
8 | a0001c0002t0001g0076 a0001c0002t0001g0197 a0001c0011t0003g0155 others(5): Show |
8 | HG01081.hp2 HG01243.hp1 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.298-374_298-373ins others(24): Show |
LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 3/38 | chr6 | 112207518 | |||||||
chr6:112207518 | A | AAACCAAC others(21): Show |
12 | a0001c0002t0001g0192 a0001c0002t0001g0254 a0001c0011t0003g0062 others(9): Show |
12 | HG00741.hp1 HG02109.hp1 HG02109.hp2 others(9): Show |
intron_variant | MODIFIER | c.298-374_298-373ins others(28): Show |
LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 3/38 | chr6 | 112207518 | |||||||
chr6:112207518 | A | AAACCAAC others(25): Show |
6 | a0001c0023t0003g0302 a0001c0037t0003g0003 a0004c0057t0003g0017 others(3): Show |
6 | HG02818.hp2 HG02970.hp1 HG03195.hp1 others(3): Show |
intron_variant | MODIFIER | c.298-374_298-373ins others(32): Show |
LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 3/38 | chr6 | 112207518 | |||||||
chr6:112207518 | A | AAACCAAC others(29): Show |
1 | a0001c0023t0003g0306 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.298-374_298-373ins others(36): Show |
LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 3/38 | chr6 | 112207518 | |||||||
chr6:112207518 | AAACCAAC others(1): Show |
A | 7 | a0001c0002t0001g0020 a0001c0011t0003g0161 a0001c0011t0003g0298 others(4): Show |
7 | HG01981.hp2 HG02257.hp1 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.298-381_298-374del others(8): Show |
LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 3/38 | chr6 | 112207518 | |||||||
chr6:112207537 | C | A | 39 | a0001c0001t0001g0069 a0001c0001t0001g0095 a0001c0002t0001g0005 others(36): Show |
39 | HG00639.hp1 HG00741.hp1 HG00741.hp2 others(36): Show |
intron_variant | MODIFIER | c.298-392G>T | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 3/38 | chr6 | 112207537 | |||||||
chr6:112207560 | G | A | 1 | a0003c0004t0001g0141 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.298-415C>T | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 3/38 | chr6 | 112207560 | |||||||
chr6:112207567 | T | C | 27 | a0001c0002t0001g0076 a0001c0002t0001g0192 a0001c0002t0001g0197 others(24): Show |
27 | HG00741.hp1 HG01081.hp2 HG01243.hp1 others(24): Show |
intron_variant | MODIFIER | c.298-422A>G | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 3/38 | chr6 | 112207567 | |||||||
chr6:112207714 | G | GT | 7 | a0001c0002t0001g0020 a0001c0011t0003g0161 a0001c0011t0003g0298 others(4): Show |
7 | HG01981.hp2 HG02257.hp1 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.298-570dupA | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 3/38 | chr6 | 112207714 | |||||||
chr6:112207735 | C | T | 27 | a0001c0002t0001g0076 a0001c0002t0001g0192 a0001c0002t0001g0197 others(24): Show |
27 | HG00741.hp1 HG01081.hp2 HG01243.hp1 others(24): Show |
intron_variant | MODIFIER | c.298-590G>A | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 3/38 | chr6 | 112207735 | |||||||
chr6:112207738 | A | G | 2 | a0001c0011t0003g0161 a0001c0011t0003g0298 |
2 | HG02257.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.298-593T>C | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 3/38 | chr6 | 112207738 | |||||||
chr6:112207777 | G | A | 27 | a0001c0002t0001g0076 a0001c0002t0001g0192 a0001c0002t0001g0197 others(24): Show |
27 | HG00741.hp1 HG01081.hp2 HG01243.hp1 others(24): Show |
intron_variant | MODIFIER | c.298-632C>T | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 3/38 | chr6 | 112207777 | |||||||
chr6:112208067 | C | T | 166 | a0001c0001t0001g0027 a0001c0001t0001g0069 a0001c0001t0001g0070 others(163): Show |
166 | HG00408.hp2 HG00621.hp1 HG00639.hp1 others(163): Show |
intron_variant | MODIFIER | c.298-922G>A | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 3/38 | chr6 | 112208067 | |||||||
chr6:112208081 | C | A | 20 | a0001c0002t0001g0192 a0001c0002t0001g0254 a0001c0011t0003g0062 others(17): Show |
20 | HG00741.hp1 HG02109.hp1 HG02109.hp2 others(17): Show |
intron_variant | MODIFIER | c.298-936G>T | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 3/38 | chr6 | 112208081 | |||||||
chr6:112208171 | G | GTTAGAA | 57 | a0001c0001t0001g0027 a0001c0001t0001g0070 a0001c0001t0001g0072 others(54): Show |
57 | HG00642.hp1 HG00741.hp1 HG01071.hp1 others(54): Show |
intron_variant | MODIFIER | c.298-1032_298-1027d others(8): Show |
LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 3/38 | chr6 | 112208171 | |||||||
chr6:112208227 | G | A | 57 | a0001c0001t0001g0027 a0001c0001t0001g0070 a0001c0001t0001g0072 others(54): Show |
57 | HG00642.hp1 HG00741.hp1 HG01071.hp1 others(54): Show |
intron_variant | MODIFIER | c.298-1082C>T | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 3/38 | chr6 | 112208227 | |||||||
chr6:112208318 | G | A | 1 | a0003c0059t0001g0259 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.298-1173C>T | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 3/38 | chr6 | 112208318 | |||||||
chr6:112208414 | C | G | 1 | a0001c0001t0001g0008 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.298-1269G>C | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 3/38 | chr6 | 112208414 | |||||||
chr6:112208431 | G | A | 1 | a0003c0058t0001g0210 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.298-1286C>T | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 3/38 | chr6 | 112208431 | |||||||
chr6:112208512 | T | G | 7 | a0001c0002t0001g0076 a0001c0002t0001g0197 a0001c0020t0005g0168 others(4): Show |
7 | HG01081.hp2 HG01243.hp1 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.298-1367A>C | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 3/38 | chr6 | 112208512 | |||||||
chr6:112208517 | G | A | 37 | a0001c0001t0001g0027 a0001c0001t0001g0070 a0001c0001t0001g0072 others(34): Show |
37 | HG00642.hp1 HG01071.hp1 HG01361.hp1 others(34): Show |
intron_variant | MODIFIER | c.298-1372C>T | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 3/38 | chr6 | 112208517 | |||||||
chr6:112208526 | C | T | 184 | a0001c0001t0001g0027 a0001c0001t0001g0069 a0001c0001t0001g0070 others(181): Show |
184 | HG00408.hp2 HG00621.hp1 HG00639.hp1 others(181): Show |
intron_variant | MODIFIER | c.298-1381G>A | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 3/38 | chr6 | 112208526 | |||||||
chr6:112208648 | G | A | 111 | a0001c0001t0001g0069 a0001c0001t0001g0090 a0001c0001t0001g0095 others(108): Show |
111 | HG00408.hp2 HG00621.hp1 HG00639.hp1 others(108): Show |
intron_variant | MODIFIER | c.298-1503C>T | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 3/38 | chr6 | 112208648 | |||||||
chr6:112208696 | T | A | 1 | a0004c0010t0001g0284 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.298-1551A>T | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 3/38 | chr6 | 112208696 | |||||||
chr6:112208816 | A | C | 1 | a0009c0017t0002g0307 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.298-1671T>G | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 3/38 | chr6 | 112208816 | |||||||
chr6:112208865 | A | G | 1 | a0005c0008t0001g0241 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.298-1720T>C | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 3/38 | chr6 | 112208865 | |||||||
chr6:112208883 | A | G | 37 | a0001c0001t0001g0027 a0001c0001t0001g0070 a0001c0001t0001g0072 others(34): Show |
37 | HG00642.hp1 HG01071.hp1 HG01361.hp1 others(34): Show |
intron_variant | MODIFIER | c.298-1738T>C | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 3/38 | chr6 | 112208883 | |||||||
chr6:112209299 | T | C | 181 | a0001c0001t0001g0027 a0001c0001t0001g0069 a0001c0001t0001g0070 others(178): Show |
181 | HG00408.hp2 HG00621.hp1 HG00639.hp1 others(178): Show |
intron_variant | MODIFIER | c.298-2154A>G | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 3/38 | chr6 | 112209299 | |||||||
chr6:112209413 | A | C | 1 | a0003c0004t0001g0176 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.298-2268T>G | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 3/38 | chr6 | 112209413 | |||||||
chr6:112209558 | T | G | 4 | a0002c0003t0002g0099 a0002c0003t0002g0100 a0004c0026t0001g0067 others(1): Show |
4 | HG00733.hp2 HG01167.hp1 HG01169.hp1 others(1): Show |
intron_variant | MODIFIER | c.298-2413A>C | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 3/38 | chr6 | 112209558 | |||||||
chr6:112209680 | C | G | 115 | a0001c0001t0001g0069 a0001c0001t0001g0090 a0001c0001t0001g0095 others(112): Show |
115 | HG00408.hp2 HG00621.hp1 HG00639.hp1 others(112): Show |
intron_variant | MODIFIER | c.298-2535G>C | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 3/38 | chr6 | 112209680 | |||||||
chr6:112209681 | C | G | 1 | a0001c0023t0003g0302 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.298-2536G>C | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 3/38 | chr6 | 112209681 | |||||||
chr6:112209692 | C | A | 6 | a0001c0023t0003g0302 a0001c0023t0003g0306 a0001c0037t0003g0003 others(3): Show |
6 | HG02818.hp2 HG02886.hp2 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.298-2547G>T | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 3/38 | chr6 | 112209692 | |||||||
chr6:112209929 | C | G | 11 | a0001c0009t0001g0134 a0003c0013t0001g0145 a0003c0013t0001g0217 others(8): Show |
11 | HG00621.hp2 HG01934.hp1 HG01981.hp1 others(8): Show |
intron_variant | MODIFIER | c.298-2784G>C | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 3/38 | chr6 | 112209929 | |||||||
chr6:112210018 | C | CCT | 17 | a0001c0002t0001g0192 a0001c0002t0001g0254 a0001c0011t0003g0062 others(14): Show |
17 | HG00642.hp2 HG00741.hp1 HG01081.hp1 others(14): Show |
intron_variant | MODIFIER | c.298-2875_298-2874d others(4): Show |
LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 3/38 | chr6 | 112210018 | |||||||
chr6:112210115 | C | A | 19 | a0001c0002t0001g0192 a0001c0002t0001g0254 a0001c0011t0003g0062 others(16): Show |
19 | HG00741.hp1 HG02109.hp1 HG02109.hp2 others(16): Show |
intron_variant | MODIFIER | c.298-2970G>T | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 3/38 | chr6 | 112210115 | |||||||
chr6:112210136 | G | A | 1 | a0001c0011t0003g0298 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.298-2991C>T | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 3/38 | chr6 | 112210136 | |||||||
chr6:112210200 | A | G | 27 | a0001c0001t0001g0095 a0001c0002t0001g0005 a0001c0002t0001g0006 others(24): Show |
27 | HG00639.hp1 HG00741.hp2 HG01168.hp2 others(24): Show |
intron_variant | MODIFIER | c.298-3055T>C | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 3/38 | chr6 | 112210200 | |||||||
chr6:112210202 | G | A | 116 | a0001c0001t0001g0069 a0001c0001t0001g0090 a0001c0001t0001g0095 others(113): Show |
116 | HG00408.hp2 HG00621.hp1 HG00639.hp1 others(113): Show |
intron_variant | MODIFIER | c.298-3057C>T | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 3/38 | chr6 | 112210202 | |||||||
chr6:112210204 | CT | C | 21 | a0001c0002t0001g0192 a0001c0002t0001g0254 a0001c0011t0003g0062 others(18): Show |
21 | HG00741.hp1 HG02109.hp1 HG02109.hp2 others(18): Show |
intron_variant | MODIFIER | c.298-3060delA | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 3/38 | chr6 | 112210204 | |||||||
chr6:112210223 | A | C | 183 | a0001c0001t0001g0027 a0001c0001t0001g0069 a0001c0001t0001g0070 others(180): Show |
183 | HG00408.hp2 HG00621.hp1 HG00639.hp1 others(180): Show |
intron_variant | MODIFIER | c.298-3078T>G | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 3/38 | chr6 | 112210223 | |||||||
chr6:112210367 | A | G | 1 | a0003c0004t0001g0176 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.298-3222T>C | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 3/38 | chr6 | 112210367 | |||||||
chr6:112210395 | T | A | 1 | a0001c0011t0003g0062 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.298-3250A>T | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 3/38 | chr6 | 112210395 | |||||||
chr6:112210459 | T | C | 37 | a0001c0001t0001g0027 a0001c0001t0001g0070 a0001c0001t0001g0072 others(34): Show |
37 | HG00642.hp1 HG01071.hp1 HG01361.hp1 others(34): Show |
intron_variant | MODIFIER | c.298-3314A>G | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 3/38 | chr6 | 112210459 | |||||||
chr6:112210747 | A | G | 1 | a0016c0042t0001g0296 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.298-3602T>C | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 3/38 | chr6 | 112210747 | |||||||
chr6:112210863 | G | A | 7 | a0001c0002t0001g0076 a0001c0002t0001g0197 a0001c0020t0005g0168 others(4): Show |
7 | HG01081.hp2 HG01243.hp1 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.298-3718C>T | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 3/38 | chr6 | 112210863 | |||||||
chr6:112211067 | A | G | 37 | a0001c0001t0001g0027 a0001c0001t0001g0070 a0001c0001t0001g0072 others(34): Show |
37 | HG00642.hp1 HG01071.hp1 HG01361.hp1 others(34): Show |
intron_variant | MODIFIER | c.298-3922T>C | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 3/38 | chr6 | 112211067 | |||||||
chr6:112211127 | T | C | 4 | a0001c0005t0001g0263 a0006c0027t0002g0130 a0006c0027t0002g0140 others(1): Show |
4 | HG02015.hp1 NA18966.hp2 NA19010.hp2 others(1): Show |
intron_variant | MODIFIER | c.298-3982A>G | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 3/38 | chr6 | 112211127 | |||||||
chr6:112211221 | A | G | 1 | a0004c0057t0003g0017 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.298-4076T>C | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 3/38 | chr6 | 112211221 | |||||||
chr6:112211295 | A | G | 10 | a0001c0002t0001g0192 a0001c0011t0003g0062 a0001c0011t0003g0155 others(7): Show |
10 | HG02109.hp1 HG02145.hp2 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.298-4150T>C | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 3/38 | chr6 | 112211295 | |||||||
chr6:112211320 | C | A | 1 | a0009c0017t0002g0021 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.298-4175G>T | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 3/38 | chr6 | 112211320 | |||||||
chr6:112211327 | T | G | 37 | a0001c0001t0001g0027 a0001c0001t0001g0070 a0001c0001t0001g0072 others(34): Show |
37 | HG00642.hp1 HG01071.hp1 HG01361.hp1 others(34): Show |
intron_variant | MODIFIER | c.298-4182A>C | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 3/38 | chr6 | 112211327 | |||||||
chr6:112211475 | G | T | 1 | a0002c0006t0002g0303 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.298-4330C>A | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 3/38 | chr6 | 112211475 | |||||||
chr6:112212147 | T | C | 7 | a0001c0002t0001g0020 a0001c0002t0001g0311 a0001c0011t0003g0313 others(4): Show |
7 | HG01891.hp1 HG01981.hp2 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.297+4221A>G | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 3/38 | chr6 | 112212147 | |||||||
chr6:112212167 | T | C | 1 | a0001c0052t0002g0295 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.297+4201A>G | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 3/38 | chr6 | 112212167 | |||||||
chr6:112212226 | A | AT | 17 | a0001c0001t0001g0136 a0001c0002t0001g0076 a0001c0002t0001g0197 others(14): Show |
17 | HG00280.hp2 HG00741.hp1 HG01081.hp2 others(14): Show |
intron_variant | MODIFIER | c.297+4141dupA | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 3/38 | chr6 | 112212226 | |||||||
chr6:112212226 | AT | A | 79 | a0001c0001t0001g0072 a0001c0001t0001g0090 a0001c0001t0001g0121 others(76): Show |
79 | HG00408.hp2 HG00639.hp2 HG01169.hp1 others(76): Show |
intron_variant | MODIFIER | c.297+4141delA | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 3/38 | chr6 | 112212226 | |||||||
chr6:112212226 | ATT | A | 100 | a0001c0001t0001g0014 a0001c0001t0001g0042 a0001c0001t0001g0069 others(97): Show |
100 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(97): Show |
intron_variant | MODIFIER | c.297+4140_297+4141d others(4): Show |
LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 3/38 | chr6 | 112212226 | |||||||
chr6:112212267 | A | G | 4 | a0001c0002t0001g0253 a0001c0002t0001g0254 a0001c0011t0003g0255 others(1): Show |
4 | HG00741.hp1 HG02109.hp2 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.297+4101T>C | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 3/38 | chr6 | 112212267 | |||||||
chr6:112212405 | G | T | 1 | a0002c0006t0002g0193 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.297+3963C>A | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 3/38 | chr6 | 112212405 | |||||||
chr6:112212517 | C | T | 9 | a0001c0002t0001g0164 a0001c0002t0001g0165 a0001c0009t0001g0134 others(6): Show |
9 | HG01934.hp1 HG01981.hp1 HG02886.hp1 others(6): Show |
intron_variant | MODIFIER | c.297+3851G>A | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 3/38 | chr6 | 112212517 | |||||||
chr6:112212674 | T | C | 2 | a0001c0005t0001g0103 a0002c0006t0002g0104 |
2 | NA18963.hp2 NA19066.hp2 |
intron_variant | MODIFIER | c.297+3694A>G | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 3/38 | chr6 | 112212674 | |||||||
chr6:112212736 | T | G | 9 | a0001c0002t0001g0020 a0001c0002t0001g0045 a0001c0002t0001g0047 others(6): Show |
9 | HG01891.hp1 HG01891.hp2 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.297+3632A>C | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 3/38 | chr6 | 112212736 | |||||||
chr6:112212749 | G | C | 1 | a0003c0058t0001g0210 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.297+3619C>G | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 3/38 | chr6 | 112212749 | |||||||
chr6:112212764 | T | A | 5 | a0001c0023t0003g0306 a0001c0037t0003g0003 a0004c0057t0003g0017 others(2): Show |
5 | HG02886.hp2 HG02970.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.297+3604A>T | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 3/38 | chr6 | 112212764 | |||||||
chr6:112212835 | C | G | 19 | a0001c0002t0001g0076 a0001c0002t0001g0197 a0001c0011t0003g0062 others(16): Show |
19 | HG01081.hp2 HG01243.hp1 HG01981.hp2 others(16): Show |
intron_variant | MODIFIER | c.297+3533G>C | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 3/38 | chr6 | 112212835 | |||||||
chr6:112212962 | C | T | 210 | a0001c0001t0001g0014 a0001c0001t0001g0042 a0001c0001t0001g0069 others(207): Show |
210 | HG00408.hp2 HG00621.hp1 HG00621.hp2 others(207): Show |
intron_variant | MODIFIER | c.297+3406G>A | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 3/38 | chr6 | 112212962 | |||||||
chr6:112213014 | A | C | 198 | a0001c0001t0001g0014 a0001c0001t0001g0042 a0001c0001t0001g0069 others(195): Show |
198 | HG00408.hp2 HG00621.hp1 HG00621.hp2 others(195): Show |
intron_variant | MODIFIER | c.297+3354T>G | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 3/38 | chr6 | 112213014 | |||||||
chr6:112213057 | C | A | 1 | a0003c0058t0001g0210 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.297+3311G>T | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 3/38 | chr6 | 112213057 | |||||||
chr6:112213284 | C | G | 6 | a0001c0002t0001g0076 a0001c0002t0001g0197 a0002c0006t0002g0199 others(3): Show |
6 | HG01081.hp2 HG01981.hp2 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.297+3084G>C | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 3/38 | chr6 | 112213284 | |||||||
chr6:112213451 | C | G | 1 | a0001c0001t0001g0228 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.297+2917G>C | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 3/38 | chr6 | 112213451 | |||||||
chr6:112213532 | T | G | 9 | a0001c0002t0001g0205 a0001c0020t0005g0168 a0001c0020t0005g0169 others(6): Show |
9 | HG01071.hp1 HG02717.hp2 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.297+2836A>C | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 3/38 | chr6 | 112213532 | |||||||
chr6:112213579 | A | G | 4 | a0001c0002t0001g0253 a0001c0002t0001g0254 a0001c0011t0003g0255 others(1): Show |
4 | HG00741.hp1 HG02109.hp2 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.297+2789T>C | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 3/38 | chr6 | 112213579 | |||||||
chr6:112213611 | TA | T | 5 | a0001c0023t0003g0306 a0001c0037t0003g0003 a0004c0057t0003g0017 others(2): Show |
5 | HG02886.hp2 HG02970.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.297+2756delT | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 3/38 | chr6 | 112213611 | |||||||
chr6:112213659 | A | G | 9 | a0003c0004t0001g0018 a0003c0004t0001g0030 a0003c0013t0001g0023 others(6): Show |
9 | HG00323.hp1 HG01071.hp2 HG01074.hp1 others(6): Show |
intron_variant | MODIFIER | c.297+2709T>C | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 3/38 | chr6 | 112213659 | |||||||
chr6:112213696 | G | C | 3 | a0002c0006t0002g0249 a0002c0006t0002g0251 a0003c0004t0001g0312 |
3 | HG02622.hp2 HG02976.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.297+2672C>G | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 3/38 | chr6 | 112213696 | |||||||
chr6:112213743 | T | G | 7 | a0001c0002t0001g0253 a0001c0002t0001g0254 a0001c0011t0003g0255 others(4): Show |
7 | HG00741.hp1 HG02109.hp2 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.297+2625A>C | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 3/38 | chr6 | 112213743 | |||||||
chr6:112213926 | C | T | 9 | a0001c0002t0001g0164 a0001c0002t0001g0165 a0001c0009t0001g0134 others(6): Show |
9 | HG01934.hp1 HG01981.hp1 HG02886.hp1 others(6): Show |
intron_variant | MODIFIER | c.297+2442G>A | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 3/38 | chr6 | 112213926 | |||||||
chr6:112213930 | C | A | 32 | a0001c0001t0001g0090 a0001c0001t0001g0095 a0001c0001t0001g0167 others(29): Show |
32 | HG00639.hp1 HG00642.hp1 HG00673.hp2 others(29): Show |
intron_variant | MODIFIER | c.297+2438G>T | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 3/38 | chr6 | 112213930 | |||||||
chr6:112213937 | T | C | 3 | a0001c0020t0005g0168 a0001c0020t0005g0169 a0002c0006t0002g0170 |
3 | HG02895.hp1 HG02897.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.297+2431A>G | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 3/38 | chr6 | 112213937 | |||||||
chr6:112214000 | C | T | 11 | a0001c0011t0003g0062 a0001c0011t0003g0155 a0001c0011t0003g0158 others(8): Show |
11 | HG01243.hp1 HG02109.hp1 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.297+2368G>A | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 3/38 | chr6 | 112214000 | |||||||
chr6:112214026 | C | T | 1 | a0001c0001t0001g0257 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.297+2342G>A | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 3/38 | chr6 | 112214026 | |||||||
chr6:112214437 | C | T | 8 | a0001c0002t0001g0076 a0001c0002t0001g0197 a0001c0011t0003g0236 others(5): Show |
8 | HG01081.hp2 HG01981.hp2 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.297+1931G>A | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 3/38 | chr6 | 112214437 | |||||||
chr6:112214452 | G | T | 78 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0015 others(75): Show |
78 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(75): Show |
intron_variant | MODIFIER | c.297+1916C>A | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 3/38 | chr6 | 112214452 | |||||||
chr6:112214476 | A | G | 1 | a0003c0058t0001g0210 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.297+1892T>C | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 3/38 | chr6 | 112214476 | |||||||
chr6:112214542 | T | G | 1 | a0013c0039t0001g0196 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.297+1826A>C | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 3/38 | chr6 | 112214542 | |||||||
chr6:112214544 | G | T | 1 | a0013c0039t0001g0196 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.297+1824C>A | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 3/38 | chr6 | 112214544 | |||||||
chr6:112214605 | G | A | 4 | a0001c0002t0001g0253 a0001c0002t0001g0254 a0001c0011t0003g0255 others(1): Show |
4 | HG00741.hp1 HG02109.hp2 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.297+1763C>T | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 3/38 | chr6 | 112214605 | |||||||
chr6:112214732 | T | C | 3 | a0001c0001t0001g0237 a0003c0004t0001g0081 a0003c0004t0001g0240 |
3 | HG00408.hp1 NA18952.hp1 NA18960.hp1 |
intron_variant | MODIFIER | c.297+1636A>G | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 3/38 | chr6 | 112214732 | |||||||
chr6:112214751 | C | T | 1 | a0001c0016t0001g0048 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.297+1617G>A | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 3/38 | chr6 | 112214751 | |||||||
chr6:112214969 | C | T | 1 | a0003c0058t0001g0210 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.297+1399G>A | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 3/38 | chr6 | 112214969 | |||||||
chr6:112215042 | A | G | 1 | a0002c0003t0002g0198 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.297+1326T>C | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 3/38 | chr6 | 112215042 | |||||||
chr6:112215043 | T | A | 1 | a0013c0039t0001g0196 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.297+1325A>T | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 3/38 | chr6 | 112215043 | |||||||
chr6:112215137 | G | A | 4 | a0003c0004t0001g0022 a0003c0004t0001g0028 a0003c0004t0001g0029 others(1): Show |
4 | HG02258.hp2 HG02615.hp1 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.297+1231C>T | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 3/38 | chr6 | 112215137 | |||||||
chr6:112215307 | A | G | 1 | a0019c0036t0001g0282 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.297+1061T>C | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 3/38 | chr6 | 112215307 | |||||||
chr6:112215340 | G | A | 3 | a0002c0006t0002g0133 a0004c0010t0001g0080 a0004c0010t0001g0152 |
3 | HG02080.hp2 NA18971.hp2 NA19062.hp2 |
intron_variant | MODIFIER | c.297+1028C>T | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 3/38 | chr6 | 112215340 | |||||||
chr6:112215530 | C | CT | 164 | a0001c0001t0001g0014 a0001c0001t0001g0070 a0001c0001t0001g0072 others(161): Show |
164 | HG00408.hp2 HG00621.hp1 HG00621.hp2 others(161): Show |
intron_variant | MODIFIER | c.297+837dupA | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 3/38 | chr6 | 112215530 | |||||||
chr6:112215789 | A | G | 51 | a0001c0001t0001g0014 a0001c0001t0001g0220 a0001c0001t0001g0222 others(48): Show |
51 | HG00621.hp2 HG01071.hp1 HG01081.hp2 others(48): Show |
intron_variant | MODIFIER | c.297+579T>C | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 3/38 | chr6 | 112215789 | |||||||
chr6:112215918 | T | C | 1 | a0003c0058t0001g0210 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.297+450A>G | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 3/38 | chr6 | 112215918 | |||||||
chr6:112216019 | A | T | 8 | a0001c0002t0001g0076 a0001c0002t0001g0197 a0001c0011t0003g0236 others(5): Show |
8 | HG01081.hp2 HG01981.hp2 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.297+349T>A | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 3/38 | chr6 | 112216019 | |||||||
chr6:112216097 | G | A | 1 | a0008c0015t0001g0058 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.297+271C>T | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 3/38 | chr6 | 112216097 | |||||||
chr6:112216108 | A | G | 5 | a0001c0002t0001g0020 a0001c0002t0001g0045 a0001c0002t0001g0047 others(2): Show |
5 | HG01891.hp2 HG02055.hp1 HG02055.hp2 others(2): Show |
intron_variant | MODIFIER | c.297+260T>C | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 3/38 | chr6 | 112216108 | |||||||
chr6:112216266 | G | A | 8 | a0001c0002t0001g0076 a0001c0002t0001g0197 a0001c0011t0003g0236 others(5): Show |
8 | HG01081.hp2 HG01981.hp2 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.297+102C>T | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 3/38 | chr6 | 112216266 | |||||||
chr6:112216296 | A | G | 164 | a0001c0001t0001g0014 a0001c0001t0001g0070 a0001c0001t0001g0072 others(161): Show |
164 | HG00408.hp2 HG00621.hp1 HG00621.hp2 others(161): Show |
intron_variant | MODIFIER | c.297+72T>C | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 3/38 | chr6 | 112216296 | |||||||
chr6:112216481 | A | G | 2 | a0004c0026t0001g0067 a0004c0026t0001g0068 |
2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.196-12T>C | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 2/38 | chr6 | 112216481 | |||||||
chr6:112216590 | C | T | 1 | a0003c0004t0008g0273 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.196-121G>A | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 2/38 | chr6 | 112216590 | |||||||
chr6:112216660 | A | G | 9 | a0001c0001t0001g0050 a0001c0001t0001g0051 a0001c0001t0001g0052 others(6): Show |
9 | HG00639.hp2 HG01074.hp2 HG01243.hp2 others(6): Show |
intron_variant | MODIFIER | c.196-191T>C | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 2/38 | chr6 | 112216660 | |||||||
chr6:112216766 | G | A | 9 | a0001c0002t0001g0076 a0001c0002t0001g0197 a0001c0011t0003g0236 others(6): Show |
9 | HG01081.hp2 HG01981.hp2 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.196-297C>T | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 2/38 | chr6 | 112216766 | |||||||
chr6:112216773 | T | C | 3 | a0002c0006t0002g0249 a0002c0006t0002g0251 a0003c0004t0001g0312 |
3 | HG02622.hp2 HG02976.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.196-304A>G | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 2/38 | chr6 | 112216773 | |||||||
chr6:112216901 | C | T | 1 | a0001c0011t0003g0009 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.196-432G>A | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 2/38 | chr6 | 112216901 | |||||||
chr6:112216927 | T | A | 1 | a0007c0060t0002g0260 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.196-458A>T | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 2/38 | chr6 | 112216927 | |||||||
chr6:112217120 | T | C | 32 | a0001c0001t0001g0042 a0001c0001t0001g0069 a0001c0001t0001g0186 others(29): Show |
32 | HG00673.hp1 HG01167.hp1 HG01169.hp1 others(29): Show |
intron_variant | MODIFIER | c.196-651A>G | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 2/38 | chr6 | 112217120 | |||||||
chr6:112217264 | G | A | 51 | a0001c0001t0001g0014 a0001c0001t0001g0220 a0001c0001t0001g0222 others(48): Show |
51 | HG00621.hp2 HG01071.hp1 HG01081.hp2 others(48): Show |
intron_variant | MODIFIER | c.196-795C>T | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 2/38 | chr6 | 112217264 | |||||||
chr6:112217337 | G | A | 1 | a0001c0005t0001g0230 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.196-868C>T | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 2/38 | chr6 | 112217337 | |||||||
chr6:112217425 | G | T | 1 | a0004c0010t0001g0166 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.196-956C>A | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 2/38 | chr6 | 112217425 | |||||||
chr6:112217501 | C | T | 3 | a0001c0016t0010g0209 a0002c0048t0002g0143 a0012c0021t0001g0144 |
3 | NA18948.hp1 NA19055.hp1 NA19085.hp2 |
intron_variant | MODIFIER | c.196-1032G>A | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 2/38 | chr6 | 112217501 | |||||||
chr6:112217644 | C | T | 4 | a0001c0002t0001g0253 a0001c0002t0001g0254 a0001c0011t0003g0255 others(1): Show |
4 | HG00741.hp1 HG02109.hp2 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.196-1175G>A | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 2/38 | chr6 | 112217644 | |||||||
chr6:112217710 | A | G | 1 | a0007c0014t0002g0250 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.196-1241T>C | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 2/38 | chr6 | 112217710 | |||||||
chr6:112217750 | G | T | 1 | a0001c0002t0001g0191 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.196-1281C>A | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 2/38 | chr6 | 112217750 | |||||||
chr6:112217758 | G | A | 4 | a0001c0002t0001g0253 a0001c0002t0001g0254 a0001c0011t0003g0255 others(1): Show |
4 | HG00741.hp1 HG02109.hp2 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.196-1289C>T | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 2/38 | chr6 | 112217758 | |||||||
chr6:112217771 | C | A | 1 | a0001c0005t0001g0043 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.196-1302G>T | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 2/38 | chr6 | 112217771 | |||||||
chr6:112217781 | T | C | 2 | a0001c0001t0001g0228 a0001c0001t0011g0229 |
2 | HG01515.hp2 HG02004.hp2 |
intron_variant | MODIFIER | c.196-1312A>G | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 2/38 | chr6 | 112217781 | |||||||
chr6:112217848 | A | G | 200 | a0001c0001t0001g0014 a0001c0001t0001g0042 a0001c0001t0001g0069 others(197): Show |
200 | HG00408.hp2 HG00621.hp1 HG00621.hp2 others(197): Show |
intron_variant | MODIFIER | c.196-1379T>C | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 2/38 | chr6 | 112217848 | |||||||
chr6:112217853 | AAGATTGC others(3): Show |
A | 1 | a0001c0002t0001g0109 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.196-1394_196-1385d others(12): Show |
LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 2/38 | chr6 | 112217853 | |||||||
chr6:112217860 | C | A | 1 | a0002c0006t0002g0173 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.196-1391G>T | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 2/38 | chr6 | 112217860 | |||||||
chr6:112217864 | A | G | 1 | a0001c0002t0001g0109 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.196-1395T>C | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 2/38 | chr6 | 112217864 | |||||||
chr6:112218219 | T | C | 1 | a0001c0005t0001g0230 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.196-1750A>G | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 2/38 | chr6 | 112218219 | |||||||
chr6:112218246 | T | C | 1 | a0012c0021t0001g0083 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.196-1777A>G | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 2/38 | chr6 | 112218246 | |||||||
chr6:112218267 | G | A | 6 | a0001c0002t0001g0076 a0001c0002t0001g0197 a0002c0006t0002g0199 others(3): Show |
6 | HG01081.hp2 HG01981.hp2 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.196-1798C>T | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 2/38 | chr6 | 112218267 | |||||||
chr6:112218306 | T | TA | 31 | a0001c0001t0001g0090 a0001c0001t0001g0095 a0001c0001t0001g0167 others(28): Show |
31 | HG00639.hp1 HG00642.hp1 HG00673.hp2 others(28): Show |
intron_variant | MODIFIER | c.196-1838dupT | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 2/38 | chr6 | 112218306 | |||||||
chr6:112218310 | A | C | 9 | a0001c0011t0003g0062 a0001c0011t0003g0155 a0001c0011t0003g0158 others(6): Show |
9 | HG01243.hp1 HG02109.hp1 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.196-1841T>G | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 2/38 | chr6 | 112218310 | |||||||
chr6:112218452 | C | T | 4 | a0001c0023t0003g0306 a0001c0037t0003g0003 a0009c0017t0002g0307 others(1): Show |
4 | HG02886.hp2 HG02970.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.196-1983G>A | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 2/38 | chr6 | 112218452 | |||||||
chr6:112218559 | C | G | 4 | a0001c0002t0001g0253 a0001c0002t0001g0254 a0001c0011t0003g0255 others(1): Show |
4 | HG00741.hp1 HG02109.hp2 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.196-2090G>C | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 2/38 | chr6 | 112218559 | |||||||
chr6:112218762 | T | C | 32 | a0001c0001t0001g0042 a0001c0001t0001g0069 a0001c0001t0001g0186 others(29): Show |
32 | HG00673.hp1 HG01167.hp1 HG01169.hp1 others(29): Show |
intron_variant | MODIFIER | c.196-2293A>G | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 2/38 | chr6 | 112218762 | |||||||
chr6:112218767 | G | A | 4 | a0001c0002t0001g0309 a0002c0003t0002g0304 a0002c0003t0002g0305 others(1): Show |
4 | HG03654.hp1 HG03942.hp2 HG04199.hp2 others(1): Show |
intron_variant | MODIFIER | c.196-2298C>T | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 2/38 | chr6 | 112218767 | |||||||
chr6:112218895 | G | T | 1 | a0001c0002t0001g0215 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.196-2426C>A | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 2/38 | chr6 | 112218895 | |||||||
chr6:112218925 | G | T | 1 | a0002c0003t0002g0079 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.196-2456C>A | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 2/38 | chr6 | 112218925 | |||||||
chr6:112218968 | C | T | 1 | a0008c0031t0001g0056 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.196-2499G>A | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 2/38 | chr6 | 112218968 | |||||||
chr6:112219011 | T | A | 2 | a0003c0004t0008g0273 a0008c0015t0001g0274 |
2 | HG03669.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.196-2542A>T | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 2/38 | chr6 | 112219011 | |||||||
chr6:112219026 | G | A | 1 | a0002c0006t0002g0303 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.196-2557C>T | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 2/38 | chr6 | 112219026 | |||||||
chr6:112219069 | T | C | 32 | a0001c0001t0001g0042 a0001c0001t0001g0069 a0001c0001t0001g0186 others(29): Show |
32 | HG00673.hp1 HG01167.hp1 HG01169.hp1 others(29): Show |
intron_variant | MODIFIER | c.196-2600A>G | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 2/38 | chr6 | 112219069 | |||||||
chr6:112219193 | C | T | 4 | a0001c0002t0001g0253 a0001c0002t0001g0254 a0001c0011t0003g0255 others(1): Show |
4 | HG00741.hp1 HG02109.hp2 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.196-2724G>A | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 2/38 | chr6 | 112219193 | |||||||
chr6:112219279 | C | A | 4 | a0001c0002t0001g0253 a0001c0002t0001g0254 a0001c0011t0003g0255 others(1): Show |
4 | HG00741.hp1 HG02109.hp2 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.196-2810G>T | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 2/38 | chr6 | 112219279 | |||||||
chr6:112219451 | C | T | 1 | a0003c0025t0001g0113 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.196-2982G>A | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 2/38 | chr6 | 112219451 | |||||||
chr6:112219608 | G | T | 4 | a0001c0002t0001g0253 a0001c0002t0001g0254 a0001c0011t0003g0255 others(1): Show |
4 | HG00741.hp1 HG02109.hp2 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.196-3139C>A | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 2/38 | chr6 | 112219608 | |||||||
chr6:112219665 | A | G | 1 | a0001c0001t0001g0042 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.196-3196T>C | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 2/38 | chr6 | 112219665 | |||||||
chr6:112219752 | G | A | 4 | a0001c0002t0001g0253 a0001c0002t0001g0254 a0001c0011t0003g0255 others(1): Show |
4 | HG00741.hp1 HG02109.hp2 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.196-3283C>T | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 2/38 | chr6 | 112219752 | |||||||
chr6:112219874 | C | A | 1 | a0003c0004t0001g0234 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.196-3405G>T | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 2/38 | chr6 | 112219874 | |||||||
chr6:112219920 | C | T | 4 | a0001c0023t0003g0306 a0001c0037t0003g0003 a0009c0017t0002g0307 others(1): Show |
4 | HG02886.hp2 HG02970.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.196-3451G>A | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 2/38 | chr6 | 112219920 | |||||||
chr6:112219932 | C | G | 4 | a0001c0002t0001g0309 a0002c0003t0002g0304 a0002c0003t0002g0305 others(1): Show |
4 | HG03654.hp1 HG03942.hp2 HG04199.hp2 others(1): Show |
intron_variant | MODIFIER | c.196-3463G>C | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 2/38 | chr6 | 112219932 | |||||||
chr6:112219986 | C | T | 1 | a0001c0002t0001g0215 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.196-3517G>A | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 2/38 | chr6 | 112219986 | |||||||
chr6:112220008 | T | G | 29 | a0001c0001t0001g0014 a0001c0001t0001g0220 a0001c0001t0001g0222 others(26): Show |
29 | HG00621.hp2 HG01071.hp1 HG01106.hp2 others(26): Show |
intron_variant | MODIFIER | c.196-3539A>C | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 2/38 | chr6 | 112220008 | |||||||
chr6:112220172 | A | C | 4 | a0001c0002t0001g0253 a0001c0002t0001g0254 a0001c0011t0003g0255 others(1): Show |
4 | HG00741.hp1 HG02109.hp2 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.196-3703T>G | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 2/38 | chr6 | 112220172 | |||||||
chr6:112220216 | T | C | 4 | a0001c0002t0001g0253 a0001c0002t0001g0254 a0001c0011t0003g0255 others(1): Show |
4 | HG00741.hp1 HG02109.hp2 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.196-3747A>G | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 2/38 | chr6 | 112220216 | |||||||
chr6:112220255 | T | C | 4 | a0001c0002t0001g0253 a0001c0002t0001g0254 a0001c0011t0003g0255 others(1): Show |
4 | HG00741.hp1 HG02109.hp2 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.196-3786A>G | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 2/38 | chr6 | 112220255 | |||||||
chr6:112220262 | A | G | 1 | a0001c0002t0001g0212 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.196-3793T>C | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 2/38 | chr6 | 112220262 | |||||||
chr6:112220266 | C | A | 1 | a0016c0042t0001g0296 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.196-3797G>T | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 2/38 | chr6 | 112220266 | |||||||
chr6:112220305 | C | A | 4 | a0001c0002t0001g0253 a0001c0002t0001g0254 a0001c0011t0003g0255 others(1): Show |
4 | HG00741.hp1 HG02109.hp2 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.196-3836G>T | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 2/38 | chr6 | 112220305 | |||||||
chr6:112220389 | G | C | 29 | a0001c0001t0001g0014 a0001c0001t0001g0220 a0001c0001t0001g0222 others(26): Show |
29 | HG00621.hp2 HG01071.hp1 HG01106.hp2 others(26): Show |
intron_variant | MODIFIER | c.196-3920C>G | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 2/38 | chr6 | 112220389 | |||||||
chr6:112220460 | G | A | 57 | a0001c0001t0001g0070 a0001c0001t0001g0072 a0001c0001t0001g0074 others(54): Show |
57 | HG00408.hp2 HG00621.hp1 HG01168.hp2 others(54): Show |
intron_variant | MODIFIER | c.196-3991C>T | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 2/38 | chr6 | 112220460 | |||||||
chr6:112220524 | A | G | 4 | a0003c0004t0001g0022 a0003c0004t0001g0028 a0003c0004t0001g0029 others(1): Show |
4 | HG02258.hp2 HG02615.hp1 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.196-4055T>C | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 2/38 | chr6 | 112220524 | |||||||
chr6:112220618 | ATTGT | A | 4 | a0001c0002t0001g0253 a0001c0002t0001g0254 a0001c0011t0003g0255 others(1): Show |
4 | HG00741.hp1 HG02109.hp2 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.196-4153_196-4150d others(6): Show |
LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 2/38 | chr6 | 112220618 | |||||||
chr6:112220632 | A | C | 4 | a0001c0002t0001g0253 a0001c0002t0001g0254 a0001c0011t0003g0255 others(1): Show |
4 | HG00741.hp1 HG02109.hp2 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.196-4163T>G | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 2/38 | chr6 | 112220632 | |||||||
chr6:112220657 | G | A | 4 | a0001c0002t0001g0253 a0001c0002t0001g0254 a0001c0011t0003g0255 others(1): Show |
4 | HG00741.hp1 HG02109.hp2 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.196-4188C>T | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 2/38 | chr6 | 112220657 | |||||||
chr6:112220907 | C | T | 4 | a0001c0002t0001g0253 a0001c0002t0001g0254 a0001c0011t0003g0255 others(1): Show |
4 | HG00741.hp1 HG02109.hp2 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.196-4438G>A | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 2/38 | chr6 | 112220907 | |||||||
chr6:112221019 | T | C | 4 | a0001c0002t0001g0253 a0001c0002t0001g0254 a0001c0011t0003g0255 others(1): Show |
4 | HG00741.hp1 HG02109.hp2 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.196-4550A>G | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 2/38 | chr6 | 112221019 | |||||||
chr6:112221041 | T | C | 32 | a0001c0001t0001g0042 a0001c0001t0001g0069 a0001c0001t0001g0186 others(29): Show |
32 | HG00673.hp1 HG01167.hp1 HG01169.hp1 others(29): Show |
intron_variant | MODIFIER | c.196-4572A>G | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 2/38 | chr6 | 112221041 | |||||||
chr6:112221102 | C | A | 4 | a0001c0002t0001g0253 a0001c0002t0001g0254 a0001c0011t0003g0255 others(1): Show |
4 | HG00741.hp1 HG02109.hp2 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.196-4633G>T | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 2/38 | chr6 | 112221102 | |||||||
chr6:112221123 | T | C | 4 | a0001c0002t0001g0253 a0001c0002t0001g0254 a0001c0011t0003g0255 others(1): Show |
4 | HG00741.hp1 HG02109.hp2 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.196-4654A>G | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 2/38 | chr6 | 112221123 | |||||||
chr6:112221268 | G | T | 37 | a0001c0001t0001g0042 a0001c0001t0001g0069 a0001c0001t0001g0186 others(34): Show |
37 | HG00673.hp1 HG01167.hp1 HG01169.hp1 others(34): Show |
intron_variant | MODIFIER | c.196-4799C>A | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 2/38 | chr6 | 112221268 | |||||||
chr6:112221269 | T | G | 4 | a0001c0002t0001g0253 a0001c0002t0001g0254 a0001c0011t0003g0255 others(1): Show |
4 | HG00741.hp1 HG02109.hp2 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.196-4800A>C | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 2/38 | chr6 | 112221269 | |||||||
chr6:112221437 | G | C | 4 | a0001c0002t0001g0253 a0001c0002t0001g0254 a0001c0011t0003g0255 others(1): Show |
4 | HG00741.hp1 HG02109.hp2 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.196-4968C>G | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 2/38 | chr6 | 112221437 | |||||||
chr6:112221471 | A | T | 2 | a0001c0002t0001g0253 a0001c0011t0003g0293 |
2 | HG02109.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.196-5002T>A | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 2/38 | chr6 | 112221471 | |||||||
chr6:112221556 | C | T | 4 | a0001c0002t0001g0253 a0001c0002t0001g0254 a0001c0011t0003g0255 others(1): Show |
4 | HG00741.hp1 HG02109.hp2 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.196-5087G>A | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 2/38 | chr6 | 112221556 | |||||||
chr6:112221701 | G | A | 4 | a0001c0002t0001g0253 a0001c0002t0001g0254 a0001c0011t0003g0255 others(1): Show |
4 | HG00741.hp1 HG02109.hp2 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.196-5232C>T | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 2/38 | chr6 | 112221701 | |||||||
chr6:112221719 | G | C | 1 | a0002c0006t0002g0251 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.196-5250C>G | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 2/38 | chr6 | 112221719 | |||||||
chr6:112222096 | C | T | 4 | a0001c0002t0001g0253 a0001c0002t0001g0254 a0001c0011t0003g0255 others(1): Show |
4 | HG00741.hp1 HG02109.hp2 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.196-5627G>A | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 2/38 | chr6 | 112222096 | |||||||
chr6:112222175 | G | A | 1 | a0001c0023t0003g0302 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.196-5706C>T | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 2/38 | chr6 | 112222175 | |||||||
chr6:112222338 | T | C | 109 | a0001c0001t0001g0070 a0001c0001t0001g0072 a0001c0001t0001g0074 others(106): Show |
109 | HG00408.hp2 HG00621.hp1 HG00639.hp1 others(106): Show |
intron_variant | MODIFIER | c.196-5869A>G | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 2/38 | chr6 | 112222338 | |||||||
chr6:112222575 | G | A | 1 | a0005c0008t0004g0245 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.196-6106C>T | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 2/38 | chr6 | 112222575 | |||||||
chr6:112222586 | T | C | 3 | a0002c0006t0002g0249 a0002c0006t0002g0251 a0003c0004t0001g0312 |
3 | HG02622.hp2 HG02976.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.196-6117A>G | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 2/38 | chr6 | 112222586 | |||||||
chr6:112222611 | G | T | 18 | a0001c0002t0001g0076 a0001c0002t0001g0197 a0001c0011t0003g0062 others(15): Show |
18 | HG01081.hp2 HG01243.hp1 HG01981.hp2 others(15): Show |
intron_variant | MODIFIER | c.196-6142C>A | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 2/38 | chr6 | 112222611 | |||||||
chr6:112222638 | G | C | 6 | a0001c0002t0001g0205 a0002c0003t0001g0171 a0002c0003t0006g0001 others(3): Show |
6 | HG01071.hp1 HG02717.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.196-6169C>G | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 2/38 | chr6 | 112222638 | |||||||
chr6:112222765 | C | T | 3 | a0001c0009t0009g0078 a0002c0003t0002g0077 a0002c0003t0002g0079 |
3 | HG00099.hp2 HG00280.hp1 HG00323.hp2 |
intron_variant | MODIFIER | c.196-6296G>A | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 2/38 | chr6 | 112222765 | |||||||
chr6:112222786 | C | T | 1 | a0001c0011t0003g0293 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.196-6317G>A | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 2/38 | chr6 | 112222786 | |||||||
chr6:112222787 | G | C | 5 | a0001c0001t0001g0256 a0001c0001t0001g0283 a0003c0004t0008g0273 others(2): Show |
5 | HG01361.hp1 HG01361.hp2 HG02004.hp1 others(2): Show |
intron_variant | MODIFIER | c.196-6318C>G | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 2/38 | chr6 | 112222787 | |||||||
chr6:112222852 | C | A | 1 | a0001c0001t0001g0069 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.196-6383G>T | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 2/38 | chr6 | 112222852 | |||||||
chr6:112222854 | T | C | 109 | a0001c0001t0001g0070 a0001c0001t0001g0072 a0001c0001t0001g0074 others(106): Show |
109 | HG00408.hp2 HG00621.hp1 HG00639.hp1 others(106): Show |
intron_variant | MODIFIER | c.196-6385A>G | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 2/38 | chr6 | 112222854 | |||||||
chr6:112223068 | C | G | 7 | a0001c0002t0001g0076 a0001c0002t0001g0197 a0001c0023t0003g0302 others(4): Show |
7 | HG01081.hp2 HG01981.hp2 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.196-6599G>C | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 2/38 | chr6 | 112223068 | |||||||
chr6:112223195 | A | T | 1 | a0002c0003t0002g0304 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.196-6726T>A | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 2/38 | chr6 | 112223195 | |||||||
chr6:112223282 | G | C | 29 | a0001c0001t0001g0014 a0001c0001t0001g0220 a0001c0001t0001g0222 others(26): Show |
29 | HG00621.hp2 HG01071.hp1 HG01106.hp2 others(26): Show |
intron_variant | MODIFIER | c.196-6813C>G | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 2/38 | chr6 | 112223282 | |||||||
chr6:112223295 | A | G | 4 | a0001c0002t0001g0253 a0001c0002t0001g0254 a0001c0011t0003g0255 others(1): Show |
4 | HG00741.hp1 HG02109.hp2 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.196-6826T>C | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 2/38 | chr6 | 112223295 | |||||||
chr6:112223372 | A | G | 4 | a0001c0023t0003g0306 a0001c0037t0003g0003 a0009c0017t0002g0307 others(1): Show |
4 | HG02886.hp2 HG02970.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.196-6903T>C | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 2/38 | chr6 | 112223372 | |||||||
chr6:112223760 | T | C | 4 | a0001c0002t0001g0253 a0001c0002t0001g0254 a0001c0011t0003g0255 others(1): Show |
4 | HG00741.hp1 HG02109.hp2 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.196-7291A>G | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 2/38 | chr6 | 112223760 | |||||||
chr6:112223762 | T | C | 5 | a0001c0002t0001g0311 a0001c0011t0003g0313 a0001c0051t0003g0314 others(2): Show |
5 | HG01891.hp1 HG02897.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.196-7293A>G | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 2/38 | chr6 | 112223762 | |||||||
chr6:112223781 | T | C | 1 | a0001c0016t0001g0048 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.196-7312A>G | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 2/38 | chr6 | 112223781 | |||||||
chr6:112223933 | A | T | 51 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0015 others(48): Show |
51 | HG00099.hp1 HG00597.hp1 HG00639.hp2 others(48): Show |
intron_variant | MODIFIER | c.196-7464T>A | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 2/38 | chr6 | 112223933 | |||||||
chr6:112224019 | T | C | 1 | a0002c0003t0001g0171 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.196-7550A>G | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 2/38 | chr6 | 112224019 | |||||||
chr6:112224078 | T | C | 4 | a0001c0002t0001g0253 a0001c0002t0001g0254 a0001c0011t0003g0255 others(1): Show |
4 | HG00741.hp1 HG02109.hp2 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.196-7609A>G | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 2/38 | chr6 | 112224078 | |||||||
chr6:112224112 | T | G | 1 | a0001c0002t0001g0107 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.196-7643A>C | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 2/38 | chr6 | 112224112 | |||||||
chr6:112224199 | C | T | 6 | a0008c0015t0001g0057 a0008c0015t0001g0058 a0008c0015t0001g0059 others(3): Show |
6 | HG02486.hp2 HG02818.hp2 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.196-7730G>A | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 2/38 | chr6 | 112224199 | |||||||
chr6:112224300 | A | G | 4 | a0001c0002t0001g0253 a0001c0002t0001g0254 a0001c0011t0003g0255 others(1): Show |
4 | HG00741.hp1 HG02109.hp2 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.196-7831T>C | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 2/38 | chr6 | 112224300 | |||||||
chr6:112224519 | C | T | 4 | a0001c0023t0003g0306 a0001c0037t0003g0003 a0009c0017t0002g0307 others(1): Show |
4 | HG02886.hp2 HG02970.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.196-8050G>A | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 2/38 | chr6 | 112224519 | |||||||
chr6:112224605 | A | C | 4 | a0001c0002t0001g0253 a0001c0002t0001g0254 a0001c0011t0003g0255 others(1): Show |
4 | HG00741.hp1 HG02109.hp2 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.196-8136T>G | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 2/38 | chr6 | 112224605 | |||||||
chr6:112224618 | C | A | 50 | a0001c0001t0001g0014 a0001c0001t0001g0220 a0001c0001t0001g0222 others(47): Show |
50 | HG00621.hp2 HG01071.hp1 HG01081.hp2 others(47): Show |
intron_variant | MODIFIER | c.196-8149G>T | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 2/38 | chr6 | 112224618 | |||||||
chr6:112224730 | C | A | 5 | a0001c0002t0001g0311 a0001c0011t0003g0313 a0001c0051t0003g0314 others(2): Show |
5 | HG01891.hp1 HG02897.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.196-8261G>T | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 2/38 | chr6 | 112224730 | |||||||
chr6:112224740 | C | T | 5 | a0001c0002t0001g0311 a0001c0011t0003g0313 a0001c0051t0003g0314 others(2): Show |
5 | HG01891.hp1 HG02897.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.196-8271G>A | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 2/38 | chr6 | 112224740 | |||||||
chr6:112224813 | C | CA | 71 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0015 others(68): Show |
71 | HG00099.hp1 HG00597.hp1 HG00639.hp2 others(68): Show |
intron_variant | MODIFIER | c.196-8345dupT | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 2/38 | chr6 | 112224813 | |||||||
chr6:112224813 | CA | C | 37 | a0001c0001t0001g0014 a0001c0001t0001g0016 a0001c0001t0001g0220 others(34): Show |
37 | HG00621.hp2 HG01071.hp1 HG01074.hp1 others(34): Show |
intron_variant | MODIFIER | c.196-8345delT | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 2/38 | chr6 | 112224813 | |||||||
chr6:112224887 | T | C | 3 | a0002c0006t0002g0249 a0002c0006t0002g0251 a0007c0014t0002g0250 |
3 | HG02622.hp2 HG02976.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.196-8418A>G | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 2/38 | chr6 | 112224887 | |||||||
chr6:112224938 | G | GT | 160 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0015 others(157): Show |
160 | HG00099.hp1 HG00408.hp2 HG00597.hp1 others(157): Show |
intron_variant | MODIFIER | c.196-8470dupA | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 2/38 | chr6 | 112224938 | |||||||
chr6:112224987 | G | A | 1 | a0001c0001t0001g0219 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.196-8518C>T | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 2/38 | chr6 | 112224987 | |||||||
chr6:112225070 | T | C | 8 | a0001c0002t0001g0258 a0001c0002t0001g0278 a0001c0002t0001g0279 others(5): Show |
8 | HG00408.hp2 HG00621.hp1 HG02074.hp2 others(5): Show |
intron_variant | MODIFIER | c.196-8601A>G | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 2/38 | chr6 | 112225070 | |||||||
chr6:112225171 | C | G | 43 | a0001c0001t0001g0014 a0001c0001t0001g0220 a0001c0001t0001g0222 others(40): Show |
43 | HG00621.hp2 HG01071.hp1 HG01106.hp2 others(40): Show |
intron_variant | MODIFIER | c.196-8702G>C | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 2/38 | chr6 | 112225171 | |||||||
chr6:112225358 | A | G | 1 | a0003c0004t0001g0225 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.196-8889T>C | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 2/38 | chr6 | 112225358 | |||||||
chr6:112225459 | G | C | 26 | a0001c0001t0001g0016 a0001c0001t0001g0027 a0001c0001t0001g0033 others(23): Show |
26 | HG00280.hp2 HG00323.hp1 HG00642.hp2 others(23): Show |
intron_variant | MODIFIER | c.196-8990C>G | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 2/38 | chr6 | 112225459 | |||||||
chr6:112225599 | C | G | 1 | a0003c0013t0001g0065 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.196-9130G>C | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 2/38 | chr6 | 112225599 | |||||||
chr6:112225637 | T | C | 1 | a0003c0004t0001g0312 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.196-9168A>G | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 2/38 | chr6 | 112225637 | |||||||
chr6:112225693 | G | T | 1 | a0007c0014t0002g0250 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.196-9224C>A | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 2/38 | chr6 | 112225693 | |||||||
chr6:112226211 | T | C | 49 | a0001c0001t0001g0014 a0001c0001t0001g0220 a0001c0001t0001g0222 others(46): Show |
49 | HG00621.hp2 HG01071.hp1 HG01106.hp2 others(46): Show |
intron_variant | MODIFIER | c.196-9742A>G | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 2/38 | chr6 | 112226211 | |||||||
chr6:112226232 | T | C | 9 | a0001c0002t0001g0205 a0001c0020t0005g0168 a0001c0020t0005g0169 others(6): Show |
9 | HG01071.hp1 HG02717.hp2 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.196-9763A>G | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 2/38 | chr6 | 112226232 | |||||||
chr6:112226255 | T | C | 1 | a0001c0005t0001g0137 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.196-9786A>G | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 2/38 | chr6 | 112226255 | |||||||
chr6:112226315 | A | G | 1 | a0007c0014t0002g0292 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.196-9846T>C | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 2/38 | chr6 | 112226315 | |||||||
chr6:112226451 | T | C | 1 | a0001c0005t0001g0280 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.196-9982A>G | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 2/38 | chr6 | 112226451 | |||||||
chr6:112226543 | C | T | 3 | a0002c0006t0002g0249 a0002c0006t0002g0251 a0007c0014t0002g0250 |
3 | HG02622.hp2 HG02976.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.196-10074G>A | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 2/38 | chr6 | 112226543 | |||||||
chr6:112226630 | C | T | 2 | a0003c0025t0001g0086 a0003c0025t0001g0113 |
2 | HG02886.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.196-10161G>A | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 2/38 | chr6 | 112226630 | |||||||
chr6:112226869 | G | T | 2 | a0001c0011t0003g0009 a0001c0050t0001g0310 |
2 | HG02055.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.196-10400C>A | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 2/38 | chr6 | 112226869 | |||||||
chr6:112227003 | G | A | 9 | a0001c0002t0001g0188 a0001c0002t0001g0191 a0001c0002t0001g0192 others(6): Show |
9 | HG01167.hp1 HG01169.hp1 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.196-10534C>T | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 2/38 | chr6 | 112227003 | |||||||
chr6:112227041 | T | TTTTA | 63 | a0001c0001t0001g0014 a0001c0001t0001g0042 a0001c0001t0001g0186 others(60): Show |
63 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(60): Show |
intron_variant | MODIFIER | c.196-10576_196-1057 others(8): Show |
LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 2/38 | chr6 | 112227041 | |||||||
chr6:112227041 | T | TTTTATTT others(1): Show |
35 | a0001c0001t0001g0224 a0001c0001t0001g0237 a0001c0002t0001g0020 others(32): Show |
35 | HG00280.hp1 HG00408.hp1 HG00621.hp2 others(32): Show |
intron_variant | MODIFIER | c.196-10580_196-1057 others(12): Show |
LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 2/38 | chr6 | 112227041 | |||||||
chr6:112227041 | T | TTTTATTT others(5): Show |
7 | a0001c0001t0001g0069 a0001c0001t0001g0246 a0001c0002t0001g0213 others(4): Show |
7 | HG00597.hp2 HG02015.hp2 HG02698.hp2 others(4): Show |
intron_variant | MODIFIER | c.196-10584_196-1057 others(16): Show |
LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 2/38 | chr6 | 112227041 | |||||||
chr6:112227041 | T | TTTTTTTT others(1): Show |
10 | a0001c0011t0003g0062 a0001c0011t0003g0155 a0001c0011t0003g0158 others(7): Show |
10 | HG01243.hp1 HG02109.hp1 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.196-10573_196-1057 others(12): Show |
LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 2/38 | chr6 | 112227041 | |||||||
chr6:112227041 | T | TTTTTTTT others(5): Show |
1 | a0004c0007t0001g0162 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.196-10573_196-1057 others(16): Show |
LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 2/38 | chr6 | 112227041 | |||||||
chr6:112227041 | TTTTA | T | 110 | a0001c0001t0001g0007 a0001c0001t0001g0015 a0001c0001t0001g0050 others(107): Show |
110 | HG00099.hp1 HG00280.hp2 HG00408.hp2 others(107): Show |
intron_variant | MODIFIER | c.196-10576_196-1057 others(8): Show |
LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 2/38 | chr6 | 112227041 | |||||||
chr6:112227041 | TTTTATTT others(9): Show |
T | 4 | a0001c0023t0003g0306 a0001c0037t0003g0003 a0009c0017t0002g0307 others(1): Show |
4 | HG02886.hp2 HG02970.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.196-10588_196-1057 others(20): Show |
LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 2/38 | chr6 | 112227041 | |||||||
chr6:112227095 | G | A | 1 | a0003c0004t0001g0141 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.196-10626C>T | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 2/38 | chr6 | 112227095 | |||||||
chr6:112227252 | G | A | 1 | a0001c0009t0001g0288 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.196-10783C>T | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 2/38 | chr6 | 112227252 | |||||||
chr6:112227430 | AAG | A | 4 | a0001c0002t0001g0020 a0001c0002t0001g0045 a0001c0002t0001g0047 others(1): Show |
4 | HG01891.hp2 HG02055.hp2 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.196-10963_196-1096 others(6): Show |
LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 2/38 | chr6 | 112227430 | |||||||
chr6:112227446 | A | T | 2 | a0001c0011t0003g0009 a0001c0050t0001g0310 |
2 | HG02055.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.196-10977T>A | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 2/38 | chr6 | 112227446 | |||||||
chr6:112227758 | ATCTG | A | 3 | a0002c0006t0002g0249 a0002c0006t0002g0251 a0007c0014t0002g0250 |
3 | HG02622.hp2 HG02976.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.196-11293_196-1129 others(8): Show |
LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 2/38 | chr6 | 112227758 | |||||||
chr6:112227901 | C | G | 226 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0014 others(223): Show |
226 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(223): Show |
intron_variant | MODIFIER | c.196-11432G>C | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 2/38 | chr6 | 112227901 | |||||||
chr6:112227906 | CTTAT | C | 34 | a0001c0001t0001g0015 a0001c0001t0001g0090 a0001c0001t0001g0095 others(31): Show |
34 | HG00639.hp1 HG00642.hp1 HG00673.hp2 others(31): Show |
intron_variant | MODIFIER | c.196-11441_196-1143 others(8): Show |
LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 2/38 | chr6 | 112227906 | |||||||
chr6:112227939 | G | C | 2 | a0003c0059t0001g0259 a0007c0060t0002g0260 |
2 | HG02280.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.196-11470C>G | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 2/38 | chr6 | 112227939 | |||||||
chr6:112227963 | A | C | 123 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0015 others(120): Show |
123 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(120): Show |
intron_variant | MODIFIER | c.196-11494T>G | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 2/38 | chr6 | 112227963 | |||||||
chr6:112228127 | C | T | 4 | a0001c0001t0001g0222 a0001c0001t0001g0223 a0001c0001t0001g0224 others(1): Show |
4 | HG02040.hp2 NA18954.hp2 NA19006.hp2 others(1): Show |
intron_variant | MODIFIER | c.196-11658G>A | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 2/38 | chr6 | 112228127 | |||||||
chr6:112228341 | A | G | 1 | a0002c0006t0002g0088 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.196-11872T>C | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 2/38 | chr6 | 112228341 | |||||||
chr6:112228385 | C | T | 102 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0015 others(99): Show |
102 | HG00099.hp1 HG00280.hp2 HG00597.hp1 others(99): Show |
intron_variant | MODIFIER | c.196-11916G>A | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 2/38 | chr6 | 112228385 | |||||||
chr6:112228721 | C | T | 3 | a0005c0008t0001g0262 a0005c0044t0001g0261 a0018c0030t0001g0004 |
3 | HG02280.hp1 HG02717.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.196-12252G>A | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 2/38 | chr6 | 112228721 | |||||||
chr6:112228739 | G | A | 4 | a0001c0023t0003g0306 a0001c0037t0003g0003 a0009c0017t0002g0307 others(1): Show |
4 | HG02886.hp2 HG02970.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.196-12270C>T | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 2/38 | chr6 | 112228739 | |||||||
chr6:112228814 | T | C | 97 | a0001c0001t0001g0016 a0001c0001t0001g0027 a0001c0001t0001g0033 others(94): Show |
97 | HG00323.hp1 HG00642.hp2 HG00673.hp1 others(94): Show |
intron_variant | MODIFIER | c.196-12345A>G | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 2/38 | chr6 | 112228814 | |||||||
chr6:112228859 | T | C | 71 | a0001c0001t0001g0042 a0001c0001t0001g0069 a0001c0001t0001g0186 others(68): Show |
71 | HG00673.hp1 HG01081.hp2 HG01167.hp1 others(68): Show |
intron_variant | MODIFIER | c.196-12390A>G | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 2/38 | chr6 | 112228859 | |||||||
chr6:112229038 | C | T | 7 | a0001c0002t0001g0076 a0001c0002t0001g0197 a0001c0023t0003g0302 others(4): Show |
7 | HG01081.hp2 HG01981.hp2 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.196-12569G>A | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 2/38 | chr6 | 112229038 | |||||||
chr6:112229316 | T | C | 19 | a0001c0002t0001g0076 a0001c0002t0001g0197 a0001c0011t0003g0009 others(16): Show |
19 | HG01081.hp2 HG01981.hp2 HG02055.hp1 others(16): Show |
intron_variant | MODIFIER | c.196-12847A>G | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 2/38 | chr6 | 112229316 | |||||||
chr6:112229367 | T | C | 3 | a0001c0001t0001g0202 a0001c0001t0001g0204 a0001c0009t0001g0203 |
3 | HG02040.hp1 HG02132.hp2 HG02155.hp1 |
intron_variant | MODIFIER | c.196-12898A>G | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 2/38 | chr6 | 112229367 | |||||||
chr6:112229455 | C | T | 1 | a0001c0011t0003g0009 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.196-12986G>A | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 2/38 | chr6 | 112229455 | |||||||
chr6:112229477 | A | C | 4 | a0001c0023t0003g0306 a0001c0037t0003g0003 a0009c0017t0002g0307 others(1): Show |
4 | HG02886.hp2 HG02970.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.196-13008T>G | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 2/38 | chr6 | 112229477 | |||||||
chr6:112229545 | G | A | 1 | a0003c0058t0001g0210 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.196-13076C>T | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 2/38 | chr6 | 112229545 | |||||||
chr6:112229603 | A | G | 3 | a0002c0006t0002g0249 a0002c0006t0002g0251 a0007c0014t0002g0250 |
3 | HG02622.hp2 HG02976.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.196-13134T>C | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 2/38 | chr6 | 112229603 | |||||||
chr6:112229751 | G | A | 2 | a0001c0002t0001g0045 a0001c0002t0001g0047 |
2 | HG02055.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.196-13282C>T | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 2/38 | chr6 | 112229751 | |||||||
chr6:112229893 | AT | A | 4 | a0006c0012t0002g0075 a0006c0012t0002g0179 a0006c0012t0002g0194 others(1): Show |
4 | NA18960.hp2 NA18968.hp2 NA19002.hp2 others(1): Show |
intron_variant | MODIFIER | c.196-13425delA | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 2/38 | chr6 | 112229893 | |||||||
chr6:112229909 | C | G | 1 | a0007c0014t0002g0041 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.196-13440G>C | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 2/38 | chr6 | 112229909 | |||||||
chr6:112230317 | G | C | 1 | a0002c0006t0002g0108 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.196-13848C>G | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 2/38 | chr6 | 112230317 | |||||||
chr6:112230363 | C | T | 1 | a0016c0042t0001g0296 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.196-13894G>A | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 2/38 | chr6 | 112230363 | |||||||
chr6:112230411 | C | T | 1 | a0009c0017t0002g0307 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.196-13942G>A | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 2/38 | chr6 | 112230411 | |||||||
chr6:112230434 | G | C | 33 | a0001c0001t0001g0042 a0001c0001t0001g0069 a0001c0001t0001g0186 others(30): Show |
33 | HG00673.hp1 HG01167.hp1 HG01169.hp1 others(30): Show |
intron_variant | MODIFIER | c.196-13965C>G | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 2/38 | chr6 | 112230434 | |||||||
chr6:112230562 | A | G | 2 | a0001c0011t0003g0009 a0001c0050t0001g0310 |
2 | HG02055.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.196-14093T>C | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 2/38 | chr6 | 112230562 | |||||||
chr6:112230732 | A | G | 1 | a0019c0036t0001g0282 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.196-14263T>C | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 2/38 | chr6 | 112230732 | |||||||
chr6:112230771 | C | T | 6 | a0008c0015t0001g0057 a0008c0015t0001g0058 a0008c0015t0001g0059 others(3): Show |
6 | HG02486.hp2 HG02818.hp2 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.196-14302G>A | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 2/38 | chr6 | 112230771 | |||||||
chr6:112230788 | T | C | 6 | a0008c0015t0001g0057 a0008c0015t0001g0058 a0008c0015t0001g0059 others(3): Show |
6 | HG02486.hp2 HG02818.hp2 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.196-14319A>G | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 2/38 | chr6 | 112230788 | |||||||
chr6:112230830 | G | T | 13 | a0001c0002t0001g0076 a0001c0002t0001g0197 a0001c0023t0003g0302 others(10): Show |
13 | HG01081.hp2 HG01981.hp2 HG02486.hp2 others(10): Show |
intron_variant | MODIFIER | c.196-14361C>A | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 2/38 | chr6 | 112230830 | |||||||
chr6:112230972 | C | G | 3 | a0002c0006t0002g0249 a0002c0006t0002g0251 a0007c0014t0002g0250 |
3 | HG02622.hp2 HG02976.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.196-14503G>C | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 2/38 | chr6 | 112230972 | |||||||
chr6:112231131 | C | T | 2 | a0001c0001t0001g0008 a0004c0007t0001g0117 |
2 | NA19012.hp2 NA19068.hp2 |
intron_variant | MODIFIER | c.196-14662G>A | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 2/38 | chr6 | 112231131 | |||||||
chr6:112231170 | T | C | 6 | a0008c0015t0001g0057 a0008c0015t0001g0058 a0008c0015t0001g0059 others(3): Show |
6 | HG02486.hp2 HG02818.hp2 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.196-14701A>G | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 2/38 | chr6 | 112231170 | |||||||
chr6:112231192 | T | C | 1 | a0001c0054t0001g0301 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.196-14723A>G | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 2/38 | chr6 | 112231192 | |||||||
chr6:112231332 | G | C | 1 | a0002c0024t0001g0172 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.196-14863C>G | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 2/38 | chr6 | 112231332 | |||||||
chr6:112231334 | G | T | 13 | a0001c0002t0001g0076 a0001c0002t0001g0197 a0001c0023t0003g0302 others(10): Show |
13 | HG01081.hp2 HG01981.hp2 HG02486.hp2 others(10): Show |
intron_variant | MODIFIER | c.196-14865C>A | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 2/38 | chr6 | 112231334 | |||||||
chr6:112231421 | A | G | 1 | a0003c0058t0001g0210 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.196-14952T>C | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 2/38 | chr6 | 112231421 | |||||||
chr6:112231439 | C | T | 19 | a0001c0002t0001g0076 a0001c0002t0001g0197 a0001c0011t0003g0009 others(16): Show |
19 | HG01081.hp2 HG01981.hp2 HG02055.hp1 others(16): Show |
intron_variant | MODIFIER | c.196-14970G>A | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 2/38 | chr6 | 112231439 | |||||||
chr6:112231442 | T | C | 7 | a0001c0002t0001g0076 a0001c0002t0001g0197 a0001c0023t0003g0302 others(4): Show |
7 | HG01081.hp2 HG01981.hp2 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.196-14973A>G | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 2/38 | chr6 | 112231442 | |||||||
chr6:112231519 | G | T | 13 | a0001c0002t0001g0076 a0001c0002t0001g0197 a0001c0023t0003g0302 others(10): Show |
13 | HG01081.hp2 HG01981.hp2 HG02486.hp2 others(10): Show |
intron_variant | MODIFIER | c.196-15050C>A | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 2/38 | chr6 | 112231519 | |||||||
chr6:112231999 | A | G | 1 | a0017c0046t0002g0233 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.196-15530T>C | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 2/38 | chr6 | 112231999 | |||||||
chr6:112232142 | A | C | 4 | a0001c0023t0003g0306 a0001c0037t0003g0003 a0009c0017t0002g0307 others(1): Show |
4 | HG02886.hp2 HG02970.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.196-15673T>G | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 2/38 | chr6 | 112232142 | |||||||
chr6:112232215 | A | C | 2 | a0002c0006t0002g0264 a0002c0006t0002g0265 |
2 | NA18979.hp1 NA18980.hp1 |
intron_variant | MODIFIER | c.196-15746T>G | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 2/38 | chr6 | 112232215 | |||||||
chr6:112232237 | C | A | 1 | a0003c0004t0001g0035 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.196-15768G>T | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 2/38 | chr6 | 112232237 | |||||||
chr6:112232240 | C | T | 3 | a0002c0006t0002g0249 a0002c0006t0002g0251 a0007c0014t0002g0250 |
3 | HG02622.hp2 HG02976.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.196-15771G>A | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 2/38 | chr6 | 112232240 | |||||||
chr6:112232323 | A | G | 3 | a0002c0006t0002g0249 a0002c0006t0002g0251 a0007c0014t0002g0250 |
3 | HG02622.hp2 HG02976.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.196-15854T>C | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 2/38 | chr6 | 112232323 | |||||||
chr6:112232669 | G | A | 3 | a0002c0006t0002g0249 a0002c0006t0002g0251 a0007c0014t0002g0250 |
3 | HG02622.hp2 HG02976.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.196-16200C>T | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 2/38 | chr6 | 112232669 | |||||||
chr6:112232835 | A | G | 28 | a0001c0002t0001g0076 a0001c0002t0001g0197 a0001c0011t0003g0009 others(25): Show |
28 | HG01081.hp2 HG01243.hp1 HG01981.hp2 others(25): Show |
intron_variant | MODIFIER | c.196-16366T>C | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 2/38 | chr6 | 112232835 | |||||||
chr6:112232860 | C | T | 1 | a0001c0005t0001g0043 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.196-16391G>A | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 2/38 | chr6 | 112232860 | |||||||
chr6:112232906 | C | T | 1 | a0001c0001t0001g0027 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.196-16437G>A | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 2/38 | chr6 | 112232906 | |||||||
chr6:112233117 | G | A | 4 | a0001c0002t0001g0020 a0001c0002t0001g0045 a0001c0002t0001g0047 others(1): Show |
4 | HG01891.hp2 HG02055.hp2 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.196-16648C>T | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 2/38 | chr6 | 112233117 | |||||||
chr6:112233138 | G | A | 1 | a0003c0058t0001g0210 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.196-16669C>T | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 2/38 | chr6 | 112233138 | |||||||
chr6:112233174 | G | C | 1 | a0003c0043t0001g0036 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.196-16705C>G | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 2/38 | chr6 | 112233174 | |||||||
chr6:112233393 | C | G | 1 | a0003c0004t0001g0114 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.196-16924G>C | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 2/38 | chr6 | 112233393 | |||||||
chr6:112233584 | G | A | 1 | a0007c0014t0002g0292 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.196-17115C>T | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 2/38 | chr6 | 112233584 | |||||||
chr6:112233753 | T | C | 13 | a0001c0002t0001g0076 a0001c0002t0001g0197 a0001c0023t0003g0302 others(10): Show |
13 | HG01081.hp2 HG01981.hp2 HG02486.hp2 others(10): Show |
intron_variant | MODIFIER | c.196-17284A>G | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 2/38 | chr6 | 112233753 | |||||||
chr6:112233939 | G | A | 1 | a0003c0058t0001g0210 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.196-17470C>T | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 2/38 | chr6 | 112233939 | |||||||
chr6:112234156 | A | AT | 15 | a0001c0001t0001g0246 a0001c0002t0001g0020 a0001c0002t0001g0045 others(12): Show |
15 | HG01891.hp2 HG02055.hp1 HG02055.hp2 others(12): Show |
intron_variant | MODIFIER | c.196-17688dupA | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 2/38 | chr6 | 112234156 | |||||||
chr6:112234261 | C | T | 1 | a0002c0003t0002g0305 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.196-17792G>A | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 2/38 | chr6 | 112234261 | |||||||
chr6:112234367 | G | A | 1 | a0001c0001t0001g0074 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.196-17898C>T | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 2/38 | chr6 | 112234367 | |||||||
chr6:112234370 | A | G | 1 | a0004c0007t0001g0211 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.196-17901T>C | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 2/38 | chr6 | 112234370 | |||||||
chr6:112234396 | C | G | 2 | a0001c0001t0001g0220 a0002c0003t0002g0221 |
2 | HG01256.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.196-17927G>C | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 2/38 | chr6 | 112234396 | |||||||
chr6:112234618 | G | C | 47 | a0001c0001t0001g0042 a0001c0001t0001g0069 a0001c0001t0001g0186 others(44): Show |
47 | HG00673.hp1 HG01081.hp2 HG01167.hp1 others(44): Show |
intron_variant | MODIFIER | c.196-18149C>G | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 2/38 | chr6 | 112234618 | |||||||
chr6:112234749 | T | A | 1 | a0006c0012t0002g0218 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.196-18280A>T | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 2/38 | chr6 | 112234749 | |||||||
chr6:112234884 | G | T | 1 | a0003c0058t0001g0210 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.196-18415C>A | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 2/38 | chr6 | 112234884 | |||||||
chr6:112234941 | C | T | 1 | a0001c0023t0003g0302 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.196-18472G>A | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 2/38 | chr6 | 112234941 | |||||||
chr6:112235017 | C | A | 1 | a0001c0001t0001g0015 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.196-18548G>T | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 2/38 | chr6 | 112235017 | |||||||
chr6:112235054 | G | A | 2 | a0001c0011t0003g0009 a0001c0050t0001g0310 |
2 | HG02055.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.196-18585C>T | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 2/38 | chr6 | 112235054 | |||||||
chr6:112235064 | C | T | 1 | a0002c0003t0002g0304 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.196-18595G>A | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 2/38 | chr6 | 112235064 | |||||||
chr6:112235290 | T | C | 1 | a0006c0012t0002g0195 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.195+18666A>G | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 2/38 | chr6 | 112235290 | |||||||
chr6:112235326 | T | A | 1 | a0005c0008t0001g0174 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.195+18630A>T | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 2/38 | chr6 | 112235326 | |||||||
chr6:112235431 | G | A | 29 | a0001c0001t0001g0014 a0001c0001t0001g0220 a0001c0001t0001g0222 others(26): Show |
29 | HG00621.hp2 HG01071.hp1 HG01106.hp2 others(26): Show |
intron_variant | MODIFIER | c.195+18525C>T | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 2/38 | chr6 | 112235431 | |||||||
chr6:112235465 | G | A | 51 | a0001c0001t0001g0070 a0001c0001t0001g0072 a0001c0001t0001g0074 others(48): Show |
51 | HG00408.hp2 HG00621.hp1 HG01168.hp2 others(48): Show |
intron_variant | MODIFIER | c.195+18491C>T | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 2/38 | chr6 | 112235465 | |||||||
chr6:112235752 | G | A | 7 | a0001c0002t0001g0076 a0001c0002t0001g0197 a0001c0023t0003g0302 others(4): Show |
7 | HG01081.hp2 HG01981.hp2 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.195+18204C>T | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 2/38 | chr6 | 112235752 | |||||||
chr6:112235823 | G | A | 2 | a0003c0025t0001g0086 a0003c0025t0001g0113 |
2 | HG02886.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.195+18133C>T | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 2/38 | chr6 | 112235823 | |||||||
chr6:112235888 | G | C | 25 | a0001c0001t0001g0016 a0001c0001t0001g0027 a0001c0001t0001g0033 others(22): Show |
25 | HG00323.hp1 HG00642.hp2 HG00733.hp1 others(22): Show |
intron_variant | MODIFIER | c.195+18068C>G | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 2/38 | chr6 | 112235888 | |||||||
chr6:112236052 | T | G | 6 | a0001c0002t0001g0076 a0001c0002t0001g0197 a0002c0006t0002g0199 others(3): Show |
6 | HG01081.hp2 HG01981.hp2 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.195+17904A>C | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 2/38 | chr6 | 112236052 | |||||||
chr6:112236091 | G | T | 4 | a0001c0002t0001g0309 a0002c0003t0002g0304 a0002c0003t0002g0305 others(1): Show |
4 | HG03654.hp1 HG03942.hp2 HG04199.hp2 others(1): Show |
intron_variant | MODIFIER | c.195+17865C>A | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 2/38 | chr6 | 112236091 | |||||||
chr6:112236117 | G | C | 2 | a0001c0011t0003g0009 a0001c0050t0001g0310 |
2 | HG02055.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.195+17839C>G | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 2/38 | chr6 | 112236117 | |||||||
chr6:112236174 | A | G | 1 | a0001c0023t0003g0302 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.195+17782T>C | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 2/38 | chr6 | 112236174 | |||||||
chr6:112236294 | A | G | 1 | a0002c0003t0002g0206 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.195+17662T>C | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 2/38 | chr6 | 112236294 | |||||||
chr6:112236295 | G | A | 4 | a0001c0002t0001g0020 a0001c0002t0001g0045 a0001c0002t0001g0047 others(1): Show |
4 | HG01891.hp2 HG02055.hp2 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.195+17661C>T | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 2/38 | chr6 | 112236295 | |||||||
chr6:112236368 | G | A | 98 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0015 others(95): Show |
98 | HG00099.hp1 HG00280.hp2 HG00597.hp1 others(95): Show |
intron_variant | MODIFIER | c.195+17588C>T | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 2/38 | chr6 | 112236368 | |||||||
chr6:112236370 | A | C | 7 | a0001c0002t0001g0076 a0001c0002t0001g0197 a0002c0006t0002g0199 others(4): Show |
7 | HG01081.hp2 HG01981.hp2 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.195+17586T>G | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 2/38 | chr6 | 112236370 | |||||||
chr6:112236416 | A | G | 2 | a0001c0002t0001g0253 a0001c0011t0003g0293 |
2 | HG02109.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.195+17540T>C | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 2/38 | chr6 | 112236416 | |||||||
chr6:112236539 | T | C | 102 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0015 others(99): Show |
102 | HG00099.hp1 HG00280.hp2 HG00597.hp1 others(99): Show |
intron_variant | MODIFIER | c.195+17417A>G | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 2/38 | chr6 | 112236539 | |||||||
chr6:112236642 | T | C | 51 | a0001c0001t0001g0070 a0001c0001t0001g0072 a0001c0001t0001g0074 others(48): Show |
51 | HG00408.hp2 HG00621.hp1 HG01168.hp2 others(48): Show |
intron_variant | MODIFIER | c.195+17314A>G | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 2/38 | chr6 | 112236642 | |||||||
chr6:112236863 | A | G | 1 | a0002c0003t0002g0206 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.195+17093T>C | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 2/38 | chr6 | 112236863 | |||||||
chr6:112237150 | A | G | 1 | a0003c0058t0001g0210 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.195+16806T>C | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 2/38 | chr6 | 112237150 | |||||||
chr6:112237181 | C | G | 1 | a0003c0004t0001g0238 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.195+16775G>C | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 2/38 | chr6 | 112237181 | |||||||
chr6:112237204 | A | G | 2 | a0003c0025t0001g0086 a0003c0025t0001g0113 |
2 | HG02886.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.195+16752T>C | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 2/38 | chr6 | 112237204 | |||||||
chr6:112237282 | A | G | 6 | a0001c0002t0001g0076 a0001c0002t0001g0197 a0002c0006t0002g0199 others(3): Show |
6 | HG01081.hp2 HG01981.hp2 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.195+16674T>C | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 2/38 | chr6 | 112237282 | |||||||
chr6:112237297 | A | C | 47 | a0001c0001t0001g0042 a0001c0001t0001g0069 a0001c0001t0001g0186 others(44): Show |
47 | HG00673.hp1 HG01081.hp2 HG01167.hp1 others(44): Show |
intron_variant | MODIFIER | c.195+16659T>G | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 2/38 | chr6 | 112237297 | |||||||
chr6:112237395 | T | C | 4 | a0001c0023t0003g0306 a0001c0037t0003g0003 a0009c0017t0002g0307 others(1): Show |
4 | HG02886.hp2 HG02970.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.195+16561A>G | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 2/38 | chr6 | 112237395 | |||||||
chr6:112237562 | C | T | 98 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0015 others(95): Show |
98 | HG00099.hp1 HG00280.hp2 HG00597.hp1 others(95): Show |
intron_variant | MODIFIER | c.195+16394G>A | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 2/38 | chr6 | 112237562 | |||||||
chr6:112237588 | C | T | 1 | a0003c0004t0001g0180 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.195+16368G>A | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 2/38 | chr6 | 112237588 | |||||||
chr6:112237746 | T | C | 1 | a0001c0001t0001g0237 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.195+16210A>G | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 2/38 | chr6 | 112237746 | |||||||
chr6:112237912 | A | G | 4 | a0001c0002t0001g0309 a0002c0003t0002g0304 a0002c0003t0002g0305 others(1): Show |
4 | HG03654.hp1 HG03942.hp2 HG04199.hp2 others(1): Show |
intron_variant | MODIFIER | c.195+16044T>C | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 2/38 | chr6 | 112237912 | |||||||
chr6:112238036 | G | T | 2 | a0005c0008t0001g0026 a0010c0029t0001g0025 |
2 | HG00642.hp2 HG01081.hp1 |
intron_variant | MODIFIER | c.195+15920C>A | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 2/38 | chr6 | 112238036 | |||||||
chr6:112238321 | T | G | 1 | a0002c0006t0002g0170 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.195+15635A>C | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 2/38 | chr6 | 112238321 | |||||||
chr6:112238432 | A | G | 47 | a0001c0001t0001g0042 a0001c0001t0001g0069 a0001c0001t0001g0186 others(44): Show |
47 | HG00673.hp1 HG01081.hp2 HG01167.hp1 others(44): Show |
intron_variant | MODIFIER | c.195+15524T>C | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 2/38 | chr6 | 112238432 | |||||||
chr6:112238545 | C | A | 285 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0014 others(282): Show |
285 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(282): Show |
intron_variant | MODIFIER | c.195+15411G>T | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 2/38 | chr6 | 112238545 | |||||||
chr6:112238552 | A | T | 1 | a0001c0016t0010g0209 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.195+15404T>A | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 2/38 | chr6 | 112238552 | |||||||
chr6:112238564 | G | C | 1 | a0003c0058t0001g0210 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.195+15392C>G | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 2/38 | chr6 | 112238564 | |||||||
chr6:112238595 | T | C | 34 | a0001c0001t0001g0042 a0001c0001t0001g0069 a0001c0001t0001g0186 others(31): Show |
34 | HG00673.hp1 HG01167.hp1 HG01169.hp1 others(31): Show |
intron_variant | MODIFIER | c.195+15361A>G | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 2/38 | chr6 | 112238595 | |||||||
chr6:112238719 | TAAAC | T | 4 | a0001c0002t0001g0020 a0001c0002t0001g0045 a0001c0002t0001g0047 others(1): Show |
4 | HG01891.hp2 HG02055.hp2 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.195+15233_195+1523 others(8): Show |
LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 2/38 | chr6 | 112238719 | |||||||
chr6:112238841 | C | G | 4 | a0001c0002t0001g0253 a0001c0002t0001g0254 a0001c0011t0003g0255 others(1): Show |
4 | HG00741.hp1 HG02109.hp2 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.195+15115G>C | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 2/38 | chr6 | 112238841 | |||||||
chr6:112239014 | A | G | 1 | a0007c0060t0002g0260 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.195+14942T>C | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 2/38 | chr6 | 112239014 | |||||||
chr6:112239081 | G | A | 5 | a0002c0003t0001g0171 a0002c0003t0006g0001 a0002c0003t0006g0002 others(2): Show |
5 | HG01071.hp1 HG02717.hp2 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.195+14875C>T | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 2/38 | chr6 | 112239081 | |||||||
chr6:112239087 | G | A | 34 | a0001c0001t0001g0042 a0001c0001t0001g0069 a0001c0001t0001g0186 others(31): Show |
34 | HG00673.hp1 HG01167.hp1 HG01169.hp1 others(31): Show |
intron_variant | MODIFIER | c.195+14869C>T | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 2/38 | chr6 | 112239087 | |||||||
chr6:112239321 | C | CA | 58 | a0001c0001t0001g0042 a0001c0001t0001g0069 a0001c0001t0001g0186 others(55): Show |
58 | HG00673.hp1 HG00733.hp1 HG01081.hp2 others(55): Show |
intron_variant | MODIFIER | c.195+14634dupT | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 2/38 | chr6 | 112239321 | |||||||
chr6:112239321 | C | CAA | 33 | a0001c0001t0001g0016 a0001c0001t0001g0027 a0001c0001t0001g0033 others(30): Show |
33 | HG00323.hp1 HG00642.hp2 HG01074.hp1 others(30): Show |
intron_variant | MODIFIER | c.195+14633_195+1463 others(6): Show |
LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 2/38 | chr6 | 112239321 | |||||||
chr6:112239321 | CA | C | 18 | a0001c0001t0001g0050 a0001c0001t0001g0051 a0001c0001t0001g0052 others(15): Show |
18 | HG00621.hp1 HG01074.hp2 HG01243.hp2 others(15): Show |
intron_variant | MODIFIER | c.195+14634delT | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 2/38 | chr6 | 112239321 | |||||||
chr6:112239460 | A | G | 6 | a0001c0002t0001g0076 a0001c0002t0001g0197 a0002c0006t0002g0199 others(3): Show |
6 | HG01081.hp2 HG01981.hp2 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.195+14496T>C | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 2/38 | chr6 | 112239460 | |||||||
chr6:112239797 | C | T | 1 | a0001c0001t0001g0237 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.195+14159G>A | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 2/38 | chr6 | 112239797 | |||||||
chr6:112239879 | C | T | 2 | a0001c0011t0003g0009 a0001c0050t0001g0310 |
2 | HG02055.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.195+14077G>A | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 2/38 | chr6 | 112239879 | |||||||
chr6:112239899 | T | C | 46 | a0001c0001t0001g0042 a0001c0001t0001g0069 a0001c0001t0001g0070 others(43): Show |
46 | HG00673.hp1 HG01167.hp1 HG01169.hp1 others(43): Show |
intron_variant | MODIFIER | c.195+14057A>G | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 2/38 | chr6 | 112239899 | |||||||
chr6:112239911 | A | C | 12 | a0001c0002t0001g0076 a0001c0002t0001g0197 a0002c0006t0002g0199 others(9): Show |
12 | HG01081.hp2 HG01981.hp2 HG02486.hp2 others(9): Show |
intron_variant | MODIFIER | c.195+14045T>G | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 2/38 | chr6 | 112239911 | |||||||
chr6:112239953 | G | A | 25 | a0001c0001t0001g0016 a0001c0001t0001g0027 a0001c0001t0001g0033 others(22): Show |
25 | HG00323.hp1 HG00642.hp2 HG00733.hp1 others(22): Show |
intron_variant | MODIFIER | c.195+14003C>T | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 2/38 | chr6 | 112239953 | |||||||
chr6:112240139 | C | T | 1 | a0003c0013t0001g0023 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.195+13817G>A | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 2/38 | chr6 | 112240139 | |||||||
chr6:112240170 | C | T | 25 | a0001c0001t0001g0016 a0001c0001t0001g0027 a0001c0001t0001g0033 others(22): Show |
25 | HG00323.hp1 HG00642.hp2 HG00733.hp1 others(22): Show |
intron_variant | MODIFIER | c.195+13786G>A | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 2/38 | chr6 | 112240170 | |||||||
chr6:112240171 | G | A | 12 | a0001c0011t0003g0062 a0001c0011t0003g0155 a0001c0011t0003g0158 others(9): Show |
12 | HG01243.hp1 HG02109.hp1 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.195+13785C>T | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 2/38 | chr6 | 112240171 | |||||||
chr6:112240229 | T | G | 45 | a0001c0001t0001g0256 a0001c0001t0001g0257 a0001c0001t0001g0281 others(42): Show |
45 | HG00408.hp2 HG00621.hp1 HG01168.hp2 others(42): Show |
intron_variant | MODIFIER | c.195+13727A>C | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 2/38 | chr6 | 112240229 | |||||||
chr6:112240264 | T | A | 1 | a0001c0052t0002g0295 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.195+13692A>T | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 2/38 | chr6 | 112240264 | |||||||
chr6:112240289 | G | T | 1 | a0003c0059t0001g0259 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.195+13667C>A | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 2/38 | chr6 | 112240289 | |||||||
chr6:112240293 | A | T | 1 | a0001c0002t0001g0258 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.195+13663T>A | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 2/38 | chr6 | 112240293 | |||||||
chr6:112240450 | G | C | 1 | a0005c0008t0001g0248 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.195+13506C>G | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 2/38 | chr6 | 112240450 | |||||||
chr6:112240563 | G | A | 1 | a0004c0010t0001g0284 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.195+13393C>T | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 2/38 | chr6 | 112240563 | |||||||
chr6:112240686 | A | G | 1 | a0003c0004t0001g0114 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.195+13270T>C | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 2/38 | chr6 | 112240686 | |||||||
chr6:112240737 | T | C | 30 | a0001c0001t0001g0014 a0001c0001t0001g0219 a0001c0001t0001g0220 others(27): Show |
30 | HG00621.hp2 HG01071.hp1 HG01106.hp2 others(27): Show |
intron_variant | MODIFIER | c.195+13219A>G | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 2/38 | chr6 | 112240737 | |||||||
chr6:112240782 | A | T | 3 | a0001c0023t0003g0306 a0001c0037t0003g0003 a0009c0017t0002g0307 |
3 | HG02886.hp2 HG03195.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.195+13174T>A | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 2/38 | chr6 | 112240782 | |||||||
chr6:112240811 | C | T | 1 | a0002c0006t0002g0303 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.195+13145G>A | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 2/38 | chr6 | 112240811 | |||||||
chr6:112241075 | C | T | 47 | a0001c0001t0001g0042 a0001c0001t0001g0069 a0001c0001t0001g0070 others(44): Show |
47 | HG00673.hp1 HG01081.hp2 HG01167.hp1 others(44): Show |
intron_variant | MODIFIER | c.195+12881G>A | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 2/38 | chr6 | 112241075 | |||||||
chr6:112241098 | A | AAT | 4 | a0001c0001t0001g0257 a0003c0025t0001g0086 a0003c0025t0001g0113 others(1): Show |
4 | HG02886.hp1 HG03486.hp2 NA18975.hp1 others(1): Show |
intron_variant | MODIFIER | c.195+12856_195+1285 others(6): Show |
LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 2/38 | chr6 | 112241098 | |||||||
chr6:112241098 | AAT | A | 25 | a0001c0001t0001g0016 a0001c0001t0001g0027 a0001c0001t0001g0033 others(22): Show |
25 | HG00323.hp1 HG00642.hp2 HG00733.hp1 others(22): Show |
intron_variant | MODIFIER | c.195+12856_195+1285 others(6): Show |
LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 2/38 | chr6 | 112241098 | |||||||
chr6:112241104 | T | TATATATA others(27): Show |
3 | a0001c0037t0003g0003 a0009c0017t0002g0307 a0009c0017t0002g0308 |
3 | HG02970.hp1 HG03195.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.195+12818_195+1285 others(38): Show |
LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 2/38 | chr6 | 112241104 | |||||||
chr6:112241136 | G | T | 84 | a0001c0001t0001g0016 a0001c0001t0001g0027 a0001c0001t0001g0033 others(81): Show |
84 | HG00323.hp1 HG00642.hp2 HG00673.hp1 others(81): Show |
intron_variant | MODIFIER | c.195+12820C>A | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 2/38 | chr6 | 112241136 | |||||||
chr6:112241136 | GGAATATA others(5): Show |
G | 1 | a0001c0002t0001g0289 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.195+12808_195+1281 others(16): Show |
LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 2/38 | chr6 | 112241136 | |||||||
chr6:112241140 | T | TATATATA others(3): Show |
40 | a0001c0001t0001g0042 a0001c0001t0001g0070 a0001c0001t0001g0072 others(37): Show |
40 | HG00673.hp1 HG00741.hp1 HG01167.hp1 others(37): Show |
intron_variant | MODIFIER | c.195+12806_195+1281 others(14): Show |
LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 2/38 | chr6 | 112241140 | |||||||
chr6:112241140 | T | TATATATA others(15): Show |
1 | a0001c0011t0003g0236 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.195+12794_195+1281 others(26): Show |
LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 2/38 | chr6 | 112241140 | |||||||
chr6:112241140 | T | TATATATA others(25): Show |
3 | a0001c0001t0001g0246 a0001c0005t0001g0247 a0005c0008t0001g0248 |
3 | NA18948.hp2 NA19062.hp1 NA19064.hp1 |
intron_variant | MODIFIER | c.195+12784_195+1281 others(36): Show |
LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 2/38 | chr6 | 112241140 | |||||||
chr6:112241140 | T | TATATATA others(35): Show |
62 | a0001c0001t0001g0008 a0001c0001t0001g0015 a0001c0001t0001g0050 others(59): Show |
62 | HG00099.hp1 HG00280.hp2 HG00639.hp2 others(59): Show |
intron_variant | MODIFIER | c.195+12815_195+1281 others(46): Show |
LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 2/38 | chr6 | 112241140 | |||||||
chr6:112241140 | T | TATATATA others(67): Show |
1 | a0001c0009t0001g0112 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.195+12815_195+1281 others(78): Show |
LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 2/38 | chr6 | 112241140 | |||||||
chr6:112241140 | T | TATATATA others(25): Show |
3 | a0001c0002t0001g0197 a0001c0023t0003g0302 a0002c0003t0002g0198 |
3 | HG03017.hp2 HG03195.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.195+12815_195+1281 others(36): Show |
LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 2/38 | chr6 | 112241140 | |||||||
chr6:112241140 | T | TATATATA others(47): Show |
7 | a0001c0002t0001g0076 a0002c0006t0002g0199 a0004c0007t0001g0201 others(4): Show |
7 | HG01081.hp2 HG01981.hp2 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.195+12815_195+1281 others(58): Show |
LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 2/38 | chr6 | 112241140 | |||||||
chr6:112241140 | T | TATATATA others(69): Show |
4 | a0001c0050t0001g0310 a0008c0015t0001g0059 a0008c0015t0001g0061 others(1): Show |
4 | HG02486.hp2 HG03139.hp2 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.195+12815_195+1281 others(80): Show |
LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 2/38 | chr6 | 112241140 | |||||||
chr6:112241140 | T | TATATATA others(81): Show |
1 | a0009c0053t0002g0178 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.195+12815_195+1281 others(92): Show |
LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 2/38 | chr6 | 112241140 | |||||||
chr6:112241140 | T | TATATATA others(79): Show |
1 | a0003c0018t0002g0038 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.195+12815_195+1281 others(90): Show |
LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 2/38 | chr6 | 112241140 | |||||||
chr6:112241140 | T | TATATATA others(79): Show |
2 | a0002c0006t0002g0037 a0004c0057t0003g0017 |
2 | HG06807.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.195+12815_195+1281 others(90): Show |
LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 2/38 | chr6 | 112241140 | |||||||
chr6:112241140 | TATATATA others(15): Show |
T | 1 | a0003c0013t0001g0217 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.195+12794_195+1281 others(26): Show |
LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 2/38 | chr6 | 112241140 | |||||||
chr6:112241140 | TATATATA others(25): Show |
T | 1 | a0004c0010t0012g0177 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.195+12784_195+1281 others(36): Show |
LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 2/38 | chr6 | 112241140 | |||||||
chr6:112241148 | T | TGAATATA others(25): Show |
1 | a0001c0001t0001g0007 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.195+12807_195+1280 others(36): Show |
LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 2/38 | chr6 | 112241148 | |||||||
chr6:112241150 | AAT | A | 4 | a0001c0001t0001g0069 a0001c0001t0001g0202 a0001c0001t0001g0204 others(1): Show |
4 | HG02040.hp1 HG02132.hp2 HG02155.hp1 others(1): Show |
intron_variant | MODIFIER | c.195+12804_195+1280 others(6): Show |
LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 2/38 | chr6 | 112241150 | |||||||
chr6:112241152 | T | TATATATA others(3): Show |
1 | a0003c0004t0001g0242 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.195+12794_195+1280 others(14): Show |
LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 2/38 | chr6 | 112241152 | |||||||
chr6:112241152 | T | TATATATA others(65): Show |
1 | a0012c0021t0001g0083 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.195+12803_195+1280 others(76): Show |
LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 2/38 | chr6 | 112241152 | |||||||
chr6:112241152 | T | TATATATG others(79): Show |
1 | a0005c0008t0001g0031 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.195+12803_195+1280 others(90): Show |
LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 2/38 | chr6 | 112241152 | |||||||
chr6:112241152 | T | TATATATG others(25): Show |
5 | a0001c0001t0001g0033 a0005c0008t0001g0026 a0005c0008t0004g0040 others(2): Show |
5 | HG00642.hp2 HG01081.hp1 HG01175.hp2 others(2): Show |
intron_variant | MODIFIER | c.195+12803_195+1280 others(36): Show |
LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 2/38 | chr6 | 112241152 | |||||||
chr6:112241152 | T | TATATATG others(79): Show |
2 | a0003c0043t0001g0036 a0007c0014t0002g0041 |
2 | HG01074.hp1 HG01261.hp2 |
intron_variant | MODIFIER | c.195+12803_195+1280 others(90): Show |
LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 2/38 | chr6 | 112241152 | |||||||
chr6:112241152 | T | TATATATG others(79): Show |
13 | a0001c0001t0001g0016 a0001c0001t0001g0027 a0003c0004t0001g0018 others(10): Show |
13 | HG00323.hp1 HG00733.hp1 HG01106.hp1 others(10): Show |
intron_variant | MODIFIER | c.195+12803_195+1280 others(90): Show |
LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 2/38 | chr6 | 112241152 | |||||||
chr6:112241152 | T | TATATATG others(123): Show |
1 | a0003c0004t0001g0022 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.195+12803_195+1280 others(134): Show |
LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 2/38 | chr6 | 112241152 | |||||||
chr6:112241152 | TATATATA others(3): Show |
T | 29 | a0001c0001t0001g0014 a0001c0001t0001g0219 a0001c0001t0001g0220 others(26): Show |
29 | HG00621.hp2 HG01071.hp1 HG01106.hp2 others(26): Show |
intron_variant | MODIFIER | c.195+12794_195+1280 others(14): Show |
LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 2/38 | chr6 | 112241152 | |||||||
chr6:112241152 | TATATATA others(13): Show |
T | 2 | a0001c0011t0003g0161 a0001c0011t0003g0298 |
2 | HG02257.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.195+12784_195+1280 others(24): Show |
LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 2/38 | chr6 | 112241152 | |||||||
chr6:112241162 | A | AATATATA others(17): Show |
1 | a0001c0023t0003g0306 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.195+12793_195+1279 others(28): Show |
LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 2/38 | chr6 | 112241162 | |||||||
chr6:112241162 | A | AATATATA others(25): Show |
1 | a0003c0025t0001g0086 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.195+12793_195+1279 others(36): Show |
LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 2/38 | chr6 | 112241162 | |||||||
chr6:112241164 | TATATATG others(1): Show |
T | 4 | a0001c0001t0001g0069 a0001c0001t0001g0202 a0001c0001t0001g0204 others(1): Show |
4 | HG02040.hp1 HG02132.hp2 HG02155.hp1 others(1): Show |
intron_variant | MODIFIER | c.195+12784_195+1279 others(12): Show |
LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 2/38 | chr6 | 112241164 | |||||||
chr6:112241170 | T | TGAATATA others(35): Show |
33 | a0001c0001t0001g0090 a0001c0001t0001g0095 a0001c0001t0001g0167 others(30): Show |
33 | HG00639.hp1 HG00642.hp1 HG00673.hp2 others(30): Show |
intron_variant | MODIFIER | c.195+12785_195+1278 others(46): Show |
LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 2/38 | chr6 | 112241170 | |||||||
chr6:112241172 | A | AAT | 79 | a0001c0001t0001g0016 a0001c0001t0001g0027 a0001c0001t0001g0033 others(76): Show |
79 | HG00323.hp1 HG00642.hp2 HG00673.hp1 others(76): Show |
intron_variant | MODIFIER | c.195+12782_195+1278 others(6): Show |
LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 2/38 | chr6 | 112241172 | |||||||
chr6:112241172 | A | AATATATA others(99): Show |
1 | a0001c0011t0003g0009 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.195+12783_195+1278 others(110): Show |
LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 2/38 | chr6 | 112241172 | |||||||
chr6:112241181 | G | T | 1 | a0003c0004t0001g0022 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.195+12775C>A | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 2/38 | chr6 | 112241181 | |||||||
chr6:112241182 | A | C | 1 | a0003c0004t0001g0022 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.195+12774T>G | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 2/38 | chr6 | 112241182 | |||||||
chr6:112241312 | G | A | 1 | a0018c0030t0001g0004 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.195+12644C>T | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 2/38 | chr6 | 112241312 | |||||||
chr6:112241600 | T | A | 25 | a0001c0001t0001g0016 a0001c0001t0001g0027 a0001c0001t0001g0033 others(22): Show |
25 | HG00323.hp1 HG00642.hp2 HG00733.hp1 others(22): Show |
intron_variant | MODIFIER | c.195+12356A>T | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 2/38 | chr6 | 112241600 | |||||||
chr6:112241752 | G | A | 1 | a0001c0011t0003g0255 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.195+12204C>T | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 2/38 | chr6 | 112241752 | |||||||
chr6:112241871 | T | C | 4 | a0001c0023t0003g0306 a0001c0037t0003g0003 a0009c0017t0002g0307 others(1): Show |
4 | HG02886.hp2 HG02970.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.195+12085A>G | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 2/38 | chr6 | 112241871 | |||||||
chr6:112241893 | C | G | 1 | a0001c0002t0001g0289 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.195+12063G>C | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 2/38 | chr6 | 112241893 | |||||||
chr6:112242169 | C | A | 1 | a0001c0001t0001g0285 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.195+11787G>T | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 2/38 | chr6 | 112242169 | |||||||
chr6:112242171 | T | C | 1 | a0001c0011t0003g0009 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.195+11785A>G | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 2/38 | chr6 | 112242171 | |||||||
chr6:112242259 | A | G | 1 | a0001c0001t0001g0149 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.195+11697T>C | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 2/38 | chr6 | 112242259 | |||||||
chr6:112242370 | C | T | 1 | a0001c0001t0001g0149 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.195+11586G>A | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 2/38 | chr6 | 112242370 | |||||||
chr6:112242832 | G | A | 1 | a0001c0001t0001g0014 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.195+11124C>T | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 2/38 | chr6 | 112242832 | |||||||
chr6:112243101 | T | C | 3 | a0001c0001t0001g0149 a0001c0016t0001g0151 a0006c0012t0002g0150 |
3 | HG02027.hp1 HG02165.hp1 NA18973.hp1 |
intron_variant | MODIFIER | c.195+10855A>G | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 2/38 | chr6 | 112243101 | |||||||
chr6:112243135 | T | C | 1 | a0003c0058t0001g0210 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.195+10821A>G | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 2/38 | chr6 | 112243135 | |||||||
chr6:112243188 | C | A | 1 | a0001c0011t0003g0009 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.195+10768G>T | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 2/38 | chr6 | 112243188 | |||||||
chr6:112243315 | T | C | 231 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0014 others(228): Show |
231 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(228): Show |
intron_variant | MODIFIER | c.195+10641A>G | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 2/38 | chr6 | 112243315 | |||||||
chr6:112243411 | G | T | 1 | a0001c0001t0001g0256 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.195+10545C>A | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 2/38 | chr6 | 112243411 | |||||||
chr6:112243426 | T | G | 1 | a0003c0058t0001g0210 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.195+10530A>C | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 2/38 | chr6 | 112243426 | |||||||
chr6:112243579 | G | A | 1 | a0004c0026t0001g0068 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.195+10377C>T | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 2/38 | chr6 | 112243579 | |||||||
chr6:112243793 | C | T | 4 | a0001c0005t0001g0286 a0001c0009t0001g0287 a0001c0009t0001g0288 others(1): Show |
4 | NA18998.hp2 NA19000.hp2 NA19002.hp1 others(1): Show |
intron_variant | MODIFIER | c.195+10163G>A | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 2/38 | chr6 | 112243793 | |||||||
chr6:112243801 | C | T | 244 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0014 others(241): Show |
244 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(241): Show |
intron_variant | MODIFIER | c.195+10155G>A | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 2/38 | chr6 | 112243801 | |||||||
chr6:112243823 | C | A | 2 | a0004c0010t0001g0080 a0004c0010t0001g0152 |
2 | NA18971.hp2 NA19062.hp2 |
intron_variant | MODIFIER | c.195+10133G>T | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 2/38 | chr6 | 112243823 | |||||||
chr6:112243882 | A | G | 31 | a0001c0001t0001g0016 a0001c0001t0001g0027 a0001c0001t0001g0033 others(28): Show |
31 | HG00323.hp1 HG00642.hp2 HG00733.hp1 others(28): Show |
intron_variant | MODIFIER | c.195+10074T>C | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 2/38 | chr6 | 112243882 | |||||||
chr6:112243927 | G | A | 4 | a0001c0002t0001g0309 a0002c0003t0002g0304 a0002c0003t0002g0305 others(1): Show |
4 | HG03654.hp1 HG03942.hp2 HG04199.hp2 others(1): Show |
intron_variant | MODIFIER | c.195+10029C>T | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 2/38 | chr6 | 112243927 | |||||||
chr6:112244045 | T | G | 1 | a0001c0011t0003g0009 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.195+9911A>C | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 2/38 | chr6 | 112244045 | |||||||
chr6:112244212 | C | T | 1 | a0001c0011t0003g0009 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.195+9744G>A | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 2/38 | chr6 | 112244212 | |||||||
chr6:112244309 | G | A | 1 | a0001c0009t0001g0049 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.195+9647C>T | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 2/38 | chr6 | 112244309 | |||||||
chr6:112244324 | T | C | 4 | a0001c0005t0001g0286 a0001c0009t0001g0287 a0001c0009t0001g0288 others(1): Show |
4 | NA18998.hp2 NA19000.hp2 NA19002.hp1 others(1): Show |
intron_variant | MODIFIER | c.195+9632A>G | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 2/38 | chr6 | 112244324 | |||||||
chr6:112244436 | G | C | 32 | a0001c0001t0001g0016 a0001c0001t0001g0027 a0001c0001t0001g0033 others(29): Show |
32 | HG00323.hp1 HG00642.hp2 HG00733.hp1 others(29): Show |
intron_variant | MODIFIER | c.195+9520C>G | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 2/38 | chr6 | 112244436 | |||||||
chr6:112244823 | A | G | 1 | a0001c0011t0003g0009 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.195+9133T>C | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 2/38 | chr6 | 112244823 | |||||||
chr6:112245045 | C | T | 1 | a0003c0058t0001g0210 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.195+8911G>A | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 2/38 | chr6 | 112245045 | |||||||
chr6:112245295 | T | C | 1 | a0001c0011t0003g0009 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.195+8661A>G | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 2/38 | chr6 | 112245295 | |||||||
chr6:112245326 | A | T | 1 | a0004c0010t0001g0080 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.195+8630T>A | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 2/38 | chr6 | 112245326 | |||||||
chr6:112245562 | A | C | 2 | a0004c0026t0001g0067 a0004c0026t0001g0068 |
2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.195+8394T>G | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 2/38 | chr6 | 112245562 | |||||||
chr6:112245669 | C | CA | 290 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0014 others(287): Show |
290 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(287): Show |
intron_variant | MODIFIER | c.195+8286dupT | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 2/38 | chr6 | 112245669 | |||||||
chr6:112245904 | G | A | 1 | a0001c0002t0001g0289 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.195+8052C>T | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 2/38 | chr6 | 112245904 | |||||||
chr6:112246006 | G | C | 51 | a0001c0001t0001g0042 a0001c0001t0001g0069 a0001c0001t0001g0070 others(48): Show |
51 | HG00673.hp1 HG00741.hp1 HG01081.hp2 others(48): Show |
intron_variant | MODIFIER | c.195+7950C>G | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 2/38 | chr6 | 112246006 | |||||||
chr6:112246010 | C | G | 98 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0015 others(95): Show |
98 | HG00099.hp1 HG00280.hp2 HG00597.hp1 others(95): Show |
intron_variant | MODIFIER | c.195+7946G>C | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 2/38 | chr6 | 112246010 | |||||||
chr6:112246036 | C | T | 1 | a0008c0031t0001g0056 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.195+7920G>A | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 2/38 | chr6 | 112246036 | |||||||
chr6:112246317 | A | G | 68 | a0001c0001t0001g0042 a0001c0001t0001g0069 a0001c0001t0001g0070 others(65): Show |
68 | HG00673.hp1 HG00741.hp1 HG01081.hp2 others(65): Show |
intron_variant | MODIFIER | c.195+7639T>C | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 2/38 | chr6 | 112246317 | |||||||
chr6:112246494 | G | A | 1 | a0002c0003t0002g0163 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.195+7462C>T | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 2/38 | chr6 | 112246494 | |||||||
chr6:112246520 | C | CT | 8 | a0001c0002t0001g0212 a0001c0002t0001g0215 a0001c0009t0001g0082 others(5): Show |
8 | HG01256.hp1 HG02027.hp2 HG02071.hp1 others(5): Show |
intron_variant | MODIFIER | c.195+7435dupA | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 2/38 | chr6 | 112246520 | |||||||
chr6:112246520 | CT | C | 140 | a0001c0001t0001g0027 a0001c0001t0001g0033 a0001c0001t0001g0042 others(137): Show |
140 | HG00323.hp1 HG00408.hp2 HG00621.hp1 others(137): Show |
intron_variant | MODIFIER | c.195+7435delA | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 2/38 | chr6 | 112246520 | |||||||
chr6:112246559 | C | T | 1 | a0002c0006t0002g0084 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.195+7397G>A | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 2/38 | chr6 | 112246559 | |||||||
chr6:112246613 | C | T | 1 | a0001c0001t0001g0007 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.195+7343G>A | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 2/38 | chr6 | 112246613 | |||||||
chr6:112246640 | C | G | 3 | a0001c0009t0009g0078 a0002c0003t0002g0077 a0002c0003t0002g0079 |
3 | HG00099.hp2 HG00280.hp1 HG00323.hp2 |
intron_variant | MODIFIER | c.195+7316G>C | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 2/38 | chr6 | 112246640 | |||||||
chr6:112246722 | A | G | 1 | a0012c0021t0001g0083 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.195+7234T>C | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 2/38 | chr6 | 112246722 | |||||||
chr6:112246777 | C | T | 1 | a0001c0009t0001g0082 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.195+7179G>A | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 2/38 | chr6 | 112246777 | |||||||
chr6:112246917 | C | G | 21 | a0001c0001t0001g0014 a0001c0001t0001g0219 a0001c0001t0001g0220 others(18): Show |
21 | HG00621.hp2 HG01106.hp2 HG01256.hp2 others(18): Show |
intron_variant | MODIFIER | c.195+7039G>C | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 2/38 | chr6 | 112246917 | |||||||
chr6:112247068 | G | A | 31 | a0001c0001t0001g0027 a0001c0001t0001g0033 a0001c0002t0001g0020 others(28): Show |
31 | HG00323.hp1 HG00642.hp2 HG00733.hp1 others(28): Show |
intron_variant | MODIFIER | c.195+6888C>T | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 2/38 | chr6 | 112247068 | |||||||
chr6:112247203 | T | A | 1 | a0004c0010t0001g0166 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.195+6753A>T | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 2/38 | chr6 | 112247203 | |||||||
chr6:112247320 | G | A | 1 | a0001c0011t0003g0009 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.195+6636C>T | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 2/38 | chr6 | 112247320 | |||||||
chr6:112247523 | A | C | 6 | a0008c0015t0001g0057 a0008c0015t0001g0058 a0008c0015t0001g0059 others(3): Show |
6 | HG02486.hp2 HG02818.hp2 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.195+6433T>G | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 2/38 | chr6 | 112247523 | |||||||
chr6:112247548 | G | T | 3 | a0001c0002t0001g0045 a0001c0002t0001g0047 a0001c0020t0005g0046 |
3 | HG01891.hp2 HG02055.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.195+6408C>A | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 2/38 | chr6 | 112247548 | |||||||
chr6:112247984 | C | CGTG | 6 | a0008c0015t0001g0057 a0008c0015t0001g0058 a0008c0015t0001g0059 others(3): Show |
6 | HG02486.hp2 HG02818.hp2 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.195+5971_195+5972i others(5): Show |
LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 2/38 | chr6 | 112247984 | |||||||
chr6:112247985 | A | C | 6 | a0008c0015t0001g0057 a0008c0015t0001g0058 a0008c0015t0001g0059 others(3): Show |
6 | HG02486.hp2 HG02818.hp2 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.195+5971T>G | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 2/38 | chr6 | 112247985 | |||||||
chr6:112248097 | T | C | 3 | a0001c0001t0001g0202 a0001c0001t0001g0204 a0001c0009t0001g0203 |
3 | HG02040.hp1 HG02132.hp2 HG02155.hp1 |
intron_variant | MODIFIER | c.195+5859A>G | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 2/38 | chr6 | 112248097 | |||||||
chr6:112248229 | A | G | 3 | a0001c0002t0001g0045 a0001c0002t0001g0047 a0001c0020t0005g0046 |
3 | HG01891.hp2 HG02055.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.195+5727T>C | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 2/38 | chr6 | 112248229 | |||||||
chr6:112248498 | C | CA | 96 | a0001c0001t0001g0007 a0001c0001t0001g0016 a0001c0001t0001g0027 others(93): Show |
96 | HG00323.hp1 HG00597.hp1 HG00642.hp2 others(93): Show |
intron_variant | MODIFIER | c.195+5457dupT | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 2/38 | chr6 | 112248498 | |||||||
chr6:112248498 | CA | C | 30 | a0001c0001t0001g0237 a0001c0001t0001g0246 a0001c0002t0001g0045 others(27): Show |
30 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(27): Show |
intron_variant | MODIFIER | c.195+5457delT | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 2/38 | chr6 | 112248498 | |||||||
chr6:112248620 | T | C | 1 | a0001c0011t0003g0009 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.195+5336A>G | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 2/38 | chr6 | 112248620 | |||||||
chr6:112248754 | A | G | 27 | a0001c0001t0001g0016 a0001c0001t0001g0027 a0001c0001t0001g0033 others(24): Show |
27 | HG00323.hp1 HG00642.hp2 HG00733.hp1 others(24): Show |
intron_variant | MODIFIER | c.195+5202T>C | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 2/38 | chr6 | 112248754 | |||||||
chr6:112248897 | T | C | 4 | a0001c0002t0001g0311 a0001c0011t0003g0313 a0001c0051t0003g0314 others(1): Show |
4 | HG01891.hp1 HG02897.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.195+5059A>G | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 2/38 | chr6 | 112248897 | |||||||
chr6:112249173 | G | A | 3 | a0001c0002t0001g0045 a0001c0002t0001g0047 a0001c0020t0005g0046 |
3 | HG01891.hp2 HG02055.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.195+4783C>T | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 2/38 | chr6 | 112249173 | |||||||
chr6:112249231 | T | A | 1 | a0001c0002t0001g0205 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.195+4725A>T | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 2/38 | chr6 | 112249231 | |||||||
chr6:112249377 | G | C | 1 | a0005c0045t0007g0039 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.195+4579C>G | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 2/38 | chr6 | 112249377 | |||||||
chr6:112249415 | A | C | 126 | a0001c0001t0001g0014 a0001c0001t0001g0016 a0001c0001t0001g0027 others(123): Show |
126 | HG00323.hp1 HG00621.hp2 HG00642.hp2 others(123): Show |
intron_variant | MODIFIER | c.195+4541T>G | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 2/38 | chr6 | 112249415 | |||||||
chr6:112249441 | C | CA | 89 | a0001c0001t0001g0014 a0001c0001t0001g0042 a0001c0001t0001g0186 others(86): Show |
89 | HG00597.hp2 HG00621.hp2 HG00673.hp1 others(86): Show |
intron_variant | MODIFIER | c.195+4514dupT | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 2/38 | chr6 | 112249441 | |||||||
chr6:112249441 | C | CAA | 7 | a0001c0002t0001g0213 a0001c0005t0001g0044 a0001c0016t0001g0048 others(4): Show |
7 | HG01891.hp1 HG02027.hp2 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.195+4513_195+4514d others(4): Show |
LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 2/38 | chr6 | 112249441 | |||||||
chr6:112249441 | CA | C | 7 | a0001c0001t0001g0016 a0001c0005t0001g0063 a0001c0011t0003g0062 others(4): Show |
7 | HG01515.hp1 HG01978.hp2 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.195+4514delT | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 2/38 | chr6 | 112249441 | |||||||
chr6:112249441 | CAA | C | 6 | a0008c0015t0001g0057 a0008c0015t0001g0058 a0008c0015t0001g0059 others(3): Show |
6 | HG02486.hp2 HG02818.hp2 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.195+4513_195+4514d others(4): Show |
LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 2/38 | chr6 | 112249441 | |||||||
chr6:112249441 | CAAAAAAA others(1): Show |
C | 6 | a0001c0001t0001g0050 a0001c0001t0001g0051 a0001c0001t0001g0052 others(3): Show |
6 | HG01074.hp2 HG01243.hp2 HG01255.hp1 others(3): Show |
intron_variant | MODIFIER | c.195+4507_195+4514d others(10): Show |
LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 2/38 | chr6 | 112249441 | |||||||
chr6:112249513 | A | G | 1 | a0001c0011t0003g0009 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.195+4443T>C | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 2/38 | chr6 | 112249513 | |||||||
chr6:112249699 | C | T | 1 | a0001c0011t0003g0009 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.195+4257G>A | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 2/38 | chr6 | 112249699 | |||||||
chr6:112249737 | A | G | 1 | a0016c0042t0001g0296 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.195+4219T>C | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 2/38 | chr6 | 112249737 | |||||||
chr6:112249881 | A | G | 1 | a0001c0009t0001g0049 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.195+4075T>C | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 2/38 | chr6 | 112249881 | |||||||
chr6:112249907 | T | C | 1 | a0001c0052t0002g0295 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.195+4049A>G | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 2/38 | chr6 | 112249907 | |||||||
chr6:112249927 | CTCTTATA others(39): Show |
C | 1 | a0003c0013t0001g0216 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.195+3983_195+4028d others(48): Show |
LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 2/38 | chr6 | 112249927 | |||||||
chr6:112249933 | T | C | 1 | a0003c0013t0001g0011 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.195+4023A>G | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 2/38 | chr6 | 112249933 | |||||||
chr6:112250012 | G | A | 1 | a0001c0001t0001g0214 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.195+3944C>T | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 2/38 | chr6 | 112250012 | |||||||
chr6:112250153 | G | T | 3 | a0001c0002t0001g0045 a0001c0002t0001g0047 a0001c0020t0005g0046 |
3 | HG01891.hp2 HG02055.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.195+3803C>A | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 2/38 | chr6 | 112250153 | |||||||
chr6:112250290 | A | G | 1 | a0001c0016t0001g0048 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.195+3666T>C | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 2/38 | chr6 | 112250290 | |||||||
chr6:112250351 | C | T | 1 | a0001c0011t0003g0009 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.195+3605G>A | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 2/38 | chr6 | 112250351 | |||||||
chr6:112250672 | G | A | 1 | a0001c0002t0001g0215 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.195+3284C>T | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 2/38 | chr6 | 112250672 | |||||||
chr6:112250749 | C | T | 3 | a0001c0002t0001g0045 a0001c0002t0001g0047 a0001c0020t0005g0046 |
3 | HG01891.hp2 HG02055.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.195+3207G>A | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 2/38 | chr6 | 112250749 | |||||||
chr6:112250769 | A | G | 1 | a0004c0057t0003g0017 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.195+3187T>C | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 2/38 | chr6 | 112250769 | |||||||
chr6:112250834 | G | GTGTTTCT others(27): Show |
1 | a0003c0013t0001g0216 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.195+3121_195+3122i others(36): Show |
LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 2/38 | chr6 | 112250834 | |||||||
chr6:112250835 | G | T | 1 | a0003c0013t0001g0216 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.195+3121C>A | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 2/38 | chr6 | 112250835 | |||||||
chr6:112250846 | T | C | 1 | a0003c0013t0001g0216 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.195+3110A>G | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 2/38 | chr6 | 112250846 | |||||||
chr6:112250880 | T | TCTACCCA others(7): Show |
1 | a0003c0013t0001g0216 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.195+3075_195+3076i others(16): Show |
LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 2/38 | chr6 | 112250880 | |||||||
chr6:112250915 | C | T | 27 | a0001c0001t0001g0016 a0001c0001t0001g0027 a0001c0001t0001g0033 others(24): Show |
27 | HG00323.hp1 HG00642.hp2 HG00733.hp1 others(24): Show |
intron_variant | MODIFIER | c.195+3041G>A | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 2/38 | chr6 | 112250915 | |||||||
chr6:112251159 | T | C | 21 | a0001c0001t0001g0014 a0001c0001t0001g0219 a0001c0001t0001g0220 others(18): Show |
21 | HG00621.hp2 HG01106.hp2 HG01256.hp2 others(18): Show |
intron_variant | MODIFIER | c.195+2797A>G | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 2/38 | chr6 | 112251159 | |||||||
chr6:112251260 | G | A | 1 | a0001c0002t0001g0309 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.195+2696C>T | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 2/38 | chr6 | 112251260 | |||||||
chr6:112251497 | T | G | 1 | a0003c0004t0001g0234 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.195+2459A>C | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 2/38 | chr6 | 112251497 | |||||||
chr6:112251554 | A | C | 1 | a0001c0011t0003g0236 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.195+2402T>G | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 2/38 | chr6 | 112251554 | |||||||
chr6:112251570 | C | G | 2 | a0001c0005t0001g0043 a0001c0005t0001g0044 |
2 | NA18947.hp2 NA19086.hp1 |
intron_variant | MODIFIER | c.195+2386G>C | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 2/38 | chr6 | 112251570 | |||||||
chr6:112251685 | T | A | 1 | a0007c0014t0002g0041 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.195+2271A>T | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 2/38 | chr6 | 112251685 | |||||||
chr6:112251686 | A | G | 1 | a0001c0001t0001g0042 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.195+2270T>C | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 2/38 | chr6 | 112251686 | |||||||
chr6:112251714 | C | T | 1 | a0001c0001t0001g0016 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.195+2242G>A | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 2/38 | chr6 | 112251714 | |||||||
chr6:112251838 | T | C | 1 | a0001c0005t0001g0235 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.195+2118A>G | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 2/38 | chr6 | 112251838 | |||||||
chr6:112252060 | T | C | 1 | a0001c0050t0001g0310 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.195+1896A>G | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 2/38 | chr6 | 112252060 | |||||||
chr6:112252087 | C | G | 27 | a0001c0001t0001g0016 a0001c0001t0001g0027 a0001c0001t0001g0033 others(24): Show |
27 | HG00323.hp1 HG00642.hp2 HG00733.hp1 others(24): Show |
intron_variant | MODIFIER | c.195+1869G>C | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 2/38 | chr6 | 112252087 | |||||||
chr6:112252203 | G | A | 1 | a0002c0003t0006g0002 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.195+1753C>T | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 2/38 | chr6 | 112252203 | |||||||
chr6:112252228 | A | T | 1 | a0001c0001t0001g0015 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.195+1728T>A | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 2/38 | chr6 | 112252228 | |||||||
chr6:112252292 | T | C | 4 | a0001c0002t0001g0311 a0001c0011t0003g0313 a0001c0051t0003g0314 others(1): Show |
4 | HG01891.hp1 HG02897.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.195+1664A>G | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 2/38 | chr6 | 112252292 | |||||||
chr6:112252354 | A | G | 3 | a0001c0001t0001g0014 a0001c0022t0002g0012 a0004c0010t0001g0013 |
3 | HG01261.hp1 HG02258.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.195+1602T>C | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 2/38 | chr6 | 112252354 | |||||||
chr6:112252578 | G | A | 68 | a0001c0001t0001g0237 a0001c0001t0001g0246 a0001c0001t0001g0256 others(65): Show |
68 | HG00408.hp1 HG00408.hp2 HG00597.hp2 others(65): Show |
intron_variant | MODIFIER | c.195+1378C>T | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 2/38 | chr6 | 112252578 | |||||||
chr6:112252796 | A | G | 2 | a0003c0013t0001g0010 a0003c0013t0001g0011 |
2 | HG02165.hp2 NA18973.hp2 |
intron_variant | MODIFIER | c.195+1160T>C | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 2/38 | chr6 | 112252796 | |||||||
chr6:112252943 | C | T | 1 | a0001c0011t0003g0009 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.195+1013G>A | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 2/38 | chr6 | 112252943 | |||||||
chr6:112253063 | A | G | 1 | a0001c0001t0001g0008 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.195+893T>C | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 2/38 | chr6 | 112253063 | |||||||
chr6:112253472 | T | C | 1 | a0016c0042t0001g0296 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.195+484A>G | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 2/38 | chr6 | 112253472 | |||||||
chr6:112253631 | A | G | 1 | a0001c0001t0001g0007 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.195+325T>C | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 2/38 | chr6 | 112253631 | |||||||
chr6:112253670 | T | C | 1 | a0005c0008t0004g0297 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.195+286A>G | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 2/38 | chr6 | 112253670 | |||||||
chr6:112253748 | C | A | 1 | a0001c0051t0003g0314 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.195+208G>T | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 2/38 | chr6 | 112253748 | |||||||
chr6:112253812 | A | G | 2 | a0001c0002t0001g0005 a0001c0002t0001g0006 |
2 | HG01168.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.195+144T>C | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 2/38 | chr6 | 112253812 | |||||||
chr6:112253825 | G | C | 1 | a0001c0011t0003g0298 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.195+131C>G | LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 2/38 | chr6 | 112253825 | |||||||
chr6:112254358 | T | TCCCCTTC others(15): Show |
14 | a0001c0002t0001g0309 a0001c0002t0001g0311 a0001c0011t0003g0313 others(11): Show |
14 | HG01891.hp1 HG02886.hp2 HG02897.hp1 others(11): Show |
intron_variant | MODIFIER | c.-142+79_-141-68dup others(22): Show |
LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 1/38 | chr6 | 112254358 | |||||||
chr6:112254380 | C | CCCCCTTC others(9): Show |
1 | a0001c0037t0003g0003 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.-142+78_-142+79ins others(16): Show |
LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 1/38 | chr6 | 112254380 |