Item | Value |
---|---|
geneid | 3909 |
ensemblid | ENSG00000053747.17 |
hgncid | 6483 |
symbol | LAMA3 |
name | laminin subunit alpha 3 |
refseq_nuc | NM_000227.6 |
refseq_prot | NP_000218.3 |
ensembl_nuc | ENST00000269217.11 |
ensembl_prot | ENSP00000269217.5 |
mane_status | MANE Plus Clinical |
chr | chr18 |
start | 23873020 |
end | 23955066 |
strand | + |
ver | v1.2 |
region | chr18:23873020-23955066 |
region5000 | chr18:23868020-23960066 |
regionname0 | LAMA3_chr18_23873020_23955066 |
regionname5000 | LAMA3_chr18_23868020_23960066 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/0 | 1724 | 228 | 62 | 38 | 85 | 11 | 31 | 69 | LAMA3_chr18_23868020_23960066 | LAMA3 | MPPAV others(1719): Show |
chr18 | 23868020 | 23960066 |
a0002 | 0/1 | 1724 | 63 | 3 | 11 | 39 | 3 | 6 | 32 | LAMA3_chr18_23868020_23960066 | LAMA3 | MPPAV others(1719): Show |
chr18 | 23868020 | 23960066 |
a0003 | 0/0 | 1724 | 8 | 0 | 3 | 5 | 0 | 0 | 4 | LAMA3_chr18_23868020_23960066 | LAMA3 | MPPAV others(1719): Show |
chr18 | 23868020 | 23960066 |
a0004 | 0/0 | 1724 | 7 | 7 | 0 | 0 | 0 | 0 | 0 | LAMA3_chr18_23868020_23960066 | LAMA3 | MPPAV others(1719): Show |
chr18 | 23868020 | 23960066 |
a0005 | 0/0 | 1724 | 3 | 2 | 1 | 0 | 0 | 0 | 0 | LAMA3_chr18_23868020_23960066 | LAMA3 | MPPAV others(1719): Show |
chr18 | 23868020 | 23960066 |
a0006 | 0/0 | 1724 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | LAMA3_chr18_23868020_23960066 | LAMA3 | MPPAV others(1719): Show |
chr18 | 23868020 | 23960066 |
a0007 | 0/0 | 1724 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | LAMA3_chr18_23868020_23960066 | LAMA3 | MPPAV others(1719): Show |
chr18 | 23868020 | 23960066 |
a0008 | 0/0 | 1724 | 2 | 0 | 0 | 0 | 0 | 2 | 0 | LAMA3_chr18_23868020_23960066 | LAMA3 | MPPAV others(1719): Show |
chr18 | 23868020 | 23960066 |
a0009 | 0/0 | 1724 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | LAMA3_chr18_23868020_23960066 | LAMA3 | MPPAV others(1719): Show |
chr18 | 23868020 | 23960066 |
a0010 | 0/0 | 1724 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | LAMA3_chr18_23868020_23960066 | LAMA3 | MPPAV others(1719): Show |
chr18 | 23868020 | 23960066 |
a0011 | 0/0 | 1724 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | LAMA3_chr18_23868020_23960066 | LAMA3 | MPPAV others(1719): Show |
chr18 | 23868020 | 23960066 |
a0012 | 0/0 | 1724 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | LAMA3_chr18_23868020_23960066 | LAMA3 | MPPAV others(1719): Show |
chr18 | 23868020 | 23960066 |
a0013 | 0/0 | 1724 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | LAMA3_chr18_23868020_23960066 | LAMA3 | MPPAV others(1719): Show |
chr18 | 23868020 | 23960066 |
a0014 | 0/0 | 1724 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | LAMA3_chr18_23868020_23960066 | LAMA3 | MPPAV others(1719): Show |
chr18 | 23868020 | 23960066 |
a0015 | 0/0 | 1724 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | LAMA3_chr18_23868020_23960066 | LAMA3 | MPPAV others(1719): Show |
chr18 | 23868020 | 23960066 |
a0016 | 0/0 | 1724 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | LAMA3_chr18_23868020_23960066 | LAMA3 | MPPAV others(1719): Show |
chr18 | 23868020 | 23960066 |
a0017 | 0/0 | 1724 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | LAMA3_chr18_23868020_23960066 | LAMA3 | MPPAV others(1719): Show |
chr18 | 23868020 | 23960066 |
a0018 | 0/0 | 1724 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | LAMA3_chr18_23868020_23960066 | LAMA3 | MPPAV others(1719): Show |
chr18 | 23868020 | 23960066 |
a0019 | 0/0 | 1724 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | LAMA3_chr18_23868020_23960066 | LAMA3 | MPPAV others(1719): Show |
chr18 | 23868020 | 23960066 |
a0020 | 0/0 | 1724 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | LAMA3_chr18_23868020_23960066 | LAMA3 | MPPAV others(1719): Show |
chr18 | 23868020 | 23960066 |
a0021 | 0/0 | 1724 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | LAMA3_chr18_23868020_23960066 | LAMA3 | MPPAV others(1719): Show |
chr18 | 23868020 | 23960066 |
a0022 | 0/0 | 1724 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | LAMA3_chr18_23868020_23960066 | LAMA3 | MPPAV others(1719): Show |
chr18 | 23868020 | 23960066 |
a0023 | 0/0 | 1724 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | LAMA3_chr18_23868020_23960066 | LAMA3 | MPPAV others(1719): Show |
chr18 | 23868020 | 23960066 |
a0024 | 0/0 | 1724 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | LAMA3_chr18_23868020_23960066 | LAMA3 | MPPAV others(1719): Show |
chr18 | 23868020 | 23960066 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/0 | 5172 | 165 | 41 | 19 | 69 | 8 | 27 | LAMA3_chr18_23868020_23960066 | LAMA3 | ATGCC others(5167): Show |
chr18 | 23868020 | 23960066 | ||
a0001c0003 | 0/0 | 5172 | 41 | 12 | 13 | 12 | 1 | 3 | LAMA3_chr18_23868020_23960066 | LAMA3 | ATGCC others(5167): Show |
chr18 | 23868020 | 23960066 | ||
a0001c0006 | 0/0 | 5172 | 7 | 7 | 0 | 0 | 0 | 0 | LAMA3_chr18_23868020_23960066 | LAMA3 | ATGCC others(5167): Show |
chr18 | 23868020 | 23960066 | ||
a0001c0007 | 0/0 | 5172 | 4 | 0 | 1 | 2 | 1 | 0 | LAMA3_chr18_23868020_23960066 | LAMA3 | ATGCC others(5167): Show |
chr18 | 23868020 | 23960066 | ||
a0001c0009 | 0/0 | 5172 | 3 | 0 | 3 | 0 | 0 | 0 | LAMA3_chr18_23868020_23960066 | LAMA3 | ATGCC others(5167): Show |
chr18 | 23868020 | 23960066 | ||
a0001c0011 | 0/0 | 5172 | 3 | 1 | 1 | 0 | 0 | 1 | LAMA3_chr18_23868020_23960066 | LAMA3 | ATGCC others(5167): Show |
chr18 | 23868020 | 23960066 | ||
a0001c0023 | 0/0 | 5172 | 1 | 0 | 1 | 0 | 0 | 0 | LAMA3_chr18_23868020_23960066 | LAMA3 | ATGCC others(5167): Show |
chr18 | 23868020 | 23960066 | ||
a0001c0025 | 0/0 | 5172 | 1 | 0 | 0 | 0 | 1 | 0 | LAMA3_chr18_23868020_23960066 | LAMA3 | ATGCC others(5167): Show |
chr18 | 23868020 | 23960066 | ||
a0001c0027 | 0/0 | 5172 | 1 | 0 | 0 | 1 | 0 | 0 | LAMA3_chr18_23868020_23960066 | LAMA3 | ATGCC others(5167): Show |
chr18 | 23868020 | 23960066 | ||
a0001c0031 | 0/0 | 5172 | 1 | 1 | 0 | 0 | 0 | 0 | LAMA3_chr18_23868020_23960066 | LAMA3 | ATGCC others(5167): Show |
chr18 | 23868020 | 23960066 | ||
a0001c0037 | 0/0 | 5172 | 1 | 0 | 0 | 1 | 0 | 0 | LAMA3_chr18_23868020_23960066 | LAMA3 | ATGCC others(5167): Show |
chr18 | 23868020 | 23960066 | ||
a0002c0002 | 0/1 | 5172 | 57 | 3 | 9 | 37 | 1 | 6 | LAMA3_chr18_23868020_23960066 | LAMA3 | ATGCC others(5167): Show |
chr18 | 23868020 | 23960066 | ||
a0002c0008 | 0/0 | 5172 | 4 | 0 | 2 | 0 | 2 | 0 | LAMA3_chr18_23868020_23960066 | LAMA3 | ATGCC others(5167): Show |
chr18 | 23868020 | 23960066 | ||
a0002c0017 | 0/0 | 5172 | 2 | 0 | 0 | 2 | 0 | 0 | LAMA3_chr18_23868020_23960066 | LAMA3 | ATGCC others(5167): Show |
chr18 | 23868020 | 23960066 | ||
a0003c0004 | 0/0 | 5172 | 8 | 0 | 3 | 5 | 0 | 0 | LAMA3_chr18_23868020_23960066 | LAMA3 | ATGCC others(5167): Show |
chr18 | 23868020 | 23960066 | ||
a0004c0005 | 0/0 | 5172 | 7 | 7 | 0 | 0 | 0 | 0 | LAMA3_chr18_23868020_23960066 | LAMA3 | ATGCC others(5167): Show |
chr18 | 23868020 | 23960066 | ||
a0005c0015 | 0/0 | 5172 | 2 | 2 | 0 | 0 | 0 | 0 | LAMA3_chr18_23868020_23960066 | LAMA3 | ATGCC others(5167): Show |
chr18 | 23868020 | 23960066 | ||
a0005c0021 | 0/0 | 5172 | 1 | 0 | 1 | 0 | 0 | 0 | LAMA3_chr18_23868020_23960066 | LAMA3 | ATGCC others(5167): Show |
chr18 | 23868020 | 23960066 | ||
a0006c0010 | 0/0 | 5172 | 3 | 3 | 0 | 0 | 0 | 0 | LAMA3_chr18_23868020_23960066 | LAMA3 | ATGCC others(5167): Show |
chr18 | 23868020 | 23960066 | ||
a0007c0012 | 0/0 | 5172 | 2 | 2 | 0 | 0 | 0 | 0 | LAMA3_chr18_23868020_23960066 | LAMA3 | ATGCC others(5167): Show |
chr18 | 23868020 | 23960066 | ||
a0008c0016 | 0/0 | 5172 | 2 | 0 | 0 | 0 | 0 | 2 | LAMA3_chr18_23868020_23960066 | LAMA3 | ATGCC others(5167): Show |
chr18 | 23868020 | 23960066 | ||
a0009c0013 | 0/0 | 5172 | 2 | 0 | 0 | 2 | 0 | 0 | LAMA3_chr18_23868020_23960066 | LAMA3 | ATGCC others(5167): Show |
chr18 | 23868020 | 23960066 | ||
a0010c0014 | 0/0 | 5172 | 2 | 0 | 0 | 2 | 0 | 0 | LAMA3_chr18_23868020_23960066 | LAMA3 | ATGCC others(5167): Show |
chr18 | 23868020 | 23960066 | ||
a0011c0022 | 0/0 | 5172 | 1 | 0 | 1 | 0 | 0 | 0 | LAMA3_chr18_23868020_23960066 | LAMA3 | ATGCC others(5167): Show |
chr18 | 23868020 | 23960066 | ||
a0012c0029 | 0/0 | 5172 | 1 | 0 | 1 | 0 | 0 | 0 | LAMA3_chr18_23868020_23960066 | LAMA3 | ATGCC others(5167): Show |
chr18 | 23868020 | 23960066 | ||
a0013c0035 | 0/0 | 5172 | 1 | 0 | 1 | 0 | 0 | 0 | LAMA3_chr18_23868020_23960066 | LAMA3 | ATGCC others(5167): Show |
chr18 | 23868020 | 23960066 | ||
a0014c0020 | 0/0 | 5172 | 1 | 1 | 0 | 0 | 0 | 0 | LAMA3_chr18_23868020_23960066 | LAMA3 | ATGCC others(5167): Show |
chr18 | 23868020 | 23960066 | ||
a0015c0032 | 0/0 | 5172 | 1 | 1 | 0 | 0 | 0 | 0 | LAMA3_chr18_23868020_23960066 | LAMA3 | ATGCC others(5167): Show |
chr18 | 23868020 | 23960066 | ||
a0016c0024 | 0/0 | 5172 | 1 | 1 | 0 | 0 | 0 | 0 | LAMA3_chr18_23868020_23960066 | LAMA3 | ATGCC others(5167): Show |
chr18 | 23868020 | 23960066 | ||
a0017c0036 | 0/0 | 5172 | 1 | 1 | 0 | 0 | 0 | 0 | LAMA3_chr18_23868020_23960066 | LAMA3 | ATGCC others(5167): Show |
chr18 | 23868020 | 23960066 | ||
a0018c0034 | 0/0 | 5172 | 1 | 1 | 0 | 0 | 0 | 0 | LAMA3_chr18_23868020_23960066 | LAMA3 | ATGCC others(5167): Show |
chr18 | 23868020 | 23960066 | ||
a0019c0019 | 0/0 | 5172 | 1 | 0 | 0 | 0 | 0 | 1 | LAMA3_chr18_23868020_23960066 | LAMA3 | ATGCC others(5167): Show |
chr18 | 23868020 | 23960066 | ||
a0020c0028 | 0/0 | 5172 | 1 | 0 | 0 | 0 | 0 | 1 | LAMA3_chr18_23868020_23960066 | LAMA3 | ATGCC others(5167): Show |
chr18 | 23868020 | 23960066 | ||
a0021c0030 | 0/0 | 5172 | 1 | 0 | 0 | 0 | 0 | 1 | LAMA3_chr18_23868020_23960066 | LAMA3 | ATGCC others(5167): Show |
chr18 | 23868020 | 23960066 | ||
a0022c0018 | 0/0 | 5172 | 1 | 0 | 0 | 1 | 0 | 0 | LAMA3_chr18_23868020_23960066 | LAMA3 | ATGCC others(5167): Show |
chr18 | 23868020 | 23960066 | ||
a0023c0033 | 0/0 | 5172 | 1 | 1 | 0 | 0 | 0 | 0 | LAMA3_chr18_23868020_23960066 | LAMA3 | ATGCC others(5167): Show |
chr18 | 23868020 | 23960066 | ||
a0024c0026 | 0/0 | 5172 | 1 | 1 | 0 | 0 | 0 | 0 | LAMA3_chr18_23868020_23960066 | LAMA3 | ATGCC others(5167): Show |
chr18 | 23868020 | 23960066 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 1/0 | 5618 | 97 | 31 | 2 | 46 | 3 | 14 | LAMA3_chr18_23868020_23960066 | LAMA3 | AGCCA others(5613): Show |
chr18 | 23868020 | 23960066 |
a0001c0001t0002 | 0/0 | 5618 | 66 | 10 | 17 | 23 | 5 | 11 | LAMA3_chr18_23868020_23960066 | LAMA3 | AGCCA others(5613): Show |
chr18 | 23868020 | 23960066 |
a0001c0001t0005 | 0/0 | 5618 | 1 | 0 | 0 | 0 | 0 | 1 | LAMA3_chr18_23868020_23960066 | LAMA3 | AGCCA others(5613): Show |
chr18 | 23868020 | 23960066 |
a0001c0001t0006 | 0/0 | 5618 | 1 | 0 | 0 | 0 | 0 | 1 | LAMA3_chr18_23868020_23960066 | LAMA3 | AGCCA others(5613): Show |
chr18 | 23868020 | 23960066 |
a0001c0003t0001 | 0/0 | 5618 | 41 | 12 | 13 | 12 | 1 | 3 | LAMA3_chr18_23868020_23960066 | LAMA3 | AGCCA others(5613): Show |
chr18 | 23868020 | 23960066 |
a0001c0006t0001 | 0/0 | 5618 | 7 | 7 | 0 | 0 | 0 | 0 | LAMA3_chr18_23868020_23960066 | LAMA3 | AGCCA others(5613): Show |
chr18 | 23868020 | 23960066 |
a0001c0007t0001 | 0/0 | 5618 | 2 | 0 | 0 | 2 | 0 | 0 | LAMA3_chr18_23868020_23960066 | LAMA3 | AGCCA others(5613): Show |
chr18 | 23868020 | 23960066 |
a0001c0007t0002 | 0/0 | 5618 | 2 | 0 | 1 | 0 | 1 | 0 | LAMA3_chr18_23868020_23960066 | LAMA3 | AGCCA others(5613): Show |
chr18 | 23868020 | 23960066 |
a0001c0009t0001 | 0/0 | 5618 | 2 | 0 | 2 | 0 | 0 | 0 | LAMA3_chr18_23868020_23960066 | LAMA3 | AGCCA others(5613): Show |
chr18 | 23868020 | 23960066 |
a0001c0009t0002 | 0/0 | 5618 | 1 | 0 | 1 | 0 | 0 | 0 | LAMA3_chr18_23868020_23960066 | LAMA3 | AGCCA others(5613): Show |
chr18 | 23868020 | 23960066 |
a0001c0011t0001 | 0/0 | 5618 | 3 | 1 | 1 | 0 | 0 | 1 | LAMA3_chr18_23868020_23960066 | LAMA3 | AGCCA others(5613): Show |
chr18 | 23868020 | 23960066 |
a0001c0023t0002 | 0/0 | 5618 | 1 | 0 | 1 | 0 | 0 | 0 | LAMA3_chr18_23868020_23960066 | LAMA3 | AGCCA others(5613): Show |
chr18 | 23868020 | 23960066 |
a0001c0025t0002 | 0/0 | 5618 | 1 | 0 | 0 | 0 | 1 | 0 | LAMA3_chr18_23868020_23960066 | LAMA3 | AGCCA others(5613): Show |
chr18 | 23868020 | 23960066 |
a0001c0027t0001 | 0/0 | 5618 | 1 | 0 | 0 | 1 | 0 | 0 | LAMA3_chr18_23868020_23960066 | LAMA3 | AGCCA others(5613): Show |
chr18 | 23868020 | 23960066 |
a0001c0031t0004 | 0/0 | 5619 | 1 | 1 | 0 | 0 | 0 | 0 | LAMA3_chr18_23868020_23960066 | LAMA3 | AGCCA others(5614): Show |
chr18 | 23868020 | 23960066 |
a0001c0037t0001 | 0/0 | 5618 | 1 | 0 | 0 | 1 | 0 | 0 | LAMA3_chr18_23868020_23960066 | LAMA3 | AGCCA others(5613): Show |
chr18 | 23868020 | 23960066 |
a0002c0002t0001 | 0/1 | 5618 | 53 | 3 | 5 | 37 | 1 | 6 | LAMA3_chr18_23868020_23960066 | LAMA3 | AGCCA others(5613): Show |
chr18 | 23868020 | 23960066 |
a0002c0002t0003 | 0/0 | 5618 | 4 | 0 | 4 | 0 | 0 | 0 | LAMA3_chr18_23868020_23960066 | LAMA3 | AGCCA others(5613): Show |
chr18 | 23868020 | 23960066 |
a0002c0008t0001 | 0/0 | 5618 | 4 | 0 | 2 | 0 | 2 | 0 | LAMA3_chr18_23868020_23960066 | LAMA3 | AGCCA others(5613): Show |
chr18 | 23868020 | 23960066 |
a0002c0017t0001 | 0/0 | 5618 | 2 | 0 | 0 | 2 | 0 | 0 | LAMA3_chr18_23868020_23960066 | LAMA3 | AGCCA others(5613): Show |
chr18 | 23868020 | 23960066 |
a0003c0004t0001 | 0/0 | 5618 | 8 | 0 | 3 | 5 | 0 | 0 | LAMA3_chr18_23868020_23960066 | LAMA3 | AGCCA others(5613): Show |
chr18 | 23868020 | 23960066 |
a0004c0005t0002 | 0/0 | 5618 | 7 | 7 | 0 | 0 | 0 | 0 | LAMA3_chr18_23868020_23960066 | LAMA3 | AGCCA others(5613): Show |
chr18 | 23868020 | 23960066 |
a0005c0015t0001 | 0/0 | 5618 | 2 | 2 | 0 | 0 | 0 | 0 | LAMA3_chr18_23868020_23960066 | LAMA3 | AGCCA others(5613): Show |
chr18 | 23868020 | 23960066 |
a0005c0021t0002 | 0/0 | 5618 | 1 | 0 | 1 | 0 | 0 | 0 | LAMA3_chr18_23868020_23960066 | LAMA3 | AGCCA others(5613): Show |
chr18 | 23868020 | 23960066 |
a0006c0010t0001 | 0/0 | 5618 | 3 | 3 | 0 | 0 | 0 | 0 | LAMA3_chr18_23868020_23960066 | LAMA3 | AGCCA others(5613): Show |
chr18 | 23868020 | 23960066 |
a0007c0012t0001 | 0/0 | 5618 | 2 | 2 | 0 | 0 | 0 | 0 | LAMA3_chr18_23868020_23960066 | LAMA3 | AGCCA others(5613): Show |
chr18 | 23868020 | 23960066 |
a0008c0016t0001 | 0/0 | 5618 | 2 | 0 | 0 | 0 | 0 | 2 | LAMA3_chr18_23868020_23960066 | LAMA3 | AGCCA others(5613): Show |
chr18 | 23868020 | 23960066 |
a0009c0013t0002 | 0/0 | 5618 | 2 | 0 | 0 | 2 | 0 | 0 | LAMA3_chr18_23868020_23960066 | LAMA3 | AGCCA others(5613): Show |
chr18 | 23868020 | 23960066 |
a0010c0014t0001 | 0/0 | 5618 | 2 | 0 | 0 | 2 | 0 | 0 | LAMA3_chr18_23868020_23960066 | LAMA3 | AGCCA others(5613): Show |
chr18 | 23868020 | 23960066 |
a0011c0022t0001 | 0/0 | 5618 | 1 | 0 | 1 | 0 | 0 | 0 | LAMA3_chr18_23868020_23960066 | LAMA3 | AGCCA others(5613): Show |
chr18 | 23868020 | 23960066 |
a0012c0029t0003 | 0/0 | 5618 | 1 | 0 | 1 | 0 | 0 | 0 | LAMA3_chr18_23868020_23960066 | LAMA3 | AGCCA others(5613): Show |
chr18 | 23868020 | 23960066 |
a0013c0035t0001 | 0/0 | 5618 | 1 | 0 | 1 | 0 | 0 | 0 | LAMA3_chr18_23868020_23960066 | LAMA3 | AGCCA others(5613): Show |
chr18 | 23868020 | 23960066 |
a0014c0020t0004 | 0/0 | 5619 | 1 | 1 | 0 | 0 | 0 | 0 | LAMA3_chr18_23868020_23960066 | LAMA3 | AGCCA others(5614): Show |
chr18 | 23868020 | 23960066 |
a0015c0032t0001 | 0/0 | 5618 | 1 | 1 | 0 | 0 | 0 | 0 | LAMA3_chr18_23868020_23960066 | LAMA3 | AGCCA others(5613): Show |
chr18 | 23868020 | 23960066 |
a0016c0024t0001 | 0/0 | 5618 | 1 | 1 | 0 | 0 | 0 | 0 | LAMA3_chr18_23868020_23960066 | LAMA3 | AGCCA others(5613): Show |
chr18 | 23868020 | 23960066 |
a0017c0036t0001 | 0/0 | 5618 | 1 | 1 | 0 | 0 | 0 | 0 | LAMA3_chr18_23868020_23960066 | LAMA3 | AGCCA others(5613): Show |
chr18 | 23868020 | 23960066 |
a0018c0034t0004 | 0/0 | 5619 | 1 | 1 | 0 | 0 | 0 | 0 | LAMA3_chr18_23868020_23960066 | LAMA3 | AGCCA others(5614): Show |
chr18 | 23868020 | 23960066 |
a0019c0019t0002 | 0/0 | 5618 | 1 | 0 | 0 | 0 | 0 | 1 | LAMA3_chr18_23868020_23960066 | LAMA3 | AGCCA others(5613): Show |
chr18 | 23868020 | 23960066 |
a0020c0028t0001 | 0/0 | 5618 | 1 | 0 | 0 | 0 | 0 | 1 | LAMA3_chr18_23868020_23960066 | LAMA3 | AGCCA others(5613): Show |
chr18 | 23868020 | 23960066 |
a0021c0030t0001 | 0/0 | 5618 | 1 | 0 | 0 | 0 | 0 | 1 | LAMA3_chr18_23868020_23960066 | LAMA3 | AGCCA others(5613): Show |
chr18 | 23868020 | 23960066 |
a0022c0018t0001 | 0/0 | 5618 | 1 | 0 | 0 | 1 | 0 | 0 | LAMA3_chr18_23868020_23960066 | LAMA3 | AGCCA others(5613): Show |
chr18 | 23868020 | 23960066 |
a0023c0033t0001 | 0/0 | 5618 | 1 | 1 | 0 | 0 | 0 | 0 | LAMA3_chr18_23868020_23960066 | LAMA3 | AGCCA others(5613): Show |
chr18 | 23868020 | 23960066 |
a0024c0026t0004 | 0/0 | 5619 | 1 | 1 | 0 | 0 | 0 | 0 | LAMA3_chr18_23868020_23960066 | LAMA3 | AGCCA others(5614): Show |
chr18 | 23868020 | 23960066 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
a0001c0001t0001g0002 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
a0001c0001t0001g0005 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
a0001c0001t0001g0014 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
a0001c0001t0001g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
a0001c0001t0001g0016 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
a0001c0001t0001g0017 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
a0001c0001t0001g0022 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
a0001c0001t0001g0023 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
a0001c0001t0001g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
a0001c0001t0001g0025 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
a0001c0001t0001g0059 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
a0001c0001t0001g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
a0001c0001t0001g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
a0001c0001t0001g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
a0001c0001t0001g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
a0001c0001t0001g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
a0001c0001t0001g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
a0001c0001t0001g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
a0001c0001t0001g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
a0001c0001t0001g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
a0001c0001t0001g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
a0001c0001t0001g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
a0001c0001t0001g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
a0001c0001t0001g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
a0001c0001t0001g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
a0001c0001t0001g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
a0001c0001t0001g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
a0001c0001t0001g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
a0001c0001t0001g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
a0001c0001t0001g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
a0001c0001t0001g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
a0001c0001t0001g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
a0001c0001t0001g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
a0001c0001t0001g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
a0001c0001t0001g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
a0001c0001t0002g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
a0001c0001t0002g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
a0001c0001t0002g0013 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
a0001c0001t0002g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
a0001c0001t0002g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
a0001c0001t0002g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
a0001c0001t0002g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
a0001c0001t0002g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
a0001c0001t0002g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
a0001c0001t0002g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
a0001c0001t0002g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
a0001c0001t0002g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
a0001c0001t0002g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
a0001c0001t0002g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
a0001c0001t0002g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
a0001c0001t0002g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
a0001c0001t0002g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
a0001c0001t0002g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
a0001c0001t0002g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
a0001c0001t0002g0108 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
a0001c0001t0002g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
a0001c0001t0002g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
a0001c0001t0002g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
a0001c0001t0002g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
a0001c0001t0002g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
a0001c0001t0002g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
a0001c0001t0002g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
a0001c0001t0002g0116 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
a0001c0001t0002g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
a0001c0001t0002g0118 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
a0001c0001t0002g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
a0001c0001t0002g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
a0001c0001t0002g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
a0001c0001t0002g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
a0001c0001t0002g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
a0001c0001t0002g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
a0001c0001t0002g0126 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
a0001c0001t0002g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
a0001c0001t0002g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
a0001c0001t0002g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
a0001c0001t0002g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
a0001c0001t0002g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
a0001c0001t0002g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
a0001c0001t0002g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
a0001c0001t0002g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
a0001c0001t0002g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
a0001c0001t0002g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
a0001c0001t0002g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
a0001c0001t0002g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
a0001c0001t0002g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
a0001c0001t0002g0143 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
a0001c0001t0002g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
a0001c0001t0002g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
a0001c0001t0002g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
a0001c0001t0002g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
a0001c0001t0002g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
a0001c0001t0002g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
a0001c0001t0002g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
a0001c0001t0002g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
a0001c0001t0002g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
a0001c0001t0002g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
a0001c0001t0002g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
a0001c0001t0002g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
a0001c0001t0002g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
a0001c0001t0002g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
a0001c0001t0005g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
a0001c0001t0006g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
a0001c0003t0001g0006 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
a0001c0003t0001g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
a0001c0003t0001g0019 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
a0001c0003t0001g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
a0001c0003t0001g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
a0001c0003t0001g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
a0001c0003t0001g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
a0001c0003t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
a0001c0003t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
a0001c0003t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
a0001c0003t0001g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
a0001c0003t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
a0001c0003t0001g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
a0001c0003t0001g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
a0001c0003t0001g0270 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
a0001c0003t0001g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
a0001c0003t0001g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
a0001c0003t0001g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
a0001c0003t0001g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
a0001c0003t0001g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
a0001c0003t0001g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
a0001c0003t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
a0001c0003t0001g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
a0001c0003t0001g0279 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
a0001c0003t0001g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
a0001c0003t0001g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
a0001c0003t0001g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
a0001c0003t0001g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
a0001c0003t0001g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
a0001c0003t0001g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
a0001c0003t0001g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
a0001c0003t0001g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
a0001c0003t0001g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
a0001c0003t0001g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
a0001c0003t0001g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
a0001c0003t0001g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
a0001c0003t0001g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
a0001c0006t0001g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
a0001c0006t0001g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
a0001c0006t0001g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
a0001c0006t0001g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
a0001c0006t0001g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
a0001c0006t0001g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
a0001c0006t0001g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
a0001c0007t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
a0001c0007t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
a0001c0007t0002g0027 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
a0001c0007t0002g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
a0001c0009t0001g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
a0001c0009t0001g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
a0001c0009t0002g0011 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
a0001c0011t0001g0243 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
a0001c0011t0001g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
a0001c0011t0001g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
a0001c0023t0002g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
a0001c0025t0002g0146 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
a0001c0027t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
a0001c0031t0004g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
a0001c0037t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
a0002c0002t0001g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
a0002c0002t0001g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
a0002c0002t0001g0010 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
a0002c0002t0001g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
a0002c0002t0001g0029 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
a0002c0002t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
a0002c0002t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
a0002c0002t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
a0002c0002t0001g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
a0002c0002t0001g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
a0002c0002t0001g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
a0002c0002t0001g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
a0002c0002t0001g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
a0002c0002t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
a0002c0002t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
a0002c0002t0001g0062 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
a0002c0002t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
a0002c0002t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
a0002c0002t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
a0002c0002t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
a0002c0002t0001g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
a0002c0002t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
a0002c0002t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
a0002c0002t0001g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
a0002c0002t0001g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
a0002c0002t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
a0002c0002t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
a0002c0002t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
a0002c0002t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
a0002c0002t0001g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
a0002c0002t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
a0002c0002t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
a0002c0002t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
a0002c0002t0001g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
a0002c0002t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
a0002c0002t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
a0002c0002t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
a0002c0002t0001g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
a0002c0002t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
a0002c0002t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
a0002c0002t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
a0002c0002t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
a0002c0002t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
a0002c0002t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
a0002c0002t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
a0002c0002t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
a0002c0002t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
a0002c0002t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
a0002c0002t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
a0002c0002t0001g0281 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
a0002c0002t0003g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
a0002c0002t0003g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
a0002c0002t0003g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
a0002c0002t0003g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
a0002c0008t0001g0007 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
a0002c0008t0001g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
a0002c0008t0001g0071 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
a0002c0017t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
a0002c0017t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
a0003c0004t0001g0003 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
a0003c0004t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
a0003c0004t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
a0003c0004t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
a0003c0004t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
a0003c0004t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
a0004c0005t0002g0004 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
a0004c0005t0002g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
a0004c0005t0002g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
a0004c0005t0002g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
a0004c0005t0002g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
a0005c0015t0001g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
a0005c0015t0001g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
a0005c0021t0002g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
a0006c0010t0001g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
a0006c0010t0001g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
a0006c0010t0001g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
a0007c0012t0001g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
a0007c0012t0001g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
a0008c0016t0001g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
a0008c0016t0001g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
a0009c0013t0002g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
a0009c0013t0002g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
a0010c0014t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
a0010c0014t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
a0011c0022t0001g0305 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
a0012c0029t0003g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
a0013c0035t0001g0003 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
a0014c0020t0004g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
a0015c0032t0001g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
a0016c0024t0001g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
a0017c0036t0001g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
a0018c0034t0004g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
a0019c0019t0002g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
a0020c0028t0001g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
a0021c0030t0001g0268 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
a0022c0018t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
a0023c0033t0001g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
a0024c0026t0004g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0007 | t0002 | g0027 | EUR | GBR | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
HG00099 | hp2 | a0001 | c0001 | t0002 | g0126 | EUR | GBR | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
HG00140 | hp1 | a0002 | c0002 | t0001 | g0062 | EUR | GBR | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
HG00140 | hp2 | a0001 | c0025 | t0002 | g0146 | EUR | GBR | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
HG00280 | hp1 | a0001 | c0001 | t0002 | g0143 | EUR | FIN | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
HG00280 | hp2 | a0001 | c0003 | t0001 | g0270 | EUR | FIN | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
HG00423 | hp1 | a0001 | c0001 | t0002 | g0038 | EAS | CHS | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
HG00423 | hp2 | a0001 | c0001 | t0001 | g0179 | EAS | CHS | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
HG00438 | hp1 | a0003 | c0004 | t0001 | g0197 | EAS | CHS | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
HG00438 | hp2 | a0001 | c0001 | t0002 | g0011 | EAS | CHS | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
HG00558 | hp1 | a0002 | c0002 | t0001 | g0009 | EAS | CHS | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
HG00558 | hp2 | a0001 | c0001 | t0001 | g0182 | EAS | CHS | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
HG00609 | hp1 | a0001 | c0001 | t0001 | g0175 | EAS | CHS | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
HG00609 | hp2 | a0002 | c0017 | t0001 | g0068 | EAS | CHS | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
HG00621 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
HG00621 | hp2 | a0002 | c0002 | t0001 | g0050 | EAS | CHS | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
HG00639 | hp1 | a0001 | c0001 | t0002 | g0013 | AMR | PUR | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
HG00639 | hp2 | a0001 | c0003 | t0001 | g0264 | AMR | PUR | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
HG00642 | hp1 | a0005 | c0021 | t0002 | g0154 | AMR | PUR | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
HG00642 | hp2 | a0001 | c0009 | t0001 | g0223 | AMR | PUR | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
HG00673 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
HG00673 | hp2 | a0002 | c0002 | t0001 | g0008 | EAS | CHS | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
HG00735 | hp1 | a0001 | c0001 | t0002 | g0242 | AMR | PUR | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
HG00735 | hp2 | a0001 | c0001 | t0002 | g0031 | AMR | PUR | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
HG00738 | hp1 | a0001 | c0003 | t0001 | g0006 | AMR | PUR | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
HG00738 | hp2 | a0001 | c0001 | t0002 | g0150 | AMR | PUR | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
HG00741 | hp1 | a0001 | c0001 | t0001 | g0191 | AMR | PUR | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
HG00741 | hp2 | a0002 | c0002 | t0001 | g0076 | AMR | PUR | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
HG01069 | hp1 | a0001 | c0009 | t0001 | g0220 | AMR | PUR | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
HG01069 | hp2 | a0002 | c0008 | t0001 | g0057 | AMR | PUR | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
HG01071 | hp1 | a0001 | c0001 | t0002 | g0240 | AMR | PUR | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
HG01071 | hp2 | a0002 | c0008 | t0001 | g0007 | AMR | PUR | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
HG01074 | hp1 | a0002 | c0002 | t0003 | g0065 | AMR | PUR | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
HG01074 | hp2 | a0001 | c0001 | t0002 | g0013 | AMR | PUR | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
HG01081 | hp1 | a0003 | c0004 | t0001 | g0003 | AMR | PUR | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
HG01081 | hp2 | a0001 | c0001 | t0002 | g0156 | AMR | PUR | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
HG01099 | hp1 | a0001 | c0003 | t0001 | g0269 | AMR | PUR | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
HG01099 | hp2 | a0001 | c0001 | t0002 | g0131 | AMR | PUR | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
HG01109 | hp1 | a0001 | c0003 | t0001 | g0293 | AMR | PUR | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
HG01109 | hp2 | a0001 | c0003 | t0001 | g0272 | AMR | PUR | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
HG01167 | hp1 | a0001 | c0003 | t0001 | g0247 | AMR | PUR | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
HG01167 | hp2 | a0001 | c0001 | t0002 | g0121 | AMR | PUR | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
HG01168 | hp1 | a0002 | c0002 | t0001 | g0055 | AMR | PUR | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
HG01168 | hp2 | a0001 | c0011 | t0001 | g0244 | AMR | PUR | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
HG01243 | hp1 | a0001 | c0001 | t0002 | g0111 | AMR | PUR | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
HG01243 | hp2 | a0011 | c0022 | t0001 | g0305 | AMR | PUR | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
HG01257 | hp1 | a0001 | c0001 | t0002 | g0138 | AMR | CLM | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
HG01257 | hp2 | a0001 | c0003 | t0001 | g0006 | AMR | CLM | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
HG01258 | hp1 | a0001 | c0001 | t0002 | g0141 | AMR | CLM | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
HG01258 | hp2 | a0001 | c0003 | t0001 | g0006 | AMR | CLM | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
HG01346 | hp1 | a0002 | c0002 | t0001 | g0026 | AMR | CLM | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
HG01346 | hp2 | a0001 | c0009 | t0002 | g0011 | AMR | CLM | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
HG01358 | hp1 | a0001 | c0003 | t0001 | g0271 | AMR | CLM | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
HG01358 | hp2 | a0002 | c0002 | t0003 | g0086 | AMR | CLM | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
HG01496 | hp1 | a0001 | c0003 | t0001 | g0276 | AMR | CLM | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
HG01496 | hp2 | a0001 | c0001 | t0002 | g0127 | AMR | CLM | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
HG01515 | hp1 | a0001 | c0001 | t0002 | g0118 | EUR | IBS | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
HG01515 | hp2 | a0001 | c0001 | t0001 | g0016 | EUR | IBS | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
HG01516 | hp1 | a0001 | c0001 | t0002 | g0108 | EUR | IBS | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
HG01516 | hp2 | a0002 | c0008 | t0001 | g0007 | EUR | IBS | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
HG01517 | hp1 | a0002 | c0008 | t0001 | g0071 | EUR | IBS | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
HG01517 | hp2 | a0001 | c0001 | t0001 | g0016 | EUR | IBS | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
HG01884 | hp1 | a0001 | c0001 | t0001 | g0259 | AFR | ACB | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
HG01884 | hp2 | a0001 | c0001 | t0002 | g0133 | AFR | ACB | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
HG01891 | hp1 | a0001 | c0001 | t0001 | g0241 | AFR | ACB | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
HG01891 | hp2 | a0001 | c0001 | t0002 | g0030 | AFR | ACB | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
HG01928 | hp1 | a0001 | c0003 | t0001 | g0274 | AMR | PEL | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
HG01928 | hp2 | a0001 | c0001 | t0002 | g0145 | AMR | PEL | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
HG01934 | hp1 | a0001 | c0003 | t0001 | g0275 | AMR | PEL | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
HG01934 | hp2 | a0001 | c0001 | t0001 | g0024 | AMR | PEL | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
HG01975 | hp1 | a0001 | c0023 | t0002 | g0157 | AMR | PEL | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
HG01975 | hp2 | a0003 | c0004 | t0001 | g0003 | AMR | PEL | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
HG01978 | hp1 | a0002 | c0002 | t0001 | g0054 | AMR | PEL | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
HG01978 | hp2 | a0001 | c0001 | t0002 | g0115 | AMR | PEL | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
HG01981 | hp1 | a0001 | c0007 | t0002 | g0028 | AMR | PEL | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
HG01981 | hp2 | a0001 | c0003 | t0001 | g0282 | AMR | PEL | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
HG01993 | hp1 | a0012 | c0029 | t0003 | g0103 | AMR | PEL | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
HG01993 | hp2 | a0013 | c0035 | t0001 | g0003 | AMR | PEL | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
HG02004 | hp1 | a0003 | c0004 | t0001 | g0003 | AMR | PEL | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
HG02004 | hp2 | a0002 | c0002 | t0003 | g0064 | AMR | PEL | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
HG02040 | hp1 | a0001 | c0003 | t0001 | g0018 | EAS | KHV | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
HG02040 | hp2 | a0002 | c0002 | t0001 | g0060 | EAS | KHV | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
HG02071 | hp1 | a0001 | c0001 | t0002 | g0139 | EAS | KHV | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
HG02071 | hp2 | a0001 | c0001 | t0001 | g0166 | EAS | KHV | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
HG02080 | hp1 | a0001 | c0001 | t0001 | g0218 | EAS | KHV | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
HG02080 | hp2 | a0001 | c0027 | t0001 | g0167 | EAS | KHV | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
HG02083 | hp1 | a0002 | c0002 | t0001 | g0105 | EAS | KHV | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
HG02083 | hp2 | a0001 | c0001 | t0001 | g0190 | EAS | KHV | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
HG02135 | hp1 | a0001 | c0001 | t0001 | g0228 | EAS | KHV | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
HG02135 | hp2 | a0002 | c0002 | t0001 | g0075 | EAS | KHV | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
HG02145 | hp1 | a0001 | c0001 | t0001 | g0258 | AFR | ACB | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
HG02145 | hp2 | a0001 | c0001 | t0001 | g0201 | AFR | ACB | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
HG02257 | hp1 | a0007 | c0012 | t0001 | g0226 | AFR | ACB | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
HG02257 | hp2 | a0001 | c0001 | t0002 | g0128 | AFR | ACB | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
HG02258 | hp1 | a0001 | c0001 | t0001 | g0213 | AFR | ACB | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
HG02258 | hp2 | a0001 | c0006 | t0001 | g0020 | AFR | ACB | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
HG02280 | hp1 | a0001 | c0001 | t0001 | g0204 | AFR | ACB | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
HG02280 | hp2 | a0001 | c0003 | t0001 | g0289 | AFR | ACB | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
HG02300 | hp1 | a0001 | c0001 | t0002 | g0134 | AMR | PEL | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
HG02300 | hp2 | a0002 | c0002 | t0003 | g0087 | AMR | PEL | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
HG02451 | hp1 | a0001 | c0001 | t0001 | g0211 | AFR | ACB | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
HG02451 | hp2 | a0014 | c0020 | t0004 | g0233 | AFR | ACB | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
HG02572 | hp1 | a0005 | c0015 | t0001 | g0045 | AFR | GWD | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
HG02572 | hp2 | a0001 | c0003 | t0001 | g0295 | AFR | GWD | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
HG02602 | hp1 | a0001 | c0003 | t0001 | g0279 | SAS | PJL | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
HG02602 | hp2 | a0002 | c0002 | t0001 | g0073 | SAS | PJL | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
HG02615 | hp1 | a0005 | c0015 | t0001 | g0046 | AFR | GWD | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
HG02615 | hp2 | a0006 | c0010 | t0001 | g0206 | AFR | GWD | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
HG02622 | hp1 | a0006 | c0010 | t0001 | g0235 | AFR | GWD | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
HG02622 | hp2 | a0001 | c0003 | t0001 | g0284 | AFR | GWD | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
HG02630 | hp1 | a0001 | c0001 | t0002 | g0122 | AFR | GWD | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
HG02630 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | GWD | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
HG02683 | hp1 | a0001 | c0001 | t0002 | g0136 | SAS | PJL | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
HG02683 | hp2 | a0001 | c0001 | t0001 | g0221 | SAS | PJL | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
HG02723 | hp1 | a0015 | c0032 | t0001 | g0266 | AFR | GWD | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
HG02723 | hp2 | a0006 | c0010 | t0001 | g0205 | AFR | GWD | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
HG02735 | hp1 | a0002 | c0002 | t0001 | g0084 | SAS | PJL | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
HG02735 | hp2 | a0001 | c0011 | t0001 | g0243 | SAS | PJL | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
HG02738 | hp1 | a0001 | c0001 | t0001 | g0196 | SAS | PJL | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
HG02738 | hp2 | a0001 | c0001 | t0002 | g0155 | SAS | PJL | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
HG02809 | hp1 | a0001 | c0006 | t0001 | g0296 | AFR | GWD | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
HG02809 | hp2 | a0004 | c0005 | t0002 | g0004 | AFR | GWD | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
HG02818 | hp1 | a0001 | c0003 | t0001 | g0302 | AFR | GWD | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
HG02818 | hp2 | a0001 | c0003 | t0001 | g0303 | AFR | GWD | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
HG02886 | hp1 | a0001 | c0006 | t0001 | g0300 | AFR | GWD | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
HG02886 | hp2 | a0002 | c0002 | t0001 | g0094 | AFR | GWD | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
HG02896 | hp1 | a0004 | c0005 | t0002 | g0004 | AFR | GWD | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
HG02896 | hp2 | a0001 | c0006 | t0001 | g0297 | AFR | GWD | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
HG02897 | hp1 | a0001 | c0001 | t0001 | g0162 | AFR | GWD | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
HG02897 | hp2 | a0004 | c0005 | t0002 | g0004 | AFR | GWD | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
HG02922 | hp1 | a0001 | c0001 | t0001 | g0249 | AFR | ESN | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
HG02922 | hp2 | a0001 | c0001 | t0001 | g0014 | AFR | ESN | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
HG02965 | hp1 | a0001 | c0003 | t0001 | g0286 | AFR | ESN | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
HG02965 | hp2 | a0001 | c0001 | t0001 | g0017 | AFR | ESN | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
HG02970 | hp1 | a0001 | c0006 | t0001 | g0298 | AFR | ESN | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
HG02970 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | ESN | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
HG02976 | hp1 | a0001 | c0001 | t0001 | g0304 | AFR | ESN | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
HG02976 | hp2 | a0016 | c0024 | t0001 | g0021 | AFR | ESN | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
HG03017 | hp1 | a0001 | c0001 | t0001 | g0231 | SAS | PJL | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
HG03017 | hp2 | a0001 | c0001 | t0002 | g0147 | SAS | PJL | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
HG03041 | hp1 | a0001 | c0001 | t0002 | g0149 | AFR | GWD | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
HG03041 | hp2 | a0001 | c0003 | t0001 | g0252 | AFR | GWD | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
HG03098 | hp1 | a0004 | c0005 | t0002 | g0152 | AFR | MSL | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
HG03098 | hp2 | a0001 | c0006 | t0001 | g0299 | AFR | MSL | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
HG03130 | hp1 | a0001 | c0006 | t0001 | g0245 | AFR | ESN | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
HG03130 | hp2 | a0001 | c0001 | t0001 | g0254 | AFR | ESN | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
HG03195 | hp1 | a0001 | c0001 | t0002 | g0120 | AFR | ESN | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
HG03195 | hp2 | a0001 | c0001 | t0001 | g0212 | AFR | ESN | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
HG03209 | hp1 | a0007 | c0012 | t0001 | g0225 | AFR | MSL | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
HG03209 | hp2 | a0001 | c0003 | t0001 | g0285 | AFR | MSL | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
HG03225 | hp1 | a0017 | c0036 | t0001 | g0290 | AFR | MSL | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
HG03225 | hp2 | a0001 | c0001 | t0001 | g0176 | AFR | MSL | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
HG03239 | hp1 | a0001 | c0001 | t0001 | g0192 | SAS | PJL | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
HG03239 | hp2 | a0002 | c0002 | t0001 | g0053 | SAS | PJL | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
HG03453 | hp1 | a0001 | c0001 | t0001 | g0207 | AFR | MSL | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
HG03453 | hp2 | a0001 | c0003 | t0001 | g0250 | AFR | MSL | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
HG03486 | hp1 | a0018 | c0034 | t0004 | g0294 | AFR | MSL | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
HG03486 | hp2 | a0004 | c0005 | t0002 | g0130 | AFR | MSL | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
HG03490 | hp1 | a0001 | c0001 | t0002 | g0113 | SAS | PJL | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
HG03490 | hp2 | a0008 | c0016 | t0001 | g0082 | SAS | PJL | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
HG03491 | hp1 | a0001 | c0003 | t0001 | g0019 | SAS | PJL | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
HG03491 | hp2 | a0002 | c0002 | t0001 | g0281 | SAS | PJL | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
HG03492 | hp1 | a0001 | c0003 | t0001 | g0019 | SAS | PJL | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
HG03492 | hp2 | a0008 | c0016 | t0001 | g0079 | SAS | PJL | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
HG03516 | hp1 | a0001 | c0011 | t0001 | g0253 | AFR | ESN | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
HG03516 | hp2 | a0001 | c0001 | t0002 | g0119 | AFR | ESN | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
HG03540 | hp1 | a0001 | c0001 | t0001 | g0209 | AFR | GWD | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
HG03540 | hp2 | a0001 | c0003 | t0001 | g0251 | AFR | GWD | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
HG03654 | hp1 | a0001 | c0001 | t0002 | g0110 | SAS | PJL | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
HG03654 | hp2 | a0001 | c0001 | t0001 | g0203 | SAS | PJL | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
HG03669 | hp1 | a0019 | c0019 | t0002 | g0125 | SAS | PJL | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
HG03669 | hp2 | a0001 | c0001 | t0001 | g0234 | SAS | PJL | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
HG03688 | hp1 | a0001 | c0001 | t0001 | g0193 | SAS | STU | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
HG03688 | hp2 | a0001 | c0001 | t0002 | g0124 | SAS | STU | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
HG03704 | hp1 | a0001 | c0001 | t0002 | g0112 | SAS | PJL | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
HG03704 | hp2 | a0001 | c0001 | t0001 | g0025 | SAS | PJL | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
HG03710 | hp1 | a0001 | c0001 | t0002 | g0140 | SAS | PJL | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
HG03710 | hp2 | a0001 | c0001 | t0001 | g0186 | SAS | PJL | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
HG03831 | hp1 | a0001 | c0001 | t0002 | g0067 | SAS | BEB | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
HG03831 | hp2 | a0001 | c0001 | t0001 | g0047 | SAS | BEB | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
HG03834 | hp1 | a0001 | c0001 | t0006 | g0200 | SAS | BEB | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
HG03834 | hp2 | a0001 | c0001 | t0001 | g0023 | SAS | BEB | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
HG04115 | hp1 | a0001 | c0001 | t0001 | g0022 | SAS | STU | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
HG04115 | hp2 | a0001 | c0001 | t0001 | g0246 | SAS | STU | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
HG04184 | hp1 | a0001 | c0001 | t0002 | g0132 | SAS | BEB | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
HG04184 | hp2 | a0020 | c0028 | t0001 | g0106 | SAS | BEB | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
HG04199 | hp1 | a0021 | c0030 | t0001 | g0268 | SAS | STU | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
HG04199 | hp2 | a0001 | c0001 | t0005 | g0137 | SAS | STU | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
HG04204 | hp1 | a0001 | c0001 | t0001 | g0227 | SAS | STU | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
HG04204 | hp2 | a0002 | c0002 | t0001 | g0090 | SAS | STU | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
NA18522 | hp1 | a0001 | c0001 | t0001 | g0257 | AFR | YRI | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
NA18522 | hp2 | a0001 | c0001 | t0001 | g0210 | AFR | YRI | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
NA18747 | hp1 | a0001 | c0003 | t0001 | g0261 | EAS | CHB | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
NA18747 | hp2 | a0001 | c0001 | t0002 | g0040 | EAS | CHB | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
NA18906 | hp1 | a0001 | c0001 | t0001 | g0208 | AFR | YRI | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
NA18906 | hp2 | a0001 | c0003 | t0001 | g0291 | AFR | YRI | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
NA18940 | hp1 | a0009 | c0013 | t0002 | g0144 | EAS | JPT | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
NA18940 | hp2 | a0001 | c0001 | t0001 | g0178 | EAS | JPT | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
NA18942 | hp1 | a0003 | c0004 | t0001 | g0188 | EAS | JPT | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
NA18942 | hp2 | a0002 | c0002 | t0001 | g0010 | EAS | JPT | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
NA18944 | hp1 | a0001 | c0001 | t0001 | g0229 | EAS | JPT | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
NA18944 | hp2 | a0002 | c0002 | t0001 | g0070 | EAS | JPT | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
NA18946 | hp1 | a0002 | c0002 | t0001 | g0085 | EAS | JPT | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
NA18946 | hp2 | a0001 | c0001 | t0001 | g0236 | EAS | JPT | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
NA18948 | hp1 | a0001 | c0001 | t0002 | g0044 | EAS | JPT | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
NA18948 | hp2 | a0002 | c0002 | t0001 | g0048 | EAS | JPT | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
NA18950 | hp1 | a0002 | c0002 | t0001 | g0063 | EAS | JPT | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
NA18950 | hp2 | a0001 | c0001 | t0001 | g0172 | EAS | JPT | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
NA18951 | hp1 | a0003 | c0004 | t0001 | g0187 | EAS | JPT | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
NA18951 | hp2 | a0002 | c0002 | t0001 | g0089 | EAS | JPT | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
NA18953 | hp1 | a0001 | c0001 | t0002 | g0036 | EAS | JPT | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
NA18953 | hp2 | a0001 | c0003 | t0001 | g0273 | EAS | JPT | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
NA18954 | hp1 | a0009 | c0013 | t0002 | g0012 | EAS | JPT | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
NA18954 | hp2 | a0001 | c0001 | t0001 | g0173 | EAS | JPT | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
NA18957 | hp1 | a0001 | c0001 | t0001 | g0177 | EAS | JPT | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
NA18957 | hp2 | a0001 | c0001 | t0002 | g0037 | EAS | JPT | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
NA18959 | hp1 | a0001 | c0003 | t0001 | g0267 | EAS | JPT | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
NA18959 | hp2 | a0001 | c0001 | t0001 | g0170 | EAS | JPT | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
NA18960 | hp1 | a0002 | c0017 | t0001 | g0069 | EAS | JPT | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
NA18960 | hp2 | a0001 | c0003 | t0001 | g0288 | EAS | JPT | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
NA18961 | hp1 | a0002 | c0002 | t0001 | g0100 | EAS | JPT | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
NA18961 | hp2 | a0001 | c0001 | t0001 | g0163 | EAS | JPT | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
NA18962 | hp1 | a0001 | c0001 | t0001 | g0222 | EAS | JPT | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
NA18962 | hp2 | a0001 | c0001 | t0002 | g0114 | EAS | JPT | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
NA18964 | hp1 | a0001 | c0001 | t0002 | g0148 | EAS | JPT | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
NA18964 | hp2 | a0001 | c0001 | t0001 | g0239 | EAS | JPT | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
NA18965 | hp1 | a0001 | c0001 | t0001 | g0181 | EAS | JPT | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
NA18965 | hp2 | a0002 | c0002 | t0001 | g0101 | EAS | JPT | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
NA18969 | hp1 | a0001 | c0001 | t0001 | g0230 | EAS | JPT | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
NA18969 | hp2 | a0001 | c0001 | t0001 | g0180 | EAS | JPT | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
NA18970 | hp1 | a0001 | c0001 | t0001 | g0183 | EAS | JPT | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
NA18970 | hp2 | a0002 | c0002 | t0001 | g0104 | EAS | JPT | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
NA18973 | hp1 | a0001 | c0001 | t0001 | g0164 | EAS | JPT | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
NA18973 | hp2 | a0002 | c0002 | t0001 | g0080 | EAS | JPT | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
NA18974 | hp1 | a0010 | c0014 | t0001 | g0232 | EAS | JPT | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
NA18974 | hp2 | a0002 | c0002 | t0001 | g0078 | EAS | JPT | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
NA18975 | hp1 | a0002 | c0002 | t0001 | g0049 | EAS | JPT | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
NA18975 | hp2 | a0001 | c0001 | t0001 | g0165 | EAS | JPT | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
NA18979 | hp1 | a0001 | c0003 | t0001 | g0280 | EAS | JPT | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
NA18979 | hp2 | a0022 | c0018 | t0001 | g0194 | EAS | JPT | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
NA18981 | hp1 | a0001 | c0001 | t0001 | g0185 | EAS | JPT | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
NA18981 | hp2 | a0002 | c0002 | t0001 | g0096 | EAS | JPT | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
NA18982 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
NA18982 | hp2 | a0001 | c0003 | t0001 | g0263 | EAS | JPT | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
NA18983 | hp1 | a0001 | c0001 | t0002 | g0034 | EAS | JPT | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
NA18983 | hp2 | a0001 | c0001 | t0001 | g0219 | EAS | JPT | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
NA18985 | hp1 | a0001 | c0001 | t0002 | g0042 | EAS | JPT | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
NA18985 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
NA18988 | hp1 | a0002 | c0002 | t0001 | g0008 | EAS | JPT | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
NA18988 | hp2 | a0001 | c0003 | t0001 | g0262 | EAS | JPT | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
NA18989 | hp1 | a0001 | c0001 | t0001 | g0171 | EAS | JPT | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
NA18989 | hp2 | a0002 | c0002 | t0001 | g0009 | EAS | JPT | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
NA18991 | hp1 | a0001 | c0007 | t0001 | g0051 | EAS | JPT | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
NA18991 | hp2 | a0001 | c0001 | t0001 | g0195 | EAS | JPT | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
NA18995 | hp1 | a0002 | c0002 | t0001 | g0107 | EAS | JPT | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
NA18995 | hp2 | a0001 | c0001 | t0001 | g0237 | EAS | JPT | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
NA18999 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
NA18999 | hp2 | a0002 | c0002 | t0001 | g0074 | EAS | JPT | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
NA19001 | hp1 | a0001 | c0001 | t0002 | g0033 | EAS | JPT | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
NA19001 | hp2 | a0002 | c0002 | t0001 | g0092 | EAS | JPT | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
NA19003 | hp1 | a0001 | c0001 | t0001 | g0169 | EAS | JPT | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
NA19003 | hp2 | a0001 | c0001 | t0002 | g0135 | EAS | JPT | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
NA19004 | hp1 | a0002 | c0002 | t0001 | g0088 | EAS | JPT | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
NA19004 | hp2 | a0001 | c0001 | t0001 | g0214 | EAS | JPT | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
NA19009 | hp1 | a0001 | c0001 | t0001 | g0174 | EAS | JPT | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
NA19009 | hp2 | a0001 | c0001 | t0002 | g0159 | EAS | JPT | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
NA19010 | hp1 | a0002 | c0002 | t0001 | g0061 | EAS | JPT | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
NA19010 | hp2 | a0010 | c0014 | t0001 | g0217 | EAS | JPT | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
NA19011 | hp1 | a0001 | c0001 | t0001 | g0238 | EAS | JPT | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
NA19011 | hp2 | a0001 | c0001 | t0002 | g0039 | EAS | JPT | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
NA19012 | hp1 | a0001 | c0003 | t0001 | g0018 | EAS | JPT | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
NA19012 | hp2 | a0003 | c0004 | t0001 | g0189 | EAS | JPT | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
NA19030 | hp1 | a0023 | c0033 | t0001 | g0283 | AFR | LWK | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
NA19030 | hp2 | a0004 | c0005 | t0002 | g0151 | AFR | LWK | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
NA19043 | hp1 | a0001 | c0001 | t0002 | g0161 | AFR | LWK | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
NA19043 | hp2 | a0001 | c0001 | t0001 | g0168 | AFR | LWK | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
NA19054 | hp1 | a0002 | c0002 | t0001 | g0099 | EAS | JPT | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
NA19054 | hp2 | a0001 | c0001 | t0001 | g0199 | EAS | JPT | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
NA19057 | hp1 | a0002 | c0002 | t0001 | g0093 | EAS | JPT | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
NA19057 | hp2 | a0001 | c0037 | t0001 | g0215 | EAS | JPT | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
NA19058 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
NA19058 | hp2 | a0001 | c0001 | t0002 | g0035 | EAS | JPT | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
NA19060 | hp1 | a0002 | c0002 | t0001 | g0081 | EAS | JPT | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
NA19060 | hp2 | a0001 | c0003 | t0001 | g0278 | EAS | JPT | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
NA19063 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
NA19063 | hp2 | a0002 | c0002 | t0001 | g0102 | EAS | JPT | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
NA19066 | hp1 | a0002 | c0002 | t0001 | g0098 | EAS | JPT | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
NA19066 | hp2 | a0001 | c0001 | t0002 | g0043 | EAS | JPT | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
NA19074 | hp1 | a0001 | c0007 | t0001 | g0052 | EAS | JPT | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
NA19074 | hp2 | a0001 | c0001 | t0002 | g0012 | EAS | JPT | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
NA19077 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
NA19077 | hp2 | a0002 | c0002 | t0001 | g0072 | EAS | JPT | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
NA19078 | hp1 | a0001 | c0001 | t0002 | g0117 | EAS | JPT | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
NA19078 | hp2 | a0001 | c0003 | t0001 | g0265 | EAS | JPT | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
NA19079 | hp1 | a0002 | c0002 | t0001 | g0095 | EAS | JPT | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
NA19079 | hp2 | a0001 | c0001 | t0001 | g0224 | EAS | JPT | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
NA19082 | hp1 | a0002 | c0002 | t0001 | g0083 | EAS | JPT | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
NA19082 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
NA19083 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
NA19083 | hp2 | a0001 | c0001 | t0002 | g0032 | EAS | JPT | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
NA19084 | hp1 | a0001 | c0001 | t0002 | g0123 | EAS | JPT | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
NA19084 | hp2 | a0002 | c0002 | t0001 | g0066 | EAS | JPT | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
NA19085 | hp1 | a0002 | c0002 | t0001 | g0091 | EAS | JPT | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
NA19085 | hp2 | a0001 | c0001 | t0002 | g0041 | EAS | JPT | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
NA19087 | hp1 | a0001 | c0001 | t0002 | g0153 | EAS | JPT | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
NA19087 | hp2 | a0001 | c0001 | t0001 | g0216 | EAS | JPT | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
NA19091 | hp1 | a0003 | c0004 | t0001 | g0198 | EAS | JPT | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
NA19091 | hp2 | a0002 | c0002 | t0001 | g0097 | EAS | JPT | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
NA19240 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | YRI | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
NA19240 | hp2 | a0001 | c0001 | t0001 | g0248 | AFR | YRI | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
NA20129 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | ASW | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
NA20129 | hp2 | a0001 | c0001 | t0002 | g0160 | AFR | ASW | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
NA20805 | hp1 | a0001 | c0001 | t0001 | g0202 | EUR | TSI | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
NA20805 | hp2 | a0001 | c0001 | t0002 | g0116 | EUR | TSI | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
NA20905 | hp1 | a0001 | c0001 | t0002 | g0109 | SAS | GIH | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
NA20905 | hp2 | a0002 | c0002 | t0001 | g0077 | SAS | GIH | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
HG01123 | hp1 | a0002 | c0002 | t0001 | g0010 | AMR | CLM | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
HG01123 | hp2 | a0001 | c0001 | t0002 | g0142 | AMR | CLM | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
HG02109 | hp1 | a0002 | c0002 | t0001 | g0056 | AFR | ACB | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
HG02109 | hp2 | a0001 | c0001 | t0001 | g0260 | AFR | ACB | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
HG02486 | hp1 | a0001 | c0001 | t0001 | g0256 | AFR | ACB | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
HG02486 | hp2 | a0001 | c0001 | t0002 | g0158 | AFR | ACB | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
HG02559 | hp1 | a0001 | c0001 | t0001 | g0017 | AFR | ACB | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
HG02559 | hp2 | a0001 | c0031 | t0004 | g0292 | AFR | ACB | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
HG03471 | hp1 | a0001 | c0003 | t0001 | g0287 | AFR | MSL | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
HG03471 | hp2 | a0001 | c0001 | t0001 | g0255 | AFR | MSL | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
NA18955 | hp1 | a0001 | c0003 | t0001 | g0277 | EAS | JPT | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
NA18955 | hp2 | a0001 | c0001 | t0001 | g0184 | EAS | JPT | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
NA20300 | hp1 | a0002 | c0002 | t0001 | g0058 | AFR | USA | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
NA20300 | hp2 | a0004 | c0005 | t0002 | g0129 | AFR | USA | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
NA21309 | hp1 | a0001 | c0001 | t0001 | g0014 | AFR | LWK | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
NA21309 | hp2 | a0024 | c0026 | t0004 | g0301 | AFR | LWK | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
homoSapiens | chm13v2 | a0002 | c0002 | t0001 | g0029 | REF | REF | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0059 | REF | REF | LAMA3_chr18_23868020_23960066 | LAMA3 | chr18 | 23868020 | 23960066 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr18:23873120 | C | A | 1 | a0007 | 2 | HG02257.hp1 HG03209.hp1 |
missense_variant | MODERATE | c.76C>A | p.Leu26Met | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 1/38 | 101/5618 | 76/5175 | 26/1724 | chr18 | 23873120 | |||
chr18:23873154 | T | G | 2 | a0019 a0022 |
2 | HG03669.hp1 NA18979.hp2 |
missense_variant | MODERATE | c.110T>G | p.Phe37Cys | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 1/38 | 135/5618 | 110/5175 | 37/1724 | chr18 | 23873154 | |||
chr18:23876307 | G | T | 1 | a0017 | 1 | HG03225.hp1 | missense_variant | MODERATE | c.185G>T | p.Gly62Val | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 2/38 | 210/5618 | 185/5175 | 62/1724 | chr18 | 23876307 | |||
chr18:23881955 | C | T | 1 | a0013 | 1 | HG01993.hp2 | missense_variant | MODERATE | c.305C>T | p.Ala102Val | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 3/38 | 330/5618 | 305/5175 | 102/1724 | chr18 | 23881955 | |||
chr18:23895017 | G | C | 1 | a0014 | 1 | HG02451.hp2 | missense_variant | MODERATE | c.745G>C | p.Glu249Gln | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 7/38 | 770/5618 | 745/5175 | 249/1724 | chr18 | 23895017 | |||
chr18:23898979 | A | C | 1 | a0008 | 2 | HG03490.hp2 HG03492.hp2 |
missense_variant | MODERATE | c.923A>C | p.Gln308Pro | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 9/38 | 948/5618 | 923/5175 | 308/1724 | chr18 | 23898979 | |||
chr18:23898991 | A | G | 1 | a0012 | 1 | HG01993.hp1 | missense_variant | MODERATE | c.935A>G | p.Asn312Ser | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 9/38 | 960/5618 | 935/5175 | 312/1724 | chr18 | 23898991 | |||
chr18:23899375 | G | A | 1 | a0014 | 1 | HG02451.hp2 | missense_variant | MODERATE | c.1097G>A | p.Arg366His | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 10/38 | 1122/5618 | 1097/5175 | 366/1724 | chr18 | 23899375 | |||
chr18:23899392 | C | T | 1 | a0005 | 2 | HG02572.hp1 HG02615.hp1 |
missense_variant | MODERATE | c.1114C>T | p.Arg372Trp | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 10/38 | 1139/5618 | 1114/5175 | 372/1724 | chr18 | 23899392 | |||
chr18:23899393 | G | A | 1 | a0005 | 1 | HG00642.hp1 | missense_variant | MODERATE | c.1115G>A | p.Arg372Gln | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 10/38 | 1140/5618 | 1115/5175 | 372/1724 | chr18 | 23899393 | |||
chr18:23901136 | G | A | 1 | a0021 | 1 | HG04199.hp1 | missense_variant | MODERATE | c.1187G>A | p.Arg396Gln | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 11/38 | 1212/5618 | 1187/5175 | 396/1724 | chr18 | 23901136 | |||
chr18:23901244 | G | A | 1 | a0011 | 1 | HG01243.hp2 | missense_variant | MODERATE | c.1295G>A | p.Arg432Gln | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 11/38 | 1320/5618 | 1295/5175 | 432/1724 | chr18 | 23901244 | |||
chr18:23907561 | G | T | 1 | a0010 | 2 | NA18974.hp1 NA19010.hp2 |
missense_variant | MODERATE | c.1903G>T | p.Ala635Ser | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 16/38 | 1928/5618 | 1903/5175 | 635/1724 | chr18 | 23907561 | |||
chr18:23912765 | A | G | 1 | a0018 | 1 | HG03486.hp1 | missense_variant | MODERATE | c.2386A>G | p.Asn796Asp | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 19/38 | 2411/5618 | 2386/5175 | 796/1724 | chr18 | 23912765 | |||
chr18:23914850 | C | G | 1 | a0024 | 1 | NA21309.hp2 | missense_variant | MODERATE | c.2807C>G | p.Pro936Arg | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 21/38 | 2832/5618 | 2807/5175 | 936/1724 | chr18 | 23914850 | |||
chr18:23921512 | A | G | 1 | a0004 | 7 | HG02809.hp2 HG02896.hp1 HG02897.hp2 others(4): Show |
missense_variant | MODERATE | c.3277A>G | p.Thr1093Ala | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 25/38 | 3302/5618 | 3277/5175 | 1093/1724 | chr18 | 23921512 | |||
chr18:23931070 | C | A | 4 | a0002 a0008 a0012 others(1): Show |
66 | HG00140.hp1 HG00558.hp1 HG00609.hp2 others(63): Show |
missense_variant | MODERATE | c.3618C>A | p.Asn1206Lys | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 28/38 | 3643/5618 | 3618/5175 | 1206/1724 | chr18 | 23931070 | |||
chr18:23932212 | C | T | 1 | a0006 | 3 | HG02615.hp2 HG02622.hp1 HG02723.hp2 |
missense_variant | MODERATE | c.3802C>T | p.His1268Tyr | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 29/38 | 3827/5618 | 3802/5175 | 1268/1724 | chr18 | 23932212 | |||
chr18:23932248 | G | A | 1 | a0009 | 2 | NA18940.hp1 NA18954.hp1 |
missense_variant | MODERATE | c.3838G>A | p.Gly1280Arg | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 29/38 | 3863/5618 | 3838/5175 | 1280/1724 | chr18 | 23932248 | |||
chr18:23933846 | G | A | 1 | a0015 | 1 | HG02723.hp1 | missense_variant | MODERATE | c.3946G>A | p.Gly1316Arg | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 30/38 | 3971/5618 | 3946/5175 | 1316/1724 | chr18 | 23933846 | |||
chr18:23939383 | C | T | 1 | a0020 | 1 | HG04184.hp2 | missense_variant | MODERATE | c.4196C>T | p.Pro1399Leu | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 31/38 | 4221/5618 | 4196/5175 | 1399/1724 | chr18 | 23939383 | |||
chr18:23949766 | G | A | 3 | a0003 a0013 a0022 |
10 | HG00438.hp1 HG01081.hp1 HG01975.hp2 others(7): Show |
missense_variant&splice_region_variant | MODERATE | c.4526G>A | p.Ser1509Asn | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 34/38 | 4551/5618 | 4526/5175 | 1509/1724 | chr18 | 23949766 | |||
chr18:23950107 | A | G | 1 | a0016 | 1 | HG02976.hp2 | missense_variant | MODERATE | c.4763A>G | p.His1588Arg | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 35/38 | 4788/5618 | 4763/5175 | 1588/1724 | chr18 | 23950107 | |||
chr18:23951690 | G | A | 1 | a0023 | 1 | NA19030.hp1 | missense_variant | MODERATE | c.4822G>A | p.Ala1608Thr | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 36/38 | 4847/5618 | 4822/5175 | 1608/1724 | chr18 | 23951690 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr18:23873074 | C | T | 1 | a0002c0008 | 4 | HG01069.hp2 HG01071.hp2 HG01516.hp2 others(1): Show |
synonymous_variant | LOW | c.30C>T | p.Cys10Cys | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 1/38 | 55/5618 | 30/5175 | 10/1724 | chr18 | 23873074 | |||
chr18:23873167 | C | G | 1 | a0001c0037 | 1 | NA19057.hp2 | synonymous_variant | LOW | c.123C>G | p.Pro41Pro | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 1/38 | 148/5618 | 123/5175 | 41/1724 | chr18 | 23873167 | |||
chr18:23882001 | C | T | 1 | a0002c0017 | 2 | HG00609.hp2 NA18960.hp1 |
synonymous_variant | LOW | c.351C>T | p.Ala117Ala | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 3/38 | 376/5618 | 351/5175 | 117/1724 | chr18 | 23882001 | |||
chr18:23890029 | C | T | 7 | a0001c0003 a0001c0031 a0015c0032 others(4): Show |
47 | HG00280.hp2 HG00639.hp2 HG00738.hp1 others(44): Show |
synonymous_variant | LOW | c.495C>T | p.Phe165Phe | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 5/38 | 520/5618 | 495/5175 | 165/1724 | chr18 | 23890029 | |||
chr18:23901269 | C | G | 7 | a0001c0007 a0002c0002 a0002c0008 others(4): Show |
70 | HG00099.hp1 HG00140.hp1 HG00558.hp1 others(67): Show |
synonymous_variant | LOW | c.1320C>G | p.Ala440Ala | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 11/38 | 1345/5618 | 1320/5175 | 440/1724 | chr18 | 23901269 | |||
chr18:23904616 | C | T | 1 | a0001c0027 | 1 | HG02080.hp2 | synonymous_variant | LOW | c.1710C>T | p.Tyr570Tyr | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 14/38 | 1735/5618 | 1710/5175 | 570/1724 | chr18 | 23904616 | |||
chr18:23904634 | C | T | 1 | a0001c0006 | 7 | HG02258.hp2 HG02809.hp1 HG02886.hp1 others(4): Show |
synonymous_variant | LOW | c.1728C>T | p.Ala576Ala | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 14/38 | 1753/5618 | 1728/5175 | 576/1724 | chr18 | 23904634 | |||
chr18:23907808 | C | T | 1 | a0011c0022 | 1 | HG01243.hp2 | synonymous_variant | LOW | c.2061C>T | p.Asn687Asn | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 17/38 | 2086/5618 | 2061/5175 | 687/1724 | chr18 | 23907808 | |||
chr18:23916569 | C | T | 1 | a0001c0025 | 1 | HG00140.hp2 | synonymous_variant | LOW | c.2970C>T | p.Asp990Asp | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 23/38 | 2995/5618 | 2970/5175 | 990/1724 | chr18 | 23916569 | |||
chr18:23916590 | G | A | 2 | a0001c0031 a0018c0034 |
2 | HG02559.hp2 HG03486.hp1 |
synonymous_variant | LOW | c.2991G>A | p.Thr997Thr | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 23/38 | 3016/5618 | 2991/5175 | 997/1724 | chr18 | 23916590 | |||
chr18:23916677 | G | C | 1 | a0001c0023 | 1 | HG01975.hp1 | synonymous_variant | LOW | c.3078G>C | p.Leu1026Leu | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 23/38 | 3103/5618 | 3078/5175 | 1026/1724 | chr18 | 23916677 | |||
chr18:23921039 | C | T | 1 | a0001c0011 | 3 | HG01168.hp2 HG02735.hp2 HG03516.hp1 |
synonymous_variant | LOW | c.3201C>T | p.Asn1067Asn | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 24/38 | 3226/5618 | 3201/5175 | 1067/1724 | chr18 | 23921039 | |||
chr18:23928228 | G | A | 1 | a0001c0009 | 3 | HG00642.hp2 HG01069.hp1 HG01346.hp2 |
synonymous_variant | LOW | c.3456G>A | p.Ser1152Ser | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 26/38 | 3481/5618 | 3456/5175 | 1152/1724 | chr18 | 23928228 | |||
chr18:23932160 | A | T | 1 | a0016c0024 | 1 | HG02976.hp2 | splice_region_variant&synonymous_variant | LOW | c.3750A>T | p.Gly1250Gly | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 29/38 | 3775/5618 | 3750/5175 | 1250/1724 | chr18 | 23932160 | |||
chr18:23933804 | C | T | 6 | a0002c0002 a0002c0008 a0002c0017 others(3): Show |
66 | HG00140.hp1 HG00558.hp1 HG00609.hp2 others(63): Show |
synonymous_variant | LOW | c.3904C>T | p.Leu1302Leu | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 30/38 | 3929/5618 | 3904/5175 | 1302/1724 | chr18 | 23933804 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr18:23954737 | C | A | 10 | a0001c0001t0002 a0001c0001t0005 a0001c0007t0002 others(7): Show |
83 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(80): Show |
3_prime_UTR_variant | MODIFIER | c.*89C>A | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 38/38 | 89 | chr18 | 23954737 | ||||||
chr18:23954739 | C | T | 10 | a0001c0001t0002 a0001c0001t0005 a0001c0007t0002 others(7): Show |
83 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(80): Show |
3_prime_UTR_variant | MODIFIER | c.*91C>T | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 38/38 | 91 | chr18 | 23954739 | ||||||
chr18:23954774 | A | G | 1 | a0001c0001t0006 | 1 | HG03834.hp1 | 3_prime_UTR_variant | MODIFIER | c.*126A>G | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 38/38 | 126 | chr18 | 23954774 | ||||||
chr18:23954908 | A | G | 1 | a0001c0001t0005 | 1 | HG04199.hp2 | 3_prime_UTR_variant | MODIFIER | c.*260A>G | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 38/38 | 260 | chr18 | 23954908 | ||||||
chr18:23954963 | T | TA | 4 | a0001c0031t0004 a0014c0020t0004 a0018c0034t0004 others(1): Show |
4 | HG02451.hp2 HG02559.hp2 HG03486.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*322dupA | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 38/38 | 323 | INFO_REALIGN_3_PRIME | chr18 | 23954963 | |||||
chr18:23955043 | A | T | 2 | a0002c0002t0003 a0012c0029t0003 |
5 | HG01074.hp1 HG01358.hp2 HG01993.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*395A>T | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 38/38 | 395 | chr18 | 23955043 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr18:23873463 | C | A | 1 | a0001c0006t0001g0020 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.171+248C>A | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 1/37 | chr18 | 23873463 | |||||||
chr18:23873490 | A | G | 1 | a0011c0022t0001g0305 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.171+275A>G | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 1/37 | chr18 | 23873490 | |||||||
chr18:23873494 | C | G | 1 | a0001c0001t0001g0304 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.171+279C>G | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 1/37 | chr18 | 23873494 | |||||||
chr18:23873939 | T | A | 1 | a0016c0024t0001g0021 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.171+724T>A | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 1/37 | chr18 | 23873939 | |||||||
chr18:23874093 | T | C | 4 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0024 others(1): Show |
4 | HG01934.hp2 HG03704.hp2 HG03834.hp2 others(1): Show |
intron_variant | MODIFIER | c.171+878T>C | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 1/37 | chr18 | 23874093 | |||||||
chr18:23874344 | C | T | 69 | a0001c0001t0001g0017 a0001c0001t0001g0022 a0001c0001t0001g0023 others(66): Show |
74 | HG00280.hp2 HG00639.hp2 HG00738.hp1 others(71): Show |
intron_variant | MODIFIER | c.171+1129C>T | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 1/37 | chr18 | 23874344 | |||||||
chr18:23874495 | G | A | 3 | a0001c0007t0002g0027 a0001c0007t0002g0028 a0002c0002t0001g0026 |
3 | HG00099.hp1 HG01346.hp1 HG01981.hp1 |
intron_variant | MODIFIER | c.171+1280G>A | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 1/37 | chr18 | 23874495 | |||||||
chr18:23874525 | G | T | 1 | a0011c0022t0001g0305 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.171+1310G>T | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 1/37 | chr18 | 23874525 | |||||||
chr18:23874581 | A | G | 1 | a0001c0003t0001g0303 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.171+1366A>G | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 1/37 | chr18 | 23874581 | |||||||
chr18:23874867 | T | C | 1 | a0001c0001t0002g0030 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.172-1427T>C | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 1/37 | chr18 | 23874867 | |||||||
chr18:23874948 | C | T | 1 | a0001c0003t0001g0302 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.172-1346C>T | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 1/37 | chr18 | 23874948 | |||||||
chr18:23874967 | G | C | 1 | a0001c0001t0002g0031 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.172-1327G>C | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 1/37 | chr18 | 23874967 | |||||||
chr18:23875025 | G | A | 2 | a0001c0006t0001g0020 a0001c0006t0001g0245 |
2 | HG02258.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.172-1269G>A | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 1/37 | chr18 | 23875025 | |||||||
chr18:23875111 | C | A | 8 | a0001c0001t0002g0032 a0001c0001t0002g0033 a0001c0001t0002g0034 others(5): Show |
8 | HG00423.hp1 NA18953.hp1 NA18957.hp2 others(5): Show |
intron_variant | MODIFIER | c.172-1183C>A | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 1/37 | chr18 | 23875111 | |||||||
chr18:23875140 | T | C | 5 | a0001c0001t0002g0040 a0001c0001t0002g0041 a0001c0001t0002g0042 others(2): Show |
5 | NA18747.hp2 NA18948.hp1 NA18985.hp1 others(2): Show |
intron_variant | MODIFIER | c.172-1154T>C | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 1/37 | chr18 | 23875140 | |||||||
chr18:23875332 | G | T | 1 | a0016c0024t0001g0021 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.172-962G>T | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 1/37 | chr18 | 23875332 | |||||||
chr18:23875389 | T | C | 2 | a0005c0015t0001g0045 a0005c0015t0001g0046 |
2 | HG02572.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.172-905T>C | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 1/37 | chr18 | 23875389 | |||||||
chr18:23875406 | A | G | 1 | a0011c0022t0001g0305 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.172-888A>G | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 1/37 | chr18 | 23875406 | |||||||
chr18:23875467 | A | G | 2 | a0001c0011t0001g0243 a0001c0011t0001g0244 |
2 | HG01168.hp2 HG02735.hp2 |
intron_variant | MODIFIER | c.172-827A>G | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 1/37 | chr18 | 23875467 | |||||||
chr18:23875515 | G | A | 1 | a0001c0001t0001g0047 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.172-779G>A | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 1/37 | chr18 | 23875515 | |||||||
chr18:23875595 | A | G | 241 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(238): Show |
263 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(260): Show |
intron_variant | MODIFIER | c.172-699A>G | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 1/37 | chr18 | 23875595 | |||||||
chr18:23875643 | C | G | 1 | a0016c0024t0001g0021 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.172-651C>G | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 1/37 | chr18 | 23875643 | |||||||
chr18:23875872 | G | A | 1 | a0002c0002t0001g0107 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.172-422G>A | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 1/37 | chr18 | 23875872 | |||||||
chr18:23876068 | C | T | 1 | a0001c0001t0002g0242 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.172-226C>T | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 1/37 | chr18 | 23876068 | |||||||
chr18:23876129 | A | G | 71 | a0001c0001t0001g0017 a0001c0001t0001g0022 a0001c0001t0001g0023 others(68): Show |
76 | HG00280.hp2 HG00639.hp2 HG00738.hp1 others(73): Show |
intron_variant | MODIFIER | c.172-165A>G | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 1/37 | chr18 | 23876129 | |||||||
chr18:23876169 | G | T | 1 | a0024c0026t0004g0301 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.172-125G>T | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 1/37 | chr18 | 23876169 | |||||||
chr18:23876579 | C | T | 1 | a0001c0001t0002g0240 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.285+172C>T | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 2/37 | chr18 | 23876579 | |||||||
chr18:23876780 | T | A | 67 | a0001c0001t0001g0017 a0001c0001t0001g0022 a0001c0001t0001g0023 others(64): Show |
72 | HG00280.hp2 HG00639.hp2 HG00738.hp1 others(69): Show |
intron_variant | MODIFIER | c.285+373T>A | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 2/37 | chr18 | 23876780 | |||||||
chr18:23876814 | C | T | 1 | a0024c0026t0004g0301 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.285+407C>T | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 2/37 | chr18 | 23876814 | |||||||
chr18:23877109 | G | A | 1 | a0001c0001t0001g0246 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.285+702G>A | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 2/37 | chr18 | 23877109 | |||||||
chr18:23877162 | T | A | 2 | a0002c0002t0001g0048 a0002c0002t0001g0049 |
2 | NA18948.hp2 NA18975.hp1 |
intron_variant | MODIFIER | c.285+755T>A | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 2/37 | chr18 | 23877162 | |||||||
chr18:23877319 | T | G | 1 | a0001c0003t0001g0247 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.285+912T>G | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 2/37 | chr18 | 23877319 | |||||||
chr18:23877366 | T | A | 1 | a0001c0001t0002g0108 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.285+959T>A | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 2/37 | chr18 | 23877366 | |||||||
chr18:23877680 | T | C | 1 | a0001c0001t0001g0248 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.285+1273T>C | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 2/37 | chr18 | 23877680 | |||||||
chr18:23877811 | A | G | 2 | a0002c0002t0001g0105 a0020c0028t0001g0106 |
2 | HG02083.hp1 HG04184.hp2 |
intron_variant | MODIFIER | c.285+1404A>G | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 2/37 | chr18 | 23877811 | |||||||
chr18:23877907 | C | T | 1 | a0002c0002t0001g0104 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.285+1500C>T | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 2/37 | chr18 | 23877907 | |||||||
chr18:23877974 | G | A | 149 | a0001c0001t0001g0017 a0001c0001t0001g0022 a0001c0001t0001g0023 others(146): Show |
157 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(154): Show |
intron_variant | MODIFIER | c.285+1567G>A | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 2/37 | chr18 | 23877974 | |||||||
chr18:23878045 | G | A | 20 | a0001c0001t0001g0017 a0001c0001t0001g0022 a0001c0001t0001g0023 others(17): Show |
21 | HG01884.hp1 HG01891.hp1 HG01934.hp2 others(18): Show |
intron_variant | MODIFIER | c.285+1638G>A | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 2/37 | chr18 | 23878045 | |||||||
chr18:23878046 | G | T | 1 | a0001c0003t0001g0019 | 2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.285+1639G>T | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 2/37 | chr18 | 23878046 | |||||||
chr18:23878063 | G | A | 1 | a0001c0003t0001g0303 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.285+1656G>A | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 2/37 | chr18 | 23878063 | |||||||
chr18:23878264 | A | G | 1 | a0016c0024t0001g0021 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.285+1857A>G | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 2/37 | chr18 | 23878264 | |||||||
chr18:23878372 | T | C | 1 | a0001c0001t0001g0249 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.285+1965T>C | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 2/37 | chr18 | 23878372 | |||||||
chr18:23878651 | A | T | 3 | a0001c0001t0001g0237 a0001c0001t0001g0238 a0001c0001t0001g0239 |
3 | NA18964.hp2 NA18995.hp2 NA19011.hp1 |
intron_variant | MODIFIER | c.285+2244A>T | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 2/37 | chr18 | 23878651 | |||||||
chr18:23878760 | A | G | 77 | a0001c0001t0002g0011 a0001c0001t0002g0012 a0001c0001t0002g0013 others(74): Show |
80 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(77): Show |
intron_variant | MODIFIER | c.285+2353A>G | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 2/37 | chr18 | 23878760 | |||||||
chr18:23878917 | A | T | 1 | a0001c0001t0001g0236 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.285+2510A>T | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 2/37 | chr18 | 23878917 | |||||||
chr18:23878932 | C | A | 1 | a0002c0002t0001g0050 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.285+2525C>A | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 2/37 | chr18 | 23878932 | |||||||
chr18:23879012 | C | G | 1 | a0001c0001t0002g0161 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.285+2605C>G | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 2/37 | chr18 | 23879012 | |||||||
chr18:23879182 | C | A | 3 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0024 |
3 | HG01934.hp2 HG03834.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.286-2754C>A | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 2/37 | chr18 | 23879182 | |||||||
chr18:23879213 | C | T | 2 | a0001c0001t0001g0023 a0001c0001t0001g0024 |
2 | HG01934.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.286-2723C>T | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 2/37 | chr18 | 23879213 | |||||||
chr18:23879282 | C | T | 1 | a0006c0010t0001g0235 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.286-2654C>T | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 2/37 | chr18 | 23879282 | |||||||
chr18:23879352 | C | T | 1 | a0001c0001t0001g0047 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.286-2584C>T | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 2/37 | chr18 | 23879352 | |||||||
chr18:23879524 | G | A | 56 | a0001c0001t0001g0017 a0001c0001t0001g0241 a0001c0001t0001g0246 others(53): Show |
61 | HG00280.hp2 HG00639.hp2 HG00738.hp1 others(58): Show |
intron_variant | MODIFIER | c.286-2412G>A | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 2/37 | chr18 | 23879524 | |||||||
chr18:23879842 | C | T | 1 | a0016c0024t0001g0021 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.286-2094C>T | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 2/37 | chr18 | 23879842 | |||||||
chr18:23880171 | A | G | 1 | a0012c0029t0003g0103 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.286-1765A>G | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 2/37 | chr18 | 23880171 | |||||||
chr18:23880393 | T | A | 1 | a0001c0001t0002g0109 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.286-1543T>A | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 2/37 | chr18 | 23880393 | |||||||
chr18:23880490 | G | A | 1 | a0016c0024t0001g0021 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.286-1446G>A | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 2/37 | chr18 | 23880490 | |||||||
chr18:23880551 | C | T | 7 | a0001c0006t0001g0020 a0001c0006t0001g0245 a0001c0006t0001g0296 others(4): Show |
7 | HG02258.hp2 HG02809.hp1 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.286-1385C>T | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 2/37 | chr18 | 23880551 | |||||||
chr18:23880606 | C | T | 1 | a0001c0001t0002g0160 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.286-1330C>T | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 2/37 | chr18 | 23880606 | |||||||
chr18:23880617 | G | A | 1 | a0001c0001t0002g0110 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.286-1319G>A | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 2/37 | chr18 | 23880617 | |||||||
chr18:23880628 | C | T | 1 | a0024c0026t0004g0301 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.286-1308C>T | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 2/37 | chr18 | 23880628 | |||||||
chr18:23880654 | G | A | 32 | a0001c0001t0002g0032 a0001c0003t0001g0006 a0001c0003t0001g0018 others(29): Show |
36 | HG00280.hp2 HG00639.hp2 HG00738.hp1 others(33): Show |
intron_variant | MODIFIER | c.286-1282G>A | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 2/37 | chr18 | 23880654 | |||||||
chr18:23880769 | C | T | 1 | a0001c0001t0001g0234 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.286-1167C>T | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 2/37 | chr18 | 23880769 | |||||||
chr18:23880770 | G | A | 1 | a0024c0026t0004g0301 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.286-1166G>A | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 2/37 | chr18 | 23880770 | |||||||
chr18:23880843 | C | T | 1 | a0001c0001t0002g0159 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.286-1093C>T | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 2/37 | chr18 | 23880843 | |||||||
chr18:23881078 | T | G | 50 | a0001c0001t0001g0002 a0001c0001t0001g0014 a0001c0001t0001g0162 others(47): Show |
56 | HG00423.hp2 HG00438.hp1 HG00558.hp2 others(53): Show |
intron_variant | MODIFIER | c.286-858T>G | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 2/37 | chr18 | 23881078 | |||||||
chr18:23881131 | C | A | 1 | a0001c0003t0001g0289 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.286-805C>A | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 2/37 | chr18 | 23881131 | |||||||
chr18:23881361 | G | T | 1 | a0024c0026t0004g0301 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.286-575G>T | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 2/37 | chr18 | 23881361 | |||||||
chr18:23881417 | C | T | 4 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0024 others(1): Show |
4 | HG01934.hp2 HG03704.hp2 HG03834.hp2 others(1): Show |
intron_variant | MODIFIER | c.286-519C>T | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 2/37 | chr18 | 23881417 | |||||||
chr18:23881477 | T | A | 3 | a0001c0003t0001g0261 a0001c0003t0001g0262 a0001c0003t0001g0263 |
3 | NA18747.hp1 NA18982.hp2 NA18988.hp2 |
intron_variant | MODIFIER | c.286-459T>A | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 2/37 | chr18 | 23881477 | |||||||
chr18:23881557 | C | T | 4 | a0001c0001t0002g0041 a0001c0001t0002g0042 a0001c0001t0002g0043 others(1): Show |
4 | NA18948.hp1 NA18985.hp1 NA19066.hp2 others(1): Show |
intron_variant | MODIFIER | c.286-379C>T | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 2/37 | chr18 | 23881557 | |||||||
chr18:23881612 | G | A | 1 | a0001c0001t0002g0111 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.286-324G>A | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 2/37 | chr18 | 23881612 | |||||||
chr18:23881653 | G | A | 2 | a0005c0015t0001g0045 a0005c0015t0001g0046 |
2 | HG02572.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.286-283G>A | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 2/37 | chr18 | 23881653 | |||||||
chr18:23881681 | G | A | 239 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(236): Show |
261 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(258): Show |
intron_variant | MODIFIER | c.286-255G>A | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 2/37 | chr18 | 23881681 | |||||||
chr18:23882269 | G | A | 1 | a0001c0001t0006g0200 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.395+224G>A | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 3/37 | chr18 | 23882269 | |||||||
chr18:23882352 | G | A | 1 | a0002c0002t0001g0053 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.395+307G>A | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 3/37 | chr18 | 23882352 | |||||||
chr18:23882395 | C | T | 1 | a0001c0001t0001g0047 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.395+350C>T | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 3/37 | chr18 | 23882395 | |||||||
chr18:23882524 | C | A | 1 | a0001c0001t0002g0040 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.395+479C>A | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 3/37 | chr18 | 23882524 | |||||||
chr18:23882609 | TA | T | 68 | a0001c0001t0001g0017 a0001c0001t0001g0022 a0001c0001t0001g0023 others(65): Show |
73 | HG00280.hp2 HG00639.hp2 HG00738.hp1 others(70): Show |
intron_variant | MODIFIER | c.395+580delA | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 3/37 | INFO_REALIGN_3_PRIME | chr18 | 23882609 | ||||||
chr18:23882609 | TAA | T | 11 | a0001c0003t0001g0288 a0001c0003t0001g0289 a0001c0003t0001g0302 others(8): Show |
11 | HG02258.hp2 HG02280.hp2 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.395+579_395+580del others(2): Show |
LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 3/37 | INFO_REALIGN_3_PRIME | chr18 | 23882609 | ||||||
chr18:23882642 | C | T | 1 | a0001c0001t0001g0047 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.395+597C>T | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 3/37 | chr18 | 23882642 | |||||||
chr18:23882678 | T | A | 1 | a0001c0001t0001g0162 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.395+633T>A | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 3/37 | chr18 | 23882678 | |||||||
chr18:23882695 | T | C | 1 | a0002c0002t0001g0054 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.395+650T>C | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 3/37 | chr18 | 23882695 | |||||||
chr18:23882709 | C | T | 76 | a0001c0001t0002g0011 a0001c0001t0002g0012 a0001c0001t0002g0013 others(73): Show |
79 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(76): Show |
intron_variant | MODIFIER | c.395+664C>T | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 3/37 | chr18 | 23882709 | |||||||
chr18:23882781 | G | A | 1 | a0001c0001t0001g0201 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.395+736G>A | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 3/37 | chr18 | 23882781 | |||||||
chr18:23882932 | A | C | 2 | a0001c0001t0002g0158 a0001c0001t0002g0161 |
2 | HG02486.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.395+887A>C | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 3/37 | chr18 | 23882932 | |||||||
chr18:23882962 | T | A | 2 | a0001c0001t0002g0158 a0001c0001t0002g0161 |
2 | HG02486.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.395+917T>A | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 3/37 | chr18 | 23882962 | |||||||
chr18:23883156 | C | T | 3 | a0001c0003t0001g0261 a0001c0003t0001g0262 a0001c0003t0001g0263 |
3 | NA18747.hp1 NA18982.hp2 NA18988.hp2 |
intron_variant | MODIFIER | c.395+1111C>T | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 3/37 | chr18 | 23883156 | |||||||
chr18:23883213 | C | T | 3 | a0001c0001t0001g0228 a0001c0001t0001g0229 a0001c0001t0001g0230 |
3 | HG02135.hp1 NA18944.hp1 NA18969.hp1 |
intron_variant | MODIFIER | c.395+1168C>T | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 3/37 | chr18 | 23883213 | |||||||
chr18:23883216 | T | A | 1 | a0001c0001t0002g0242 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.395+1171T>A | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 3/37 | chr18 | 23883216 | |||||||
chr18:23883304 | C | A | 7 | a0001c0006t0001g0020 a0001c0006t0001g0245 a0001c0006t0001g0296 others(4): Show |
7 | HG02258.hp2 HG02809.hp1 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.395+1259C>A | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 3/37 | chr18 | 23883304 | |||||||
chr18:23883372 | C | T | 2 | a0002c0002t0001g0105 a0020c0028t0001g0106 |
2 | HG02083.hp1 HG04184.hp2 |
intron_variant | MODIFIER | c.395+1327C>T | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 3/37 | chr18 | 23883372 | |||||||
chr18:23883463 | C | T | 1 | a0002c0002t0001g0099 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.396-1310C>T | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 3/37 | chr18 | 23883463 | |||||||
chr18:23883627 | C | T | 1 | a0002c0002t0001g0098 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.396-1146C>T | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 3/37 | chr18 | 23883627 | |||||||
chr18:23883762 | C | A | 60 | a0001c0001t0001g0017 a0001c0001t0001g0241 a0001c0001t0001g0246 others(57): Show |
65 | HG00280.hp2 HG00639.hp2 HG00738.hp1 others(62): Show |
intron_variant | MODIFIER | c.396-1011C>A | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 3/37 | chr18 | 23883762 | |||||||
chr18:23883970 | A | G | 72 | a0001c0001t0001g0017 a0001c0001t0001g0022 a0001c0001t0001g0023 others(69): Show |
77 | HG00280.hp2 HG00639.hp2 HG00738.hp1 others(74): Show |
intron_variant | MODIFIER | c.396-803A>G | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 3/37 | chr18 | 23883970 | |||||||
chr18:23884047 | G | GGTGTGTG others(3): Show |
1 | a0001c0001t0001g0022 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.396-683_396-674dup others(10): Show |
LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 3/37 | INFO_REALIGN_3_PRIME | chr18 | 23884047 | ||||||
chr18:23884047 | GGT | G | 33 | a0001c0001t0001g0163 a0001c0001t0002g0032 a0001c0001t0002g0033 others(30): Show |
33 | HG00099.hp2 HG00735.hp1 HG01099.hp2 others(30): Show |
intron_variant | MODIFIER | c.396-675_396-674del others(2): Show |
LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 3/37 | INFO_REALIGN_3_PRIME | chr18 | 23884047 | ||||||
chr18:23884047 | GGTGT | G | 50 | a0001c0001t0001g0025 a0001c0001t0002g0011 a0001c0001t0002g0012 others(47): Show |
51 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(48): Show |
intron_variant | MODIFIER | c.396-677_396-674del others(4): Show |
LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 3/37 | INFO_REALIGN_3_PRIME | chr18 | 23884047 | ||||||
chr18:23884047 | GGTGTGT | G | 49 | a0001c0001t0002g0030 a0001c0001t0002g0039 a0001c0001t0002g0153 others(46): Show |
54 | HG00558.hp1 HG00609.hp2 HG00642.hp1 others(51): Show |
intron_variant | MODIFIER | c.396-679_396-674del others(6): Show |
LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 3/37 | INFO_REALIGN_3_PRIME | chr18 | 23884047 | ||||||
chr18:23884047 | GGTGTGTG others(1): Show |
G | 8 | a0001c0001t0002g0031 a0001c0001t0002g0156 a0001c0023t0002g0157 others(5): Show |
8 | HG00621.hp2 HG00735.hp2 HG01081.hp2 others(5): Show |
intron_variant | MODIFIER | c.396-681_396-674del others(8): Show |
LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 3/37 | INFO_REALIGN_3_PRIME | chr18 | 23884047 | ||||||
chr18:23884047 | GGTGTGTG others(3): Show |
G | 8 | a0002c0002t0001g0010 a0002c0002t0001g0094 a0002c0002t0001g0095 others(5): Show |
9 | HG01123.hp1 HG02886.hp2 NA18942.hp2 others(6): Show |
intron_variant | MODIFIER | c.396-683_396-674del others(10): Show |
LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 3/37 | INFO_REALIGN_3_PRIME | chr18 | 23884047 | ||||||
chr18:23884047 | GGTGTGTG others(7): Show |
G | 1 | a0011c0022t0001g0305 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.396-687_396-674del others(14): Show |
LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 3/37 | INFO_REALIGN_3_PRIME | chr18 | 23884047 | ||||||
chr18:23884047 | GGTGTGTG others(9): Show |
G | 2 | a0001c0001t0001g0047 a0001c0003t0001g0261 |
2 | HG03831.hp2 NA18747.hp1 |
intron_variant | MODIFIER | c.396-689_396-674del others(16): Show |
LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 3/37 | INFO_REALIGN_3_PRIME | chr18 | 23884047 | ||||||
chr18:23884047 | GGTGTGTG others(11): Show |
G | 47 | a0001c0001t0001g0017 a0001c0001t0001g0202 a0001c0001t0001g0203 others(44): Show |
52 | HG00280.hp2 HG00639.hp2 HG00738.hp1 others(49): Show |
intron_variant | MODIFIER | c.396-691_396-674del others(18): Show |
LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 3/37 | INFO_REALIGN_3_PRIME | chr18 | 23884047 | ||||||
chr18:23884047 | GGTGTGTG others(13): Show |
G | 8 | a0001c0001t0001g0015 a0001c0001t0001g0164 a0001c0001t0001g0165 others(5): Show |
9 | NA18964.hp2 NA18973.hp1 NA18975.hp2 others(6): Show |
intron_variant | MODIFIER | c.396-693_396-674del others(20): Show |
LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 3/37 | INFO_REALIGN_3_PRIME | chr18 | 23884047 | ||||||
chr18:23884047 | GGTGTGTG others(15): Show |
G | 79 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(76): Show |
92 | HG00423.hp2 HG00558.hp2 HG00609.hp1 others(89): Show |
intron_variant | MODIFIER | c.396-695_396-674del others(22): Show |
LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 3/37 | INFO_REALIGN_3_PRIME | chr18 | 23884047 | ||||||
chr18:23884047 | GGTGTGTG others(17): Show |
G | 3 | a0002c0002t0001g0107 a0003c0004t0001g0197 a0003c0004t0001g0198 |
3 | HG00438.hp1 NA18995.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.396-697_396-674del others(24): Show |
LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 3/37 | INFO_REALIGN_3_PRIME | chr18 | 23884047 | ||||||
chr18:23884153 | A | G | 150 | a0001c0001t0001g0017 a0001c0001t0001g0022 a0001c0001t0001g0023 others(147): Show |
158 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(155): Show |
intron_variant | MODIFIER | c.396-620A>G | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 3/37 | chr18 | 23884153 | |||||||
chr18:23884235 | A | G | 4 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0024 others(1): Show |
4 | HG01934.hp2 HG03704.hp2 HG03834.hp2 others(1): Show |
intron_variant | MODIFIER | c.396-538A>G | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 3/37 | chr18 | 23884235 | |||||||
chr18:23884388 | T | G | 12 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0024 others(9): Show |
12 | HG01934.hp2 HG02258.hp2 HG02451.hp2 others(9): Show |
intron_variant | MODIFIER | c.396-385T>G | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 3/37 | chr18 | 23884388 | |||||||
chr18:23884390 | T | C | 1 | a0001c0001t0001g0047 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.396-383T>C | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 3/37 | chr18 | 23884390 | |||||||
chr18:23884760 | G | C | 1 | a0001c0001t0002g0132 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.396-13G>C | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 3/37 | chr18 | 23884760 | |||||||
chr18:23884875 | C | T | 1 | a0001c0001t0002g0112 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.476+22C>T | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 4/37 | chr18 | 23884875 | |||||||
chr18:23884941 | G | C | 1 | a0001c0001t0002g0158 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.476+88G>C | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 4/37 | chr18 | 23884941 | |||||||
chr18:23885191 | C | A | 2 | a0006c0010t0001g0205 a0006c0010t0001g0206 |
2 | HG02615.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.476+338C>A | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 4/37 | chr18 | 23885191 | |||||||
chr18:23885287 | C | T | 1 | a0001c0001t0002g0036 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.476+434C>T | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 4/37 | chr18 | 23885287 | |||||||
chr18:23885316 | T | C | 1 | a0001c0001t0002g0133 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.476+463T>C | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 4/37 | chr18 | 23885316 | |||||||
chr18:23885330 | A | AC | 11 | a0001c0001t0001g0047 a0001c0001t0001g0196 a0001c0001t0001g0227 others(8): Show |
11 | HG01099.hp2 HG02109.hp2 HG02257.hp1 others(8): Show |
intron_variant | MODIFIER | c.476+484dupC | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 4/37 | INFO_REALIGN_3_PRIME | chr18 | 23885330 | ||||||
chr18:23885365 | C | G | 1 | a0001c0003t0001g0295 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.476+512C>G | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 4/37 | chr18 | 23885365 | |||||||
chr18:23885463 | G | A | 1 | a0002c0002t0001g0101 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.476+610G>A | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 4/37 | chr18 | 23885463 | |||||||
chr18:23885576 | A | C | 1 | a0011c0022t0001g0305 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.476+723A>C | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 4/37 | chr18 | 23885576 | |||||||
chr18:23885705 | A | G | 12 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0024 others(9): Show |
12 | HG01934.hp2 HG02258.hp2 HG02451.hp2 others(9): Show |
intron_variant | MODIFIER | c.476+852A>G | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 4/37 | chr18 | 23885705 | |||||||
chr18:23885739 | T | C | 1 | a0011c0022t0001g0305 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.476+886T>C | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 4/37 | chr18 | 23885739 | |||||||
chr18:23885775 | C | T | 5 | a0001c0003t0001g0284 a0001c0003t0001g0285 a0001c0003t0001g0286 others(2): Show |
5 | HG02622.hp2 HG02965.hp1 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.476+922C>T | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 4/37 | chr18 | 23885775 | |||||||
chr18:23885828 | G | A | 1 | a0001c0003t0001g0295 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.476+975G>A | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 4/37 | chr18 | 23885828 | |||||||
chr18:23885875 | A | G | 1 | a0001c0003t0001g0263 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.476+1022A>G | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 4/37 | chr18 | 23885875 | |||||||
chr18:23885989 | A | G | 1 | a0011c0022t0001g0305 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.476+1136A>G | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 4/37 | chr18 | 23885989 | |||||||
chr18:23886253 | C | T | 1 | a0016c0024t0001g0021 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.476+1400C>T | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 4/37 | chr18 | 23886253 | |||||||
chr18:23886293 | G | A | 6 | a0001c0001t0002g0119 a0001c0001t0002g0120 a0001c0001t0002g0121 others(3): Show |
6 | HG01167.hp2 HG02486.hp2 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.476+1440G>A | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 4/37 | chr18 | 23886293 | |||||||
chr18:23886351 | T | G | 78 | a0001c0001t0002g0011 a0001c0001t0002g0012 a0001c0001t0002g0013 others(75): Show |
81 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(78): Show |
intron_variant | MODIFIER | c.476+1498T>G | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 4/37 | chr18 | 23886351 | |||||||
chr18:23886625 | G | GA | 7 | a0001c0001t0001g0166 a0001c0003t0001g0250 a0001c0003t0001g0251 others(4): Show |
7 | HG01109.hp1 HG02071.hp2 HG03041.hp2 others(4): Show |
intron_variant | MODIFIER | c.476+1782dupA | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 4/37 | INFO_REALIGN_3_PRIME | chr18 | 23886625 | ||||||
chr18:23887071 | C | G | 13 | a0001c0001t0001g0017 a0001c0001t0001g0241 a0001c0001t0001g0246 others(10): Show |
14 | HG01884.hp1 HG01891.hp1 HG02109.hp2 others(11): Show |
intron_variant | MODIFIER | c.476+2218C>G | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 4/37 | chr18 | 23887071 | |||||||
chr18:23887311 | G | A | 2 | a0002c0017t0001g0068 a0002c0017t0001g0069 |
2 | HG00609.hp2 NA18960.hp1 |
intron_variant | MODIFIER | c.476+2458G>A | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 4/37 | chr18 | 23887311 | |||||||
chr18:23887428 | G | A | 1 | a0001c0003t0001g0264 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.476+2575G>A | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 4/37 | chr18 | 23887428 | |||||||
chr18:23887653 | A | G | 13 | a0001c0001t0001g0017 a0001c0001t0001g0241 a0001c0001t0001g0246 others(10): Show |
14 | HG01884.hp1 HG01891.hp1 HG02109.hp2 others(11): Show |
intron_variant | MODIFIER | c.477-2358A>G | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 4/37 | chr18 | 23887653 | |||||||
chr18:23887701 | T | C | 1 | a0001c0003t0001g0302 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.477-2310T>C | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 4/37 | chr18 | 23887701 | |||||||
chr18:23887729 | A | G | 78 | a0001c0001t0002g0011 a0001c0001t0002g0012 a0001c0001t0002g0013 others(75): Show |
81 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(78): Show |
intron_variant | MODIFIER | c.477-2282A>G | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 4/37 | chr18 | 23887729 | |||||||
chr18:23887754 | G | A | 1 | a0014c0020t0004g0233 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.477-2257G>A | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 4/37 | chr18 | 23887754 | |||||||
chr18:23887808 | A | G | 1 | a0001c0001t0001g0204 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.477-2203A>G | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 4/37 | chr18 | 23887808 | |||||||
chr18:23887865 | G | A | 1 | a0014c0020t0004g0233 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.477-2146G>A | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 4/37 | chr18 | 23887865 | |||||||
chr18:23888033 | G | C | 1 | a0001c0001t0001g0207 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.477-1978G>C | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 4/37 | chr18 | 23888033 | |||||||
chr18:23888067 | G | A | 1 | a0011c0022t0001g0305 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.477-1944G>A | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 4/37 | chr18 | 23888067 | |||||||
chr18:23888092 | A | C | 1 | a0011c0022t0001g0305 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.477-1919A>C | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 4/37 | chr18 | 23888092 | |||||||
chr18:23888107 | C | T | 2 | a0002c0002t0001g0105 a0020c0028t0001g0106 |
2 | HG02083.hp1 HG04184.hp2 |
intron_variant | MODIFIER | c.477-1904C>T | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 4/37 | chr18 | 23888107 | |||||||
chr18:23888276 | A | C | 1 | a0007c0012t0001g0225 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.477-1735A>C | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 4/37 | chr18 | 23888276 | |||||||
chr18:23888511 | T | A | 1 | a0001c0001t0002g0033 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.477-1500T>A | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 4/37 | chr18 | 23888511 | |||||||
chr18:23888544 | G | T | 3 | a0001c0001t0001g0195 a0001c0007t0001g0051 a0001c0007t0001g0052 |
3 | NA18991.hp1 NA18991.hp2 NA19074.hp1 |
intron_variant | MODIFIER | c.477-1467G>T | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 4/37 | chr18 | 23888544 | |||||||
chr18:23888788 | T | A | 5 | a0001c0003t0001g0250 a0001c0003t0001g0251 a0001c0003t0001g0252 others(2): Show |
5 | HG01109.hp1 HG03041.hp2 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.477-1223T>A | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 4/37 | chr18 | 23888788 | |||||||
chr18:23888938 | T | A | 1 | a0001c0001t0001g0047 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.477-1073T>A | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 4/37 | chr18 | 23888938 | |||||||
chr18:23888938 | T | TA | 48 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0024 others(45): Show |
53 | HG00280.hp2 HG00639.hp1 HG00639.hp2 others(50): Show |
intron_variant | MODIFIER | c.477-1058dupA | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 4/37 | INFO_REALIGN_3_PRIME | chr18 | 23888938 | ||||||
chr18:23888938 | T | TAA | 82 | a0001c0001t0002g0011 a0001c0001t0002g0012 a0001c0001t0002g0030 others(79): Show |
84 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(81): Show |
intron_variant | MODIFIER | c.477-1059_477-1058d others(4): Show |
LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 4/37 | INFO_REALIGN_3_PRIME | chr18 | 23888938 | ||||||
chr18:23889179 | G | A | 1 | a0014c0020t0004g0233 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.477-832G>A | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 4/37 | chr18 | 23889179 | |||||||
chr18:23889281 | A | G | 71 | a0001c0001t0001g0017 a0001c0001t0001g0022 a0001c0001t0001g0023 others(68): Show |
76 | HG00280.hp2 HG00639.hp2 HG00738.hp1 others(73): Show |
intron_variant | MODIFIER | c.477-730A>G | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 4/37 | chr18 | 23889281 | |||||||
chr18:23889342 | G | T | 4 | a0001c0003t0001g0289 a0001c0003t0001g0302 a0001c0031t0004g0292 others(1): Show |
4 | HG02280.hp2 HG02559.hp2 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.477-669G>T | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 4/37 | chr18 | 23889342 | |||||||
chr18:23889351 | C | A | 1 | a0024c0026t0004g0301 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.477-660C>A | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 4/37 | chr18 | 23889351 | |||||||
chr18:23889597 | A | G | 4 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0024 others(1): Show |
4 | HG01934.hp2 HG03704.hp2 HG03834.hp2 others(1): Show |
intron_variant | MODIFIER | c.477-414A>G | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 4/37 | chr18 | 23889597 | |||||||
chr18:23889664 | A | AG | 12 | a0001c0001t0002g0155 a0001c0003t0001g0262 a0001c0003t0001g0273 others(9): Show |
12 | HG01109.hp1 HG01496.hp1 HG01928.hp1 others(9): Show |
intron_variant | MODIFIER | c.477-341dupG | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 4/37 | INFO_REALIGN_3_PRIME | chr18 | 23889664 | ||||||
chr18:23889674 | GAGGA | G | 6 | a0001c0001t0001g0224 a0001c0001t0001g0238 a0001c0001t0001g0239 others(3): Show |
6 | HG01884.hp1 HG01891.hp1 HG02145.hp1 others(3): Show |
intron_variant | MODIFIER | c.477-317_477-314del others(4): Show |
LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 4/37 | INFO_REALIGN_3_PRIME | chr18 | 23889674 | ||||||
chr18:23889678 | A | G | 44 | a0001c0003t0001g0006 a0001c0003t0001g0018 a0001c0003t0001g0019 others(41): Show |
48 | HG00280.hp2 HG00639.hp2 HG00738.hp1 others(45): Show |
intron_variant | MODIFIER | c.477-333A>G | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 4/37 | chr18 | 23889678 | |||||||
chr18:23889689 | GAAGGAAG others(29): Show |
G | 2 | a0006c0010t0001g0205 a0006c0010t0001g0206 |
2 | HG02615.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.477-313_477-278del others(36): Show |
LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 4/37 | INFO_REALIGN_3_PRIME | chr18 | 23889689 | ||||||
chr18:23889690 | AAGGAAGG others(5): Show |
A | 9 | a0001c0006t0001g0296 a0002c0002t0001g0010 a0002c0002t0001g0050 others(6): Show |
9 | HG00621.hp2 HG02809.hp1 NA18942.hp2 others(6): Show |
intron_variant | MODIFIER | c.477-309_477-298del others(12): Show |
LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 4/37 | INFO_REALIGN_3_PRIME | chr18 | 23889690 | ||||||
chr18:23889698 | GAGGGAGG others(1): Show |
G | 89 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0024 others(86): Show |
92 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(89): Show |
intron_variant | MODIFIER | c.477-301_477-294del others(8): Show |
LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 4/37 | INFO_REALIGN_3_PRIME | chr18 | 23889698 | ||||||
chr18:23889706 | A | G | 1 | a0001c0006t0001g0296 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.477-305A>G | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 4/37 | chr18 | 23889706 | |||||||
chr18:23889710 | G | A | 8 | a0001c0001t0001g0017 a0001c0001t0001g0241 a0001c0001t0001g0249 others(5): Show |
9 | HG01884.hp1 HG01891.hp1 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.477-301G>A | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 4/37 | chr18 | 23889710 | |||||||
chr18:23889717 | G | A | 1 | a0001c0001t0002g0033 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.477-294G>A | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 4/37 | chr18 | 23889717 | |||||||
chr18:23889717 | GAAGGAAG others(1): Show |
G | 49 | a0001c0001t0002g0119 a0001c0001t0002g0120 a0001c0001t0002g0121 others(46): Show |
53 | HG00280.hp2 HG00639.hp2 HG00738.hp1 others(50): Show |
intron_variant | MODIFIER | c.477-286_477-279del others(8): Show |
LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 4/37 | INFO_REALIGN_3_PRIME | chr18 | 23889717 | ||||||
chr18:23889865 | G | A | 1 | a0001c0006t0001g0245 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.477-146G>A | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 4/37 | chr18 | 23889865 | |||||||
chr18:23890190 | C | T | 14 | a0001c0001t0001g0017 a0001c0001t0001g0241 a0001c0001t0001g0246 others(11): Show |
15 | HG01884.hp1 HG01891.hp1 HG02109.hp2 others(12): Show |
intron_variant | MODIFIER | c.583+73C>T | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 5/37 | chr18 | 23890190 | |||||||
chr18:23890225 | C | T | 7 | a0001c0001t0001g0017 a0001c0001t0001g0241 a0001c0001t0001g0249 others(4): Show |
8 | HG01884.hp1 HG01891.hp1 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.583+108C>T | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 5/37 | chr18 | 23890225 | |||||||
chr18:23890234 | T | A | 7 | a0001c0001t0001g0207 a0001c0001t0001g0208 a0001c0001t0001g0209 others(4): Show |
7 | HG02258.hp1 HG02451.hp1 HG03195.hp2 others(4): Show |
intron_variant | MODIFIER | c.583+117T>A | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 5/37 | chr18 | 23890234 | |||||||
chr18:23890360 | T | A | 97 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0024 others(94): Show |
100 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(97): Show |
intron_variant | MODIFIER | c.583+243T>A | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 5/37 | chr18 | 23890360 | |||||||
chr18:23890643 | C | T | 1 | a0001c0003t0001g0289 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.583+526C>T | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 5/37 | chr18 | 23890643 | |||||||
chr18:23890648 | C | T | 1 | a0001c0006t0001g0299 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.583+531C>T | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 5/37 | chr18 | 23890648 | |||||||
chr18:23890689 | C | T | 1 | a0024c0026t0004g0301 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.583+572C>T | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 5/37 | chr18 | 23890689 | |||||||
chr18:23890773 | A | T | 1 | a0001c0001t0002g0067 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.583+656A>T | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 5/37 | chr18 | 23890773 | |||||||
chr18:23891051 | G | A | 43 | a0001c0003t0001g0006 a0001c0003t0001g0018 a0001c0003t0001g0019 others(40): Show |
47 | HG00280.hp2 HG00639.hp2 HG00738.hp1 others(44): Show |
intron_variant | MODIFIER | c.583+934G>A | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 5/37 | chr18 | 23891051 | |||||||
chr18:23891245 | G | A | 1 | a0016c0024t0001g0021 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.583+1128G>A | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 5/37 | chr18 | 23891245 | |||||||
chr18:23891422 | G | T | 4 | a0002c0002t0001g0066 a0002c0002t0001g0089 a0002c0017t0001g0068 others(1): Show |
4 | HG00609.hp2 NA18951.hp2 NA18960.hp1 others(1): Show |
intron_variant | MODIFIER | c.583+1305G>T | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 5/37 | chr18 | 23891422 | |||||||
chr18:23891515 | T | G | 1 | a0001c0003t0001g0247 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.583+1398T>G | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 5/37 | chr18 | 23891515 | |||||||
chr18:23891677 | C | A | 2 | a0007c0012t0001g0225 a0007c0012t0001g0226 |
2 | HG02257.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.583+1560C>A | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 5/37 | chr18 | 23891677 | |||||||
chr18:23891679 | T | C | 1 | a0001c0001t0001g0016 | 2 | HG01515.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.583+1562T>C | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 5/37 | chr18 | 23891679 | |||||||
chr18:23891739 | T | G | 1 | a0001c0001t0001g0224 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.583+1622T>G | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 5/37 | chr18 | 23891739 | |||||||
chr18:23891759 | G | A | 2 | a0001c0003t0001g0289 a0001c0003t0001g0302 |
2 | HG02280.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.583+1642G>A | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 5/37 | chr18 | 23891759 | |||||||
chr18:23891804 | C | T | 71 | a0001c0001t0001g0017 a0001c0001t0001g0022 a0001c0001t0001g0023 others(68): Show |
76 | HG00280.hp2 HG00639.hp2 HG00738.hp1 others(73): Show |
intron_variant | MODIFIER | c.583+1687C>T | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 5/37 | chr18 | 23891804 | |||||||
chr18:23891830 | C | G | 1 | a0001c0025t0002g0146 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.583+1713C>G | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 5/37 | chr18 | 23891830 | |||||||
chr18:23892047 | TCTGAGAC others(13): Show |
T | 1 | a0001c0003t0001g0280 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.583+1933_583+1952d others(22): Show |
LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 5/37 | INFO_REALIGN_3_PRIME | chr18 | 23892047 | ||||||
chr18:23892109 | A | G | 2 | a0002c0002t0001g0066 a0002c0002t0001g0089 |
2 | NA18951.hp2 NA19084.hp2 |
intron_variant | MODIFIER | c.583+1992A>G | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 5/37 | chr18 | 23892109 | |||||||
chr18:23892211 | C | G | 1 | a0022c0018t0001g0194 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.584-2087C>G | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 5/37 | chr18 | 23892211 | |||||||
chr18:23892320 | T | A | 14 | a0001c0001t0001g0017 a0001c0001t0001g0241 a0001c0001t0001g0246 others(11): Show |
15 | HG01884.hp1 HG01891.hp1 HG02109.hp2 others(12): Show |
intron_variant | MODIFIER | c.584-1978T>A | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 5/37 | chr18 | 23892320 | |||||||
chr18:23892488 | C | G | 43 | a0001c0003t0001g0006 a0001c0003t0001g0018 a0001c0003t0001g0019 others(40): Show |
47 | HG00280.hp2 HG00639.hp2 HG00738.hp1 others(44): Show |
intron_variant | MODIFIER | c.584-1810C>G | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 5/37 | chr18 | 23892488 | |||||||
chr18:23892630 | T | C | 1 | a0002c0002t0001g0094 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.584-1668T>C | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 5/37 | chr18 | 23892630 | |||||||
chr18:23892679 | G | T | 1 | a0002c0002t0001g0060 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.584-1619G>T | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 5/37 | chr18 | 23892679 | |||||||
chr18:23892725 | A | C | 4 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0024 others(1): Show |
4 | HG01934.hp2 HG03704.hp2 HG03834.hp2 others(1): Show |
intron_variant | MODIFIER | c.584-1573A>C | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 5/37 | chr18 | 23892725 | |||||||
chr18:23892781 | T | C | 1 | a0001c0001t0002g0134 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.584-1517T>C | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 5/37 | chr18 | 23892781 | |||||||
chr18:23892795 | T | C | 244 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(241): Show |
266 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(263): Show |
intron_variant | MODIFIER | c.584-1503T>C | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 5/37 | chr18 | 23892795 | |||||||
chr18:23892796 | G | A | 1 | a0001c0027t0001g0167 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.584-1502G>A | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 5/37 | chr18 | 23892796 | |||||||
chr18:23892830 | G | C | 2 | a0005c0015t0001g0045 a0005c0015t0001g0046 |
2 | HG02572.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.584-1468G>C | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 5/37 | chr18 | 23892830 | |||||||
chr18:23892862 | C | T | 1 | a0011c0022t0001g0305 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.584-1436C>T | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 5/37 | chr18 | 23892862 | |||||||
chr18:23892903 | C | CA | 121 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(118): Show |
135 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(132): Show |
intron_variant | MODIFIER | c.584-1376dupA | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 5/37 | INFO_REALIGN_3_PRIME | chr18 | 23892903 | ||||||
chr18:23892903 | C | CAA | 6 | a0001c0001t0001g0015 a0001c0001t0001g0166 a0001c0001t0001g0168 others(3): Show |
7 | HG01891.hp1 HG02071.hp2 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.584-1377_584-1376d others(4): Show |
LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 5/37 | INFO_REALIGN_3_PRIME | chr18 | 23892903 | ||||||
chr18:23893155 | T | C | 7 | a0001c0006t0001g0020 a0001c0006t0001g0245 a0001c0006t0001g0296 others(4): Show |
7 | HG02258.hp2 HG02809.hp1 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.584-1143T>C | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 5/37 | chr18 | 23893155 | |||||||
chr18:23893275 | A | G | 14 | a0001c0001t0001g0017 a0001c0001t0001g0241 a0001c0001t0001g0246 others(11): Show |
15 | HG01884.hp1 HG01891.hp1 HG02109.hp2 others(12): Show |
intron_variant | MODIFIER | c.584-1023A>G | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 5/37 | chr18 | 23893275 | |||||||
chr18:23893550 | T | C | 1 | a0001c0003t0001g0295 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.584-748T>C | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 5/37 | chr18 | 23893550 | |||||||
chr18:23893569 | T | C | 1 | a0001c0001t0002g0113 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.584-729T>C | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 5/37 | chr18 | 23893569 | |||||||
chr18:23893576 | C | T | 1 | a0002c0002t0001g0088 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.584-722C>T | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 5/37 | chr18 | 23893576 | |||||||
chr18:23893657 | A | G | 73 | a0001c0001t0001g0017 a0001c0001t0001g0022 a0001c0001t0001g0023 others(70): Show |
78 | HG00280.hp2 HG00639.hp2 HG00738.hp1 others(75): Show |
intron_variant | MODIFIER | c.584-641A>G | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 5/37 | chr18 | 23893657 | |||||||
chr18:23893706 | G | A | 1 | a0007c0012t0001g0225 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.584-592G>A | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 5/37 | chr18 | 23893706 | |||||||
chr18:23893803 | T | C | 243 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(240): Show |
265 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(262): Show |
intron_variant | MODIFIER | c.584-495T>C | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 5/37 | chr18 | 23893803 | |||||||
chr18:23893913 | C | T | 44 | a0001c0003t0001g0006 a0001c0003t0001g0018 a0001c0003t0001g0019 others(41): Show |
48 | HG00280.hp2 HG00639.hp2 HG00738.hp1 others(45): Show |
intron_variant | MODIFIER | c.584-385C>T | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 5/37 | chr18 | 23893913 | |||||||
chr18:23893999 | G | A | 78 | a0001c0001t0002g0011 a0001c0001t0002g0012 a0001c0001t0002g0013 others(75): Show |
81 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(78): Show |
intron_variant | MODIFIER | c.584-299G>A | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 5/37 | chr18 | 23893999 | |||||||
chr18:23894406 | T | A | 1 | a0001c0001t0005g0137 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.634+58T>A | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 6/37 | chr18 | 23894406 | |||||||
chr18:23894601 | G | A | 250 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(247): Show |
272 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(269): Show |
intron_variant | MODIFIER | c.634+253G>A | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 6/37 | chr18 | 23894601 | |||||||
chr18:23894785 | G | T | 1 | a0002c0002t0001g0090 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.635-122G>T | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 6/37 | chr18 | 23894785 | |||||||
chr18:23894796 | C | T | 1 | a0016c0024t0001g0021 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.635-111C>T | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 6/37 | chr18 | 23894796 | |||||||
chr18:23894863 | G | A | 65 | a0001c0007t0001g0051 a0001c0007t0001g0052 a0001c0007t0002g0027 others(62): Show |
69 | HG00099.hp1 HG00140.hp1 HG00558.hp1 others(66): Show |
intron_variant | MODIFIER | c.635-44G>A | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 6/37 | chr18 | 23894863 | |||||||
chr18:23895189 | G | A | 6 | a0001c0007t0002g0027 a0001c0007t0002g0028 a0002c0002t0001g0026 others(3): Show |
6 | HG00099.hp1 HG00140.hp1 HG01168.hp1 others(3): Show |
intron_variant | MODIFIER | c.786+131G>A | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 7/37 | chr18 | 23895189 | |||||||
chr18:23895595 | T | G | 65 | a0001c0007t0001g0051 a0001c0007t0001g0052 a0001c0007t0002g0027 others(62): Show |
69 | HG00099.hp1 HG00140.hp1 HG00558.hp1 others(66): Show |
intron_variant | MODIFIER | c.786+537T>G | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 7/37 | chr18 | 23895595 | |||||||
chr18:23895680 | G | A | 64 | a0001c0007t0001g0051 a0001c0007t0001g0052 a0001c0007t0002g0027 others(61): Show |
68 | HG00099.hp1 HG00140.hp1 HG00558.hp1 others(65): Show |
intron_variant | MODIFIER | c.786+622G>A | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 7/37 | chr18 | 23895680 | |||||||
chr18:23895802 | T | A | 1 | a0001c0003t0001g0295 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.786+744T>A | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 7/37 | chr18 | 23895802 | |||||||
chr18:23896054 | G | C | 4 | a0001c0001t0002g0032 a0001c0001t0002g0034 a0001c0001t0002g0036 others(1): Show |
4 | NA18953.hp1 NA18983.hp1 NA19011.hp2 others(1): Show |
intron_variant | MODIFIER | c.786+996G>C | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 7/37 | chr18 | 23896054 | |||||||
chr18:23896152 | A | G | 1 | a0002c0002t0001g0100 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.786+1094A>G | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 7/37 | chr18 | 23896152 | |||||||
chr18:23896344 | A | G | 1 | a0001c0003t0001g0295 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.786+1286A>G | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 7/37 | chr18 | 23896344 | |||||||
chr18:23896698 | A | T | 8 | a0001c0001t0002g0031 a0001c0001t0002g0112 a0001c0001t0002g0127 others(5): Show |
8 | HG00140.hp2 HG00735.hp2 HG01099.hp2 others(5): Show |
intron_variant | MODIFIER | c.786+1640A>T | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 7/37 | chr18 | 23896698 | |||||||
chr18:23896911 | C | T | 13 | a0001c0001t0001g0017 a0001c0001t0001g0241 a0001c0001t0001g0246 others(10): Show |
14 | HG01884.hp1 HG01891.hp1 HG02109.hp2 others(11): Show |
intron_variant | MODIFIER | c.787-1827C>T | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 7/37 | chr18 | 23896911 | |||||||
chr18:23896916 | C | T | 44 | a0001c0001t0002g0117 a0001c0003t0001g0006 a0001c0003t0001g0018 others(41): Show |
48 | HG00280.hp2 HG00639.hp2 HG00738.hp1 others(45): Show |
intron_variant | MODIFIER | c.787-1822C>T | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 7/37 | chr18 | 23896916 | |||||||
chr18:23896965 | C | G | 1 | a0002c0002t0001g0281 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.787-1773C>G | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 7/37 | chr18 | 23896965 | |||||||
chr18:23896982 | T | C | 233 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(230): Show |
254 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(251): Show |
intron_variant | MODIFIER | c.787-1756T>C | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 7/37 | chr18 | 23896982 | |||||||
chr18:23897406 | T | C | 1 | a0011c0022t0001g0305 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.787-1332T>C | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 7/37 | chr18 | 23897406 | |||||||
chr18:23897408 | A | G | 1 | a0017c0036t0001g0290 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.787-1330A>G | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 7/37 | chr18 | 23897408 | |||||||
chr18:23897618 | G | T | 59 | a0001c0001t0001g0017 a0001c0001t0001g0241 a0001c0001t0001g0246 others(56): Show |
64 | HG00280.hp2 HG00639.hp2 HG00738.hp1 others(61): Show |
intron_variant | MODIFIER | c.787-1120G>T | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 7/37 | chr18 | 23897618 | |||||||
chr18:23897673 | T | G | 1 | a0002c0002t0001g0099 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.787-1065T>G | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 7/37 | chr18 | 23897673 | |||||||
chr18:23897674 | C | T | 1 | a0002c0002t0001g0099 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.787-1064C>T | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 7/37 | chr18 | 23897674 | |||||||
chr18:23897760 | A | C | 4 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0024 others(1): Show |
4 | HG01934.hp2 HG03704.hp2 HG03834.hp2 others(1): Show |
intron_variant | MODIFIER | c.787-978A>C | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 7/37 | chr18 | 23897760 | |||||||
chr18:23897825 | T | C | 1 | a0001c0001t0001g0164 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.787-913T>C | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 7/37 | chr18 | 23897825 | |||||||
chr18:23897845 | A | T | 292 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(289): Show |
318 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(315): Show |
intron_variant | MODIFIER | c.787-893A>T | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 7/37 | chr18 | 23897845 | |||||||
chr18:23898073 | ACT | A | 47 | a0001c0001t0001g0002 a0001c0001t0001g0014 a0001c0001t0001g0015 others(44): Show |
54 | HG00423.hp2 HG00438.hp1 HG00558.hp2 others(51): Show |
intron_variant | MODIFIER | c.787-664_787-663del others(2): Show |
LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 7/37 | chr18 | 23898073 | |||||||
chr18:23898116 | C | T | 292 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(289): Show |
318 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(315): Show |
intron_variant | MODIFIER | c.787-622C>T | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 7/37 | chr18 | 23898116 | |||||||
chr18:23898323 | C | T | 1 | a0001c0027t0001g0167 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.787-415C>T | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 7/37 | chr18 | 23898323 | |||||||
chr18:23898539 | A | G | 1 | a0002c0002t0001g0056 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.787-199A>G | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 7/37 | chr18 | 23898539 | |||||||
chr18:23898552 | G | T | 1 | a0001c0001t0001g0190 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.787-186G>T | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 7/37 | chr18 | 23898552 | |||||||
chr18:23898569 | A | G | 5 | a0002c0002t0003g0064 a0002c0002t0003g0065 a0002c0002t0003g0086 others(2): Show |
5 | HG01074.hp1 HG01358.hp2 HG01993.hp1 others(2): Show |
intron_variant | MODIFIER | c.787-169A>G | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 7/37 | chr18 | 23898569 | |||||||
chr18:23898590 | G | A | 1 | a0001c0003t0001g0303 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.787-148G>A | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 7/37 | chr18 | 23898590 | |||||||
chr18:23898597 | A | G | 2 | a0001c0001t0002g0134 a0001c0001t0002g0145 |
2 | HG01928.hp2 HG02300.hp1 |
intron_variant | MODIFIER | c.787-141A>G | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 7/37 | chr18 | 23898597 | |||||||
chr18:23898926 | G | C | 2 | a0005c0015t0001g0045 a0005c0015t0001g0046 |
2 | HG02572.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.898-28G>C | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 8/37 | chr18 | 23898926 | |||||||
chr18:23899544 | A | G | 3 | a0002c0002t0001g0008 a0002c0002t0001g0009 a0002c0002t0001g0070 |
5 | HG00558.hp1 HG00673.hp2 NA18944.hp2 others(2): Show |
intron_variant | MODIFIER | c.1177+89A>G | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 10/37 | chr18 | 23899544 | |||||||
chr18:23899825 | A | G | 1 | a0017c0036t0001g0290 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1177+370A>G | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 10/37 | chr18 | 23899825 | |||||||
chr18:23899922 | G | A | 1 | a0001c0003t0001g0288 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.1177+467G>A | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 10/37 | chr18 | 23899922 | |||||||
chr18:23899947 | G | A | 1 | a0006c0010t0001g0205 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1177+492G>A | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 10/37 | chr18 | 23899947 | |||||||
chr18:23900070 | C | CGT | 156 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(153): Show |
174 | HG00099.hp1 HG00140.hp1 HG00423.hp2 others(171): Show |
intron_variant | MODIFIER | c.1177+630_1177+631d others(4): Show |
LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 10/37 | INFO_REALIGN_3_PRIME | chr18 | 23900070 | ||||||
chr18:23900070 | C | CGTGT | 76 | a0001c0001t0002g0011 a0001c0001t0002g0012 a0001c0001t0002g0013 others(73): Show |
79 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(76): Show |
intron_variant | MODIFIER | c.1177+628_1177+631d others(6): Show |
LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 10/37 | INFO_REALIGN_3_PRIME | chr18 | 23900070 | ||||||
chr18:23900070 | C | T | 1 | a0001c0001t0002g0124 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1177+615C>T | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 10/37 | chr18 | 23900070 | |||||||
chr18:23900173 | C | T | 7 | a0001c0006t0001g0020 a0001c0006t0001g0245 a0001c0006t0001g0296 others(4): Show |
7 | HG02258.hp2 HG02809.hp1 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.1177+718C>T | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 10/37 | chr18 | 23900173 | |||||||
chr18:23900360 | C | T | 1 | a0016c0024t0001g0021 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1178-767C>T | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 10/37 | chr18 | 23900360 | |||||||
chr18:23900397 | T | C | 3 | a0001c0001t0001g0208 a0001c0001t0001g0209 a0001c0001t0001g0210 |
3 | HG03540.hp1 NA18522.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1178-730T>C | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 10/37 | chr18 | 23900397 | |||||||
chr18:23900510 | G | A | 13 | a0001c0001t0001g0017 a0001c0001t0001g0241 a0001c0001t0001g0246 others(10): Show |
14 | HG01884.hp1 HG01891.hp1 HG02109.hp2 others(11): Show |
intron_variant | MODIFIER | c.1178-617G>A | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 10/37 | chr18 | 23900510 | |||||||
chr18:23900705 | G | T | 2 | a0005c0015t0001g0045 a0005c0015t0001g0046 |
2 | HG02572.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.1178-422G>T | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 10/37 | chr18 | 23900705 | |||||||
chr18:23900775 | G | C | 1 | a0001c0001t0001g0204 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1178-352G>C | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 10/37 | chr18 | 23900775 | |||||||
chr18:23901376 | A | G | 154 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(151): Show |
172 | HG00099.hp1 HG00423.hp2 HG00438.hp1 others(169): Show |
intron_variant | MODIFIER | c.1374+53A>G | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 11/37 | chr18 | 23901376 | |||||||
chr18:23901914 | G | A | 2 | a0001c0001t0001g0254 a0001c0011t0001g0253 |
2 | HG03130.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.1374+591G>A | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 11/37 | chr18 | 23901914 | |||||||
chr18:23901992 | C | G | 1 | a0001c0001t0002g0118 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.1374+669C>G | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 11/37 | chr18 | 23901992 | |||||||
chr18:23902089 | A | T | 2 | a0014c0020t0004g0233 a0024c0026t0004g0301 |
2 | HG02451.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1374+766A>T | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 11/37 | chr18 | 23902089 | |||||||
chr18:23902167 | T | A | 1 | a0001c0001t0001g0201 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1375-842T>A | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 11/37 | chr18 | 23902167 | |||||||
chr18:23902171 | T | A | 1 | a0001c0001t0002g0127 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.1375-838T>A | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 11/37 | chr18 | 23902171 | |||||||
chr18:23902252 | C | T | 155 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(152): Show |
173 | HG00099.hp1 HG00140.hp1 HG00423.hp2 others(170): Show |
intron_variant | MODIFIER | c.1375-757C>T | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 11/37 | chr18 | 23902252 | |||||||
chr18:23902289 | C | T | 1 | a0002c0002t0001g0085 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.1375-720C>T | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 11/37 | chr18 | 23902289 | |||||||
chr18:23902292 | G | A | 1 | a0001c0003t0001g0302 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1375-717G>A | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 11/37 | chr18 | 23902292 | |||||||
chr18:23902361 | A | G | 1 | a0016c0024t0001g0021 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1375-648A>G | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 11/37 | chr18 | 23902361 | |||||||
chr18:23902655 | G | A | 1 | a0017c0036t0001g0290 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1375-354G>A | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 11/37 | chr18 | 23902655 | |||||||
chr18:23902781 | C | T | 2 | a0005c0015t0001g0045 a0005c0015t0001g0046 |
2 | HG02572.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.1375-228C>T | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 11/37 | chr18 | 23902781 | |||||||
chr18:23902818 | G | T | 1 | a0006c0010t0001g0235 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1375-191G>T | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 11/37 | chr18 | 23902818 | |||||||
chr18:23903242 | G | A | 67 | a0001c0007t0001g0051 a0001c0007t0001g0052 a0001c0007t0002g0027 others(64): Show |
71 | HG00099.hp1 HG00140.hp1 HG00558.hp1 others(68): Show |
intron_variant | MODIFIER | c.1491+117G>A | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 12/37 | chr18 | 23903242 | |||||||
chr18:23903278 | C | T | 8 | a0003c0004t0001g0003 a0003c0004t0001g0187 a0003c0004t0001g0188 others(5): Show |
10 | HG00438.hp1 HG01081.hp1 HG01975.hp2 others(7): Show |
intron_variant | MODIFIER | c.1491+153C>T | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 12/37 | chr18 | 23903278 | |||||||
chr18:23903392 | T | A | 2 | a0001c0001t0001g0202 a0001c0001t0001g0203 |
2 | HG03654.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.1491+267T>A | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 12/37 | chr18 | 23903392 | |||||||
chr18:23903471 | C | G | 17 | a0001c0001t0001g0017 a0001c0001t0001g0241 a0001c0001t0001g0246 others(14): Show |
18 | HG01884.hp1 HG01891.hp1 HG02109.hp2 others(15): Show |
intron_variant | MODIFIER | c.1491+346C>G | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 12/37 | chr18 | 23903471 | |||||||
chr18:23903540 | A | G | 4 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0024 others(1): Show |
4 | HG01934.hp2 HG03704.hp2 HG03834.hp2 others(1): Show |
intron_variant | MODIFIER | c.1492-393A>G | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 12/37 | chr18 | 23903540 | |||||||
chr18:23903631 | T | C | 1 | a0002c0002t0001g0104 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.1492-302T>C | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 12/37 | chr18 | 23903631 | |||||||
chr18:23903640 | A | C | 15 | a0001c0001t0001g0017 a0001c0001t0001g0241 a0001c0001t0001g0246 others(12): Show |
16 | HG01884.hp1 HG01891.hp1 HG02109.hp2 others(13): Show |
intron_variant | MODIFIER | c.1492-293A>C | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 12/37 | chr18 | 23903640 | |||||||
chr18:23903657 | C | T | 3 | a0001c0001t0002g0012 a0009c0013t0002g0012 a0009c0013t0002g0144 |
3 | NA18940.hp1 NA18954.hp1 NA19074.hp2 |
intron_variant | MODIFIER | c.1492-276C>T | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 12/37 | chr18 | 23903657 | |||||||
chr18:23904110 | C | T | 2 | a0006c0010t0001g0205 a0006c0010t0001g0206 |
2 | HG02615.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.1646+23C>T | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 13/37 | chr18 | 23904110 | |||||||
chr18:23904280 | G | A | 89 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(86): Show |
103 | HG00423.hp2 HG00438.hp1 HG00558.hp2 others(100): Show |
intron_variant | MODIFIER | c.1646+193G>A | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 13/37 | chr18 | 23904280 | |||||||
chr18:23904289 | G | T | 2 | a0007c0012t0001g0225 a0007c0012t0001g0226 |
2 | HG02257.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.1646+202G>T | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 13/37 | chr18 | 23904289 | |||||||
chr18:23904303 | G | A | 3 | a0001c0001t0001g0241 a0001c0001t0001g0258 a0001c0001t0001g0259 |
3 | HG01884.hp1 HG01891.hp1 HG02145.hp1 |
intron_variant | MODIFIER | c.1646+216G>A | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 13/37 | chr18 | 23904303 | |||||||
chr18:23904357 | G | A | 1 | a0016c0024t0001g0021 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1647-196G>A | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 13/37 | chr18 | 23904357 | |||||||
chr18:23904408 | T | G | 2 | a0002c0002t0001g0048 a0002c0002t0001g0049 |
2 | NA18948.hp2 NA18975.hp1 |
intron_variant | MODIFIER | c.1647-145T>G | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 13/37 | chr18 | 23904408 | |||||||
chr18:23904441 | TA | T | 7 | a0001c0001t0001g0203 a0001c0001t0001g0304 a0001c0001t0002g0108 others(4): Show |
7 | HG01168.hp1 HG01168.hp2 HG01516.hp1 others(4): Show |
intron_variant | MODIFIER | c.1647-100delA | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 13/37 | INFO_REALIGN_3_PRIME | chr18 | 23904441 | ||||||
chr18:23904705 | G | A | 1 | a0001c0001t0002g0042 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.1788+11G>A | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 14/37 | chr18 | 23904705 | |||||||
chr18:23904968 | G | A | 1 | a0001c0001t0002g0147 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1788+274G>A | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 14/37 | chr18 | 23904968 | |||||||
chr18:23905157 | G | A | 1 | a0001c0001t0002g0124 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1789-365G>A | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 14/37 | chr18 | 23905157 | |||||||
chr18:23905170 | T | C | 2 | a0014c0020t0004g0233 a0024c0026t0004g0301 |
2 | HG02451.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1789-352T>C | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 14/37 | chr18 | 23905170 | |||||||
chr18:23905248 | G | A | 1 | a0001c0001t0002g0138 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.1789-274G>A | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 14/37 | chr18 | 23905248 | |||||||
chr18:23905875 | C | T | 7 | a0001c0006t0001g0020 a0001c0006t0001g0245 a0001c0006t0001g0296 others(4): Show |
7 | HG02258.hp2 HG02809.hp1 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.1891+251C>T | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 15/37 | chr18 | 23905875 | |||||||
chr18:23905910 | G | A | 15 | a0001c0001t0001g0017 a0001c0001t0001g0241 a0001c0001t0001g0246 others(12): Show |
16 | HG01884.hp1 HG01891.hp1 HG02109.hp2 others(13): Show |
intron_variant | MODIFIER | c.1891+286G>A | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 15/37 | chr18 | 23905910 | |||||||
chr18:23905939 | AT | A | 13 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0214 others(10): Show |
19 | HG00621.hp1 HG00673.hp1 HG02080.hp1 others(16): Show |
intron_variant | MODIFIER | c.1891+323delT | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 15/37 | INFO_REALIGN_3_PRIME | chr18 | 23905939 | ||||||
chr18:23906049 | G | A | 78 | a0001c0001t0002g0011 a0001c0001t0002g0012 a0001c0001t0002g0013 others(75): Show |
81 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(78): Show |
intron_variant | MODIFIER | c.1891+425G>A | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 15/37 | chr18 | 23906049 | |||||||
chr18:23906157 | A | T | 1 | a0016c0024t0001g0021 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1891+533A>T | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 15/37 | chr18 | 23906157 | |||||||
chr18:23906452 | A | T | 14 | a0001c0001t0001g0017 a0001c0001t0001g0241 a0001c0001t0001g0246 others(11): Show |
15 | HG01884.hp1 HG01891.hp1 HG02109.hp2 others(12): Show |
intron_variant | MODIFIER | c.1891+828A>T | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 15/37 | chr18 | 23906452 | |||||||
chr18:23906565 | T | C | 234 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(231): Show |
255 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(252): Show |
intron_variant | MODIFIER | c.1891+941T>C | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 15/37 | chr18 | 23906565 | |||||||
chr18:23906778 | C | T | 1 | a0016c0024t0001g0021 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1892-772C>T | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 15/37 | chr18 | 23906778 | |||||||
chr18:23906865 | C | T | 1 | a0001c0003t0001g0295 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1892-685C>T | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 15/37 | chr18 | 23906865 | |||||||
chr18:23906948 | G | T | 1 | a0001c0001t0001g0219 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.1892-602G>T | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 15/37 | chr18 | 23906948 | |||||||
chr18:23907089 | T | G | 78 | a0001c0001t0002g0011 a0001c0001t0002g0012 a0001c0001t0002g0013 others(75): Show |
81 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(78): Show |
intron_variant | MODIFIER | c.1892-461T>G | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 15/37 | chr18 | 23907089 | |||||||
chr18:23907135 | T | C | 1 | a0001c0001t0001g0047 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1892-415T>C | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 15/37 | chr18 | 23907135 | |||||||
chr18:23907139 | G | A | 250 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(247): Show |
272 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(269): Show |
intron_variant | MODIFIER | c.1892-411G>A | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 15/37 | chr18 | 23907139 | |||||||
chr18:23907207 | G | C | 2 | a0005c0015t0001g0045 a0005c0015t0001g0046 |
2 | HG02572.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.1892-343G>C | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 15/37 | chr18 | 23907207 | |||||||
chr18:23907302 | A | G | 1 | a0001c0023t0002g0157 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.1892-248A>G | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 15/37 | chr18 | 23907302 | |||||||
chr18:23907303 | G | T | 1 | a0001c0001t0002g0030 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1892-247G>T | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 15/37 | chr18 | 23907303 | |||||||
chr18:23907482 | G | A | 1 | a0002c0002t0003g0064 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.1892-68G>A | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 15/37 | chr18 | 23907482 | |||||||
chr18:23908101 | G | A | 7 | a0001c0001t0001g0169 a0001c0001t0001g0170 a0001c0001t0001g0171 others(4): Show |
7 | HG00609.hp1 NA18950.hp2 NA18954.hp2 others(4): Show |
intron_variant | MODIFIER | c.2188+166G>A | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 17/37 | chr18 | 23908101 | |||||||
chr18:23908142 | A | G | 78 | a0001c0001t0002g0011 a0001c0001t0002g0012 a0001c0001t0002g0013 others(75): Show |
81 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(78): Show |
intron_variant | MODIFIER | c.2188+207A>G | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 17/37 | chr18 | 23908142 | |||||||
chr18:23908264 | CTCATGCC others(5): Show |
C | 5 | a0001c0003t0001g0250 a0001c0003t0001g0251 a0001c0003t0001g0252 others(2): Show |
5 | HG01109.hp2 HG03041.hp2 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.2188+332_2188+343d others(14): Show |
LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 17/37 | INFO_REALIGN_3_PRIME | chr18 | 23908264 | ||||||
chr18:23908297 | G | A | 1 | a0001c0001t0001g0015 | 2 | NA19058.hp1 NA19077.hp1 |
intron_variant | MODIFIER | c.2188+362G>A | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 17/37 | chr18 | 23908297 | |||||||
chr18:23908402 | C | T | 1 | a0001c0001t0002g0155 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.2188+467C>T | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 17/37 | chr18 | 23908402 | |||||||
chr18:23908438 | G | A | 2 | a0005c0015t0001g0045 a0005c0015t0001g0046 |
2 | HG02572.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.2188+503G>A | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 17/37 | chr18 | 23908438 | |||||||
chr18:23908447 | G | A | 1 | a0016c0024t0001g0021 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.2188+512G>A | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 17/37 | chr18 | 23908447 | |||||||
chr18:23908458 | A | G | 1 | a0001c0006t0001g0298 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.2188+523A>G | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 17/37 | chr18 | 23908458 | |||||||
chr18:23908517 | G | A | 1 | a0001c0001t0005g0137 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.2188+582G>A | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 17/37 | chr18 | 23908517 | |||||||
chr18:23908525 | A | G | 1 | a0001c0001t0005g0137 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.2188+590A>G | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 17/37 | chr18 | 23908525 | |||||||
chr18:23908533 | C | A | 2 | a0001c0001t0001g0169 a0001c0001t0001g0170 |
2 | NA18959.hp2 NA19003.hp1 |
intron_variant | MODIFIER | c.2188+598C>A | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 17/37 | chr18 | 23908533 | |||||||
chr18:23908533 | C | CA | 29 | a0001c0001t0001g0017 a0001c0001t0001g0022 a0001c0001t0001g0047 others(26): Show |
33 | HG00438.hp2 HG01081.hp1 HG01346.hp2 others(30): Show |
intron_variant | MODIFIER | c.2189-601dupA | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 17/37 | INFO_REALIGN_3_PRIME | chr18 | 23908533 | ||||||
chr18:23908585 | A | G | 2 | a0004c0005t0002g0129 a0004c0005t0002g0130 |
2 | HG03486.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.2189-568A>G | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 17/37 | chr18 | 23908585 | |||||||
chr18:23908900 | A | C | 1 | a0002c0002t0001g0085 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.2189-253A>C | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 17/37 | chr18 | 23908900 | |||||||
chr18:23908907 | A | C | 3 | a0001c0001t0001g0208 a0001c0001t0001g0209 a0001c0001t0001g0210 |
3 | HG03540.hp1 NA18522.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.2189-246A>C | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 17/37 | chr18 | 23908907 | |||||||
chr18:23908925 | G | A | 169 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(166): Show |
186 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(183): Show |
intron_variant | MODIFIER | c.2189-228G>A | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 17/37 | chr18 | 23908925 | |||||||
chr18:23908983 | G | A | 229 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(226): Show |
251 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(248): Show |
intron_variant | MODIFIER | c.2189-170G>A | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 17/37 | chr18 | 23908983 | |||||||
chr18:23909035 | C | T | 1 | a0001c0001t0001g0047 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.2189-118C>T | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 17/37 | chr18 | 23909035 | |||||||
chr18:23909141 | T | C | 1 | a0001c0001t0001g0241 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.2189-12T>C | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 17/37 | chr18 | 23909141 | |||||||
chr18:23909525 | C | T | 3 | a0006c0010t0001g0205 a0006c0010t0001g0206 a0006c0010t0001g0235 |
3 | HG02615.hp2 HG02622.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.2331+230C>T | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 18/37 | chr18 | 23909525 | |||||||
chr18:23909700 | G | A | 1 | a0011c0022t0001g0305 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.2331+405G>A | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 18/37 | chr18 | 23909700 | |||||||
chr18:23909922 | T | C | 234 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(231): Show |
256 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(253): Show |
intron_variant | MODIFIER | c.2331+627T>C | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 18/37 | chr18 | 23909922 | |||||||
chr18:23909999 | A | G | 1 | a0002c0002t0001g0084 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.2331+704A>G | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 18/37 | chr18 | 23909999 | |||||||
chr18:23910070 | C | T | 132 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(129): Show |
150 | HG00280.hp2 HG00423.hp2 HG00438.hp1 others(147): Show |
intron_variant | MODIFIER | c.2331+775C>T | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 18/37 | chr18 | 23910070 | |||||||
chr18:23910121 | T | C | 1 | a0001c0001t0001g0176 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.2331+826T>C | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 18/37 | chr18 | 23910121 | |||||||
chr18:23910124 | A | T | 1 | a0001c0003t0001g0303 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.2331+829A>T | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 18/37 | chr18 | 23910124 | |||||||
chr18:23910199 | T | C | 1 | a0001c0001t0002g0110 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.2331+904T>C | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 18/37 | chr18 | 23910199 | |||||||
chr18:23910335 | A | G | 1 | a0002c0002t0001g0026 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.2331+1040A>G | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 18/37 | chr18 | 23910335 | |||||||
chr18:23910399 | C | T | 4 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0024 others(1): Show |
4 | HG01934.hp2 HG03704.hp2 HG03834.hp2 others(1): Show |
intron_variant | MODIFIER | c.2331+1104C>T | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 18/37 | chr18 | 23910399 | |||||||
chr18:23910400 | G | A | 80 | a0001c0001t0001g0047 a0001c0001t0002g0011 a0001c0001t0002g0012 others(77): Show |
83 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(80): Show |
intron_variant | MODIFIER | c.2331+1105G>A | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 18/37 | chr18 | 23910400 | |||||||
chr18:23910419 | A | G | 5 | a0001c0001t0001g0248 a0001c0001t0001g0254 a0001c0001t0001g0255 others(2): Show |
5 | HG02109.hp2 HG03130.hp2 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.2331+1124A>G | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 18/37 | chr18 | 23910419 | |||||||
chr18:23910692 | A | G | 2 | a0002c0002t0001g0105 a0020c0028t0001g0106 |
2 | HG02083.hp1 HG04184.hp2 |
intron_variant | MODIFIER | c.2331+1397A>G | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 18/37 | chr18 | 23910692 | |||||||
chr18:23910875 | G | A | 1 | a0001c0001t0001g0231 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.2331+1580G>A | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 18/37 | chr18 | 23910875 | |||||||
chr18:23911014 | CAGTCATG others(136): Show |
C | 45 | a0001c0001t0001g0002 a0001c0001t0001g0014 a0001c0001t0001g0015 others(42): Show |
52 | HG00423.hp2 HG00438.hp1 HG00558.hp2 others(49): Show |
intron_variant | MODIFIER | c.2332-1696_2332-155 others(4): Show |
LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 18/37 | chr18 | 23911014 | |||||||
chr18:23911096 | T | C | 1 | a0001c0003t0001g0302 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.2332-1615T>C | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 18/37 | chr18 | 23911096 | |||||||
chr18:23911135 | C | T | 2 | a0004c0005t0002g0129 a0004c0005t0002g0130 |
2 | HG03486.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.2332-1576C>T | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 18/37 | chr18 | 23911135 | |||||||
chr18:23911431 | T | C | 1 | a0002c0017t0001g0068 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.2332-1280T>C | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 18/37 | chr18 | 23911431 | |||||||
chr18:23911681 | A | T | 4 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0024 others(1): Show |
4 | HG01934.hp2 HG03704.hp2 HG03834.hp2 others(1): Show |
intron_variant | MODIFIER | c.2332-1030A>T | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 18/37 | chr18 | 23911681 | |||||||
chr18:23911770 | G | A | 290 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(287): Show |
316 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(313): Show |
intron_variant | MODIFIER | c.2332-941G>A | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 18/37 | chr18 | 23911770 | |||||||
chr18:23911833 | A | G | 13 | a0001c0001t0001g0017 a0001c0001t0001g0241 a0001c0001t0001g0246 others(10): Show |
14 | HG01884.hp1 HG01891.hp1 HG02109.hp2 others(11): Show |
intron_variant | MODIFIER | c.2332-878A>G | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 18/37 | chr18 | 23911833 | |||||||
chr18:23911930 | T | A | 2 | a0001c0001t0002g0114 a0001c0001t0002g0117 |
2 | NA18962.hp2 NA19078.hp1 |
intron_variant | MODIFIER | c.2332-781T>A | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 18/37 | chr18 | 23911930 | |||||||
chr18:23911996 | AT | A | 14 | a0001c0001t0001g0017 a0001c0001t0001g0241 a0001c0001t0001g0246 others(11): Show |
15 | HG01884.hp1 HG01891.hp1 HG02109.hp2 others(12): Show |
intron_variant | MODIFIER | c.2332-712delT | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 18/37 | INFO_REALIGN_3_PRIME | chr18 | 23911996 | ||||||
chr18:23912108 | A | G | 1 | a0002c0002t0001g0099 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.2332-603A>G | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 18/37 | chr18 | 23912108 | |||||||
chr18:23912139 | G | GT | 143 | a0001c0001t0001g0213 a0001c0001t0002g0011 a0001c0001t0002g0012 others(140): Show |
150 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(147): Show |
intron_variant | MODIFIER | c.2332-560dupT | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 18/37 | INFO_REALIGN_3_PRIME | chr18 | 23912139 | ||||||
chr18:23912152 | G | T | 1 | a0001c0001t0001g0218 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.2332-559G>T | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 18/37 | chr18 | 23912152 | |||||||
chr18:23912235 | G | C | 30 | a0001c0003t0001g0006 a0001c0003t0001g0018 a0001c0003t0001g0019 others(27): Show |
34 | HG00280.hp2 HG00639.hp2 HG00738.hp1 others(31): Show |
intron_variant | MODIFIER | c.2332-476G>C | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 18/37 | chr18 | 23912235 | |||||||
chr18:23912356 | G | A | 5 | a0001c0003t0001g0250 a0001c0003t0001g0251 a0001c0003t0001g0252 others(2): Show |
5 | HG01109.hp2 HG03041.hp2 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.2332-355G>A | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 18/37 | chr18 | 23912356 | |||||||
chr18:23912383 | CA | C | 4 | a0001c0003t0001g0270 a0001c0003t0001g0271 a0001c0003t0001g0279 others(1): Show |
4 | HG00280.hp2 HG01109.hp1 HG01358.hp1 others(1): Show |
intron_variant | MODIFIER | c.2332-323delA | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 18/37 | INFO_REALIGN_3_PRIME | chr18 | 23912383 | ||||||
chr18:23912470 | A | G | 2 | a0001c0001t0001g0186 a0001c0001t0001g0236 |
2 | HG03710.hp2 NA18946.hp2 |
intron_variant | MODIFIER | c.2332-241A>G | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 18/37 | chr18 | 23912470 | |||||||
chr18:23912585 | C | T | 1 | a0016c0024t0001g0021 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.2332-126C>T | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 18/37 | chr18 | 23912585 | |||||||
chr18:23912597 | T | A | 1 | a0001c0001t0001g0255 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.2332-114T>A | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 18/37 | chr18 | 23912597 | |||||||
chr18:23912611 | G | A | 1 | a0001c0003t0001g0273 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.2332-100G>A | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 18/37 | chr18 | 23912611 | |||||||
chr18:23913070 | T | C | 5 | a0004c0005t0002g0004 a0004c0005t0002g0129 a0004c0005t0002g0130 others(2): Show |
7 | HG02809.hp2 HG02896.hp1 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.2502+189T>C | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 19/37 | chr18 | 23913070 | |||||||
chr18:23913259 | A | G | 1 | a0001c0006t0001g0297 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.2502+378A>G | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 19/37 | chr18 | 23913259 | |||||||
chr18:23913342 | G | A | 1 | a0001c0003t0001g0247 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.2502+461G>A | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 19/37 | chr18 | 23913342 | |||||||
chr18:23913510 | A | C | 1 | a0011c0022t0001g0305 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.2502+629A>C | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 19/37 | chr18 | 23913510 | |||||||
chr18:23913711 | A | G | 78 | a0001c0001t0002g0011 a0001c0001t0002g0012 a0001c0001t0002g0013 others(75): Show |
81 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(78): Show |
intron_variant | MODIFIER | c.2503-699A>G | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 19/37 | chr18 | 23913711 | |||||||
chr18:23913774 | C | A | 65 | a0001c0007t0002g0027 a0001c0007t0002g0028 a0002c0002t0001g0008 others(62): Show |
69 | HG00099.hp1 HG00140.hp1 HG00558.hp1 others(66): Show |
intron_variant | MODIFIER | c.2503-636C>A | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 19/37 | chr18 | 23913774 | |||||||
chr18:23913926 | G | A | 65 | a0001c0007t0002g0027 a0001c0007t0002g0028 a0002c0002t0001g0008 others(62): Show |
69 | HG00099.hp1 HG00140.hp1 HG00558.hp1 others(66): Show |
intron_variant | MODIFIER | c.2503-484G>A | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 19/37 | chr18 | 23913926 | |||||||
chr18:23914018 | T | C | 1 | a0001c0003t0001g0302 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.2503-392T>C | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 19/37 | chr18 | 23914018 | |||||||
chr18:23914254 | A | G | 144 | a0001c0001t0001g0047 a0001c0001t0002g0011 a0001c0001t0002g0012 others(141): Show |
151 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(148): Show |
intron_variant | MODIFIER | c.2503-156A>G | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 19/37 | chr18 | 23914254 | |||||||
chr18:23914930 | C | T | 1 | a0005c0021t0002g0154 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.2817+70C>T | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 21/37 | chr18 | 23914930 | |||||||
chr18:23915230 | T | C | 10 | a0002c0002t0001g0058 a0002c0002t0001g0281 a0002c0002t0003g0064 others(7): Show |
11 | HG01069.hp2 HG01071.hp2 HG01074.hp1 others(8): Show |
intron_variant | MODIFIER | c.2818-59T>C | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 21/37 | chr18 | 23915230 | |||||||
chr18:23915519 | T | C | 144 | a0001c0001t0001g0047 a0001c0001t0002g0011 a0001c0001t0002g0012 others(141): Show |
151 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(148): Show |
intron_variant | MODIFIER | c.2951+97T>C | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 22/37 | chr18 | 23915519 | |||||||
chr18:23915792 | G | A | 3 | a0006c0010t0001g0205 a0006c0010t0001g0206 a0006c0010t0001g0235 |
3 | HG02615.hp2 HG02622.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.2951+370G>A | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 22/37 | chr18 | 23915792 | |||||||
chr18:23915826 | C | T | 2 | a0010c0014t0001g0217 a0010c0014t0001g0232 |
2 | NA18974.hp1 NA19010.hp2 |
intron_variant | MODIFIER | c.2951+404C>T | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 22/37 | chr18 | 23915826 | |||||||
chr18:23915828 | A | G | 17 | a0001c0001t0001g0017 a0001c0001t0001g0241 a0001c0001t0001g0246 others(14): Show |
18 | HG01884.hp1 HG01891.hp1 HG02109.hp2 others(15): Show |
intron_variant | MODIFIER | c.2951+406A>G | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 22/37 | chr18 | 23915828 | |||||||
chr18:23916004 | TC | T | 9 | a0001c0006t0001g0245 a0001c0006t0001g0296 a0001c0006t0001g0297 others(6): Show |
9 | HG01243.hp2 HG02615.hp1 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.2952-545delC | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 22/37 | INFO_REALIGN_3_PRIME | chr18 | 23916004 | ||||||
chr18:23916005 | C | CA | 3 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0001c0001t0001g0025 |
3 | HG01934.hp2 HG03704.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.2952-546_2952-545i others(3): Show |
LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 22/37 | chr18 | 23916005 | |||||||
chr18:23916005 | C | CAAAAAAA others(5): Show |
1 | a0001c0001t0001g0017 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.2952-546_2952-545i others(14): Show |
LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 22/37 | chr18 | 23916005 | |||||||
chr18:23916005 | C | CAAAAAAA others(6): Show |
6 | a0001c0001t0001g0017 a0001c0001t0001g0241 a0001c0001t0001g0246 others(3): Show |
6 | HG01884.hp1 HG01891.hp1 HG02145.hp1 others(3): Show |
intron_variant | MODIFIER | c.2952-546_2952-545i others(15): Show |
LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 22/37 | chr18 | 23916005 | |||||||
chr18:23916005 | C | CAAAAAAA others(15): Show |
2 | a0001c0001t0001g0249 a0001c0001t0001g0257 |
2 | HG02922.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.2952-546_2952-545i others(24): Show |
LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 22/37 | chr18 | 23916005 | |||||||
chr18:23916005 | CCA | C | 6 | a0001c0003t0001g0289 a0001c0003t0001g0291 a0001c0031t0004g0292 others(3): Show |
6 | HG02280.hp2 HG02451.hp2 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.2952-545_2952-544d others(4): Show |
LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 22/37 | chr18 | 23916005 | |||||||
chr18:23916005 | CCAA | C | 26 | a0001c0001t0002g0067 a0001c0001t0002g0110 a0001c0001t0002g0114 others(23): Show |
28 | HG01109.hp2 HG02135.hp2 HG02622.hp1 others(25): Show |
intron_variant | MODIFIER | c.2952-545_2952-543d others(5): Show |
LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 22/37 | chr18 | 23916005 | |||||||
chr18:23916005 | CCAAA | C | 152 | a0001c0001t0001g0005 a0001c0001t0001g0047 a0001c0001t0001g0173 others(149): Show |
159 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(156): Show |
intron_variant | MODIFIER | c.2952-545_2952-542d others(6): Show |
LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 22/37 | chr18 | 23916005 | |||||||
chr18:23916005 | CCAAAA | C | 66 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0015 others(63): Show |
73 | HG00423.hp2 HG00438.hp1 HG00609.hp1 others(70): Show |
intron_variant | MODIFIER | c.2952-545_2952-541d others(7): Show |
LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 22/37 | chr18 | 23916005 | |||||||
chr18:23916005 | CCAAAAA | C | 18 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0014 others(15): Show |
22 | HG00558.hp2 HG00741.hp1 HG01081.hp1 others(19): Show |
intron_variant | MODIFIER | c.2952-545_2952-540d others(8): Show |
LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 22/37 | chr18 | 23916005 | |||||||
chr18:23916006 | C | A | 30 | a0001c0001t0001g0017 a0001c0001t0001g0022 a0001c0001t0001g0023 others(27): Show |
33 | HG00099.hp1 HG00558.hp1 HG00673.hp2 others(30): Show |
intron_variant | MODIFIER | c.2952-545C>A | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 22/37 | chr18 | 23916006 | |||||||
chr18:23916027 | A | G | 10 | a0001c0001t0002g0121 a0001c0001t0002g0143 a0001c0001t0002g0150 others(7): Show |
12 | HG00280.hp1 HG00558.hp1 HG00673.hp2 others(9): Show |
intron_variant | MODIFIER | c.2952-524A>G | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 22/37 | chr18 | 23916027 | |||||||
chr18:23916029 | A | G | 1 | a0003c0004t0001g0189 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.2952-522A>G | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 22/37 | chr18 | 23916029 | |||||||
chr18:23916032 | G | A | 105 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(102): Show |
120 | HG00423.hp2 HG00438.hp1 HG00558.hp2 others(117): Show |
intron_variant | MODIFIER | c.2952-519G>A | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 22/37 | chr18 | 23916032 | |||||||
chr18:23916033 | AAAAG | A | 8 | a0001c0001t0002g0121 a0001c0003t0001g0274 a0001c0003t0001g0295 others(5): Show |
10 | HG00558.hp1 HG00673.hp2 HG01167.hp2 others(7): Show |
intron_variant | MODIFIER | c.2952-514_2952-511d others(6): Show |
LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 22/37 | INFO_REALIGN_3_PRIME | chr18 | 23916033 | ||||||
chr18:23916037 | G | GA | 177 | a0001c0001t0001g0047 a0001c0001t0001g0249 a0001c0001t0001g0257 others(174): Show |
186 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(183): Show |
intron_variant | MODIFIER | c.2952-510dupA | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 22/37 | INFO_REALIGN_3_PRIME | chr18 | 23916037 | ||||||
chr18:23916042 | G | A | 1 | a0001c0007t0002g0027 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.2952-509G>A | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 22/37 | chr18 | 23916042 | |||||||
chr18:23916043 | A | G | 1 | a0001c0007t0002g0027 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.2952-508A>G | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 22/37 | chr18 | 23916043 | |||||||
chr18:23916048 | GA | G | 184 | a0001c0001t0001g0047 a0001c0001t0002g0011 a0001c0001t0002g0012 others(181): Show |
195 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(192): Show |
intron_variant | MODIFIER | c.2952-498delA | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 22/37 | INFO_REALIGN_3_PRIME | chr18 | 23916048 | ||||||
chr18:23916049 | A | AAAAAG | 12 | a0001c0001t0001g0246 a0001c0001t0001g0248 a0001c0001t0001g0249 others(9): Show |
12 | HG02109.hp2 HG02451.hp2 HG02559.hp2 others(9): Show |
intron_variant | MODIFIER | c.2952-482_2952-478d others(7): Show |
LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 22/37 | INFO_REALIGN_3_PRIME | chr18 | 23916049 | ||||||
chr18:23916049 | A | AAAAAGAA others(4): Show |
5 | a0001c0001t0001g0017 a0001c0001t0001g0241 a0001c0001t0001g0256 others(2): Show |
6 | HG01884.hp1 HG01891.hp1 HG02145.hp1 others(3): Show |
intron_variant | MODIFIER | c.2952-493_2952-492i others(13): Show |
LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 22/37 | INFO_REALIGN_3_PRIME | chr18 | 23916049 | ||||||
chr18:23916049 | AAAAAGAA others(3): Show |
A | 2 | a0001c0001t0001g0163 a0001c0001t0001g0181 |
2 | NA18961.hp2 NA18965.hp1 |
intron_variant | MODIFIER | c.2952-487_2952-478d others(12): Show |
LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 22/37 | INFO_REALIGN_3_PRIME | chr18 | 23916049 | ||||||
chr18:23916202 | C | T | 90 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(87): Show |
104 | HG00423.hp2 HG00438.hp1 HG00558.hp2 others(101): Show |
intron_variant | MODIFIER | c.2952-349C>T | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 22/37 | chr18 | 23916202 | |||||||
chr18:23916214 | T | C | 1 | a0016c0024t0001g0021 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.2952-337T>C | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 22/37 | chr18 | 23916214 | |||||||
chr18:23916260 | A | T | 4 | a0001c0031t0004g0292 a0014c0020t0004g0233 a0018c0034t0004g0294 others(1): Show |
4 | HG02451.hp2 HG02559.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.2952-291A>T | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 22/37 | chr18 | 23916260 | |||||||
chr18:23916299 | A | G | 1 | a0001c0001t0002g0126 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.2952-252A>G | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 22/37 | chr18 | 23916299 | |||||||
chr18:23916363 | A | C | 1 | a0001c0003t0001g0271 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.2952-188A>C | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 22/37 | chr18 | 23916363 | |||||||
chr18:23916495 | C | A | 1 | a0001c0001t0002g0040 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.2952-56C>A | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 22/37 | chr18 | 23916495 | |||||||
chr18:23916714 | C | T | 1 | a0001c0001t0001g0185 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.3096+19C>T | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 23/37 | chr18 | 23916714 | |||||||
chr18:23916781 | C | T | 1 | a0001c0001t0001g0047 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.3096+86C>T | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 23/37 | chr18 | 23916781 | |||||||
chr18:23916865 | CT | C | 18 | a0001c0001t0001g0173 a0001c0001t0001g0177 a0001c0001t0001g0211 others(15): Show |
20 | HG00438.hp1 HG01081.hp1 HG01257.hp1 others(17): Show |
intron_variant | MODIFIER | c.3096+185delT | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 23/37 | INFO_REALIGN_3_PRIME | chr18 | 23916865 | ||||||
chr18:23916890 | A | G | 64 | a0001c0007t0002g0027 a0001c0007t0002g0028 a0002c0002t0001g0008 others(61): Show |
68 | HG00099.hp1 HG00140.hp1 HG00558.hp1 others(65): Show |
intron_variant | MODIFIER | c.3096+195A>G | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 23/37 | chr18 | 23916890 | |||||||
chr18:23917001 | AT | A | 252 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(249): Show |
274 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(271): Show |
intron_variant | MODIFIER | c.3096+312delT | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 23/37 | INFO_REALIGN_3_PRIME | chr18 | 23917001 | ||||||
chr18:23917227 | T | G | 17 | a0001c0001t0001g0017 a0001c0001t0001g0241 a0001c0001t0001g0246 others(14): Show |
18 | HG01884.hp1 HG01891.hp1 HG02109.hp2 others(15): Show |
intron_variant | MODIFIER | c.3096+532T>G | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 23/37 | chr18 | 23917227 | |||||||
chr18:23917344 | T | C | 1 | a0001c0001t0002g0148 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.3096+649T>C | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 23/37 | chr18 | 23917344 | |||||||
chr18:23917358 | C | T | 1 | a0001c0001t0002g0147 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.3096+663C>T | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 23/37 | chr18 | 23917358 | |||||||
chr18:23917395 | A | T | 2 | a0002c0002t0001g0105 a0020c0028t0001g0106 |
2 | HG02083.hp1 HG04184.hp2 |
intron_variant | MODIFIER | c.3096+700A>T | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 23/37 | chr18 | 23917395 | |||||||
chr18:23917646 | C | T | 1 | a0001c0001t0001g0047 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.3096+951C>T | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 23/37 | chr18 | 23917646 | |||||||
chr18:23917964 | T | C | 1 | a0011c0022t0001g0305 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.3096+1269T>C | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 23/37 | chr18 | 23917964 | |||||||
chr18:23917982 | C | A | 5 | a0001c0003t0001g0250 a0001c0003t0001g0251 a0001c0003t0001g0252 others(2): Show |
5 | HG01109.hp2 HG03041.hp2 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.3096+1287C>A | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 23/37 | chr18 | 23917982 | |||||||
chr18:23918780 | G | A | 3 | a0004c0005t0002g0004 a0004c0005t0002g0151 a0004c0005t0002g0152 |
5 | HG02809.hp2 HG02896.hp1 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.3096+2085G>A | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 23/37 | chr18 | 23918780 | |||||||
chr18:23918829 | C | T | 1 | a0001c0001t0001g0193 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.3097-2106C>T | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 23/37 | chr18 | 23918829 | |||||||
chr18:23918993 | G | A | 1 | a0001c0001t0002g0110 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.3097-1942G>A | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 23/37 | chr18 | 23918993 | |||||||
chr18:23919011 | G | T | 1 | a0001c0003t0001g0289 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.3097-1924G>T | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 23/37 | chr18 | 23919011 | |||||||
chr18:23919242 | C | T | 1 | a0003c0004t0001g0188 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.3097-1693C>T | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 23/37 | chr18 | 23919242 | |||||||
chr18:23919268 | A | T | 4 | a0001c0031t0004g0292 a0014c0020t0004g0233 a0018c0034t0004g0294 others(1): Show |
4 | HG02451.hp2 HG02559.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.3097-1667A>T | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 23/37 | chr18 | 23919268 | |||||||
chr18:23919278 | G | C | 4 | a0001c0031t0004g0292 a0014c0020t0004g0233 a0018c0034t0004g0294 others(1): Show |
4 | HG02451.hp2 HG02559.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.3097-1657G>C | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 23/37 | chr18 | 23919278 | |||||||
chr18:23919324 | G | A | 1 | a0001c0001t0002g0031 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.3097-1611G>A | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 23/37 | chr18 | 23919324 | |||||||
chr18:23919376 | A | G | 3 | a0001c0001t0002g0013 a0001c0001t0002g0111 a0001c0001t0002g0118 |
4 | HG00639.hp1 HG01074.hp2 HG01243.hp1 others(1): Show |
intron_variant | MODIFIER | c.3097-1559A>G | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 23/37 | chr18 | 23919376 | |||||||
chr18:23919522 | A | G | 1 | a0001c0001t0001g0175 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.3097-1413A>G | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 23/37 | chr18 | 23919522 | |||||||
chr18:23919723 | C | A | 6 | a0001c0007t0002g0027 a0001c0007t0002g0028 a0002c0002t0001g0026 others(3): Show |
6 | HG00099.hp1 HG00140.hp1 HG01168.hp1 others(3): Show |
intron_variant | MODIFIER | c.3097-1212C>A | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 23/37 | chr18 | 23919723 | |||||||
chr18:23919863 | G | C | 1 | a0001c0001t0001g0025 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.3097-1072G>C | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 23/37 | chr18 | 23919863 | |||||||
chr18:23919898 | C | T | 1 | a0001c0001t0001g0204 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.3097-1037C>T | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 23/37 | chr18 | 23919898 | |||||||
chr18:23919917 | C | T | 5 | a0001c0001t0001g0248 a0001c0001t0001g0254 a0001c0001t0001g0255 others(2): Show |
5 | HG02109.hp2 HG03130.hp2 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.3097-1018C>T | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 23/37 | chr18 | 23919917 | |||||||
chr18:23920580 | C | A | 1 | a0001c0001t0002g0147 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.3097-355C>A | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 23/37 | chr18 | 23920580 | |||||||
chr18:23920583 | C | T | 2 | a0001c0003t0001g0265 a0001c0003t0001g0278 |
2 | NA19060.hp2 NA19078.hp2 |
intron_variant | MODIFIER | c.3097-352C>T | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 23/37 | chr18 | 23920583 | |||||||
chr18:23920657 | C | T | 2 | a0001c0001t0001g0173 a0001c0001t0001g0174 |
2 | NA18954.hp2 NA19009.hp1 |
intron_variant | MODIFIER | c.3097-278C>T | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 23/37 | chr18 | 23920657 | |||||||
chr18:23920723 | G | C | 1 | a0002c0002t0001g0053 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.3097-212G>C | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 23/37 | chr18 | 23920723 | |||||||
chr18:23920750 | G | A | 4 | a0001c0001t0001g0191 a0001c0001t0001g0192 a0001c0001t0001g0193 others(1): Show |
4 | HG00741.hp1 HG02738.hp1 HG03239.hp1 others(1): Show |
intron_variant | MODIFIER | c.3097-185G>A | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 23/37 | chr18 | 23920750 | |||||||
chr18:23920750 | G | T | 1 | a0024c0026t0004g0301 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.3097-185G>T | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 23/37 | chr18 | 23920750 | |||||||
chr18:23920759 | A | G | 3 | a0001c0001t0002g0116 a0001c0001t0002g0126 a0001c0001t0002g0240 |
3 | HG00099.hp2 HG01071.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.3097-176A>G | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 23/37 | chr18 | 23920759 | |||||||
chr18:23920866 | G | A | 3 | a0001c0001t0002g0135 a0001c0001t0002g0148 a0001c0001t0002g0159 |
3 | NA18964.hp1 NA19003.hp2 NA19009.hp2 |
intron_variant | MODIFIER | c.3097-69G>A | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 23/37 | chr18 | 23920866 | |||||||
chr18:23921148 | A | G | 2 | a0001c0001t0001g0023 a0001c0001t0001g0024 |
2 | HG01934.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.3216+94A>G | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 24/37 | chr18 | 23921148 | |||||||
chr18:23921239 | T | C | 1 | a0001c0003t0001g0303 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.3216+185T>C | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 24/37 | chr18 | 23921239 | |||||||
chr18:23921365 | T | C | 2 | a0001c0001t0002g0143 a0001c0001t0002g0150 |
2 | HG00280.hp1 HG00738.hp2 |
intron_variant | MODIFIER | c.3217-87T>C | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 24/37 | chr18 | 23921365 | |||||||
chr18:23922095 | C | T | 80 | a0001c0001t0002g0011 a0001c0001t0002g0012 a0001c0001t0002g0013 others(77): Show |
83 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(80): Show |
intron_variant | MODIFIER | c.3350+510C>T | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 25/37 | chr18 | 23922095 | |||||||
chr18:23922100 | G | A | 156 | a0001c0001t0001g0017 a0001c0001t0001g0047 a0001c0001t0001g0241 others(153): Show |
164 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(161): Show |
intron_variant | MODIFIER | c.3350+515G>A | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 25/37 | chr18 | 23922100 | |||||||
chr18:23922173 | A | G | 4 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0024 others(1): Show |
4 | HG01934.hp2 HG03704.hp2 HG03834.hp2 others(1): Show |
intron_variant | MODIFIER | c.3350+588A>G | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 25/37 | chr18 | 23922173 | |||||||
chr18:23922230 | C | T | 1 | a0016c0024t0001g0021 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.3350+645C>T | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 25/37 | chr18 | 23922230 | |||||||
chr18:23922412 | G | T | 10 | a0001c0001t0001g0016 a0001c0001t0001g0202 a0001c0001t0001g0203 others(7): Show |
11 | HG00642.hp2 HG01069.hp1 HG01515.hp2 others(8): Show |
intron_variant | MODIFIER | c.3350+827G>T | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 25/37 | chr18 | 23922412 | |||||||
chr18:23922448 | G | A | 293 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(290): Show |
319 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(316): Show |
intron_variant | MODIFIER | c.3350+863G>A | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 25/37 | chr18 | 23922448 | |||||||
chr18:23922455 | C | T | 1 | a0001c0001t0001g0047 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.3350+870C>T | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 25/37 | chr18 | 23922455 | |||||||
chr18:23922692 | A | G | 1 | a0001c0001t0001g0172 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.3350+1107A>G | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 25/37 | chr18 | 23922692 | |||||||
chr18:23922785 | C | T | 2 | a0002c0002t0001g0083 a0016c0024t0001g0021 |
2 | HG02976.hp2 NA19082.hp1 |
intron_variant | MODIFIER | c.3350+1200C>T | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 25/37 | chr18 | 23922785 | |||||||
chr18:23922843 | T | C | 133 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(130): Show |
151 | HG00280.hp2 HG00423.hp2 HG00438.hp1 others(148): Show |
intron_variant | MODIFIER | c.3350+1258T>C | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 25/37 | chr18 | 23922843 | |||||||
chr18:23922862 | C | T | 2 | a0002c0017t0001g0068 a0002c0017t0001g0069 |
2 | HG00609.hp2 NA18960.hp1 |
intron_variant | MODIFIER | c.3350+1277C>T | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 25/37 | chr18 | 23922862 | |||||||
chr18:23922884 | G | T | 5 | a0004c0005t0002g0004 a0004c0005t0002g0129 a0004c0005t0002g0130 others(2): Show |
7 | HG02809.hp2 HG02896.hp1 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.3350+1299G>T | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 25/37 | chr18 | 23922884 | |||||||
chr18:23922955 | G | A | 4 | a0001c0001t0001g0191 a0001c0001t0001g0192 a0001c0001t0001g0193 others(1): Show |
4 | HG00741.hp1 HG02738.hp1 HG03239.hp1 others(1): Show |
intron_variant | MODIFIER | c.3350+1370G>A | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 25/37 | chr18 | 23922955 | |||||||
chr18:23922972 | G | C | 1 | a0001c0007t0001g0051 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.3350+1387G>C | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 25/37 | chr18 | 23922972 | |||||||
chr18:23922982 | C | T | 4 | a0001c0001t0001g0207 a0001c0001t0001g0211 a0001c0001t0001g0212 others(1): Show |
4 | HG02258.hp1 HG02451.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.3350+1397C>T | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 25/37 | chr18 | 23922982 | |||||||
chr18:23923151 | C | T | 80 | a0001c0001t0002g0011 a0001c0001t0002g0012 a0001c0001t0002g0013 others(77): Show |
83 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(80): Show |
intron_variant | MODIFIER | c.3350+1566C>T | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 25/37 | chr18 | 23923151 | |||||||
chr18:23923184 | C | T | 4 | a0002c0002t0001g0026 a0002c0002t0001g0055 a0002c0002t0001g0056 others(1): Show |
4 | HG00140.hp1 HG01168.hp1 HG01346.hp1 others(1): Show |
intron_variant | MODIFIER | c.3350+1599C>T | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 25/37 | chr18 | 23923184 | |||||||
chr18:23923207 | A | G | 74 | a0001c0001t0002g0011 a0001c0001t0002g0012 a0001c0001t0002g0013 others(71): Show |
77 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(74): Show |
intron_variant | MODIFIER | c.3350+1622A>G | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 25/37 | chr18 | 23923207 | |||||||
chr18:23923341 | C | T | 1 | a0001c0001t0001g0164 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.3350+1756C>T | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 25/37 | chr18 | 23923341 | |||||||
chr18:23923394 | A | G | 4 | a0001c0031t0004g0292 a0014c0020t0004g0233 a0018c0034t0004g0294 others(1): Show |
4 | HG02451.hp2 HG02559.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.3350+1809A>G | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 25/37 | chr18 | 23923394 | |||||||
chr18:23923447 | G | A | 4 | a0001c0001t0001g0207 a0001c0001t0001g0211 a0001c0001t0001g0212 others(1): Show |
4 | HG02258.hp1 HG02451.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.3350+1862G>A | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 25/37 | chr18 | 23923447 | |||||||
chr18:23923457 | A | C | 1 | a0001c0001t0001g0210 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.3350+1872A>C | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 25/37 | chr18 | 23923457 | |||||||
chr18:23923530 | C | T | 137 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(134): Show |
155 | HG00280.hp2 HG00423.hp2 HG00438.hp1 others(152): Show |
intron_variant | MODIFIER | c.3350+1945C>T | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 25/37 | chr18 | 23923530 | |||||||
chr18:23923723 | G | A | 1 | a0002c0002t0001g0091 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.3350+2138G>A | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 25/37 | chr18 | 23923723 | |||||||
chr18:23923937 | C | T | 1 | a0001c0003t0001g0291 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.3350+2352C>T | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 25/37 | chr18 | 23923937 | |||||||
chr18:23924027 | C | G | 4 | a0001c0031t0004g0292 a0014c0020t0004g0233 a0018c0034t0004g0294 others(1): Show |
4 | HG02451.hp2 HG02559.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.3350+2442C>G | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 25/37 | chr18 | 23924027 | |||||||
chr18:23924104 | C | T | 1 | a0001c0001t0001g0237 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.3350+2519C>T | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 25/37 | chr18 | 23924104 | |||||||
chr18:23924342 | G | A | 2 | a0001c0001t0002g0032 a0001c0001t0002g0036 |
2 | NA18953.hp1 NA19083.hp2 |
intron_variant | MODIFIER | c.3350+2757G>A | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 25/37 | chr18 | 23924342 | |||||||
chr18:23924436 | G | A | 1 | a0001c0001t0001g0227 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.3350+2851G>A | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 25/37 | chr18 | 23924436 | |||||||
chr18:23924513 | G | A | 4 | a0001c0031t0004g0292 a0014c0020t0004g0233 a0018c0034t0004g0294 others(1): Show |
4 | HG02451.hp2 HG02559.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.3350+2928G>A | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 25/37 | chr18 | 23924513 | |||||||
chr18:23924543 | CT | C | 224 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0015 others(221): Show |
241 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(238): Show |
intron_variant | MODIFIER | c.3350+2976delT | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 25/37 | INFO_REALIGN_3_PRIME | chr18 | 23924543 | ||||||
chr18:23924549 | T | C | 2 | a0001c0001t0001g0047 a0001c0001t0002g0158 |
2 | HG02486.hp2 HG03831.hp2 |
intron_variant | MODIFIER | c.3350+2964T>C | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 25/37 | chr18 | 23924549 | |||||||
chr18:23924566 | C | T | 1 | a0001c0003t0001g0286 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.3350+2981C>T | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 25/37 | chr18 | 23924566 | |||||||
chr18:23924611 | C | G | 1 | a0001c0006t0001g0245 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.3350+3026C>G | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 25/37 | chr18 | 23924611 | |||||||
chr18:23924704 | C | T | 1 | a0001c0001t0001g0216 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.3350+3119C>T | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 25/37 | chr18 | 23924704 | |||||||
chr18:23924705 | G | A | 4 | a0001c0001t0001g0177 a0001c0001t0001g0185 a0001c0001t0001g0186 others(1): Show |
4 | HG03710.hp2 NA18946.hp2 NA18957.hp1 others(1): Show |
intron_variant | MODIFIER | c.3350+3120G>A | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 25/37 | chr18 | 23924705 | |||||||
chr18:23924755 | C | G | 1 | a0001c0003t0001g0261 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.3350+3170C>G | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 25/37 | chr18 | 23924755 | |||||||
chr18:23924762 | C | T | 1 | a0011c0022t0001g0305 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.3350+3177C>T | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 25/37 | chr18 | 23924762 | |||||||
chr18:23925097 | G | T | 4 | a0001c0001t0001g0191 a0001c0001t0001g0192 a0001c0001t0001g0193 others(1): Show |
4 | HG00741.hp1 HG02738.hp1 HG03239.hp1 others(1): Show |
intron_variant | MODIFIER | c.3351-3026G>T | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 25/37 | chr18 | 23925097 | |||||||
chr18:23925130 | G | C | 1 | a0001c0001t0001g0164 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.3351-2993G>C | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 25/37 | chr18 | 23925130 | |||||||
chr18:23925261 | T | C | 3 | a0002c0008t0001g0007 a0002c0008t0001g0057 a0002c0008t0001g0071 |
4 | HG01069.hp2 HG01071.hp2 HG01516.hp2 others(1): Show |
intron_variant | MODIFIER | c.3351-2862T>C | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 25/37 | chr18 | 23925261 | |||||||
chr18:23925300 | C | T | 293 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(290): Show |
319 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(316): Show |
intron_variant | MODIFIER | c.3351-2823C>T | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 25/37 | chr18 | 23925300 | |||||||
chr18:23925454 | A | G | 1 | a0001c0001t0001g0256 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.3351-2669A>G | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 25/37 | chr18 | 23925454 | |||||||
chr18:23925630 | C | T | 89 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(86): Show |
103 | HG00423.hp2 HG00438.hp1 HG00558.hp2 others(100): Show |
intron_variant | MODIFIER | c.3351-2493C>T | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 25/37 | chr18 | 23925630 | |||||||
chr18:23925937 | G | A | 1 | a0001c0001t0001g0204 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.3351-2186G>A | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 25/37 | chr18 | 23925937 | |||||||
chr18:23926049 | A | G | 1 | a0001c0001t0001g0222 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.3351-2074A>G | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 25/37 | chr18 | 23926049 | |||||||
chr18:23926255 | G | T | 157 | a0001c0001t0001g0017 a0001c0001t0001g0047 a0001c0001t0001g0241 others(154): Show |
165 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(162): Show |
intron_variant | MODIFIER | c.3351-1868G>T | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 25/37 | chr18 | 23926255 | |||||||
chr18:23926312 | T | C | 3 | a0001c0031t0004g0292 a0014c0020t0004g0233 a0018c0034t0004g0294 |
3 | HG02451.hp2 HG02559.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.3351-1811T>C | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 25/37 | chr18 | 23926312 | |||||||
chr18:23926320 | C | T | 1 | a0001c0001t0002g0110 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.3351-1803C>T | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 25/37 | chr18 | 23926320 | |||||||
chr18:23926339 | G | T | 80 | a0001c0001t0002g0011 a0001c0001t0002g0012 a0001c0001t0002g0013 others(77): Show |
83 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(80): Show |
intron_variant | MODIFIER | c.3351-1784G>T | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 25/37 | chr18 | 23926339 | |||||||
chr18:23926842 | A | G | 1 | a0001c0003t0001g0247 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.3351-1281A>G | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 25/37 | chr18 | 23926842 | |||||||
chr18:23926875 | C | A | 82 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(79): Show |
96 | HG00423.hp2 HG00438.hp1 HG00558.hp2 others(93): Show |
intron_variant | MODIFIER | c.3351-1248C>A | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 25/37 | chr18 | 23926875 | |||||||
chr18:23927325 | C | T | 1 | a0001c0003t0001g0295 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.3351-798C>T | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 25/37 | chr18 | 23927325 | |||||||
chr18:23927361 | T | G | 161 | a0001c0001t0001g0017 a0001c0001t0001g0047 a0001c0001t0001g0241 others(158): Show |
169 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(166): Show |
intron_variant | MODIFIER | c.3351-762T>G | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 25/37 | chr18 | 23927361 | |||||||
chr18:23927409 | T | A | 1 | a0001c0001t0002g0119 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.3351-714T>A | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 25/37 | chr18 | 23927409 | |||||||
chr18:23927451 | G | C | 10 | a0002c0002t0001g0058 a0002c0002t0001g0281 a0002c0002t0003g0064 others(7): Show |
11 | HG01069.hp2 HG01071.hp2 HG01074.hp1 others(8): Show |
intron_variant | MODIFIER | c.3351-672G>C | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 25/37 | chr18 | 23927451 | |||||||
chr18:23927465 | G | A | 80 | a0001c0001t0002g0011 a0001c0001t0002g0012 a0001c0001t0002g0013 others(77): Show |
83 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(80): Show |
intron_variant | MODIFIER | c.3351-658G>A | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 25/37 | chr18 | 23927465 | |||||||
chr18:23927526 | A | G | 1 | a0016c0024t0001g0021 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.3351-597A>G | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 25/37 | chr18 | 23927526 | |||||||
chr18:23927586 | A | G | 1 | a0001c0001t0001g0047 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.3351-537A>G | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 25/37 | chr18 | 23927586 | |||||||
chr18:23927593 | G | A | 49 | a0001c0003t0001g0006 a0001c0003t0001g0018 a0001c0003t0001g0019 others(46): Show |
53 | HG00280.hp2 HG00639.hp2 HG00738.hp1 others(50): Show |
intron_variant | MODIFIER | c.3351-530G>A | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 25/37 | chr18 | 23927593 | |||||||
chr18:23927609 | T | G | 3 | a0001c0001t0001g0208 a0001c0001t0001g0209 a0001c0001t0001g0210 |
3 | HG03540.hp1 NA18522.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.3351-514T>G | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 25/37 | chr18 | 23927609 | |||||||
chr18:23927639 | T | C | 4 | a0001c0031t0004g0292 a0014c0020t0004g0233 a0018c0034t0004g0294 others(1): Show |
4 | HG02451.hp2 HG02559.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.3351-484T>C | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 25/37 | chr18 | 23927639 | |||||||
chr18:23928268 | G | C | 1 | a0001c0027t0001g0167 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.3468+28G>C | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 26/37 | chr18 | 23928268 | |||||||
chr18:23928307 | C | T | 2 | a0001c0001t0002g0158 a0001c0001t0002g0161 |
2 | HG02486.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.3468+67C>T | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 26/37 | chr18 | 23928307 | |||||||
chr18:23928322 | C | T | 24 | a0001c0003t0001g0006 a0001c0003t0001g0018 a0001c0003t0001g0019 others(21): Show |
28 | HG00280.hp2 HG00639.hp2 HG00738.hp1 others(25): Show |
intron_variant | MODIFIER | c.3468+82C>T | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 26/37 | chr18 | 23928322 | |||||||
chr18:23928364 | A | G | 5 | a0001c0001t0001g0248 a0001c0001t0001g0254 a0001c0001t0001g0255 others(2): Show |
5 | HG02109.hp2 HG03130.hp2 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.3468+124A>G | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 26/37 | chr18 | 23928364 | |||||||
chr18:23928967 | A | G | 1 | a0005c0021t0002g0154 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.3609+202A>G | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 27/37 | chr18 | 23928967 | |||||||
chr18:23929000 | C | T | 1 | a0001c0001t0001g0246 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.3609+235C>T | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 27/37 | chr18 | 23929000 | |||||||
chr18:23929003 | G | A | 1 | a0001c0003t0001g0303 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.3609+238G>A | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 27/37 | chr18 | 23929003 | |||||||
chr18:23929183 | C | T | 1 | a0004c0005t0002g0151 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.3609+418C>T | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 27/37 | chr18 | 23929183 | |||||||
chr18:23929256 | A | G | 1 | a0001c0001t0001g0236 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.3609+491A>G | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 27/37 | chr18 | 23929256 | |||||||
chr18:23929344 | A | C | 1 | a0001c0001t0001g0047 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.3609+579A>C | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 27/37 | chr18 | 23929344 | |||||||
chr18:23929513 | C | CAGGAAGG others(42): Show |
1 | a0001c0001t0002g0153 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.3609+796_3609+844d others(51): Show |
LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 27/37 | INFO_REALIGN_3_PRIME | chr18 | 23929513 | ||||||
chr18:23929536 | T | C | 1 | a0011c0022t0001g0305 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.3609+771T>C | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 27/37 | chr18 | 23929536 | |||||||
chr18:23929576 | C | T | 1 | a0001c0003t0001g0302 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.3609+811C>T | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 27/37 | chr18 | 23929576 | |||||||
chr18:23929676 | C | T | 1 | a0001c0001t0001g0162 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.3609+911C>T | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 27/37 | chr18 | 23929676 | |||||||
chr18:23929704 | A | C | 74 | a0001c0001t0002g0011 a0001c0001t0002g0012 a0001c0001t0002g0013 others(71): Show |
77 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(74): Show |
intron_variant | MODIFIER | c.3609+939A>C | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 27/37 | chr18 | 23929704 | |||||||
chr18:23929773 | A | G | 1 | a0001c0003t0001g0303 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.3609+1008A>G | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 27/37 | chr18 | 23929773 | |||||||
chr18:23929910 | C | T | 1 | a0001c0003t0001g0272 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.3609+1145C>T | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 27/37 | chr18 | 23929910 | |||||||
chr18:23930236 | C | G | 1 | a0001c0003t0001g0295 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.3610-826C>G | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 27/37 | chr18 | 23930236 | |||||||
chr18:23930499 | GCAC | G | 4 | a0001c0031t0004g0292 a0014c0020t0004g0233 a0018c0034t0004g0294 others(1): Show |
4 | HG02451.hp2 HG02559.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.3610-561_3610-559d others(5): Show |
LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 27/37 | INFO_REALIGN_3_PRIME | chr18 | 23930499 | ||||||
chr18:23930707 | C | G | 293 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(290): Show |
319 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(316): Show |
intron_variant | MODIFIER | c.3610-355C>G | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 27/37 | chr18 | 23930707 | |||||||
chr18:23930717 | C | G | 2 | a0003c0004t0001g0197 a0003c0004t0001g0198 |
2 | HG00438.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.3610-345C>G | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 27/37 | chr18 | 23930717 | |||||||
chr18:23930870 | A | G | 1 | a0001c0001t0002g0123 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.3610-192A>G | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 27/37 | chr18 | 23930870 | |||||||
chr18:23931208 | G | C | 293 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(290): Show |
319 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(316): Show |
splice_region_variant&intron_variant | LOW | c.3749+7G>C | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 28/37 | chr18 | 23931208 | |||||||
chr18:23931547 | T | C | 1 | a0001c0001t0002g0123 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.3749+346T>C | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 28/37 | chr18 | 23931547 | |||||||
chr18:23931728 | C | T | 1 | a0001c0027t0001g0167 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.3750-432C>T | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 28/37 | chr18 | 23931728 | |||||||
chr18:23931942 | G | A | 1 | a0001c0001t0001g0214 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.3750-218G>A | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 28/37 | chr18 | 23931942 | |||||||
chr18:23932711 | G | C | 1 | a0001c0003t0001g0303 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.3881+420G>C | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 29/37 | chr18 | 23932711 | |||||||
chr18:23932715 | G | C | 4 | a0001c0031t0004g0292 a0014c0020t0004g0233 a0018c0034t0004g0294 others(1): Show |
4 | HG02451.hp2 HG02559.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.3881+424G>C | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 29/37 | chr18 | 23932715 | |||||||
chr18:23932771 | T | G | 5 | a0001c0003t0001g0250 a0001c0003t0001g0251 a0001c0003t0001g0252 others(2): Show |
5 | HG01109.hp2 HG03041.hp2 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.3881+480T>G | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 29/37 | chr18 | 23932771 | |||||||
chr18:23932774 | T | C | 1 | a0001c0037t0001g0215 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.3881+483T>C | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 29/37 | chr18 | 23932774 | |||||||
chr18:23932808 | G | A | 1 | a0001c0001t0002g0031 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.3881+517G>A | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 29/37 | chr18 | 23932808 | |||||||
chr18:23932843 | G | A | 9 | a0001c0006t0001g0020 a0001c0006t0001g0245 a0001c0006t0001g0296 others(6): Show |
9 | HG02258.hp2 HG02572.hp1 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.3881+552G>A | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 29/37 | chr18 | 23932843 | |||||||
chr18:23933031 | G | A | 80 | a0001c0001t0002g0011 a0001c0001t0002g0012 a0001c0001t0002g0013 others(77): Show |
83 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(80): Show |
intron_variant | MODIFIER | c.3881+740G>A | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 29/37 | chr18 | 23933031 | |||||||
chr18:23933155 | A | G | 1 | a0001c0001t0002g0111 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.3882-627A>G | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 29/37 | chr18 | 23933155 | |||||||
chr18:23933208 | C | T | 1 | a0001c0003t0001g0286 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.3882-574C>T | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 29/37 | chr18 | 23933208 | |||||||
chr18:23933294 | G | A | 2 | a0001c0001t0002g0119 a0001c0001t0002g0120 |
2 | HG03195.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.3882-488G>A | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 29/37 | chr18 | 23933294 | |||||||
chr18:23933338 | A | C | 30 | a0001c0003t0001g0006 a0001c0003t0001g0018 a0001c0003t0001g0019 others(27): Show |
34 | HG00280.hp2 HG00639.hp2 HG00738.hp1 others(31): Show |
intron_variant | MODIFIER | c.3882-444A>C | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 29/37 | chr18 | 23933338 | |||||||
chr18:23933389 | A | T | 297 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(294): Show |
323 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(320): Show |
intron_variant | MODIFIER | c.3882-393A>T | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 29/37 | chr18 | 23933389 | |||||||
chr18:23934017 | G | A | 4 | a0001c0031t0004g0292 a0014c0020t0004g0233 a0018c0034t0004g0294 others(1): Show |
4 | HG02451.hp2 HG02559.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.4035+82G>A | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 30/37 | chr18 | 23934017 | |||||||
chr18:23934289 | C | A | 1 | a0002c0002t0001g0094 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.4035+354C>A | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 30/37 | chr18 | 23934289 | |||||||
chr18:23934396 | T | C | 293 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(290): Show |
319 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(316): Show |
intron_variant | MODIFIER | c.4035+461T>C | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 30/37 | chr18 | 23934396 | |||||||
chr18:23934457 | G | A | 1 | a0001c0001t0001g0169 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.4035+522G>A | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 30/37 | chr18 | 23934457 | |||||||
chr18:23934562 | G | A | 1 | a0002c0002t0003g0064 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.4035+627G>A | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 30/37 | chr18 | 23934562 | |||||||
chr18:23934616 | A | T | 2 | a0001c0001t0002g0143 a0001c0001t0002g0150 |
2 | HG00280.hp1 HG00738.hp2 |
intron_variant | MODIFIER | c.4035+681A>T | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 30/37 | chr18 | 23934616 | |||||||
chr18:23934936 | T | A | 1 | a0001c0001t0002g0123 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.4035+1001T>A | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 30/37 | chr18 | 23934936 | |||||||
chr18:23934977 | G | A | 1 | a0001c0011t0001g0243 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.4035+1042G>A | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 30/37 | chr18 | 23934977 | |||||||
chr18:23935027 | T | C | 2 | a0001c0003t0001g0265 a0001c0003t0001g0278 |
2 | NA19060.hp2 NA19078.hp2 |
intron_variant | MODIFIER | c.4035+1092T>C | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 30/37 | chr18 | 23935027 | |||||||
chr18:23935193 | G | T | 9 | a0001c0006t0001g0020 a0001c0006t0001g0245 a0001c0006t0001g0296 others(6): Show |
9 | HG02258.hp2 HG02572.hp1 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.4035+1258G>T | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 30/37 | chr18 | 23935193 | |||||||
chr18:23935225 | G | A | 75 | a0001c0001t0001g0017 a0001c0001t0001g0241 a0001c0001t0001g0246 others(72): Show |
80 | HG00140.hp1 HG00558.hp1 HG00609.hp2 others(77): Show |
intron_variant | MODIFIER | c.4035+1290G>A | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 30/37 | chr18 | 23935225 | |||||||
chr18:23935427 | G | A | 252 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(249): Show |
274 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(271): Show |
intron_variant | MODIFIER | c.4035+1492G>A | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 30/37 | chr18 | 23935427 | |||||||
chr18:23935565 | C | T | 3 | a0001c0001t0002g0116 a0001c0001t0002g0126 a0001c0001t0002g0240 |
3 | HG00099.hp2 HG01071.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.4035+1630C>T | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 30/37 | chr18 | 23935565 | |||||||
chr18:23936185 | ACT | A | 248 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(245): Show |
270 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(267): Show |
intron_variant | MODIFIER | c.4035+2253_4035+225 others(6): Show |
LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 30/37 | INFO_REALIGN_3_PRIME | chr18 | 23936185 | ||||||
chr18:23936245 | A | T | 9 | a0001c0006t0001g0020 a0001c0006t0001g0245 a0001c0006t0001g0296 others(6): Show |
9 | HG02258.hp2 HG02572.hp1 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.4035+2310A>T | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 30/37 | chr18 | 23936245 | |||||||
chr18:23936305 | T | C | 1 | a0001c0001t0001g0047 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.4035+2370T>C | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 30/37 | chr18 | 23936305 | |||||||
chr18:23936476 | G | A | 4 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0024 others(1): Show |
4 | HG01934.hp2 HG03704.hp2 HG03834.hp2 others(1): Show |
intron_variant | MODIFIER | c.4035+2541G>A | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 30/37 | chr18 | 23936476 | |||||||
chr18:23936705 | A | G | 1 | a0001c0001t0001g0219 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.4036-2518A>G | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 30/37 | chr18 | 23936705 | |||||||
chr18:23937028 | GC | G | 9 | a0001c0006t0001g0020 a0001c0006t0001g0245 a0001c0006t0001g0296 others(6): Show |
9 | HG02258.hp2 HG02572.hp1 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.4036-2193delC | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 30/37 | INFO_REALIGN_3_PRIME | chr18 | 23937028 | ||||||
chr18:23937113 | C | G | 40 | a0001c0003t0001g0006 a0001c0003t0001g0018 a0001c0003t0001g0019 others(37): Show |
44 | HG00280.hp2 HG00639.hp2 HG00738.hp1 others(41): Show |
intron_variant | MODIFIER | c.4036-2110C>G | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 30/37 | chr18 | 23937113 | |||||||
chr18:23937132 | A | G | 252 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(249): Show |
274 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(271): Show |
intron_variant | MODIFIER | c.4036-2091A>G | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 30/37 | chr18 | 23937132 | |||||||
chr18:23937152 | G | A | 1 | a0002c0002t0001g0073 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.4036-2071G>A | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 30/37 | chr18 | 23937152 | |||||||
chr18:23937288 | C | A | 1 | a0011c0022t0001g0305 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.4036-1935C>A | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 30/37 | chr18 | 23937288 | |||||||
chr18:23937341 | G | A | 4 | a0001c0001t0001g0191 a0001c0001t0001g0192 a0001c0001t0001g0193 others(1): Show |
4 | HG00741.hp1 HG02738.hp1 HG03239.hp1 others(1): Show |
intron_variant | MODIFIER | c.4036-1882G>A | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 30/37 | chr18 | 23937341 | |||||||
chr18:23937358 | T | A | 3 | a0002c0002t0001g0008 a0002c0002t0001g0009 a0002c0002t0001g0070 |
5 | HG00558.hp1 HG00673.hp2 NA18944.hp2 others(2): Show |
intron_variant | MODIFIER | c.4036-1865T>A | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 30/37 | chr18 | 23937358 | |||||||
chr18:23937371 | CA | C | 173 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(170): Show |
195 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(192): Show |
intron_variant | MODIFIER | c.4036-1825delA | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 30/37 | INFO_REALIGN_3_PRIME | chr18 | 23937371 | ||||||
chr18:23937371 | CAAAAAAA others(4): Show |
C | 2 | a0001c0001t0002g0030 a0001c0001t0002g0132 |
2 | HG01891.hp2 HG04184.hp1 |
intron_variant | MODIFIER | c.4036-1835_4036-182 others(15): Show |
LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 30/37 | INFO_REALIGN_3_PRIME | chr18 | 23937371 | ||||||
chr18:23937371 | CAAAAAAA others(5): Show |
C | 82 | a0001c0001t0001g0191 a0001c0001t0001g0192 a0001c0001t0001g0193 others(79): Show |
85 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(82): Show |
intron_variant | MODIFIER | c.4036-1836_4036-182 others(16): Show |
LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 30/37 | INFO_REALIGN_3_PRIME | chr18 | 23937371 | ||||||
chr18:23937371 | CAAAAAAA others(7): Show |
C | 2 | a0001c0003t0001g0289 a0001c0003t0001g0302 |
2 | HG02280.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.4036-1838_4036-182 others(18): Show |
LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 30/37 | INFO_REALIGN_3_PRIME | chr18 | 23937371 | ||||||
chr18:23937482 | C | G | 4 | a0001c0001t0001g0191 a0001c0001t0001g0192 a0001c0001t0001g0193 others(1): Show |
4 | HG00741.hp1 HG02738.hp1 HG03239.hp1 others(1): Show |
intron_variant | MODIFIER | c.4036-1741C>G | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 30/37 | chr18 | 23937482 | |||||||
chr18:23937580 | C | A | 4 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0024 others(1): Show |
4 | HG01934.hp2 HG03704.hp2 HG03834.hp2 others(1): Show |
intron_variant | MODIFIER | c.4036-1643C>A | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 30/37 | chr18 | 23937580 | |||||||
chr18:23937854 | G | A | 4 | a0001c0001t0001g0191 a0001c0001t0001g0192 a0001c0001t0001g0193 others(1): Show |
4 | HG00741.hp1 HG02738.hp1 HG03239.hp1 others(1): Show |
intron_variant | MODIFIER | c.4036-1369G>A | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 30/37 | chr18 | 23937854 | |||||||
chr18:23938137 | G | A | 249 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(246): Show |
269 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(266): Show |
intron_variant | MODIFIER | c.4036-1086G>A | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 30/37 | chr18 | 23938137 | |||||||
chr18:23938542 | C | T | 2 | a0001c0001t0001g0184 a0001c0001t0001g0190 |
2 | HG02083.hp2 NA18955.hp2 |
intron_variant | MODIFIER | c.4036-681C>T | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 30/37 | chr18 | 23938542 | |||||||
chr18:23938667 | G | A | 1 | a0001c0011t0001g0253 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.4036-556G>A | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 30/37 | chr18 | 23938667 | |||||||
chr18:23938672 | C | T | 156 | a0001c0001t0001g0017 a0001c0001t0001g0047 a0001c0001t0001g0173 others(153): Show |
162 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(159): Show |
intron_variant | MODIFIER | c.4036-551C>T | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 30/37 | chr18 | 23938672 | |||||||
chr18:23938731 | G | A | 154 | a0001c0001t0001g0017 a0001c0001t0001g0047 a0001c0001t0001g0241 others(151): Show |
160 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(157): Show |
intron_variant | MODIFIER | c.4036-492G>A | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 30/37 | chr18 | 23938731 | |||||||
chr18:23938813 | C | T | 1 | a0001c0001t0002g0033 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.4036-410C>T | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 30/37 | chr18 | 23938813 | |||||||
chr18:23938819 | A | AAAG | 295 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(292): Show |
321 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(318): Show |
intron_variant | MODIFIER | c.4036-403_4036-401d others(5): Show |
LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 30/37 | INFO_REALIGN_3_PRIME | chr18 | 23938819 | ||||||
chr18:23938976 | A | C | 1 | a0001c0001t0002g0135 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.4036-247A>C | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 30/37 | chr18 | 23938976 | |||||||
chr18:23938993 | G | T | 2 | a0001c0003t0001g0265 a0001c0003t0001g0278 |
2 | NA19060.hp2 NA19078.hp2 |
intron_variant | MODIFIER | c.4036-230G>T | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 30/37 | chr18 | 23938993 | |||||||
chr18:23939493 | G | A | 2 | a0001c0001t0001g0238 a0001c0001t0001g0239 |
2 | NA18964.hp2 NA19011.hp1 |
intron_variant | MODIFIER | c.4199+107G>A | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 31/37 | chr18 | 23939493 | |||||||
chr18:23939546 | G | A | 1 | a0001c0001t0001g0258 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.4199+160G>A | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 31/37 | chr18 | 23939546 | |||||||
chr18:23939593 | G | A | 1 | a0001c0001t0001g0047 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.4199+207G>A | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 31/37 | chr18 | 23939593 | |||||||
chr18:23939672 | A | C | 86 | a0001c0001t0001g0017 a0001c0001t0001g0201 a0001c0001t0001g0207 others(83): Show |
91 | HG00140.hp1 HG00558.hp1 HG00609.hp2 others(88): Show |
intron_variant | MODIFIER | c.4199+286A>C | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 31/37 | chr18 | 23939672 | |||||||
chr18:23939756 | T | C | 2 | a0001c0001t0002g0127 a0001c0001t0002g0131 |
2 | HG01099.hp2 HG01496.hp2 |
intron_variant | MODIFIER | c.4199+370T>C | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 31/37 | chr18 | 23939756 | |||||||
chr18:23940189 | G | A | 1 | a0002c0002t0001g0077 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.4199+803G>A | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 31/37 | chr18 | 23940189 | |||||||
chr18:23940216 | G | A | 63 | a0002c0002t0001g0008 a0002c0002t0001g0009 a0002c0002t0001g0010 others(60): Show |
67 | HG00140.hp1 HG00558.hp1 HG00609.hp2 others(64): Show |
intron_variant | MODIFIER | c.4199+830G>A | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 31/37 | chr18 | 23940216 | |||||||
chr18:23940309 | G | C | 4 | a0001c0001t0002g0119 a0001c0001t0002g0120 a0001c0001t0002g0121 others(1): Show |
4 | HG01167.hp2 HG02630.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.4199+923G>C | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 31/37 | chr18 | 23940309 | |||||||
chr18:23940690 | A | G | 2 | a0001c0001t0001g0202 a0001c0001t0001g0203 |
2 | HG03654.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.4199+1304A>G | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 31/37 | chr18 | 23940690 | |||||||
chr18:23940695 | T | C | 1 | a0001c0001t0001g0165 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.4199+1309T>C | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 31/37 | chr18 | 23940695 | |||||||
chr18:23940788 | A | G | 13 | a0001c0001t0001g0017 a0001c0001t0001g0241 a0001c0001t0001g0246 others(10): Show |
14 | HG01884.hp1 HG01891.hp1 HG02109.hp2 others(11): Show |
intron_variant | MODIFIER | c.4199+1402A>G | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 31/37 | chr18 | 23940788 | |||||||
chr18:23940845 | TC | T | 289 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(286): Show |
315 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(312): Show |
intron_variant | MODIFIER | c.4199+1463delC | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 31/37 | INFO_REALIGN_3_PRIME | chr18 | 23940845 | ||||||
chr18:23940858 | C | T | 10 | a0001c0001t0001g0201 a0001c0001t0001g0207 a0001c0001t0001g0208 others(7): Show |
10 | HG02145.hp2 HG02257.hp1 HG02258.hp1 others(7): Show |
intron_variant | MODIFIER | c.4199+1472C>T | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 31/37 | chr18 | 23940858 | |||||||
chr18:23940865 | A | G | 293 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(290): Show |
319 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(316): Show |
intron_variant | MODIFIER | c.4199+1479A>G | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 31/37 | chr18 | 23940865 | |||||||
chr18:23940934 | CTTTT | C | 4 | a0001c0031t0004g0292 a0014c0020t0004g0233 a0018c0034t0004g0294 others(1): Show |
4 | HG02451.hp2 HG02559.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.4199+1549_4199+155 others(8): Show |
LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 31/37 | chr18 | 23940934 | |||||||
chr18:23940939 | C | CT | 158 | a0001c0001t0001g0017 a0001c0001t0001g0173 a0001c0001t0001g0174 others(155): Show |
166 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(163): Show |
intron_variant | MODIFIER | c.4199+1568dupT | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 31/37 | INFO_REALIGN_3_PRIME | chr18 | 23940939 | ||||||
chr18:23940939 | CT | C | 10 | a0001c0001t0001g0170 a0001c0006t0001g0020 a0001c0006t0001g0245 others(7): Show |
10 | HG02258.hp2 HG02572.hp1 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.4199+1568delT | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 31/37 | INFO_REALIGN_3_PRIME | chr18 | 23940939 | ||||||
chr18:23940960 | G | A | 289 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(286): Show |
315 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(312): Show |
intron_variant | MODIFIER | c.4199+1574G>A | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 31/37 | chr18 | 23940960 | |||||||
chr18:23941099 | C | T | 4 | a0001c0001t0001g0191 a0001c0001t0001g0192 a0001c0001t0001g0193 others(1): Show |
4 | HG00741.hp1 HG02738.hp1 HG03239.hp1 others(1): Show |
intron_variant | MODIFIER | c.4199+1713C>T | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 31/37 | chr18 | 23941099 | |||||||
chr18:23941157 | C | A | 1 | a0001c0001t0002g0044 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.4199+1771C>A | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 31/37 | chr18 | 23941157 | |||||||
chr18:23941226 | G | A | 1 | a0002c0002t0001g0094 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.4199+1840G>A | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 31/37 | chr18 | 23941226 | |||||||
chr18:23941285 | C | T | 1 | a0002c0002t0001g0084 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.4199+1899C>T | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 31/37 | chr18 | 23941285 | |||||||
chr18:23941323 | GGC | G | 174 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(171): Show |
195 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(192): Show |
intron_variant | MODIFIER | c.4199+1940_4199+194 others(6): Show |
LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 31/37 | INFO_REALIGN_3_PRIME | chr18 | 23941323 | ||||||
chr18:23941324 | G | GC | 22 | a0002c0002t0001g0048 a0002c0002t0001g0053 a0002c0002t0001g0060 others(19): Show |
23 | HG00140.hp1 HG00609.hp2 HG01069.hp2 others(20): Show |
intron_variant | MODIFIER | c.4199+1939dupC | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 31/37 | INFO_REALIGN_3_PRIME | chr18 | 23941324 | ||||||
chr18:23941324 | G | GCC | 30 | a0002c0002t0001g0010 a0002c0002t0001g0026 a0002c0002t0001g0049 others(27): Show |
31 | HG00621.hp2 HG00741.hp2 HG01123.hp1 others(28): Show |
intron_variant | MODIFIER | c.4199+1939_4199+194 others(6): Show |
LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 31/37 | INFO_REALIGN_3_PRIME | chr18 | 23941324 | ||||||
chr18:23941324 | G | GCCC | 10 | a0002c0002t0001g0008 a0002c0002t0001g0009 a0002c0002t0001g0055 others(7): Show |
12 | HG00558.hp1 HG00673.hp2 HG01168.hp1 others(9): Show |
intron_variant | MODIFIER | c.4199+1939_4199+194 others(7): Show |
LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 31/37 | INFO_REALIGN_3_PRIME | chr18 | 23941324 | ||||||
chr18:23941325 | CG | C | 46 | a0001c0001t0001g0017 a0001c0001t0001g0171 a0001c0001t0001g0178 others(43): Show |
47 | HG00438.hp1 HG00642.hp1 HG01099.hp2 others(44): Show |
intron_variant | MODIFIER | c.4199+1940delG | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 31/37 | chr18 | 23941325 | |||||||
chr18:23941326 | G | C | 72 | a0001c0001t0001g0047 a0001c0001t0001g0166 a0001c0001t0001g0179 others(69): Show |
76 | HG00140.hp1 HG00423.hp2 HG00558.hp1 others(73): Show |
intron_variant | MODIFIER | c.4199+1940G>C | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 31/37 | chr18 | 23941326 | |||||||
chr18:23941330 | C | A | 1 | a0001c0003t0001g0295 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.4199+1944C>A | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 31/37 | chr18 | 23941330 | |||||||
chr18:23941331 | C | A | 1 | a0002c0002t0001g0094 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.4199+1945C>A | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 31/37 | chr18 | 23941331 | |||||||
chr18:23941333 | C | G | 3 | a0001c0003t0001g0018 a0001c0003t0001g0273 a0001c0003t0001g0288 |
4 | HG02040.hp1 NA18953.hp2 NA18960.hp2 others(1): Show |
intron_variant | MODIFIER | c.4199+1947C>G | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 31/37 | chr18 | 23941333 | |||||||
chr18:23941334 | C | A | 13 | a0001c0001t0001g0017 a0001c0001t0001g0241 a0001c0001t0001g0246 others(10): Show |
14 | HG01884.hp1 HG01891.hp1 HG02109.hp2 others(11): Show |
intron_variant | MODIFIER | c.4199+1948C>A | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 31/37 | chr18 | 23941334 | |||||||
chr18:23941334 | C | G | 1 | a0001c0001t0001g0014 | 2 | HG02922.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.4199+1948C>G | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 31/37 | chr18 | 23941334 | |||||||
chr18:23941337 | G | C | 1 | a0001c0001t0002g0121 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.4199+1951G>C | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 31/37 | chr18 | 23941337 | |||||||
chr18:23941337 | G | T | 1 | a0023c0033t0001g0283 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.4199+1951G>T | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 31/37 | chr18 | 23941337 | |||||||
chr18:23941617 | C | T | 1 | a0001c0001t0001g0246 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.4200-2171C>T | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 31/37 | chr18 | 23941617 | |||||||
chr18:23942017 | G | A | 1 | a0001c0001t0002g0139 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.4200-1771G>A | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 31/37 | chr18 | 23942017 | |||||||
chr18:23942231 | G | T | 4 | a0001c0001t0001g0191 a0001c0001t0001g0192 a0001c0001t0001g0193 others(1): Show |
4 | HG00741.hp1 HG02738.hp1 HG03239.hp1 others(1): Show |
intron_variant | MODIFIER | c.4200-1557G>T | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 31/37 | chr18 | 23942231 | |||||||
chr18:23942352 | T | C | 1 | a0001c0001t0001g0204 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.4200-1436T>C | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 31/37 | chr18 | 23942352 | |||||||
chr18:23942580 | CT | C | 248 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(245): Show |
270 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(267): Show |
intron_variant | MODIFIER | c.4200-1190delT | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 31/37 | INFO_REALIGN_3_PRIME | chr18 | 23942580 | ||||||
chr18:23942735 | G | A | 1 | a0001c0006t0001g0298 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.4200-1053G>A | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 31/37 | chr18 | 23942735 | |||||||
chr18:23942876 | C | T | 4 | a0001c0031t0004g0292 a0014c0020t0004g0233 a0018c0034t0004g0294 others(1): Show |
4 | HG02451.hp2 HG02559.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.4200-912C>T | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 31/37 | chr18 | 23942876 | |||||||
chr18:23943005 | C | T | 6 | a0001c0003t0001g0250 a0001c0003t0001g0251 a0001c0003t0001g0252 others(3): Show |
6 | HG01109.hp2 HG03041.hp2 HG03225.hp1 others(3): Show |
intron_variant | MODIFIER | c.4200-783C>T | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 31/37 | chr18 | 23943005 | |||||||
chr18:23943085 | C | G | 1 | a0012c0029t0003g0103 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.4200-703C>G | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 31/37 | chr18 | 23943085 | |||||||
chr18:23943099 | C | A | 86 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(83): Show |
100 | HG00423.hp2 HG00438.hp1 HG00558.hp2 others(97): Show |
intron_variant | MODIFIER | c.4200-689C>A | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 31/37 | chr18 | 23943099 | |||||||
chr18:23943115 | G | A | 1 | a0001c0001t0001g0047 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.4200-673G>A | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 31/37 | chr18 | 23943115 | |||||||
chr18:23943179 | A | C | 3 | a0006c0010t0001g0205 a0006c0010t0001g0206 a0006c0010t0001g0235 |
3 | HG02615.hp2 HG02622.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.4200-609A>C | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 31/37 | chr18 | 23943179 | |||||||
chr18:23943305 | G | T | 1 | a0001c0003t0001g0269 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.4200-483G>T | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 31/37 | chr18 | 23943305 | |||||||
chr18:23943418 | A | T | 297 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(294): Show |
323 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(320): Show |
intron_variant | MODIFIER | c.4200-370A>T | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 31/37 | chr18 | 23943418 | |||||||
chr18:23943475 | A | G | 1 | a0001c0001t0001g0196 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.4200-313A>G | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 31/37 | chr18 | 23943475 | |||||||
chr18:23943568 | C | G | 40 | a0001c0003t0001g0006 a0001c0003t0001g0018 a0001c0003t0001g0019 others(37): Show |
44 | HG00280.hp2 HG00639.hp2 HG00738.hp1 others(41): Show |
intron_variant | MODIFIER | c.4200-220C>G | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 31/37 | chr18 | 23943568 | |||||||
chr18:23943601 | T | C | 1 | a0001c0001t0002g0148 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.4200-187T>C | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 31/37 | chr18 | 23943601 | |||||||
chr18:23943777 | G | A | 3 | a0001c0003t0001g0018 a0001c0003t0001g0273 a0001c0003t0001g0288 |
4 | HG02040.hp1 NA18953.hp2 NA18960.hp2 others(1): Show |
intron_variant | MODIFIER | c.4200-11G>A | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 31/37 | chr18 | 23943777 | |||||||
chr18:23944053 | C | T | 2 | a0008c0016t0001g0079 a0008c0016t0001g0082 |
2 | HG03490.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.4383+82C>T | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 32/37 | chr18 | 23944053 | |||||||
chr18:23944071 | G | A | 1 | a0001c0001t0001g0304 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.4383+100G>A | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 32/37 | chr18 | 23944071 | |||||||
chr18:23944101 | C | T | 1 | a0001c0003t0001g0303 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.4383+130C>T | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 32/37 | chr18 | 23944101 | |||||||
chr18:23944586 | A | T | 88 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(85): Show |
102 | HG00423.hp2 HG00438.hp1 HG00558.hp2 others(99): Show |
intron_variant | MODIFIER | c.4383+615A>T | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 32/37 | chr18 | 23944586 | |||||||
chr18:23944675 | G | A | 62 | a0002c0002t0001g0008 a0002c0002t0001g0009 a0002c0002t0001g0010 others(59): Show |
66 | HG00140.hp1 HG00558.hp1 HG00609.hp2 others(63): Show |
intron_variant | MODIFIER | c.4383+704G>A | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 32/37 | chr18 | 23944675 | |||||||
chr18:23944796 | G | A | 77 | a0001c0001t0002g0011 a0001c0001t0002g0012 a0001c0001t0002g0013 others(74): Show |
80 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(77): Show |
intron_variant | MODIFIER | c.4383+825G>A | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 32/37 | chr18 | 23944796 | |||||||
chr18:23944993 | C | A | 2 | a0002c0002t0001g0105 a0020c0028t0001g0106 |
2 | HG02083.hp1 HG04184.hp2 |
intron_variant | MODIFIER | c.4383+1022C>A | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 32/37 | chr18 | 23944993 | |||||||
chr18:23944994 | A | G | 2 | a0002c0002t0001g0105 a0020c0028t0001g0106 |
2 | HG02083.hp1 HG04184.hp2 |
intron_variant | MODIFIER | c.4383+1023A>G | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 32/37 | chr18 | 23944994 | |||||||
chr18:23945237 | C | T | 1 | a0014c0020t0004g0233 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.4384-907C>T | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 32/37 | chr18 | 23945237 | |||||||
chr18:23945297 | G | A | 8 | a0001c0001t0001g0166 a0001c0001t0001g0178 a0001c0001t0001g0179 others(5): Show |
8 | HG00423.hp2 HG02071.hp2 HG02083.hp2 others(5): Show |
intron_variant | MODIFIER | c.4384-847G>A | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 32/37 | chr18 | 23945297 | |||||||
chr18:23945325 | C | T | 1 | a0016c0024t0001g0021 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.4384-819C>T | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 32/37 | chr18 | 23945325 | |||||||
chr18:23945547 | C | G | 4 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0024 others(1): Show |
4 | HG01934.hp2 HG03704.hp2 HG03834.hp2 others(1): Show |
intron_variant | MODIFIER | c.4384-597C>G | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 32/37 | chr18 | 23945547 | |||||||
chr18:23945759 | C | T | 4 | a0001c0001t0001g0191 a0001c0001t0001g0192 a0001c0001t0001g0193 others(1): Show |
4 | HG00741.hp1 HG02738.hp1 HG03239.hp1 others(1): Show |
intron_variant | MODIFIER | c.4384-385C>T | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 32/37 | chr18 | 23945759 | |||||||
chr18:23945788 | T | A | 4 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0024 others(1): Show |
4 | HG01934.hp2 HG03704.hp2 HG03834.hp2 others(1): Show |
intron_variant | MODIFIER | c.4384-356T>A | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 32/37 | chr18 | 23945788 | |||||||
chr18:23946001 | G | A | 2 | a0001c0003t0001g0289 a0001c0003t0001g0302 |
2 | HG02280.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.4384-143G>A | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 32/37 | chr18 | 23946001 | |||||||
chr18:23946042 | C | G | 2 | a0001c0001t0001g0202 a0001c0001t0001g0203 |
2 | HG03654.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.4384-102C>G | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 32/37 | chr18 | 23946042 | |||||||
chr18:23946123 | C | T | 79 | a0001c0001t0002g0011 a0001c0001t0002g0012 a0001c0001t0002g0013 others(76): Show |
82 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(79): Show |
intron_variant | MODIFIER | c.4384-21C>T | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 32/37 | chr18 | 23946123 | |||||||
chr18:23946729 | A | G | 1 | a0011c0022t0001g0305 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.4524+445A>G | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 33/37 | chr18 | 23946729 | |||||||
chr18:23946832 | A | G | 1 | a0001c0001t0001g0047 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.4524+548A>G | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 33/37 | chr18 | 23946832 | |||||||
chr18:23946889 | C | T | 1 | a0001c0001t0001g0165 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.4524+605C>T | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 33/37 | chr18 | 23946889 | |||||||
chr18:23946890 | G | A | 4 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0024 others(1): Show |
4 | HG01934.hp2 HG03704.hp2 HG03834.hp2 others(1): Show |
intron_variant | MODIFIER | c.4524+606G>A | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 33/37 | chr18 | 23946890 | |||||||
chr18:23946891 | T | C | 1 | a0001c0001t0001g0222 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.4524+607T>C | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 33/37 | chr18 | 23946891 | |||||||
chr18:23947200 | C | G | 36 | a0001c0001t0001g0229 a0001c0003t0001g0006 a0001c0003t0001g0018 others(33): Show |
40 | HG00280.hp2 HG00639.hp2 HG00738.hp1 others(37): Show |
intron_variant | MODIFIER | c.4524+916C>G | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 33/37 | chr18 | 23947200 | |||||||
chr18:23947291 | G | T | 1 | a0017c0036t0001g0290 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.4524+1007G>T | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 33/37 | chr18 | 23947291 | |||||||
chr18:23947302 | C | G | 1 | a0001c0003t0001g0286 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.4524+1018C>G | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 33/37 | chr18 | 23947302 | |||||||
chr18:23947327 | G | T | 1 | a0024c0026t0004g0301 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.4524+1043G>T | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 33/37 | chr18 | 23947327 | |||||||
chr18:23947482 | G | A | 1 | a0016c0024t0001g0021 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.4524+1198G>A | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 33/37 | chr18 | 23947482 | |||||||
chr18:23947486 | G | A | 2 | a0001c0003t0001g0289 a0001c0003t0001g0302 |
2 | HG02280.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.4524+1202G>A | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 33/37 | chr18 | 23947486 | |||||||
chr18:23947545 | C | T | 1 | a0001c0001t0002g0124 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.4524+1261C>T | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 33/37 | chr18 | 23947545 | |||||||
chr18:23947721 | C | T | 86 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(83): Show |
100 | HG00423.hp2 HG00438.hp1 HG00558.hp2 others(97): Show |
intron_variant | MODIFIER | c.4524+1437C>T | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 33/37 | chr18 | 23947721 | |||||||
chr18:23947812 | CT | C | 149 | a0001c0001t0001g0047 a0001c0001t0001g0169 a0001c0001t0001g0191 others(146): Show |
156 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(153): Show |
intron_variant | MODIFIER | c.4524+1545delT | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 33/37 | INFO_REALIGN_3_PRIME | chr18 | 23947812 | ||||||
chr18:23947812 | CTT | C | 7 | a0001c0001t0002g0037 a0001c0001t0002g0044 a0001c0001t0002g0117 others(4): Show |
7 | HG00280.hp1 HG03491.hp2 NA18946.hp1 others(4): Show |
intron_variant | MODIFIER | c.4524+1544_4524+154 others(6): Show |
LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 33/37 | INFO_REALIGN_3_PRIME | chr18 | 23947812 | ||||||
chr18:23947898 | G | A | 63 | a0002c0002t0001g0008 a0002c0002t0001g0009 a0002c0002t0001g0010 others(60): Show |
67 | HG00140.hp1 HG00558.hp1 HG00609.hp2 others(64): Show |
intron_variant | MODIFIER | c.4524+1614G>A | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 33/37 | chr18 | 23947898 | |||||||
chr18:23948048 | G | A | 1 | a0002c0002t0001g0072 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.4525-1717G>A | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 33/37 | chr18 | 23948048 | |||||||
chr18:23948107 | C | T | 7 | a0001c0001t0001g0017 a0001c0001t0001g0241 a0001c0001t0001g0249 others(4): Show |
8 | HG01884.hp1 HG01891.hp1 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.4525-1658C>T | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 33/37 | chr18 | 23948107 | |||||||
chr18:23948180 | C | A | 1 | a0001c0003t0001g0264 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.4525-1585C>A | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 33/37 | chr18 | 23948180 | |||||||
chr18:23948377 | G | A | 63 | a0002c0002t0001g0008 a0002c0002t0001g0009 a0002c0002t0001g0010 others(60): Show |
67 | HG00140.hp1 HG00558.hp1 HG00609.hp2 others(64): Show |
intron_variant | MODIFIER | c.4525-1388G>A | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 33/37 | chr18 | 23948377 | |||||||
chr18:23948383 | G | A | 1 | a0001c0001t0001g0175 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.4525-1382G>A | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 33/37 | chr18 | 23948383 | |||||||
chr18:23948560 | T | C | 1 | a0001c0003t0001g0303 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.4525-1205T>C | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 33/37 | chr18 | 23948560 | |||||||
chr18:23948639 | G | A | 86 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(83): Show |
100 | HG00423.hp2 HG00438.hp1 HG00558.hp2 others(97): Show |
intron_variant | MODIFIER | c.4525-1126G>A | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 33/37 | chr18 | 23948639 | |||||||
chr18:23948759 | G | A | 2 | a0001c0001t0001g0204 a0001c0006t0001g0298 |
2 | HG02280.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.4525-1006G>A | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 33/37 | chr18 | 23948759 | |||||||
chr18:23948964 | G | C | 1 | a0001c0001t0001g0175 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.4525-801G>C | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 33/37 | chr18 | 23948964 | |||||||
chr18:23948974 | C | T | 1 | a0010c0014t0001g0217 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.4525-791C>T | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 33/37 | chr18 | 23948974 | |||||||
chr18:23949026 | G | A | 1 | a0011c0022t0001g0305 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.4525-739G>A | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 33/37 | chr18 | 23949026 | |||||||
chr18:23949043 | A | G | 40 | a0001c0003t0001g0006 a0001c0003t0001g0018 a0001c0003t0001g0019 others(37): Show |
44 | HG00280.hp2 HG00639.hp2 HG00738.hp1 others(41): Show |
intron_variant | MODIFIER | c.4525-722A>G | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 33/37 | chr18 | 23949043 | |||||||
chr18:23949329 | C | T | 1 | a0014c0020t0004g0233 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.4525-436C>T | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 33/37 | chr18 | 23949329 | |||||||
chr18:23949413 | TCCATCTG others(6): Show |
T | 1 | a0001c0001t0001g0047 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.4525-348_4525-336d others(15): Show |
LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 33/37 | INFO_REALIGN_3_PRIME | chr18 | 23949413 | ||||||
chr18:23949556 | A | C | 1 | a0002c0002t0001g0072 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.4525-209A>C | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 33/37 | chr18 | 23949556 | |||||||
chr18:23949758 | G | A | 80 | a0001c0001t0002g0011 a0001c0001t0002g0012 a0001c0001t0002g0013 others(77): Show |
83 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(80): Show |
splice_region_variant&intron_variant | LOW | c.4525-7G>A | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 33/37 | chr18 | 23949758 | |||||||
chr18:23949996 | G | A | 1 | a0002c0002t0001g0060 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.4685-33G>A | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 34/37 | chr18 | 23949996 | |||||||
chr18:23950294 | TA | T | 14 | a0002c0002t0001g0010 a0002c0002t0001g0048 a0002c0002t0001g0049 others(11): Show |
15 | HG00621.hp2 HG01123.hp1 NA18942.hp2 others(12): Show |
intron_variant | MODIFIER | c.4815+136delA | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 35/37 | chr18 | 23950294 | |||||||
chr18:23950558 | A | G | 1 | a0016c0024t0001g0021 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.4815+399A>G | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 35/37 | chr18 | 23950558 | |||||||
chr18:23950573 | G | A | 1 | a0001c0001t0002g0117 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.4815+414G>A | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 35/37 | chr18 | 23950573 | |||||||
chr18:23950702 | T | A | 86 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(83): Show |
100 | HG00423.hp2 HG00438.hp1 HG00558.hp2 others(97): Show |
intron_variant | MODIFIER | c.4815+543T>A | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 35/37 | chr18 | 23950702 | |||||||
chr18:23950786 | G | A | 5 | a0001c0003t0001g0250 a0001c0003t0001g0251 a0001c0003t0001g0252 others(2): Show |
5 | HG01109.hp2 HG03041.hp2 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.4815+627G>A | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 35/37 | chr18 | 23950786 | |||||||
chr18:23950827 | C | A | 1 | a0001c0001t0001g0162 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.4815+668C>A | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 35/37 | chr18 | 23950827 | |||||||
chr18:23951053 | T | C | 1 | a0003c0004t0001g0188 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.4816-631T>C | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 35/37 | chr18 | 23951053 | |||||||
chr18:23951093 | T | C | 4 | a0001c0001t0001g0191 a0001c0001t0001g0192 a0001c0001t0001g0193 others(1): Show |
4 | HG00741.hp1 HG02738.hp1 HG03239.hp1 others(1): Show |
intron_variant | MODIFIER | c.4816-591T>C | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 35/37 | chr18 | 23951093 | |||||||
chr18:23951182 | C | T | 2 | a0001c0001t0002g0123 a0001c0001t0002g0139 |
2 | HG02071.hp1 NA19084.hp1 |
intron_variant | MODIFIER | c.4816-502C>T | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 35/37 | chr18 | 23951182 | |||||||
chr18:23951195 | C | T | 45 | a0001c0001t0001g0002 a0001c0001t0001g0014 a0001c0001t0001g0015 others(42): Show |
52 | HG00423.hp2 HG00438.hp1 HG00558.hp2 others(49): Show |
intron_variant | MODIFIER | c.4816-489C>T | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 35/37 | chr18 | 23951195 | |||||||
chr18:23951300 | C | A | 1 | a0001c0003t0001g0289 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.4816-384C>A | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 35/37 | chr18 | 23951300 | |||||||
chr18:23951367 | AG | A | 7 | a0001c0003t0001g0006 a0001c0003t0001g0264 a0001c0003t0001g0269 others(4): Show |
9 | HG00639.hp2 HG00738.hp1 HG01099.hp1 others(6): Show |
intron_variant | MODIFIER | c.4816-315delG | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 35/37 | INFO_REALIGN_3_PRIME | chr18 | 23951367 | ||||||
chr18:23951488 | C | A | 2 | a0001c0003t0001g0265 a0001c0003t0001g0278 |
2 | NA19060.hp2 NA19078.hp2 |
intron_variant | MODIFIER | c.4816-196C>A | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 35/37 | chr18 | 23951488 | |||||||
chr18:23951548 | T | C | 100 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(97): Show |
115 | HG00423.hp2 HG00438.hp1 HG00558.hp2 others(112): Show |
intron_variant | MODIFIER | c.4816-136T>C | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 35/37 | chr18 | 23951548 | |||||||
chr18:23951558 | A | G | 4 | a0001c0001t0001g0191 a0001c0001t0001g0192 a0001c0001t0001g0193 others(1): Show |
4 | HG00741.hp1 HG02738.hp1 HG03239.hp1 others(1): Show |
intron_variant | MODIFIER | c.4816-126A>G | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 35/37 | chr18 | 23951558 | |||||||
chr18:23951670 | C | T | 4 | a0001c0001t0001g0191 a0001c0001t0001g0192 a0001c0001t0001g0193 others(1): Show |
4 | HG00741.hp1 HG02738.hp1 HG03239.hp1 others(1): Show |
intron_variant | MODIFIER | c.4816-14C>T | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 35/37 | chr18 | 23951670 | |||||||
chr18:23951937 | C | T | 8 | a0001c0003t0001g0006 a0001c0003t0001g0264 a0001c0003t0001g0267 others(5): Show |
10 | HG00639.hp2 HG00738.hp1 HG01099.hp1 others(7): Show |
intron_variant | MODIFIER | c.4909+160C>T | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 36/37 | chr18 | 23951937 | |||||||
chr18:23951942 | C | T | 79 | a0001c0001t0002g0011 a0001c0001t0002g0012 a0001c0001t0002g0013 others(76): Show |
82 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(79): Show |
intron_variant | MODIFIER | c.4909+165C>T | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 36/37 | chr18 | 23951942 | |||||||
chr18:23952002 | G | T | 1 | a0001c0001t0002g0149 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.4909+225G>T | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 36/37 | chr18 | 23952002 | |||||||
chr18:23952469 | C | T | 4 | a0001c0001t0001g0191 a0001c0001t0001g0192 a0001c0001t0001g0193 others(1): Show |
4 | HG00741.hp1 HG02738.hp1 HG03239.hp1 others(1): Show |
intron_variant | MODIFIER | c.4910-521C>T | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 36/37 | chr18 | 23952469 | |||||||
chr18:23952495 | C | T | 133 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0024 others(130): Show |
140 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(137): Show |
intron_variant | MODIFIER | c.4910-495C>T | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 36/37 | chr18 | 23952495 | |||||||
chr18:23952569 | C | T | 1 | a0001c0001t0002g0145 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.4910-421C>T | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 36/37 | chr18 | 23952569 | |||||||
chr18:23952592 | G | A | 3 | a0001c0001t0002g0035 a0001c0001t0002g0037 a0001c0001t0002g0038 |
3 | HG00423.hp1 NA18957.hp2 NA19058.hp2 |
intron_variant | MODIFIER | c.4910-398G>A | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 36/37 | chr18 | 23952592 | |||||||
chr18:23952957 | C | T | 4 | a0001c0031t0004g0292 a0014c0020t0004g0233 a0018c0034t0004g0294 others(1): Show |
4 | HG02451.hp2 HG02559.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.4910-33C>T | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 36/37 | chr18 | 23952957 | |||||||
chr18:23953195 | G | A | 1 | a0002c0002t0001g0063 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.5029+86G>A | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 37/37 | chr18 | 23953195 | |||||||
chr18:23953320 | ATTTTGTT others(6): Show |
A | 1 | a0001c0003t0001g0250 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.5029+228_5029+240d others(15): Show |
LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 37/37 | INFO_REALIGN_3_PRIME | chr18 | 23953320 | ||||||
chr18:23953325 | GT | G | 284 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(281): Show |
310 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(307): Show |
intron_variant | MODIFIER | c.5029+228delT | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 37/37 | INFO_REALIGN_3_PRIME | chr18 | 23953325 | ||||||
chr18:23953327 | T | G | 4 | a0001c0001t0001g0017 a0001c0001t0001g0249 a0001c0001t0001g0256 others(1): Show |
5 | HG02486.hp1 HG02559.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.5029+218T>G | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 37/37 | chr18 | 23953327 | |||||||
chr18:23953328 | T | G | 1 | a0002c0002t0001g0098 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.5029+219T>G | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 37/37 | chr18 | 23953328 | |||||||
chr18:23953334 | T | G | 1 | a0001c0003t0001g0302 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.5029+225T>G | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 37/37 | chr18 | 23953334 | |||||||
chr18:23953335 | T | G | 1 | a0001c0003t0001g0018 | 2 | HG02040.hp1 NA19012.hp1 |
intron_variant | MODIFIER | c.5029+226T>G | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 37/37 | chr18 | 23953335 | |||||||
chr18:23953337 | T | G | 1 | a0001c0001t0002g0123 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.5029+228T>G | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 37/37 | chr18 | 23953337 | |||||||
chr18:23953338 | G | T | 5 | a0001c0001t0001g0191 a0001c0001t0001g0192 a0001c0001t0001g0193 others(2): Show |
5 | HG00741.hp1 HG02738.hp1 HG03239.hp1 others(2): Show |
intron_variant | MODIFIER | c.5029+229G>T | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 37/37 | chr18 | 23953338 | |||||||
chr18:23953339 | T | G | 5 | a0001c0001t0001g0191 a0001c0001t0001g0192 a0001c0001t0001g0193 others(2): Show |
5 | HG00741.hp1 HG02738.hp1 HG03239.hp1 others(2): Show |
intron_variant | MODIFIER | c.5029+230T>G | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 37/37 | chr18 | 23953339 | |||||||
chr18:23953350 | G | GT | 14 | a0001c0001t0001g0017 a0001c0001t0001g0241 a0001c0001t0001g0246 others(11): Show |
15 | HG01123.hp2 HG01884.hp1 HG01891.hp1 others(12): Show |
intron_variant | MODIFIER | c.5029+250dupT | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 37/37 | INFO_REALIGN_3_PRIME | chr18 | 23953350 | ||||||
chr18:23953395 | G | A | 4 | a0001c0001t0001g0191 a0001c0001t0001g0192 a0001c0001t0001g0193 others(1): Show |
4 | HG00741.hp1 HG02738.hp1 HG03239.hp1 others(1): Show |
intron_variant | MODIFIER | c.5029+286G>A | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 37/37 | chr18 | 23953395 | |||||||
chr18:23953516 | G | A | 4 | a0001c0001t0001g0191 a0001c0001t0001g0192 a0001c0001t0001g0193 others(1): Show |
4 | HG00741.hp1 HG02738.hp1 HG03239.hp1 others(1): Show |
intron_variant | MODIFIER | c.5029+407G>A | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 37/37 | chr18 | 23953516 | |||||||
chr18:23953589 | G | A | 1 | a0004c0005t0002g0129 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.5029+480G>A | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 37/37 | chr18 | 23953589 | |||||||
chr18:23953734 | G | T | 1 | a0001c0003t0001g0302 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.5029+625G>T | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 37/37 | chr18 | 23953734 | |||||||
chr18:23953782 | T | C | 1 | a0001c0001t0001g0023 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.5029+673T>C | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 37/37 | chr18 | 23953782 | |||||||
chr18:23954105 | A | G | 1 | a0001c0001t0001g0228 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.5030-398A>G | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 37/37 | chr18 | 23954105 | |||||||
chr18:23954107 | T | C | 1 | a0001c0001t0001g0246 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.5030-396T>C | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 37/37 | chr18 | 23954107 | |||||||
chr18:23954173 | G | A | 8 | a0001c0001t0002g0031 a0001c0001t0002g0112 a0001c0001t0002g0127 others(5): Show |
8 | HG00140.hp2 HG00735.hp2 HG01099.hp2 others(5): Show |
intron_variant | MODIFIER | c.5030-330G>A | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 37/37 | chr18 | 23954173 | |||||||
chr18:23954401 | T | TA | 116 | a0001c0001t0001g0005 a0001c0001t0001g0166 a0001c0001t0001g0170 others(113): Show |
125 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(122): Show |
intron_variant | MODIFIER | c.5030-80dupA | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 37/37 | INFO_REALIGN_3_PRIME | chr18 | 23954401 | ||||||
chr18:23954401 | T | TAA | 10 | a0001c0001t0002g0032 a0001c0001t0002g0043 a0001c0001t0002g0117 others(7): Show |
10 | HG02572.hp2 HG03516.hp2 HG04199.hp1 others(7): Show |
intron_variant | MODIFIER | c.5030-81_5030-80dup others(2): Show |
LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 37/37 | INFO_REALIGN_3_PRIME | chr18 | 23954401 | ||||||
chr18:23954401 | TA | T | 6 | a0001c0001t0001g0182 a0001c0001t0001g0221 a0001c0001t0001g0227 others(3): Show |
6 | HG00558.hp2 HG02135.hp2 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.5030-80delA | LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 37/37 | INFO_REALIGN_3_PRIME | chr18 | 23954401 | ||||||
chr18:23954401 | TAA | T | 61 | a0001c0001t0001g0047 a0002c0002t0001g0008 a0002c0002t0001g0009 others(58): Show |
65 | HG00140.hp1 HG00558.hp1 HG00609.hp2 others(62): Show |
intron_variant | MODIFIER | c.5030-81_5030-80del others(2): Show |
LAMA3 | ENSG00000053747.17 | transcript | ENST00000269217.11 | protein_coding | 37/37 | INFO_REALIGN_3_PRIME | chr18 | 23954401 |