Item | Value |
---|---|
geneid | 4000 |
ensemblid | ENSG00000160789.24 |
hgncid | 6636 |
symbol | LMNA |
name | lamin A/C |
refseq_nuc | NM_005572.4 |
refseq_prot | NP_005563.1 |
ensembl_nuc | ENST00000677389.1 |
ensembl_prot | ENSP00000503633.1 |
mane_status | MANE Plus Clinical |
chr | chr1 |
start | 156114711 |
end | 156137866 |
strand | + |
ver | v1.2 |
region | chr1:156114711-156137866 |
region5000 | chr1:156109711-156142866 |
regionname0 | LMNA_chr1_156114711_156137866 |
regionname5000 | LMNA_chr1_156109711_156142866 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 572 | 285 | 86 | 64 | 97 | 6 | 30 | 66 | LMNA_chr1_156109711_156142866 | LMNA | METPS others(567): Show |
chr1 | 156109711 | 156142866 |
a0002 | 0/0 | 572 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | LMNA_chr1_156109711_156142866 | LMNA | METPS others(567): Show |
chr1 | 156109711 | 156142866 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/0 | 1716 | 132 | 12 | 36 | 64 | 4 | 15 | LMNA_chr1_156109711_156142866 | LMNA | ATGGA others(1711): Show |
chr1 | 156109711 | 156142866 | ||
a0001c0002 | 0/1 | 1716 | 64 | 6 | 19 | 28 | 2 | 8 | LMNA_chr1_156109711_156142866 | LMNA | ATGGA others(1711): Show |
chr1 | 156109711 | 156142866 | ||
a0001c0003 | 0/0 | 1716 | 63 | 46 | 6 | 4 | 0 | 7 | LMNA_chr1_156109711_156142866 | LMNA | ATGGA others(1711): Show |
chr1 | 156109711 | 156142866 | ||
a0001c0004 | 0/0 | 1716 | 21 | 21 | 0 | 0 | 0 | 0 | LMNA_chr1_156109711_156142866 | LMNA | ATGGA others(1711): Show |
chr1 | 156109711 | 156142866 | ||
a0001c0005 | 0/0 | 1716 | 1 | 1 | 0 | 0 | 0 | 0 | LMNA_chr1_156109711_156142866 | LMNA | ATGGA others(1711): Show |
chr1 | 156109711 | 156142866 | ||
a0001c0006 | 0/0 | 1716 | 1 | 0 | 1 | 0 | 0 | 0 | LMNA_chr1_156109711_156142866 | LMNA | ATGGA others(1711): Show |
chr1 | 156109711 | 156142866 | ||
a0001c0007 | 0/0 | 1716 | 1 | 0 | 0 | 1 | 0 | 0 | LMNA_chr1_156109711_156142866 | LMNA | ATGGA others(1711): Show |
chr1 | 156109711 | 156142866 | ||
a0001c0009 | 0/0 | 1716 | 1 | 0 | 1 | 0 | 0 | 0 | LMNA_chr1_156109711_156142866 | LMNA | ATGGA others(1711): Show |
chr1 | 156109711 | 156142866 | ||
a0001c0010 | 0/0 | 1716 | 1 | 0 | 1 | 0 | 0 | 0 | LMNA_chr1_156109711_156142866 | LMNA | ATGGA others(1711): Show |
chr1 | 156109711 | 156142866 | ||
a0002c0008 | 0/0 | 1716 | 1 | 0 | 0 | 1 | 0 | 0 | LMNA_chr1_156109711_156142866 | LMNA | ATGGA others(1711): Show |
chr1 | 156109711 | 156142866 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 1/0 | 2029 | 131 | 11 | 36 | 64 | 4 | 15 | LMNA_chr1_156109711_156142866 | LMNA | AGTGT others(2024): Show |
chr1 | 156109711 | 156142866 |
a0001c0001t0002 | 0/0 | 2029 | 1 | 1 | 0 | 0 | 0 | 0 | LMNA_chr1_156109711_156142866 | LMNA | AGTGT others(2024): Show |
chr1 | 156109711 | 156142866 |
a0001c0002t0001 | 0/1 | 2029 | 64 | 6 | 19 | 28 | 2 | 8 | LMNA_chr1_156109711_156142866 | LMNA | AGTGT others(2024): Show |
chr1 | 156109711 | 156142866 |
a0001c0003t0001 | 0/0 | 2029 | 63 | 46 | 6 | 4 | 0 | 7 | LMNA_chr1_156109711_156142866 | LMNA | AGTGT others(2024): Show |
chr1 | 156109711 | 156142866 |
a0001c0004t0001 | 0/0 | 2029 | 15 | 15 | 0 | 0 | 0 | 0 | LMNA_chr1_156109711_156142866 | LMNA | AGTGT others(2024): Show |
chr1 | 156109711 | 156142866 |
a0001c0004t0002 | 0/0 | 2029 | 6 | 6 | 0 | 0 | 0 | 0 | LMNA_chr1_156109711_156142866 | LMNA | AGTGT others(2024): Show |
chr1 | 156109711 | 156142866 |
a0001c0005t0001 | 0/0 | 2029 | 1 | 1 | 0 | 0 | 0 | 0 | LMNA_chr1_156109711_156142866 | LMNA | AGTGT others(2024): Show |
chr1 | 156109711 | 156142866 |
a0001c0006t0001 | 0/0 | 2029 | 1 | 0 | 1 | 0 | 0 | 0 | LMNA_chr1_156109711_156142866 | LMNA | AGTGT others(2024): Show |
chr1 | 156109711 | 156142866 |
a0001c0007t0001 | 0/0 | 2029 | 1 | 0 | 0 | 1 | 0 | 0 | LMNA_chr1_156109711_156142866 | LMNA | AGTGT others(2024): Show |
chr1 | 156109711 | 156142866 |
a0001c0009t0001 | 0/0 | 2029 | 1 | 0 | 1 | 0 | 0 | 0 | LMNA_chr1_156109711_156142866 | LMNA | AGTGT others(2024): Show |
chr1 | 156109711 | 156142866 |
a0001c0010t0001 | 0/0 | 2029 | 1 | 0 | 1 | 0 | 0 | 0 | LMNA_chr1_156109711_156142866 | LMNA | AGTGT others(2024): Show |
chr1 | 156109711 | 156142866 |
a0002c0008t0001 | 0/0 | 2029 | 1 | 0 | 0 | 1 | 0 | 0 | LMNA_chr1_156109711_156142866 | LMNA | AGTGT others(2024): Show |
chr1 | 156109711 | 156142866 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 19 | 0 | 11 | 6 | 1 | 1 | LMNA_chr1_156109711_156142866 | LMNA | chr1 | 156109711 | 156142866 |
a0001c0001t0001g0002 | 0/0 | 14 | 0 | 4 | 9 | 0 | 1 | LMNA_chr1_156109711_156142866 | LMNA | chr1 | 156109711 | 156142866 |
a0001c0001t0001g0006 | 0/0 | 3 | 1 | 1 | 0 | 1 | 0 | LMNA_chr1_156109711_156142866 | LMNA | chr1 | 156109711 | 156142866 |
a0001c0001t0001g0007 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | LMNA_chr1_156109711_156142866 | LMNA | chr1 | 156109711 | 156142866 |
a0001c0001t0001g0008 | 0/0 | 3 | 0 | 2 | 0 | 0 | 1 | LMNA_chr1_156109711_156142866 | LMNA | chr1 | 156109711 | 156142866 |
a0001c0001t0001g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LMNA_chr1_156109711_156142866 | LMNA | chr1 | 156109711 | 156142866 |
a0001c0001t0001g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMNA_chr1_156109711_156142866 | LMNA | chr1 | 156109711 | 156142866 |
a0001c0001t0001g0014 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | LMNA_chr1_156109711_156142866 | LMNA | chr1 | 156109711 | 156142866 |
a0001c0001t0001g0015 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LMNA_chr1_156109711_156142866 | LMNA | chr1 | 156109711 | 156142866 |
a0001c0001t0001g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LMNA_chr1_156109711_156142866 | LMNA | chr1 | 156109711 | 156142866 |
a0001c0001t0001g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LMNA_chr1_156109711_156142866 | LMNA | chr1 | 156109711 | 156142866 |
a0001c0001t0001g0019 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | LMNA_chr1_156109711_156142866 | LMNA | chr1 | 156109711 | 156142866 |
a0001c0001t0001g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LMNA_chr1_156109711_156142866 | LMNA | chr1 | 156109711 | 156142866 |
a0001c0001t0001g0024 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | LMNA_chr1_156109711_156142866 | LMNA | chr1 | 156109711 | 156142866 |
a0001c0001t0001g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMNA_chr1_156109711_156142866 | LMNA | chr1 | 156109711 | 156142866 |
a0001c0001t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMNA_chr1_156109711_156142866 | LMNA | chr1 | 156109711 | 156142866 |
a0001c0001t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMNA_chr1_156109711_156142866 | LMNA | chr1 | 156109711 | 156142866 |
a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMNA_chr1_156109711_156142866 | LMNA | chr1 | 156109711 | 156142866 |
a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMNA_chr1_156109711_156142866 | LMNA | chr1 | 156109711 | 156142866 |
a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMNA_chr1_156109711_156142866 | LMNA | chr1 | 156109711 | 156142866 |
a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LMNA_chr1_156109711_156142866 | LMNA | chr1 | 156109711 | 156142866 |
a0001c0001t0001g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMNA_chr1_156109711_156142866 | LMNA | chr1 | 156109711 | 156142866 |
a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMNA_chr1_156109711_156142866 | LMNA | chr1 | 156109711 | 156142866 |
a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMNA_chr1_156109711_156142866 | LMNA | chr1 | 156109711 | 156142866 |
a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMNA_chr1_156109711_156142866 | LMNA | chr1 | 156109711 | 156142866 |
a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMNA_chr1_156109711_156142866 | LMNA | chr1 | 156109711 | 156142866 |
a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMNA_chr1_156109711_156142866 | LMNA | chr1 | 156109711 | 156142866 |
a0001c0001t0001g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMNA_chr1_156109711_156142866 | LMNA | chr1 | 156109711 | 156142866 |
a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMNA_chr1_156109711_156142866 | LMNA | chr1 | 156109711 | 156142866 |
a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMNA_chr1_156109711_156142866 | LMNA | chr1 | 156109711 | 156142866 |
a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMNA_chr1_156109711_156142866 | LMNA | chr1 | 156109711 | 156142866 |
a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMNA_chr1_156109711_156142866 | LMNA | chr1 | 156109711 | 156142866 |
a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LMNA_chr1_156109711_156142866 | LMNA | chr1 | 156109711 | 156142866 |
a0001c0001t0001g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMNA_chr1_156109711_156142866 | LMNA | chr1 | 156109711 | 156142866 |
a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LMNA_chr1_156109711_156142866 | LMNA | chr1 | 156109711 | 156142866 |
a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMNA_chr1_156109711_156142866 | LMNA | chr1 | 156109711 | 156142866 |
a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMNA_chr1_156109711_156142866 | LMNA | chr1 | 156109711 | 156142866 |
a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMNA_chr1_156109711_156142866 | LMNA | chr1 | 156109711 | 156142866 |
a0001c0001t0001g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMNA_chr1_156109711_156142866 | LMNA | chr1 | 156109711 | 156142866 |
a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMNA_chr1_156109711_156142866 | LMNA | chr1 | 156109711 | 156142866 |
a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMNA_chr1_156109711_156142866 | LMNA | chr1 | 156109711 | 156142866 |
a0001c0001t0001g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMNA_chr1_156109711_156142866 | LMNA | chr1 | 156109711 | 156142866 |
a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMNA_chr1_156109711_156142866 | LMNA | chr1 | 156109711 | 156142866 |
a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LMNA_chr1_156109711_156142866 | LMNA | chr1 | 156109711 | 156142866 |
a0001c0001t0001g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMNA_chr1_156109711_156142866 | LMNA | chr1 | 156109711 | 156142866 |
a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMNA_chr1_156109711_156142866 | LMNA | chr1 | 156109711 | 156142866 |
a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMNA_chr1_156109711_156142866 | LMNA | chr1 | 156109711 | 156142866 |
a0001c0001t0001g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMNA_chr1_156109711_156142866 | LMNA | chr1 | 156109711 | 156142866 |
a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LMNA_chr1_156109711_156142866 | LMNA | chr1 | 156109711 | 156142866 |
a0001c0001t0001g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMNA_chr1_156109711_156142866 | LMNA | chr1 | 156109711 | 156142866 |
a0001c0001t0001g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMNA_chr1_156109711_156142866 | LMNA | chr1 | 156109711 | 156142866 |
a0001c0001t0001g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMNA_chr1_156109711_156142866 | LMNA | chr1 | 156109711 | 156142866 |
a0001c0001t0001g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMNA_chr1_156109711_156142866 | LMNA | chr1 | 156109711 | 156142866 |
a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMNA_chr1_156109711_156142866 | LMNA | chr1 | 156109711 | 156142866 |
a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMNA_chr1_156109711_156142866 | LMNA | chr1 | 156109711 | 156142866 |
a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMNA_chr1_156109711_156142866 | LMNA | chr1 | 156109711 | 156142866 |
a0001c0001t0001g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMNA_chr1_156109711_156142866 | LMNA | chr1 | 156109711 | 156142866 |
a0001c0001t0001g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMNA_chr1_156109711_156142866 | LMNA | chr1 | 156109711 | 156142866 |
a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LMNA_chr1_156109711_156142866 | LMNA | chr1 | 156109711 | 156142866 |
a0001c0001t0001g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMNA_chr1_156109711_156142866 | LMNA | chr1 | 156109711 | 156142866 |
a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMNA_chr1_156109711_156142866 | LMNA | chr1 | 156109711 | 156142866 |
a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LMNA_chr1_156109711_156142866 | LMNA | chr1 | 156109711 | 156142866 |
a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMNA_chr1_156109711_156142866 | LMNA | chr1 | 156109711 | 156142866 |
a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LMNA_chr1_156109711_156142866 | LMNA | chr1 | 156109711 | 156142866 |
a0001c0001t0001g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMNA_chr1_156109711_156142866 | LMNA | chr1 | 156109711 | 156142866 |
a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMNA_chr1_156109711_156142866 | LMNA | chr1 | 156109711 | 156142866 |
a0001c0001t0001g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMNA_chr1_156109711_156142866 | LMNA | chr1 | 156109711 | 156142866 |
a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMNA_chr1_156109711_156142866 | LMNA | chr1 | 156109711 | 156142866 |
a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMNA_chr1_156109711_156142866 | LMNA | chr1 | 156109711 | 156142866 |
a0001c0001t0001g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMNA_chr1_156109711_156142866 | LMNA | chr1 | 156109711 | 156142866 |
a0001c0001t0001g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMNA_chr1_156109711_156142866 | LMNA | chr1 | 156109711 | 156142866 |
a0001c0001t0001g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMNA_chr1_156109711_156142866 | LMNA | chr1 | 156109711 | 156142866 |
a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LMNA_chr1_156109711_156142866 | LMNA | chr1 | 156109711 | 156142866 |
a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMNA_chr1_156109711_156142866 | LMNA | chr1 | 156109711 | 156142866 |
a0001c0001t0001g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMNA_chr1_156109711_156142866 | LMNA | chr1 | 156109711 | 156142866 |
a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMNA_chr1_156109711_156142866 | LMNA | chr1 | 156109711 | 156142866 |
a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMNA_chr1_156109711_156142866 | LMNA | chr1 | 156109711 | 156142866 |
a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMNA_chr1_156109711_156142866 | LMNA | chr1 | 156109711 | 156142866 |
a0001c0001t0001g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMNA_chr1_156109711_156142866 | LMNA | chr1 | 156109711 | 156142866 |
a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMNA_chr1_156109711_156142866 | LMNA | chr1 | 156109711 | 156142866 |
a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LMNA_chr1_156109711_156142866 | LMNA | chr1 | 156109711 | 156142866 |
a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMNA_chr1_156109711_156142866 | LMNA | chr1 | 156109711 | 156142866 |
a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LMNA_chr1_156109711_156142866 | LMNA | chr1 | 156109711 | 156142866 |
a0001c0001t0001g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMNA_chr1_156109711_156142866 | LMNA | chr1 | 156109711 | 156142866 |
a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LMNA_chr1_156109711_156142866 | LMNA | chr1 | 156109711 | 156142866 |
a0001c0001t0001g0172 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | LMNA_chr1_156109711_156142866 | LMNA | chr1 | 156109711 | 156142866 |
a0001c0001t0002g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMNA_chr1_156109711_156142866 | LMNA | chr1 | 156109711 | 156142866 |
a0001c0002t0001g0003 | 0/0 | 9 | 0 | 9 | 0 | 0 | 0 | LMNA_chr1_156109711_156142866 | LMNA | chr1 | 156109711 | 156142866 |
a0001c0002t0001g0006 | 0/0 | 4 | 0 | 1 | 1 | 0 | 2 | LMNA_chr1_156109711_156142866 | LMNA | chr1 | 156109711 | 156142866 |
a0001c0002t0001g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMNA_chr1_156109711_156142866 | LMNA | chr1 | 156109711 | 156142866 |
a0001c0002t0001g0009 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | LMNA_chr1_156109711_156142866 | LMNA | chr1 | 156109711 | 156142866 |
a0001c0002t0001g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMNA_chr1_156109711_156142866 | LMNA | chr1 | 156109711 | 156142866 |
a0001c0002t0001g0015 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LMNA_chr1_156109711_156142866 | LMNA | chr1 | 156109711 | 156142866 |
a0001c0002t0001g0018 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LMNA_chr1_156109711_156142866 | LMNA | chr1 | 156109711 | 156142866 |
a0001c0002t0001g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LMNA_chr1_156109711_156142866 | LMNA | chr1 | 156109711 | 156142866 |
a0001c0002t0001g0022 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | LMNA_chr1_156109711_156142866 | LMNA | chr1 | 156109711 | 156142866 |
a0001c0002t0001g0023 | 0/0 | 2 | 1 | 0 | 1 | 0 | 0 | LMNA_chr1_156109711_156142866 | LMNA | chr1 | 156109711 | 156142866 |
a0001c0002t0001g0026 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | LMNA_chr1_156109711_156142866 | LMNA | chr1 | 156109711 | 156142866 |
a0001c0002t0001g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMNA_chr1_156109711_156142866 | LMNA | chr1 | 156109711 | 156142866 |
a0001c0002t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMNA_chr1_156109711_156142866 | LMNA | chr1 | 156109711 | 156142866 |
a0001c0002t0001g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMNA_chr1_156109711_156142866 | LMNA | chr1 | 156109711 | 156142866 |
a0001c0002t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMNA_chr1_156109711_156142866 | LMNA | chr1 | 156109711 | 156142866 |
a0001c0002t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMNA_chr1_156109711_156142866 | LMNA | chr1 | 156109711 | 156142866 |
a0001c0002t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMNA_chr1_156109711_156142866 | LMNA | chr1 | 156109711 | 156142866 |
a0001c0002t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMNA_chr1_156109711_156142866 | LMNA | chr1 | 156109711 | 156142866 |
a0001c0002t0001g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMNA_chr1_156109711_156142866 | LMNA | chr1 | 156109711 | 156142866 |
a0001c0002t0001g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMNA_chr1_156109711_156142866 | LMNA | chr1 | 156109711 | 156142866 |
a0001c0002t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMNA_chr1_156109711_156142866 | LMNA | chr1 | 156109711 | 156142866 |
a0001c0002t0001g0096 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LMNA_chr1_156109711_156142866 | LMNA | chr1 | 156109711 | 156142866 |
a0001c0002t0001g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMNA_chr1_156109711_156142866 | LMNA | chr1 | 156109711 | 156142866 |
a0001c0002t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMNA_chr1_156109711_156142866 | LMNA | chr1 | 156109711 | 156142866 |
a0001c0002t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMNA_chr1_156109711_156142866 | LMNA | chr1 | 156109711 | 156142866 |
a0001c0002t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMNA_chr1_156109711_156142866 | LMNA | chr1 | 156109711 | 156142866 |
a0001c0002t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMNA_chr1_156109711_156142866 | LMNA | chr1 | 156109711 | 156142866 |
a0001c0002t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMNA_chr1_156109711_156142866 | LMNA | chr1 | 156109711 | 156142866 |
a0001c0002t0001g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMNA_chr1_156109711_156142866 | LMNA | chr1 | 156109711 | 156142866 |
a0001c0002t0001g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMNA_chr1_156109711_156142866 | LMNA | chr1 | 156109711 | 156142866 |
a0001c0002t0001g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LMNA_chr1_156109711_156142866 | LMNA | chr1 | 156109711 | 156142866 |
a0001c0002t0001g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LMNA_chr1_156109711_156142866 | LMNA | chr1 | 156109711 | 156142866 |
a0001c0002t0001g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LMNA_chr1_156109711_156142866 | LMNA | chr1 | 156109711 | 156142866 |
a0001c0002t0001g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMNA_chr1_156109711_156142866 | LMNA | chr1 | 156109711 | 156142866 |
a0001c0002t0001g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMNA_chr1_156109711_156142866 | LMNA | chr1 | 156109711 | 156142866 |
a0001c0002t0001g0121 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | LMNA_chr1_156109711_156142866 | LMNA | chr1 | 156109711 | 156142866 |
a0001c0002t0001g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMNA_chr1_156109711_156142866 | LMNA | chr1 | 156109711 | 156142866 |
a0001c0002t0001g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMNA_chr1_156109711_156142866 | LMNA | chr1 | 156109711 | 156142866 |
a0001c0002t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMNA_chr1_156109711_156142866 | LMNA | chr1 | 156109711 | 156142866 |
a0001c0002t0001g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMNA_chr1_156109711_156142866 | LMNA | chr1 | 156109711 | 156142866 |
a0001c0002t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMNA_chr1_156109711_156142866 | LMNA | chr1 | 156109711 | 156142866 |
a0001c0002t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMNA_chr1_156109711_156142866 | LMNA | chr1 | 156109711 | 156142866 |
a0001c0002t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMNA_chr1_156109711_156142866 | LMNA | chr1 | 156109711 | 156142866 |
a0001c0002t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMNA_chr1_156109711_156142866 | LMNA | chr1 | 156109711 | 156142866 |
a0001c0002t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMNA_chr1_156109711_156142866 | LMNA | chr1 | 156109711 | 156142866 |
a0001c0002t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMNA_chr1_156109711_156142866 | LMNA | chr1 | 156109711 | 156142866 |
a0001c0002t0001g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMNA_chr1_156109711_156142866 | LMNA | chr1 | 156109711 | 156142866 |
a0001c0003t0001g0004 | 0/0 | 9 | 6 | 3 | 0 | 0 | 0 | LMNA_chr1_156109711_156142866 | LMNA | chr1 | 156109711 | 156142866 |
a0001c0003t0001g0005 | 0/0 | 7 | 6 | 0 | 1 | 0 | 0 | LMNA_chr1_156109711_156142866 | LMNA | chr1 | 156109711 | 156142866 |
a0001c0003t0001g0011 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | LMNA_chr1_156109711_156142866 | LMNA | chr1 | 156109711 | 156142866 |
a0001c0003t0001g0025 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | LMNA_chr1_156109711_156142866 | LMNA | chr1 | 156109711 | 156142866 |
a0001c0003t0001g0028 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | LMNA_chr1_156109711_156142866 | LMNA | chr1 | 156109711 | 156142866 |
a0001c0003t0001g0029 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | LMNA_chr1_156109711_156142866 | LMNA | chr1 | 156109711 | 156142866 |
a0001c0003t0001g0030 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | LMNA_chr1_156109711_156142866 | LMNA | chr1 | 156109711 | 156142866 |
a0001c0003t0001g0031 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | LMNA_chr1_156109711_156142866 | LMNA | chr1 | 156109711 | 156142866 |
a0001c0003t0001g0034 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | LMNA_chr1_156109711_156142866 | LMNA | chr1 | 156109711 | 156142866 |
a0001c0003t0001g0036 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | LMNA_chr1_156109711_156142866 | LMNA | chr1 | 156109711 | 156142866 |
a0001c0003t0001g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMNA_chr1_156109711_156142866 | LMNA | chr1 | 156109711 | 156142866 |
a0001c0003t0001g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMNA_chr1_156109711_156142866 | LMNA | chr1 | 156109711 | 156142866 |
a0001c0003t0001g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMNA_chr1_156109711_156142866 | LMNA | chr1 | 156109711 | 156142866 |
a0001c0003t0001g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LMNA_chr1_156109711_156142866 | LMNA | chr1 | 156109711 | 156142866 |
a0001c0003t0001g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMNA_chr1_156109711_156142866 | LMNA | chr1 | 156109711 | 156142866 |
a0001c0003t0001g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMNA_chr1_156109711_156142866 | LMNA | chr1 | 156109711 | 156142866 |
a0001c0003t0001g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMNA_chr1_156109711_156142866 | LMNA | chr1 | 156109711 | 156142866 |
a0001c0003t0001g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMNA_chr1_156109711_156142866 | LMNA | chr1 | 156109711 | 156142866 |
a0001c0003t0001g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMNA_chr1_156109711_156142866 | LMNA | chr1 | 156109711 | 156142866 |
a0001c0003t0001g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMNA_chr1_156109711_156142866 | LMNA | chr1 | 156109711 | 156142866 |
a0001c0003t0001g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMNA_chr1_156109711_156142866 | LMNA | chr1 | 156109711 | 156142866 |
a0001c0003t0001g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMNA_chr1_156109711_156142866 | LMNA | chr1 | 156109711 | 156142866 |
a0001c0003t0001g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMNA_chr1_156109711_156142866 | LMNA | chr1 | 156109711 | 156142866 |
a0001c0003t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMNA_chr1_156109711_156142866 | LMNA | chr1 | 156109711 | 156142866 |
a0001c0003t0001g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMNA_chr1_156109711_156142866 | LMNA | chr1 | 156109711 | 156142866 |
a0001c0003t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMNA_chr1_156109711_156142866 | LMNA | chr1 | 156109711 | 156142866 |
a0001c0003t0001g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LMNA_chr1_156109711_156142866 | LMNA | chr1 | 156109711 | 156142866 |
a0001c0003t0001g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LMNA_chr1_156109711_156142866 | LMNA | chr1 | 156109711 | 156142866 |
a0001c0003t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMNA_chr1_156109711_156142866 | LMNA | chr1 | 156109711 | 156142866 |
a0001c0003t0001g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMNA_chr1_156109711_156142866 | LMNA | chr1 | 156109711 | 156142866 |
a0001c0003t0001g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMNA_chr1_156109711_156142866 | LMNA | chr1 | 156109711 | 156142866 |
a0001c0003t0001g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMNA_chr1_156109711_156142866 | LMNA | chr1 | 156109711 | 156142866 |
a0001c0003t0001g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMNA_chr1_156109711_156142866 | LMNA | chr1 | 156109711 | 156142866 |
a0001c0003t0001g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMNA_chr1_156109711_156142866 | LMNA | chr1 | 156109711 | 156142866 |
a0001c0003t0001g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMNA_chr1_156109711_156142866 | LMNA | chr1 | 156109711 | 156142866 |
a0001c0003t0001g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMNA_chr1_156109711_156142866 | LMNA | chr1 | 156109711 | 156142866 |
a0001c0003t0001g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LMNA_chr1_156109711_156142866 | LMNA | chr1 | 156109711 | 156142866 |
a0001c0003t0001g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LMNA_chr1_156109711_156142866 | LMNA | chr1 | 156109711 | 156142866 |
a0001c0003t0001g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMNA_chr1_156109711_156142866 | LMNA | chr1 | 156109711 | 156142866 |
a0001c0003t0001g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMNA_chr1_156109711_156142866 | LMNA | chr1 | 156109711 | 156142866 |
a0001c0004t0001g0010 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | LMNA_chr1_156109711_156142866 | LMNA | chr1 | 156109711 | 156142866 |
a0001c0004t0001g0032 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | LMNA_chr1_156109711_156142866 | LMNA | chr1 | 156109711 | 156142866 |
a0001c0004t0001g0035 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | LMNA_chr1_156109711_156142866 | LMNA | chr1 | 156109711 | 156142866 |
a0001c0004t0001g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMNA_chr1_156109711_156142866 | LMNA | chr1 | 156109711 | 156142866 |
a0001c0004t0001g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMNA_chr1_156109711_156142866 | LMNA | chr1 | 156109711 | 156142866 |
a0001c0004t0001g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMNA_chr1_156109711_156142866 | LMNA | chr1 | 156109711 | 156142866 |
a0001c0004t0001g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMNA_chr1_156109711_156142866 | LMNA | chr1 | 156109711 | 156142866 |
a0001c0004t0001g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMNA_chr1_156109711_156142866 | LMNA | chr1 | 156109711 | 156142866 |
a0001c0004t0001g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMNA_chr1_156109711_156142866 | LMNA | chr1 | 156109711 | 156142866 |
a0001c0004t0001g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMNA_chr1_156109711_156142866 | LMNA | chr1 | 156109711 | 156142866 |
a0001c0004t0001g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMNA_chr1_156109711_156142866 | LMNA | chr1 | 156109711 | 156142866 |
a0001c0004t0002g0033 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | LMNA_chr1_156109711_156142866 | LMNA | chr1 | 156109711 | 156142866 |
a0001c0004t0002g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMNA_chr1_156109711_156142866 | LMNA | chr1 | 156109711 | 156142866 |
a0001c0004t0002g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMNA_chr1_156109711_156142866 | LMNA | chr1 | 156109711 | 156142866 |
a0001c0004t0002g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMNA_chr1_156109711_156142866 | LMNA | chr1 | 156109711 | 156142866 |
a0001c0004t0002g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMNA_chr1_156109711_156142866 | LMNA | chr1 | 156109711 | 156142866 |
a0001c0005t0001g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMNA_chr1_156109711_156142866 | LMNA | chr1 | 156109711 | 156142866 |
a0001c0006t0001g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMNA_chr1_156109711_156142866 | LMNA | chr1 | 156109711 | 156142866 |
a0001c0007t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMNA_chr1_156109711_156142866 | LMNA | chr1 | 156109711 | 156142866 |
a0001c0009t0001g0001 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMNA_chr1_156109711_156142866 | LMNA | chr1 | 156109711 | 156142866 |
a0001c0010t0001g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMNA_chr1_156109711_156142866 | LMNA | chr1 | 156109711 | 156142866 |
a0002c0008t0001g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMNA_chr1_156109711_156142866 | LMNA | chr1 | 156109711 | 156142866 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00140 | hp1 | a0001 | c0001 | t0001 | g0006 | EUR | GBR | LMNA_chr1_156109711_156142866 | LMNA | chr1 | 156109711 | 156142866 |
HG00140 | hp2 | a0001 | c0002 | t0001 | g0018 | EUR | GBR | LMNA_chr1_156109711_156142866 | LMNA | chr1 | 156109711 | 156142866 |
HG00280 | hp1 | a0001 | c0001 | t0001 | g0116 | EUR | FIN | LMNA_chr1_156109711_156142866 | LMNA | chr1 | 156109711 | 156142866 |
HG00280 | hp2 | a0001 | c0002 | t0001 | g0096 | EUR | FIN | LMNA_chr1_156109711_156142866 | LMNA | chr1 | 156109711 | 156142866 |
HG00408 | hp1 | a0001 | c0002 | t0001 | g0009 | EAS | CHS | LMNA_chr1_156109711_156142866 | LMNA | chr1 | 156109711 | 156142866 |
HG00408 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | LMNA_chr1_156109711_156142866 | LMNA | chr1 | 156109711 | 156142866 |
HG00438 | hp1 | a0001 | c0001 | t0001 | g0122 | EAS | CHS | LMNA_chr1_156109711_156142866 | LMNA | chr1 | 156109711 | 156142866 |
HG00438 | hp2 | a0001 | c0002 | t0001 | g0060 | EAS | CHS | LMNA_chr1_156109711_156142866 | LMNA | chr1 | 156109711 | 156142866 |
HG00544 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | CHS | LMNA_chr1_156109711_156142866 | LMNA | chr1 | 156109711 | 156142866 |
HG00544 | hp2 | a0001 | c0001 | t0001 | g0020 | EAS | CHS | LMNA_chr1_156109711_156142866 | LMNA | chr1 | 156109711 | 156142866 |
HG00621 | hp1 | a0001 | c0001 | t0001 | g0077 | EAS | CHS | LMNA_chr1_156109711_156142866 | LMNA | chr1 | 156109711 | 156142866 |
HG00621 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | CHS | LMNA_chr1_156109711_156142866 | LMNA | chr1 | 156109711 | 156142866 |
HG00639 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | LMNA_chr1_156109711_156142866 | LMNA | chr1 | 156109711 | 156142866 |
HG00639 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | LMNA_chr1_156109711_156142866 | LMNA | chr1 | 156109711 | 156142866 |
HG00642 | hp1 | a0001 | c0001 | t0001 | g0052 | AMR | PUR | LMNA_chr1_156109711_156142866 | LMNA | chr1 | 156109711 | 156142866 |
HG00642 | hp2 | a0001 | c0002 | t0001 | g0065 | AMR | PUR | LMNA_chr1_156109711_156142866 | LMNA | chr1 | 156109711 | 156142866 |
HG00733 | hp1 | a0001 | c0001 | t0001 | g0081 | AMR | PUR | LMNA_chr1_156109711_156142866 | LMNA | chr1 | 156109711 | 156142866 |
HG00733 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | LMNA_chr1_156109711_156142866 | LMNA | chr1 | 156109711 | 156142866 |
HG00735 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | LMNA_chr1_156109711_156142866 | LMNA | chr1 | 156109711 | 156142866 |
HG00735 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | LMNA_chr1_156109711_156142866 | LMNA | chr1 | 156109711 | 156142866 |
HG00741 | hp1 | a0001 | c0001 | t0001 | g0019 | AMR | PUR | LMNA_chr1_156109711_156142866 | LMNA | chr1 | 156109711 | 156142866 |
HG00741 | hp2 | a0001 | c0002 | t0001 | g0003 | AMR | PUR | LMNA_chr1_156109711_156142866 | LMNA | chr1 | 156109711 | 156142866 |
HG01074 | hp1 | a0001 | c0002 | t0001 | g0003 | AMR | PUR | LMNA_chr1_156109711_156142866 | LMNA | chr1 | 156109711 | 156142866 |
HG01074 | hp2 | a0001 | c0001 | t0001 | g0107 | AMR | PUR | LMNA_chr1_156109711_156142866 | LMNA | chr1 | 156109711 | 156142866 |
HG01099 | hp1 | a0001 | c0010 | t0001 | g0018 | AMR | PUR | LMNA_chr1_156109711_156142866 | LMNA | chr1 | 156109711 | 156142866 |
HG01099 | hp2 | a0001 | c0001 | t0001 | g0013 | AMR | PUR | LMNA_chr1_156109711_156142866 | LMNA | chr1 | 156109711 | 156142866 |
HG01106 | hp1 | a0001 | c0001 | t0001 | g0072 | AMR | PUR | LMNA_chr1_156109711_156142866 | LMNA | chr1 | 156109711 | 156142866 |
HG01106 | hp2 | a0001 | c0001 | t0001 | g0132 | AMR | PUR | LMNA_chr1_156109711_156142866 | LMNA | chr1 | 156109711 | 156142866 |
HG01167 | hp1 | a0001 | c0002 | t0001 | g0118 | AMR | PUR | LMNA_chr1_156109711_156142866 | LMNA | chr1 | 156109711 | 156142866 |
HG01167 | hp2 | a0001 | c0003 | t0001 | g0004 | AMR | PUR | LMNA_chr1_156109711_156142866 | LMNA | chr1 | 156109711 | 156142866 |
HG01169 | hp1 | a0001 | c0002 | t0001 | g0104 | AMR | PUR | LMNA_chr1_156109711_156142866 | LMNA | chr1 | 156109711 | 156142866 |
HG01169 | hp2 | a0001 | c0003 | t0001 | g0034 | AMR | PUR | LMNA_chr1_156109711_156142866 | LMNA | chr1 | 156109711 | 156142866 |
HG01175 | hp1 | a0001 | c0001 | t0001 | g0123 | AMR | PUR | LMNA_chr1_156109711_156142866 | LMNA | chr1 | 156109711 | 156142866 |
HG01175 | hp2 | a0001 | c0002 | t0001 | g0003 | AMR | PUR | LMNA_chr1_156109711_156142866 | LMNA | chr1 | 156109711 | 156142866 |
HG01192 | hp1 | a0001 | c0001 | t0001 | g0024 | AMR | PUR | LMNA_chr1_156109711_156142866 | LMNA | chr1 | 156109711 | 156142866 |
HG01192 | hp2 | a0001 | c0001 | t0001 | g0008 | AMR | PUR | LMNA_chr1_156109711_156142866 | LMNA | chr1 | 156109711 | 156142866 |
HG01243 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | LMNA_chr1_156109711_156142866 | LMNA | chr1 | 156109711 | 156142866 |
HG01243 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | LMNA_chr1_156109711_156142866 | LMNA | chr1 | 156109711 | 156142866 |
HG01255 | hp1 | a0001 | c0001 | t0001 | g0151 | AMR | CLM | LMNA_chr1_156109711_156142866 | LMNA | chr1 | 156109711 | 156142866 |
HG01255 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | LMNA_chr1_156109711_156142866 | LMNA | chr1 | 156109711 | 156142866 |
HG01256 | hp1 | a0001 | c0002 | t0001 | g0064 | AMR | CLM | LMNA_chr1_156109711_156142866 | LMNA | chr1 | 156109711 | 156142866 |
HG01256 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | LMNA_chr1_156109711_156142866 | LMNA | chr1 | 156109711 | 156142866 |
HG01257 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | LMNA_chr1_156109711_156142866 | LMNA | chr1 | 156109711 | 156142866 |
HG01257 | hp2 | a0001 | c0003 | t0001 | g0004 | AMR | CLM | LMNA_chr1_156109711_156142866 | LMNA | chr1 | 156109711 | 156142866 |
HG01258 | hp1 | a0001 | c0003 | t0001 | g0004 | AMR | CLM | LMNA_chr1_156109711_156142866 | LMNA | chr1 | 156109711 | 156142866 |
HG01258 | hp2 | a0001 | c0002 | t0001 | g0003 | AMR | CLM | LMNA_chr1_156109711_156142866 | LMNA | chr1 | 156109711 | 156142866 |
HG01261 | hp1 | a0001 | c0003 | t0001 | g0134 | AMR | CLM | LMNA_chr1_156109711_156142866 | LMNA | chr1 | 156109711 | 156142866 |
HG01261 | hp2 | a0001 | c0009 | t0001 | g0001 | AMR | CLM | LMNA_chr1_156109711_156142866 | LMNA | chr1 | 156109711 | 156142866 |
HG01346 | hp1 | a0001 | c0002 | t0001 | g0003 | AMR | CLM | LMNA_chr1_156109711_156142866 | LMNA | chr1 | 156109711 | 156142866 |
HG01346 | hp2 | a0001 | c0001 | t0001 | g0119 | AMR | CLM | LMNA_chr1_156109711_156142866 | LMNA | chr1 | 156109711 | 156142866 |
HG01361 | hp1 | a0001 | c0002 | t0001 | g0003 | AMR | CLM | LMNA_chr1_156109711_156142866 | LMNA | chr1 | 156109711 | 156142866 |
HG01361 | hp2 | a0001 | c0001 | t0001 | g0084 | AMR | CLM | LMNA_chr1_156109711_156142866 | LMNA | chr1 | 156109711 | 156142866 |
HG01433 | hp1 | a0001 | c0002 | t0001 | g0131 | AMR | CLM | LMNA_chr1_156109711_156142866 | LMNA | chr1 | 156109711 | 156142866 |
HG01433 | hp2 | a0001 | c0003 | t0001 | g0147 | AMR | CLM | LMNA_chr1_156109711_156142866 | LMNA | chr1 | 156109711 | 156142866 |
HG01496 | hp1 | a0001 | c0006 | t0001 | g0068 | AMR | CLM | LMNA_chr1_156109711_156142866 | LMNA | chr1 | 156109711 | 156142866 |
HG01496 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | LMNA_chr1_156109711_156142866 | LMNA | chr1 | 156109711 | 156142866 |
HG01516 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | IBS | LMNA_chr1_156109711_156142866 | LMNA | chr1 | 156109711 | 156142866 |
HG01516 | hp2 | a0001 | c0001 | t0001 | g0086 | EUR | IBS | LMNA_chr1_156109711_156142866 | LMNA | chr1 | 156109711 | 156142866 |
HG01884 | hp1 | a0001 | c0004 | t0001 | g0162 | AFR | ACB | LMNA_chr1_156109711_156142866 | LMNA | chr1 | 156109711 | 156142866 |
HG01884 | hp2 | a0001 | c0002 | t0001 | g0097 | AFR | ACB | LMNA_chr1_156109711_156142866 | LMNA | chr1 | 156109711 | 156142866 |
HG01943 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | LMNA_chr1_156109711_156142866 | LMNA | chr1 | 156109711 | 156142866 |
HG01943 | hp2 | a0001 | c0002 | t0001 | g0051 | AMR | PEL | LMNA_chr1_156109711_156142866 | LMNA | chr1 | 156109711 | 156142866 |
HG01952 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | PEL | LMNA_chr1_156109711_156142866 | LMNA | chr1 | 156109711 | 156142866 |
HG01952 | hp2 | a0001 | c0002 | t0001 | g0006 | AMR | PEL | LMNA_chr1_156109711_156142866 | LMNA | chr1 | 156109711 | 156142866 |
HG01975 | hp1 | a0001 | c0002 | t0001 | g0156 | AMR | PEL | LMNA_chr1_156109711_156142866 | LMNA | chr1 | 156109711 | 156142866 |
HG01975 | hp2 | a0001 | c0001 | t0001 | g0014 | AMR | PEL | LMNA_chr1_156109711_156142866 | LMNA | chr1 | 156109711 | 156142866 |
HG01978 | hp1 | a0001 | c0001 | t0001 | g0094 | AMR | PEL | LMNA_chr1_156109711_156142866 | LMNA | chr1 | 156109711 | 156142866 |
HG01978 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | LMNA_chr1_156109711_156142866 | LMNA | chr1 | 156109711 | 156142866 |
HG01981 | hp1 | a0001 | c0002 | t0001 | g0117 | AMR | PEL | LMNA_chr1_156109711_156142866 | LMNA | chr1 | 156109711 | 156142866 |
HG01981 | hp2 | a0001 | c0001 | t0001 | g0137 | AMR | PEL | LMNA_chr1_156109711_156142866 | LMNA | chr1 | 156109711 | 156142866 |
HG01993 | hp1 | a0001 | c0002 | t0001 | g0106 | AMR | PEL | LMNA_chr1_156109711_156142866 | LMNA | chr1 | 156109711 | 156142866 |
HG01993 | hp2 | a0001 | c0002 | t0001 | g0003 | AMR | PEL | LMNA_chr1_156109711_156142866 | LMNA | chr1 | 156109711 | 156142866 |
HG02004 | hp1 | a0001 | c0001 | t0001 | g0014 | AMR | PEL | LMNA_chr1_156109711_156142866 | LMNA | chr1 | 156109711 | 156142866 |
HG02004 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | LMNA_chr1_156109711_156142866 | LMNA | chr1 | 156109711 | 156142866 |
HG02015 | hp1 | a0001 | c0002 | t0001 | g0098 | EAS | KHV | LMNA_chr1_156109711_156142866 | LMNA | chr1 | 156109711 | 156142866 |
HG02015 | hp2 | a0001 | c0001 | t0001 | g0073 | EAS | KHV | LMNA_chr1_156109711_156142866 | LMNA | chr1 | 156109711 | 156142866 |
HG02027 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | LMNA_chr1_156109711_156142866 | LMNA | chr1 | 156109711 | 156142866 |
HG02027 | hp2 | a0001 | c0001 | t0001 | g0027 | EAS | KHV | LMNA_chr1_156109711_156142866 | LMNA | chr1 | 156109711 | 156142866 |
HG02055 | hp1 | a0001 | c0001 | t0001 | g0133 | AFR | ACB | LMNA_chr1_156109711_156142866 | LMNA | chr1 | 156109711 | 156142866 |
HG02055 | hp2 | a0001 | c0003 | t0001 | g0125 | AFR | ACB | LMNA_chr1_156109711_156142866 | LMNA | chr1 | 156109711 | 156142866 |
HG02056 | hp1 | a0001 | c0007 | t0001 | g0140 | EAS | KHV | LMNA_chr1_156109711_156142866 | LMNA | chr1 | 156109711 | 156142866 |
HG02056 | hp2 | a0001 | c0002 | t0001 | g0143 | EAS | KHV | LMNA_chr1_156109711_156142866 | LMNA | chr1 | 156109711 | 156142866 |
HG02071 | hp1 | a0001 | c0002 | t0001 | g0006 | EAS | KHV | LMNA_chr1_156109711_156142866 | LMNA | chr1 | 156109711 | 156142866 |
HG02071 | hp2 | a0001 | c0001 | t0001 | g0149 | EAS | KHV | LMNA_chr1_156109711_156142866 | LMNA | chr1 | 156109711 | 156142866 |
HG02074 | hp1 | a0001 | c0002 | t0001 | g0027 | EAS | KHV | LMNA_chr1_156109711_156142866 | LMNA | chr1 | 156109711 | 156142866 |
HG02074 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | LMNA_chr1_156109711_156142866 | LMNA | chr1 | 156109711 | 156142866 |
HG02083 | hp1 | a0001 | c0002 | t0001 | g0021 | EAS | KHV | LMNA_chr1_156109711_156142866 | LMNA | chr1 | 156109711 | 156142866 |
HG02083 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | LMNA_chr1_156109711_156142866 | LMNA | chr1 | 156109711 | 156142866 |
HG02129 | hp1 | a0001 | c0002 | t0001 | g0100 | EAS | KHV | LMNA_chr1_156109711_156142866 | LMNA | chr1 | 156109711 | 156142866 |
HG02129 | hp2 | a0001 | c0001 | t0001 | g0126 | EAS | KHV | LMNA_chr1_156109711_156142866 | LMNA | chr1 | 156109711 | 156142866 |
HG02132 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | KHV | LMNA_chr1_156109711_156142866 | LMNA | chr1 | 156109711 | 156142866 |
HG02132 | hp2 | a0001 | c0003 | t0001 | g0163 | EAS | KHV | LMNA_chr1_156109711_156142866 | LMNA | chr1 | 156109711 | 156142866 |
HG02135 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | LMNA_chr1_156109711_156142866 | LMNA | chr1 | 156109711 | 156142866 |
HG02135 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | KHV | LMNA_chr1_156109711_156142866 | LMNA | chr1 | 156109711 | 156142866 |
HG02145 | hp1 | a0001 | c0001 | t0001 | g0090 | AFR | ACB | LMNA_chr1_156109711_156142866 | LMNA | chr1 | 156109711 | 156142866 |
HG02145 | hp2 | a0001 | c0003 | t0001 | g0186 | AFR | ACB | LMNA_chr1_156109711_156142866 | LMNA | chr1 | 156109711 | 156142866 |
HG02155 | hp1 | a0002 | c0008 | t0001 | g0005 | EAS | CDX | LMNA_chr1_156109711_156142866 | LMNA | chr1 | 156109711 | 156142866 |
HG02155 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | CDX | LMNA_chr1_156109711_156142866 | LMNA | chr1 | 156109711 | 156142866 |
HG02165 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | CDX | LMNA_chr1_156109711_156142866 | LMNA | chr1 | 156109711 | 156142866 |
HG02165 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | CDX | LMNA_chr1_156109711_156142866 | LMNA | chr1 | 156109711 | 156142866 |
HG02257 | hp1 | a0001 | c0004 | t0001 | g0010 | AFR | ACB | LMNA_chr1_156109711_156142866 | LMNA | chr1 | 156109711 | 156142866 |
HG02257 | hp2 | a0001 | c0004 | t0001 | g0175 | AFR | ACB | LMNA_chr1_156109711_156142866 | LMNA | chr1 | 156109711 | 156142866 |
HG02258 | hp1 | a0001 | c0003 | t0001 | g0005 | AFR | ACB | LMNA_chr1_156109711_156142866 | LMNA | chr1 | 156109711 | 156142866 |
HG02258 | hp2 | a0001 | c0003 | t0001 | g0004 | AFR | ACB | LMNA_chr1_156109711_156142866 | LMNA | chr1 | 156109711 | 156142866 |
HG02273 | hp1 | a0001 | c0001 | t0001 | g0008 | AMR | PEL | LMNA_chr1_156109711_156142866 | LMNA | chr1 | 156109711 | 156142866 |
HG02273 | hp2 | a0001 | c0002 | t0001 | g0003 | AMR | PEL | LMNA_chr1_156109711_156142866 | LMNA | chr1 | 156109711 | 156142866 |
HG02293 | hp1 | a0001 | c0002 | t0001 | g0003 | AMR | PEL | LMNA_chr1_156109711_156142866 | LMNA | chr1 | 156109711 | 156142866 |
HG02293 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | LMNA_chr1_156109711_156142866 | LMNA | chr1 | 156109711 | 156142866 |
HG02300 | hp1 | a0001 | c0001 | t0001 | g0044 | AMR | PEL | LMNA_chr1_156109711_156142866 | LMNA | chr1 | 156109711 | 156142866 |
HG02300 | hp2 | a0001 | c0001 | t0001 | g0144 | AMR | PEL | LMNA_chr1_156109711_156142866 | LMNA | chr1 | 156109711 | 156142866 |
HG02572 | hp1 | a0001 | c0004 | t0001 | g0010 | AFR | GWD | LMNA_chr1_156109711_156142866 | LMNA | chr1 | 156109711 | 156142866 |
HG02572 | hp2 | a0001 | c0004 | t0002 | g0033 | AFR | GWD | LMNA_chr1_156109711_156142866 | LMNA | chr1 | 156109711 | 156142866 |
HG02602 | hp1 | a0001 | c0003 | t0001 | g0184 | SAS | PJL | LMNA_chr1_156109711_156142866 | LMNA | chr1 | 156109711 | 156142866 |
HG02602 | hp2 | a0001 | c0001 | t0001 | g0079 | SAS | PJL | LMNA_chr1_156109711_156142866 | LMNA | chr1 | 156109711 | 156142866 |
HG02615 | hp1 | a0001 | c0002 | t0001 | g0026 | AFR | GWD | LMNA_chr1_156109711_156142866 | LMNA | chr1 | 156109711 | 156142866 |
HG02615 | hp2 | a0001 | c0003 | t0001 | g0028 | AFR | GWD | LMNA_chr1_156109711_156142866 | LMNA | chr1 | 156109711 | 156142866 |
HG02622 | hp1 | a0001 | c0003 | t0001 | g0183 | AFR | GWD | LMNA_chr1_156109711_156142866 | LMNA | chr1 | 156109711 | 156142866 |
HG02622 | hp2 | a0001 | c0004 | t0002 | g0178 | AFR | GWD | LMNA_chr1_156109711_156142866 | LMNA | chr1 | 156109711 | 156142866 |
HG02630 | hp1 | a0001 | c0005 | t0001 | g0170 | AFR | GWD | LMNA_chr1_156109711_156142866 | LMNA | chr1 | 156109711 | 156142866 |
HG02630 | hp2 | a0001 | c0003 | t0001 | g0005 | AFR | GWD | LMNA_chr1_156109711_156142866 | LMNA | chr1 | 156109711 | 156142866 |
HG02647 | hp1 | a0001 | c0004 | t0002 | g0176 | AFR | GWD | LMNA_chr1_156109711_156142866 | LMNA | chr1 | 156109711 | 156142866 |
HG02647 | hp2 | a0001 | c0003 | t0001 | g0146 | AFR | GWD | LMNA_chr1_156109711_156142866 | LMNA | chr1 | 156109711 | 156142866 |
HG02698 | hp1 | a0001 | c0001 | t0001 | g0105 | SAS | PJL | LMNA_chr1_156109711_156142866 | LMNA | chr1 | 156109711 | 156142866 |
HG02698 | hp2 | a0001 | c0003 | t0001 | g0030 | SAS | PJL | LMNA_chr1_156109711_156142866 | LMNA | chr1 | 156109711 | 156142866 |
HG02723 | hp1 | a0001 | c0003 | t0001 | g0120 | AFR | GWD | LMNA_chr1_156109711_156142866 | LMNA | chr1 | 156109711 | 156142866 |
HG02723 | hp2 | a0001 | c0004 | t0001 | g0010 | AFR | GWD | LMNA_chr1_156109711_156142866 | LMNA | chr1 | 156109711 | 156142866 |
HG02809 | hp1 | a0001 | c0004 | t0001 | g0067 | AFR | GWD | LMNA_chr1_156109711_156142866 | LMNA | chr1 | 156109711 | 156142866 |
HG02809 | hp2 | a0001 | c0003 | t0001 | g0169 | AFR | GWD | LMNA_chr1_156109711_156142866 | LMNA | chr1 | 156109711 | 156142866 |
HG02818 | hp1 | a0001 | c0004 | t0001 | g0032 | AFR | GWD | LMNA_chr1_156109711_156142866 | LMNA | chr1 | 156109711 | 156142866 |
HG02818 | hp2 | a0001 | c0003 | t0001 | g0005 | AFR | GWD | LMNA_chr1_156109711_156142866 | LMNA | chr1 | 156109711 | 156142866 |
HG02895 | hp1 | a0001 | c0001 | t0001 | g0095 | AFR | GWD | LMNA_chr1_156109711_156142866 | LMNA | chr1 | 156109711 | 156142866 |
HG02895 | hp2 | a0001 | c0003 | t0001 | g0161 | AFR | GWD | LMNA_chr1_156109711_156142866 | LMNA | chr1 | 156109711 | 156142866 |
HG02896 | hp1 | a0001 | c0002 | t0001 | g0026 | AFR | GWD | LMNA_chr1_156109711_156142866 | LMNA | chr1 | 156109711 | 156142866 |
HG02896 | hp2 | a0001 | c0004 | t0001 | g0180 | AFR | GWD | LMNA_chr1_156109711_156142866 | LMNA | chr1 | 156109711 | 156142866 |
HG02897 | hp1 | a0001 | c0003 | t0001 | g0029 | AFR | GWD | LMNA_chr1_156109711_156142866 | LMNA | chr1 | 156109711 | 156142866 |
HG02897 | hp2 | a0001 | c0004 | t0001 | g0035 | AFR | GWD | LMNA_chr1_156109711_156142866 | LMNA | chr1 | 156109711 | 156142866 |
HG02922 | hp1 | a0001 | c0003 | t0001 | g0028 | AFR | ESN | LMNA_chr1_156109711_156142866 | LMNA | chr1 | 156109711 | 156142866 |
HG02922 | hp2 | a0001 | c0003 | t0001 | g0157 | AFR | ESN | LMNA_chr1_156109711_156142866 | LMNA | chr1 | 156109711 | 156142866 |
HG02965 | hp1 | a0001 | c0004 | t0001 | g0070 | AFR | ESN | LMNA_chr1_156109711_156142866 | LMNA | chr1 | 156109711 | 156142866 |
HG02965 | hp2 | a0001 | c0004 | t0001 | g0080 | AFR | ESN | LMNA_chr1_156109711_156142866 | LMNA | chr1 | 156109711 | 156142866 |
HG02970 | hp1 | a0001 | c0004 | t0001 | g0032 | AFR | ESN | LMNA_chr1_156109711_156142866 | LMNA | chr1 | 156109711 | 156142866 |
HG02970 | hp2 | a0001 | c0003 | t0001 | g0011 | AFR | ESN | LMNA_chr1_156109711_156142866 | LMNA | chr1 | 156109711 | 156142866 |
HG02976 | hp1 | a0001 | c0001 | t0001 | g0076 | AFR | ESN | LMNA_chr1_156109711_156142866 | LMNA | chr1 | 156109711 | 156142866 |
HG02976 | hp2 | a0001 | c0003 | t0001 | g0158 | AFR | ESN | LMNA_chr1_156109711_156142866 | LMNA | chr1 | 156109711 | 156142866 |
HG03041 | hp1 | a0001 | c0003 | t0001 | g0159 | AFR | GWD | LMNA_chr1_156109711_156142866 | LMNA | chr1 | 156109711 | 156142866 |
HG03041 | hp2 | a0001 | c0003 | t0001 | g0004 | AFR | GWD | LMNA_chr1_156109711_156142866 | LMNA | chr1 | 156109711 | 156142866 |
HG03098 | hp1 | a0001 | c0003 | t0001 | g0078 | AFR | MSL | LMNA_chr1_156109711_156142866 | LMNA | chr1 | 156109711 | 156142866 |
HG03098 | hp2 | a0001 | c0003 | t0001 | g0025 | AFR | MSL | LMNA_chr1_156109711_156142866 | LMNA | chr1 | 156109711 | 156142866 |
HG03130 | hp1 | a0001 | c0003 | t0001 | g0004 | AFR | ESN | LMNA_chr1_156109711_156142866 | LMNA | chr1 | 156109711 | 156142866 |
HG03130 | hp2 | a0001 | c0003 | t0001 | g0005 | AFR | ESN | LMNA_chr1_156109711_156142866 | LMNA | chr1 | 156109711 | 156142866 |
HG03139 | hp1 | a0001 | c0004 | t0002 | g0033 | AFR | ESN | LMNA_chr1_156109711_156142866 | LMNA | chr1 | 156109711 | 156142866 |
HG03139 | hp2 | a0001 | c0003 | t0001 | g0005 | AFR | ESN | LMNA_chr1_156109711_156142866 | LMNA | chr1 | 156109711 | 156142866 |
HG03195 | hp1 | a0001 | c0004 | t0001 | g0174 | AFR | ESN | LMNA_chr1_156109711_156142866 | LMNA | chr1 | 156109711 | 156142866 |
HG03195 | hp2 | a0001 | c0004 | t0002 | g0177 | AFR | ESN | LMNA_chr1_156109711_156142866 | LMNA | chr1 | 156109711 | 156142866 |
HG03209 | hp1 | a0001 | c0001 | t0001 | g0006 | AFR | MSL | LMNA_chr1_156109711_156142866 | LMNA | chr1 | 156109711 | 156142866 |
HG03209 | hp2 | a0001 | c0003 | t0001 | g0004 | AFR | MSL | LMNA_chr1_156109711_156142866 | LMNA | chr1 | 156109711 | 156142866 |
HG03239 | hp1 | a0001 | c0002 | t0001 | g0110 | SAS | PJL | LMNA_chr1_156109711_156142866 | LMNA | chr1 | 156109711 | 156142866 |
HG03239 | hp2 | a0001 | c0001 | t0001 | g0008 | SAS | PJL | LMNA_chr1_156109711_156142866 | LMNA | chr1 | 156109711 | 156142866 |
HG03453 | hp1 | a0001 | c0003 | t0001 | g0109 | AFR | MSL | LMNA_chr1_156109711_156142866 | LMNA | chr1 | 156109711 | 156142866 |
HG03453 | hp2 | a0001 | c0001 | t0002 | g0188 | AFR | MSL | LMNA_chr1_156109711_156142866 | LMNA | chr1 | 156109711 | 156142866 |
HG03486 | hp1 | a0001 | c0003 | t0001 | g0025 | AFR | MSL | LMNA_chr1_156109711_156142866 | LMNA | chr1 | 156109711 | 156142866 |
HG03486 | hp2 | a0001 | c0003 | t0001 | g0171 | AFR | MSL | LMNA_chr1_156109711_156142866 | LMNA | chr1 | 156109711 | 156142866 |
HG03490 | hp1 | a0001 | c0003 | t0001 | g0164 | SAS | PJL | LMNA_chr1_156109711_156142866 | LMNA | chr1 | 156109711 | 156142866 |
HG03490 | hp2 | a0001 | c0002 | t0001 | g0022 | SAS | PJL | LMNA_chr1_156109711_156142866 | LMNA | chr1 | 156109711 | 156142866 |
HG03491 | hp1 | a0001 | c0001 | t0001 | g0043 | SAS | PJL | LMNA_chr1_156109711_156142866 | LMNA | chr1 | 156109711 | 156142866 |
HG03491 | hp2 | a0001 | c0001 | t0001 | g0061 | SAS | PJL | LMNA_chr1_156109711_156142866 | LMNA | chr1 | 156109711 | 156142866 |
HG03492 | hp1 | a0001 | c0001 | t0001 | g0024 | SAS | PJL | LMNA_chr1_156109711_156142866 | LMNA | chr1 | 156109711 | 156142866 |
HG03492 | hp2 | a0001 | c0002 | t0001 | g0022 | SAS | PJL | LMNA_chr1_156109711_156142866 | LMNA | chr1 | 156109711 | 156142866 |
HG03516 | hp1 | a0001 | c0001 | t0001 | g0088 | AFR | ESN | LMNA_chr1_156109711_156142866 | LMNA | chr1 | 156109711 | 156142866 |
HG03516 | hp2 | a0001 | c0001 | t0001 | g0087 | AFR | ESN | LMNA_chr1_156109711_156142866 | LMNA | chr1 | 156109711 | 156142866 |
HG03540 | hp1 | a0001 | c0002 | t0001 | g0128 | AFR | GWD | LMNA_chr1_156109711_156142866 | LMNA | chr1 | 156109711 | 156142866 |
HG03540 | hp2 | a0001 | c0004 | t0001 | g0035 | AFR | GWD | LMNA_chr1_156109711_156142866 | LMNA | chr1 | 156109711 | 156142866 |
HG03579 | hp1 | a0001 | c0003 | t0001 | g0004 | AFR | MSL | LMNA_chr1_156109711_156142866 | LMNA | chr1 | 156109711 | 156142866 |
HG03579 | hp2 | a0001 | c0001 | t0001 | g0019 | AFR | MSL | LMNA_chr1_156109711_156142866 | LMNA | chr1 | 156109711 | 156142866 |
HG03669 | hp1 | a0001 | c0003 | t0001 | g0185 | SAS | PJL | LMNA_chr1_156109711_156142866 | LMNA | chr1 | 156109711 | 156142866 |
HG03669 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | LMNA_chr1_156109711_156142866 | LMNA | chr1 | 156109711 | 156142866 |
HG03704 | hp1 | a0001 | c0002 | t0001 | g0015 | SAS | PJL | LMNA_chr1_156109711_156142866 | LMNA | chr1 | 156109711 | 156142866 |
HG03704 | hp2 | a0001 | c0001 | t0001 | g0015 | SAS | PJL | LMNA_chr1_156109711_156142866 | LMNA | chr1 | 156109711 | 156142866 |
HG03834 | hp1 | a0001 | c0002 | t0001 | g0006 | SAS | BEB | LMNA_chr1_156109711_156142866 | LMNA | chr1 | 156109711 | 156142866 |
HG03834 | hp2 | a0001 | c0001 | t0001 | g0150 | SAS | BEB | LMNA_chr1_156109711_156142866 | LMNA | chr1 | 156109711 | 156142866 |
HG03927 | hp1 | a0001 | c0001 | t0001 | g0135 | SAS | BEB | LMNA_chr1_156109711_156142866 | LMNA | chr1 | 156109711 | 156142866 |
HG03927 | hp2 | a0001 | c0001 | t0001 | g0148 | SAS | BEB | LMNA_chr1_156109711_156142866 | LMNA | chr1 | 156109711 | 156142866 |
HG03942 | hp1 | a0001 | c0001 | t0001 | g0112 | SAS | BEB | LMNA_chr1_156109711_156142866 | LMNA | chr1 | 156109711 | 156142866 |
HG03942 | hp2 | a0001 | c0001 | t0001 | g0166 | SAS | BEB | LMNA_chr1_156109711_156142866 | LMNA | chr1 | 156109711 | 156142866 |
HG04115 | hp1 | a0001 | c0002 | t0001 | g0115 | SAS | STU | LMNA_chr1_156109711_156142866 | LMNA | chr1 | 156109711 | 156142866 |
HG04115 | hp2 | a0001 | c0003 | t0001 | g0108 | SAS | STU | LMNA_chr1_156109711_156142866 | LMNA | chr1 | 156109711 | 156142866 |
HG04199 | hp1 | a0001 | c0003 | t0001 | g0165 | SAS | STU | LMNA_chr1_156109711_156142866 | LMNA | chr1 | 156109711 | 156142866 |
HG04199 | hp2 | a0001 | c0002 | t0001 | g0113 | SAS | STU | LMNA_chr1_156109711_156142866 | LMNA | chr1 | 156109711 | 156142866 |
HG04228 | hp1 | a0001 | c0003 | t0001 | g0030 | SAS | STU | LMNA_chr1_156109711_156142866 | LMNA | chr1 | 156109711 | 156142866 |
HG04228 | hp2 | a0001 | c0002 | t0001 | g0006 | SAS | STU | LMNA_chr1_156109711_156142866 | LMNA | chr1 | 156109711 | 156142866 |
NA18522 | hp1 | a0001 | c0003 | t0001 | g0168 | AFR | YRI | LMNA_chr1_156109711_156142866 | LMNA | chr1 | 156109711 | 156142866 |
NA18522 | hp2 | a0001 | c0003 | t0001 | g0034 | AFR | YRI | LMNA_chr1_156109711_156142866 | LMNA | chr1 | 156109711 | 156142866 |
NA18747 | hp1 | a0001 | c0002 | t0001 | g0009 | EAS | CHB | LMNA_chr1_156109711_156142866 | LMNA | chr1 | 156109711 | 156142866 |
NA18747 | hp2 | a0001 | c0001 | t0001 | g0048 | EAS | CHB | LMNA_chr1_156109711_156142866 | LMNA | chr1 | 156109711 | 156142866 |
NA18906 | hp1 | a0001 | c0001 | t0001 | g0089 | AFR | YRI | LMNA_chr1_156109711_156142866 | LMNA | chr1 | 156109711 | 156142866 |
NA18906 | hp2 | a0001 | c0003 | t0001 | g0036 | AFR | YRI | LMNA_chr1_156109711_156142866 | LMNA | chr1 | 156109711 | 156142866 |
NA18941 | hp1 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | LMNA_chr1_156109711_156142866 | LMNA | chr1 | 156109711 | 156142866 |
NA18941 | hp2 | a0001 | c0002 | t0001 | g0155 | EAS | JPT | LMNA_chr1_156109711_156142866 | LMNA | chr1 | 156109711 | 156142866 |
NA18945 | hp1 | a0001 | c0003 | t0001 | g0005 | EAS | JPT | LMNA_chr1_156109711_156142866 | LMNA | chr1 | 156109711 | 156142866 |
NA18945 | hp2 | a0001 | c0002 | t0001 | g0101 | EAS | JPT | LMNA_chr1_156109711_156142866 | LMNA | chr1 | 156109711 | 156142866 |
NA18946 | hp1 | a0001 | c0001 | t0001 | g0071 | EAS | JPT | LMNA_chr1_156109711_156142866 | LMNA | chr1 | 156109711 | 156142866 |
NA18946 | hp2 | a0001 | c0001 | t0001 | g0054 | EAS | JPT | LMNA_chr1_156109711_156142866 | LMNA | chr1 | 156109711 | 156142866 |
NA18949 | hp1 | a0001 | c0002 | t0001 | g0130 | EAS | JPT | LMNA_chr1_156109711_156142866 | LMNA | chr1 | 156109711 | 156142866 |
NA18949 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | LMNA_chr1_156109711_156142866 | LMNA | chr1 | 156109711 | 156142866 |
NA18950 | hp1 | a0001 | c0002 | t0001 | g0138 | EAS | JPT | LMNA_chr1_156109711_156142866 | LMNA | chr1 | 156109711 | 156142866 |
NA18950 | hp2 | a0001 | c0002 | t0001 | g0152 | EAS | JPT | LMNA_chr1_156109711_156142866 | LMNA | chr1 | 156109711 | 156142866 |
NA18951 | hp1 | a0001 | c0001 | t0001 | g0059 | EAS | JPT | LMNA_chr1_156109711_156142866 | LMNA | chr1 | 156109711 | 156142866 |
NA18951 | hp2 | a0001 | c0002 | t0001 | g0013 | EAS | JPT | LMNA_chr1_156109711_156142866 | LMNA | chr1 | 156109711 | 156142866 |
NA18964 | hp1 | a0001 | c0001 | t0001 | g0082 | EAS | JPT | LMNA_chr1_156109711_156142866 | LMNA | chr1 | 156109711 | 156142866 |
NA18964 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | LMNA_chr1_156109711_156142866 | LMNA | chr1 | 156109711 | 156142866 |
NA18968 | hp1 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | LMNA_chr1_156109711_156142866 | LMNA | chr1 | 156109711 | 156142866 |
NA18968 | hp2 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | LMNA_chr1_156109711_156142866 | LMNA | chr1 | 156109711 | 156142866 |
NA18969 | hp1 | a0001 | c0002 | t0001 | g0057 | EAS | JPT | LMNA_chr1_156109711_156142866 | LMNA | chr1 | 156109711 | 156142866 |
NA18969 | hp2 | a0001 | c0001 | t0001 | g0055 | EAS | JPT | LMNA_chr1_156109711_156142866 | LMNA | chr1 | 156109711 | 156142866 |
NA18971 | hp1 | a0001 | c0001 | t0001 | g0069 | EAS | JPT | LMNA_chr1_156109711_156142866 | LMNA | chr1 | 156109711 | 156142866 |
NA18971 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | LMNA_chr1_156109711_156142866 | LMNA | chr1 | 156109711 | 156142866 |
NA18974 | hp1 | a0001 | c0002 | t0001 | g0053 | EAS | JPT | LMNA_chr1_156109711_156142866 | LMNA | chr1 | 156109711 | 156142866 |
NA18974 | hp2 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | LMNA_chr1_156109711_156142866 | LMNA | chr1 | 156109711 | 156142866 |
NA18978 | hp1 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | LMNA_chr1_156109711_156142866 | LMNA | chr1 | 156109711 | 156142866 |
NA18978 | hp2 | a0001 | c0001 | t0001 | g0145 | EAS | JPT | LMNA_chr1_156109711_156142866 | LMNA | chr1 | 156109711 | 156142866 |
NA18979 | hp1 | a0001 | c0002 | t0001 | g0103 | EAS | JPT | LMNA_chr1_156109711_156142866 | LMNA | chr1 | 156109711 | 156142866 |
NA18979 | hp2 | a0001 | c0002 | t0001 | g0009 | EAS | JPT | LMNA_chr1_156109711_156142866 | LMNA | chr1 | 156109711 | 156142866 |
NA18983 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | LMNA_chr1_156109711_156142866 | LMNA | chr1 | 156109711 | 156142866 |
NA18983 | hp2 | a0001 | c0001 | t0001 | g0074 | EAS | JPT | LMNA_chr1_156109711_156142866 | LMNA | chr1 | 156109711 | 156142866 |
NA18984 | hp1 | a0001 | c0001 | t0001 | g0049 | EAS | JPT | LMNA_chr1_156109711_156142866 | LMNA | chr1 | 156109711 | 156142866 |
NA18984 | hp2 | a0001 | c0002 | t0001 | g0023 | EAS | JPT | LMNA_chr1_156109711_156142866 | LMNA | chr1 | 156109711 | 156142866 |
NA18989 | hp1 | a0001 | c0001 | t0001 | g0046 | EAS | JPT | LMNA_chr1_156109711_156142866 | LMNA | chr1 | 156109711 | 156142866 |
NA18989 | hp2 | a0001 | c0001 | t0001 | g0045 | EAS | JPT | LMNA_chr1_156109711_156142866 | LMNA | chr1 | 156109711 | 156142866 |
NA18995 | hp1 | a0001 | c0002 | t0001 | g0008 | EAS | JPT | LMNA_chr1_156109711_156142866 | LMNA | chr1 | 156109711 | 156142866 |
NA18995 | hp2 | a0001 | c0001 | t0001 | g0111 | EAS | JPT | LMNA_chr1_156109711_156142866 | LMNA | chr1 | 156109711 | 156142866 |
NA18999 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | LMNA_chr1_156109711_156142866 | LMNA | chr1 | 156109711 | 156142866 |
NA18999 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | LMNA_chr1_156109711_156142866 | LMNA | chr1 | 156109711 | 156142866 |
NA19003 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | LMNA_chr1_156109711_156142866 | LMNA | chr1 | 156109711 | 156142866 |
NA19003 | hp2 | a0001 | c0003 | t0001 | g0167 | EAS | JPT | LMNA_chr1_156109711_156142866 | LMNA | chr1 | 156109711 | 156142866 |
NA19004 | hp1 | a0001 | c0002 | t0001 | g0037 | EAS | JPT | LMNA_chr1_156109711_156142866 | LMNA | chr1 | 156109711 | 156142866 |
NA19004 | hp2 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | LMNA_chr1_156109711_156142866 | LMNA | chr1 | 156109711 | 156142866 |
NA19005 | hp1 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | LMNA_chr1_156109711_156142866 | LMNA | chr1 | 156109711 | 156142866 |
NA19005 | hp2 | a0001 | c0002 | t0001 | g0102 | EAS | JPT | LMNA_chr1_156109711_156142866 | LMNA | chr1 | 156109711 | 156142866 |
NA19010 | hp1 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | LMNA_chr1_156109711_156142866 | LMNA | chr1 | 156109711 | 156142866 |
NA19010 | hp2 | a0001 | c0001 | t0001 | g0056 | EAS | JPT | LMNA_chr1_156109711_156142866 | LMNA | chr1 | 156109711 | 156142866 |
NA19030 | hp1 | a0001 | c0003 | t0001 | g0031 | AFR | LWK | LMNA_chr1_156109711_156142866 | LMNA | chr1 | 156109711 | 156142866 |
NA19030 | hp2 | a0001 | c0003 | t0001 | g0099 | AFR | LWK | LMNA_chr1_156109711_156142866 | LMNA | chr1 | 156109711 | 156142866 |
NA19043 | hp1 | a0001 | c0003 | t0001 | g0047 | AFR | LWK | LMNA_chr1_156109711_156142866 | LMNA | chr1 | 156109711 | 156142866 |
NA19043 | hp2 | a0001 | c0001 | t0001 | g0129 | AFR | LWK | LMNA_chr1_156109711_156142866 | LMNA | chr1 | 156109711 | 156142866 |
NA19054 | hp1 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | LMNA_chr1_156109711_156142866 | LMNA | chr1 | 156109711 | 156142866 |
NA19054 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | LMNA_chr1_156109711_156142866 | LMNA | chr1 | 156109711 | 156142866 |
NA19056 | hp1 | a0001 | c0002 | t0001 | g0058 | EAS | JPT | LMNA_chr1_156109711_156142866 | LMNA | chr1 | 156109711 | 156142866 |
NA19056 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | LMNA_chr1_156109711_156142866 | LMNA | chr1 | 156109711 | 156142866 |
NA19057 | hp1 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | LMNA_chr1_156109711_156142866 | LMNA | chr1 | 156109711 | 156142866 |
NA19057 | hp2 | a0001 | c0001 | t0001 | g0066 | EAS | JPT | LMNA_chr1_156109711_156142866 | LMNA | chr1 | 156109711 | 156142866 |
NA19063 | hp1 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | LMNA_chr1_156109711_156142866 | LMNA | chr1 | 156109711 | 156142866 |
NA19063 | hp2 | a0001 | c0002 | t0001 | g0075 | EAS | JPT | LMNA_chr1_156109711_156142866 | LMNA | chr1 | 156109711 | 156142866 |
NA19066 | hp1 | a0001 | c0001 | t0001 | g0083 | EAS | JPT | LMNA_chr1_156109711_156142866 | LMNA | chr1 | 156109711 | 156142866 |
NA19066 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | LMNA_chr1_156109711_156142866 | LMNA | chr1 | 156109711 | 156142866 |
NA19084 | hp1 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | LMNA_chr1_156109711_156142866 | LMNA | chr1 | 156109711 | 156142866 |
NA19084 | hp2 | a0001 | c0001 | t0001 | g0050 | EAS | JPT | LMNA_chr1_156109711_156142866 | LMNA | chr1 | 156109711 | 156142866 |
NA19085 | hp1 | a0001 | c0002 | t0001 | g0153 | EAS | JPT | LMNA_chr1_156109711_156142866 | LMNA | chr1 | 156109711 | 156142866 |
NA19085 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | LMNA_chr1_156109711_156142866 | LMNA | chr1 | 156109711 | 156142866 |
NA19087 | hp1 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | LMNA_chr1_156109711_156142866 | LMNA | chr1 | 156109711 | 156142866 |
NA19087 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | LMNA_chr1_156109711_156142866 | LMNA | chr1 | 156109711 | 156142866 |
NA19088 | hp1 | a0001 | c0002 | t0001 | g0021 | EAS | JPT | LMNA_chr1_156109711_156142866 | LMNA | chr1 | 156109711 | 156142866 |
NA19088 | hp2 | a0001 | c0001 | t0001 | g0091 | EAS | JPT | LMNA_chr1_156109711_156142866 | LMNA | chr1 | 156109711 | 156142866 |
NA19089 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | LMNA_chr1_156109711_156142866 | LMNA | chr1 | 156109711 | 156142866 |
NA19089 | hp2 | a0001 | c0003 | t0001 | g0160 | EAS | JPT | LMNA_chr1_156109711_156142866 | LMNA | chr1 | 156109711 | 156142866 |
NA19090 | hp1 | a0001 | c0002 | t0001 | g0154 | EAS | JPT | LMNA_chr1_156109711_156142866 | LMNA | chr1 | 156109711 | 156142866 |
NA19090 | hp2 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | LMNA_chr1_156109711_156142866 | LMNA | chr1 | 156109711 | 156142866 |
NA19240 | hp1 | a0001 | c0003 | t0001 | g0182 | AFR | YRI | LMNA_chr1_156109711_156142866 | LMNA | chr1 | 156109711 | 156142866 |
NA19240 | hp2 | a0001 | c0003 | t0001 | g0187 | AFR | YRI | LMNA_chr1_156109711_156142866 | LMNA | chr1 | 156109711 | 156142866 |
NA20129 | hp1 | a0001 | c0001 | t0001 | g0062 | AFR | ASW | LMNA_chr1_156109711_156142866 | LMNA | chr1 | 156109711 | 156142866 |
NA20129 | hp2 | a0001 | c0003 | t0001 | g0181 | AFR | ASW | LMNA_chr1_156109711_156142866 | LMNA | chr1 | 156109711 | 156142866 |
NA20905 | hp1 | a0001 | c0001 | t0001 | g0063 | SAS | GIH | LMNA_chr1_156109711_156142866 | LMNA | chr1 | 156109711 | 156142866 |
NA20905 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | GIH | LMNA_chr1_156109711_156142866 | LMNA | chr1 | 156109711 | 156142866 |
HG02109 | hp1 | a0001 | c0003 | t0001 | g0011 | AFR | ACB | LMNA_chr1_156109711_156142866 | LMNA | chr1 | 156109711 | 156142866 |
HG02109 | hp2 | a0001 | c0003 | t0001 | g0029 | AFR | ACB | LMNA_chr1_156109711_156142866 | LMNA | chr1 | 156109711 | 156142866 |
HG02486 | hp1 | a0001 | c0003 | t0001 | g0036 | AFR | ACB | LMNA_chr1_156109711_156142866 | LMNA | chr1 | 156109711 | 156142866 |
HG02486 | hp2 | a0001 | c0003 | t0001 | g0004 | AFR | ACB | LMNA_chr1_156109711_156142866 | LMNA | chr1 | 156109711 | 156142866 |
HG02559 | hp1 | a0001 | c0004 | t0001 | g0085 | AFR | ACB | LMNA_chr1_156109711_156142866 | LMNA | chr1 | 156109711 | 156142866 |
HG02559 | hp2 | a0001 | c0002 | t0001 | g0124 | AFR | ACB | LMNA_chr1_156109711_156142866 | LMNA | chr1 | 156109711 | 156142866 |
HG06807 | hp1 | a0001 | c0003 | t0001 | g0005 | AFR | USA | LMNA_chr1_156109711_156142866 | LMNA | chr1 | 156109711 | 156142866 |
HG06807 | hp2 | a0001 | c0004 | t0002 | g0173 | AFR | USA | LMNA_chr1_156109711_156142866 | LMNA | chr1 | 156109711 | 156142866 |
NA20300 | hp1 | a0001 | c0002 | t0001 | g0023 | AFR | USA | LMNA_chr1_156109711_156142866 | LMNA | chr1 | 156109711 | 156142866 |
NA20300 | hp2 | a0001 | c0003 | t0001 | g0011 | AFR | USA | LMNA_chr1_156109711_156142866 | LMNA | chr1 | 156109711 | 156142866 |
NA21309 | hp1 | a0001 | c0003 | t0001 | g0179 | AFR | LWK | LMNA_chr1_156109711_156142866 | LMNA | chr1 | 156109711 | 156142866 |
NA21309 | hp2 | a0001 | c0003 | t0001 | g0031 | AFR | LWK | LMNA_chr1_156109711_156142866 | LMNA | chr1 | 156109711 | 156142866 |
homoSapiens | chm13v2 | a0001 | c0002 | t0001 | g0121 | REF | REF | LMNA_chr1_156109711_156142866 | LMNA | chr1 | 156109711 | 156142866 |
homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0172 | REF | REF | LMNA_chr1_156109711_156142866 | LMNA | chr1 | 156109711 | 156142866 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:156134454 | C | T | 1 | a0002 | 1 | HG02155.hp1 | missense_variant | MODERATE | c.565C>T | p.Arg189Trp | LMNA | ENSG00000160789.24 | transcript | ENST00000677389.1 | protein_coding | 3/10 | 773/2029 | 565/1719 | 189/572 | chr1 | 156134454 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:156114969 | C | T | 2 | a0001c0009 a0001c0010 |
2 | HG01099.hp1 HG01261.hp2 |
synonymous_variant | LOW | c.51C>T | p.Ser17Ser | LMNA | ENSG00000160789.24 | transcript | ENST00000677389.1 | protein_coding | 1/10 | 259/2029 | 51/1719 | 17/572 | chr1 | 156114969 | |||
chr1:156135237 | T | C | 3 | a0001c0003 a0001c0005 a0002c0008 |
65 | HG01167.hp2 HG01169.hp2 HG01257.hp2 others(62): Show |
synonymous_variant | LOW | c.861T>C | p.Ala287Ala | LMNA | ENSG00000160789.24 | transcript | ENST00000677389.1 | protein_coding | 5/10 | 1069/2029 | 861/1719 | 287/572 | chr1 | 156135237 | |||
chr1:156136394 | T | C | 4 | a0001c0003 a0001c0004 a0001c0006 others(1): Show |
86 | HG01167.hp2 HG01169.hp2 HG01257.hp2 others(83): Show |
synonymous_variant | LOW | c.1338T>C | p.Asp446Asp | LMNA | ENSG00000160789.24 | transcript | ENST00000677389.1 | protein_coding | 7/10 | 1546/2029 | 1338/1719 | 446/572 | chr1 | 156136394 | |||
chr1:156137190 | C | T | 1 | a0001c0006 | 1 | HG01496.hp1 | synonymous_variant | LOW | c.1566C>T | p.Cys522Cys | LMNA | ENSG00000160789.24 | transcript | ENST00000677389.1 | protein_coding | 9/10 | 1774/2029 | 1566/1719 | 522/572 | chr1 | 156137190 | |||
chr1:156137208 | G | A | 1 | a0001c0007 | 1 | HG02056.hp1 | synonymous_variant | LOW | c.1584G>A | p.Thr528Thr | LMNA | ENSG00000160789.24 | transcript | ENST00000677389.1 | protein_coding | 9/10 | 1792/2029 | 1584/1719 | 528/572 | chr1 | 156137208 | |||
chr1:156137743 | C | T | 3 | a0001c0002 a0001c0007 a0001c0010 |
65 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(62): Show |
synonymous_variant | LOW | c.1698C>T | p.His566His | LMNA | ENSG00000160789.24 | transcript | ENST00000677389.1 | protein_coding | 10/10 | 1906/2029 | 1698/1719 | 566/572 | chr1 | 156137743 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:156114831 | G | T | 2 | a0001c0001t0002 a0001c0004t0002 |
7 | HG02572.hp2 HG02622.hp2 HG02647.hp1 others(4): Show |
5_prime_UTR_variant | MODIFIER | c.-88G>T | LMNA | ENSG00000160789.24 | transcript | ENST00000677389.1 | protein_coding | 1/10 | 88 | chr1 | 156114831 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:156115309 | G | A | 1 | a0001c0002t0001g0037 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.356+35G>A | LMNA | ENSG00000160789.24 | transcript | ENST00000677389.1 | protein_coding | 1/9 | chr1 | 156115309 | |||||||
chr1:156115584 | T | C | 150 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(147): Show |
215 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(212): Show |
intron_variant | MODIFIER | c.356+310T>C | LMNA | ENSG00000160789.24 | transcript | ENST00000677389.1 | protein_coding | 1/9 | chr1 | 156115584 | |||||||
chr1:156115702 | G | A | 4 | a0001c0001t0001g0012 a0001c0001t0001g0038 a0001c0001t0001g0039 others(1): Show |
5 | HG02135.hp2 NA18968.hp2 NA18978.hp1 others(2): Show |
intron_variant | MODIFIER | c.356+428G>A | LMNA | ENSG00000160789.24 | transcript | ENST00000677389.1 | protein_coding | 1/9 | chr1 | 156115702 | |||||||
chr1:156115917 | T | C | 1 | a0001c0003t0001g0157 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.356+643T>C | LMNA | ENSG00000160789.24 | transcript | ENST00000677389.1 | protein_coding | 1/9 | chr1 | 156115917 | |||||||
chr1:156116024 | C | T | 1 | a0001c0002t0001g0156 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.356+750C>T | LMNA | ENSG00000160789.24 | transcript | ENST00000677389.1 | protein_coding | 1/9 | chr1 | 156116024 | |||||||
chr1:156116075 | G | C | 1 | a0001c0003t0001g0158 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.356+801G>C | LMNA | ENSG00000160789.24 | transcript | ENST00000677389.1 | protein_coding | 1/9 | chr1 | 156116075 | |||||||
chr1:156116328 | A | G | 1 | a0001c0002t0001g0155 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.356+1054A>G | LMNA | ENSG00000160789.24 | transcript | ENST00000677389.1 | protein_coding | 1/9 | chr1 | 156116328 | |||||||
chr1:156116608 | A | C | 3 | a0001c0002t0001g0152 a0001c0002t0001g0153 a0001c0002t0001g0154 |
3 | NA18950.hp2 NA19085.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.356+1334A>C | LMNA | ENSG00000160789.24 | transcript | ENST00000677389.1 | protein_coding | 1/9 | chr1 | 156116608 | |||||||
chr1:156116769 | C | T | 1 | a0001c0001t0001g0151 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.356+1495C>T | LMNA | ENSG00000160789.24 | transcript | ENST00000677389.1 | protein_coding | 1/9 | chr1 | 156116769 | |||||||
chr1:156116787 | C | T | 1 | a0001c0001t0001g0150 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.356+1513C>T | LMNA | ENSG00000160789.24 | transcript | ENST00000677389.1 | protein_coding | 1/9 | chr1 | 156116787 | |||||||
chr1:156116810 | C | T | 1 | a0001c0001t0002g0188 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.356+1536C>T | LMNA | ENSG00000160789.24 | transcript | ENST00000677389.1 | protein_coding | 1/9 | chr1 | 156116810 | |||||||
chr1:156116843 | C | T | 1 | a0001c0001t0001g0149 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.356+1569C>T | LMNA | ENSG00000160789.24 | transcript | ENST00000677389.1 | protein_coding | 1/9 | chr1 | 156116843 | |||||||
chr1:156116889 | A | G | 1 | a0001c0001t0001g0148 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.356+1615A>G | LMNA | ENSG00000160789.24 | transcript | ENST00000677389.1 | protein_coding | 1/9 | chr1 | 156116889 | |||||||
chr1:156116922 | G | GT | 17 | a0001c0001t0001g0027 a0001c0001t0001g0135 a0001c0001t0001g0136 others(14): Show |
17 | HG01433.hp2 HG01981.hp2 HG02027.hp2 others(14): Show |
intron_variant | MODIFIER | c.356+1657dupT | LMNA | ENSG00000160789.24 | transcript | ENST00000677389.1 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 156116922 | ||||||
chr1:156117073 | A | C | 25 | a0001c0001t0002g0188 a0001c0003t0001g0004 a0001c0003t0001g0011 others(22): Show |
40 | HG01167.hp2 HG01169.hp2 HG01257.hp2 others(37): Show |
intron_variant | MODIFIER | c.356+1799A>C | LMNA | ENSG00000160789.24 | transcript | ENST00000677389.1 | protein_coding | 1/9 | chr1 | 156117073 | |||||||
chr1:156117079 | A | AT | 11 | a0001c0001t0001g0129 a0001c0001t0001g0132 a0001c0001t0001g0133 others(8): Show |
14 | HG01106.hp2 HG01433.hp1 HG01433.hp2 others(11): Show |
intron_variant | MODIFIER | c.356+1828dupT | LMNA | ENSG00000160789.24 | transcript | ENST00000677389.1 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 156117079 | ||||||
chr1:156117079 | AT | A | 85 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(82): Show |
128 | HG00140.hp2 HG00408.hp2 HG00438.hp2 others(125): Show |
intron_variant | MODIFIER | c.356+1828delT | LMNA | ENSG00000160789.24 | transcript | ENST00000677389.1 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 156117079 | ||||||
chr1:156117079 | ATT | A | 28 | a0001c0001t0001g0038 a0001c0001t0001g0041 a0001c0001t0001g0042 others(25): Show |
36 | HG01255.hp1 HG02132.hp2 HG02155.hp1 others(33): Show |
intron_variant | MODIFIER | c.356+1827_356+1828d others(4): Show |
LMNA | ENSG00000160789.24 | transcript | ENST00000677389.1 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 156117079 | ||||||
chr1:156117079 | ATTT | A | 7 | a0001c0003t0001g0028 a0001c0003t0001g0029 a0001c0003t0001g0159 others(4): Show |
9 | HG01884.hp1 HG02109.hp2 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.356+1826_356+1828d others(5): Show |
LMNA | ENSG00000160789.24 | transcript | ENST00000677389.1 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 156117079 | ||||||
chr1:156117102 | T | A | 1 | a0001c0003t0001g0187 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.356+1828T>A | LMNA | ENSG00000160789.24 | transcript | ENST00000677389.1 | protein_coding | 1/9 | chr1 | 156117102 | |||||||
chr1:156117113 | A | G | 1 | a0001c0004t0001g0175 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.356+1839A>G | LMNA | ENSG00000160789.24 | transcript | ENST00000677389.1 | protein_coding | 1/9 | chr1 | 156117113 | |||||||
chr1:156117327 | C | G | 1 | a0001c0001t0001g0094 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.356+2053C>G | LMNA | ENSG00000160789.24 | transcript | ENST00000677389.1 | protein_coding | 1/9 | chr1 | 156117327 | |||||||
chr1:156117415 | A | G | 13 | a0001c0003t0001g0004 a0001c0003t0001g0011 a0001c0003t0001g0034 others(10): Show |
25 | HG01167.hp2 HG01169.hp2 HG01257.hp2 others(22): Show |
intron_variant | MODIFIER | c.356+2141A>G | LMNA | ENSG00000160789.24 | transcript | ENST00000677389.1 | protein_coding | 1/9 | chr1 | 156117415 | |||||||
chr1:156117423 | C | T | 1 | a0001c0001t0001g0133 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.356+2149C>T | LMNA | ENSG00000160789.24 | transcript | ENST00000677389.1 | protein_coding | 1/9 | chr1 | 156117423 | |||||||
chr1:156117689 | C | T | 9 | a0001c0001t0001g0020 a0001c0001t0001g0048 a0001c0001t0001g0091 others(6): Show |
10 | HG00544.hp2 HG02129.hp2 NA18747.hp2 others(7): Show |
intron_variant | MODIFIER | c.356+2415C>T | LMNA | ENSG00000160789.24 | transcript | ENST00000677389.1 | protein_coding | 1/9 | chr1 | 156117689 | |||||||
chr1:156117781 | A | G | 1 | a0001c0005t0001g0170 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.356+2507A>G | LMNA | ENSG00000160789.24 | transcript | ENST00000677389.1 | protein_coding | 1/9 | chr1 | 156117781 | |||||||
chr1:156117820 | G | C | 1 | a0001c0003t0001g0171 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.356+2546G>C | LMNA | ENSG00000160789.24 | transcript | ENST00000677389.1 | protein_coding | 1/9 | chr1 | 156117820 | |||||||
chr1:156117915 | G | A | 11 | a0001c0001t0001g0020 a0001c0001t0001g0048 a0001c0001t0001g0049 others(8): Show |
12 | HG00544.hp2 HG02129.hp2 NA18747.hp2 others(9): Show |
intron_variant | MODIFIER | c.356+2641G>A | LMNA | ENSG00000160789.24 | transcript | ENST00000677389.1 | protein_coding | 1/9 | chr1 | 156117915 | |||||||
chr1:156117962 | T | C | 17 | a0001c0001t0001g0166 a0001c0002t0001g0026 a0001c0002t0001g0128 others(14): Show |
26 | HG02132.hp2 HG02155.hp1 HG02258.hp1 others(23): Show |
intron_variant | MODIFIER | c.356+2688T>C | LMNA | ENSG00000160789.24 | transcript | ENST00000677389.1 | protein_coding | 1/9 | chr1 | 156117962 | |||||||
chr1:156117969 | AT | A | 114 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(111): Show |
164 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(161): Show |
intron_variant | MODIFIER | c.356+2720delT | LMNA | ENSG00000160789.24 | transcript | ENST00000677389.1 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 156117969 | ||||||
chr1:156117969 | ATT | A | 24 | a0001c0001t0001g0052 a0001c0001t0001g0054 a0001c0001t0001g0095 others(21): Show |
35 | HG00642.hp1 HG01167.hp2 HG01169.hp2 others(32): Show |
intron_variant | MODIFIER | c.356+2719_356+2720d others(4): Show |
LMNA | ENSG00000160789.24 | transcript | ENST00000677389.1 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 156117969 | ||||||
chr1:156118285 | G | A | 2 | a0001c0002t0001g0096 a0001c0002t0001g0097 |
2 | HG00280.hp2 HG01884.hp2 |
intron_variant | MODIFIER | c.356+3011G>A | LMNA | ENSG00000160789.24 | transcript | ENST00000677389.1 | protein_coding | 1/9 | chr1 | 156118285 | |||||||
chr1:156118389 | C | G | 1 | a0001c0001t0001g0077 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.356+3115C>G | LMNA | ENSG00000160789.24 | transcript | ENST00000677389.1 | protein_coding | 1/9 | chr1 | 156118389 | |||||||
chr1:156118465 | C | G | 26 | a0001c0001t0002g0188 a0001c0003t0001g0004 a0001c0003t0001g0011 others(23): Show |
41 | HG01167.hp2 HG01169.hp2 HG01257.hp2 others(38): Show |
intron_variant | MODIFIER | c.356+3191C>G | LMNA | ENSG00000160789.24 | transcript | ENST00000677389.1 | protein_coding | 1/9 | chr1 | 156118465 | |||||||
chr1:156118524 | G | A | 1 | a0001c0004t0001g0162 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.356+3250G>A | LMNA | ENSG00000160789.24 | transcript | ENST00000677389.1 | protein_coding | 1/9 | chr1 | 156118524 | |||||||
chr1:156118592 | G | A | 5 | a0001c0001t0001g0007 a0001c0001t0001g0041 a0001c0001t0001g0042 others(2): Show |
8 | HG00544.hp1 HG02132.hp1 NA18969.hp2 others(5): Show |
intron_variant | MODIFIER | c.356+3318G>A | LMNA | ENSG00000160789.24 | transcript | ENST00000677389.1 | protein_coding | 1/9 | chr1 | 156118592 | |||||||
chr1:156118686 | A | G | 2 | a0001c0004t0001g0035 a0001c0004t0001g0180 |
3 | HG02896.hp2 HG02897.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.356+3412A>G | LMNA | ENSG00000160789.24 | transcript | ENST00000677389.1 | protein_coding | 1/9 | chr1 | 156118686 | |||||||
chr1:156118735 | C | T | 27 | a0001c0001t0002g0188 a0001c0003t0001g0004 a0001c0003t0001g0011 others(24): Show |
44 | HG01167.hp2 HG01169.hp2 HG01257.hp2 others(41): Show |
intron_variant | MODIFIER | c.356+3461C>T | LMNA | ENSG00000160789.24 | transcript | ENST00000677389.1 | protein_coding | 1/9 | chr1 | 156118735 | |||||||
chr1:156119243 | G | A | 6 | a0001c0002t0001g0009 a0001c0002t0001g0021 a0001c0002t0001g0037 others(3): Show |
9 | HG00408.hp1 HG02015.hp1 HG02056.hp2 others(6): Show |
intron_variant | MODIFIER | c.356+3969G>A | LMNA | ENSG00000160789.24 | transcript | ENST00000677389.1 | protein_coding | 1/9 | chr1 | 156119243 | |||||||
chr1:156119359 | G | A | 5 | a0001c0003t0001g0031 a0001c0003t0001g0158 a0001c0004t0001g0010 others(2): Show |
9 | HG02257.hp1 HG02572.hp1 HG02723.hp2 others(6): Show |
intron_variant | MODIFIER | c.356+4085G>A | LMNA | ENSG00000160789.24 | transcript | ENST00000677389.1 | protein_coding | 1/9 | chr1 | 156119359 | |||||||
chr1:156119533 | G | T | 28 | a0001c0001t0002g0188 a0001c0003t0001g0004 a0001c0003t0001g0011 others(25): Show |
46 | HG01167.hp2 HG01169.hp2 HG01257.hp2 others(43): Show |
intron_variant | MODIFIER | c.356+4259G>T | LMNA | ENSG00000160789.24 | transcript | ENST00000677389.1 | protein_coding | 1/9 | chr1 | 156119533 | |||||||
chr1:156119548 | A | G | 1 | a0001c0003t0001g0187 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.356+4274A>G | LMNA | ENSG00000160789.24 | transcript | ENST00000677389.1 | protein_coding | 1/9 | chr1 | 156119548 | |||||||
chr1:156119733 | C | A | 1 | a0001c0003t0001g0163 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.356+4459C>A | LMNA | ENSG00000160789.24 | transcript | ENST00000677389.1 | protein_coding | 1/9 | chr1 | 156119733 | |||||||
chr1:156119782 | G | A | 1 | a0001c0003t0001g0099 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.356+4508G>A | LMNA | ENSG00000160789.24 | transcript | ENST00000677389.1 | protein_coding | 1/9 | chr1 | 156119782 | |||||||
chr1:156119818 | T | C | 29 | a0001c0001t0002g0188 a0001c0003t0001g0004 a0001c0003t0001g0011 others(26): Show |
47 | HG01167.hp2 HG01169.hp2 HG01257.hp2 others(44): Show |
intron_variant | MODIFIER | c.356+4544T>C | LMNA | ENSG00000160789.24 | transcript | ENST00000677389.1 | protein_coding | 1/9 | chr1 | 156119818 | |||||||
chr1:156119840 | C | G | 21 | a0001c0001t0002g0188 a0001c0003t0001g0004 a0001c0003t0001g0011 others(18): Show |
35 | HG01167.hp2 HG01169.hp2 HG01257.hp2 others(32): Show |
intron_variant | MODIFIER | c.356+4566C>G | LMNA | ENSG00000160789.24 | transcript | ENST00000677389.1 | protein_coding | 1/9 | chr1 | 156119840 | |||||||
chr1:156119843 | T | A | 12 | a0001c0001t0001g0059 a0001c0002t0001g0057 a0001c0002t0001g0058 others(9): Show |
12 | HG02129.hp1 NA18941.hp2 NA18945.hp2 others(9): Show |
intron_variant | MODIFIER | c.356+4569T>A | LMNA | ENSG00000160789.24 | transcript | ENST00000677389.1 | protein_coding | 1/9 | chr1 | 156119843 | |||||||
chr1:156120082 | C | T | 28 | a0001c0001t0002g0188 a0001c0003t0001g0004 a0001c0003t0001g0011 others(25): Show |
46 | HG01167.hp2 HG01169.hp2 HG01257.hp2 others(43): Show |
intron_variant | MODIFIER | c.356+4808C>T | LMNA | ENSG00000160789.24 | transcript | ENST00000677389.1 | protein_coding | 1/9 | chr1 | 156120082 | |||||||
chr1:156120129 | C | T | 21 | a0001c0001t0002g0188 a0001c0003t0001g0004 a0001c0003t0001g0011 others(18): Show |
35 | HG01167.hp2 HG01169.hp2 HG01257.hp2 others(32): Show |
intron_variant | MODIFIER | c.356+4855C>T | LMNA | ENSG00000160789.24 | transcript | ENST00000677389.1 | protein_coding | 1/9 | chr1 | 156120129 | |||||||
chr1:156120152 | C | T | 2 | a0001c0003t0001g0120 a0001c0003t0001g0125 |
2 | HG02055.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.356+4878C>T | LMNA | ENSG00000160789.24 | transcript | ENST00000677389.1 | protein_coding | 1/9 | chr1 | 156120152 | |||||||
chr1:156120359 | G | T | 1 | a0001c0001t0001g0094 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.356+5085G>T | LMNA | ENSG00000160789.24 | transcript | ENST00000677389.1 | protein_coding | 1/9 | chr1 | 156120359 | |||||||
chr1:156120457 | C | T | 1 | a0001c0003t0001g0187 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.356+5183C>T | LMNA | ENSG00000160789.24 | transcript | ENST00000677389.1 | protein_coding | 1/9 | chr1 | 156120457 | |||||||
chr1:156120504 | G | A | 2 | a0001c0003t0001g0047 a0001c0004t0001g0175 |
2 | HG02257.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.356+5230G>A | LMNA | ENSG00000160789.24 | transcript | ENST00000677389.1 | protein_coding | 1/9 | chr1 | 156120504 | |||||||
chr1:156120554 | C | T | 5 | a0001c0001t0001g0076 a0001c0001t0001g0087 a0001c0001t0001g0088 others(2): Show |
5 | HG02145.hp1 HG02976.hp1 HG03516.hp1 others(2): Show |
intron_variant | MODIFIER | c.356+5280C>T | LMNA | ENSG00000160789.24 | transcript | ENST00000677389.1 | protein_coding | 1/9 | chr1 | 156120554 | |||||||
chr1:156120652 | A | G | 2 | a0001c0001t0001g0086 a0001c0001t0001g0148 |
2 | HG01516.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.356+5378A>G | LMNA | ENSG00000160789.24 | transcript | ENST00000677389.1 | protein_coding | 1/9 | chr1 | 156120652 | |||||||
chr1:156120721 | AAAAAC | A | 5 | a0001c0003t0001g0031 a0001c0003t0001g0158 a0001c0004t0001g0010 others(2): Show |
9 | HG02257.hp1 HG02572.hp1 HG02723.hp2 others(6): Show |
intron_variant | MODIFIER | c.356+5458_356+5462d others(7): Show |
LMNA | ENSG00000160789.24 | transcript | ENST00000677389.1 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 156120721 | ||||||
chr1:156121046 | C | CT | 27 | a0001c0001t0001g0012 a0001c0001t0001g0017 a0001c0001t0001g0040 others(24): Show |
34 | HG01167.hp1 HG01346.hp2 HG01361.hp2 others(31): Show |
intron_variant | MODIFIER | c.356+5797dupT | LMNA | ENSG00000160789.24 | transcript | ENST00000677389.1 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 156121046 | ||||||
chr1:156121046 | CT | C | 10 | a0001c0001t0001g0043 a0001c0001t0001g0061 a0001c0001t0001g0062 others(7): Show |
11 | HG00438.hp2 HG01169.hp1 HG02109.hp2 others(8): Show |
intron_variant | MODIFIER | c.356+5797delT | LMNA | ENSG00000160789.24 | transcript | ENST00000677389.1 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 156121046 | ||||||
chr1:156121046 | CTT | C | 19 | a0001c0001t0001g0091 a0001c0001t0001g0166 a0001c0002t0001g0026 others(16): Show |
28 | HG01884.hp1 HG02132.hp2 HG02155.hp1 others(25): Show |
intron_variant | MODIFIER | c.356+5796_356+5797d others(4): Show |
LMNA | ENSG00000160789.24 | transcript | ENST00000677389.1 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 156121046 | ||||||
chr1:156121046 | CTTTTTTT others(5): Show |
C | 1 | a0001c0003t0001g0187 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.356+5786_356+5797d others(14): Show |
LMNA | ENSG00000160789.24 | transcript | ENST00000677389.1 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 156121046 | ||||||
chr1:156121130 | A | G | 1 | a0001c0001t0001g0077 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.356+5856A>G | LMNA | ENSG00000160789.24 | transcript | ENST00000677389.1 | protein_coding | 1/9 | chr1 | 156121130 | |||||||
chr1:156121209 | C | T | 2 | a0001c0003t0001g0187 a0001c0005t0001g0170 |
2 | HG02630.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.356+5935C>T | LMNA | ENSG00000160789.24 | transcript | ENST00000677389.1 | protein_coding | 1/9 | chr1 | 156121209 | |||||||
chr1:156121263 | G | T | 1 | a0001c0001t0001g0093 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.356+5989G>T | LMNA | ENSG00000160789.24 | transcript | ENST00000677389.1 | protein_coding | 1/9 | chr1 | 156121263 | |||||||
chr1:156121324 | A | T | 2 | a0001c0001t0001g0054 a0001c0001t0001g0074 |
2 | NA18946.hp2 NA18983.hp2 |
intron_variant | MODIFIER | c.356+6050A>T | LMNA | ENSG00000160789.24 | transcript | ENST00000677389.1 | protein_coding | 1/9 | chr1 | 156121324 | |||||||
chr1:156121642 | C | A | 4 | a0001c0001t0001g0166 a0001c0003t0001g0030 a0001c0003t0001g0164 others(1): Show |
5 | HG02698.hp2 HG03490.hp1 HG03942.hp2 others(2): Show |
intron_variant | MODIFIER | c.356+6368C>A | LMNA | ENSG00000160789.24 | transcript | ENST00000677389.1 | protein_coding | 1/9 | chr1 | 156121642 | |||||||
chr1:156121798 | T | C | 1 | a0001c0001t0001g0063 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.356+6524T>C | LMNA | ENSG00000160789.24 | transcript | ENST00000677389.1 | protein_coding | 1/9 | chr1 | 156121798 | |||||||
chr1:156121833 | A | G | 5 | a0001c0003t0001g0169 a0001c0004t0001g0035 a0001c0004t0001g0085 others(2): Show |
6 | HG02257.hp2 HG02559.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.356+6559A>G | LMNA | ENSG00000160789.24 | transcript | ENST00000677389.1 | protein_coding | 1/9 | chr1 | 156121833 | |||||||
chr1:156121892 | C | T | 1 | a0001c0001t0001g0073 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.356+6618C>T | LMNA | ENSG00000160789.24 | transcript | ENST00000677389.1 | protein_coding | 1/9 | chr1 | 156121892 | |||||||
chr1:156122099 | C | T | 2 | a0001c0003t0001g0187 a0001c0005t0001g0170 |
2 | HG02630.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.356+6825C>T | LMNA | ENSG00000160789.24 | transcript | ENST00000677389.1 | protein_coding | 1/9 | chr1 | 156122099 | |||||||
chr1:156122146 | G | A | 5 | a0001c0003t0001g0036 a0001c0003t0001g0147 a0001c0003t0001g0157 others(2): Show |
6 | HG01433.hp2 HG02486.hp1 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.356+6872G>A | LMNA | ENSG00000160789.24 | transcript | ENST00000677389.1 | protein_coding | 1/9 | chr1 | 156122146 | |||||||
chr1:156122357 | C | T | 1 | a0001c0005t0001g0170 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.356+7083C>T | LMNA | ENSG00000160789.24 | transcript | ENST00000677389.1 | protein_coding | 1/9 | chr1 | 156122357 | |||||||
chr1:156122492 | C | A | 7 | a0001c0002t0001g0003 a0001c0002t0001g0051 a0001c0002t0001g0064 others(4): Show |
15 | HG00642.hp2 HG00741.hp2 HG01074.hp1 others(12): Show |
intron_variant | MODIFIER | c.356+7218C>A | LMNA | ENSG00000160789.24 | transcript | ENST00000677389.1 | protein_coding | 1/9 | chr1 | 156122492 | |||||||
chr1:156122615 | C | G | 1 | a0001c0001t0001g0054 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.356+7341C>G | LMNA | ENSG00000160789.24 | transcript | ENST00000677389.1 | protein_coding | 1/9 | chr1 | 156122615 | |||||||
chr1:156122664 | G | A | 1 | a0001c0002t0001g0022 | 2 | HG03490.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.356+7390G>A | LMNA | ENSG00000160789.24 | transcript | ENST00000677389.1 | protein_coding | 1/9 | chr1 | 156122664 | |||||||
chr1:156122848 | C | T | 33 | a0001c0003t0001g0004 a0001c0003t0001g0011 a0001c0003t0001g0029 others(30): Show |
52 | HG01167.hp2 HG01169.hp2 HG01257.hp2 others(49): Show |
intron_variant | MODIFIER | c.356+7574C>T | LMNA | ENSG00000160789.24 | transcript | ENST00000677389.1 | protein_coding | 1/9 | chr1 | 156122848 | |||||||
chr1:156123015 | G | A | 2 | a0001c0001t0001g0079 a0001c0001t0001g0107 |
2 | HG01074.hp2 HG02602.hp2 |
intron_variant | MODIFIER | c.357-7602G>A | LMNA | ENSG00000160789.24 | transcript | ENST00000677389.1 | protein_coding | 1/9 | chr1 | 156123015 | |||||||
chr1:156123040 | G | A | 20 | a0001c0003t0001g0004 a0001c0003t0001g0011 a0001c0003t0001g0029 others(17): Show |
37 | HG01167.hp2 HG01169.hp2 HG01257.hp2 others(34): Show |
intron_variant | MODIFIER | c.357-7577G>A | LMNA | ENSG00000160789.24 | transcript | ENST00000677389.1 | protein_coding | 1/9 | chr1 | 156123040 | |||||||
chr1:156123139 | CAAG | C | 21 | a0001c0003t0001g0004 a0001c0003t0001g0011 a0001c0003t0001g0029 others(18): Show |
38 | HG01167.hp2 HG01169.hp2 HG01257.hp2 others(35): Show |
intron_variant | MODIFIER | c.357-7474_357-7472d others(5): Show |
LMNA | ENSG00000160789.24 | transcript | ENST00000677389.1 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 156123139 | ||||||
chr1:156123200 | T | C | 30 | a0001c0001t0001g0166 a0001c0003t0001g0005 a0001c0003t0001g0028 others(27): Show |
40 | HG01884.hp1 HG02132.hp2 HG02155.hp1 others(37): Show |
intron_variant | MODIFIER | c.357-7417T>C | LMNA | ENSG00000160789.24 | transcript | ENST00000677389.1 | protein_coding | 1/9 | chr1 | 156123200 | |||||||
chr1:156123322 | C | T | 1 | a0001c0002t0001g0053 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.357-7295C>T | LMNA | ENSG00000160789.24 | transcript | ENST00000677389.1 | protein_coding | 1/9 | chr1 | 156123322 | |||||||
chr1:156123404 | T | C | 33 | a0001c0003t0001g0004 a0001c0003t0001g0011 a0001c0003t0001g0029 others(30): Show |
52 | HG01167.hp2 HG01169.hp2 HG01257.hp2 others(49): Show |
intron_variant | MODIFIER | c.357-7213T>C | LMNA | ENSG00000160789.24 | transcript | ENST00000677389.1 | protein_coding | 1/9 | chr1 | 156123404 | |||||||
chr1:156123437 | C | G | 1 | a0001c0001t0001g0083 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.357-7180C>G | LMNA | ENSG00000160789.24 | transcript | ENST00000677389.1 | protein_coding | 1/9 | chr1 | 156123437 | |||||||
chr1:156123463 | A | C | 1 | a0001c0001t0001g0116 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.357-7154A>C | LMNA | ENSG00000160789.24 | transcript | ENST00000677389.1 | protein_coding | 1/9 | chr1 | 156123463 | |||||||
chr1:156123615 | C | T | 20 | a0001c0003t0001g0004 a0001c0003t0001g0011 a0001c0003t0001g0029 others(17): Show |
37 | HG01167.hp2 HG01169.hp2 HG01257.hp2 others(34): Show |
intron_variant | MODIFIER | c.357-7002C>T | LMNA | ENSG00000160789.24 | transcript | ENST00000677389.1 | protein_coding | 1/9 | chr1 | 156123615 | |||||||
chr1:156123629 | T | C | 2 | a0001c0003t0001g0187 a0001c0005t0001g0170 |
2 | HG02630.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.357-6988T>C | LMNA | ENSG00000160789.24 | transcript | ENST00000677389.1 | protein_coding | 1/9 | chr1 | 156123629 | |||||||
chr1:156123798 | C | T | 1 | a0001c0005t0001g0170 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.357-6819C>T | LMNA | ENSG00000160789.24 | transcript | ENST00000677389.1 | protein_coding | 1/9 | chr1 | 156123798 | |||||||
chr1:156123842 | G | A | 1 | a0001c0002t0001g0096 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.357-6775G>A | LMNA | ENSG00000160789.24 | transcript | ENST00000677389.1 | protein_coding | 1/9 | chr1 | 156123842 | |||||||
chr1:156123937 | T | C | 2 | a0001c0003t0001g0134 a0001c0003t0001g0184 |
2 | HG01261.hp1 HG02602.hp1 |
intron_variant | MODIFIER | c.357-6680T>C | LMNA | ENSG00000160789.24 | transcript | ENST00000677389.1 | protein_coding | 1/9 | chr1 | 156123937 | |||||||
chr1:156124146 | C | T | 1 | a0001c0003t0001g0169 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.357-6471C>T | LMNA | ENSG00000160789.24 | transcript | ENST00000677389.1 | protein_coding | 1/9 | chr1 | 156124146 | |||||||
chr1:156124266 | G | C | 21 | a0001c0003t0001g0004 a0001c0003t0001g0011 a0001c0003t0001g0029 others(18): Show |
38 | HG01167.hp2 HG01169.hp2 HG01257.hp2 others(35): Show |
intron_variant | MODIFIER | c.357-6351G>C | LMNA | ENSG00000160789.24 | transcript | ENST00000677389.1 | protein_coding | 1/9 | chr1 | 156124266 | |||||||
chr1:156124282 | C | CCT | 9 | a0001c0004t0001g0035 a0001c0004t0001g0085 a0001c0004t0001g0162 others(6): Show |
11 | HG01884.hp1 HG02559.hp1 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.357-6320_357-6319d others(4): Show |
LMNA | ENSG00000160789.24 | transcript | ENST00000677389.1 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 156124282 | ||||||
chr1:156124297 | C | T | 21 | a0001c0003t0001g0004 a0001c0003t0001g0011 a0001c0003t0001g0029 others(18): Show |
38 | HG01167.hp2 HG01169.hp2 HG01257.hp2 others(35): Show |
intron_variant | MODIFIER | c.357-6320C>T | LMNA | ENSG00000160789.24 | transcript | ENST00000677389.1 | protein_coding | 1/9 | chr1 | 156124297 | |||||||
chr1:156124408 | C | T | 21 | a0001c0003t0001g0004 a0001c0003t0001g0011 a0001c0003t0001g0029 others(18): Show |
38 | HG01167.hp2 HG01169.hp2 HG01257.hp2 others(35): Show |
intron_variant | MODIFIER | c.357-6209C>T | LMNA | ENSG00000160789.24 | transcript | ENST00000677389.1 | protein_coding | 1/9 | chr1 | 156124408 | |||||||
chr1:156124512 | C | T | 4 | a0001c0003t0001g0031 a0001c0004t0001g0010 a0001c0004t0001g0032 others(1): Show |
8 | HG02257.hp1 HG02572.hp1 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.357-6105C>T | LMNA | ENSG00000160789.24 | transcript | ENST00000677389.1 | protein_coding | 1/9 | chr1 | 156124512 | |||||||
chr1:156124576 | T | C | 21 | a0001c0003t0001g0004 a0001c0003t0001g0011 a0001c0003t0001g0029 others(18): Show |
38 | HG01167.hp2 HG01169.hp2 HG01257.hp2 others(35): Show |
intron_variant | MODIFIER | c.357-6041T>C | LMNA | ENSG00000160789.24 | transcript | ENST00000677389.1 | protein_coding | 1/9 | chr1 | 156124576 | |||||||
chr1:156124652 | T | G | 21 | a0001c0003t0001g0004 a0001c0003t0001g0011 a0001c0003t0001g0029 others(18): Show |
38 | HG01167.hp2 HG01169.hp2 HG01257.hp2 others(35): Show |
intron_variant | MODIFIER | c.357-5965T>G | LMNA | ENSG00000160789.24 | transcript | ENST00000677389.1 | protein_coding | 1/9 | chr1 | 156124652 | |||||||
chr1:156124674 | C | T | 1 | a0001c0004t0001g0162 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.357-5943C>T | LMNA | ENSG00000160789.24 | transcript | ENST00000677389.1 | protein_coding | 1/9 | chr1 | 156124674 | |||||||
chr1:156124675 | G | A | 1 | a0001c0003t0001g0169 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.357-5942G>A | LMNA | ENSG00000160789.24 | transcript | ENST00000677389.1 | protein_coding | 1/9 | chr1 | 156124675 | |||||||
chr1:156124735 | G | C | 3 | a0001c0003t0001g0187 a0001c0004t0002g0176 a0001c0005t0001g0170 |
3 | HG02630.hp1 HG02647.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.357-5882G>C | LMNA | ENSG00000160789.24 | transcript | ENST00000677389.1 | protein_coding | 1/9 | chr1 | 156124735 | |||||||
chr1:156124745 | A | G | 21 | a0001c0003t0001g0004 a0001c0003t0001g0011 a0001c0003t0001g0029 others(18): Show |
38 | HG01167.hp2 HG01169.hp2 HG01257.hp2 others(35): Show |
intron_variant | MODIFIER | c.357-5872A>G | LMNA | ENSG00000160789.24 | transcript | ENST00000677389.1 | protein_coding | 1/9 | chr1 | 156124745 | |||||||
chr1:156124787 | A | G | 51 | a0001c0001t0001g0166 a0001c0003t0001g0004 a0001c0003t0001g0005 others(48): Show |
78 | HG01167.hp2 HG01169.hp2 HG01257.hp2 others(75): Show |
intron_variant | MODIFIER | c.357-5830A>G | LMNA | ENSG00000160789.24 | transcript | ENST00000677389.1 | protein_coding | 1/9 | chr1 | 156124787 | |||||||
chr1:156124820 | C | T | 1 | a0001c0001t0002g0188 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.357-5797C>T | LMNA | ENSG00000160789.24 | transcript | ENST00000677389.1 | protein_coding | 1/9 | chr1 | 156124820 | |||||||
chr1:156124890 | G | A | 21 | a0001c0003t0001g0004 a0001c0003t0001g0011 a0001c0003t0001g0029 others(18): Show |
38 | HG01167.hp2 HG01169.hp2 HG01257.hp2 others(35): Show |
intron_variant | MODIFIER | c.357-5727G>A | LMNA | ENSG00000160789.24 | transcript | ENST00000677389.1 | protein_coding | 1/9 | chr1 | 156124890 | |||||||
chr1:156124949 | C | G | 1 | a0001c0001t0001g0086 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.357-5668C>G | LMNA | ENSG00000160789.24 | transcript | ENST00000677389.1 | protein_coding | 1/9 | chr1 | 156124949 | |||||||
chr1:156124982 | G | C | 1 | a0001c0003t0001g0158 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.357-5635G>C | LMNA | ENSG00000160789.24 | transcript | ENST00000677389.1 | protein_coding | 1/9 | chr1 | 156124982 | |||||||
chr1:156124990 | C | G | 1 | a0001c0001t0001g0141 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.357-5627C>G | LMNA | ENSG00000160789.24 | transcript | ENST00000677389.1 | protein_coding | 1/9 | chr1 | 156124990 | |||||||
chr1:156125081 | A | G | 21 | a0001c0003t0001g0004 a0001c0003t0001g0011 a0001c0003t0001g0029 others(18): Show |
38 | HG01167.hp2 HG01169.hp2 HG01257.hp2 others(35): Show |
intron_variant | MODIFIER | c.357-5536A>G | LMNA | ENSG00000160789.24 | transcript | ENST00000677389.1 | protein_coding | 1/9 | chr1 | 156125081 | |||||||
chr1:156125158 | C | T | 1 | a0001c0002t0001g0106 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.357-5459C>T | LMNA | ENSG00000160789.24 | transcript | ENST00000677389.1 | protein_coding | 1/9 | chr1 | 156125158 | |||||||
chr1:156125403 | AG | A | 21 | a0001c0003t0001g0004 a0001c0003t0001g0011 a0001c0003t0001g0029 others(18): Show |
38 | HG01167.hp2 HG01169.hp2 HG01257.hp2 others(35): Show |
intron_variant | MODIFIER | c.357-5210delG | LMNA | ENSG00000160789.24 | transcript | ENST00000677389.1 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 156125403 | ||||||
chr1:156125470 | G | C | 1 | a0001c0003t0001g0187 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.357-5147G>C | LMNA | ENSG00000160789.24 | transcript | ENST00000677389.1 | protein_coding | 1/9 | chr1 | 156125470 | |||||||
chr1:156125543 | G | T | 1 | a0001c0005t0001g0170 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.357-5074G>T | LMNA | ENSG00000160789.24 | transcript | ENST00000677389.1 | protein_coding | 1/9 | chr1 | 156125543 | |||||||
chr1:156125568 | A | C | 6 | a0001c0002t0001g0009 a0001c0002t0001g0021 a0001c0002t0001g0037 others(3): Show |
9 | HG00408.hp1 HG02015.hp1 HG02056.hp2 others(6): Show |
intron_variant | MODIFIER | c.357-5049A>C | LMNA | ENSG00000160789.24 | transcript | ENST00000677389.1 | protein_coding | 1/9 | chr1 | 156125568 | |||||||
chr1:156125573 | C | T | 7 | a0001c0002t0001g0003 a0001c0002t0001g0051 a0001c0002t0001g0064 others(4): Show |
15 | HG00642.hp2 HG00741.hp2 HG01074.hp1 others(12): Show |
intron_variant | MODIFIER | c.357-5044C>T | LMNA | ENSG00000160789.24 | transcript | ENST00000677389.1 | protein_coding | 1/9 | chr1 | 156125573 | |||||||
chr1:156125622 | G | A | 21 | a0001c0003t0001g0004 a0001c0003t0001g0011 a0001c0003t0001g0029 others(18): Show |
38 | HG01167.hp2 HG01169.hp2 HG01257.hp2 others(35): Show |
intron_variant | MODIFIER | c.357-4995G>A | LMNA | ENSG00000160789.24 | transcript | ENST00000677389.1 | protein_coding | 1/9 | chr1 | 156125622 | |||||||
chr1:156125645 | C | T | 3 | a0001c0004t0001g0010 a0001c0004t0001g0032 a0001c0004t0001g0174 |
6 | HG02257.hp1 HG02572.hp1 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.357-4972C>T | LMNA | ENSG00000160789.24 | transcript | ENST00000677389.1 | protein_coding | 1/9 | chr1 | 156125645 | |||||||
chr1:156125646 | G | A | 1 | a0001c0001t0001g0086 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.357-4971G>A | LMNA | ENSG00000160789.24 | transcript | ENST00000677389.1 | protein_coding | 1/9 | chr1 | 156125646 | |||||||
chr1:156125652 | C | G | 33 | a0001c0003t0001g0004 a0001c0003t0001g0011 a0001c0003t0001g0029 others(30): Show |
52 | HG01167.hp2 HG01169.hp2 HG01257.hp2 others(49): Show |
intron_variant | MODIFIER | c.357-4965C>G | LMNA | ENSG00000160789.24 | transcript | ENST00000677389.1 | protein_coding | 1/9 | chr1 | 156125652 | |||||||
chr1:156125675 | T | C | 50 | a0001c0003t0001g0004 a0001c0003t0001g0005 a0001c0003t0001g0011 others(47): Show |
77 | HG01167.hp2 HG01169.hp2 HG01257.hp2 others(74): Show |
intron_variant | MODIFIER | c.357-4942T>C | LMNA | ENSG00000160789.24 | transcript | ENST00000677389.1 | protein_coding | 1/9 | chr1 | 156125675 | |||||||
chr1:156125857 | T | C | 21 | a0001c0003t0001g0004 a0001c0003t0001g0011 a0001c0003t0001g0029 others(18): Show |
38 | HG01167.hp2 HG01169.hp2 HG01257.hp2 others(35): Show |
intron_variant | MODIFIER | c.357-4760T>C | LMNA | ENSG00000160789.24 | transcript | ENST00000677389.1 | protein_coding | 1/9 | chr1 | 156125857 | |||||||
chr1:156125904 | C | T | 1 | a0001c0001t0001g0045 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.357-4713C>T | LMNA | ENSG00000160789.24 | transcript | ENST00000677389.1 | protein_coding | 1/9 | chr1 | 156125904 | |||||||
chr1:156125921 | T | C | 50 | a0001c0003t0001g0004 a0001c0003t0001g0005 a0001c0003t0001g0011 others(47): Show |
77 | HG01167.hp2 HG01169.hp2 HG01257.hp2 others(74): Show |
intron_variant | MODIFIER | c.357-4696T>C | LMNA | ENSG00000160789.24 | transcript | ENST00000677389.1 | protein_coding | 1/9 | chr1 | 156125921 | |||||||
chr1:156125965 | C | T | 21 | a0001c0003t0001g0004 a0001c0003t0001g0011 a0001c0003t0001g0029 others(18): Show |
38 | HG01167.hp2 HG01169.hp2 HG01257.hp2 others(35): Show |
intron_variant | MODIFIER | c.357-4652C>T | LMNA | ENSG00000160789.24 | transcript | ENST00000677389.1 | protein_coding | 1/9 | chr1 | 156125965 | |||||||
chr1:156125970 | AAAT | A | 10 | a0001c0004t0001g0035 a0001c0004t0001g0085 a0001c0004t0001g0162 others(7): Show |
12 | HG01884.hp1 HG02257.hp2 HG02559.hp1 others(9): Show |
intron_variant | MODIFIER | c.357-4636_357-4634d others(5): Show |
LMNA | ENSG00000160789.24 | transcript | ENST00000677389.1 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 156125970 | ||||||
chr1:156126018 | C | A | 21 | a0001c0003t0001g0004 a0001c0003t0001g0011 a0001c0003t0001g0029 others(18): Show |
38 | HG01167.hp2 HG01169.hp2 HG01257.hp2 others(35): Show |
intron_variant | MODIFIER | c.357-4599C>A | LMNA | ENSG00000160789.24 | transcript | ENST00000677389.1 | protein_coding | 1/9 | chr1 | 156126018 | |||||||
chr1:156126057 | C | T | 21 | a0001c0003t0001g0004 a0001c0003t0001g0011 a0001c0003t0001g0029 others(18): Show |
38 | HG01167.hp2 HG01169.hp2 HG01257.hp2 others(35): Show |
intron_variant | MODIFIER | c.357-4560C>T | LMNA | ENSG00000160789.24 | transcript | ENST00000677389.1 | protein_coding | 1/9 | chr1 | 156126057 | |||||||
chr1:156126091 | C | T | 1 | a0001c0002t0001g0115 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.357-4526C>T | LMNA | ENSG00000160789.24 | transcript | ENST00000677389.1 | protein_coding | 1/9 | chr1 | 156126091 | |||||||
chr1:156126340 | T | C | 1 | a0001c0001t0001g0087 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.357-4277T>C | LMNA | ENSG00000160789.24 | transcript | ENST00000677389.1 | protein_coding | 1/9 | chr1 | 156126340 | |||||||
chr1:156126371 | CGG | C | 2 | a0001c0003t0001g0029 a0001c0003t0001g0161 |
3 | HG02109.hp2 HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.357-4245_357-4244d others(4): Show |
LMNA | ENSG00000160789.24 | transcript | ENST00000677389.1 | protein_coding | 1/9 | chr1 | 156126371 | |||||||
chr1:156126388 | G | A | 1 | a0001c0001t0001g0126 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.357-4229G>A | LMNA | ENSG00000160789.24 | transcript | ENST00000677389.1 | protein_coding | 1/9 | chr1 | 156126388 | |||||||
chr1:156126414 | C | T | 1 | a0001c0001t0001g0044 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.357-4203C>T | LMNA | ENSG00000160789.24 | transcript | ENST00000677389.1 | protein_coding | 1/9 | chr1 | 156126414 | |||||||
chr1:156126585 | G | A | 14 | a0001c0003t0001g0005 a0001c0003t0001g0028 a0001c0003t0001g0030 others(11): Show |
22 | HG02132.hp2 HG02155.hp1 HG02258.hp1 others(19): Show |
intron_variant | MODIFIER | c.357-4032G>A | LMNA | ENSG00000160789.24 | transcript | ENST00000677389.1 | protein_coding | 1/9 | chr1 | 156126585 | |||||||
chr1:156126596 | G | A | 20 | a0001c0003t0001g0004 a0001c0003t0001g0011 a0001c0003t0001g0029 others(17): Show |
37 | HG01167.hp2 HG01169.hp2 HG01257.hp2 others(34): Show |
intron_variant | MODIFIER | c.357-4021G>A | LMNA | ENSG00000160789.24 | transcript | ENST00000677389.1 | protein_coding | 1/9 | chr1 | 156126596 | |||||||
chr1:156126626 | T | G | 50 | a0001c0003t0001g0004 a0001c0003t0001g0005 a0001c0003t0001g0011 others(47): Show |
77 | HG01167.hp2 HG01169.hp2 HG01257.hp2 others(74): Show |
intron_variant | MODIFIER | c.357-3991T>G | LMNA | ENSG00000160789.24 | transcript | ENST00000677389.1 | protein_coding | 1/9 | chr1 | 156126626 | |||||||
chr1:156127023 | ACCCTGTC others(2): Show |
A | 15 | a0001c0003t0001g0004 a0001c0003t0001g0011 a0001c0003t0001g0029 others(12): Show |
28 | HG01167.hp2 HG01169.hp2 HG01257.hp2 others(25): Show |
intron_variant | MODIFIER | c.357-3588_357-3580d others(11): Show |
LMNA | ENSG00000160789.24 | transcript | ENST00000677389.1 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 156127023 | ||||||
chr1:156127082 | T | C | 21 | a0001c0003t0001g0004 a0001c0003t0001g0011 a0001c0003t0001g0029 others(18): Show |
38 | HG01167.hp2 HG01169.hp2 HG01257.hp2 others(35): Show |
intron_variant | MODIFIER | c.357-3535T>C | LMNA | ENSG00000160789.24 | transcript | ENST00000677389.1 | protein_coding | 1/9 | chr1 | 156127082 | |||||||
chr1:156127101 | A | G | 1 | a0001c0003t0001g0185 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.357-3516A>G | LMNA | ENSG00000160789.24 | transcript | ENST00000677389.1 | protein_coding | 1/9 | chr1 | 156127101 | |||||||
chr1:156127128 | G | A | 15 | a0001c0003t0001g0004 a0001c0003t0001g0011 a0001c0003t0001g0029 others(12): Show |
28 | HG01167.hp2 HG01169.hp2 HG01257.hp2 others(25): Show |
intron_variant | MODIFIER | c.357-3489G>A | LMNA | ENSG00000160789.24 | transcript | ENST00000677389.1 | protein_coding | 1/9 | chr1 | 156127128 | |||||||
chr1:156127186 | G | A | 4 | a0001c0003t0001g0031 a0001c0004t0001g0010 a0001c0004t0001g0032 others(1): Show |
8 | HG02257.hp1 HG02572.hp1 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.357-3431G>A | LMNA | ENSG00000160789.24 | transcript | ENST00000677389.1 | protein_coding | 1/9 | chr1 | 156127186 | |||||||
chr1:156127268 | G | A | 1 | a0001c0001t0001g0127 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.357-3349G>A | LMNA | ENSG00000160789.24 | transcript | ENST00000677389.1 | protein_coding | 1/9 | chr1 | 156127268 | |||||||
chr1:156127343 | G | A | 1 | a0001c0004t0001g0162 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.357-3274G>A | LMNA | ENSG00000160789.24 | transcript | ENST00000677389.1 | protein_coding | 1/9 | chr1 | 156127343 | |||||||
chr1:156127431 | T | A | 1 | a0001c0003t0001g0158 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.357-3186T>A | LMNA | ENSG00000160789.24 | transcript | ENST00000677389.1 | protein_coding | 1/9 | chr1 | 156127431 | |||||||
chr1:156127462 | G | A | 2 | a0001c0003t0001g0163 a0001c0003t0001g0167 |
2 | HG02132.hp2 NA19003.hp2 |
intron_variant | MODIFIER | c.357-3155G>A | LMNA | ENSG00000160789.24 | transcript | ENST00000677389.1 | protein_coding | 1/9 | chr1 | 156127462 | |||||||
chr1:156127509 | G | GT | 36 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0017 others(33): Show |
43 | HG00408.hp1 HG00621.hp1 HG00621.hp2 others(40): Show |
intron_variant | MODIFIER | c.357-3081dupT | LMNA | ENSG00000160789.24 | transcript | ENST00000677389.1 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 156127509 | ||||||
chr1:156127509 | G | GTT | 14 | a0001c0001t0001g0072 a0001c0001t0001g0127 a0001c0002t0001g0003 others(11): Show |
23 | HG00642.hp2 HG00741.hp2 HG01074.hp1 others(20): Show |
intron_variant | MODIFIER | c.357-3082_357-3081d others(4): Show |
LMNA | ENSG00000160789.24 | transcript | ENST00000677389.1 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 156127509 | ||||||
chr1:156127509 | GT | G | 8 | a0001c0001t0001g0049 a0001c0001t0001g0066 a0001c0001t0002g0188 others(5): Show |
9 | HG01884.hp1 HG03041.hp1 HG03453.hp1 others(6): Show |
intron_variant | MODIFIER | c.357-3081delT | LMNA | ENSG00000160789.24 | transcript | ENST00000677389.1 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 156127509 | ||||||
chr1:156127509 | GTTTTTT | G | 19 | a0001c0003t0001g0004 a0001c0003t0001g0011 a0001c0003t0001g0029 others(16): Show |
36 | HG01167.hp2 HG01169.hp2 HG01257.hp2 others(33): Show |
intron_variant | MODIFIER | c.357-3086_357-3081d others(8): Show |
LMNA | ENSG00000160789.24 | transcript | ENST00000677389.1 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 156127509 | ||||||
chr1:156127612 | A | G | 22 | a0001c0003t0001g0004 a0001c0003t0001g0011 a0001c0003t0001g0029 others(19): Show |
39 | HG01167.hp2 HG01169.hp2 HG01257.hp2 others(36): Show |
intron_variant | MODIFIER | c.357-3005A>G | LMNA | ENSG00000160789.24 | transcript | ENST00000677389.1 | protein_coding | 1/9 | chr1 | 156127612 | |||||||
chr1:156127686 | AT | A | 81 | a0001c0001t0001g0006 a0001c0001t0001g0013 a0001c0001t0001g0015 others(78): Show |
118 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(115): Show |
intron_variant | MODIFIER | c.357-2913delT | LMNA | ENSG00000160789.24 | transcript | ENST00000677389.1 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 156127686 | ||||||
chr1:156127773 | G | A | 12 | a0001c0003t0001g0187 a0001c0004t0001g0035 a0001c0004t0001g0085 others(9): Show |
14 | HG01884.hp1 HG02257.hp2 HG02559.hp1 others(11): Show |
intron_variant | MODIFIER | c.357-2844G>A | LMNA | ENSG00000160789.24 | transcript | ENST00000677389.1 | protein_coding | 1/9 | chr1 | 156127773 | |||||||
chr1:156127796 | C | T | 1 | a0001c0002t0001g0098 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.357-2821C>T | LMNA | ENSG00000160789.24 | transcript | ENST00000677389.1 | protein_coding | 1/9 | chr1 | 156127796 | |||||||
chr1:156127831 | C | A | 2 | a0001c0003t0001g0187 a0001c0005t0001g0170 |
2 | HG02630.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.357-2786C>A | LMNA | ENSG00000160789.24 | transcript | ENST00000677389.1 | protein_coding | 1/9 | chr1 | 156127831 | |||||||
chr1:156127841 | C | T | 1 | a0001c0001t0001g0071 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.357-2776C>T | LMNA | ENSG00000160789.24 | transcript | ENST00000677389.1 | protein_coding | 1/9 | chr1 | 156127841 | |||||||
chr1:156127842 | T | A | 21 | a0001c0003t0001g0004 a0001c0003t0001g0011 a0001c0003t0001g0029 others(18): Show |
38 | HG01167.hp2 HG01169.hp2 HG01257.hp2 others(35): Show |
intron_variant | MODIFIER | c.357-2775T>A | LMNA | ENSG00000160789.24 | transcript | ENST00000677389.1 | protein_coding | 1/9 | chr1 | 156127842 | |||||||
chr1:156127844 | G | C | 21 | a0001c0003t0001g0004 a0001c0003t0001g0011 a0001c0003t0001g0029 others(18): Show |
38 | HG01167.hp2 HG01169.hp2 HG01257.hp2 others(35): Show |
intron_variant | MODIFIER | c.357-2773G>C | LMNA | ENSG00000160789.24 | transcript | ENST00000677389.1 | protein_coding | 1/9 | chr1 | 156127844 | |||||||
chr1:156128166 | A | T | 12 | a0001c0003t0001g0187 a0001c0004t0001g0035 a0001c0004t0001g0085 others(9): Show |
14 | HG01884.hp1 HG02257.hp2 HG02559.hp1 others(11): Show |
intron_variant | MODIFIER | c.357-2451A>T | LMNA | ENSG00000160789.24 | transcript | ENST00000677389.1 | protein_coding | 1/9 | chr1 | 156128166 | |||||||
chr1:156128348 | A | G | 14 | a0001c0003t0001g0005 a0001c0003t0001g0028 a0001c0003t0001g0030 others(11): Show |
22 | HG02132.hp2 HG02155.hp1 HG02258.hp1 others(19): Show |
intron_variant | MODIFIER | c.357-2269A>G | LMNA | ENSG00000160789.24 | transcript | ENST00000677389.1 | protein_coding | 1/9 | chr1 | 156128348 | |||||||
chr1:156128540 | C | T | 1 | a0001c0001t0001g0112 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.357-2077C>T | LMNA | ENSG00000160789.24 | transcript | ENST00000677389.1 | protein_coding | 1/9 | chr1 | 156128540 | |||||||
chr1:156128541 | G | A | 2 | a0001c0002t0001g0096 a0001c0002t0001g0097 |
2 | HG00280.hp2 HG01884.hp2 |
intron_variant | MODIFIER | c.357-2076G>A | LMNA | ENSG00000160789.24 | transcript | ENST00000677389.1 | protein_coding | 1/9 | chr1 | 156128541 | |||||||
chr1:156128829 | A | G | 50 | a0001c0003t0001g0004 a0001c0003t0001g0005 a0001c0003t0001g0011 others(47): Show |
77 | HG01167.hp2 HG01169.hp2 HG01257.hp2 others(74): Show |
intron_variant | MODIFIER | c.357-1788A>G | LMNA | ENSG00000160789.24 | transcript | ENST00000677389.1 | protein_coding | 1/9 | chr1 | 156128829 | |||||||
chr1:156128899 | G | A | 21 | a0001c0003t0001g0004 a0001c0003t0001g0011 a0001c0003t0001g0029 others(18): Show |
38 | HG01167.hp2 HG01169.hp2 HG01257.hp2 others(35): Show |
intron_variant | MODIFIER | c.357-1718G>A | LMNA | ENSG00000160789.24 | transcript | ENST00000677389.1 | protein_coding | 1/9 | chr1 | 156128899 | |||||||
chr1:156128982 | G | A | 10 | a0001c0004t0001g0035 a0001c0004t0001g0085 a0001c0004t0001g0162 others(7): Show |
12 | HG01884.hp1 HG02257.hp2 HG02559.hp1 others(9): Show |
intron_variant | MODIFIER | c.357-1635G>A | LMNA | ENSG00000160789.24 | transcript | ENST00000677389.1 | protein_coding | 1/9 | chr1 | 156128982 | |||||||
chr1:156129039 | G | A | 14 | a0001c0003t0001g0031 a0001c0004t0001g0010 a0001c0004t0001g0032 others(11): Show |
20 | HG01884.hp1 HG02257.hp1 HG02257.hp2 others(17): Show |
intron_variant | MODIFIER | c.357-1578G>A | LMNA | ENSG00000160789.24 | transcript | ENST00000677389.1 | protein_coding | 1/9 | chr1 | 156129039 | |||||||
chr1:156129121 | G | A | 2 | a0001c0003t0001g0187 a0001c0005t0001g0170 |
2 | HG02630.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.357-1496G>A | LMNA | ENSG00000160789.24 | transcript | ENST00000677389.1 | protein_coding | 1/9 | chr1 | 156129121 | |||||||
chr1:156129217 | G | C | 1 | a0001c0001t0001g0056 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.357-1400G>C | LMNA | ENSG00000160789.24 | transcript | ENST00000677389.1 | protein_coding | 1/9 | chr1 | 156129217 | |||||||
chr1:156129226 | G | A | 1 | a0001c0001t0001g0046 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.357-1391G>A | LMNA | ENSG00000160789.24 | transcript | ENST00000677389.1 | protein_coding | 1/9 | chr1 | 156129226 | |||||||
chr1:156129307 | G | A | 4 | a0001c0001t0001g0012 a0001c0001t0001g0038 a0001c0001t0001g0039 others(1): Show |
5 | HG02135.hp2 NA18968.hp2 NA18978.hp1 others(2): Show |
intron_variant | MODIFIER | c.357-1310G>A | LMNA | ENSG00000160789.24 | transcript | ENST00000677389.1 | protein_coding | 1/9 | chr1 | 156129307 | |||||||
chr1:156129599 | T | C | 1 | a0001c0004t0001g0162 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.357-1018T>C | LMNA | ENSG00000160789.24 | transcript | ENST00000677389.1 | protein_coding | 1/9 | chr1 | 156129599 | |||||||
chr1:156129603 | C | T | 14 | a0001c0003t0001g0031 a0001c0004t0001g0010 a0001c0004t0001g0032 others(11): Show |
20 | HG01884.hp1 HG02257.hp1 HG02257.hp2 others(17): Show |
intron_variant | MODIFIER | c.357-1014C>T | LMNA | ENSG00000160789.24 | transcript | ENST00000677389.1 | protein_coding | 1/9 | chr1 | 156129603 | |||||||
chr1:156129652 | A | G | 1 | a0001c0001t0001g0137 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.357-965A>G | LMNA | ENSG00000160789.24 | transcript | ENST00000677389.1 | protein_coding | 1/9 | chr1 | 156129652 | |||||||
chr1:156129765 | G | A | 1 | a0001c0001t0001g0081 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.357-852G>A | LMNA | ENSG00000160789.24 | transcript | ENST00000677389.1 | protein_coding | 1/9 | chr1 | 156129765 | |||||||
chr1:156129839 | C | G | 28 | a0001c0003t0001g0004 a0001c0003t0001g0011 a0001c0003t0001g0029 others(25): Show |
44 | HG01167.hp2 HG01169.hp2 HG01257.hp2 others(41): Show |
intron_variant | MODIFIER | c.357-778C>G | LMNA | ENSG00000160789.24 | transcript | ENST00000677389.1 | protein_coding | 1/9 | chr1 | 156129839 | |||||||
chr1:156129878 | T | G | 42 | a0001c0001t0002g0188 a0001c0003t0001g0004 a0001c0003t0001g0005 others(39): Show |
67 | HG01167.hp2 HG01169.hp2 HG01257.hp2 others(64): Show |
intron_variant | MODIFIER | c.357-739T>G | LMNA | ENSG00000160789.24 | transcript | ENST00000677389.1 | protein_coding | 1/9 | chr1 | 156129878 | |||||||
chr1:156130039 | A | G | 34 | a0001c0003t0001g0004 a0001c0003t0001g0011 a0001c0003t0001g0029 others(31): Show |
53 | HG01167.hp2 HG01169.hp2 HG01257.hp2 others(50): Show |
intron_variant | MODIFIER | c.357-578A>G | LMNA | ENSG00000160789.24 | transcript | ENST00000677389.1 | protein_coding | 1/9 | chr1 | 156130039 | |||||||
chr1:156130162 | A | G | 1 | a0001c0001t0001g0135 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.357-455A>G | LMNA | ENSG00000160789.24 | transcript | ENST00000677389.1 | protein_coding | 1/9 | chr1 | 156130162 | |||||||
chr1:156130258 | C | A | 23 | a0001c0003t0001g0004 a0001c0003t0001g0011 a0001c0003t0001g0029 others(20): Show |
40 | HG01167.hp2 HG01169.hp2 HG01257.hp2 others(37): Show |
intron_variant | MODIFIER | c.357-359C>A | LMNA | ENSG00000160789.24 | transcript | ENST00000677389.1 | protein_coding | 1/9 | chr1 | 156130258 | |||||||
chr1:156130348 | T | C | 14 | a0001c0003t0001g0004 a0001c0003t0001g0011 a0001c0003t0001g0029 others(11): Show |
27 | HG01167.hp2 HG01169.hp2 HG01257.hp2 others(24): Show |
intron_variant | MODIFIER | c.357-269T>C | LMNA | ENSG00000160789.24 | transcript | ENST00000677389.1 | protein_coding | 1/9 | chr1 | 156130348 | |||||||
chr1:156130443 | T | TG | 15 | a0001c0003t0001g0004 a0001c0003t0001g0011 a0001c0003t0001g0029 others(12): Show |
28 | HG01167.hp2 HG01169.hp2 HG01257.hp2 others(25): Show |
intron_variant | MODIFIER | c.357-171dupG | LMNA | ENSG00000160789.24 | transcript | ENST00000677389.1 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 156130443 | ||||||
chr1:156130452 | A | G | 1 | a0001c0002t0001g0110 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.357-165A>G | LMNA | ENSG00000160789.24 | transcript | ENST00000677389.1 | protein_coding | 1/9 | chr1 | 156130452 | |||||||
chr1:156130809 | C | T | 1 | a0001c0001t0001g0144 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.513+36C>T | LMNA | ENSG00000160789.24 | transcript | ENST00000677389.1 | protein_coding | 2/9 | chr1 | 156130809 | |||||||
chr1:156130948 | T | C | 51 | a0001c0003t0001g0004 a0001c0003t0001g0005 a0001c0003t0001g0011 others(48): Show |
78 | HG01167.hp2 HG01169.hp2 HG01257.hp2 others(75): Show |
intron_variant | MODIFIER | c.513+175T>C | LMNA | ENSG00000160789.24 | transcript | ENST00000677389.1 | protein_coding | 2/9 | chr1 | 156130948 | |||||||
chr1:156131004 | G | T | 1 | a0001c0001t0001g0042 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.513+231G>T | LMNA | ENSG00000160789.24 | transcript | ENST00000677389.1 | protein_coding | 2/9 | chr1 | 156131004 | |||||||
chr1:156131047 | C | G | 34 | a0001c0003t0001g0004 a0001c0003t0001g0011 a0001c0003t0001g0029 others(31): Show |
53 | HG01167.hp2 HG01169.hp2 HG01257.hp2 others(50): Show |
intron_variant | MODIFIER | c.513+274C>G | LMNA | ENSG00000160789.24 | transcript | ENST00000677389.1 | protein_coding | 2/9 | chr1 | 156131047 | |||||||
chr1:156131157 | A | G | 35 | a0001c0003t0001g0004 a0001c0003t0001g0011 a0001c0003t0001g0029 others(32): Show |
54 | HG01167.hp2 HG01169.hp2 HG01257.hp2 others(51): Show |
intron_variant | MODIFIER | c.513+384A>G | LMNA | ENSG00000160789.24 | transcript | ENST00000677389.1 | protein_coding | 2/9 | chr1 | 156131157 | |||||||
chr1:156131197 | C | T | 6 | a0001c0003t0001g0025 a0001c0003t0001g0099 a0001c0003t0001g0109 others(3): Show |
7 | HG02055.hp2 HG02622.hp1 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.513+424C>T | LMNA | ENSG00000160789.24 | transcript | ENST00000677389.1 | protein_coding | 2/9 | chr1 | 156131197 | |||||||
chr1:156131278 | T | A | 52 | a0001c0001t0001g0072 a0001c0003t0001g0004 a0001c0003t0001g0005 others(49): Show |
79 | HG01106.hp1 HG01167.hp2 HG01169.hp2 others(76): Show |
intron_variant | MODIFIER | c.513+505T>A | LMNA | ENSG00000160789.24 | transcript | ENST00000677389.1 | protein_coding | 2/9 | chr1 | 156131278 | |||||||
chr1:156131281 | T | A | 28 | a0001c0003t0001g0004 a0001c0003t0001g0011 a0001c0003t0001g0029 others(25): Show |
46 | HG01167.hp2 HG01169.hp2 HG01257.hp2 others(43): Show |
intron_variant | MODIFIER | c.513+508T>A | LMNA | ENSG00000160789.24 | transcript | ENST00000677389.1 | protein_coding | 2/9 | chr1 | 156131281 | |||||||
chr1:156131284 | T | A | 2 | a0001c0003t0001g0031 a0001c0005t0001g0170 |
3 | HG02630.hp1 NA19030.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.513+511T>A | LMNA | ENSG00000160789.24 | transcript | ENST00000677389.1 | protein_coding | 2/9 | chr1 | 156131284 | |||||||
chr1:156131372 | G | T | 3 | a0001c0004t0001g0010 a0001c0004t0001g0032 a0001c0004t0001g0174 |
6 | HG02257.hp1 HG02572.hp1 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.513+599G>T | LMNA | ENSG00000160789.24 | transcript | ENST00000677389.1 | protein_coding | 2/9 | chr1 | 156131372 | |||||||
chr1:156131431 | T | C | 2 | a0001c0003t0001g0031 a0001c0003t0001g0169 |
3 | HG02809.hp2 NA19030.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.513+658T>C | LMNA | ENSG00000160789.24 | transcript | ENST00000677389.1 | protein_coding | 2/9 | chr1 | 156131431 | |||||||
chr1:156131690 | C | T | 1 | a0001c0001t0001g0092 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.513+917C>T | LMNA | ENSG00000160789.24 | transcript | ENST00000677389.1 | protein_coding | 2/9 | chr1 | 156131690 | |||||||
chr1:156131758 | T | C | 23 | a0001c0003t0001g0004 a0001c0003t0001g0011 a0001c0003t0001g0029 others(20): Show |
40 | HG01167.hp2 HG01169.hp2 HG01257.hp2 others(37): Show |
intron_variant | MODIFIER | c.513+985T>C | LMNA | ENSG00000160789.24 | transcript | ENST00000677389.1 | protein_coding | 2/9 | chr1 | 156131758 | |||||||
chr1:156131777 | C | T | 1 | a0001c0006t0001g0068 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.513+1004C>T | LMNA | ENSG00000160789.24 | transcript | ENST00000677389.1 | protein_coding | 2/9 | chr1 | 156131777 | |||||||
chr1:156131940 | C | T | 23 | a0001c0003t0001g0004 a0001c0003t0001g0011 a0001c0003t0001g0029 others(20): Show |
40 | HG01167.hp2 HG01169.hp2 HG01257.hp2 others(37): Show |
intron_variant | MODIFIER | c.513+1167C>T | LMNA | ENSG00000160789.24 | transcript | ENST00000677389.1 | protein_coding | 2/9 | chr1 | 156131940 | |||||||
chr1:156131943 | G | A | 1 | a0001c0001t0001g0069 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.513+1170G>A | LMNA | ENSG00000160789.24 | transcript | ENST00000677389.1 | protein_coding | 2/9 | chr1 | 156131943 | |||||||
chr1:156132038 | A | G | 23 | a0001c0003t0001g0004 a0001c0003t0001g0011 a0001c0003t0001g0029 others(20): Show |
40 | HG01167.hp2 HG01169.hp2 HG01257.hp2 others(37): Show |
intron_variant | MODIFIER | c.513+1265A>G | LMNA | ENSG00000160789.24 | transcript | ENST00000677389.1 | protein_coding | 2/9 | chr1 | 156132038 | |||||||
chr1:156132042 | A | G | 23 | a0001c0003t0001g0004 a0001c0003t0001g0011 a0001c0003t0001g0029 others(20): Show |
40 | HG01167.hp2 HG01169.hp2 HG01257.hp2 others(37): Show |
intron_variant | MODIFIER | c.513+1269A>G | LMNA | ENSG00000160789.24 | transcript | ENST00000677389.1 | protein_coding | 2/9 | chr1 | 156132042 | |||||||
chr1:156132309 | C | A | 23 | a0001c0003t0001g0004 a0001c0003t0001g0011 a0001c0003t0001g0029 others(20): Show |
40 | HG01167.hp2 HG01169.hp2 HG01257.hp2 others(37): Show |
intron_variant | MODIFIER | c.513+1536C>A | LMNA | ENSG00000160789.24 | transcript | ENST00000677389.1 | protein_coding | 2/9 | chr1 | 156132309 | |||||||
chr1:156132341 | C | G | 23 | a0001c0003t0001g0004 a0001c0003t0001g0011 a0001c0003t0001g0029 others(20): Show |
40 | HG01167.hp2 HG01169.hp2 HG01257.hp2 others(37): Show |
intron_variant | MODIFIER | c.513+1568C>G | LMNA | ENSG00000160789.24 | transcript | ENST00000677389.1 | protein_coding | 2/9 | chr1 | 156132341 | |||||||
chr1:156132647 | C | T | 23 | a0001c0003t0001g0004 a0001c0003t0001g0011 a0001c0003t0001g0029 others(20): Show |
40 | HG01167.hp2 HG01169.hp2 HG01257.hp2 others(37): Show |
intron_variant | MODIFIER | c.514-1756C>T | LMNA | ENSG00000160789.24 | transcript | ENST00000677389.1 | protein_coding | 2/9 | chr1 | 156132647 | |||||||
chr1:156132662 | G | A | 1 | a0001c0002t0001g0100 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.514-1741G>A | LMNA | ENSG00000160789.24 | transcript | ENST00000677389.1 | protein_coding | 2/9 | chr1 | 156132662 | |||||||
chr1:156132685 | G | A | 51 | a0001c0003t0001g0004 a0001c0003t0001g0005 a0001c0003t0001g0011 others(48): Show |
78 | HG01167.hp2 HG01169.hp2 HG01257.hp2 others(75): Show |
intron_variant | MODIFIER | c.514-1718G>A | LMNA | ENSG00000160789.24 | transcript | ENST00000677389.1 | protein_coding | 2/9 | chr1 | 156132685 | |||||||
chr1:156132813 | C | A | 23 | a0001c0003t0001g0004 a0001c0003t0001g0011 a0001c0003t0001g0029 others(20): Show |
40 | HG01167.hp2 HG01169.hp2 HG01257.hp2 others(37): Show |
intron_variant | MODIFIER | c.514-1590C>A | LMNA | ENSG00000160789.24 | transcript | ENST00000677389.1 | protein_coding | 2/9 | chr1 | 156132813 | |||||||
chr1:156132829 | C | T | 1 | a0001c0006t0001g0068 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.514-1574C>T | LMNA | ENSG00000160789.24 | transcript | ENST00000677389.1 | protein_coding | 2/9 | chr1 | 156132829 | |||||||
chr1:156132835 | C | CT | 3 | a0001c0003t0001g0147 a0001c0003t0001g0157 a0001c0003t0001g0182 |
3 | HG01433.hp2 HG02922.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.514-1567dupT | LMNA | ENSG00000160789.24 | transcript | ENST00000677389.1 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr1 | 156132835 | ||||||
chr1:156132836 | TC | T | 5 | a0001c0003t0001g0031 a0001c0003t0001g0158 a0001c0003t0001g0169 others(2): Show |
6 | HG02630.hp1 HG02809.hp2 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.514-1566delC | LMNA | ENSG00000160789.24 | transcript | ENST00000677389.1 | protein_coding | 2/9 | chr1 | 156132836 | |||||||
chr1:156132837 | C | T | 17 | a0001c0003t0001g0004 a0001c0003t0001g0011 a0001c0003t0001g0029 others(14): Show |
33 | HG01167.hp2 HG01169.hp2 HG01257.hp2 others(30): Show |
intron_variant | MODIFIER | c.514-1566C>T | LMNA | ENSG00000160789.24 | transcript | ENST00000677389.1 | protein_coding | 2/9 | chr1 | 156132837 | |||||||
chr1:156132837 | CT | C | 128 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(125): Show |
182 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(179): Show |
intron_variant | MODIFIER | c.514-1546delT | LMNA | ENSG00000160789.24 | transcript | ENST00000677389.1 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr1 | 156132837 | ||||||
chr1:156132837 | CTT | C | 6 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(3): Show |
6 | HG01943.hp1 HG01943.hp2 HG02273.hp2 others(3): Show |
intron_variant | MODIFIER | c.514-1547_514-1546d others(4): Show |
LMNA | ENSG00000160789.24 | transcript | ENST00000677389.1 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr1 | 156132837 | ||||||
chr1:156132839 | T | C | 1 | a0001c0006t0001g0068 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.514-1564T>C | LMNA | ENSG00000160789.24 | transcript | ENST00000677389.1 | protein_coding | 2/9 | chr1 | 156132839 | |||||||
chr1:156132902 | C | T | 1 | a0001c0004t0001g0070 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.514-1501C>T | LMNA | ENSG00000160789.24 | transcript | ENST00000677389.1 | protein_coding | 2/9 | chr1 | 156132902 | |||||||
chr1:156132903 | G | A | 23 | a0001c0003t0001g0004 a0001c0003t0001g0011 a0001c0003t0001g0029 others(20): Show |
40 | HG01167.hp2 HG01169.hp2 HG01257.hp2 others(37): Show |
intron_variant | MODIFIER | c.514-1500G>A | LMNA | ENSG00000160789.24 | transcript | ENST00000677389.1 | protein_coding | 2/9 | chr1 | 156132903 | |||||||
chr1:156132965 | G | A | 23 | a0001c0003t0001g0004 a0001c0003t0001g0011 a0001c0003t0001g0029 others(20): Show |
40 | HG01167.hp2 HG01169.hp2 HG01257.hp2 others(37): Show |
intron_variant | MODIFIER | c.514-1438G>A | LMNA | ENSG00000160789.24 | transcript | ENST00000677389.1 | protein_coding | 2/9 | chr1 | 156132965 | |||||||
chr1:156132991 | C | G | 1 | a0001c0001t0001g0149 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.514-1412C>G | LMNA | ENSG00000160789.24 | transcript | ENST00000677389.1 | protein_coding | 2/9 | chr1 | 156132991 | |||||||
chr1:156133190 | A | G | 1 | a0001c0003t0001g0158 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.514-1213A>G | LMNA | ENSG00000160789.24 | transcript | ENST00000677389.1 | protein_coding | 2/9 | chr1 | 156133190 | |||||||
chr1:156133235 | A | G | 1 | a0001c0003t0001g0164 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.514-1168A>G | LMNA | ENSG00000160789.24 | transcript | ENST00000677389.1 | protein_coding | 2/9 | chr1 | 156133235 | |||||||
chr1:156133383 | C | T | 1 | a0001c0002t0001g0060 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.514-1020C>T | LMNA | ENSG00000160789.24 | transcript | ENST00000677389.1 | protein_coding | 2/9 | chr1 | 156133383 | |||||||
chr1:156133401 | T | C | 15 | a0001c0003t0001g0004 a0001c0003t0001g0011 a0001c0003t0001g0029 others(12): Show |
28 | HG01167.hp2 HG01169.hp2 HG01257.hp2 others(25): Show |
intron_variant | MODIFIER | c.514-1002T>C | LMNA | ENSG00000160789.24 | transcript | ENST00000677389.1 | protein_coding | 2/9 | chr1 | 156133401 | |||||||
chr1:156133412 | G | A | 51 | a0001c0003t0001g0004 a0001c0003t0001g0005 a0001c0003t0001g0011 others(48): Show |
78 | HG01167.hp2 HG01169.hp2 HG01257.hp2 others(75): Show |
intron_variant | MODIFIER | c.514-991G>A | LMNA | ENSG00000160789.24 | transcript | ENST00000677389.1 | protein_coding | 2/9 | chr1 | 156133412 | |||||||
chr1:156133444 | G | A | 20 | a0001c0003t0001g0004 a0001c0003t0001g0011 a0001c0003t0001g0029 others(17): Show |
34 | HG01167.hp2 HG01169.hp2 HG01257.hp2 others(31): Show |
intron_variant | MODIFIER | c.514-959G>A | LMNA | ENSG00000160789.24 | transcript | ENST00000677389.1 | protein_coding | 2/9 | chr1 | 156133444 | |||||||
chr1:156133463 | C | T | 14 | a0001c0004t0001g0010 a0001c0004t0001g0032 a0001c0004t0001g0035 others(11): Show |
19 | HG01884.hp1 HG02257.hp1 HG02257.hp2 others(16): Show |
intron_variant | MODIFIER | c.514-940C>T | LMNA | ENSG00000160789.24 | transcript | ENST00000677389.1 | protein_coding | 2/9 | chr1 | 156133463 | |||||||
chr1:156133805 | G | C | 14 | a0001c0003t0001g0005 a0001c0003t0001g0028 a0001c0003t0001g0030 others(11): Show |
22 | HG02132.hp2 HG02155.hp1 HG02258.hp1 others(19): Show |
intron_variant | MODIFIER | c.514-598G>C | LMNA | ENSG00000160789.24 | transcript | ENST00000677389.1 | protein_coding | 2/9 | chr1 | 156133805 | |||||||
chr1:156133851 | A | G | 1 | a0001c0006t0001g0068 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.514-552A>G | LMNA | ENSG00000160789.24 | transcript | ENST00000677389.1 | protein_coding | 2/9 | chr1 | 156133851 | |||||||
chr1:156134016 | G | T | 1 | a0001c0002t0001g0138 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.514-387G>T | LMNA | ENSG00000160789.24 | transcript | ENST00000677389.1 | protein_coding | 2/9 | chr1 | 156134016 | |||||||
chr1:156134029 | CTTTTT | C | 26 | a0001c0003t0001g0004 a0001c0003t0001g0011 a0001c0003t0001g0025 others(23): Show |
41 | HG01167.hp2 HG01169.hp2 HG01257.hp2 others(38): Show |
intron_variant | MODIFIER | c.514-373_514-369del others(5): Show |
LMNA | ENSG00000160789.24 | transcript | ENST00000677389.1 | protein_coding | 2/9 | chr1 | 156134029 | |||||||
chr1:156134035 | G | A | 2 | a0001c0004t0001g0035 a0001c0004t0001g0180 |
3 | HG02896.hp2 HG02897.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.514-368G>A | LMNA | ENSG00000160789.24 | transcript | ENST00000677389.1 | protein_coding | 2/9 | chr1 | 156134035 | |||||||
chr1:156134085 | C | T | 1 | a0001c0002t0001g0022 | 2 | HG03490.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.514-318C>T | LMNA | ENSG00000160789.24 | transcript | ENST00000677389.1 | protein_coding | 2/9 | chr1 | 156134085 | |||||||
chr1:156134162 | G | A | 1 | a0001c0001t0001g0135 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.514-241G>A | LMNA | ENSG00000160789.24 | transcript | ENST00000677389.1 | protein_coding | 2/9 | chr1 | 156134162 | |||||||
chr1:156134206 | A | C | 57 | a0001c0003t0001g0004 a0001c0003t0001g0005 a0001c0003t0001g0011 others(54): Show |
85 | HG01167.hp2 HG01169.hp2 HG01257.hp2 others(82): Show |
intron_variant | MODIFIER | c.514-197A>C | LMNA | ENSG00000160789.24 | transcript | ENST00000677389.1 | protein_coding | 2/9 | chr1 | 156134206 | |||||||
chr1:156134292 | C | T | 3 | a0001c0004t0001g0010 a0001c0004t0001g0032 a0001c0004t0001g0174 |
6 | HG02257.hp1 HG02572.hp1 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.514-111C>T | LMNA | ENSG00000160789.24 | transcript | ENST00000677389.1 | protein_coding | 2/9 | chr1 | 156134292 | |||||||
chr1:156134584 | G | T | 17 | a0001c0003t0001g0005 a0001c0003t0001g0028 a0001c0003t0001g0030 others(14): Show |
25 | HG01496.hp1 HG02132.hp2 HG02155.hp1 others(22): Show |
intron_variant | MODIFIER | c.639+56G>T | LMNA | ENSG00000160789.24 | transcript | ENST00000677389.1 | protein_coding | 3/9 | chr1 | 156134584 | |||||||
chr1:156134601 | C | T | 16 | a0001c0003t0001g0005 a0001c0003t0001g0028 a0001c0003t0001g0030 others(13): Show |
24 | HG02132.hp2 HG02155.hp1 HG02258.hp1 others(21): Show |
intron_variant | MODIFIER | c.639+73C>T | LMNA | ENSG00000160789.24 | transcript | ENST00000677389.1 | protein_coding | 3/9 | chr1 | 156134601 | |||||||
chr1:156134988 | G | T | 14 | a0001c0004t0001g0010 a0001c0004t0001g0032 a0001c0004t0001g0035 others(11): Show |
19 | HG01884.hp1 HG02257.hp1 HG02257.hp2 others(16): Show |
intron_variant | MODIFIER | c.810+13G>T | LMNA | ENSG00000160789.24 | transcript | ENST00000677389.1 | protein_coding | 4/9 | chr1 | 156134988 | |||||||
chr1:156135032 | C | A | 1 | a0001c0004t0001g0162 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.810+57C>A | LMNA | ENSG00000160789.24 | transcript | ENST00000677389.1 | protein_coding | 4/9 | chr1 | 156135032 | |||||||
chr1:156135036 | C | T | 14 | a0001c0004t0001g0010 a0001c0004t0001g0032 a0001c0004t0001g0035 others(11): Show |
19 | HG01884.hp1 HG02257.hp1 HG02257.hp2 others(16): Show |
intron_variant | MODIFIER | c.810+61C>T | LMNA | ENSG00000160789.24 | transcript | ENST00000677389.1 | protein_coding | 4/9 | chr1 | 156135036 | |||||||
chr1:156135086 | G | C | 1 | a0001c0003t0001g0158 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.811-101G>C | LMNA | ENSG00000160789.24 | transcript | ENST00000677389.1 | protein_coding | 4/9 | chr1 | 156135086 | |||||||
chr1:156135378 | C | T | 1 | a0001c0001t0001g0111 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.936+66C>T | LMNA | ENSG00000160789.24 | transcript | ENST00000677389.1 | protein_coding | 5/9 | chr1 | 156135378 | |||||||
chr1:156135546 | C | T | 42 | a0001c0003t0001g0004 a0001c0003t0001g0005 a0001c0003t0001g0011 others(39): Show |
65 | HG01167.hp2 HG01169.hp2 HG01257.hp2 others(62): Show |
intron_variant | MODIFIER | c.936+234C>T | LMNA | ENSG00000160789.24 | transcript | ENST00000677389.1 | protein_coding | 5/9 | chr1 | 156135546 | |||||||
chr1:156135626 | A | G | 10 | a0001c0001t0001g0014 a0001c0001t0001g0024 a0001c0001t0001g0043 others(7): Show |
12 | HG00280.hp1 HG00733.hp1 HG01074.hp2 others(9): Show |
intron_variant | MODIFIER | c.937-275A>G | LMNA | ENSG00000160789.24 | transcript | ENST00000677389.1 | protein_coding | 5/9 | chr1 | 156135626 | |||||||
chr1:156135743 | C | G | 1 | a0001c0001t0001g0088 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.937-158C>G | LMNA | ENSG00000160789.24 | transcript | ENST00000677389.1 | protein_coding | 5/9 | chr1 | 156135743 | |||||||
chr1:156135744 | T | G | 1 | a0001c0001t0001g0088 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.937-157T>G | LMNA | ENSG00000160789.24 | transcript | ENST00000677389.1 | protein_coding | 5/9 | chr1 | 156135744 | |||||||
chr1:156135745 | T | G | 1 | a0001c0001t0001g0088 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.937-156T>G | LMNA | ENSG00000160789.24 | transcript | ENST00000677389.1 | protein_coding | 5/9 | chr1 | 156135745 | |||||||
chr1:156135747 | T | G | 1 | a0001c0001t0001g0088 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.937-154T>G | LMNA | ENSG00000160789.24 | transcript | ENST00000677389.1 | protein_coding | 5/9 | chr1 | 156135747 | |||||||
chr1:156135749 | A | G | 1 | a0001c0001t0001g0088 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.937-152A>G | LMNA | ENSG00000160789.24 | transcript | ENST00000677389.1 | protein_coding | 5/9 | chr1 | 156135749 | |||||||
chr1:156135750 | T | G | 1 | a0001c0001t0001g0088 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.937-151T>G | LMNA | ENSG00000160789.24 | transcript | ENST00000677389.1 | protein_coding | 5/9 | chr1 | 156135750 | |||||||
chr1:156135752 | T | G | 1 | a0001c0001t0001g0088 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.937-149T>G | LMNA | ENSG00000160789.24 | transcript | ENST00000677389.1 | protein_coding | 5/9 | chr1 | 156135752 | |||||||
chr1:156135753 | T | G | 1 | a0001c0001t0001g0088 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.937-148T>G | LMNA | ENSG00000160789.24 | transcript | ENST00000677389.1 | protein_coding | 5/9 | chr1 | 156135753 | |||||||
chr1:156135754 | C | G | 1 | a0001c0001t0001g0088 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.937-147C>G | LMNA | ENSG00000160789.24 | transcript | ENST00000677389.1 | protein_coding | 5/9 | chr1 | 156135754 | |||||||
chr1:156135755 | A | G | 1 | a0001c0001t0001g0088 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.937-146A>G | LMNA | ENSG00000160789.24 | transcript | ENST00000677389.1 | protein_coding | 5/9 | chr1 | 156135755 | |||||||
chr1:156135757 | A | G | 1 | a0001c0001t0001g0088 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.937-144A>G | LMNA | ENSG00000160789.24 | transcript | ENST00000677389.1 | protein_coding | 5/9 | chr1 | 156135757 | |||||||
chr1:156135759 | C | G | 1 | a0001c0001t0001g0088 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.937-142C>G | LMNA | ENSG00000160789.24 | transcript | ENST00000677389.1 | protein_coding | 5/9 | chr1 | 156135759 | |||||||
chr1:156135760 | T | G | 1 | a0001c0001t0001g0088 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.937-141T>G | LMNA | ENSG00000160789.24 | transcript | ENST00000677389.1 | protein_coding | 5/9 | chr1 | 156135760 | |||||||
chr1:156135763 | C | G | 1 | a0001c0001t0001g0088 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.937-138C>G | LMNA | ENSG00000160789.24 | transcript | ENST00000677389.1 | protein_coding | 5/9 | chr1 | 156135763 | |||||||
chr1:156135764 | T | G | 1 | a0001c0001t0001g0088 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.937-137T>G | LMNA | ENSG00000160789.24 | transcript | ENST00000677389.1 | protein_coding | 5/9 | chr1 | 156135764 | |||||||
chr1:156135765 | C | G | 1 | a0001c0001t0001g0088 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.937-136C>G | LMNA | ENSG00000160789.24 | transcript | ENST00000677389.1 | protein_coding | 5/9 | chr1 | 156135765 | |||||||
chr1:156135766 | T | G | 1 | a0001c0001t0001g0088 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.937-135T>G | LMNA | ENSG00000160789.24 | transcript | ENST00000677389.1 | protein_coding | 5/9 | chr1 | 156135766 | |||||||
chr1:156135768 | A | G | 1 | a0001c0001t0001g0088 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.937-133A>G | LMNA | ENSG00000160789.24 | transcript | ENST00000677389.1 | protein_coding | 5/9 | chr1 | 156135768 | |||||||
chr1:156135769 | T | G | 1 | a0001c0001t0001g0088 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.937-132T>G | LMNA | ENSG00000160789.24 | transcript | ENST00000677389.1 | protein_coding | 5/9 | chr1 | 156135769 | |||||||
chr1:156135771 | A | G | 1 | a0001c0001t0001g0088 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.937-130A>G | LMNA | ENSG00000160789.24 | transcript | ENST00000677389.1 | protein_coding | 5/9 | chr1 | 156135771 | |||||||
chr1:156135775 | C | G | 1 | a0001c0001t0001g0088 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.937-126C>G | LMNA | ENSG00000160789.24 | transcript | ENST00000677389.1 | protein_coding | 5/9 | chr1 | 156135775 | |||||||
chr1:156135776 | T | G | 1 | a0001c0001t0001g0088 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.937-125T>G | LMNA | ENSG00000160789.24 | transcript | ENST00000677389.1 | protein_coding | 5/9 | chr1 | 156135776 | |||||||
chr1:156135777 | C | G | 1 | a0001c0001t0001g0088 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.937-124C>G | LMNA | ENSG00000160789.24 | transcript | ENST00000677389.1 | protein_coding | 5/9 | chr1 | 156135777 | |||||||
chr1:156135778 | T | G | 1 | a0001c0001t0001g0088 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.937-123T>G | LMNA | ENSG00000160789.24 | transcript | ENST00000677389.1 | protein_coding | 5/9 | chr1 | 156135778 | |||||||
chr1:156135789 | T | A | 1 | a0001c0001t0001g0088 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.937-112T>A | LMNA | ENSG00000160789.24 | transcript | ENST00000677389.1 | protein_coding | 5/9 | chr1 | 156135789 | |||||||
chr1:156135818 | G | T | 42 | a0001c0003t0001g0004 a0001c0003t0001g0005 a0001c0003t0001g0011 others(39): Show |
65 | HG01167.hp2 HG01169.hp2 HG01257.hp2 others(62): Show |
intron_variant | MODIFIER | c.937-83G>T | LMNA | ENSG00000160789.24 | transcript | ENST00000677389.1 | protein_coding | 5/9 | chr1 | 156135818 | |||||||
chr1:156136137 | G | A | 42 | a0001c0003t0001g0004 a0001c0003t0001g0005 a0001c0003t0001g0011 others(39): Show |
65 | HG01167.hp2 HG01169.hp2 HG01257.hp2 others(62): Show |
intron_variant | MODIFIER | c.1157+16G>A | LMNA | ENSG00000160789.24 | transcript | ENST00000677389.1 | protein_coding | 6/9 | chr1 | 156136137 | |||||||
chr1:156136171 | A | G | 5 | a0001c0004t0001g0010 a0001c0004t0001g0032 a0001c0004t0001g0162 others(2): Show |
8 | HG01496.hp1 HG01884.hp1 HG02257.hp1 others(5): Show |
intron_variant | MODIFIER | c.1158-43A>G | LMNA | ENSG00000160789.24 | transcript | ENST00000677389.1 | protein_coding | 6/9 | chr1 | 156136171 | |||||||
chr1:156136578 | G | A | 55 | a0001c0003t0001g0004 a0001c0003t0001g0005 a0001c0003t0001g0011 others(52): Show |
83 | HG01167.hp2 HG01169.hp2 HG01257.hp2 others(80): Show |
intron_variant | MODIFIER | c.1380+142G>A | LMNA | ENSG00000160789.24 | transcript | ENST00000677389.1 | protein_coding | 7/9 | chr1 | 156136578 | |||||||
chr1:156136776 | C | T | 1 | a0001c0001t0001g0111 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.1381-145C>T | LMNA | ENSG00000160789.24 | transcript | ENST00000677389.1 | protein_coding | 7/9 | chr1 | 156136776 | |||||||
chr1:156136796 | G | A | 1 | a0001c0001t0001g0084 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.1381-125G>A | LMNA | ENSG00000160789.24 | transcript | ENST00000677389.1 | protein_coding | 7/9 | chr1 | 156136796 | |||||||
chr1:156136867 | C | A | 4 | a0001c0001t0001g0054 a0001c0001t0001g0059 a0001c0001t0001g0074 others(1): Show |
4 | NA18946.hp2 NA18951.hp1 NA18964.hp1 others(1): Show |
intron_variant | MODIFIER | c.1381-54C>A | LMNA | ENSG00000160789.24 | transcript | ENST00000677389.1 | protein_coding | 7/9 | chr1 | 156136867 | |||||||
chr1:156137072 | C | T | 37 | a0001c0003t0001g0004 a0001c0003t0001g0005 a0001c0003t0001g0011 others(34): Show |
59 | HG01167.hp2 HG01169.hp2 HG01257.hp2 others(56): Show |
intron_variant | MODIFIER | c.1489-41C>T | LMNA | ENSG00000160789.24 | transcript | ENST00000677389.1 | protein_coding | 8/9 | chr1 | 156137072 | |||||||
chr1:156137082 | G | T | 1 | a0001c0006t0001g0068 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.1489-31G>T | LMNA | ENSG00000160789.24 | transcript | ENST00000677389.1 | protein_coding | 8/9 | chr1 | 156137082 | |||||||
chr1:156137097 | C | G | 1 | a0001c0006t0001g0068 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.1489-16C>G | LMNA | ENSG00000160789.24 | transcript | ENST00000677389.1 | protein_coding | 8/9 | chr1 | 156137097 | |||||||
chr1:156137375 | A | G | 10 | a0001c0001t0001g0014 a0001c0001t0001g0024 a0001c0001t0001g0043 others(7): Show |
12 | HG00280.hp1 HG00733.hp1 HG01074.hp2 others(9): Show |
intron_variant | MODIFIER | c.1608+143A>G | LMNA | ENSG00000160789.24 | transcript | ENST00000677389.1 | protein_coding | 9/9 | chr1 | 156137375 | |||||||
chr1:156137384 | A | G | 3 | a0001c0004t0001g0010 a0001c0004t0001g0032 a0001c0004t0001g0174 |
6 | HG02257.hp1 HG02572.hp1 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.1608+152A>G | LMNA | ENSG00000160789.24 | transcript | ENST00000677389.1 | protein_coding | 9/9 | chr1 | 156137384 | |||||||
chr1:156137464 | C | G | 1 | a0001c0001t0001g0054 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.1609-190C>G | LMNA | ENSG00000160789.24 | transcript | ENST00000677389.1 | protein_coding | 9/9 | chr1 | 156137464 | |||||||
chr1:156137465 | G | C | 1 | a0001c0001t0001g0054 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.1609-189G>C | LMNA | ENSG00000160789.24 | transcript | ENST00000677389.1 | protein_coding | 9/9 | chr1 | 156137465 | |||||||
chr1:156137546 | G | A | 6 | a0001c0003t0001g0025 a0001c0003t0001g0099 a0001c0003t0001g0109 others(3): Show |
7 | HG02055.hp2 HG02622.hp1 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.1609-108G>A | LMNA | ENSG00000160789.24 | transcript | ENST00000677389.1 | protein_coding | 9/9 | chr1 | 156137546 |