Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 347404 |
|---|---|
| ensemblid | ENSG00000147036.12 |
| hgncid | 24767 |
| symbol | LANCL3 |
| name | LanC like family member 3 |
| refseq_nuc | NM_001170331.2 |
| refseq_prot | NP_001163802.1 |
| ensembl_nuc | ENST00000378619.4 |
| ensembl_prot | ENSP00000367882.4 |
| mane_status | MANE Select |
| chr | chrX |
| start | 37571661 |
| end | 37684463 |
| strand | + |
| ver | v1.2 |
| region | chrX:37571661-37684463 |
| region5000 | chrX:37566661-37689463 |
| regionname0 | LANCL3_chrX_37571661_37684463 |
| regionname5000 | LANCL3_chrX_37566661_37689463 |
| ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 420 | 196 | 66 | 34 | 70 | 5 | 19 | 55 | LANCL3_chrX_37566661_37689463 | LANCL3 | copy fasta | chrX | 37566661 | 37689463 |
| a0002 | 0/0 | 420 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | LANCL3_chrX_37566661_37689463 | LANCL3 | copy fasta | chrX | 37566661 | 37689463 |
| a0003 | 0/0 | 420 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | LANCL3_chrX_37566661_37689463 | LANCL3 | copy fasta | chrX | 37566661 | 37689463 |
| a0004 | 0/0 | 249 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | LANCL3_chrX_37566661_37689463 | LANCL3 | copy fasta | chrX | 37566661 | 37689463 |
| a0005 | 0/0 | 420 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | LANCL3_chrX_37566661_37689463 | LANCL3 | copy fasta | chrX | 37566661 | 37689463 |
| a0006 | 0/0 | 420 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | LANCL3_chrX_37566661_37689463 | LANCL3 | copy fasta | chrX | 37566661 | 37689463 |
| chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 1/1 | 1263 | 126 | 17 | 22 | 64 | 5 | 16 | LANCL3_chrX_37566661_37689463 | LANCL3 | copy fasta | chrX | 37566661 | 37689463 |
| c0002 | 0/0 | 1263 | 42 | 24 | 11 | 4 | 0 | 3 | LANCL3_chrX_37566661_37689463 | LANCL3 | copy fasta | chrX | 37566661 | 37689463 |
| c0003 | 0/0 | 1263 | 20 | 20 | 0 | 0 | 0 | 0 | LANCL3_chrX_37566661_37689463 | LANCL3 | copy fasta | chrX | 37566661 | 37689463 |
| c0004 | 0/0 | 1263 | 5 | 5 | 0 | 0 | 0 | 0 | LANCL3_chrX_37566661_37689463 | LANCL3 | copy fasta | chrX | 37566661 | 37689463 |
| c0005 | 0/0 | 1263 | 2 | 0 | 0 | 2 | 0 | 0 | LANCL3_chrX_37566661_37689463 | LANCL3 | copy fasta | chrX | 37566661 | 37689463 |
| c0006 | 0/0 | 1263 | 1 | 1 | 0 | 0 | 0 | 0 | LANCL3_chrX_37566661_37689463 | LANCL3 | copy fasta | chrX | 37566661 | 37689463 |
| c0007 | 0/0 | 1263 | 1 | 1 | 0 | 0 | 0 | 0 | LANCL3_chrX_37566661_37689463 | LANCL3 | copy fasta | chrX | 37566661 | 37689463 |
| c0008 | 0/0 | 1264 | 1 | 0 | 0 | 1 | 0 | 0 | LANCL3_chrX_37566661_37689463 | LANCL3 | copy fasta | chrX | 37566661 | 37689463 |
| c0009 | 0/0 | 1263 | 1 | 0 | 0 | 0 | 0 | 1 | LANCL3_chrX_37566661_37689463 | LANCL3 | copy fasta | chrX | 37566661 | 37689463 |
| c0010 | 0/0 | 1263 | 1 | 0 | 1 | 0 | 0 | 0 | LANCL3_chrX_37566661_37689463 | LANCL3 | copy fasta | chrX | 37566661 | 37689463 |
| c0011 | 0/0 | 1263 | 1 | 0 | 1 | 0 | 0 | 0 | LANCL3_chrX_37566661_37689463 | LANCL3 | copy fasta | chrX | 37566661 | 37689463 |
| thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 0/1 | 8861 | 98 | 3 | 20 | 60 | 4 | 10 | LANCL3_chrX_37566661_37689463 | LANCL3 | copy fasta | chrX | 37566661 | 37689463 |
| t0002 | 0/0 | 8868 | 9 | 6 | 3 | 0 | 0 | 0 | LANCL3_chrX_37566661_37689463 | LANCL3 | copy fasta | chrX | 37566661 | 37689463 |
| t0003 | 0/0 | 8871 | 8 | 0 | 6 | 2 | 0 | 0 | LANCL3_chrX_37566661_37689463 | LANCL3 | copy fasta | chrX | 37566661 | 37689463 |
| t0004 | 0/0 | 8870 | 5 | 4 | 0 | 0 | 0 | 1 | LANCL3_chrX_37566661_37689463 | LANCL3 | copy fasta | chrX | 37566661 | 37689463 |
| t0005 | 0/0 | 8873 | 5 | 5 | 0 | 0 | 0 | 0 | LANCL3_chrX_37566661_37689463 | LANCL3 | copy fasta | chrX | 37566661 | 37689463 |
| t0006 | 0/0 | 8854 | 4 | 0 | 0 | 2 | 0 | 2 | LANCL3_chrX_37566661_37689463 | LANCL3 | copy fasta | chrX | 37566661 | 37689463 |
| t0007 | 0/0 | 8866 | 4 | 4 | 0 | 0 | 0 | 0 | LANCL3_chrX_37566661_37689463 | LANCL3 | copy fasta | chrX | 37566661 | 37689463 |
| t0008 | 0/0 | 8861 | 4 | 4 | 0 | 0 | 0 | 0 | LANCL3_chrX_37566661_37689463 | LANCL3 | copy fasta | chrX | 37566661 | 37689463 |
| t0009 | 0/0 | 8870 | 4 | 4 | 0 | 0 | 0 | 0 | LANCL3_chrX_37566661_37689463 | LANCL3 | copy fasta | chrX | 37566661 | 37689463 |
| t0010 | 0/0 | 8855 | 3 | 3 | 0 | 0 | 0 | 0 | LANCL3_chrX_37566661_37689463 | LANCL3 | copy fasta | chrX | 37566661 | 37689463 |
| t0011 | 0/0 | 8864 | 3 | 0 | 1 | 2 | 0 | 0 | LANCL3_chrX_37566661_37689463 | LANCL3 | copy fasta | chrX | 37566661 | 37689463 |
| t0012 | 0/0 | 8864 | 2 | 2 | 0 | 0 | 0 | 0 | LANCL3_chrX_37566661_37689463 | LANCL3 | copy fasta | chrX | 37566661 | 37689463 |
| t0013 | 0/0 | 8866 | 2 | 2 | 0 | 0 | 0 | 0 | LANCL3_chrX_37566661_37689463 | LANCL3 | copy fasta | chrX | 37566661 | 37689463 |
| t0014 | 0/0 | 8868 | 2 | 2 | 0 | 0 | 0 | 0 | LANCL3_chrX_37566661_37689463 | LANCL3 | copy fasta | chrX | 37566661 | 37689463 |
| t0015 | 0/0 | 8868 | 2 | 2 | 0 | 0 | 0 | 0 | LANCL3_chrX_37566661_37689463 | LANCL3 | copy fasta | chrX | 37566661 | 37689463 |
| t0016 | 0/0 | 8865 | 2 | 2 | 0 | 0 | 0 | 0 | LANCL3_chrX_37566661_37689463 | LANCL3 | copy fasta | chrX | 37566661 | 37689463 |
| t0017 | 0/0 | 8861 | 2 | 0 | 0 | 0 | 0 | 2 | LANCL3_chrX_37566661_37689463 | LANCL3 | copy fasta | chrX | 37566661 | 37689463 |
| t0018 | 0/0 | 8863 | 2 | 0 | 0 | 1 | 0 | 1 | LANCL3_chrX_37566661_37689463 | LANCL3 | copy fasta | chrX | 37566661 | 37689463 |
| t0019 | 0/0 | 8873 | 2 | 2 | 0 | 0 | 0 | 0 | LANCL3_chrX_37566661_37689463 | LANCL3 | copy fasta | chrX | 37566661 | 37689463 |
| t0020 | 0/0 | 8877 | 2 | 2 | 0 | 0 | 0 | 0 | LANCL3_chrX_37566661_37689463 | LANCL3 | copy fasta | chrX | 37566661 | 37689463 |
| t0021 | 0/0 | 8877 | 2 | 1 | 0 | 0 | 0 | 1 | LANCL3_chrX_37566661_37689463 | LANCL3 | copy fasta | chrX | 37566661 | 37689463 |
| t0022 | 0/0 | 8854 | 1 | 1 | 0 | 0 | 0 | 0 | LANCL3_chrX_37566661_37689463 | LANCL3 | copy fasta | chrX | 37566661 | 37689463 |
| t0023 | 0/0 | 8856 | 1 | 1 | 0 | 0 | 0 | 0 | LANCL3_chrX_37566661_37689463 | LANCL3 | copy fasta | chrX | 37566661 | 37689463 |
| t0024 | 0/0 | 8858 | 1 | 1 | 0 | 0 | 0 | 0 | LANCL3_chrX_37566661_37689463 | LANCL3 | copy fasta | chrX | 37566661 | 37689463 |
| t0025 | 0/0 | 8866 | 1 | 0 | 1 | 0 | 0 | 0 | LANCL3_chrX_37566661_37689463 | LANCL3 | copy fasta | chrX | 37566661 | 37689463 |
| t0026 | 0/0 | 8868 | 1 | 0 | 0 | 0 | 0 | 1 | LANCL3_chrX_37566661_37689463 | LANCL3 | copy fasta | chrX | 37566661 | 37689463 |
| t0027 | 0/0 | 8870 | 1 | 1 | 0 | 0 | 0 | 0 | LANCL3_chrX_37566661_37689463 | LANCL3 | copy fasta | chrX | 37566661 | 37689463 |
| t0028 | 0/0 | 8870 | 1 | 0 | 0 | 0 | 0 | 1 | LANCL3_chrX_37566661_37689463 | LANCL3 | copy fasta | chrX | 37566661 | 37689463 |
| t0029 | 0/0 | 8870 | 1 | 1 | 0 | 0 | 0 | 0 | LANCL3_chrX_37566661_37689463 | LANCL3 | copy fasta | chrX | 37566661 | 37689463 |
| t0030 | 0/0 | 8872 | 1 | 0 | 1 | 0 | 0 | 0 | LANCL3_chrX_37566661_37689463 | LANCL3 | copy fasta | chrX | 37566661 | 37689463 |
| t0031 | 0/0 | 8872 | 1 | 1 | 0 | 0 | 0 | 0 | LANCL3_chrX_37566661_37689463 | LANCL3 | copy fasta | chrX | 37566661 | 37689463 |
| t0032 | 0/0 | 8870 | 1 | 1 | 0 | 0 | 0 | 0 | LANCL3_chrX_37566661_37689463 | LANCL3 | copy fasta | chrX | 37566661 | 37689463 |
| t0033 | 0/0 | 8863 | 1 | 1 | 0 | 0 | 0 | 0 | LANCL3_chrX_37566661_37689463 | LANCL3 | copy fasta | chrX | 37566661 | 37689463 |
| t0034 | 0/0 | 8861 | 1 | 0 | 0 | 1 | 0 | 0 | LANCL3_chrX_37566661_37689463 | LANCL3 | copy fasta | chrX | 37566661 | 37689463 |
| t0035 | 0/0 | 8861 | 1 | 0 | 1 | 0 | 0 | 0 | LANCL3_chrX_37566661_37689463 | LANCL3 | copy fasta | chrX | 37566661 | 37689463 |
| t0036 | 0/0 | 8861 | 1 | 0 | 0 | 0 | 1 | 0 | LANCL3_chrX_37566661_37689463 | LANCL3 | copy fasta | chrX | 37566661 | 37689463 |
| t0037 | 0/0 | 8861 | 1 | 0 | 0 | 1 | 0 | 0 | LANCL3_chrX_37566661_37689463 | LANCL3 | copy fasta | chrX | 37566661 | 37689463 |
| t0038 | 0/0 | 8861 | 1 | 0 | 1 | 0 | 0 | 0 | LANCL3_chrX_37566661_37689463 | LANCL3 | copy fasta | chrX | 37566661 | 37689463 |
| t0039 | 0/0 | 8862 | 1 | 0 | 0 | 0 | 0 | 1 | LANCL3_chrX_37566661_37689463 | LANCL3 | copy fasta | chrX | 37566661 | 37689463 |
| t0040 | 0/0 | 8863 | 1 | 1 | 0 | 0 | 0 | 0 | LANCL3_chrX_37566661_37689463 | LANCL3 | copy fasta | chrX | 37566661 | 37689463 |
| t0041 | 1/0 | 8861 | 1 | 0 | 0 | 0 | 0 | 0 | LANCL3_chrX_37566661_37689463 | LANCL3 | copy fasta | chrX | 37566661 | 37689463 |
| t0042 | 0/0 | 8858 | 1 | 0 | 1 | 0 | 0 | 0 | LANCL3_chrX_37566661_37689463 | LANCL3 | copy fasta | chrX | 37566661 | 37689463 |
| t0043 | 0/0 | 8859 | 1 | 1 | 0 | 0 | 0 | 0 | LANCL3_chrX_37566661_37689463 | LANCL3 | copy fasta | chrX | 37566661 | 37689463 |
| t0044 | 0/0 | 8867 | 1 | 1 | 0 | 0 | 0 | 0 | LANCL3_chrX_37566661_37689463 | LANCL3 | copy fasta | chrX | 37566661 | 37689463 |
| t0045 | 0/0 | 8869 | 1 | 1 | 0 | 0 | 0 | 0 | LANCL3_chrX_37566661_37689463 | LANCL3 | copy fasta | chrX | 37566661 | 37689463 |
| t0046 | 0/0 | 8869 | 1 | 1 | 0 | 0 | 0 | 0 | LANCL3_chrX_37566661_37689463 | LANCL3 | copy fasta | chrX | 37566661 | 37689463 |
| t0047 | 0/0 | 8871 | 1 | 1 | 0 | 0 | 0 | 0 | LANCL3_chrX_37566661_37689463 | LANCL3 | copy fasta | chrX | 37566661 | 37689463 |
| t0048 | 0/0 | 8873 | 1 | 1 | 0 | 0 | 0 | 0 | LANCL3_chrX_37566661_37689463 | LANCL3 | copy fasta | chrX | 37566661 | 37689463 |
| t0049 | 0/0 | 8871 | 1 | 1 | 0 | 0 | 0 | 0 | LANCL3_chrX_37566661_37689463 | LANCL3 | copy fasta | chrX | 37566661 | 37689463 |
| t0050 | 0/0 | 8875 | 1 | 1 | 0 | 0 | 0 | 0 | LANCL3_chrX_37566661_37689463 | LANCL3 | copy fasta | chrX | 37566661 | 37689463 |
| t0051 | 0/0 | 8875 | 1 | 1 | 0 | 0 | 0 | 0 | LANCL3_chrX_37566661_37689463 | LANCL3 | copy fasta | chrX | 37566661 | 37689463 |
| t0052 | 0/0 | 8875 | 1 | 0 | 0 | 1 | 0 | 0 | LANCL3_chrX_37566661_37689463 | LANCL3 | copy fasta | chrX | 37566661 | 37689463 |
| t0053 | 0/0 | 8877 | 1 | 1 | 0 | 0 | 0 | 0 | LANCL3_chrX_37566661_37689463 | LANCL3 | copy fasta | chrX | 37566661 | 37689463 |
| t0054 | 0/0 | 8877 | 1 | 1 | 0 | 0 | 0 | 0 | LANCL3_chrX_37566661_37689463 | LANCL3 | copy fasta | chrX | 37566661 | 37689463 |
| t0055 | 0/0 | 8859 | 1 | 0 | 0 | 1 | 0 | 0 | LANCL3_chrX_37566661_37689463 | LANCL3 | copy fasta | chrX | 37566661 | 37689463 |
| ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 4 | 0 | 1 | 3 | 0 | 0 | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| g0002 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| g0003 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| g0004 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| g0005 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| g0006 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| g0018 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| g0049 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| g0066 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| g0076 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| g0105 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| g0110 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| g0121 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| g0174 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1263 | 126 | 17 | 22 | 64 | 5 | 16 | LANCL3_chrX_37566661_37689463 | LANCL3 | copy fasta | chrX | 37566661 | 37689463 |
| a0001c0002 | 0/0 | 1263 | 42 | 24 | 11 | 4 | 0 | 3 | LANCL3_chrX_37566661_37689463 | LANCL3 | copy fasta | chrX | 37566661 | 37689463 |
| a0001c0003 | 0/0 | 1263 | 20 | 20 | 0 | 0 | 0 | 0 | LANCL3_chrX_37566661_37689463 | LANCL3 | copy fasta | chrX | 37566661 | 37689463 |
| a0001c0004 | 0/0 | 1263 | 5 | 5 | 0 | 0 | 0 | 0 | LANCL3_chrX_37566661_37689463 | LANCL3 | copy fasta | chrX | 37566661 | 37689463 |
| a0001c0005 | 0/0 | 1263 | 2 | 0 | 0 | 2 | 0 | 0 | LANCL3_chrX_37566661_37689463 | LANCL3 | copy fasta | chrX | 37566661 | 37689463 |
| a0001c0011 | 0/0 | 1263 | 1 | 0 | 1 | 0 | 0 | 0 | LANCL3_chrX_37566661_37689463 | LANCL3 | copy fasta | chrX | 37566661 | 37689463 |
| a0002c0010 | 0/0 | 1263 | 1 | 0 | 1 | 0 | 0 | 0 | LANCL3_chrX_37566661_37689463 | LANCL3 | copy fasta | chrX | 37566661 | 37689463 |
| a0003c0009 | 0/0 | 1263 | 1 | 0 | 0 | 0 | 0 | 1 | LANCL3_chrX_37566661_37689463 | LANCL3 | copy fasta | chrX | 37566661 | 37689463 |
| a0004c0008 | 0/0 | 1264 | 1 | 0 | 0 | 1 | 0 | 0 | LANCL3_chrX_37566661_37689463 | LANCL3 | copy fasta | chrX | 37566661 | 37689463 |
| a0005c0007 | 0/0 | 1263 | 1 | 1 | 0 | 0 | 0 | 0 | LANCL3_chrX_37566661_37689463 | LANCL3 | copy fasta | chrX | 37566661 | 37689463 |
| a0006c0006 | 0/0 | 1263 | 1 | 1 | 0 | 0 | 0 | 0 | LANCL3_chrX_37566661_37689463 | LANCL3 | copy fasta | chrX | 37566661 | 37689463 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/1 | 10123 | 95 | 3 | 19 | 58 | 4 | 10 | LANCL3_chrX_37566661_37689463 | LANCL3 | copy fasta | chrX | 37566661 | 37689463 |
| a0001c0001t0006 | 0/0 | 10116 | 4 | 0 | 0 | 2 | 0 | 2 | LANCL3_chrX_37566661_37689463 | LANCL3 | copy fasta | chrX | 37566661 | 37689463 |
| a0001c0001t0008 | 0/0 | 10123 | 4 | 4 | 0 | 0 | 0 | 0 | LANCL3_chrX_37566661_37689463 | LANCL3 | copy fasta | chrX | 37566661 | 37689463 |
| a0001c0001t0010 | 0/0 | 10117 | 3 | 3 | 0 | 0 | 0 | 0 | LANCL3_chrX_37566661_37689463 | LANCL3 | copy fasta | chrX | 37566661 | 37689463 |
| a0001c0001t0017 | 0/0 | 10123 | 2 | 0 | 0 | 0 | 0 | 2 | LANCL3_chrX_37566661_37689463 | LANCL3 | copy fasta | chrX | 37566661 | 37689463 |
| a0001c0001t0018 | 0/0 | 10125 | 2 | 0 | 0 | 1 | 0 | 1 | LANCL3_chrX_37566661_37689463 | LANCL3 | copy fasta | chrX | 37566661 | 37689463 |
| a0001c0001t0020 | 0/0 | 10139 | 2 | 2 | 0 | 0 | 0 | 0 | LANCL3_chrX_37566661_37689463 | LANCL3 | copy fasta | chrX | 37566661 | 37689463 |
| a0001c0001t0022 | 0/0 | 10116 | 1 | 1 | 0 | 0 | 0 | 0 | LANCL3_chrX_37566661_37689463 | LANCL3 | copy fasta | chrX | 37566661 | 37689463 |
| a0001c0001t0031 | 0/0 | 10134 | 1 | 1 | 0 | 0 | 0 | 0 | LANCL3_chrX_37566661_37689463 | LANCL3 | copy fasta | chrX | 37566661 | 37689463 |
| a0001c0001t0034 | 0/0 | 10123 | 1 | 0 | 0 | 1 | 0 | 0 | LANCL3_chrX_37566661_37689463 | LANCL3 | copy fasta | chrX | 37566661 | 37689463 |
| a0001c0001t0035 | 0/0 | 10123 | 1 | 0 | 1 | 0 | 0 | 0 | LANCL3_chrX_37566661_37689463 | LANCL3 | copy fasta | chrX | 37566661 | 37689463 |
| a0001c0001t0036 | 0/0 | 10123 | 1 | 0 | 0 | 0 | 1 | 0 | LANCL3_chrX_37566661_37689463 | LANCL3 | copy fasta | chrX | 37566661 | 37689463 |
| a0001c0001t0037 | 0/0 | 10123 | 1 | 0 | 0 | 1 | 0 | 0 | LANCL3_chrX_37566661_37689463 | LANCL3 | copy fasta | chrX | 37566661 | 37689463 |
| a0001c0001t0038 | 0/0 | 10123 | 1 | 0 | 1 | 0 | 0 | 0 | LANCL3_chrX_37566661_37689463 | LANCL3 | copy fasta | chrX | 37566661 | 37689463 |
| a0001c0001t0039 | 0/0 | 10124 | 1 | 0 | 0 | 0 | 0 | 1 | LANCL3_chrX_37566661_37689463 | LANCL3 | copy fasta | chrX | 37566661 | 37689463 |
| a0001c0001t0040 | 0/0 | 10125 | 1 | 1 | 0 | 0 | 0 | 0 | LANCL3_chrX_37566661_37689463 | LANCL3 | copy fasta | chrX | 37566661 | 37689463 |
| a0001c0001t0041 | 1/0 | 10123 | 1 | 0 | 0 | 0 | 0 | 0 | LANCL3_chrX_37566661_37689463 | LANCL3 | copy fasta | chrX | 37566661 | 37689463 |
| a0001c0001t0042 | 0/0 | 10120 | 1 | 0 | 1 | 0 | 0 | 0 | LANCL3_chrX_37566661_37689463 | LANCL3 | copy fasta | chrX | 37566661 | 37689463 |
| a0001c0001t0043 | 0/0 | 10121 | 1 | 1 | 0 | 0 | 0 | 0 | LANCL3_chrX_37566661_37689463 | LANCL3 | copy fasta | chrX | 37566661 | 37689463 |
| a0001c0001t0048 | 0/0 | 10135 | 1 | 1 | 0 | 0 | 0 | 0 | LANCL3_chrX_37566661_37689463 | LANCL3 | copy fasta | chrX | 37566661 | 37689463 |
| a0001c0001t0055 | 0/0 | 10121 | 1 | 0 | 0 | 1 | 0 | 0 | LANCL3_chrX_37566661_37689463 | LANCL3 | copy fasta | chrX | 37566661 | 37689463 |
| a0001c0002t0002 | 0/0 | 10130 | 9 | 6 | 3 | 0 | 0 | 0 | LANCL3_chrX_37566661_37689463 | LANCL3 | copy fasta | chrX | 37566661 | 37689463 |
| a0001c0002t0003 | 0/0 | 10133 | 8 | 0 | 6 | 2 | 0 | 0 | LANCL3_chrX_37566661_37689463 | LANCL3 | copy fasta | chrX | 37566661 | 37689463 |
| a0001c0002t0004 | 0/0 | 10132 | 5 | 4 | 0 | 0 | 0 | 1 | LANCL3_chrX_37566661_37689463 | LANCL3 | copy fasta | chrX | 37566661 | 37689463 |
| a0001c0002t0011 | 0/0 | 10126 | 2 | 0 | 1 | 1 | 0 | 0 | LANCL3_chrX_37566661_37689463 | LANCL3 | copy fasta | chrX | 37566661 | 37689463 |
| a0001c0002t0014 | 0/0 | 10130 | 2 | 2 | 0 | 0 | 0 | 0 | LANCL3_chrX_37566661_37689463 | LANCL3 | copy fasta | chrX | 37566661 | 37689463 |
| a0001c0002t0016 | 0/0 | 10127 | 2 | 2 | 0 | 0 | 0 | 0 | LANCL3_chrX_37566661_37689463 | LANCL3 | copy fasta | chrX | 37566661 | 37689463 |
| a0001c0002t0019 | 0/0 | 10135 | 1 | 1 | 0 | 0 | 0 | 0 | LANCL3_chrX_37566661_37689463 | LANCL3 | copy fasta | chrX | 37566661 | 37689463 |
| a0001c0002t0021 | 0/0 | 10139 | 1 | 1 | 0 | 0 | 0 | 0 | LANCL3_chrX_37566661_37689463 | LANCL3 | copy fasta | chrX | 37566661 | 37689463 |
| a0001c0002t0026 | 0/0 | 10130 | 1 | 0 | 0 | 0 | 0 | 1 | LANCL3_chrX_37566661_37689463 | LANCL3 | copy fasta | chrX | 37566661 | 37689463 |
| a0001c0002t0027 | 0/0 | 10132 | 1 | 1 | 0 | 0 | 0 | 0 | LANCL3_chrX_37566661_37689463 | LANCL3 | copy fasta | chrX | 37566661 | 37689463 |
| a0001c0002t0028 | 0/0 | 10132 | 1 | 0 | 0 | 0 | 0 | 1 | LANCL3_chrX_37566661_37689463 | LANCL3 | copy fasta | chrX | 37566661 | 37689463 |
| a0001c0002t0030 | 0/0 | 10134 | 1 | 0 | 1 | 0 | 0 | 0 | LANCL3_chrX_37566661_37689463 | LANCL3 | copy fasta | chrX | 37566661 | 37689463 |
| a0001c0002t0032 | 0/0 | 10132 | 1 | 1 | 0 | 0 | 0 | 0 | LANCL3_chrX_37566661_37689463 | LANCL3 | copy fasta | chrX | 37566661 | 37689463 |
| a0001c0002t0033 | 0/0 | 10125 | 1 | 1 | 0 | 0 | 0 | 0 | LANCL3_chrX_37566661_37689463 | LANCL3 | copy fasta | chrX | 37566661 | 37689463 |
| a0001c0002t0045 | 0/0 | 10131 | 1 | 1 | 0 | 0 | 0 | 0 | LANCL3_chrX_37566661_37689463 | LANCL3 | copy fasta | chrX | 37566661 | 37689463 |
| a0001c0002t0049 | 0/0 | 10133 | 1 | 1 | 0 | 0 | 0 | 0 | LANCL3_chrX_37566661_37689463 | LANCL3 | copy fasta | chrX | 37566661 | 37689463 |
| a0001c0002t0051 | 0/0 | 10137 | 1 | 1 | 0 | 0 | 0 | 0 | LANCL3_chrX_37566661_37689463 | LANCL3 | copy fasta | chrX | 37566661 | 37689463 |
| a0001c0002t0052 | 0/0 | 10137 | 1 | 0 | 0 | 1 | 0 | 0 | LANCL3_chrX_37566661_37689463 | LANCL3 | copy fasta | chrX | 37566661 | 37689463 |
| a0001c0002t0053 | 0/0 | 10139 | 1 | 1 | 0 | 0 | 0 | 0 | LANCL3_chrX_37566661_37689463 | LANCL3 | copy fasta | chrX | 37566661 | 37689463 |
| a0001c0002t0054 | 0/0 | 10139 | 1 | 1 | 0 | 0 | 0 | 0 | LANCL3_chrX_37566661_37689463 | LANCL3 | copy fasta | chrX | 37566661 | 37689463 |
| a0001c0003t0005 | 0/0 | 10135 | 5 | 5 | 0 | 0 | 0 | 0 | LANCL3_chrX_37566661_37689463 | LANCL3 | copy fasta | chrX | 37566661 | 37689463 |
| a0001c0003t0007 | 0/0 | 10128 | 4 | 4 | 0 | 0 | 0 | 0 | LANCL3_chrX_37566661_37689463 | LANCL3 | copy fasta | chrX | 37566661 | 37689463 |
| a0001c0003t0012 | 0/0 | 10126 | 2 | 2 | 0 | 0 | 0 | 0 | LANCL3_chrX_37566661_37689463 | LANCL3 | copy fasta | chrX | 37566661 | 37689463 |
| a0001c0003t0013 | 0/0 | 10128 | 2 | 2 | 0 | 0 | 0 | 0 | LANCL3_chrX_37566661_37689463 | LANCL3 | copy fasta | chrX | 37566661 | 37689463 |
| a0001c0003t0015 | 0/0 | 10130 | 2 | 2 | 0 | 0 | 0 | 0 | LANCL3_chrX_37566661_37689463 | LANCL3 | copy fasta | chrX | 37566661 | 37689463 |
| a0001c0003t0024 | 0/0 | 10120 | 1 | 1 | 0 | 0 | 0 | 0 | LANCL3_chrX_37566661_37689463 | LANCL3 | copy fasta | chrX | 37566661 | 37689463 |
| a0001c0003t0029 | 0/0 | 10132 | 1 | 1 | 0 | 0 | 0 | 0 | LANCL3_chrX_37566661_37689463 | LANCL3 | copy fasta | chrX | 37566661 | 37689463 |
| a0001c0003t0046 | 0/0 | 10131 | 1 | 1 | 0 | 0 | 0 | 0 | LANCL3_chrX_37566661_37689463 | LANCL3 | copy fasta | chrX | 37566661 | 37689463 |
| a0001c0003t0047 | 0/0 | 10133 | 1 | 1 | 0 | 0 | 0 | 0 | LANCL3_chrX_37566661_37689463 | LANCL3 | copy fasta | chrX | 37566661 | 37689463 |
| a0001c0003t0050 | 0/0 | 10137 | 1 | 1 | 0 | 0 | 0 | 0 | LANCL3_chrX_37566661_37689463 | LANCL3 | copy fasta | chrX | 37566661 | 37689463 |
| a0001c0004t0009 | 0/0 | 10132 | 4 | 4 | 0 | 0 | 0 | 0 | LANCL3_chrX_37566661_37689463 | LANCL3 | copy fasta | chrX | 37566661 | 37689463 |
| a0001c0004t0023 | 0/0 | 10118 | 1 | 1 | 0 | 0 | 0 | 0 | LANCL3_chrX_37566661_37689463 | LANCL3 | copy fasta | chrX | 37566661 | 37689463 |
| a0001c0005t0001 | 0/0 | 10123 | 2 | 0 | 0 | 2 | 0 | 0 | LANCL3_chrX_37566661_37689463 | LANCL3 | copy fasta | chrX | 37566661 | 37689463 |
| a0001c0011t0001 | 0/0 | 10123 | 1 | 0 | 1 | 0 | 0 | 0 | LANCL3_chrX_37566661_37689463 | LANCL3 | copy fasta | chrX | 37566661 | 37689463 |
| a0002c0010t0025 | 0/0 | 10128 | 1 | 0 | 1 | 0 | 0 | 0 | LANCL3_chrX_37566661_37689463 | LANCL3 | copy fasta | chrX | 37566661 | 37689463 |
| a0003c0009t0021 | 0/0 | 10139 | 1 | 0 | 0 | 0 | 0 | 1 | LANCL3_chrX_37566661_37689463 | LANCL3 | copy fasta | chrX | 37566661 | 37689463 |
| a0004c0008t0011 | 0/0 | 10127 | 1 | 0 | 0 | 1 | 0 | 0 | LANCL3_chrX_37566661_37689463 | LANCL3 | copy fasta | chrX | 37566661 | 37689463 |
| a0005c0007t0044 | 0/0 | 10129 | 1 | 1 | 0 | 0 | 0 | 0 | LANCL3_chrX_37566661_37689463 | LANCL3 | copy fasta | chrX | 37566661 | 37689463 |
| a0006c0006t0019 | 0/0 | 10135 | 1 | 1 | 0 | 0 | 0 | 0 | LANCL3_chrX_37566661_37689463 | LANCL3 | copy fasta | chrX | 37566661 | 37689463 |
| actghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| a0001c0001t0001g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| a0001c0001t0001g0004 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| a0001c0001t0001g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| a0001c0001t0001g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| a0001c0001t0001g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| a0001c0001t0001g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| a0001c0001t0001g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| a0001c0001t0001g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| a0001c0001t0001g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| a0001c0001t0001g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| a0001c0001t0001g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| a0001c0001t0001g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| a0001c0001t0001g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| a0001c0001t0001g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| a0001c0001t0001g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| a0001c0001t0001g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| a0001c0001t0001g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| a0001c0001t0001g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| a0001c0001t0001g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| a0001c0001t0001g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| a0001c0001t0001g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| a0001c0001t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| a0001c0001t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| a0001c0001t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| a0001c0001t0001g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| a0001c0001t0001g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| a0001c0001t0001g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| a0001c0001t0001g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| a0001c0001t0001g0174 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| a0001c0001t0006g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| a0001c0001t0006g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| a0001c0001t0006g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| a0001c0001t0006g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| a0001c0001t0008g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| a0001c0001t0008g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| a0001c0001t0008g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| a0001c0001t0008g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| a0001c0001t0010g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| a0001c0001t0010g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| a0001c0001t0010g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| a0001c0001t0017g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| a0001c0001t0017g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| a0001c0001t0018g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| a0001c0001t0018g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| a0001c0001t0020g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| a0001c0001t0020g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| a0001c0001t0022g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| a0001c0001t0031g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| a0001c0001t0034g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| a0001c0001t0035g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| a0001c0001t0036g0110 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| a0001c0001t0037g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| a0001c0001t0038g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| a0001c0001t0039g0018 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| a0001c0001t0040g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| a0001c0001t0041g0066 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| a0001c0001t0042g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| a0001c0001t0043g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| a0001c0001t0048g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| a0001c0001t0055g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| a0001c0002t0002g0002 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| a0001c0002t0002g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| a0001c0002t0002g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| a0001c0002t0002g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| a0001c0002t0002g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| a0001c0002t0002g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| a0001c0002t0003g0005 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| a0001c0002t0003g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| a0001c0002t0003g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| a0001c0002t0003g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| a0001c0002t0003g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| a0001c0002t0003g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| a0001c0002t0003g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| a0001c0002t0004g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| a0001c0002t0004g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| a0001c0002t0004g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| a0001c0002t0004g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| a0001c0002t0004g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| a0001c0002t0011g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| a0001c0002t0011g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| a0001c0002t0014g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| a0001c0002t0014g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| a0001c0002t0016g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| a0001c0002t0016g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| a0001c0002t0019g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| a0001c0002t0021g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| a0001c0002t0026g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| a0001c0002t0027g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| a0001c0002t0028g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| a0001c0002t0030g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| a0001c0002t0032g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| a0001c0002t0033g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| a0001c0002t0045g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| a0001c0002t0049g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| a0001c0002t0051g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| a0001c0002t0052g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| a0001c0002t0053g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| a0001c0002t0054g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| a0001c0003t0005g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| a0001c0003t0005g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| a0001c0003t0005g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| a0001c0003t0005g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| a0001c0003t0005g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| a0001c0003t0007g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| a0001c0003t0007g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| a0001c0003t0007g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| a0001c0003t0007g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| a0001c0003t0012g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| a0001c0003t0012g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| a0001c0003t0013g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| a0001c0003t0013g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| a0001c0003t0015g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| a0001c0003t0015g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| a0001c0003t0024g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| a0001c0003t0029g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| a0001c0003t0046g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| a0001c0003t0047g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| a0001c0003t0050g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| a0001c0004t0009g0006 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| a0001c0004t0009g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| a0001c0004t0009g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| a0001c0004t0023g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| a0001c0005t0001g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| a0001c0005t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| a0001c0011t0001g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| a0002c0010t0025g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| a0003c0009t0021g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| a0004c0008t0011g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| a0005c0007t0044g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| a0006c0006t0019g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0076 | EUR | GBR | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| HG00280 | hp1 | a0001 | c0001 | t0036 | g0110 | EUR | FIN | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0074 | EAS | CHS | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0022 | EAS | CHS | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| HG00639 | hp1 | a0001 | c0002 | t0003 | g0005 | AMR | PUR | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| HG00639 | hp2 | a0001 | c0002 | t0011 | g0140 | AMR | PUR | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0039 | AMR | PUR | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0032 | EAS | CHS | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| HG00735 | hp1 | a0001 | c0002 | t0002 | g0135 | AMR | PUR | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0067 | AMR | PUR | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| HG00738 | hp1 | a0001 | c0001 | t0042 | g0087 | AMR | PUR | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| HG01069 | hp1 | a0001 | c0002 | t0003 | g0117 | AMR | PUR | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| HG01070 | hp1 | a0001 | c0002 | t0002 | g0158 | AMR | PUR | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| HG01071 | hp1 | a0001 | c0002 | t0003 | g0005 | AMR | PUR | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0078 | AMR | PUR | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| HG01081 | hp1 | a0001 | c0002 | t0002 | g0159 | AMR | PUR | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0093 | AMR | PUR | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0118 | AMR | PUR | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0114 | AMR | PUR | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0020 | AMR | PUR | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| HG01167 | hp1 | a0001 | c0001 | t0035 | g0112 | AMR | PUR | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0175 | AMR | PUR | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| HG01243 | hp1 | a0001 | c0002 | t0003 | g0061 | AMR | PUR | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| HG01255 | hp1 | a0001 | c0002 | t0030 | g0153 | AMR | CLM | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0068 | AMR | CLM | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| HG01258 | hp1 | a0001 | c0011 | t0001 | g0123 | AMR | CLM | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0060 | AMR | CLM | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0059 | AMR | CLM | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| HG01361 | hp1 | a0001 | c0002 | t0003 | g0069 | AMR | CLM | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0051 | AMR | CLM | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| HG01433 | hp1 | a0001 | c0001 | t0038 | g0109 | AMR | CLM | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0105 | EUR | IBS | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| HG01884 | hp1 | a0001 | c0001 | t0008 | g0186 | AFR | ACB | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| HG01884 | hp2 | a0001 | c0002 | t0019 | g0057 | AFR | ACB | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| HG01891 | hp1 | a0001 | c0002 | t0004 | g0133 | AFR | ACB | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| HG01891 | hp2 | a0001 | c0003 | t0007 | g0152 | AFR | ACB | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0098 | AMR | PEL | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0095 | AMR | PEL | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0100 | AMR | PEL | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0036 | EAS | KHV | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0037 | EAS | KHV | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0092 | EAS | KHV | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| HG02055 | hp1 | a0001 | c0004 | t0023 | g0165 | AFR | ACB | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0042 | EAS | KHV | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0089 | EAS | KHV | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0094 | EAS | KHV | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| HG02083 | hp1 | a0001 | c0001 | t0006 | g0143 | EAS | KHV | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0103 | EAS | KHV | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0070 | EAS | KHV | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | KHV | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| HG02145 | hp1 | a0001 | c0001 | t0010 | g0148 | AFR | ACB | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| HG02148 | hp1 | a0001 | c0002 | t0003 | g0040 | AMR | PEL | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0017 | AMR | PEL | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| HG02257 | hp1 | a0001 | c0002 | t0049 | g0127 | AFR | ACB | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| HG02257 | hp2 | a0001 | c0002 | t0002 | g0160 | AFR | ACB | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| HG02258 | hp1 | a0001 | c0001 | t0022 | g0150 | AFR | ACB | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| HG02300 | hp1 | a0002 | c0010 | t0025 | g0145 | AMR | PEL | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| HG02451 | hp1 | a0001 | c0002 | t0002 | g0002 | AFR | ACB | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| HG02451 | hp2 | a0001 | c0001 | t0040 | g0072 | AFR | ACB | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| HG02572 | hp1 | a0001 | c0002 | t0032 | g0166 | AFR | GWD | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| HG02602 | hp1 | a0001 | c0001 | t0017 | g0086 | SAS | PJL | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| HG02615 | hp1 | a0001 | c0004 | t0009 | g0179 | AFR | GWD | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| HG02615 | hp2 | a0001 | c0003 | t0024 | g0136 | AFR | GWD | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| HG02622 | hp1 | a0001 | c0003 | t0012 | g0161 | AFR | GWD | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| HG02622 | hp2 | a0001 | c0003 | t0005 | g0119 | AFR | GWD | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| HG02630 | hp1 | a0001 | c0001 | t0008 | g0184 | AFR | GWD | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| HG02630 | hp2 | a0005 | c0007 | t0044 | g0064 | AFR | GWD | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| HG02647 | hp1 | a0001 | c0003 | t0005 | g0010 | AFR | GWD | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0046 | SAS | PJL | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| HG02683 | hp2 | a0001 | c0002 | t0028 | g0139 | SAS | PJL | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| HG02698 | hp1 | a0001 | c0002 | t0026 | g0142 | SAS | PJL | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| HG02717 | hp1 | a0001 | c0001 | t0043 | g0056 | AFR | GWD | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| HG02723 | hp1 | a0001 | c0002 | t0021 | g0054 | AFR | GWD | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| HG02723 | hp2 | a0001 | c0002 | t0002 | g0002 | AFR | GWD | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| HG02735 | hp1 | a0001 | c0001 | t0017 | g0083 | SAS | PJL | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| HG02738 | hp1 | a0001 | c0001 | t0039 | g0018 | SAS | PJL | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| HG02809 | hp1 | a0001 | c0001 | t0020 | g0104 | AFR | GWD | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| HG02809 | hp2 | a0001 | c0002 | t0014 | g0156 | AFR | GWD | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| HG02818 | hp1 | a0001 | c0001 | t0008 | g0088 | AFR | GWD | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| HG02818 | hp2 | a0001 | c0003 | t0015 | g0168 | AFR | GWD | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| HG02895 | hp1 | a0001 | c0003 | t0013 | g0170 | AFR | GWD | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0071 | AFR | GWD | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| HG02896 | hp2 | a0001 | c0004 | t0009 | g0006 | AFR | GWD | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| HG02897 | hp1 | a0001 | c0004 | t0009 | g0006 | AFR | GWD | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| HG02897 | hp2 | a0001 | c0003 | t0013 | g0171 | AFR | GWD | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| HG02922 | hp1 | a0001 | c0002 | t0004 | g0138 | AFR | ESN | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| HG02922 | hp2 | a0001 | c0003 | t0007 | g0151 | AFR | ESN | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| HG02965 | hp1 | a0001 | c0003 | t0005 | g0183 | AFR | ESN | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| HG02970 | hp1 | a0001 | c0002 | t0016 | g0177 | AFR | ESN | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| HG02970 | hp2 | a0001 | c0002 | t0051 | g0180 | AFR | ESN | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0122 | SAS | PJL | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| HG03041 | hp1 | a0001 | c0003 | t0015 | g0169 | AFR | GWD | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| HG03041 | hp2 | a0001 | c0002 | t0002 | g0002 | AFR | GWD | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| HG03098 | hp1 | a0001 | c0003 | t0007 | g0134 | AFR | MSL | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| HG03130 | hp1 | a0001 | c0001 | t0048 | g0009 | AFR | ESN | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| HG03139 | hp1 | a0001 | c0001 | t0010 | g0146 | AFR | ESN | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| HG03195 | hp1 | a0001 | c0003 | t0005 | g0007 | AFR | ESN | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| HG03195 | hp2 | a0001 | c0002 | t0053 | g0181 | AFR | ESN | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| HG03209 | hp1 | a0001 | c0002 | t0045 | g0008 | AFR | MSL | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| HG03225 | hp1 | a0001 | c0002 | t0033 | g0172 | AFR | MSL | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| HG03453 | hp1 | a0001 | c0003 | t0050 | g0188 | AFR | MSL | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| HG03453 | hp2 | a0001 | c0003 | t0007 | g0154 | AFR | MSL | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| HG03486 | hp1 | a0001 | c0002 | t0002 | g0157 | AFR | MSL | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| HG03486 | hp2 | a0001 | c0002 | t0004 | g0149 | AFR | MSL | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| HG03490 | hp1 | a0001 | c0001 | t0006 | g0137 | SAS | PJL | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| HG03492 | hp1 | a0001 | c0001 | t0006 | g0144 | SAS | PJL | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| HG03516 | hp1 | a0001 | c0003 | t0029 | g0132 | AFR | ESN | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| HG03516 | hp2 | a0001 | c0002 | t0014 | g0131 | AFR | ESN | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| HG03540 | hp1 | a0001 | c0001 | t0020 | g0052 | AFR | GWD | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| HG03540 | hp2 | a0001 | c0003 | t0047 | g0189 | AFR | GWD | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| HG03579 | hp1 | a0001 | c0003 | t0005 | g0182 | AFR | MSL | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0045 | SAS | PJL | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| HG03669 | hp1 | a0001 | c0002 | t0004 | g0141 | SAS | PJL | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0126 | SAS | PJL | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0062 | SAS | STU | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0111 | SAS | PJL | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| HG03942 | hp1 | a0001 | c0001 | t0018 | g0116 | SAS | BEB | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0091 | SAS | STU | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0113 | SAS | STU | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0102 | SAS | STU | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| HG04228 | hp1 | a0003 | c0009 | t0021 | g0190 | SAS | STU | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0065 | AFR | YRI | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| NA18612 | hp1 | a0001 | c0001 | t0006 | g0164 | EAS | CHB | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0081 | EAS | CHB | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| NA18906 | hp1 | a0001 | c0002 | t0027 | g0155 | AFR | YRI | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| NA18906 | hp2 | a0001 | c0003 | t0012 | g0163 | AFR | YRI | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0044 | EAS | JPT | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0043 | EAS | JPT | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0047 | EAS | JPT | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| NA18960 | hp1 | a0001 | c0001 | t0037 | g0001 | EAS | JPT | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| NA18965 | hp1 | a0001 | c0001 | t0034 | g0048 | EAS | JPT | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| NA18966 | hp1 | a0001 | c0005 | t0001 | g0096 | EAS | JPT | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| NA18974 | hp1 | a0004 | c0008 | t0011 | g0130 | EAS | JPT | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0097 | EAS | JPT | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| NA18984 | hp1 | a0001 | c0002 | t0003 | g0075 | EAS | JPT | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| NA18985 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| NA18986 | hp1 | a0001 | c0005 | t0001 | g0003 | EAS | JPT | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| NA18988 | hp1 | a0001 | c0001 | t0001 | g0079 | EAS | JPT | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0099 | EAS | JPT | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0063 | EAS | JPT | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0084 | EAS | JPT | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0077 | EAS | JPT | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| NA19006 | hp1 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| NA19030 | hp1 | a0001 | c0002 | t0004 | g0167 | AFR | LWK | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| NA19030 | hp2 | a0001 | c0002 | t0016 | g0176 | AFR | LWK | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| NA19043 | hp1 | a0001 | c0002 | t0054 | g0185 | AFR | LWK | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0125 | EAS | JPT | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| NA19058 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0058 | EAS | JPT | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0055 | EAS | JPT | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| NA19072 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| NA19075 | hp1 | a0001 | c0001 | t0001 | g0082 | EAS | JPT | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| NA19076 | hp1 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| NA19077 | hp1 | a0001 | c0002 | t0052 | g0023 | EAS | JPT | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0053 | EAS | JPT | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0073 | EAS | JPT | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| NA19082 | hp1 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| NA19083 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| NA19086 | hp1 | a0001 | c0001 | t0018 | g0128 | EAS | JPT | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| NA19089 | hp2 | a0001 | c0002 | t0003 | g0026 | EAS | JPT | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| NA19091 | hp1 | a0001 | c0002 | t0011 | g0173 | EAS | JPT | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| NA19240 | hp1 | a0001 | c0001 | t0031 | g0162 | AFR | YRI | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| NA19240 | hp2 | a0001 | c0001 | t0008 | g0187 | AFR | YRI | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| NA20129 | hp1 | a0006 | c0006 | t0019 | g0038 | AFR | ASW | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| NA20129 | hp2 | a0001 | c0002 | t0002 | g0002 | AFR | ASW | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0049 | EUR | TSI | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0121 | EUR | TSI | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0115 | SAS | GIH | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| HG02109 | hp1 | a0001 | c0001 | t0010 | g0147 | AFR | ACB | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| HG02109 | hp2 | a0001 | c0004 | t0009 | g0178 | AFR | ACB | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0050 | AFR | ACB | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| HG03471 | hp1 | a0001 | c0003 | t0046 | g0011 | AFR | MSL | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| NA18955 | hp1 | a0001 | c0001 | t0055 | g0035 | EAS | JPT | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0174 | REF | REF | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0041 | g0066 | REF | REF | LANCL3_chrX_37566661_37689463 | LANCL3 | chrX | 37566661 | 37689463 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chrX:37572324
|
G | A | 1 | a0006 | 1 | NA20129.hp1 | missense_variant | MODERATE | c.454G>A | p.Ala152Thr | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/5 | 664/10123 | 454/1263 | 152/420 | chrX | 37572324 | ||
| chrX:37572363
|
T | C | 1 | a0005 | 1 | HG02630.hp2 | missense_variant | MODERATE | c.493T>C | p.Cys165Arg | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/5 | 703/10123 | 493/1263 | 165/420 | chrX | 37572363 | ||
| chrX:37659479
|
T | TC | 1 | a0004 | 1 | NA18974.hp1 | frameshift_variant | HIGH | c.716dupC | p.Ser240fs | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 3/5 | 927/10123 | 717/1263 | 239/420 | INFO_REALIGN_3_PRIME | chrX | 37659479 | |
| chrX:37659585
|
G | A | 1 | a0003 | 1 | HG04228.hp1 | missense_variant | MODERATE | c.821G>A | p.Cys274Tyr | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 3/5 | 1031/10123 | 821/1263 | 274/420 | chrX | 37659585 | ||
| chrX:37659626
|
A | T | 1 | a0002 | 1 | HG02300.hp1 | missense_variant | MODERATE | c.862A>T | p.Asn288Tyr | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 3/5 | 1072/10123 | 862/1263 | 288/420 | chrX | 37659626 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chrX:37571981
|
C | T | 1 | a0001c0005 | 2 | NA18966.hp1 NA18986.hp1 |
synonymous_variant | LOW | c.111C>T | p.Arg37Arg | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/5 | 321/10123 | 111/1263 | 37/420 | chrX | 37571981 | ||
| chrX:37572344
|
G | T | 1 | a0001c0011 | 1 | HG01258.hp1 | synonymous_variant | LOW | c.474G>T | p.Ala158Ala | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/5 | 684/10123 | 474/1263 | 158/420 | chrX | 37572344 | ||
| chrX:37659553
|
C | T | 8 | a0001c0002a0001c0003a0001c0004others(5): Show | 72 | HG00639.hp1 HG00639.hp2 HG00735.hp1 others(69): Show |
synonymous_variant | LOW | c.789C>T | p.Ser263Ser | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 3/5 | 999/10123 | 789/1263 | 263/420 | chrX | 37659553 | ||
| chrX:37659631
|
G | A | 1 | a0001c0004 | 5 | HG02055.hp1 HG02109.hp2 HG02615.hp1 others(2): Show |
synonymous_variant | LOW | c.867G>A | p.Glu289Glu | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 3/5 | 1077/10123 | 867/1263 | 289/420 | chrX | 37659631 | ||
| chrX:37675663
|
A | G | 1 | a0001c0003 | 20 | HG01891.hp2 HG02615.hp2 HG02622.hp1 others(17): Show |
synonymous_variant | LOW | c.1113A>G | p.Gln371Gln | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 5/5 | 1323/10123 | 1113/1263 | 371/420 | chrX | 37675663 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chrX:37571679
|
AGCCCGGC | A | 24 | a0001c0001t0006a0001c0001t0010a0001c0001t0022others(21): Show | 50 | HG00639.hp2 HG00735.hp1 HG01070.hp1 others(47): Show |
5_prime_UTR_variant | MODIFIER | c.-187_-181delGGCGCC others(1): Show |
LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/5 | 181 | INFO_REALIGN_3_PRIME | chrX | 37571679 | ||||
| chrX:37675850
|
CCT | C | 1 | a0001c0001t0055 | 1 | NA18955.hp1 | 3_prime_UTR_variant | MODIFIER | c.*38_*39delCT | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 5/5 | 38 | chrX | 37675850 | |||||
| chrX:37675894
|
GT | G | 1 | a0001c0001t0010 | 3 | HG02109.hp1 HG02145.hp1 HG03139.hp1 |
3_prime_UTR_variant | MODIFIER | c.*82delT | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 5/5 | 82 | chrX | 37675894 | |||||
| chrX:37676231
|
A | G | 2 | a0001c0002t0016a0001c0002t0033 | 3 | HG02970.hp1 HG03225.hp1 NA19030.hp2 |
3_prime_UTR_variant | MODIFIER | c.*418A>G | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 5/5 | 418 | chrX | 37676231 | |||||
| chrX:37677138
|
A | ATG | 3 | a0001c0001t0010a0001c0001t0018a0001c0004t0023 | 6 | HG02055.hp1 HG02109.hp1 HG02145.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1353_*1354dupGT | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 5/5 | 1355 | INFO_REALIGN_3_PRIME | chrX | 37677138 | ||||
| chrX:37677138
|
A | ATGTG | 1 | a0001c0003t0024 | 1 | HG02615.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1351_*1354dupGTGT | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 5/5 | 1355 | INFO_REALIGN_3_PRIME | chrX | 37677138 | ||||
| chrX:37677138
|
A | ATGTGTG | 1 | a0005c0007t0044 | 1 | HG02630.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1349_*1354dupGTGT others(2): Show |
LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 5/5 | 1355 | INFO_REALIGN_3_PRIME | chrX | 37677138 | ||||
| chrX:37677138
|
A | ATGTGTGT others(1): Show |
2 | a0001c0002t0045a0001c0003t0046 | 2 | HG03209.hp1 HG03471.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1347_*1354dupGTGT others(4): Show |
LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 5/5 | 1355 | INFO_REALIGN_3_PRIME | chrX | 37677138 | ||||
| chrX:37677138
|
A | ATGTGTGT others(3): Show |
9 | a0001c0001t0048a0001c0002t0003a0001c0002t0011others(6): Show | 21 | HG00639.hp1 HG00639.hp2 HG01069.hp1 others(18): Show |
3_prime_UTR_variant | MODIFIER | c.*1345_*1354dupGTGT others(6): Show |
LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 5/5 | 1355 | INFO_REALIGN_3_PRIME | chrX | 37677138 | ||||
| chrX:37677138
|
A | ATGTGTGT others(5): Show |
7 | a0001c0002t0016a0001c0002t0019a0001c0003t0005others(4): Show | 16 | HG01884.hp2 HG01891.hp2 HG02300.hp1 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*1343_*1354dupGTGT others(8): Show |
LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 5/5 | 1355 | INFO_REALIGN_3_PRIME | chrX | 37677138 | ||||
| chrX:37677138
|
A | ATGTGTGT others(7): Show |
8 | a0001c0001t0020a0001c0002t0002a0001c0002t0014others(5): Show | 19 | HG00735.hp1 HG01070.hp1 HG01081.hp1 others(16): Show |
3_prime_UTR_variant | MODIFIER | c.*1341_*1354dupGTGT others(10): Show |
LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 5/5 | 1355 | INFO_REALIGN_3_PRIME | chrX | 37677138 | ||||
| chrX:37677138
|
A | ATGTGTGT others(9): Show |
11 | a0001c0001t0031a0001c0002t0004a0001c0002t0021others(8): Show | 15 | HG01255.hp1 HG01891.hp1 HG02572.hp1 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*1339_*1354dupGTGT others(12): Show |
LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 5/5 | 1355 | INFO_REALIGN_3_PRIME | chrX | 37677138 | ||||
| chrX:37677236
|
C | T | 3 | a0001c0001t0008a0001c0001t0022a0001c0001t0043 | 6 | HG01884.hp1 HG02258.hp1 HG02630.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1423C>T | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 5/5 | 1423 | chrX | 37677236 | |||||
| chrX:37677313
|
G | C | 3 | a0001c0003t0005a0001c0003t0007a0001c0003t0013 | 11 | HG01891.hp2 HG02622.hp2 HG02647.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*1500G>C | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 5/5 | 1500 | chrX | 37677313 | |||||
| chrX:37678156
|
AAAC | A | 1 | a0001c0001t0042 | 1 | HG00738.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2349_*2351delCAA | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 5/5 | 2349 | INFO_REALIGN_3_PRIME | chrX | 37678156 | ||||
| chrX:37678179
|
C | A | 40 | a0001c0001t0020a0001c0001t0031a0001c0001t0048others(37): Show | 76 | HG00639.hp1 HG00639.hp2 HG00735.hp1 others(73): Show |
3_prime_UTR_variant | MODIFIER | c.*2366C>A | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 5/5 | 2366 | chrX | 37678179 | |||||
| chrX:37678306
|
T | A | 40 | a0001c0001t0020a0001c0001t0031a0001c0001t0048others(37): Show | 76 | HG00639.hp1 HG00639.hp2 HG00735.hp1 others(73): Show |
3_prime_UTR_variant | MODIFIER | c.*2493T>A | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 5/5 | 2493 | chrX | 37678306 | |||||
| chrX:37678491
|
T | C | 2 | a0001c0002t0014a0001c0002t0027 | 3 | HG02809.hp2 HG03516.hp2 NA18906.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2678T>C | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 5/5 | 2678 | chrX | 37678491 | |||||
| chrX:37678809
|
T | C | 59 | a0001c0001t0001a0001c0001t0006a0001c0001t0008others(56): Show | 200 | HG00140.hp1 HG00280.hp1 HG00609.hp1 others(197): Show |
3_prime_UTR_variant | MODIFIER | c.*2996T>C | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 5/5 | 2996 | chrX | 37678809 | |||||
| chrX:37679286
|
A | G | 1 | a0001c0004t0009 | 4 | HG02109.hp2 HG02615.hp1 HG02896.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*3473A>G | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 5/5 | 3473 | chrX | 37679286 | |||||
| chrX:37679337
|
G | A | 1 | a0001c0002t0028 | 1 | HG02683.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3524G>A | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 5/5 | 3524 | chrX | 37679337 | |||||
| chrX:37679613
|
C | T | 14 | a0001c0002t0003a0001c0002t0004a0001c0002t0011others(11): Show | 26 | HG00639.hp1 HG00639.hp2 HG01069.hp1 others(23): Show |
3_prime_UTR_variant | MODIFIER | c.*3800C>T | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 5/5 | 3800 | chrX | 37679613 | |||||
| chrX:37679649
|
G | A | 1 | a0001c0001t0010 | 3 | HG02109.hp1 HG02145.hp1 HG03139.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3836G>A | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 5/5 | 3836 | chrX | 37679649 | |||||
| chrX:37679654
|
T | C | 1 | a0001c0001t0010 | 3 | HG02109.hp1 HG02145.hp1 HG03139.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3841T>C | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 5/5 | 3841 | chrX | 37679654 | |||||
| chrX:37679851
|
G | A | 1 | a0001c0001t0010 | 3 | HG02109.hp1 HG02145.hp1 HG03139.hp1 |
3_prime_UTR_variant | MODIFIER | c.*4038G>A | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 5/5 | 4038 | chrX | 37679851 | |||||
| chrX:37680315
|
A | G | 7 | a0001c0002t0004a0001c0002t0021a0001c0002t0026others(4): Show | 11 | HG01891.hp1 HG02257.hp1 HG02572.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*4502A>G | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 5/5 | 4502 | chrX | 37680315 | |||||
| chrX:37680587
|
AC | A | 2 | a0001c0002t0016a0001c0002t0033 | 3 | HG02970.hp1 HG03225.hp1 NA19030.hp2 |
3_prime_UTR_variant | MODIFIER | c.*4776delC | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 5/5 | 4776 | INFO_REALIGN_3_PRIME | chrX | 37680587 | ||||
| chrX:37680836
|
A | AGT | 5 | a0001c0001t0020a0001c0001t0031a0001c0001t0040others(2): Show | 6 | HG01255.hp1 HG02451.hp2 HG02809.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*5042_*5043dupGT | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 5/5 | 5044 | INFO_REALIGN_3_PRIME | chrX | 37680836 | ||||
| chrX:37680865
|
G | A | 1 | a0001c0001t0034 | 1 | NA18965.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5052G>A | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 5/5 | 5052 | chrX | 37680865 | |||||
| chrX:37681000
|
T | C | 2 | a0001c0001t0020a0001c0002t0030 | 3 | HG01255.hp1 HG02809.hp1 HG03540.hp1 |
3_prime_UTR_variant | MODIFIER | c.*5187T>C | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 5/5 | 5187 | chrX | 37681000 | |||||
| chrX:37681294
|
T | A | 4 | a0001c0003t0015a0001c0003t0029a0001c0003t0047others(1): Show | 5 | HG02818.hp2 HG03041.hp1 HG03453.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*5481T>A | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 5/5 | 5481 | chrX | 37681294 | |||||
| chrX:37681852
|
T | C | 1 | a0001c0003t0013 | 2 | HG02895.hp1 HG02897.hp2 |
3_prime_UTR_variant | MODIFIER | c.*6039T>C | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 5/5 | 6039 | chrX | 37681852 | |||||
| chrX:37682056
|
T | C | 1 | a0001c0001t0017 | 2 | HG02602.hp1 HG02735.hp1 |
3_prime_UTR_variant | MODIFIER | c.*6243T>C | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 5/5 | 6243 | chrX | 37682056 | |||||
| chrX:37682101
|
T | A | 1 | a0001c0003t0012 | 2 | HG02622.hp1 NA18906.hp2 |
3_prime_UTR_variant | MODIFIER | c.*6288T>A | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 5/5 | 6288 | chrX | 37682101 | |||||
| chrX:37682105
|
A | AT | 1 | a0001c0001t0039 | 1 | HG02738.hp1 | 3_prime_UTR_variant | MODIFIER | c.*6307dupT | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 5/5 | 6308 | INFO_REALIGN_3_PRIME | chrX | 37682105 | ||||
| chrX:37682105
|
AT | A | 1 | a0001c0004t0009 | 4 | HG02109.hp2 HG02615.hp1 HG02896.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*6307delT | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 5/5 | 6307 | INFO_REALIGN_3_PRIME | chrX | 37682105 | ||||
| chrX:37682155
|
T | G | 1 | a0001c0002t0032 | 1 | HG02572.hp1 | 3_prime_UTR_variant | MODIFIER | c.*6342T>G | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 5/5 | 6342 | chrX | 37682155 | |||||
| chrX:37682329
|
C | T | 1 | a0001c0001t0038 | 1 | HG01433.hp1 | 3_prime_UTR_variant | MODIFIER | c.*6516C>T | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 5/5 | 6516 | chrX | 37682329 | |||||
| chrX:37682662
|
CAT | C | 1 | a0001c0001t0043 | 1 | HG02717.hp1 | 3_prime_UTR_variant | MODIFIER | c.*6850_*6851delAT | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 5/5 | 6850 | chrX | 37682662 | |||||
| chrX:37682882
|
A | G | 1 | a0001c0001t0037 | 1 | NA18960.hp1 | 3_prime_UTR_variant | MODIFIER | c.*7069A>G | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 5/5 | 7069 | chrX | 37682882 | |||||
| chrX:37683039
|
C | T | 15 | a0001c0002t0003a0001c0002t0004a0001c0002t0011others(12): Show | 27 | HG00639.hp1 HG00639.hp2 HG01069.hp1 others(24): Show |
3_prime_UTR_variant | MODIFIER | c.*7226C>T | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 5/5 | 7226 | chrX | 37683039 | |||||
| chrX:37683105
|
C | T | 2 | a0001c0003t0047a0001c0003t0050 | 2 | HG03453.hp1 HG03540.hp2 |
3_prime_UTR_variant | MODIFIER | c.*7292C>T | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 5/5 | 7292 | chrX | 37683105 | |||||
| chrX:37683403
|
A | G | 11 | a0001c0001t0010a0001c0003t0005a0001c0003t0007others(8): Show | 23 | HG01891.hp2 HG02109.hp1 HG02145.hp1 others(20): Show |
3_prime_UTR_variant | MODIFIER | c.*7590A>G | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 5/5 | 7590 | chrX | 37683403 | |||||
| chrX:37683447
|
A | T | 1 | a0001c0001t0036 | 1 | HG00280.hp1 | 3_prime_UTR_variant | MODIFIER | c.*7634A>T | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 5/5 | 7634 | chrX | 37683447 | |||||
| chrX:37683538
|
A | G | 20 | a0001c0002t0002a0001c0002t0003a0001c0002t0004others(17): Show | 41 | HG00639.hp1 HG00639.hp2 HG00735.hp1 others(38): Show |
3_prime_UTR_variant | MODIFIER | c.*7725A>G | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 5/5 | 7725 | chrX | 37683538 | |||||
| chrX:37684158
|
G | A | 1 | a0001c0001t0035 | 1 | HG01167.hp1 | 3_prime_UTR_variant | MODIFIER | c.*8345G>A | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 5/5 | 8345 | chrX | 37684158 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chrX:37572638
|
C | T | 14 | a0001c0001t0008g0184a0001c0001t0008g0186a0001c0001t0008g0187others(11): Show | 15 | HG01884.hp1 HG02109.hp2 HG02615.hp1 others(12): Show |
intron_variant | MODIFIER | c.573+195C>T | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37572638 | ||||||
| chrX:37572872
|
G | T | 2 | a0001c0002t0016g0176a0001c0002t0016g0177 | 2 | HG02970.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.573+429G>T | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37572872 | ||||||
| chrX:37572908
|
A | G | 2 | a0001c0001t0001g0174a0001c0001t0001g0175 | 2 | HG01192.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.573+465A>G | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37572908 | ||||||
| chrX:37572941
|
T | C | 14 | a0001c0001t0008g0184a0001c0001t0008g0186a0001c0001t0008g0187others(11): Show | 15 | HG01884.hp1 HG02109.hp2 HG02615.hp1 others(12): Show |
intron_variant | MODIFIER | c.573+498T>C | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37572941 | ||||||
| chrX:37573069
|
A | T | 1 | a0003c0009t0021g0190 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.573+626A>T | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37573069 | ||||||
| chrX:37573188
|
A | G | 1 | a0003c0009t0021g0190 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.573+745A>G | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37573188 | ||||||
| chrX:37573383
|
A | G | 47 | a0001c0001t0006g0137a0001c0001t0006g0143a0001c0001t0006g0144others(44): Show | 50 | HG00639.hp2 HG00735.hp1 HG01070.hp1 others(47): Show |
intron_variant | MODIFIER | c.573+940A>G | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37573383 | ||||||
| chrX:37573437
|
AAG | A | 2 | a0001c0001t0001g0129a0001c0001t0018g0128 | 2 | NA19062.hp1 NA19086.hp1 |
intron_variant | MODIFIER | c.573+997_573+998del others(2): Show |
LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chrX | 37573437 | |||||
| chrX:37573700
|
T | C | 5 | a0001c0002t0051g0180a0001c0002t0053g0181a0001c0004t0009g0006others(2): Show | 6 | HG02109.hp2 HG02615.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.573+1257T>C | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37573700 | ||||||
| chrX:37573735
|
G | A | 8 | a0001c0001t0008g0184a0001c0001t0008g0186a0001c0001t0008g0187others(5): Show | 8 | HG01884.hp1 HG02630.hp1 HG02965.hp1 others(5): Show |
intron_variant | MODIFIER | c.573+1292G>A | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37573735 | ||||||
| chrX:37573753
|
A | AT | 1 | a0001c0002t0011g0173 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.573+1319dupT | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chrX | 37573753 | |||||
| chrX:37573754
|
T | A | 1 | a0001c0003t0005g0007 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.573+1311T>A | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37573754 | ||||||
| chrX:37573765
|
A | G | 1 | a0001c0001t0001g0129 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.573+1322A>G | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37573765 | ||||||
| chrX:37573853
|
A | G | 1 | a0001c0002t0049g0127 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.573+1410A>G | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37573853 | ||||||
| chrX:37573972
|
C | G | 1 | a0001c0001t0001g0126 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.573+1529C>G | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37573972 | ||||||
| chrX:37573978
|
C | CT | 8 | a0001c0001t0001g0124a0001c0001t0001g0125a0001c0002t0049g0127others(5): Show | 9 | HG02109.hp2 HG02257.hp1 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.573+1548dupT | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chrX | 37573978 | |||||
| chrX:37573999
|
G | A | 4 | a0001c0001t0048g0009a0001c0002t0045g0008a0001c0003t0005g0010others(1): Show | 4 | HG02647.hp1 HG03130.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.573+1556G>A | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37573999 | ||||||
| chrX:37574054
|
C | CA | 39 | a0001c0001t0001g0001a0001c0001t0001g0017a0001c0001t0001g0019others(36): Show | 41 | HG00621.hp1 HG00642.hp1 HG00673.hp1 others(38): Show |
intron_variant | MODIFIER | c.573+1632dupA | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chrX | 37574054 | |||||
| chrX:37574054
|
C | CAA | 6 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(3): Show | 6 | HG02135.hp1 HG04228.hp1 NA18953.hp1 others(3): Show |
intron_variant | MODIFIER | c.573+1631_573+1632d others(4): Show |
LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chrX | 37574054 | |||||
| chrX:37574054
|
C | CAAA | 1 | a0001c0002t0049g0127 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.573+1630_573+1632d others(5): Show |
LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chrX | 37574054 | |||||
| chrX:37574054
|
C | CAAAAAAA others(3): Show |
1 | a0001c0002t0053g0181 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.573+1623_573+1632d others(12): Show |
LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chrX | 37574054 | |||||
| chrX:37574054
|
C | CAAAAAAA others(4): Show |
3 | a0001c0002t0051g0180a0001c0003t0047g0189a0001c0003t0050g0188 | 3 | HG02970.hp2 HG03453.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.573+1622_573+1632d others(13): Show |
LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chrX | 37574054 | |||||
| chrX:37574054
|
C | CAAAAAAA others(5): Show |
4 | a0001c0001t0008g0186a0001c0001t0008g0187a0001c0002t0054g0185others(1): Show | 5 | HG01884.hp1 HG02896.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.573+1621_573+1632d others(14): Show |
LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chrX | 37574054 | |||||
| chrX:37574054
|
C | CAAAAAAA others(6): Show |
2 | a0001c0004t0009g0178a0001c0004t0009g0179 | 2 | HG02109.hp2 HG02615.hp1 |
intron_variant | MODIFIER | c.573+1620_573+1632d others(15): Show |
LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chrX | 37574054 | |||||
| chrX:37574054
|
C | CAAAAAAA others(7): Show |
1 | a0001c0001t0008g0184 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.573+1619_573+1632d others(16): Show |
LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chrX | 37574054 | |||||
| chrX:37574054
|
C | CAAAAAAA others(8): Show |
1 | a0001c0003t0005g0183 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.573+1618_573+1632d others(17): Show |
LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chrX | 37574054 | |||||
| chrX:37574054
|
C | CAAAAAAA others(9): Show |
1 | a0001c0003t0005g0182 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.573+1617_573+1632d others(18): Show |
LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chrX | 37574054 | |||||
| chrX:37574054
|
CA | C | 37 | a0001c0001t0006g0137a0001c0001t0006g0143a0001c0001t0006g0144others(34): Show | 40 | HG00639.hp2 HG00735.hp1 HG01070.hp1 others(37): Show |
intron_variant | MODIFIER | c.573+1632delA | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chrX | 37574054 | |||||
| chrX:37574054
|
CAA | C | 5 | a0001c0002t0033g0172a0001c0003t0013g0170a0001c0003t0013g0171others(2): Show | 5 | HG02818.hp2 HG02895.hp1 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.573+1631_573+1632d others(4): Show |
LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chrX | 37574054 | |||||
| chrX:37574127
|
A | T | 1 | a0001c0003t0046g0011 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.573+1684A>T | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37574127 | ||||||
| chrX:37574278
|
A | T | 1 | a0001c0011t0001g0123 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.573+1835A>T | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37574278 | ||||||
| chrX:37574562
|
G | A | 1 | a0001c0003t0005g0007 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.573+2119G>A | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37574562 | ||||||
| chrX:37574633
|
C | G | 1 | a0001c0002t0049g0127 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.573+2190C>G | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37574633 | ||||||
| chrX:37574828
|
G | C | 1 | a0001c0001t0001g0051 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.573+2385G>C | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37574828 | ||||||
| chrX:37574888
|
G | GGT | 5 | a0001c0001t0001g0050a0001c0001t0001g0120a0001c0001t0001g0121others(2): Show | 5 | HG02486.hp1 HG03017.hp1 HG03669.hp2 others(2): Show |
intron_variant | MODIFIER | c.573+2468_573+2469d others(4): Show |
LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chrX | 37574888 | |||||
| chrX:37574888
|
GGT | G | 53 | a0001c0001t0006g0137a0001c0001t0006g0143a0001c0001t0006g0144others(50): Show | 56 | HG00639.hp2 HG00735.hp1 HG01070.hp1 others(53): Show |
intron_variant | MODIFIER | c.573+2468_573+2469d others(4): Show |
LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chrX | 37574888 | |||||
| chrX:37574888
|
GGTGT | G | 8 | a0001c0002t0054g0185a0001c0003t0005g0182a0001c0003t0005g0183others(5): Show | 9 | HG02109.hp2 HG02615.hp1 HG02896.hp2 others(6): Show |
intron_variant | MODIFIER | c.573+2466_573+2469d others(6): Show |
LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chrX | 37574888 | |||||
| chrX:37574907
|
G | A | 5 | a0001c0002t0054g0185a0001c0003t0005g0182a0001c0003t0005g0183others(2): Show | 5 | HG02965.hp1 HG03453.hp1 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.573+2464G>A | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37574907 | ||||||
| chrX:37574909
|
G | A | 3 | a0001c0001t0008g0184a0001c0001t0008g0186a0001c0001t0008g0187 | 3 | HG01884.hp1 HG02630.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.573+2466G>A | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37574909 | ||||||
| chrX:37574911
|
G | A | 6 | a0001c0002t0054g0185a0001c0003t0005g0007a0001c0003t0005g0182others(3): Show | 6 | HG02965.hp1 HG03195.hp1 HG03453.hp1 others(3): Show |
intron_variant | MODIFIER | c.573+2468G>A | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37574911 | ||||||
| chrX:37574913
|
A | G | 1 | a0001c0003t0005g0007 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.573+2470A>G | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37574913 | ||||||
| chrX:37574915
|
G | A | 9 | a0001c0001t0008g0184a0001c0001t0008g0186a0001c0001t0008g0187others(6): Show | 9 | HG01884.hp1 HG02630.hp1 HG02965.hp1 others(6): Show |
intron_variant | MODIFIER | c.573+2472G>A | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37574915 | ||||||
| chrX:37575045
|
C | T | 5 | a0001c0002t0051g0180a0001c0002t0053g0181a0001c0004t0009g0006others(2): Show | 6 | HG02109.hp2 HG02615.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.573+2602C>T | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37575045 | ||||||
| chrX:37575102
|
C | T | 63 | a0001c0001t0006g0137a0001c0001t0006g0143a0001c0001t0006g0144others(60): Show | 67 | HG00639.hp2 HG00735.hp1 HG01070.hp1 others(64): Show |
intron_variant | MODIFIER | c.573+2659C>T | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37575102 | ||||||
| chrX:37575128
|
C | T | 63 | a0001c0001t0006g0137a0001c0001t0006g0143a0001c0001t0006g0144others(60): Show | 67 | HG00639.hp2 HG00735.hp1 HG01070.hp1 others(64): Show |
intron_variant | MODIFIER | c.573+2685C>T | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37575128 | ||||||
| chrX:37575174
|
G | A | 1 | a0001c0001t0001g0053 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.573+2731G>A | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37575174 | ||||||
| chrX:37575379
|
A | G | 1 | a0001c0001t0001g0124 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.573+2936A>G | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37575379 | ||||||
| chrX:37575584
|
G | A | 8 | a0001c0001t0008g0184a0001c0001t0008g0186a0001c0001t0008g0187others(5): Show | 8 | HG01884.hp1 HG02630.hp1 HG02965.hp1 others(5): Show |
intron_variant | MODIFIER | c.573+3141G>A | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37575584 | ||||||
| chrX:37575681
|
T | C | 5 | a0001c0002t0051g0180a0001c0002t0053g0181a0001c0004t0009g0006others(2): Show | 6 | HG02109.hp2 HG02615.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.573+3238T>C | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37575681 | ||||||
| chrX:37575727
|
G | A | 1 | a0001c0002t0021g0054 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.573+3284G>A | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37575727 | ||||||
| chrX:37575733
|
G | A | 4 | a0001c0001t0048g0009a0001c0002t0045g0008a0001c0003t0005g0010others(1): Show | 4 | HG02647.hp1 HG03130.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.573+3290G>A | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37575733 | ||||||
| chrX:37576045
|
G | A | 1 | a0001c0003t0005g0007 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.573+3602G>A | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37576045 | ||||||
| chrX:37576121
|
G | A | 5 | a0001c0002t0054g0185a0001c0003t0005g0182a0001c0003t0005g0183others(2): Show | 5 | HG02965.hp1 HG03453.hp1 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.573+3678G>A | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37576121 | ||||||
| chrX:37576305
|
A | G | 1 | a0001c0003t0005g0119 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.573+3862A>G | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37576305 | ||||||
| chrX:37576309
|
T | C | 1 | a0001c0003t0005g0119 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.573+3866T>C | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37576309 | ||||||
| chrX:37576317
|
G | A | 1 | a0001c0003t0005g0119 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.573+3874G>A | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37576317 | ||||||
| chrX:37576461
|
G | A | 1 | a0001c0001t0001g0055 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.573+4018G>A | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37576461 | ||||||
| chrX:37576577
|
G | A | 1 | a0001c0003t0005g0007 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.573+4134G>A | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37576577 | ||||||
| chrX:37576862
|
G | A | 1 | a0001c0002t0049g0127 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.573+4419G>A | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37576862 | ||||||
| chrX:37576881
|
A | G | 4 | a0001c0001t0048g0009a0001c0002t0045g0008a0001c0003t0005g0010others(1): Show | 4 | HG02647.hp1 HG03130.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.573+4438A>G | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37576881 | ||||||
| chrX:37576910
|
C | T | 2 | a0001c0003t0005g0182a0001c0003t0005g0183 | 2 | HG02965.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.573+4467C>T | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37576910 | ||||||
| chrX:37577165
|
G | T | 5 | a0001c0002t0054g0185a0001c0003t0005g0182a0001c0003t0005g0183others(2): Show | 5 | HG02965.hp1 HG03453.hp1 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.573+4722G>T | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37577165 | ||||||
| chrX:37577251
|
A | G | 8 | a0001c0001t0008g0184a0001c0001t0008g0186a0001c0001t0008g0187others(5): Show | 8 | HG01884.hp1 HG02630.hp1 HG02965.hp1 others(5): Show |
intron_variant | MODIFIER | c.573+4808A>G | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37577251 | ||||||
| chrX:37577571
|
A | G | 1 | a0001c0002t0049g0127 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.573+5128A>G | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37577571 | ||||||
| chrX:37577810
|
A | G | 1 | a0001c0001t0001g0049 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.573+5367A>G | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37577810 | ||||||
| chrX:37577892
|
A | G | 1 | a0003c0009t0021g0190 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.573+5449A>G | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37577892 | ||||||
| chrX:37578234
|
A | G | 1 | a0001c0002t0045g0008 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.573+5791A>G | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37578234 | ||||||
| chrX:37578292
|
G | GT | 1 | a0001c0001t0034g0048 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.573+5854dupT | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chrX | 37578292 | |||||
| chrX:37578327
|
G | A | 2 | a0001c0001t0043g0056a0001c0002t0019g0057 | 2 | HG01884.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.573+5884G>A | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37578327 | ||||||
| chrX:37578514
|
T | A | 1 | a0001c0002t0049g0127 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.573+6071T>A | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37578514 | ||||||
| chrX:37578514
|
T | TG | 1 | a0001c0001t0034g0048 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.573+6072dupG | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chrX | 37578514 | |||||
| chrX:37578658
|
TA | T | 1 | a0001c0001t0034g0048 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.573+6219delA | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chrX | 37578658 | |||||
| chrX:37578702
|
A | G | 70 | a0001c0001t0006g0137a0001c0001t0006g0143a0001c0001t0006g0144others(67): Show | 74 | HG00639.hp2 HG00735.hp1 HG01070.hp1 others(71): Show |
intron_variant | MODIFIER | c.573+6259A>G | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37578702 | ||||||
| chrX:37578928
|
C | T | 9 | a0001c0001t0008g0184a0001c0001t0008g0186a0001c0001t0008g0187others(6): Show | 9 | HG01884.hp1 HG02055.hp1 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.573+6485C>T | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37578928 | ||||||
| chrX:37578980
|
T | TA | 19 | a0001c0001t0001g0012a0001c0001t0001g0017a0001c0001t0001g0019others(16): Show | 19 | HG00735.hp1 HG01109.hp1 HG01243.hp1 others(16): Show |
intron_variant | MODIFIER | c.573+6561dupA | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chrX | 37578980 | |||||
| chrX:37578980
|
TA | T | 10 | a0001c0001t0001g0118a0001c0001t0006g0164a0001c0001t0034g0048others(7): Show | 10 | HG01069.hp1 HG01099.hp1 HG02818.hp2 others(7): Show |
intron_variant | MODIFIER | c.573+6561delA | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chrX | 37578980 | |||||
| chrX:37579080
|
A | T | 1 | a0001c0003t0012g0163 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.573+6637A>T | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37579080 | ||||||
| chrX:37579149
|
G | A | 1 | a0001c0003t0024g0136 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.573+6706G>A | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37579149 | ||||||
| chrX:37579191
|
TG | T | 1 | a0001c0001t0034g0048 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.573+6750delG | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chrX | 37579191 | |||||
| chrX:37579256
|
TC | T | 1 | a0001c0001t0034g0048 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.573+6815delC | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chrX | 37579256 | |||||
| chrX:37579273
|
C | CA | 1 | a0001c0001t0034g0048 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.573+6833dupA | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chrX | 37579273 | |||||
| chrX:37579353
|
G | A | 1 | a0001c0001t0001g0021 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.573+6910G>A | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37579353 | ||||||
| chrX:37579517
|
T | TC | 1 | a0001c0001t0034g0048 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.573+7078dupC | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chrX | 37579517 | |||||
| chrX:37579530
|
T | C | 2 | a0001c0002t0016g0176a0001c0002t0016g0177 | 2 | HG02970.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.573+7087T>C | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37579530 | ||||||
| chrX:37579530
|
T | TC | 1 | a0001c0001t0034g0048 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.573+7088dupC | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chrX | 37579530 | |||||
| chrX:37579540
|
CA | C | 1 | a0001c0001t0034g0048 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.573+7101delA | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chrX | 37579540 | |||||
| chrX:37579823
|
A | AT | 1 | a0001c0001t0034g0048 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.573+7386dupT | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chrX | 37579823 | |||||
| chrX:37579881
|
A | G | 1 | a0001c0002t0049g0127 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.573+7438A>G | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37579881 | ||||||
| chrX:37579884
|
G | C | 1 | a0001c0002t0049g0127 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.573+7441G>C | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37579884 | ||||||
| chrX:37580039
|
C | T | 3 | a0001c0001t0008g0184a0001c0001t0008g0186a0001c0001t0008g0187 | 3 | HG01884.hp1 HG02630.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.573+7596C>T | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37580039 | ||||||
| chrX:37580178
|
TG | T | 1 | a0001c0001t0034g0048 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.573+7738delG | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chrX | 37580178 | |||||
| chrX:37580268
|
C | CA | 1 | a0001c0001t0034g0048 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.573+7826dupA | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chrX | 37580268 | |||||
| chrX:37580285
|
TA | T | 1 | a0001c0001t0034g0048 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.573+7846delA | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chrX | 37580285 | |||||
| chrX:37580395
|
A | AT | 1 | a0001c0001t0034g0048 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.573+7956dupT | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chrX | 37580395 | |||||
| chrX:37580437
|
A | G | 4 | a0001c0003t0005g0182a0001c0003t0005g0183a0001c0003t0047g0189others(1): Show | 4 | HG02965.hp1 HG03453.hp1 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.573+7994A>G | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37580437 | ||||||
| chrX:37580594
|
T | TA | 1 | a0001c0001t0034g0048 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.573+8152dupA | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chrX | 37580594 | |||||
| chrX:37580702
|
C | A | 26 | a0001c0001t0006g0137a0001c0001t0006g0143a0001c0001t0006g0144others(23): Show | 26 | HG00639.hp2 HG01255.hp1 HG01891.hp2 others(23): Show |
intron_variant | MODIFIER | c.573+8259C>A | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37580702 | ||||||
| chrX:37580740
|
AC | A | 1 | a0001c0001t0034g0048 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.573+8299delC | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chrX | 37580740 | |||||
| chrX:37581086
|
G | A | 1 | a0001c0001t0001g0058 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.573+8643G>A | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37581086 | ||||||
| chrX:37581101
|
C | T | 9 | a0001c0001t0008g0184a0001c0001t0008g0186a0001c0001t0008g0187others(6): Show | 9 | HG01884.hp1 HG02055.hp1 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.573+8658C>T | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37581101 | ||||||
| chrX:37581112
|
A | G | 1 | a0001c0002t0049g0127 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.573+8669A>G | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37581112 | ||||||
| chrX:37581130
|
ACT | A | 8 | a0001c0001t0001g0049a0001c0001t0001g0050a0001c0001t0001g0113others(5): Show | 8 | HG01106.hp1 HG01167.hp1 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.573+8690_573+8691d others(4): Show |
LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chrX | 37581130 | |||||
| chrX:37581186
|
AC | A | 1 | a0001c0001t0001g0111 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.573+8744delC | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37581186 | ||||||
| chrX:37581603
|
T | C | 1 | a0003c0009t0021g0190 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.573+9160T>C | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37581603 | ||||||
| chrX:37581931
|
G | C | 17 | a0001c0001t0008g0184a0001c0001t0008g0186a0001c0001t0008g0187others(14): Show | 18 | HG01884.hp1 HG02055.hp1 HG02109.hp2 others(15): Show |
intron_variant | MODIFIER | c.573+9488G>C | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37581931 | ||||||
| chrX:37582050
|
C | A | 1 | a0001c0001t0001g0062 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.573+9607C>A | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37582050 | ||||||
| chrX:37582116
|
CT | C | 2 | a0001c0001t0001g0111a0001c0002t0049g0127 | 2 | HG02257.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.573+9680delT | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chrX | 37582116 | |||||
| chrX:37582230
|
C | T | 1 | a0001c0001t0036g0110 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.573+9787C>T | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37582230 | ||||||
| chrX:37582498
|
C | A | 40 | a0001c0001t0001g0022a0001c0001t0006g0137a0001c0001t0006g0143others(37): Show | 43 | HG00621.hp1 HG00639.hp2 HG00735.hp1 others(40): Show |
intron_variant | MODIFIER | c.573+10055C>A | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37582498 | ||||||
| chrX:37582520
|
C | T | 62 | a0001c0001t0001g0022a0001c0001t0006g0137a0001c0001t0006g0143others(59): Show | 66 | HG00621.hp1 HG00639.hp2 HG00735.hp1 others(63): Show |
intron_variant | MODIFIER | c.573+10077C>T | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37582520 | ||||||
| chrX:37582949
|
G | T | 1 | a0001c0001t0034g0048 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.573+10506G>T | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37582949 | ||||||
| chrX:37583022
|
C | G | 45 | a0001c0001t0001g0022a0001c0001t0006g0137a0001c0001t0006g0143others(42): Show | 48 | HG00621.hp1 HG00639.hp2 HG00735.hp1 others(45): Show |
intron_variant | MODIFIER | c.573+10579C>G | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37583022 | ||||||
| chrX:37583023
|
C | G | 1 | a0001c0002t0049g0127 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.573+10580C>G | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37583023 | ||||||
| chrX:37583098
|
G | C | 4 | a0001c0001t0048g0009a0001c0002t0045g0008a0001c0003t0005g0010others(1): Show | 4 | HG02647.hp1 HG03130.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.573+10655G>C | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37583098 | ||||||
| chrX:37583173
|
G | T | 15 | a0001c0001t0008g0184a0001c0001t0008g0186a0001c0001t0008g0187others(12): Show | 16 | HG01884.hp1 HG02055.hp1 HG02109.hp2 others(13): Show |
intron_variant | MODIFIER | c.573+10730G>T | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37583173 | ||||||
| chrX:37583175
|
T | G | 15 | a0001c0001t0008g0184a0001c0001t0008g0186a0001c0001t0008g0187others(12): Show | 16 | HG01884.hp1 HG02055.hp1 HG02109.hp2 others(13): Show |
intron_variant | MODIFIER | c.573+10732T>G | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37583175 | ||||||
| chrX:37583249
|
G | T | 1 | a0001c0001t0038g0109 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.573+10806G>T | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37583249 | ||||||
| chrX:37583296
|
G | A | 25 | a0001c0001t0001g0022a0001c0001t0006g0137a0001c0001t0006g0143others(22): Show | 25 | HG00621.hp1 HG00639.hp2 HG01255.hp1 others(22): Show |
intron_variant | MODIFIER | c.573+10853G>A | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37583296 | ||||||
| chrX:37583411
|
A | G | 3 | a0001c0001t0020g0052a0001c0001t0043g0056a0001c0002t0019g0057 | 3 | HG01884.hp2 HG02717.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.573+10968A>G | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37583411 | ||||||
| chrX:37583470
|
C | G | 27 | a0001c0001t0001g0022a0001c0001t0006g0137a0001c0001t0006g0143others(24): Show | 27 | HG00621.hp1 HG00639.hp2 HG01255.hp1 others(24): Show |
intron_variant | MODIFIER | c.573+11027C>G | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37583470 | ||||||
| chrX:37583579
|
A | G | 1 | a0001c0001t0001g0108 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.573+11136A>G | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37583579 | ||||||
| chrX:37583686
|
C | G | 62 | a0001c0001t0001g0022a0001c0001t0006g0137a0001c0001t0006g0143others(59): Show | 66 | HG00621.hp1 HG00639.hp2 HG00735.hp1 others(63): Show |
intron_variant | MODIFIER | c.573+11243C>G | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37583686 | ||||||
| chrX:37583738
|
A | C | 1 | a0001c0002t0049g0127 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.573+11295A>C | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37583738 | ||||||
| chrX:37583763
|
G | A | 1 | a0001c0002t0049g0127 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.573+11320G>A | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37583763 | ||||||
| chrX:37584065
|
G | C | 2 | a0001c0003t0015g0168a0001c0003t0015g0169 | 2 | HG02818.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.573+11622G>C | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37584065 | ||||||
| chrX:37584077
|
G | A | 1 | a0001c0002t0011g0173 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.573+11634G>A | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37584077 | ||||||
| chrX:37584237
|
T | C | 2 | a0001c0001t0043g0056a0001c0002t0019g0057 | 2 | HG01884.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.573+11794T>C | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37584237 | ||||||
| chrX:37584284
|
C | T | 17 | a0001c0001t0008g0184a0001c0001t0008g0186a0001c0001t0008g0187others(14): Show | 18 | HG01884.hp1 HG02055.hp1 HG02109.hp2 others(15): Show |
intron_variant | MODIFIER | c.573+11841C>T | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37584284 | ||||||
| chrX:37584286
|
T | G | 17 | a0001c0001t0008g0184a0001c0001t0008g0186a0001c0001t0008g0187others(14): Show | 18 | HG01884.hp1 HG02055.hp1 HG02109.hp2 others(15): Show |
intron_variant | MODIFIER | c.573+11843T>G | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37584286 | ||||||
| chrX:37584290
|
T | G | 17 | a0001c0001t0008g0184a0001c0001t0008g0186a0001c0001t0008g0187others(14): Show | 18 | HG01884.hp1 HG02055.hp1 HG02109.hp2 others(15): Show |
intron_variant | MODIFIER | c.573+11847T>G | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37584290 | ||||||
| chrX:37584294
|
T | C | 17 | a0001c0001t0008g0184a0001c0001t0008g0186a0001c0001t0008g0187others(14): Show | 18 | HG01884.hp1 HG02055.hp1 HG02109.hp2 others(15): Show |
intron_variant | MODIFIER | c.573+11851T>C | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37584294 | ||||||
| chrX:37584296
|
T | C | 17 | a0001c0001t0008g0184a0001c0001t0008g0186a0001c0001t0008g0187others(14): Show | 18 | HG01884.hp1 HG02055.hp1 HG02109.hp2 others(15): Show |
intron_variant | MODIFIER | c.573+11853T>C | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37584296 | ||||||
| chrX:37584311
|
G | A | 17 | a0001c0001t0008g0184a0001c0001t0008g0186a0001c0001t0008g0187others(14): Show | 18 | HG01884.hp1 HG02055.hp1 HG02109.hp2 others(15): Show |
intron_variant | MODIFIER | c.573+11868G>A | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37584311 | ||||||
| chrX:37584325
|
C | G | 17 | a0001c0001t0008g0184a0001c0001t0008g0186a0001c0001t0008g0187others(14): Show | 18 | HG01884.hp1 HG02055.hp1 HG02109.hp2 others(15): Show |
intron_variant | MODIFIER | c.573+11882C>G | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37584325 | ||||||
| chrX:37584460
|
T | G | 4 | a0001c0001t0008g0184a0001c0001t0008g0186a0001c0001t0008g0187others(1): Show | 4 | HG01884.hp1 HG02055.hp1 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.573+12017T>G | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37584460 | ||||||
| chrX:37584485
|
T | C | 23 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0013others(20): Show | 25 | HG00673.hp1 HG01934.hp1 HG02135.hp1 others(22): Show |
intron_variant | MODIFIER | c.573+12042T>C | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37584485 | ||||||
| chrX:37584503
|
A | T | 1 | a0003c0009t0021g0190 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.573+12060A>T | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37584503 | ||||||
| chrX:37584604
|
G | A | 1 | a0001c0003t0005g0007 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.573+12161G>A | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37584604 | ||||||
| chrX:37584654
|
C | T | 1 | a0001c0001t0001g0125 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.573+12211C>T | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37584654 | ||||||
| chrX:37584655
|
G | A | 2 | a0001c0003t0015g0168a0001c0003t0015g0169 | 2 | HG02818.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.573+12212G>A | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37584655 | ||||||
| chrX:37584705
|
A | G | 1 | a0001c0003t0015g0169 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.573+12262A>G | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37584705 | ||||||
| chrX:37584720
|
G | A | 7 | a0001c0001t0020g0052a0001c0001t0043g0056a0001c0001t0048g0009others(4): Show | 7 | HG01884.hp2 HG02647.hp1 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.573+12277G>A | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37584720 | ||||||
| chrX:37584854
|
C | G | 1 | a0003c0009t0021g0190 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.573+12411C>G | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37584854 | ||||||
| chrX:37584864
|
C | T | 1 | a0003c0009t0021g0190 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.573+12421C>T | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37584864 | ||||||
| chrX:37584970
|
G | T | 1 | a0001c0002t0049g0127 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.573+12527G>T | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37584970 | ||||||
| chrX:37585008
|
A | G | 16 | a0001c0001t0008g0184a0001c0001t0008g0186a0001c0001t0008g0187others(13): Show | 17 | HG01884.hp1 HG02055.hp1 HG02109.hp2 others(14): Show |
intron_variant | MODIFIER | c.573+12565A>G | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37585008 | ||||||
| chrX:37585096
|
T | C | 1 | a0001c0001t0001g0120 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.573+12653T>C | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37585096 | ||||||
| chrX:37585108
|
G | C | 61 | a0001c0001t0006g0137a0001c0001t0006g0143a0001c0001t0006g0144others(58): Show | 65 | HG00639.hp2 HG00735.hp1 HG01070.hp1 others(62): Show |
intron_variant | MODIFIER | c.573+12665G>C | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37585108 | ||||||
| chrX:37585265
|
C | A | 17 | a0001c0001t0008g0184a0001c0001t0008g0186a0001c0001t0008g0187others(14): Show | 18 | HG01884.hp1 HG02055.hp1 HG02109.hp2 others(15): Show |
intron_variant | MODIFIER | c.573+12822C>A | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37585265 | ||||||
| chrX:37585315
|
C | A | 1 | a0001c0001t0001g0062 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.573+12872C>A | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37585315 | ||||||
| chrX:37585349
|
C | A | 5 | a0001c0002t0054g0185a0001c0003t0005g0182a0001c0003t0005g0183others(2): Show | 5 | HG02965.hp1 HG03453.hp1 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.573+12906C>A | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37585349 | ||||||
| chrX:37585372
|
A | G | 11 | a0001c0001t0010g0146a0001c0001t0010g0147a0001c0001t0010g0148others(8): Show | 11 | HG01255.hp1 HG01891.hp2 HG02109.hp1 others(8): Show |
intron_variant | MODIFIER | c.573+12929A>G | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37585372 | ||||||
| chrX:37585631
|
T | G | 1 | a0001c0001t0038g0109 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.573+13188T>G | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37585631 | ||||||
| chrX:37585649
|
G | T | 1 | a0001c0002t0054g0185 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.573+13206G>T | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37585649 | ||||||
| chrX:37585980
|
A | C | 5 | a0001c0002t0054g0185a0001c0003t0005g0182a0001c0003t0005g0183others(2): Show | 5 | HG02965.hp1 HG03453.hp1 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.573+13537A>C | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37585980 | ||||||
| chrX:37586058
|
CT | C | 1 | a0001c0001t0001g0013 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.573+13617delT | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chrX | 37586058 | |||||
| chrX:37586084
|
C | G | 1 | a0001c0001t0001g0118 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.573+13641C>G | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37586084 | ||||||
| chrX:37586139
|
G | A | 1 | a0005c0007t0044g0064 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.573+13696G>A | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37586139 | ||||||
| chrX:37586210
|
T | C | 71 | a0001c0001t0001g0065a0001c0001t0006g0137a0001c0001t0006g0143others(68): Show | 75 | HG00639.hp2 HG00735.hp1 HG01070.hp1 others(72): Show |
intron_variant | MODIFIER | c.573+13767T>C | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37586210 | ||||||
| chrX:37586228
|
C | T | 1 | a0001c0001t0001g0124 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.573+13785C>T | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37586228 | ||||||
| chrX:37586265
|
G | A | 4 | a0001c0001t0008g0184a0001c0001t0008g0186a0001c0001t0008g0187others(1): Show | 4 | HG01884.hp1 HG02055.hp1 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.573+13822G>A | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37586265 | ||||||
| chrX:37586492
|
G | A | 9 | a0001c0001t0008g0184a0001c0001t0008g0186a0001c0001t0008g0187others(6): Show | 9 | HG01884.hp1 HG02055.hp1 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.573+14049G>A | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37586492 | ||||||
| chrX:37586505
|
C | CT | 1 | a0002c0010t0025g0145 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.573+14068dupT | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chrX | 37586505 | |||||
| chrX:37586530
|
G | A | 26 | a0001c0001t0006g0137a0001c0001t0006g0143a0001c0001t0006g0144others(23): Show | 26 | HG00639.hp2 HG01255.hp1 HG01891.hp2 others(23): Show |
intron_variant | MODIFIER | c.573+14087G>A | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37586530 | ||||||
| chrX:37586601
|
C | G | 2 | a0001c0003t0015g0168a0001c0003t0015g0169 | 2 | HG02818.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.573+14158C>G | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37586601 | ||||||
| chrX:37586816
|
C | A | 1 | a0001c0003t0005g0007 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.573+14373C>A | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37586816 | ||||||
| chrX:37586828
|
C | T | 1 | a0001c0002t0053g0181 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.573+14385C>T | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37586828 | ||||||
| chrX:37586870
|
G | A | 1 | a0003c0009t0021g0190 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.573+14427G>A | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37586870 | ||||||
| chrX:37586873
|
C | CT | 71 | a0001c0001t0001g0065a0001c0001t0006g0137a0001c0001t0006g0143others(68): Show | 75 | HG00639.hp2 HG00735.hp1 HG01070.hp1 others(72): Show |
intron_variant | MODIFIER | c.573+14430_573+1443 others(5): Show |
LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37586873 | ||||||
| chrX:37586989
|
T | A | 5 | a0001c0002t0054g0185a0001c0003t0005g0182a0001c0003t0005g0183others(2): Show | 5 | HG02965.hp1 HG03453.hp1 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.573+14546T>A | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37586989 | ||||||
| chrX:37586990
|
C | T | 3 | a0001c0002t0033g0172a0001c0003t0013g0170a0001c0003t0013g0171 | 3 | HG02895.hp1 HG02897.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.573+14547C>T | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37586990 | ||||||
| chrX:37587198
|
C | T | 1 | a0001c0001t0001g0107 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.573+14755C>T | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37587198 | ||||||
| chrX:37587201
|
C | T | 2 | a0001c0001t0001g0046a0001c0001t0001g0047 | 2 | HG02683.hp1 NA18959.hp1 |
intron_variant | MODIFIER | c.573+14758C>T | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37587201 | ||||||
| chrX:37587272
|
G | A | 1 | a0001c0001t0006g0137 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.573+14829G>A | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37587272 | ||||||
| chrX:37587293
|
T | C | 3 | a0001c0004t0009g0006a0001c0004t0009g0178a0001c0004t0009g0179 | 4 | HG02109.hp2 HG02615.hp1 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.573+14850T>C | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37587293 | ||||||
| chrX:37587373
|
G | A | 44 | a0001c0001t0006g0137a0001c0001t0006g0143a0001c0001t0006g0144others(41): Show | 47 | HG00639.hp2 HG00735.hp1 HG01070.hp1 others(44): Show |
intron_variant | MODIFIER | c.573+14930G>A | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37587373 | ||||||
| chrX:37587392
|
T | A | 61 | a0001c0001t0006g0137a0001c0001t0006g0143a0001c0001t0006g0144others(58): Show | 65 | HG00639.hp2 HG00735.hp1 HG01070.hp1 others(62): Show |
intron_variant | MODIFIER | c.573+14949T>A | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37587392 | ||||||
| chrX:37587412
|
G | A | 2 | a0001c0001t0031g0162a0001c0002t0014g0131 | 2 | HG03516.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.573+14969G>A | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37587412 | ||||||
| chrX:37587430
|
G | T | 1 | a0001c0003t0024g0136 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.573+14987G>T | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37587430 | ||||||
| chrX:37587431
|
C | T | 1 | a0003c0009t0021g0190 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.573+14988C>T | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37587431 | ||||||
| chrX:37587475
|
C | T | 1 | a0003c0009t0021g0190 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.573+15032C>T | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37587475 | ||||||
| chrX:37587674
|
G | T | 1 | a0001c0001t0001g0045 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.573+15231G>T | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37587674 | ||||||
| chrX:37587717
|
G | T | 1 | a0001c0002t0049g0127 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.573+15274G>T | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37587717 | ||||||
| chrX:37587759
|
C | A | 1 | a0001c0002t0051g0180 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.573+15316C>A | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37587759 | ||||||
| chrX:37587882
|
A | G | 60 | a0001c0001t0006g0137a0001c0001t0006g0143a0001c0001t0006g0144others(57): Show | 64 | HG00639.hp2 HG00735.hp1 HG01070.hp1 others(61): Show |
intron_variant | MODIFIER | c.573+15439A>G | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37587882 | ||||||
| chrX:37587888
|
C | T | 1 | a0001c0001t0001g0065 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.573+15445C>T | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37587888 | ||||||
| chrX:37588445
|
C | T | 2 | a0001c0003t0012g0161a0001c0003t0012g0163 | 2 | HG02622.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.573+16002C>T | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37588445 | ||||||
| chrX:37588446
|
G | T | 1 | a0001c0001t0001g0106 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.573+16003G>T | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37588446 | ||||||
| chrX:37588686
|
T | C | 9 | a0001c0001t0008g0184a0001c0001t0008g0186a0001c0001t0008g0187others(6): Show | 9 | HG01884.hp1 HG02055.hp1 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.573+16243T>C | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37588686 | ||||||
| chrX:37588706
|
A | G | 189 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(186): Show | 198 | HG00140.hp1 HG00280.hp1 HG00609.hp1 others(195): Show |
intron_variant | MODIFIER | c.573+16263A>G | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37588706 | ||||||
| chrX:37588716
|
T | C | 9 | a0001c0001t0008g0184a0001c0001t0008g0186a0001c0001t0008g0187others(6): Show | 9 | HG01884.hp1 HG02055.hp1 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.573+16273T>C | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37588716 | ||||||
| chrX:37588722
|
T | C | 9 | a0001c0001t0008g0184a0001c0001t0008g0186a0001c0001t0008g0187others(6): Show | 9 | HG01884.hp1 HG02055.hp1 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.573+16279T>C | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37588722 | ||||||
| chrX:37588723
|
G | A | 9 | a0001c0001t0008g0184a0001c0001t0008g0186a0001c0001t0008g0187others(6): Show | 9 | HG01884.hp1 HG02055.hp1 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.573+16280G>A | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37588723 | ||||||
| chrX:37588727
|
T | C | 9 | a0001c0001t0008g0184a0001c0001t0008g0186a0001c0001t0008g0187others(6): Show | 9 | HG01884.hp1 HG02055.hp1 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.573+16284T>C | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37588727 | ||||||
| chrX:37588733
|
A | T | 9 | a0001c0001t0008g0184a0001c0001t0008g0186a0001c0001t0008g0187others(6): Show | 9 | HG01884.hp1 HG02055.hp1 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.573+16290A>T | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37588733 | ||||||
| chrX:37588767
|
G | T | 16 | a0001c0001t0008g0184a0001c0001t0008g0186a0001c0001t0008g0187others(13): Show | 17 | HG01884.hp1 HG02055.hp1 HG02109.hp2 others(14): Show |
intron_variant | MODIFIER | c.573+16324G>T | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37588767 | ||||||
| chrX:37588827
|
G | A | 1 | a0001c0002t0049g0127 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.573+16384G>A | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37588827 | ||||||
| chrX:37588921
|
C | T | 1 | a0001c0002t0049g0127 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.573+16478C>T | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37588921 | ||||||
| chrX:37588944
|
C | T | 9 | a0001c0001t0008g0184a0001c0001t0008g0186a0001c0001t0008g0187others(6): Show | 9 | HG01884.hp1 HG02055.hp1 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.573+16501C>T | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37588944 | ||||||
| chrX:37589098
|
A | G | 1 | a0001c0002t0049g0127 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.573+16655A>G | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37589098 | ||||||
| chrX:37589136
|
C | T | 4 | a0001c0001t0001g0105a0001c0002t0003g0005a0001c0002t0003g0061others(1): Show | 5 | HG00639.hp1 HG01069.hp1 HG01071.hp1 others(2): Show |
intron_variant | MODIFIER | c.573+16693C>T | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37589136 | ||||||
| chrX:37589151
|
G | GT | 1 | a0001c0002t0049g0127 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.573+16718dupT | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chrX | 37589151 | |||||
| chrX:37589292
|
C | A | 1 | a0001c0002t0032g0166 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.573+16849C>A | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37589292 | ||||||
| chrX:37589375
|
T | C | 2 | a0001c0001t0010g0146a0001c0002t0004g0138 | 2 | HG02922.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.573+16932T>C | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37589375 | ||||||
| chrX:37589408
|
A | G | 1 | a0001c0002t0049g0127 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.573+16965A>G | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37589408 | ||||||
| chrX:37589576
|
G | T | 1 | a0001c0001t0001g0020 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.573+17133G>T | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37589576 | ||||||
| chrX:37589637
|
A | G | 9 | a0001c0001t0008g0184a0001c0001t0008g0186a0001c0001t0008g0187others(6): Show | 9 | HG01884.hp1 HG02055.hp1 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.573+17194A>G | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37589637 | ||||||
| chrX:37589717
|
G | C | 9 | a0001c0001t0008g0184a0001c0001t0008g0186a0001c0001t0008g0187others(6): Show | 9 | HG01884.hp1 HG02055.hp1 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.573+17274G>C | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37589717 | ||||||
| chrX:37589966
|
G | T | 1 | a0001c0001t0038g0109 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.573+17523G>T | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37589966 | ||||||
| chrX:37590086
|
A | G | 1 | a0001c0002t0051g0180 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.573+17643A>G | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37590086 | ||||||
| chrX:37590148
|
C | G | 1 | a0003c0009t0021g0190 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.573+17705C>G | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37590148 | ||||||
| chrX:37590200
|
C | A | 1 | a0001c0002t0049g0127 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.573+17757C>A | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37590200 | ||||||
| chrX:37590223
|
G | T | 9 | a0001c0001t0008g0184a0001c0001t0008g0186a0001c0001t0008g0187others(6): Show | 9 | HG01884.hp1 HG02055.hp1 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.573+17780G>T | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37590223 | ||||||
| chrX:37590258
|
C | T | 2 | a0001c0002t0016g0176a0001c0002t0016g0177 | 2 | HG02970.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.573+17815C>T | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37590258 | ||||||
| chrX:37590373
|
A | G | 1 | a0003c0009t0021g0190 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.573+17930A>G | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37590373 | ||||||
| chrX:37590503
|
TC | T | 1 | a0001c0001t0001g0107 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.573+18061delC | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37590503 | ||||||
| chrX:37590832
|
C | T | 2 | a0001c0001t0020g0104a0005c0007t0044g0064 | 2 | HG02630.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.573+18389C>T | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37590832 | ||||||
| chrX:37590962
|
A | G | 1 | a0001c0001t0006g0144 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.573+18519A>G | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37590962 | ||||||
| chrX:37590995
|
G | A | 1 | a0001c0002t0032g0166 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.573+18552G>A | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37590995 | ||||||
| chrX:37591154
|
CCTATCAT others(7): Show |
C | 5 | a0001c0002t0051g0180a0001c0002t0053g0181a0001c0004t0009g0006others(2): Show | 6 | HG02109.hp2 HG02615.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.573+18715_573+1872 others(18): Show |
LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chrX | 37591154 | |||||
| chrX:37591519
|
A | T | 9 | a0001c0001t0008g0184a0001c0001t0008g0186a0001c0001t0008g0187others(6): Show | 9 | HG01884.hp1 HG02055.hp1 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.573+19076A>T | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37591519 | ||||||
| chrX:37591565
|
A | G | 2 | a0001c0001t0001g0125a0001c0001t0018g0116 | 2 | HG03942.hp1 NA19056.hp1 |
intron_variant | MODIFIER | c.573+19122A>G | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37591565 | ||||||
| chrX:37591571
|
G | A | 1 | a0001c0002t0049g0127 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.573+19128G>A | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37591571 | ||||||
| chrX:37591616
|
T | G | 2 | a0001c0001t0018g0116a0001c0004t0009g0178 | 2 | HG02109.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.573+19173T>G | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37591616 | ||||||
| chrX:37591663
|
C | T | 8 | a0001c0001t0001g0042a0001c0001t0001g0043a0001c0001t0001g0044others(5): Show | 8 | HG02056.hp1 HG02129.hp1 HG02683.hp1 others(5): Show |
intron_variant | MODIFIER | c.573+19220C>T | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37591663 | ||||||
| chrX:37591665
|
A | G | 8 | a0001c0001t0001g0042a0001c0001t0001g0043a0001c0001t0001g0044others(5): Show | 8 | HG02056.hp1 HG02129.hp1 HG02683.hp1 others(5): Show |
intron_variant | MODIFIER | c.573+19222A>G | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37591665 | ||||||
| chrX:37591700
|
G | T | 8 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0001g0046others(5): Show | 8 | HG02129.hp1 HG02683.hp1 HG02738.hp1 others(5): Show |
intron_variant | MODIFIER | c.573+19257G>T | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37591700 | ||||||
| chrX:37591701
|
T | TTG | 8 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0001g0046others(5): Show | 8 | HG02129.hp1 HG02683.hp1 HG02738.hp1 others(5): Show |
intron_variant | MODIFIER | c.573+19260_573+1926 others(6): Show |
LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chrX | 37591701 | |||||
| chrX:37591707
|
C | CTGA | 7 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0001g0046others(4): Show | 7 | HG02129.hp1 HG02683.hp1 HG04204.hp1 others(4): Show |
intron_variant | MODIFIER | c.573+19264_573+1926 others(7): Show |
LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37591707 | ||||||
| chrX:37591719
|
C | T | 23 | a0001c0001t0001g0003a0001c0001t0001g0020a0001c0001t0001g0022others(20): Show | 24 | HG00621.hp1 HG01109.hp1 HG01928.hp1 others(21): Show |
intron_variant | MODIFIER | c.573+19276C>T | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37591719 | ||||||
| chrX:37591730
|
TG | T | 100 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0020others(97): Show | 106 | HG00621.hp1 HG00639.hp2 HG00642.hp1 others(103): Show |
intron_variant | MODIFIER | c.573+19295delG | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chrX | 37591730 | |||||
| chrX:37591745
|
C | A | 38 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0020others(35): Show | 41 | HG00621.hp1 HG00642.hp1 HG01070.hp2 others(38): Show |
intron_variant | MODIFIER | c.573+19302C>A | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37591745 | ||||||
| chrX:37591763
|
A | T | 32 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0020others(29): Show | 34 | HG00621.hp1 HG00642.hp1 HG01070.hp2 others(31): Show |
intron_variant | MODIFIER | c.573+19320A>T | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37591763 | ||||||
| chrX:37591800
|
C | CA | 72 | a0001c0001t0001g0065a0001c0001t0006g0137a0001c0001t0006g0143others(69): Show | 76 | HG00639.hp2 HG00735.hp1 HG01070.hp1 others(73): Show |
intron_variant | MODIFIER | c.573+19360dupA | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chrX | 37591800 | |||||
| chrX:37591854
|
T | C | 4 | a0001c0001t0001g0059a0001c0001t0001g0068a0001c0001t0001g0070others(1): Show | 4 | HG01256.hp1 HG01358.hp1 HG02132.hp1 others(1): Show |
intron_variant | MODIFIER | c.573+19411T>C | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37591854 | ||||||
| chrX:37591993
|
A | G | 1 | a0001c0003t0047g0189 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.573+19550A>G | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37591993 | ||||||
| chrX:37592026
|
C | A | 1 | a0001c0002t0049g0127 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.573+19583C>A | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37592026 | ||||||
| chrX:37592614
|
TA | T | 1 | a0001c0001t0001g0106 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.573+20179delA | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chrX | 37592614 | |||||
| chrX:37592619
|
A | G | 1 | a0001c0002t0049g0127 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.573+20176A>G | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37592619 | ||||||
| chrX:37592729
|
A | T | 9 | a0001c0001t0008g0184a0001c0001t0008g0186a0001c0001t0008g0187others(6): Show | 9 | HG01884.hp1 HG02055.hp1 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.573+20286A>T | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37592729 | ||||||
| chrX:37592934
|
T | C | 61 | a0001c0001t0006g0137a0001c0001t0006g0143a0001c0001t0006g0144others(58): Show | 65 | HG00639.hp2 HG00735.hp1 HG01070.hp1 others(62): Show |
intron_variant | MODIFIER | c.573+20491T>C | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37592934 | ||||||
| chrX:37592947
|
A | C | 1 | a0001c0002t0049g0127 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.573+20504A>C | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37592947 | ||||||
| chrX:37593062
|
G | A | 5 | a0001c0002t0051g0180a0001c0002t0053g0181a0001c0004t0009g0006others(2): Show | 6 | HG02109.hp2 HG02615.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.573+20619G>A | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37593062 | ||||||
| chrX:37593191
|
T | A | 9 | a0001c0001t0008g0184a0001c0001t0008g0186a0001c0001t0008g0187others(6): Show | 9 | HG01884.hp1 HG02055.hp1 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.573+20748T>A | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37593191 | ||||||
| chrX:37593225
|
C | G | 1 | a0001c0001t0001g0053 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.573+20782C>G | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37593225 | ||||||
| chrX:37593226
|
T | G | 1 | a0001c0001t0001g0053 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.573+20783T>G | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37593226 | ||||||
| chrX:37593248
|
C | T | 3 | a0001c0002t0030g0153a0001c0003t0007g0134a0001c0003t0007g0154 | 3 | HG01255.hp1 HG03098.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.573+20805C>T | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37593248 | ||||||
| chrX:37593255
|
G | A | 1 | a0001c0001t0001g0115 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.573+20812G>A | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37593255 | ||||||
| chrX:37593273
|
G | GA | 2 | a0001c0001t0043g0056a0001c0002t0019g0057 | 2 | HG01884.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.573+20835dupA | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chrX | 37593273 | |||||
| chrX:37593727
|
A | G | 1 | a0001c0002t0049g0127 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.573+21284A>G | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37593727 | ||||||
| chrX:37593820
|
A | G | 6 | a0001c0001t0022g0150a0001c0002t0030g0153a0001c0003t0007g0134others(3): Show | 6 | HG01255.hp1 HG01891.hp2 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.573+21377A>G | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37593820 | ||||||
| chrX:37594019
|
C | T | 2 | a0001c0003t0015g0168a0001c0003t0015g0169 | 2 | HG02818.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.573+21576C>T | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37594019 | ||||||
| chrX:37594334
|
C | T | 1 | a0001c0001t0001g0118 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.573+21891C>T | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37594334 | ||||||
| chrX:37594341
|
T | C | 4 | a0001c0001t0048g0009a0001c0002t0045g0008a0001c0003t0005g0010others(1): Show | 4 | HG02647.hp1 HG03130.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.573+21898T>C | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37594341 | ||||||
| chrX:37594381
|
G | C | 1 | a0001c0002t0049g0127 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.573+21938G>C | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37594381 | ||||||
| chrX:37594418
|
T | C | 1 | a0001c0001t0001g0115 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.573+21975T>C | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37594418 | ||||||
| chrX:37594548
|
A | G | 1 | a0001c0002t0053g0181 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.573+22105A>G | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37594548 | ||||||
| chrX:37595100
|
C | T | 1 | a0001c0002t0054g0185 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.573+22657C>T | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37595100 | ||||||
| chrX:37595354
|
A | G | 1 | a0001c0002t0049g0127 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.573+22911A>G | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37595354 | ||||||
| chrX:37595374
|
T | C | 1 | a0001c0002t0049g0127 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.573+22931T>C | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37595374 | ||||||
| chrX:37595627
|
G | C | 1 | a0001c0002t0049g0127 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.573+23184G>C | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37595627 | ||||||
| chrX:37595678
|
A | G | 9 | a0001c0001t0008g0184a0001c0001t0008g0186a0001c0001t0008g0187others(6): Show | 9 | HG01884.hp1 HG02055.hp1 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.573+23235A>G | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37595678 | ||||||
| chrX:37595759
|
T | A | 1 | a0001c0001t0001g0053 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.573+23316T>A | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37595759 | ||||||
| chrX:37596201
|
A | C | 3 | a0001c0004t0009g0006a0001c0004t0009g0178a0001c0004t0009g0179 | 4 | HG02109.hp2 HG02615.hp1 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.573+23758A>C | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37596201 | ||||||
| chrX:37596622
|
AT | A | 1 | a0001c0002t0049g0127 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.573+24184delT | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chrX | 37596622 | |||||
| chrX:37596855
|
G | A | 1 | a0003c0009t0021g0190 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.573+24412G>A | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37596855 | ||||||
| chrX:37596922
|
T | G | 2 | a0001c0002t0014g0156a0001c0002t0027g0155 | 2 | HG02809.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.573+24479T>G | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37596922 | ||||||
| chrX:37597130
|
T | C | 3 | a0001c0002t0033g0172a0001c0003t0013g0170a0001c0003t0013g0171 | 3 | HG02895.hp1 HG02897.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.573+24687T>C | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37597130 | ||||||
| chrX:37597192
|
A | G | 1 | a0001c0002t0049g0127 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.573+24749A>G | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37597192 | ||||||
| chrX:37597657
|
G | A | 1 | a0001c0001t0001g0012 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.573+25214G>A | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37597657 | ||||||
| chrX:37597668
|
C | CT | 34 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0016others(31): Show | 34 | HG00673.hp1 HG00735.hp2 HG01106.hp1 others(31): Show |
intron_variant | MODIFIER | c.573+25253dupT | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chrX | 37597668 | |||||
| chrX:37597668
|
C | CTT | 2 | a0001c0001t0001g0059a0001c0002t0016g0177 | 2 | HG01358.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.573+25252_573+2525 others(6): Show |
LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chrX | 37597668 | |||||
| chrX:37597668
|
C | CTTT | 1 | a0001c0002t0016g0176 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.573+25251_573+2525 others(7): Show |
LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chrX | 37597668 | |||||
| chrX:37597668
|
CT | C | 12 | a0001c0001t0008g0184a0001c0001t0008g0186a0001c0001t0008g0187others(9): Show | 13 | HG01884.hp1 HG02109.hp2 HG02630.hp1 others(10): Show |
intron_variant | MODIFIER | c.573+25253delT | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chrX | 37597668 | |||||
| chrX:37597668
|
CTTTTTTT others(4): Show |
C | 2 | a0001c0002t0051g0180a0001c0002t0053g0181 | 2 | HG02970.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.573+25243_573+2525 others(15): Show |
LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chrX | 37597668 | |||||
| chrX:37597668
|
CTTTTTTT others(5): Show |
C | 1 | a0001c0003t0005g0007 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.573+25242_573+2525 others(16): Show |
LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chrX | 37597668 | |||||
| chrX:37597758
|
C | T | 9 | a0001c0001t0008g0184a0001c0001t0008g0186a0001c0001t0008g0187others(6): Show | 9 | HG01884.hp1 HG02055.hp1 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.573+25315C>T | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37597758 | ||||||
| chrX:37597930
|
A | G | 1 | a0003c0009t0021g0190 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.573+25487A>G | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37597930 | ||||||
| chrX:37598217
|
A | G | 16 | a0001c0001t0008g0184a0001c0001t0008g0186a0001c0001t0008g0187others(13): Show | 17 | HG01884.hp1 HG02055.hp1 HG02109.hp2 others(14): Show |
intron_variant | MODIFIER | c.573+25774A>G | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37598217 | ||||||
| chrX:37598323
|
A | G | 2 | a0001c0002t0016g0176a0001c0002t0016g0177 | 2 | HG02970.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.573+25880A>G | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37598323 | ||||||
| chrX:37598898
|
A | C | 1 | a0001c0001t0008g0088 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.573+26455A>C | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37598898 | ||||||
| chrX:37598988
|
T | A | 1 | a0001c0002t0049g0127 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.573+26545T>A | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37598988 | ||||||
| chrX:37599051
|
C | T | 5 | a0001c0002t0051g0180a0001c0002t0053g0181a0001c0004t0009g0006others(2): Show | 6 | HG02109.hp2 HG02615.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.573+26608C>T | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37599051 | ||||||
| chrX:37599196
|
G | C | 1 | a0001c0002t0049g0127 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.573+26753G>C | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37599196 | ||||||
| chrX:37599373
|
C | G | 1 | a0001c0002t0004g0167 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.573+26930C>G | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37599373 | ||||||
| chrX:37599603
|
C | T | 1 | a0001c0001t0008g0088 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.573+27160C>T | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37599603 | ||||||
| chrX:37599680
|
G | A | 1 | a0006c0006t0019g0038 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.573+27237G>A | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37599680 | ||||||
| chrX:37599689
|
A | G | 1 | a0001c0003t0005g0119 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.573+27246A>G | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37599689 | ||||||
| chrX:37599955
|
TATTTGTA others(3): Show |
T | 4 | a0001c0001t0008g0184a0001c0001t0008g0186a0001c0001t0008g0187others(1): Show | 4 | HG01884.hp1 HG02055.hp1 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.573+27513_573+2752 others(14): Show |
LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37599955 | ||||||
| chrX:37599971
|
T | C | 2 | a0001c0001t0001g0118a0001c0001t0001g0121 | 2 | HG01099.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.573+27528T>C | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37599971 | ||||||
| chrX:37600279
|
T | G | 1 | a0001c0001t0043g0056 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.573+27836T>G | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37600279 | ||||||
| chrX:37600480
|
C | A | 1 | a0001c0002t0004g0167 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.573+28037C>A | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37600480 | ||||||
| chrX:37600634
|
C | T | 71 | a0001c0001t0006g0137a0001c0001t0006g0143a0001c0001t0006g0144others(68): Show | 75 | HG00639.hp2 HG00735.hp1 HG01070.hp1 others(72): Show |
intron_variant | MODIFIER | c.573+28191C>T | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37600634 | ||||||
| chrX:37601109
|
G | A | 1 | a0003c0009t0021g0190 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.573+28666G>A | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37601109 | ||||||
| chrX:37601362
|
G | C | 5 | a0001c0002t0051g0180a0001c0002t0053g0181a0001c0004t0009g0006others(2): Show | 6 | HG02109.hp2 HG02615.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.573+28919G>C | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37601362 | ||||||
| chrX:37601471
|
AG | A | 20 | a0001c0001t0006g0137a0001c0001t0006g0143a0001c0001t0006g0144others(17): Show | 20 | HG00639.hp2 HG02083.hp1 HG02109.hp1 others(17): Show |
intron_variant | MODIFIER | c.573+29031delG | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chrX | 37601471 | |||||
| chrX:37601633
|
T | C | 6 | a0001c0001t0001g0071a0001c0001t0008g0088a0001c0001t0020g0104others(3): Show | 6 | HG02451.hp2 HG02630.hp2 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.573+29190T>C | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37601633 | ||||||
| chrX:37601689
|
C | T | 3 | a0001c0001t0001g0029a0001c0001t0001g0030a0001c0001t0001g0031 | 3 | NA18970.hp1 NA19066.hp1 NA19088.hp1 |
intron_variant | MODIFIER | c.573+29246C>T | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37601689 | ||||||
| chrX:37601958
|
C | G | 1 | a0001c0001t0042g0087 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.573+29515C>G | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37601958 | ||||||
| chrX:37602114
|
A | C | 1 | a0001c0001t0017g0086 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.573+29671A>C | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37602114 | ||||||
| chrX:37602232
|
G | T | 1 | a0001c0003t0005g0007 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.573+29789G>T | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37602232 | ||||||
| chrX:37602610
|
T | C | 54 | a0001c0001t0006g0137a0001c0001t0006g0143a0001c0001t0006g0144others(51): Show | 58 | HG00639.hp2 HG00735.hp1 HG01070.hp1 others(55): Show |
intron_variant | MODIFIER | c.573+30167T>C | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37602610 | ||||||
| chrX:37602889
|
T | A | 20 | a0001c0001t0006g0137a0001c0001t0006g0143a0001c0001t0006g0144others(17): Show | 20 | HG00639.hp2 HG02083.hp1 HG02109.hp1 others(17): Show |
intron_variant | MODIFIER | c.573+30446T>A | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37602889 | ||||||
| chrX:37602915
|
G | T | 54 | a0001c0001t0006g0137a0001c0001t0006g0143a0001c0001t0006g0144others(51): Show | 58 | HG00639.hp2 HG00735.hp1 HG01070.hp1 others(55): Show |
intron_variant | MODIFIER | c.573+30472G>T | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37602915 | ||||||
| chrX:37602936
|
AC | A | 15 | a0001c0001t0008g0184a0001c0001t0008g0186a0001c0001t0008g0187others(12): Show | 16 | HG01884.hp1 HG02055.hp1 HG02109.hp2 others(13): Show |
intron_variant | MODIFIER | c.573+30495delC | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chrX | 37602936 | |||||
| chrX:37603010
|
C | T | 54 | a0001c0001t0006g0137a0001c0001t0006g0143a0001c0001t0006g0144others(51): Show | 58 | HG00639.hp2 HG00735.hp1 HG01070.hp1 others(55): Show |
intron_variant | MODIFIER | c.573+30567C>T | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37603010 | ||||||
| chrX:37603282
|
G | A | 4 | a0001c0001t0020g0052a0001c0001t0043g0056a0001c0002t0019g0057others(1): Show | 4 | HG01884.hp2 HG02622.hp2 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.573+30839G>A | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37603282 | ||||||
| chrX:37603523
|
T | C | 11 | a0001c0002t0002g0002a0001c0002t0002g0135a0001c0002t0002g0157others(8): Show | 14 | HG00735.hp1 HG01070.hp1 HG01081.hp1 others(11): Show |
intron_variant | MODIFIER | c.573+31080T>C | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37603523 | ||||||
| chrX:37603556
|
GATGA | G | 21 | a0001c0001t0006g0137a0001c0001t0006g0143a0001c0001t0006g0144others(18): Show | 21 | HG00639.hp2 HG02083.hp1 HG02109.hp1 others(18): Show |
intron_variant | MODIFIER | c.573+31123_573+3112 others(8): Show |
LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chrX | 37603556 | |||||
| chrX:37603833
|
A | G | 71 | a0001c0001t0006g0137a0001c0001t0006g0143a0001c0001t0006g0144others(68): Show | 75 | HG00639.hp2 HG00735.hp1 HG01070.hp1 others(72): Show |
intron_variant | MODIFIER | c.573+31390A>G | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37603833 | ||||||
| chrX:37604086
|
C | G | 9 | a0001c0001t0008g0184a0001c0001t0008g0186a0001c0001t0008g0187others(6): Show | 9 | HG01884.hp1 HG02055.hp1 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.573+31643C>G | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37604086 | ||||||
| chrX:37604214
|
C | G | 1 | a0001c0001t0042g0087 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.573+31771C>G | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37604214 | ||||||
| chrX:37604435
|
G | T | 1 | a0001c0004t0023g0165 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.573+31992G>T | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37604435 | ||||||
| chrX:37604567
|
G | T | 1 | a0001c0002t0054g0185 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.573+32124G>T | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37604567 | ||||||
| chrX:37604977
|
G | T | 8 | a0001c0001t0001g0037a0001c0001t0001g0042a0001c0001t0001g0055others(5): Show | 8 | HG02027.hp1 HG02056.hp1 HG03669.hp2 others(5): Show |
intron_variant | MODIFIER | c.573+32534G>T | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37604977 | ||||||
| chrX:37605146
|
A | G | 1 | a0001c0002t0051g0180 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.573+32703A>G | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37605146 | ||||||
| chrX:37605230
|
C | G | 1 | a0001c0001t0040g0072 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.573+32787C>G | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37605230 | ||||||
| chrX:37605280
|
T | C | 73 | a0001c0001t0001g0089a0001c0001t0006g0137a0001c0001t0006g0143others(70): Show | 77 | HG00639.hp2 HG00735.hp1 HG01070.hp1 others(74): Show |
intron_variant | MODIFIER | c.573+32837T>C | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37605280 | ||||||
| chrX:37605449
|
G | A | 1 | a0001c0001t0001g0118 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.573+33006G>A | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37605449 | ||||||
| chrX:37605636
|
C | G | 5 | a0001c0002t0002g0135a0001c0002t0002g0157a0001c0002t0002g0158others(2): Show | 5 | HG00735.hp1 HG01070.hp1 HG01081.hp1 others(2): Show |
intron_variant | MODIFIER | c.573+33193C>G | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37605636 | ||||||
| chrX:37605959
|
C | T | 1 | a0001c0002t0049g0127 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.573+33516C>T | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37605959 | ||||||
| chrX:37606206
|
G | C | 1 | a0001c0003t0005g0007 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.573+33763G>C | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37606206 | ||||||
| chrX:37606232
|
C | T | 1 | a0001c0001t0020g0052 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.573+33789C>T | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37606232 | ||||||
| chrX:37606473
|
G | A | 1 | a0001c0003t0005g0007 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.573+34030G>A | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37606473 | ||||||
| chrX:37606610
|
C | T | 14 | a0001c0002t0002g0002a0001c0002t0002g0135a0001c0002t0002g0157others(11): Show | 17 | HG00735.hp1 HG01070.hp1 HG01081.hp1 others(14): Show |
intron_variant | MODIFIER | c.573+34167C>T | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37606610 | ||||||
| chrX:37606718
|
G | A | 26 | a0001c0001t0001g0089a0001c0001t0006g0143a0001c0001t0006g0144others(23): Show | 27 | HG00639.hp2 HG02071.hp1 HG02083.hp1 others(24): Show |
intron_variant | MODIFIER | c.573+34275G>A | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37606718 | ||||||
| chrX:37606908
|
G | A | 1 | a0001c0003t0024g0136 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.573+34465G>A | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37606908 | ||||||
| chrX:37607171
|
C | G | 30 | a0001c0001t0001g0089a0001c0001t0006g0143a0001c0001t0006g0144others(27): Show | 31 | HG00639.hp2 HG02071.hp1 HG02083.hp1 others(28): Show |
intron_variant | MODIFIER | c.573+34728C>G | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37607171 | ||||||
| chrX:37607265
|
A | G | 2 | a0001c0001t0020g0052a0001c0002t0045g0008 | 2 | HG03209.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.573+34822A>G | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37607265 | ||||||
| chrX:37608215
|
C | T | 2 | a0001c0003t0015g0168a0001c0003t0015g0169 | 2 | HG02818.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.573+35772C>T | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37608215 | ||||||
| chrX:37608479
|
G | C | 2 | a0001c0002t0051g0180a0001c0002t0053g0181 | 2 | HG02970.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.573+36036G>C | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37608479 | ||||||
| chrX:37609691
|
T | TA | 18 | a0001c0001t0031g0162a0001c0001t0043g0056a0001c0002t0002g0002others(15): Show | 21 | HG00735.hp1 HG01070.hp1 HG01081.hp1 others(18): Show |
intron_variant | MODIFIER | c.573+37257dupA | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chrX | 37609691 | |||||
| chrX:37609898
|
T | TA | 4 | a0001c0003t0005g0182a0001c0003t0005g0183a0001c0003t0047g0189others(1): Show | 4 | HG02965.hp1 HG03453.hp1 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.573+37461dupA | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chrX | 37609898 | |||||
| chrX:37610093
|
G | A | 1 | a0001c0001t0001g0073 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.573+37650G>A | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37610093 | ||||||
| chrX:37610259
|
G | A | 28 | a0001c0001t0001g0089a0001c0001t0006g0143a0001c0001t0006g0144others(25): Show | 29 | HG00639.hp2 HG02055.hp1 HG02071.hp1 others(26): Show |
intron_variant | MODIFIER | c.573+37816G>A | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37610259 | ||||||
| chrX:37610336
|
C | T | 2 | a0001c0003t0015g0168a0001c0003t0015g0169 | 2 | HG02818.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.573+37893C>T | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37610336 | ||||||
| chrX:37610363
|
A | G | 11 | a0001c0001t0022g0150a0001c0001t0048g0009a0001c0002t0014g0131others(8): Show | 11 | HG01255.hp1 HG01891.hp2 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.573+37920A>G | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37610363 | ||||||
| chrX:37610467
|
A | C | 70 | a0001c0001t0001g0065a0001c0001t0001g0089a0001c0001t0006g0143others(67): Show | 73 | HG00639.hp2 HG00735.hp1 HG01070.hp1 others(70): Show |
intron_variant | MODIFIER | c.573+38024A>C | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37610467 | ||||||
| chrX:37610621
|
G | A | 1 | a0001c0002t0019g0057 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.573+38178G>A | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37610621 | ||||||
| chrX:37610695
|
G | C | 2 | a0001c0003t0013g0170a0001c0003t0013g0171 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.573+38252G>C | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37610695 | ||||||
| chrX:37611271
|
C | A | 1 | a0001c0001t0001g0103 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.573+38828C>A | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37611271 | ||||||
| chrX:37611371
|
G | GT | 1 | a0001c0001t0039g0018 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.573+38936dupT | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chrX | 37611371 | |||||
| chrX:37611526
|
T | G | 1 | a0001c0001t0001g0043 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.573+39083T>G | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37611526 | ||||||
| chrX:37611711
|
G | A | 7 | a0001c0002t0004g0133a0001c0002t0004g0167a0001c0002t0021g0054others(4): Show | 7 | HG01891.hp1 HG02615.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.573+39268G>A | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37611711 | ||||||
| chrX:37611860
|
A | C | 28 | a0001c0001t0017g0086a0001c0001t0018g0116a0001c0002t0004g0133others(25): Show | 28 | HG01255.hp1 HG01884.hp2 HG01891.hp1 others(25): Show |
intron_variant | MODIFIER | c.573+39417A>C | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37611860 | ||||||
| chrX:37612130
|
C | T | 1 | a0001c0001t0001g0102 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.573+39687C>T | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37612130 | ||||||
| chrX:37612378
|
T | A | 1 | a0001c0001t0001g0174 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.573+39935T>A | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37612378 | ||||||
| chrX:37612559
|
T | C | 5 | a0001c0001t0017g0086a0001c0001t0018g0116a0001c0002t0014g0131others(2): Show | 5 | HG02602.hp1 HG02809.hp2 HG03516.hp2 others(2): Show |
intron_variant | MODIFIER | c.573+40116T>C | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37612559 | ||||||
| chrX:37613136
|
T | C | 5 | a0001c0001t0017g0086a0001c0001t0018g0116a0001c0002t0014g0131others(2): Show | 5 | HG02602.hp1 HG02809.hp2 HG03516.hp2 others(2): Show |
intron_variant | MODIFIER | c.573+40693T>C | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37613136 | ||||||
| chrX:37613896
|
A | AC | 1 | a0001c0001t0001g0012 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.573+41457dupC | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chrX | 37613896 | |||||
| chrX:37614350
|
A | G | 9 | a0001c0002t0016g0176a0001c0002t0016g0177a0001c0002t0032g0166others(6): Show | 9 | HG02572.hp1 HG02818.hp2 HG02970.hp1 others(6): Show |
intron_variant | MODIFIER | c.574-41338A>G | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37614350 | ||||||
| chrX:37614661
|
A | G | 11 | a0001c0002t0004g0133a0001c0002t0004g0167a0001c0002t0019g0057others(8): Show | 11 | HG01884.hp2 HG01891.hp1 HG02055.hp1 others(8): Show |
intron_variant | MODIFIER | c.574-41027A>G | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37614661 | ||||||
| chrX:37614734
|
A | T | 1 | a0001c0001t0001g0126 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.574-40954A>T | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37614734 | ||||||
| chrX:37615107
|
A | G | 1 | a0001c0002t0019g0057 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.574-40581A>G | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37615107 | ||||||
| chrX:37615128
|
C | T | 1 | a0001c0004t0009g0179 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.574-40560C>T | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37615128 | ||||||
| chrX:37615205
|
G | A | 16 | a0001c0001t0010g0146a0001c0001t0010g0147a0001c0001t0017g0086others(13): Show | 16 | HG01891.hp1 HG02055.hp1 HG02109.hp1 others(13): Show |
intron_variant | MODIFIER | c.574-40483G>A | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37615205 | ||||||
| chrX:37615318
|
T | C | 1 | a0001c0001t0001g0114 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.574-40370T>C | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37615318 | ||||||
| chrX:37615336
|
T | C | 3 | a0001c0002t0014g0131a0001c0002t0014g0156a0001c0002t0027g0155 | 3 | HG02809.hp2 HG03516.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.574-40352T>C | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37615336 | ||||||
| chrX:37615618
|
T | G | 1 | a0001c0001t0001g0058 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.574-40070T>G | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37615618 | ||||||
| chrX:37615880
|
G | A | 74 | a0001c0001t0001g0074a0001c0001t0001g0089a0001c0001t0010g0146others(71): Show | 79 | HG00609.hp1 HG00639.hp1 HG00639.hp2 others(76): Show |
intron_variant | MODIFIER | c.574-39808G>A | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37615880 | ||||||
| chrX:37616012
|
C | T | 3 | a0001c0003t0012g0161a0001c0003t0012g0163a0001c0003t0046g0011 | 3 | HG02622.hp1 HG03471.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.574-39676C>T | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37616012 | ||||||
| chrX:37616232
|
C | CAT | 17 | a0001c0001t0017g0086a0001c0001t0018g0116a0001c0002t0004g0133others(14): Show | 17 | HG01884.hp2 HG01891.hp1 HG02055.hp1 others(14): Show |
intron_variant | MODIFIER | c.574-39447_574-3944 others(6): Show |
LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chrX | 37616232 | |||||
| chrX:37616315
|
A | G | 1 | a0001c0001t0001g0031 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.574-39373A>G | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37616315 | ||||||
| chrX:37616391
|
CAG | C | 6 | a0001c0002t0002g0002a0001c0002t0002g0135a0001c0002t0002g0157others(3): Show | 9 | HG00735.hp1 HG01070.hp1 HG01081.hp1 others(6): Show |
intron_variant | MODIFIER | c.574-39296_574-3929 others(6): Show |
LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37616391 | ||||||
| chrX:37616488
|
C | T | 1 | a0001c0001t0018g0116 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.574-39200C>T | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37616488 | ||||||
| chrX:37616643
|
G | A | 1 | a0001c0002t0019g0057 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.574-39045G>A | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37616643 | ||||||
| chrX:37616945
|
T | C | 1 | a0001c0001t0001g0071 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.574-38743T>C | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37616945 | ||||||
| chrX:37617038
|
C | CA | 3 | a0001c0001t0001g0059a0001c0001t0001g0068a0001c0001t0055g0035 | 3 | HG01256.hp1 HG01358.hp1 NA18955.hp1 |
intron_variant | MODIFIER | c.574-38643dupA | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chrX | 37617038 | |||||
| chrX:37617058
|
G | A | 3 | a0001c0002t0016g0176a0001c0002t0016g0177a0001c0002t0033g0172 | 3 | HG02970.hp1 HG03225.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.574-38630G>A | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37617058 | ||||||
| chrX:37617101
|
T | C | 5 | a0001c0001t0017g0086a0001c0001t0018g0116a0001c0001t0040g0072others(2): Show | 5 | HG02451.hp2 HG02602.hp1 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.574-38587T>C | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37617101 | ||||||
| chrX:37617121
|
T | TG | 4 | a0001c0001t0001g0028a0001c0001t0001g0060a0001c0001t0038g0109others(1): Show | 4 | HG01261.hp1 HG01433.hp1 HG02738.hp1 others(1): Show |
intron_variant | MODIFIER | c.574-38560dupG | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chrX | 37617121 | |||||
| chrX:37617474
|
A | C | 2 | a0001c0001t0020g0052a0001c0001t0020g0104 | 2 | HG02809.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.574-38214A>C | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37617474 | ||||||
| chrX:37617599
|
C | T | 12 | a0001c0002t0030g0153a0001c0003t0005g0007a0001c0003t0005g0010others(9): Show | 12 | HG01255.hp1 HG01891.hp2 HG02622.hp2 others(9): Show |
intron_variant | MODIFIER | c.574-38089C>T | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37617599 | ||||||
| chrX:37617601
|
A | G | 1 | a0001c0001t0001g0027 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.574-38087A>G | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37617601 | ||||||
| chrX:37617609
|
A | G | 1 | a0001c0002t0019g0057 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.574-38079A>G | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37617609 | ||||||
| chrX:37618171
|
C | A | 2 | a0001c0001t0020g0052a0001c0001t0020g0104 | 2 | HG02809.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.574-37517C>A | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37618171 | ||||||
| chrX:37618404
|
GCCCTTAC others(2): Show |
G | 1 | a0001c0001t0001g0029 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.574-37279_574-3727 others(13): Show |
LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chrX | 37618404 | |||||
| chrX:37618616
|
T | C | 3 | a0001c0001t0010g0146a0001c0001t0010g0147a0001c0001t0010g0148 | 3 | HG02109.hp1 HG02145.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.574-37072T>C | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37618616 | ||||||
| chrX:37618957
|
A | G | 61 | a0001c0001t0017g0083a0001c0001t0017g0086a0001c0001t0018g0116others(58): Show | 66 | HG00639.hp1 HG00639.hp2 HG00735.hp1 others(63): Show |
intron_variant | MODIFIER | c.574-36731A>G | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37618957 | ||||||
| chrX:37619384
|
G | A | 1 | a0001c0001t0001g0100 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.574-36304G>A | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37619384 | ||||||
| chrX:37619396
|
A | G | 1 | a0001c0002t0053g0181 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.574-36292A>G | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37619396 | ||||||
| chrX:37619571
|
A | AATTTGGT others(1): Show |
60 | a0001c0001t0017g0083a0001c0001t0017g0086a0001c0001t0018g0116others(57): Show | 65 | HG00639.hp1 HG00639.hp2 HG00735.hp1 others(62): Show |
intron_variant | MODIFIER | c.574-36117_574-3611 others(12): Show |
LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37619571 | ||||||
| chrX:37619656
|
G | A | 1 | a0001c0001t0001g0174 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.574-36032G>A | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37619656 | ||||||
| chrX:37619930
|
C | T | 25 | a0001c0001t0031g0162a0001c0001t0048g0009a0001c0002t0003g0005others(22): Show | 26 | HG00639.hp1 HG00639.hp2 HG01069.hp1 others(23): Show |
intron_variant | MODIFIER | c.574-35758C>T | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37619930 | ||||||
| chrX:37620754
|
A | G | 1 | a0001c0003t0029g0132 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.574-34934A>G | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37620754 | ||||||
| chrX:37620902
|
T | TC | 1 | a0001c0001t0039g0018 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.574-34783dupC | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chrX | 37620902 | |||||
| chrX:37620933
|
G | C | 1 | a0001c0003t0024g0136 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.574-34755G>C | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37620933 | ||||||
| chrX:37620977
|
A | G | 65 | a0001c0001t0001g0050a0001c0001t0001g0122a0001c0001t0017g0083others(62): Show | 70 | HG00639.hp1 HG00639.hp2 HG00735.hp1 others(67): Show |
intron_variant | MODIFIER | c.574-34711A>G | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37620977 | ||||||
| chrX:37621064
|
G | GC | 1 | a0001c0001t0001g0012 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.574-34619dupC | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chrX | 37621064 | |||||
| chrX:37621167
|
T | C | 1 | a0001c0003t0024g0136 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.574-34521T>C | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37621167 | ||||||
| chrX:37621202
|
C | T | 15 | a0001c0001t0017g0083a0001c0001t0017g0086a0001c0001t0018g0116others(12): Show | 19 | HG00735.hp1 HG01070.hp1 HG01081.hp1 others(16): Show |
intron_variant | MODIFIER | c.574-34486C>T | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37621202 | ||||||
| chrX:37622114
|
C | T | 7 | a0001c0001t0020g0052a0001c0001t0020g0104a0001c0002t0016g0176others(4): Show | 7 | HG02055.hp1 HG02630.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.574-33574C>T | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37622114 | ||||||
| chrX:37622225
|
T | C | 7 | a0001c0001t0020g0052a0001c0001t0020g0104a0001c0002t0016g0176others(4): Show | 7 | HG02055.hp1 HG02630.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.574-33463T>C | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37622225 | ||||||
| chrX:37622319
|
C | G | 1 | a0001c0001t0001g0111 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.574-33369C>G | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37622319 | ||||||
| chrX:37622393
|
C | CT | 1 | a0001c0001t0001g0115 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.574-33282dupT | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chrX | 37622393 | |||||
| chrX:37622393
|
CT | C | 61 | a0001c0001t0001g0076a0001c0001t0001g0129a0001c0001t0010g0146others(58): Show | 66 | HG00140.hp1 HG00639.hp1 HG00639.hp2 others(63): Show |
intron_variant | MODIFIER | c.574-33282delT | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chrX | 37622393 | |||||
| chrX:37622393
|
CTT | C | 2 | a0001c0003t0015g0168a0001c0003t0015g0169 | 2 | HG02818.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.574-33283_574-3328 others(6): Show |
LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chrX | 37622393 | |||||
| chrX:37622522
|
TTATACTA others(19): Show |
T | 1 | a0001c0002t0053g0181 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.574-33163_574-3313 others(30): Show |
LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chrX | 37622522 | |||||
| chrX:37622598
|
T | C | 2 | a0001c0001t0001g0037a0001c0001t0001g0084 | 2 | HG02027.hp1 NA18995.hp1 |
intron_variant | MODIFIER | c.574-33090T>C | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37622598 | ||||||
| chrX:37622837
|
T | C | 65 | a0001c0001t0020g0052a0001c0001t0020g0104a0001c0001t0031g0162others(62): Show | 70 | HG00639.hp1 HG00639.hp2 HG00735.hp1 others(67): Show |
intron_variant | MODIFIER | c.574-32851T>C | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37622837 | ||||||
| chrX:37622947
|
A | G | 1 | a0001c0002t0032g0166 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.574-32741A>G | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37622947 | ||||||
| chrX:37623266
|
C | T | 57 | a0001c0001t0031g0162a0001c0001t0048g0009a0001c0002t0002g0002others(54): Show | 62 | HG00639.hp1 HG00639.hp2 HG00735.hp1 others(59): Show |
intron_variant | MODIFIER | c.574-32422C>T | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37623266 | ||||||
| chrX:37623282
|
C | T | 1 | a0001c0001t0001g0033 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.574-32406C>T | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37623282 | ||||||
| chrX:37624265
|
A | G | 3 | a0001c0001t0010g0146a0001c0001t0010g0147a0001c0001t0010g0148 | 3 | HG02109.hp1 HG02145.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.574-31423A>G | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37624265 | ||||||
| chrX:37624393
|
TC | T | 1 | a0004c0008t0011g0130 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.574-31292delC | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chrX | 37624393 | |||||
| chrX:37624782
|
T | C | 1 | a0001c0001t0001g0062 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.574-30906T>C | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37624782 | ||||||
| chrX:37624809
|
A | G | 2 | a0001c0004t0023g0165a0005c0007t0044g0064 | 2 | HG02055.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.574-30879A>G | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37624809 | ||||||
| chrX:37624855
|
G | A | 1 | a0001c0002t0003g0075 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.574-30833G>A | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37624855 | ||||||
| chrX:37624957
|
C | A | 1 | a0001c0002t0028g0139 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.574-30731C>A | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37624957 | ||||||
| chrX:37625288
|
T | C | 5 | a0001c0003t0015g0168a0001c0003t0015g0169a0001c0003t0029g0132others(2): Show | 5 | HG02818.hp2 HG03041.hp1 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.574-30400T>C | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37625288 | ||||||
| chrX:37625662
|
G | A | 1 | a0001c0001t0001g0073 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.574-30026G>A | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37625662 | ||||||
| chrX:37625723
|
C | G | 2 | a0001c0001t0020g0052a0001c0001t0020g0104 | 2 | HG02809.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.574-29965C>G | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37625723 | ||||||
| chrX:37625855
|
A | G | 1 | a0001c0001t0001g0042 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.574-29833A>G | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37625855 | ||||||
| chrX:37625922
|
C | T | 6 | a0001c0002t0002g0002a0001c0002t0002g0135a0001c0002t0002g0157others(3): Show | 9 | HG00735.hp1 HG01070.hp1 HG01081.hp1 others(6): Show |
intron_variant | MODIFIER | c.574-29766C>T | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37625922 | ||||||
| chrX:37626106
|
A | G | 3 | a0001c0002t0014g0131a0001c0002t0014g0156a0001c0002t0027g0155 | 3 | HG02809.hp2 HG03516.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.574-29582A>G | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37626106 | ||||||
| chrX:37626156
|
C | T | 1 | a0001c0002t0026g0142 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.574-29532C>T | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37626156 | ||||||
| chrX:37626197
|
C | T | 2 | a0001c0003t0047g0189a0001c0003t0050g0188 | 2 | HG03453.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.574-29491C>T | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37626197 | ||||||
| chrX:37626390
|
A | G | 1 | a0001c0002t0051g0180 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.574-29298A>G | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37626390 | ||||||
| chrX:37626405
|
A | G | 42 | a0001c0001t0031g0162a0001c0001t0048g0009a0001c0002t0002g0002others(39): Show | 47 | HG00639.hp1 HG00639.hp2 HG00735.hp1 others(44): Show |
intron_variant | MODIFIER | c.574-29283A>G | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37626405 | ||||||
| chrX:37626553
|
G | T | 2 | a0001c0003t0012g0161a0001c0003t0012g0163 | 2 | HG02622.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.574-29135G>T | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37626553 | ||||||
| chrX:37626578
|
GATC | G | 1 | a0005c0007t0044g0064 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.574-29107_574-2910 others(7): Show |
LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chrX | 37626578 | |||||
| chrX:37626838
|
T | G | 42 | a0001c0001t0031g0162a0001c0001t0048g0009a0001c0002t0002g0002others(39): Show | 47 | HG00639.hp1 HG00639.hp2 HG00735.hp1 others(44): Show |
intron_variant | MODIFIER | c.574-28850T>G | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37626838 | ||||||
| chrX:37626904
|
G | A | 4 | a0001c0001t0001g0024a0001c0001t0001g0027a0001c0001t0001g0063others(1): Show | 4 | NA18945.hp1 NA18990.hp1 NA19076.hp1 others(1): Show |
intron_variant | MODIFIER | c.574-28784G>A | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37626904 | ||||||
| chrX:37626904
|
G | GC | 1 | a0004c0008t0011g0130 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.574-28781dupC | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chrX | 37626904 | |||||
| chrX:37627324
|
A | G | 1 | a0001c0001t0001g0082 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.574-28364A>G | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37627324 | ||||||
| chrX:37627727
|
T | C | 4 | a0001c0003t0015g0168a0001c0003t0015g0169a0001c0003t0047g0189others(1): Show | 4 | HG02818.hp2 HG03041.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.574-27961T>C | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37627727 | ||||||
| chrX:37627747
|
G | T | 1 | a0001c0002t0003g0069 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.574-27941G>T | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37627747 | ||||||
| chrX:37627748
|
T | C | 1 | a0001c0001t0010g0148 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.574-27940T>C | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37627748 | ||||||
| chrX:37627801
|
C | G | 1 | a0001c0003t0029g0132 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.574-27887C>G | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37627801 | ||||||
| chrX:37628063
|
TA | T | 1 | a0004c0008t0011g0130 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.574-27621delA | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chrX | 37628063 | |||||
| chrX:37628151
|
A | G | 2 | a0001c0002t0019g0057a0001c0002t0045g0008 | 2 | HG01884.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.574-27537A>G | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37628151 | ||||||
| chrX:37628166
|
A | AG | 1 | a0004c0008t0011g0130 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.574-27517dupG | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chrX | 37628166 | |||||
| chrX:37628271
|
CTT | C | 1 | a0001c0002t0004g0149 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.574-27415_574-2741 others(6): Show |
LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chrX | 37628271 | |||||
| chrX:37628309
|
G | T | 1 | a0005c0007t0044g0064 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.574-27379G>T | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37628309 | ||||||
| chrX:37628393
|
G | A | 1 | a0001c0001t0001g0111 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.574-27295G>A | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37628393 | ||||||
| chrX:37628442
|
G | T | 73 | a0001c0001t0010g0146a0001c0001t0010g0147a0001c0001t0010g0148others(70): Show | 78 | HG00639.hp1 HG00639.hp2 HG00735.hp1 others(75): Show |
intron_variant | MODIFIER | c.574-27246G>T | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37628442 | ||||||
| chrX:37628482
|
A | G | 1 | a0001c0001t0001g0113 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.574-27206A>G | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37628482 | ||||||
| chrX:37628591
|
T | TC | 5 | a0001c0001t0001g0014a0001c0001t0001g0094a0001c0001t0017g0086others(2): Show | 5 | HG02074.hp1 HG02135.hp1 HG02602.hp1 others(2): Show |
intron_variant | MODIFIER | c.574-27091dupC | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chrX | 37628591 | |||||
| chrX:37628592
|
C | A | 1 | a0001c0001t0001g0126 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.574-27096C>A | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37628592 | ||||||
| chrX:37628598
|
T | TC | 2 | a0001c0001t0001g0027a0001c0004t0023g0165 | 2 | HG02055.hp1 NA19076.hp1 |
intron_variant | MODIFIER | c.574-27084dupC | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chrX | 37628598 | |||||
| chrX:37628649
|
C | CA | 1 | a0001c0001t0001g0027 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.574-27038dupA | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chrX | 37628649 | |||||
| chrX:37628695
|
G | A | 3 | a0001c0001t0010g0146a0001c0001t0010g0147a0001c0001t0010g0148 | 3 | HG02109.hp1 HG02145.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.574-26993G>A | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37628695 | ||||||
| chrX:37628739
|
T | C | 3 | a0001c0001t0010g0146a0001c0001t0010g0147a0001c0001t0010g0148 | 3 | HG02109.hp1 HG02145.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.574-26949T>C | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37628739 | ||||||
| chrX:37628757
|
T | TC | 1 | a0004c0008t0011g0130 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.574-26928dupC | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chrX | 37628757 | |||||
| chrX:37628990
|
A | G | 22 | a0001c0002t0014g0131a0001c0002t0030g0153a0001c0003t0005g0007others(19): Show | 22 | HG01255.hp1 HG01891.hp2 HG02615.hp2 others(19): Show |
intron_variant | MODIFIER | c.574-26698A>G | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37628990 | ||||||
| chrX:37629017
|
C | T | 46 | a0001c0001t0031g0162a0001c0001t0048g0009a0001c0002t0002g0002others(43): Show | 51 | HG00639.hp1 HG00639.hp2 HG00735.hp1 others(48): Show |
intron_variant | MODIFIER | c.574-26671C>T | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37629017 | ||||||
| chrX:37629037
|
T | G | 3 | a0001c0001t0010g0146a0001c0001t0010g0147a0001c0001t0010g0148 | 3 | HG02109.hp1 HG02145.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.574-26651T>G | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37629037 | ||||||
| chrX:37629052
|
A | C | 1 | a0001c0001t0001g0004 | 2 | HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.574-26636A>C | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37629052 | ||||||
| chrX:37629274
|
C | T | 1 | a0001c0001t0001g0115 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.574-26414C>T | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37629274 | ||||||
| chrX:37629310
|
G | A | 11 | a0001c0002t0002g0002a0001c0002t0002g0135a0001c0002t0002g0157others(8): Show | 15 | HG00735.hp1 HG01070.hp1 HG01081.hp1 others(12): Show |
intron_variant | MODIFIER | c.574-26378G>A | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37629310 | ||||||
| chrX:37629324
|
G | GT | 1 | a0001c0001t0001g0027 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.574-26362dupT | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chrX | 37629324 | |||||
| chrX:37629588
|
T | C | 47 | a0001c0001t0031g0162a0001c0001t0048g0009a0001c0002t0002g0002others(44): Show | 52 | HG00639.hp1 HG00639.hp2 HG00735.hp1 others(49): Show |
intron_variant | MODIFIER | c.574-26100T>C | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37629588 | ||||||
| chrX:37629589
|
G | A | 47 | a0001c0001t0031g0162a0001c0001t0048g0009a0001c0002t0002g0002others(44): Show | 52 | HG00639.hp1 HG00639.hp2 HG00735.hp1 others(49): Show |
intron_variant | MODIFIER | c.574-26099G>A | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37629589 | ||||||
| chrX:37629642
|
G | T | 23 | a0001c0001t0020g0052a0001c0001t0020g0104a0001c0002t0030g0153others(20): Show | 23 | HG01255.hp1 HG01891.hp2 HG02615.hp2 others(20): Show |
intron_variant | MODIFIER | c.574-26046G>T | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37629642 | ||||||
| chrX:37629907
|
G | A | 2 | a0001c0001t0020g0052a0001c0001t0020g0104 | 2 | HG02809.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.574-25781G>A | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37629907 | ||||||
| chrX:37630103
|
C | G | 1 | a0001c0001t0001g0175 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.574-25585C>G | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37630103 | ||||||
| chrX:37630185
|
C | G | 2 | a0001c0001t0001g0070a0001c0001t0001g0092 | 2 | HG02040.hp1 HG02132.hp1 |
intron_variant | MODIFIER | c.574-25503C>G | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37630185 | ||||||
| chrX:37630376
|
T | C | 1 | a0001c0001t0001g0077 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.574-25312T>C | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37630376 | ||||||
| chrX:37630426
|
A | T | 1 | a0001c0001t0001g0099 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.574-25262A>T | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37630426 | ||||||
| chrX:37630457
|
A | G | 1 | a0001c0001t0001g0111 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.574-25231A>G | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37630457 | ||||||
| chrX:37630606
|
T | C | 24 | a0001c0001t0020g0052a0001c0001t0020g0104a0001c0002t0014g0131others(21): Show | 24 | HG01255.hp1 HG01891.hp2 HG02615.hp2 others(21): Show |
intron_variant | MODIFIER | c.574-25082T>C | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37630606 | ||||||
| chrX:37630641
|
T | C | 46 | a0001c0001t0031g0162a0001c0001t0048g0009a0001c0002t0002g0002others(43): Show | 51 | HG00639.hp1 HG00639.hp2 HG00735.hp1 others(48): Show |
intron_variant | MODIFIER | c.574-25047T>C | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37630641 | ||||||
| chrX:37630678
|
C | T | 1 | a0001c0002t0028g0139 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.574-25010C>T | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37630678 | ||||||
| chrX:37630684
|
C | T | 1 | a0001c0002t0045g0008 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.574-25004C>T | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37630684 | ||||||
| chrX:37630713
|
C | T | 1 | a0001c0001t0040g0072 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.574-24975C>T | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37630713 | ||||||
| chrX:37630738
|
C | T | 1 | a0001c0001t0001g0129 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.574-24950C>T | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37630738 | ||||||
| chrX:37630765
|
G | A | 49 | a0001c0001t0031g0162a0001c0001t0048g0009a0001c0002t0002g0002others(46): Show | 54 | HG00639.hp1 HG00639.hp2 HG00735.hp1 others(51): Show |
intron_variant | MODIFIER | c.574-24923G>A | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37630765 | ||||||
| chrX:37630911
|
T | G | 1 | a0001c0001t0039g0018 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.574-24777T>G | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37630911 | ||||||
| chrX:37630934
|
C | T | 2 | a0001c0001t0020g0052a0001c0001t0020g0104 | 2 | HG02809.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.574-24754C>T | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37630934 | ||||||
| chrX:37631157
|
A | G | 1 | a0001c0003t0015g0169 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.574-24531A>G | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37631157 | ||||||
| chrX:37631168
|
G | A | 2 | a0001c0001t0020g0052a0001c0001t0020g0104 | 2 | HG02809.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.574-24520G>A | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37631168 | ||||||
| chrX:37631204
|
A | T | 1 | a0001c0001t0001g0055 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.574-24484A>T | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37631204 | ||||||
| chrX:37631259
|
C | G | 1 | a0005c0007t0044g0064 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.574-24429C>G | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37631259 | ||||||
| chrX:37631264
|
G | A | 46 | a0001c0001t0031g0162a0001c0001t0048g0009a0001c0002t0002g0002others(43): Show | 51 | HG00639.hp1 HG00639.hp2 HG00735.hp1 others(48): Show |
intron_variant | MODIFIER | c.574-24424G>A | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37631264 | ||||||
| chrX:37631279
|
T | C | 24 | a0001c0001t0020g0052a0001c0001t0020g0104a0001c0002t0014g0131others(21): Show | 24 | HG01255.hp1 HG01891.hp2 HG02615.hp2 others(21): Show |
intron_variant | MODIFIER | c.574-24409T>C | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37631279 | ||||||
| chrX:37631323
|
C | T | 1 | a0001c0001t0034g0048 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.574-24365C>T | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37631323 | ||||||
| chrX:37631419
|
T | C | 4 | a0001c0002t0004g0133a0001c0002t0004g0167a0001c0002t0021g0054others(1): Show | 4 | HG01891.hp1 HG02572.hp1 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.574-24269T>C | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37631419 | ||||||
| chrX:37631621
|
G | A | 2 | a0001c0001t0001g0050a0001c0001t0001g0122 | 2 | HG02486.hp1 HG03017.hp1 |
intron_variant | MODIFIER | c.574-24067G>A | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37631621 | ||||||
| chrX:37631789
|
C | T | 1 | a0001c0002t0016g0177 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.574-23899C>T | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37631789 | ||||||
| chrX:37631833
|
CTGT | C | 1 | a0001c0001t0001g0053 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.574-23853_574-2385 others(7): Show |
LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chrX | 37631833 | |||||
| chrX:37631899
|
G | A | 2 | a0001c0001t0010g0146a0001c0001t0010g0147 | 2 | HG02109.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.574-23789G>A | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37631899 | ||||||
| chrX:37631904
|
G | A | 46 | a0001c0001t0031g0162a0001c0001t0048g0009a0001c0002t0002g0002others(43): Show | 51 | HG00639.hp1 HG00639.hp2 HG00735.hp1 others(48): Show |
intron_variant | MODIFIER | c.574-23784G>A | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37631904 | ||||||
| chrX:37631922
|
C | A | 70 | a0001c0001t0020g0052a0001c0001t0020g0104a0001c0001t0031g0162others(67): Show | 75 | HG00639.hp1 HG00639.hp2 HG00735.hp1 others(72): Show |
intron_variant | MODIFIER | c.574-23766C>A | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37631922 | ||||||
| chrX:37632064
|
C | A | 23 | a0001c0001t0020g0052a0001c0001t0020g0104a0001c0002t0030g0153others(20): Show | 23 | HG01255.hp1 HG01891.hp2 HG02615.hp2 others(20): Show |
intron_variant | MODIFIER | c.574-23624C>A | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37632064 | ||||||
| chrX:37632413
|
C | T | 2 | a0001c0002t0003g0005a0001c0002t0003g0117 | 3 | HG00639.hp1 HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.574-23275C>T | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37632413 | ||||||
| chrX:37632496
|
G | A | 70 | a0001c0001t0020g0052a0001c0001t0020g0104a0001c0001t0031g0162others(67): Show | 75 | HG00639.hp1 HG00639.hp2 HG00735.hp1 others(72): Show |
intron_variant | MODIFIER | c.574-23192G>A | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37632496 | ||||||
| chrX:37632509
|
G | T | 3 | a0001c0001t0010g0146a0001c0001t0010g0147a0001c0001t0010g0148 | 3 | HG02109.hp1 HG02145.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.574-23179G>T | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37632509 | ||||||
| chrX:37632511
|
T | G | 6 | a0001c0001t0008g0088a0001c0001t0008g0184a0001c0001t0008g0186others(3): Show | 6 | HG01884.hp1 HG02258.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.574-23177T>G | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37632511 | ||||||
| chrX:37632602
|
T | A | 1 | a0001c0001t0034g0048 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.574-23086T>A | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37632602 | ||||||
| chrX:37632612
|
T | G | 25 | a0001c0001t0001g0082a0001c0001t0020g0052a0001c0001t0020g0104others(22): Show | 25 | HG01255.hp1 HG01891.hp2 HG02615.hp2 others(22): Show |
intron_variant | MODIFIER | c.574-23076T>G | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37632612 | ||||||
| chrX:37632761
|
T | G | 12 | a0001c0002t0030g0153a0001c0003t0005g0007a0001c0003t0005g0010others(9): Show | 12 | HG01255.hp1 HG01891.hp2 HG02622.hp2 others(9): Show |
intron_variant | MODIFIER | c.574-22927T>G | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37632761 | ||||||
| chrX:37632786
|
C | G | 47 | a0001c0001t0031g0162a0001c0001t0048g0009a0001c0002t0002g0002others(44): Show | 52 | HG00639.hp1 HG00639.hp2 HG00735.hp1 others(49): Show |
intron_variant | MODIFIER | c.574-22902C>G | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37632786 | ||||||
| chrX:37632861
|
A | T | 23 | a0001c0001t0020g0052a0001c0001t0020g0104a0001c0002t0030g0153others(20): Show | 23 | HG01255.hp1 HG01891.hp2 HG02615.hp2 others(20): Show |
intron_variant | MODIFIER | c.574-22827A>T | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37632861 | ||||||
| chrX:37632879
|
C | T | 1 | a0001c0002t0014g0131 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.574-22809C>T | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37632879 | ||||||
| chrX:37632916
|
C | A | 47 | a0001c0001t0031g0162a0001c0001t0048g0009a0001c0002t0002g0002others(44): Show | 52 | HG00639.hp1 HG00639.hp2 HG00735.hp1 others(49): Show |
intron_variant | MODIFIER | c.574-22772C>A | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37632916 | ||||||
| chrX:37633072
|
C | T | 1 | a0001c0001t0008g0088 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.574-22616C>T | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37633072 | ||||||
| chrX:37633125
|
C | T | 1 | a0001c0004t0023g0165 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.574-22563C>T | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37633125 | ||||||
| chrX:37633149
|
G | GT | 4 | a0001c0001t0001g0024a0001c0001t0001g0027a0001c0001t0001g0063others(1): Show | 4 | NA18945.hp1 NA18990.hp1 NA19076.hp1 others(1): Show |
intron_variant | MODIFIER | c.574-22526dupT | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chrX | 37633149 | |||||
| chrX:37633149
|
GT | G | 47 | a0001c0001t0031g0162a0001c0001t0048g0009a0001c0002t0002g0002others(44): Show | 52 | HG00639.hp1 HG00639.hp2 HG00735.hp1 others(49): Show |
intron_variant | MODIFIER | c.574-22526delT | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chrX | 37633149 | |||||
| chrX:37633183
|
C | T | 1 | a0001c0002t0011g0173 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.574-22505C>T | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37633183 | ||||||
| chrX:37633286
|
C | T | 2 | a0001c0003t0047g0189a0001c0003t0050g0188 | 2 | HG03453.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.574-22402C>T | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37633286 | ||||||
| chrX:37633298
|
T | C | 1 | a0001c0002t0002g0157 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.574-22390T>C | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37633298 | ||||||
| chrX:37633324
|
A | G | 1 | a0001c0002t0019g0057 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.574-22364A>G | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37633324 | ||||||
| chrX:37633393
|
G | A | 12 | a0001c0002t0030g0153a0001c0003t0005g0007a0001c0003t0005g0010others(9): Show | 12 | HG01255.hp1 HG01891.hp2 HG02622.hp2 others(9): Show |
intron_variant | MODIFIER | c.574-22295G>A | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37633393 | ||||||
| chrX:37633432
|
C | T | 47 | a0001c0001t0031g0162a0001c0001t0048g0009a0001c0002t0002g0002others(44): Show | 52 | HG00639.hp1 HG00639.hp2 HG00735.hp1 others(49): Show |
intron_variant | MODIFIER | c.574-22256C>T | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37633432 | ||||||
| chrX:37633522
|
C | T | 47 | a0001c0001t0031g0162a0001c0001t0048g0009a0001c0002t0002g0002others(44): Show | 52 | HG00639.hp1 HG00639.hp2 HG00735.hp1 others(49): Show |
intron_variant | MODIFIER | c.574-22166C>T | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37633522 | ||||||
| chrX:37633714
|
G | T | 1 | a0001c0002t0051g0180 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.574-21974G>T | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37633714 | ||||||
| chrX:37633809
|
C | T | 1 | a0001c0002t0051g0180 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.574-21879C>T | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37633809 | ||||||
| chrX:37634024
|
C | G | 1 | a0001c0001t0022g0150 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.574-21664C>G | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37634024 | ||||||
| chrX:37634166
|
G | A | 2 | a0001c0001t0020g0052a0001c0001t0020g0104 | 2 | HG02809.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.574-21522G>A | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37634166 | ||||||
| chrX:37634179
|
G | A | 47 | a0001c0001t0031g0162a0001c0001t0048g0009a0001c0002t0002g0002others(44): Show | 52 | HG00639.hp1 HG00639.hp2 HG00735.hp1 others(49): Show |
intron_variant | MODIFIER | c.574-21509G>A | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37634179 | ||||||
| chrX:37634279
|
C | T | 1 | a0001c0002t0004g0149 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.574-21409C>T | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37634279 | ||||||
| chrX:37634280
|
G | A | 1 | a0005c0007t0044g0064 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.574-21408G>A | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37634280 | ||||||
| chrX:37634496
|
C | T | 1 | a0001c0001t0001g0126 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.574-21192C>T | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37634496 | ||||||
| chrX:37634542
|
C | T | 47 | a0001c0001t0031g0162a0001c0001t0048g0009a0001c0002t0002g0002others(44): Show | 52 | HG00639.hp1 HG00639.hp2 HG00735.hp1 others(49): Show |
intron_variant | MODIFIER | c.574-21146C>T | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37634542 | ||||||
| chrX:37634687
|
CTAGAT | C | 1 | a0001c0004t0023g0165 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.574-20995_574-2099 others(9): Show |
LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chrX | 37634687 | |||||
| chrX:37634969
|
G | A | 3 | a0001c0001t0010g0146a0001c0001t0010g0147a0001c0001t0010g0148 | 3 | HG02109.hp1 HG02145.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.574-20719G>A | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37634969 | ||||||
| chrX:37634980
|
A | C | 1 | a0001c0001t0001g0014 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.574-20708A>C | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37634980 | ||||||
| chrX:37635027
|
T | TA | 2 | a0001c0001t0001g0067a0001c0002t0032g0166 | 2 | HG00735.hp2 HG02572.hp1 |
intron_variant | MODIFIER | c.574-20651dupA | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chrX | 37635027 | |||||
| chrX:37635027
|
TA | T | 1 | a0001c0003t0029g0132 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.574-20651delA | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chrX | 37635027 | |||||
| chrX:37635186
|
C | T | 4 | a0001c0001t0008g0184a0001c0001t0008g0186a0001c0001t0008g0187others(1): Show | 4 | HG01884.hp1 HG02258.hp1 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.574-20502C>T | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37635186 | ||||||
| chrX:37635191
|
C | T | 1 | a0001c0001t0001g0113 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.574-20497C>T | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37635191 | ||||||
| chrX:37635332
|
T | C | 26 | a0001c0001t0031g0162a0001c0001t0048g0009a0001c0002t0003g0005others(23): Show | 27 | HG00639.hp1 HG00639.hp2 HG01069.hp1 others(24): Show |
intron_variant | MODIFIER | c.574-20356T>C | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37635332 | ||||||
| chrX:37635365
|
AAATT | A | 1 | a0001c0001t0001g0019 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.574-20320_574-2031 others(8): Show |
LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chrX | 37635365 | |||||
| chrX:37635465
|
A | T | 1 | a0001c0001t0001g0077 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.574-20223A>T | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37635465 | ||||||
| chrX:37635502
|
C | T | 1 | a0005c0007t0044g0064 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.574-20186C>T | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37635502 | ||||||
| chrX:37635603
|
TCTA | T | 6 | a0001c0002t0002g0002a0001c0002t0002g0135a0001c0002t0002g0157others(3): Show | 9 | HG00735.hp1 HG01070.hp1 HG01081.hp1 others(6): Show |
intron_variant | MODIFIER | c.574-20082_574-2008 others(7): Show |
LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chrX | 37635603 | |||||
| chrX:37635837
|
A | G | 2 | a0001c0001t0001g0071a0001c0001t0040g0072 | 2 | HG02451.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.574-19851A>G | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37635837 | ||||||
| chrX:37635902
|
CA | C | 1 | a0001c0001t0020g0052 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.574-19785delA | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37635902 | ||||||
| chrX:37635949
|
C | A | 4 | a0001c0001t0001g0012a0001c0001t0001g0016a0001c0001t0001g0025others(1): Show | 4 | HG00673.hp1 NA18967.hp1 NA18983.hp1 others(1): Show |
intron_variant | MODIFIER | c.574-19739C>A | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37635949 | ||||||
| chrX:37636214
|
T | G | 23 | a0001c0001t0020g0052a0001c0001t0020g0104a0001c0002t0030g0153others(20): Show | 23 | HG01255.hp1 HG01891.hp2 HG02615.hp2 others(20): Show |
intron_variant | MODIFIER | c.574-19474T>G | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37636214 | ||||||
| chrX:37636361
|
C | T | 3 | a0001c0001t0006g0164a0001c0001t0036g0110a0001c0001t0039g0018 | 3 | HG00280.hp1 HG02738.hp1 NA18612.hp1 |
intron_variant | MODIFIER | c.574-19327C>T | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37636361 | ||||||
| chrX:37636555
|
A | T | 1 | a0001c0001t0001g0053 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.574-19133A>T | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37636555 | ||||||
| chrX:37637030
|
C | A | 47 | a0001c0001t0031g0162a0001c0001t0048g0009a0001c0002t0002g0002others(44): Show | 52 | HG00639.hp1 HG00639.hp2 HG00735.hp1 others(49): Show |
intron_variant | MODIFIER | c.574-18658C>A | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37637030 | ||||||
| chrX:37637117
|
A | G | 68 | a0001c0001t0031g0162a0001c0001t0048g0009a0001c0002t0002g0002others(65): Show | 73 | HG00639.hp1 HG00639.hp2 HG00735.hp1 others(70): Show |
intron_variant | MODIFIER | c.574-18571A>G | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37637117 | ||||||
| chrX:37637244
|
A | T | 47 | a0001c0001t0031g0162a0001c0001t0048g0009a0001c0002t0002g0002others(44): Show | 52 | HG00639.hp1 HG00639.hp2 HG00735.hp1 others(49): Show |
intron_variant | MODIFIER | c.574-18444A>T | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37637244 | ||||||
| chrX:37637248
|
TG | T | 1 | a0004c0008t0011g0130 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.574-18438delG | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chrX | 37637248 | |||||
| chrX:37637274
|
C | T | 3 | a0001c0002t0014g0131a0001c0002t0014g0156a0001c0002t0027g0155 | 3 | HG02809.hp2 HG03516.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.574-18414C>T | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37637274 | ||||||
| chrX:37637372
|
A | AT | 1 | a0004c0008t0011g0130 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.574-18311dupT | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chrX | 37637372 | |||||
| chrX:37637465
|
CT | C | 1 | a0004c0008t0011g0130 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.574-18219delT | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chrX | 37637465 | |||||
| chrX:37637499
|
G | A | 16 | a0001c0002t0030g0153a0001c0003t0005g0007a0001c0003t0005g0010others(13): Show | 16 | HG01255.hp1 HG01891.hp2 HG02615.hp2 others(13): Show |
intron_variant | MODIFIER | c.574-18189G>A | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37637499 | ||||||
| chrX:37637565
|
A | AT | 1 | a0004c0008t0011g0130 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.574-18119dupT | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chrX | 37637565 | |||||
| chrX:37637786
|
T | A | 23 | a0001c0001t0020g0052a0001c0001t0020g0104a0001c0002t0030g0153others(20): Show | 23 | HG01255.hp1 HG01891.hp2 HG02615.hp2 others(20): Show |
intron_variant | MODIFIER | c.574-17902T>A | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37637786 | ||||||
| chrX:37637853
|
C | T | 12 | a0001c0002t0030g0153a0001c0003t0005g0007a0001c0003t0005g0010others(9): Show | 12 | HG01255.hp1 HG01891.hp2 HG02622.hp2 others(9): Show |
intron_variant | MODIFIER | c.574-17835C>T | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37637853 | ||||||
| chrX:37637880
|
C | CT | 1 | a0004c0008t0011g0130 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.574-17808_574-1780 others(5): Show |
LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37637880 | ||||||
| chrX:37637934
|
GA | G | 1 | a0004c0008t0011g0130 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.574-17752delA | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chrX | 37637934 | |||||
| chrX:37637947
|
G | T | 3 | a0001c0002t0016g0176a0001c0002t0016g0177a0001c0002t0033g0172 | 3 | HG02970.hp1 HG03225.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.574-17741G>T | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37637947 | ||||||
| chrX:37637982
|
T | TG | 1 | a0004c0008t0011g0130 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.574-17703dupG | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chrX | 37637982 | |||||
| chrX:37638117
|
A | G | 3 | a0001c0003t0012g0161a0001c0003t0012g0163a0001c0003t0046g0011 | 3 | HG02622.hp1 HG03471.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.574-17571A>G | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37638117 | ||||||
| chrX:37638156
|
A | AC | 1 | a0004c0008t0011g0130 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.574-17529dupC | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chrX | 37638156 | |||||
| chrX:37638193
|
TG | T | 1 | a0004c0008t0011g0130 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.574-17493delG | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chrX | 37638193 | |||||
| chrX:37638196
|
A | T | 2 | a0001c0004t0023g0165a0005c0007t0044g0064 | 2 | HG02055.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.574-17492A>T | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37638196 | ||||||
| chrX:37638239
|
GC | G | 1 | a0004c0008t0011g0130 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.574-17446delC | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chrX | 37638239 | |||||
| chrX:37638279
|
A | AG | 1 | a0004c0008t0011g0130 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.574-17404dupG | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chrX | 37638279 | |||||
| chrX:37638334
|
G | C | 1 | a0001c0001t0001g0095 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.574-17354G>C | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37638334 | ||||||
| chrX:37638334
|
G | GA | 1 | a0004c0008t0011g0130 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.574-17352dupA | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chrX | 37638334 | |||||
| chrX:37638358
|
C | T | 1 | a0001c0001t0001g0099 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.574-17330C>T | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37638358 | ||||||
| chrX:37638643
|
G | A | 25 | a0001c0001t0031g0162a0001c0001t0048g0009a0001c0002t0003g0005others(22): Show | 26 | HG00639.hp1 HG00639.hp2 HG01069.hp1 others(23): Show |
intron_variant | MODIFIER | c.574-17045G>A | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37638643 | ||||||
| chrX:37638648
|
G | GT | 1 | a0004c0008t0011g0130 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.574-17037dupT | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chrX | 37638648 | |||||
| chrX:37638671
|
A | G | 1 | a0001c0001t0001g0051 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.574-17017A>G | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37638671 | ||||||
| chrX:37638794
|
A | C | 1 | a0001c0002t0032g0166 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.574-16894A>C | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37638794 | ||||||
| chrX:37638856
|
C | CT | 1 | a0004c0008t0011g0130 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.574-16829dupT | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chrX | 37638856 | |||||
| chrX:37639107
|
AT | A | 1 | a0004c0008t0011g0130 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.574-16580delT | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37639107 | ||||||
| chrX:37639109
|
G | A | 2 | a0001c0001t0020g0052a0001c0001t0020g0104 | 2 | HG02809.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.574-16579G>A | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37639109 | ||||||
| chrX:37639115
|
AG | A | 1 | a0004c0008t0011g0130 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.574-16571delG | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chrX | 37639115 | |||||
| chrX:37639175
|
C | T | 1 | a0001c0001t0001g0175 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.574-16513C>T | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37639175 | ||||||
| chrX:37639215
|
G | GTA | 1 | a0001c0001t0001g0034 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.574-16465_574-1646 others(6): Show |
LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chrX | 37639215 | |||||
| chrX:37639295
|
G | A | 4 | a0001c0003t0012g0161a0001c0003t0012g0163a0001c0003t0024g0136others(1): Show | 4 | HG02615.hp2 HG02622.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.574-16393G>A | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37639295 | ||||||
| chrX:37639300
|
T | TTA | 1 | a0001c0003t0007g0154 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.574-16375_574-1637 others(6): Show |
LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chrX | 37639300 | |||||
| chrX:37639300
|
TTA | T | 1 | a0004c0008t0011g0130 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.574-16375_574-1637 others(6): Show |
LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chrX | 37639300 | |||||
| chrX:37639323
|
G | A | 11 | a0001c0002t0002g0002a0001c0002t0002g0135a0001c0002t0002g0157others(8): Show | 15 | HG00735.hp1 HG01070.hp1 HG01081.hp1 others(12): Show |
intron_variant | MODIFIER | c.574-16365G>A | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37639323 | ||||||
| chrX:37639436
|
A | G | 1 | a0001c0002t0028g0139 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.574-16252A>G | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37639436 | ||||||
| chrX:37639520
|
GT | G | 1 | a0004c0008t0011g0130 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.574-16166delT | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chrX | 37639520 | |||||
| chrX:37639557
|
TG | T | 1 | a0004c0008t0011g0130 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.574-16129delG | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chrX | 37639557 | |||||
| chrX:37639573
|
AT | A | 1 | a0004c0008t0011g0130 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.574-16113delT | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chrX | 37639573 | |||||
| chrX:37639782
|
TCTTA | T | 1 | a0001c0002t0014g0156 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.574-15902_574-1589 others(8): Show |
LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chrX | 37639782 | |||||
| chrX:37639797
|
A | C | 3 | a0001c0002t0014g0131a0001c0002t0014g0156a0001c0002t0027g0155 | 3 | HG02809.hp2 HG03516.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.574-15891A>C | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37639797 | ||||||
| chrX:37639826
|
GTTTGT | G | 21 | a0001c0002t0030g0153a0001c0003t0005g0007a0001c0003t0005g0010others(18): Show | 21 | HG01255.hp1 HG01891.hp2 HG02615.hp2 others(18): Show |
intron_variant | MODIFIER | c.574-15838_574-1583 others(9): Show |
LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chrX | 37639826 | |||||
| chrX:37639826
|
GTTTGTTT others(3): Show |
G | 27 | a0001c0001t0031g0162a0001c0001t0048g0009a0001c0002t0003g0005others(24): Show | 28 | HG00639.hp1 HG00639.hp2 HG01069.hp1 others(25): Show |
intron_variant | MODIFIER | c.574-15843_574-1583 others(14): Show |
LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chrX | 37639826 | |||||
| chrX:37639925
|
G | A | 6 | a0001c0001t0001g0050a0001c0001t0001g0122a0001c0001t0006g0144others(3): Show | 6 | HG02486.hp1 HG02602.hp1 HG02735.hp1 others(3): Show |
intron_variant | MODIFIER | c.574-15763G>A | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37639925 | ||||||
| chrX:37639947
|
AT | A | 1 | a0004c0008t0011g0130 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.574-15739delT | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chrX | 37639947 | |||||
| chrX:37640055
|
TA | T | 1 | a0004c0008t0011g0130 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.574-15629delA | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chrX | 37640055 | |||||
| chrX:37640252
|
TG | T | 1 | a0004c0008t0011g0130 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.574-15432delG | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chrX | 37640252 | |||||
| chrX:37641170
|
T | C | 1 | a0001c0002t0051g0180 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.574-14518T>C | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37641170 | ||||||
| chrX:37641201
|
C | CA | 1 | a0004c0008t0011g0130 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.574-14486dupA | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chrX | 37641201 | |||||
| chrX:37641378
|
GC | G | 1 | a0004c0008t0011g0130 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.574-14308delC | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chrX | 37641378 | |||||
| chrX:37641382
|
T | C | 47 | a0001c0001t0031g0162a0001c0001t0048g0009a0001c0002t0002g0002others(44): Show | 52 | HG00639.hp1 HG00639.hp2 HG00735.hp1 others(49): Show |
intron_variant | MODIFIER | c.574-14306T>C | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37641382 | ||||||
| chrX:37641388
|
G | A | 1 | a0001c0003t0047g0189 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.574-14300G>A | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37641388 | ||||||
| chrX:37641437
|
G | C | 47 | a0001c0001t0031g0162a0001c0001t0048g0009a0001c0002t0002g0002others(44): Show | 52 | HG00639.hp1 HG00639.hp2 HG00735.hp1 others(49): Show |
intron_variant | MODIFIER | c.574-14251G>C | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37641437 | ||||||
| chrX:37641492
|
G | GC | 1 | a0004c0008t0011g0130 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.574-14193dupC | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chrX | 37641492 | |||||
| chrX:37641638
|
A | AG | 1 | a0004c0008t0011g0130 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.574-14047dupG | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chrX | 37641638 | |||||
| chrX:37641677
|
T | TG | 1 | a0004c0008t0011g0130 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.574-14008dupG | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chrX | 37641677 | |||||
| chrX:37641739
|
C | CT | 1 | a0004c0008t0011g0130 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.574-13947dupT | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chrX | 37641739 | |||||
| chrX:37641929
|
TC | T | 1 | a0004c0008t0011g0130 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.574-13756delC | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chrX | 37641929 | |||||
| chrX:37642005
|
G | GA | 1 | a0004c0008t0011g0130 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.574-13681dupA | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chrX | 37642005 | |||||
| chrX:37642219
|
G | T | 2 | a0001c0001t0020g0052a0001c0001t0020g0104 | 2 | HG02809.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.574-13469G>T | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37642219 | ||||||
| chrX:37642233
|
C | T | 47 | a0001c0001t0031g0162a0001c0001t0048g0009a0001c0002t0002g0002others(44): Show | 52 | HG00639.hp1 HG00639.hp2 HG00735.hp1 others(49): Show |
intron_variant | MODIFIER | c.574-13455C>T | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37642233 | ||||||
| chrX:37642257
|
G | A | 3 | a0001c0002t0014g0131a0001c0002t0014g0156a0001c0002t0027g0155 | 3 | HG02809.hp2 HG03516.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.574-13431G>A | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37642257 | ||||||
| chrX:37642290
|
C | G | 1 | a0001c0001t0001g0126 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.574-13398C>G | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37642290 | ||||||
| chrX:37642362
|
T | C | 1 | a0001c0002t0003g0069 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.574-13326T>C | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37642362 | ||||||
| chrX:37642549
|
AT | A | 1 | a0004c0008t0011g0130 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.574-13137delT | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chrX | 37642549 | |||||
| chrX:37642561
|
C | CA | 4 | a0001c0003t0012g0161a0001c0003t0012g0163a0001c0003t0024g0136others(1): Show | 4 | HG02615.hp2 HG02622.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.574-13119dupA | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chrX | 37642561 | |||||
| chrX:37642624
|
A | C | 1 | a0001c0001t0001g0126 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.574-13064A>C | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37642624 | ||||||
| chrX:37642701
|
A | T | 1 | a0001c0001t0001g0081 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.574-12987A>T | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37642701 | ||||||
| chrX:37642713
|
TG | T | 1 | a0004c0008t0011g0130 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.574-12973delG | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chrX | 37642713 | |||||
| chrX:37642847
|
T | C | 2 | a0001c0001t0020g0052a0001c0001t0020g0104 | 2 | HG02809.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.574-12841T>C | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37642847 | ||||||
| chrX:37642871
|
AAT | A | 1 | a0004c0008t0011g0130 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.574-12816_574-1281 others(6): Show |
LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37642871 | ||||||
| chrX:37642875
|
G | T | 1 | a0004c0008t0011g0130 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.574-12813G>T | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37642875 | ||||||
| chrX:37642912
|
G | C | 1 | a0001c0002t0045g0008 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.574-12776G>C | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37642912 | ||||||
| chrX:37643048
|
A | AG | 1 | a0004c0008t0011g0130 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.574-12638dupG | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chrX | 37643048 | |||||
| chrX:37643153
|
GC | G | 1 | a0004c0008t0011g0130 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.574-12533delC | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chrX | 37643153 | |||||
| chrX:37643184
|
A | C | 4 | a0001c0002t0004g0133a0001c0002t0004g0167a0001c0002t0021g0054others(1): Show | 4 | HG01891.hp1 HG02572.hp1 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.574-12504A>C | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37643184 | ||||||
| chrX:37643446
|
G | A | 1 | a0001c0001t0001g0090 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.574-12242G>A | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37643446 | ||||||
| chrX:37643477
|
A | G | 3 | a0001c0002t0014g0131a0001c0002t0014g0156a0001c0002t0027g0155 | 3 | HG02809.hp2 HG03516.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.574-12211A>G | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37643477 | ||||||
| chrX:37643707
|
A | AG | 1 | a0004c0008t0011g0130 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.574-11979dupG | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chrX | 37643707 | |||||
| chrX:37643887
|
G | C | 3 | a0001c0001t0010g0146a0001c0001t0010g0147a0001c0001t0010g0148 | 3 | HG02109.hp1 HG02145.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.574-11801G>C | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37643887 | ||||||
| chrX:37643954
|
C | CT | 1 | a0004c0008t0011g0130 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.574-11729dupT | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chrX | 37643954 | |||||
| chrX:37644139
|
G | T | 4 | a0001c0003t0005g0182a0001c0003t0005g0183a0001c0003t0007g0151others(1): Show | 4 | HG01891.hp2 HG02922.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.574-11549G>T | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37644139 | ||||||
| chrX:37644223
|
AC | A | 1 | a0004c0008t0011g0130 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.574-11462delC | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chrX | 37644223 | |||||
| chrX:37644458
|
T | TC | 1 | a0004c0008t0011g0130 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.574-11229dupC | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chrX | 37644458 | |||||
| chrX:37644592
|
AC | A | 1 | a0004c0008t0011g0130 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.574-11093delC | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chrX | 37644592 | |||||
| chrX:37644680
|
TC | T | 1 | a0004c0008t0011g0130 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.574-11007delC | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37644680 | ||||||
| chrX:37644686
|
C | T | 1 | a0004c0008t0011g0130 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.574-11002C>T | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37644686 | ||||||
| chrX:37644752
|
AAAACT | A | 1 | a0004c0008t0011g0130 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.574-10934_574-1093 others(9): Show |
LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chrX | 37644752 | |||||
| chrX:37644887
|
C | G | 87 | a0001c0001t0001g0050a0001c0001t0001g0071a0001c0001t0001g0122others(84): Show | 92 | HG00639.hp1 HG00639.hp2 HG00735.hp1 others(89): Show |
intron_variant | MODIFIER | c.574-10801C>G | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37644887 | ||||||
| chrX:37645073
|
G | A | 1 | a0001c0002t0011g0140 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.574-10615G>A | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37645073 | ||||||
| chrX:37645127
|
G | A | 2 | a0001c0001t0020g0052a0001c0001t0020g0104 | 2 | HG02809.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.574-10561G>A | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37645127 | ||||||
| chrX:37645212
|
A | G | 2 | a0001c0001t0020g0052a0001c0001t0020g0104 | 2 | HG02809.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.574-10476A>G | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37645212 | ||||||
| chrX:37645905
|
G | T | 21 | a0001c0002t0030g0153a0001c0003t0005g0007a0001c0003t0005g0010others(18): Show | 21 | HG01255.hp1 HG01891.hp2 HG02615.hp2 others(18): Show |
intron_variant | MODIFIER | c.574-9783G>T | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37645905 | ||||||
| chrX:37646382
|
T | A | 2 | a0001c0001t0020g0052a0001c0001t0020g0104 | 2 | HG02809.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.574-9306T>A | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37646382 | ||||||
| chrX:37646756
|
C | T | 1 | a0001c0001t0006g0144 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.574-8932C>T | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37646756 | ||||||
| chrX:37646867
|
G | A | 2 | a0001c0001t0010g0146a0001c0001t0010g0147 | 2 | HG02109.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.574-8821G>A | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37646867 | ||||||
| chrX:37646974
|
A | C | 68 | a0001c0001t0031g0162a0001c0001t0048g0009a0001c0002t0002g0002others(65): Show | 73 | HG00639.hp1 HG00639.hp2 HG00735.hp1 others(70): Show |
intron_variant | MODIFIER | c.574-8714A>C | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37646974 | ||||||
| chrX:37647023
|
A | G | 13 | a0001c0002t0003g0005a0001c0002t0003g0040a0001c0002t0003g0061others(10): Show | 14 | HG00639.hp1 HG00639.hp2 HG01069.hp1 others(11): Show |
intron_variant | MODIFIER | c.574-8665A>G | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37647023 | ||||||
| chrX:37647038
|
G | A | 2 | a0001c0001t0020g0052a0001c0001t0020g0104 | 2 | HG02809.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.574-8650G>A | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37647038 | ||||||
| chrX:37647117
|
A | G | 1 | a0001c0004t0023g0165 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.574-8571A>G | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37647117 | ||||||
| chrX:37647296
|
A | T | 1 | a0001c0001t0001g0120 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.574-8392A>T | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37647296 | ||||||
| chrX:37647310
|
TCAAAAAA others(1): Show |
T | 68 | a0001c0001t0031g0162a0001c0001t0048g0009a0001c0002t0002g0002others(65): Show | 73 | HG00639.hp1 HG00639.hp2 HG00735.hp1 others(70): Show |
intron_variant | MODIFIER | c.574-8356_574-8349d others(10): Show |
LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chrX | 37647310 | |||||
| chrX:37647477
|
A | C | 1 | a0001c0001t0001g0125 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.574-8211A>C | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37647477 | ||||||
| chrX:37647662
|
G | A | 1 | a0001c0001t0001g0065 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.574-8026G>A | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37647662 | ||||||
| chrX:37647858
|
C | T | 1 | a0001c0001t0001g0027 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.574-7830C>T | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37647858 | ||||||
| chrX:37648506
|
C | A | 1 | a0004c0008t0011g0130 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.574-7182C>A | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37648506 | ||||||
| chrX:37648599
|
A | G | 1 | a0001c0002t0003g0075 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.574-7089A>G | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37648599 | ||||||
| chrX:37648655
|
T | A | 70 | a0001c0001t0020g0052a0001c0001t0020g0104a0001c0001t0031g0162others(67): Show | 75 | HG00639.hp1 HG00639.hp2 HG00735.hp1 others(72): Show |
intron_variant | MODIFIER | c.574-7033T>A | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37648655 | ||||||
| chrX:37648782
|
A | G | 1 | a0001c0001t0001g0062 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.574-6906A>G | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37648782 | ||||||
| chrX:37649417
|
A | G | 48 | a0001c0001t0031g0162a0001c0001t0048g0009a0001c0002t0002g0002others(45): Show | 53 | HG00639.hp1 HG00639.hp2 HG00735.hp1 others(50): Show |
intron_variant | MODIFIER | c.574-6271A>G | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37649417 | ||||||
| chrX:37649501
|
A | G | 14 | a0001c0002t0030g0153a0001c0003t0005g0007a0001c0003t0005g0010others(11): Show | 14 | HG01255.hp1 HG01891.hp2 HG02055.hp1 others(11): Show |
intron_variant | MODIFIER | c.574-6187A>G | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37649501 | ||||||
| chrX:37650112
|
G | A | 1 | a0001c0001t0001g0058 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.574-5576G>A | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37650112 | ||||||
| chrX:37650258
|
G | A | 12 | a0001c0002t0030g0153a0001c0003t0005g0007a0001c0003t0005g0010others(9): Show | 12 | HG01255.hp1 HG01891.hp2 HG02622.hp2 others(9): Show |
intron_variant | MODIFIER | c.574-5430G>A | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37650258 | ||||||
| chrX:37650306
|
G | GA | 13 | a0001c0001t0001g0016a0001c0001t0001g0020a0001c0001t0001g0021others(10): Show | 13 | HG01109.hp1 HG01433.hp1 HG02056.hp1 others(10): Show |
intron_variant | MODIFIER | c.574-5366dupA | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chrX | 37650306 | |||||
| chrX:37650306
|
GA | G | 1 | a0001c0001t0001g0050 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.574-5366delA | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chrX | 37650306 | |||||
| chrX:37650465
|
C | T | 2 | a0001c0001t0020g0052a0001c0001t0020g0104 | 2 | HG02809.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.574-5223C>T | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37650465 | ||||||
| chrX:37650603
|
C | A | 3 | a0001c0004t0009g0006a0001c0004t0009g0178a0001c0004t0009g0179 | 4 | HG02109.hp2 HG02615.hp1 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.574-5085C>A | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37650603 | ||||||
| chrX:37650672
|
T | C | 45 | a0001c0001t0031g0162a0001c0001t0048g0009a0001c0002t0002g0002others(42): Show | 49 | HG00639.hp1 HG00639.hp2 HG00735.hp1 others(46): Show |
intron_variant | MODIFIER | c.574-5016T>C | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37650672 | ||||||
| chrX:37650886
|
C | G | 1 | a0001c0001t0001g0032 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.574-4802C>G | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37650886 | ||||||
| chrX:37650902
|
C | T | 1 | a0001c0002t0032g0166 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.574-4786C>T | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37650902 | ||||||
| chrX:37650914
|
G | T | 3 | a0001c0001t0010g0146a0001c0001t0010g0147a0001c0001t0010g0148 | 3 | HG02109.hp1 HG02145.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.574-4774G>T | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37650914 | ||||||
| chrX:37650926
|
G | A | 2 | a0001c0001t0020g0052a0001c0001t0020g0104 | 2 | HG02809.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.574-4762G>A | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37650926 | ||||||
| chrX:37651129
|
C | T | 74 | a0001c0001t0010g0146a0001c0001t0010g0147a0001c0001t0010g0148others(71): Show | 79 | HG00639.hp1 HG00639.hp2 HG00735.hp1 others(76): Show |
intron_variant | MODIFIER | c.574-4559C>T | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37651129 | ||||||
| chrX:37651209
|
C | T | 1 | a0001c0002t0052g0023 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.574-4479C>T | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37651209 | ||||||
| chrX:37651210
|
G | A | 3 | a0001c0002t0016g0176a0001c0002t0016g0177a0001c0002t0033g0172 | 3 | HG02970.hp1 HG03225.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.574-4478G>A | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37651210 | ||||||
| chrX:37651304
|
C | T | 1 | a0006c0006t0019g0038 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.574-4384C>T | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37651304 | ||||||
| chrX:37651450
|
A | T | 1 | a0001c0001t0040g0072 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.574-4238A>T | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37651450 | ||||||
| chrX:37651805
|
G | A | 74 | a0001c0001t0010g0146a0001c0001t0010g0147a0001c0001t0010g0148others(71): Show | 79 | HG00639.hp1 HG00639.hp2 HG00735.hp1 others(76): Show |
intron_variant | MODIFIER | c.574-3883G>A | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37651805 | ||||||
| chrX:37651982
|
A | G | 3 | a0001c0002t0003g0005a0001c0002t0003g0061a0001c0002t0003g0117 | 4 | HG00639.hp1 HG01069.hp1 HG01071.hp1 others(1): Show |
intron_variant | MODIFIER | c.574-3706A>G | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37651982 | ||||||
| chrX:37651986
|
C | T | 2 | a0001c0001t0020g0052a0001c0001t0020g0104 | 2 | HG02809.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.574-3702C>T | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37651986 | ||||||
| chrX:37652025
|
TC | T | 13 | a0001c0002t0003g0005a0001c0002t0003g0026a0001c0002t0003g0040others(10): Show | 14 | HG00639.hp1 HG00639.hp2 HG01069.hp1 others(11): Show |
intron_variant | MODIFIER | c.574-3662delC | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37652025 | ||||||
| chrX:37652027
|
A | AT | 6 | a0001c0001t0001g0051a0001c0001t0001g0089a0001c0001t0001g0098others(3): Show | 6 | HG01361.hp2 HG01928.hp1 HG02071.hp1 others(3): Show |
intron_variant | MODIFIER | c.574-3647dupT | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chrX | 37652027 | |||||
| chrX:37652027
|
A | C | 4 | a0001c0002t0004g0133a0001c0002t0004g0167a0001c0002t0021g0054others(1): Show | 4 | HG01891.hp1 HG02572.hp1 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.574-3661A>C | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37652027 | ||||||
| chrX:37652027
|
AT | A | 11 | a0001c0001t0001g0044a0001c0001t0001g0055a0001c0001t0001g0068others(8): Show | 11 | HG01255.hp1 HG01256.hp1 HG02896.hp1 others(8): Show |
intron_variant | MODIFIER | c.574-3647delT | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chrX | 37652027 | |||||
| chrX:37652028
|
T | A | 13 | a0001c0002t0003g0005a0001c0002t0003g0026a0001c0002t0003g0040others(10): Show | 14 | HG00639.hp1 HG00639.hp2 HG01069.hp1 others(11): Show |
intron_variant | MODIFIER | c.574-3660T>A | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37652028 | ||||||
| chrX:37652437
|
C | T | 2 | a0001c0001t0020g0052a0001c0001t0020g0104 | 2 | HG02809.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.574-3251C>T | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37652437 | ||||||
| chrX:37652471
|
C | G | 1 | a0001c0002t0032g0166 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.574-3217C>G | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37652471 | ||||||
| chrX:37652507
|
C | T | 190 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(187): Show | 199 | HG00140.hp1 HG00280.hp1 HG00609.hp1 others(196): Show |
intron_variant | MODIFIER | c.574-3181C>T | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37652507 | ||||||
| chrX:37652551
|
G | GA | 1 | a0001c0001t0001g0098 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.574-3133dupA | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chrX | 37652551 | |||||
| chrX:37652702
|
G | A | 1 | a0001c0001t0001g0118 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.574-2986G>A | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37652702 | ||||||
| chrX:37652711
|
G | T | 3 | a0001c0001t0010g0146a0001c0001t0010g0147a0001c0001t0010g0148 | 3 | HG02109.hp1 HG02145.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.574-2977G>T | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37652711 | ||||||
| chrX:37652736
|
G | A | 1 | a0001c0001t0001g0098 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.574-2952G>A | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37652736 | ||||||
| chrX:37652759
|
T | C | 1 | a0001c0001t0001g0126 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.574-2929T>C | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37652759 | ||||||
| chrX:37652986
|
G | A | 1 | a0001c0004t0009g0006 | 2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.574-2702G>A | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37652986 | ||||||
| chrX:37653069
|
C | T | 2 | a0001c0003t0015g0168a0001c0003t0015g0169 | 2 | HG02818.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.574-2619C>T | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37653069 | ||||||
| chrX:37653294
|
G | GCA | 2 | a0001c0001t0020g0052a0001c0001t0020g0104 | 2 | HG02809.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.574-2377_574-2376d others(4): Show |
LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chrX | 37653294 | |||||
| chrX:37653919
|
G | GA | 6 | a0001c0001t0020g0052a0001c0001t0020g0104a0001c0004t0009g0006others(3): Show | 7 | HG02055.hp1 HG02109.hp2 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.574-1757dupA | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chrX | 37653919 | |||||
| chrX:37653919
|
GA | G | 1 | a0004c0008t0011g0130 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.574-1757delA | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chrX | 37653919 | |||||
| chrX:37654671
|
G | A | 2 | a0001c0001t0001g0071a0001c0001t0040g0072 | 2 | HG02451.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.574-1017G>A | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37654671 | ||||||
| chrX:37654840
|
C | G | 1 | a0001c0001t0001g0043 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.574-848C>G | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37654840 | ||||||
| chrX:37655012
|
T | A | 1 | a0001c0003t0005g0119 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.574-676T>A | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37655012 | ||||||
| chrX:37655368
|
TGAGC | T | 1 | a0004c0008t0011g0130 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.574-319_574-316del others(4): Show |
LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37655368 | ||||||
| chrX:37655483
|
G | A | 1 | a0001c0001t0020g0104 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.574-205G>A | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37655483 | ||||||
| chrX:37655619
|
A | G | 2 | a0001c0001t0020g0052a0001c0001t0020g0104 | 2 | HG02809.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.574-69A>G | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 1/4 | chrX | 37655619 | ||||||
| chrX:37655913
|
G | T | 74 | a0001c0001t0010g0146a0001c0001t0010g0147a0001c0001t0010g0148others(71): Show | 79 | HG00639.hp1 HG00639.hp2 HG00735.hp1 others(76): Show |
intron_variant | MODIFIER | c.697+102G>T | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 2/4 | chrX | 37655913 | ||||||
| chrX:37656247
|
C | CA | 5 | a0001c0001t0001g0042a0001c0001t0001g0113a0001c0001t0001g0129others(2): Show | 5 | HG02056.hp1 HG04199.hp1 NA18984.hp1 others(2): Show |
intron_variant | MODIFIER | c.697+449dupA | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chrX | 37656247 | |||||
| chrX:37656247
|
C | CAA | 2 | a0001c0001t0031g0162a0001c0001t0048g0009 | 2 | HG03130.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.697+448_697+449dup others(2): Show |
LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chrX | 37656247 | |||||
| chrX:37656247
|
C | CAAA | 1 | a0001c0001t0020g0052 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.697+447_697+449dup others(3): Show |
LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chrX | 37656247 | |||||
| chrX:37656247
|
C | CAAAA | 1 | a0001c0001t0020g0104 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.697+446_697+449dup others(4): Show |
LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chrX | 37656247 | |||||
| chrX:37656382
|
T | TC | 1 | a0004c0008t0011g0130 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.697+573dupC | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chrX | 37656382 | |||||
| chrX:37656459
|
G | GC | 1 | a0004c0008t0011g0130 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.697+651dupC | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chrX | 37656459 | |||||
| chrX:37656486
|
A | G | 3 | a0001c0003t0012g0161a0001c0003t0012g0163a0001c0003t0046g0011 | 3 | HG02622.hp1 HG03471.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.697+675A>G | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 2/4 | chrX | 37656486 | ||||||
| chrX:37656542
|
GA | G | 1 | a0004c0008t0011g0130 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.697+736delA | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chrX | 37656542 | |||||
| chrX:37656804
|
G | A | 67 | a0001c0002t0002g0002a0001c0002t0002g0135a0001c0002t0002g0157others(64): Show | 72 | HG00639.hp1 HG00639.hp2 HG00735.hp1 others(69): Show |
intron_variant | MODIFIER | c.697+993G>A | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 2/4 | chrX | 37656804 | ||||||
| chrX:37656964
|
A | G | 74 | a0001c0001t0010g0146a0001c0001t0010g0147a0001c0001t0010g0148others(71): Show | 79 | HG00639.hp1 HG00639.hp2 HG00735.hp1 others(76): Show |
intron_variant | MODIFIER | c.697+1153A>G | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 2/4 | chrX | 37656964 | ||||||
| chrX:37657267
|
G | A | 1 | a0001c0001t0001g0175 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.697+1456G>A | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 2/4 | chrX | 37657267 | ||||||
| chrX:37657291
|
T | C | 3 | a0001c0002t0016g0176a0001c0002t0016g0177a0001c0002t0033g0172 | 3 | HG02970.hp1 HG03225.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.697+1480T>C | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 2/4 | chrX | 37657291 | ||||||
| chrX:37657340
|
T | TC | 1 | a0004c0008t0011g0130 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.697+1533dupC | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chrX | 37657340 | |||||
| chrX:37657402
|
A | AC | 1 | a0004c0008t0011g0130 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.697+1594dupC | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chrX | 37657402 | |||||
| chrX:37657542
|
A | AT | 1 | a0001c0001t0001g0041 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.697+1749dupT | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chrX | 37657542 | |||||
| chrX:37657542
|
AT | A | 3 | a0001c0001t0001g0071a0001c0001t0001g0082a0001c0011t0001g0123 | 3 | HG01258.hp1 HG02896.hp1 NA19075.hp1 |
intron_variant | MODIFIER | c.697+1749delT | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chrX | 37657542 | |||||
| chrX:37657542
|
ATT | A | 35 | a0001c0001t0020g0052a0001c0001t0020g0104a0001c0001t0031g0162others(32): Show | 39 | HG00735.hp1 HG01070.hp1 HG01081.hp1 others(36): Show |
intron_variant | MODIFIER | c.697+1748_697+1749d others(4): Show |
LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chrX | 37657542 | |||||
| chrX:37657542
|
ATTT | A | 35 | a0001c0002t0003g0005a0001c0002t0003g0040a0001c0002t0003g0061others(32): Show | 36 | HG00639.hp1 HG00639.hp2 HG01071.hp1 others(33): Show |
intron_variant | MODIFIER | c.697+1747_697+1749d others(5): Show |
LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chrX | 37657542 | |||||
| chrX:37657542
|
ATTTT | A | 1 | a0001c0002t0003g0117 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.697+1746_697+1749d others(6): Show |
LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chrX | 37657542 | |||||
| chrX:37657622
|
T | TA | 1 | a0004c0008t0011g0130 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.697+1812dupA | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chrX | 37657622 | |||||
| chrX:37657684
|
T | C | 12 | a0001c0002t0002g0002a0001c0002t0002g0135a0001c0002t0002g0157others(9): Show | 15 | HG00735.hp1 HG01070.hp1 HG01081.hp1 others(12): Show |
intron_variant | MODIFIER | c.698-1778T>C | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 2/4 | chrX | 37657684 | ||||||
| chrX:37657887
|
A | T | 1 | a0004c0008t0011g0130 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.698-1575A>T | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 2/4 | chrX | 37657887 | ||||||
| chrX:37658373
|
A | G | 71 | a0001c0001t0020g0052a0001c0001t0020g0104a0001c0001t0031g0162others(68): Show | 76 | HG00639.hp1 HG00639.hp2 HG00735.hp1 others(73): Show |
intron_variant | MODIFIER | c.698-1089A>G | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 2/4 | chrX | 37658373 | ||||||
| chrX:37658895
|
T | C | 1 | a0001c0001t0031g0162 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.698-567T>C | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 2/4 | chrX | 37658895 | ||||||
| chrX:37658932
|
G | T | 3 | a0001c0003t0012g0161a0001c0003t0012g0163a0001c0003t0046g0011 | 3 | HG02622.hp1 HG03471.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.698-530G>T | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 2/4 | chrX | 37658932 | ||||||
| chrX:37658942
|
G | A | 1 | a0001c0001t0001g0060 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.698-520G>A | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 2/4 | chrX | 37658942 | ||||||
| chrX:37658970
|
T | TA | 1 | a0004c0008t0011g0130 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.698-485dupA | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chrX | 37658970 | |||||
| chrX:37659161
|
C | T | 74 | a0001c0001t0010g0146a0001c0001t0010g0147a0001c0001t0010g0148others(71): Show | 79 | HG00639.hp1 HG00639.hp2 HG00735.hp1 others(76): Show |
intron_variant | MODIFIER | c.698-301C>T | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 2/4 | chrX | 37659161 | ||||||
| chrX:37659319
|
C | T | 1 | a0001c0003t0029g0132 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.698-143C>T | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 2/4 | chrX | 37659319 | ||||||
| chrX:37659408
|
C | T | 1 | a0001c0001t0001g0058 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.698-54C>T | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 2/4 | chrX | 37659408 | ||||||
| chrX:37659795
|
C | T | 2 | a0001c0001t0001g0037a0001c0001t0001g0084 | 2 | HG02027.hp1 NA18995.hp1 |
intron_variant | MODIFIER | c.895+136C>T | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 3/4 | chrX | 37659795 | ||||||
| chrX:37659864
|
A | G | 5 | a0001c0002t0003g0005a0001c0002t0003g0061a0001c0002t0003g0069others(2): Show | 6 | HG00639.hp1 HG01069.hp1 HG01071.hp1 others(3): Show |
intron_variant | MODIFIER | c.895+205A>G | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 3/4 | chrX | 37659864 | ||||||
| chrX:37659895
|
T | C | 4 | a0001c0001t0020g0052a0001c0001t0020g0104a0001c0001t0031g0162others(1): Show | 4 | HG02809.hp1 HG03130.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.895+236T>C | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 3/4 | chrX | 37659895 | ||||||
| chrX:37659974
|
A | C | 12 | a0001c0002t0030g0153a0001c0003t0005g0007a0001c0003t0005g0010others(9): Show | 12 | HG01255.hp1 HG01891.hp2 HG02622.hp2 others(9): Show |
intron_variant | MODIFIER | c.895+315A>C | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 3/4 | chrX | 37659974 | ||||||
| chrX:37660196
|
CA | C | 1 | a0004c0008t0011g0130 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.895+541delA | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chrX | 37660196 | |||||
| chrX:37660510
|
CT | C | 1 | a0004c0008t0011g0130 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.895+853delT | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chrX | 37660510 | |||||
| chrX:37660563
|
AT | A | 1 | a0004c0008t0011g0130 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.895+906delT | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chrX | 37660563 | |||||
| chrX:37661003
|
T | TGGG | 1 | a0001c0001t0020g0104 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.895+1345_895+1347d others(5): Show |
LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chrX | 37661003 | |||||
| chrX:37661003
|
T | TGGGG | 1 | a0001c0001t0020g0052 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.895+1347_895+1348i others(6): Show |
LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chrX | 37661003 | |||||
| chrX:37661006
|
GC | G | 23 | a0001c0002t0030g0153a0001c0003t0005g0007a0001c0003t0005g0010others(20): Show | 24 | HG01255.hp1 HG02055.hp1 HG02109.hp2 others(21): Show |
intron_variant | MODIFIER | c.895+1348delC | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 3/4 | chrX | 37661006 | ||||||
| chrX:37661007
|
C | CG | 1 | a0001c0001t0001g0016 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.895+1356dupG | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chrX | 37661007 | |||||
| chrX:37661007
|
C | G | 48 | a0001c0001t0020g0052a0001c0001t0020g0104a0001c0001t0031g0162others(45): Show | 52 | HG00639.hp1 HG00639.hp2 HG00735.hp1 others(49): Show |
intron_variant | MODIFIER | c.895+1348C>G | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 3/4 | chrX | 37661007 | ||||||
| chrX:37661010
|
G | T | 2 | a0001c0001t0001g0097a0001c0001t0001g0101 | 2 | NA18961.hp1 NA18982.hp1 |
intron_variant | MODIFIER | c.895+1351G>T | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 3/4 | chrX | 37661010 | ||||||
| chrX:37661011
|
G | GT | 42 | a0001c0002t0002g0002a0001c0002t0002g0135a0001c0002t0002g0157others(39): Show | 46 | HG00639.hp1 HG00639.hp2 HG00735.hp1 others(43): Show |
intron_variant | MODIFIER | c.895+1352_895+1353i others(3): Show |
LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 3/4 | chrX | 37661011 | ||||||
| chrX:37661011
|
G | T | 1 | a0001c0002t0019g0057 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.895+1352G>T | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 3/4 | chrX | 37661011 | ||||||
| chrX:37661340
|
C | A | 1 | a0001c0001t0001g0015 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.895+1681C>A | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 3/4 | chrX | 37661340 | ||||||
| chrX:37661420
|
TA | T | 1 | a0004c0008t0011g0130 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.895+1764delA | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chrX | 37661420 | |||||
| chrX:37661732
|
G | A | 1 | a0001c0001t0001g0070 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.895+2073G>A | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 3/4 | chrX | 37661732 | ||||||
| chrX:37661856
|
A | G | 3 | a0001c0001t0001g0059a0001c0001t0001g0068a0001c0001t0055g0035 | 3 | HG01256.hp1 HG01358.hp1 NA18955.hp1 |
intron_variant | MODIFIER | c.895+2197A>G | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 3/4 | chrX | 37661856 | ||||||
| chrX:37662016
|
CT | C | 1 | a0004c0008t0011g0130 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.895+2360delT | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chrX | 37662016 | |||||
| chrX:37662630
|
A | G | 68 | a0001c0001t0020g0052a0001c0001t0020g0104a0001c0001t0031g0162others(65): Show | 73 | HG00639.hp1 HG00639.hp2 HG00735.hp1 others(70): Show |
intron_variant | MODIFIER | c.895+2971A>G | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 3/4 | chrX | 37662630 | ||||||
| chrX:37662753
|
T | C | 66 | a0001c0002t0002g0002a0001c0002t0002g0135a0001c0002t0002g0157others(63): Show | 71 | HG00639.hp1 HG00639.hp2 HG00735.hp1 others(68): Show |
intron_variant | MODIFIER | c.895+3094T>C | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 3/4 | chrX | 37662753 | ||||||
| chrX:37662815
|
C | CT | 4 | a0001c0001t0001g0041a0001c0002t0030g0153a0001c0002t0045g0008others(1): Show | 4 | HG01255.hp1 HG02630.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.895+3171dupT | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chrX | 37662815 | |||||
| chrX:37662815
|
CT | C | 7 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0070others(4): Show | 7 | HG00280.hp1 HG01070.hp1 HG02040.hp1 others(4): Show |
intron_variant | MODIFIER | c.895+3171delT | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chrX | 37662815 | |||||
| chrX:37663003
|
G | A | 1 | a0001c0004t0023g0165 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.895+3344G>A | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 3/4 | chrX | 37663003 | ||||||
| chrX:37663302
|
A | G | 8 | a0001c0002t0016g0176a0001c0002t0016g0177a0001c0002t0033g0172others(5): Show | 8 | HG02818.hp2 HG02970.hp1 HG03041.hp1 others(5): Show |
intron_variant | MODIFIER | c.895+3643A>G | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 3/4 | chrX | 37663302 | ||||||
| chrX:37663458
|
T | A | 20 | a0001c0003t0005g0007a0001c0003t0005g0010a0001c0003t0005g0119others(17): Show | 20 | HG01891.hp2 HG02615.hp2 HG02622.hp1 others(17): Show |
intron_variant | MODIFIER | c.895+3799T>A | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 3/4 | chrX | 37663458 | ||||||
| chrX:37663585
|
G | C | 6 | a0001c0001t0001g0050a0001c0001t0001g0122a0001c0001t0006g0144others(3): Show | 6 | HG02486.hp1 HG02602.hp1 HG02735.hp1 others(3): Show |
intron_variant | MODIFIER | c.896-3697G>C | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 3/4 | chrX | 37663585 | ||||||
| chrX:37663606
|
AG | A | 1 | a0004c0008t0011g0130 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.896-3672delG | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chrX | 37663606 | |||||
| chrX:37663685
|
TG | T | 1 | a0004c0008t0011g0130 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.896-3593delG | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chrX | 37663685 | |||||
| chrX:37663756
|
T | C | 71 | a0001c0001t0020g0052a0001c0001t0020g0104a0001c0001t0031g0162others(68): Show | 76 | HG00639.hp1 HG00639.hp2 HG00735.hp1 others(73): Show |
intron_variant | MODIFIER | c.896-3526T>C | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 3/4 | chrX | 37663756 | ||||||
| chrX:37663966
|
T | TG | 1 | a0004c0008t0011g0130 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.896-3313dupG | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chrX | 37663966 | |||||
| chrX:37664046
|
C | T | 1 | a0001c0001t0001g0041 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.896-3236C>T | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 3/4 | chrX | 37664046 | ||||||
| chrX:37664208
|
C | A | 3 | a0001c0002t0016g0176a0001c0002t0016g0177a0001c0002t0033g0172 | 3 | HG02970.hp1 HG03225.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.896-3074C>A | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 3/4 | chrX | 37664208 | ||||||
| chrX:37664504
|
CT | C | 1 | a0004c0008t0011g0130 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.896-2770delT | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chrX | 37664504 | |||||
| chrX:37664684
|
G | A | 2 | a0001c0002t0045g0008a0005c0007t0044g0064 | 2 | HG02630.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.896-2598G>A | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 3/4 | chrX | 37664684 | ||||||
| chrX:37664720
|
C | T | 3 | a0001c0001t0001g0042a0001c0001t0001g0129a0001c0001t0018g0128 | 3 | HG02056.hp1 NA19062.hp1 NA19086.hp1 |
intron_variant | MODIFIER | c.896-2562C>T | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 3/4 | chrX | 37664720 | ||||||
| chrX:37664813
|
TG | T | 1 | a0004c0008t0011g0130 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.896-2467delG | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chrX | 37664813 | |||||
| chrX:37665437
|
GA | G | 1 | a0004c0008t0011g0130 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.896-1840delA | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chrX | 37665437 | |||||
| chrX:37665549
|
C | A | 20 | a0001c0003t0005g0007a0001c0003t0005g0010a0001c0003t0005g0119others(17): Show | 20 | HG01891.hp2 HG02615.hp2 HG02622.hp1 others(17): Show |
intron_variant | MODIFIER | c.896-1733C>A | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 3/4 | chrX | 37665549 | ||||||
| chrX:37665770
|
A | C | 1 | a0001c0002t0003g0075 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.896-1512A>C | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 3/4 | chrX | 37665770 | ||||||
| chrX:37665983
|
T | TA | 1 | a0004c0008t0011g0130 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.896-1295dupA | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chrX | 37665983 | |||||
| chrX:37666339
|
C | G | 3 | a0001c0002t0016g0176a0001c0002t0016g0177a0001c0002t0033g0172 | 3 | HG02970.hp1 HG03225.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.896-943C>G | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 3/4 | chrX | 37666339 | ||||||
| chrX:37666906
|
C | CG | 1 | a0004c0008t0011g0130 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.896-376_896-375ins others(1): Show |
LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 3/4 | chrX | 37666906 | ||||||
| chrX:37667510
|
C | CT | 68 | a0001c0001t0020g0052a0001c0001t0020g0104a0001c0002t0002g0002others(65): Show | 73 | HG00639.hp1 HG00639.hp2 HG00735.hp1 others(70): Show |
intron_variant | MODIFIER | c.1103+32dupT | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chrX | 37667510 | |||||
| chrX:37667510
|
C | CTT | 2 | a0001c0001t0031g0162a0001c0001t0048g0009 | 2 | HG03130.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.1103+31_1103+32dup others(2): Show |
LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chrX | 37667510 | |||||
| chrX:37667691
|
T | C | 3 | a0001c0001t0020g0052a0001c0001t0020g0104a0001c0002t0030g0153 | 3 | HG01255.hp1 HG02809.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.1103+202T>C | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 4/4 | chrX | 37667691 | ||||||
| chrX:37667733
|
T | TG | 1 | a0004c0008t0011g0130 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.1103+247dupG | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chrX | 37667733 | |||||
| chrX:37667748
|
G | GA | 1 | a0001c0001t0001g0016 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.1103+264dupA | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chrX | 37667748 | |||||
| chrX:37667748
|
GA | G | 1 | a0004c0008t0011g0130 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.1103+264delA | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chrX | 37667748 | |||||
| chrX:37667784
|
T | TACAATA | 1 | a0004c0008t0011g0130 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.1103+299_1103+300i others(8): Show |
LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chrX | 37667784 | |||||
| chrX:37667818
|
A | G | 71 | a0001c0001t0020g0052a0001c0001t0020g0104a0001c0001t0031g0162others(68): Show | 76 | HG00639.hp1 HG00639.hp2 HG00735.hp1 others(73): Show |
intron_variant | MODIFIER | c.1103+329A>G | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 4/4 | chrX | 37667818 | ||||||
| chrX:37668011
|
A | T | 71 | a0001c0001t0020g0052a0001c0001t0020g0104a0001c0001t0031g0162others(68): Show | 76 | HG00639.hp1 HG00639.hp2 HG00735.hp1 others(73): Show |
intron_variant | MODIFIER | c.1103+522A>T | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 4/4 | chrX | 37668011 | ||||||
| chrX:37668074
|
G | C | 1 | a0001c0003t0005g0010 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1103+585G>C | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 4/4 | chrX | 37668074 | ||||||
| chrX:37668148
|
A | C | 1 | a0001c0001t0001g0106 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.1103+659A>C | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 4/4 | chrX | 37668148 | ||||||
| chrX:37668257
|
C | CTA | 45 | a0001c0002t0002g0002a0001c0002t0002g0135a0001c0002t0002g0157others(42): Show | 50 | HG00639.hp1 HG00639.hp2 HG00735.hp1 others(47): Show |
intron_variant | MODIFIER | c.1103+786_1103+787d others(4): Show |
LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chrX | 37668257 | |||||
| chrX:37668257
|
C | CTATA | 6 | a0001c0002t0004g0149a0001c0002t0045g0008a0001c0003t0015g0168others(3): Show | 6 | HG02630.hp2 HG02818.hp2 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.1103+784_1103+787d others(6): Show |
LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chrX | 37668257 | |||||
| chrX:37668257
|
C | CTATATA | 3 | a0001c0001t0020g0052a0001c0001t0020g0104a0001c0002t0030g0153 | 3 | HG01255.hp1 HG02809.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.1103+782_1103+787d others(8): Show |
LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chrX | 37668257 | |||||
| chrX:37668257
|
C | CTATATAT others(1): Show |
13 | a0001c0003t0005g0010a0001c0003t0005g0119a0001c0003t0005g0182others(10): Show | 13 | HG01891.hp2 HG02622.hp1 HG02622.hp2 others(10): Show |
intron_variant | MODIFIER | c.1103+780_1103+787d others(10): Show |
LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chrX | 37668257 | |||||
| chrX:37668257
|
C | CTATATAT others(3): Show |
2 | a0001c0003t0005g0007a0001c0003t0024g0136 | 2 | HG02615.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.1103+778_1103+787d others(12): Show |
LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chrX | 37668257 | |||||
| chrX:37668270
|
TATATATC others(16): Show |
T | 2 | a0001c0001t0031g0162a0001c0001t0048g0009 | 2 | HG03130.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.1103+788_1103+810d others(25): Show |
LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chrX | 37668270 | |||||
| chrX:37668358
|
TC | T | 1 | a0004c0008t0011g0130 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.1103+871delC | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chrX | 37668358 | |||||
| chrX:37668406
|
T | C | 25 | a0001c0002t0003g0005a0001c0002t0003g0026a0001c0002t0003g0040others(22): Show | 26 | HG00639.hp1 HG00639.hp2 HG01069.hp1 others(23): Show |
intron_variant | MODIFIER | c.1103+917T>C | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 4/4 | chrX | 37668406 | ||||||
| chrX:37668506
|
A | G | 1 | a0001c0001t0006g0143 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.1103+1017A>G | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 4/4 | chrX | 37668506 | ||||||
| chrX:37668718
|
A | AG | 1 | a0001c0001t0001g0016 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.1103+1234dupG | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chrX | 37668718 | |||||
| chrX:37669004
|
T | C | 1 | a0001c0002t0019g0057 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1103+1515T>C | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 4/4 | chrX | 37669004 | ||||||
| chrX:37669120
|
G | A | 1 | a0001c0001t0001g0046 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.1103+1631G>A | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 4/4 | chrX | 37669120 | ||||||
| chrX:37669386
|
C | T | 42 | a0001c0002t0002g0002a0001c0002t0002g0135a0001c0002t0002g0157others(39): Show | 46 | HG00639.hp1 HG00639.hp2 HG00735.hp1 others(43): Show |
intron_variant | MODIFIER | c.1103+1897C>T | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 4/4 | chrX | 37669386 | ||||||
| chrX:37669397
|
C | A | 1 | a0001c0002t0045g0008 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1103+1908C>A | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 4/4 | chrX | 37669397 | ||||||
| chrX:37669787
|
C | T | 71 | a0001c0001t0020g0052a0001c0001t0020g0104a0001c0001t0031g0162others(68): Show | 76 | HG00639.hp1 HG00639.hp2 HG00735.hp1 others(73): Show |
intron_variant | MODIFIER | c.1103+2298C>T | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 4/4 | chrX | 37669787 | ||||||
| chrX:37669799
|
A | G | 1 | a0001c0002t0014g0156 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1103+2310A>G | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 4/4 | chrX | 37669799 | ||||||
| chrX:37669976
|
AT | A | 1 | a0004c0008t0011g0130 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.1103+2493delT | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chrX | 37669976 | |||||
| chrX:37669994
|
ATAGT | A | 3 | a0001c0002t0014g0131a0001c0002t0014g0156a0001c0002t0027g0155 | 3 | HG02809.hp2 HG03516.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1103+2508_1103+251 others(8): Show |
LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chrX | 37669994 | |||||
| chrX:37670234
|
A | G | 2 | a0001c0001t0001g0043a0001c0001t0001g0094 | 2 | HG02074.hp1 NA18948.hp1 |
intron_variant | MODIFIER | c.1103+2745A>G | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 4/4 | chrX | 37670234 | ||||||
| chrX:37670265
|
C | CT | 1 | a0004c0008t0011g0130 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.1103+2777dupT | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chrX | 37670265 | |||||
| chrX:37670270
|
A | ATTAT | 1 | a0004c0008t0011g0130 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.1103+2781_1103+278 others(8): Show |
LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 4/4 | chrX | 37670270 | ||||||
| chrX:37670271
|
A | T | 1 | a0004c0008t0011g0130 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.1103+2782A>T | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 4/4 | chrX | 37670271 | ||||||
| chrX:37670309
|
T | C | 74 | a0001c0001t0010g0146a0001c0001t0010g0147a0001c0001t0010g0148others(71): Show | 79 | HG00639.hp1 HG00639.hp2 HG00735.hp1 others(76): Show |
intron_variant | MODIFIER | c.1103+2820T>C | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 4/4 | chrX | 37670309 | ||||||
| chrX:37670350
|
CA | C | 1 | a0004c0008t0011g0130 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.1103+2864delA | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chrX | 37670350 | |||||
| chrX:37670452
|
T | C | 71 | a0001c0001t0020g0052a0001c0001t0020g0104a0001c0001t0031g0162others(68): Show | 76 | HG00639.hp1 HG00639.hp2 HG00735.hp1 others(73): Show |
intron_variant | MODIFIER | c.1103+2963T>C | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 4/4 | chrX | 37670452 | ||||||
| chrX:37670464
|
G | GATTTT | 71 | a0001c0001t0020g0052a0001c0001t0020g0104a0001c0001t0031g0162others(68): Show | 76 | HG00639.hp1 HG00639.hp2 HG00735.hp1 others(73): Show |
intron_variant | MODIFIER | c.1103+2977_1103+298 others(9): Show |
LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chrX | 37670464 | |||||
| chrX:37670517
|
CAGAT | C | 1 | a0001c0002t0004g0167 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1103+3031_1103+303 others(8): Show |
LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chrX | 37670517 | |||||
| chrX:37670597
|
AT | A | 1 | a0001c0001t0040g0072 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1103+3115delT | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chrX | 37670597 | |||||
| chrX:37670612
|
G | A | 3 | a0001c0001t0001g0076a0001c0001t0001g0078a0001c0001t0001g0105 | 3 | HG00140.hp1 HG01074.hp1 HG01515.hp1 |
intron_variant | MODIFIER | c.1103+3123G>A | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 4/4 | chrX | 37670612 | ||||||
| chrX:37670714
|
TA | T | 1 | a0004c0008t0011g0130 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.1103+3231delA | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chrX | 37670714 | |||||
| chrX:37670715
|
A | T | 2 | a0001c0001t0031g0162a0001c0001t0048g0009 | 2 | HG03130.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.1103+3226A>T | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 4/4 | chrX | 37670715 | ||||||
| chrX:37670763
|
G | A | 71 | a0001c0001t0020g0052a0001c0001t0020g0104a0001c0001t0031g0162others(68): Show | 76 | HG00639.hp1 HG00639.hp2 HG00735.hp1 others(73): Show |
intron_variant | MODIFIER | c.1103+3274G>A | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 4/4 | chrX | 37670763 | ||||||
| chrX:37671032
|
A | AT | 1 | a0004c0008t0011g0130 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.1103+3545dupT | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chrX | 37671032 | |||||
| chrX:37671173
|
TA | T | 1 | a0004c0008t0011g0130 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.1103+3687delA | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chrX | 37671173 | |||||
| chrX:37671405
|
A | C | 4 | a0001c0001t0001g0016a0001c0001t0001g0044a0001c0001t0001g0046others(1): Show | 4 | HG02683.hp1 NA18943.hp1 NA18959.hp1 others(1): Show |
intron_variant | MODIFIER | c.1103+3916A>C | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 4/4 | chrX | 37671405 | ||||||
| chrX:37671435
|
C | A | 23 | a0001c0002t0003g0005a0001c0002t0003g0026a0001c0002t0003g0040others(20): Show | 24 | HG00639.hp1 HG00639.hp2 HG01069.hp1 others(21): Show |
intron_variant | MODIFIER | c.1103+3946C>A | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 4/4 | chrX | 37671435 | ||||||
| chrX:37671520
|
GA | G | 3 | a0001c0004t0009g0006a0001c0004t0009g0178a0001c0004t0009g0179 | 4 | HG02109.hp2 HG02615.hp1 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.1103+4032delA | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 4/4 | chrX | 37671520 | ||||||
| chrX:37671762
|
T | G | 13 | a0001c0002t0003g0005a0001c0002t0003g0026a0001c0002t0003g0040others(10): Show | 14 | HG00639.hp1 HG00639.hp2 HG01069.hp1 others(11): Show |
intron_variant | MODIFIER | c.1104-3892T>G | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 4/4 | chrX | 37671762 | ||||||
| chrX:37671836
|
C | G | 71 | a0001c0001t0020g0052a0001c0001t0020g0104a0001c0001t0031g0162others(68): Show | 76 | HG00639.hp1 HG00639.hp2 HG00735.hp1 others(73): Show |
intron_variant | MODIFIER | c.1104-3818C>G | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 4/4 | chrX | 37671836 | ||||||
| chrX:37672191
|
A | G | 1 | a0001c0002t0053g0181 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1104-3463A>G | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 4/4 | chrX | 37672191 | ||||||
| chrX:37672730
|
G | A | 71 | a0001c0001t0020g0052a0001c0001t0020g0104a0001c0001t0031g0162others(68): Show | 76 | HG00639.hp1 HG00639.hp2 HG00735.hp1 others(73): Show |
intron_variant | MODIFIER | c.1104-2924G>A | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 4/4 | chrX | 37672730 | ||||||
| chrX:37672972
|
C | T | 1 | a0001c0003t0005g0182 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1104-2682C>T | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 4/4 | chrX | 37672972 | ||||||
| chrX:37673190
|
CT | C | 1 | a0001c0001t0001g0082 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.1104-2461delT | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chrX | 37673190 | |||||
| chrX:37673277
|
G | T | 1 | a0001c0002t0004g0167 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1104-2377G>T | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 4/4 | chrX | 37673277 | ||||||
| chrX:37673679
|
AT | A | 1 | a0004c0008t0011g0130 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.1104-1971delT | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chrX | 37673679 | |||||
| chrX:37673725
|
GA | G | 1 | a0001c0003t0005g0007 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1104-1924delA | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chrX | 37673725 | |||||
| chrX:37674672
|
G | T | 5 | a0001c0001t0020g0052a0001c0001t0020g0104a0001c0001t0031g0162others(2): Show | 5 | HG01255.hp1 HG02809.hp1 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.1104-982G>T | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 4/4 | chrX | 37674672 | ||||||
| chrX:37674739
|
C | G | 3 | a0001c0001t0010g0146a0001c0001t0010g0147a0001c0001t0010g0148 | 3 | HG02109.hp1 HG02145.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.1104-915C>G | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 4/4 | chrX | 37674739 | ||||||
| chrX:37674935
|
T | C | 1 | a0001c0001t0001g0091 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1104-719T>C | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 4/4 | chrX | 37674935 | ||||||
| chrX:37675010
|
A | T | 1 | a0001c0002t0019g0057 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1104-644A>T | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 4/4 | chrX | 37675010 | ||||||
| chrX:37675096
|
G | A | 1 | a0001c0001t0001g0089 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.1104-558G>A | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 4/4 | chrX | 37675096 | ||||||
| chrX:37675162
|
T | G | 1 | a0001c0002t0003g0075 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.1104-492T>G | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 4/4 | chrX | 37675162 | ||||||
| chrX:37675226
|
A | G | 1 | a0001c0001t0001g0080 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.1104-428A>G | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 4/4 | chrX | 37675226 | ||||||
| chrX:37675280
|
C | T | 71 | a0001c0001t0020g0052a0001c0001t0020g0104a0001c0001t0031g0162others(68): Show | 76 | HG00639.hp1 HG00639.hp2 HG00735.hp1 others(73): Show |
intron_variant | MODIFIER | c.1104-374C>T | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 4/4 | chrX | 37675280 | ||||||
| chrX:37675390
|
G | A | 74 | a0001c0001t0010g0146a0001c0001t0010g0147a0001c0001t0010g0148others(71): Show | 79 | HG00639.hp1 HG00639.hp2 HG00735.hp1 others(76): Show |
intron_variant | MODIFIER | c.1104-264G>A | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 4/4 | chrX | 37675390 | ||||||
| chrX:37675424
|
A | G | 1 | a0001c0003t0029g0132 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1104-230A>G | LANCL3 | ENSG00000147036.12 | transcript | ENST00000378619.4 | protein_coding | 4/4 | chrX | 37675424 |