geneid | 81562 |
---|---|
ensemblid | ENSG00000114988.12 |
hgncid | 19263 |
symbol | LMAN2L |
name | lectin, mannose binding 2 like |
refseq_nuc | NM_030805.4 |
refseq_prot | NP_110432.1 |
ensembl_nuc | ENST00000264963.9 |
ensembl_prot | ENSP00000264963.4 |
mane_status | MANE Select |
chr | chr2 |
start | 96705929 |
end | 96740064 |
strand | - |
ver | v1.2 |
region | chr2:96705929-96740064 |
region5000 | chr2:96700929-96745064 |
regionname0 | LMAN2L_chr2_96705929_96740064 |
regionname5000 | LMAN2L_chr2_96700929_96745064 |
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 | 348 | 266 | 84 | 53 | 95 | 14 | 18 | 73 | LMAN2L_chr2_96700929_96745064 | LMAN2L | copy fasta | chr2 | 96700929 | 96745064 |
a0002 | 0/0 | 348 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | LMAN2L_chr2_96700929_96745064 | LMAN2L | copy fasta | chr2 | 96700929 | 96745064 |
a0003 | 0/0 | 348 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | LMAN2L_chr2_96700929_96745064 | LMAN2L | copy fasta | chr2 | 96700929 | 96745064 |
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 | 1047 | 265 | 84 | 52 | 95 | 14 | 18 | LMAN2L_chr2_96700929_96745064 | LMAN2L | copy fasta | chr2 | 96700929 | 96745064 |
c0002 | 0/0 | 1047 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN2L_chr2_96700929_96745064 | LMAN2L | copy fasta | chr2 | 96700929 | 96745064 |
c0003 | 0/0 | 1047 | 1 | 0 | 1 | 0 | 0 | 0 | LMAN2L_chr2_96700929_96745064 | LMAN2L | copy fasta | chr2 | 96700929 | 96745064 |
c0004 | 0/0 | 1047 | 1 | 0 | 1 | 0 | 0 | 0 | LMAN2L_chr2_96700929_96745064 | LMAN2L | copy fasta | chr2 | 96700929 | 96745064 |
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 | 1/1 | 1352 | 253 | 72 | 52 | 96 | 13 | 18 | LMAN2L_chr2_96700929_96745064 | LMAN2L | copy fasta | chr2 | 96700929 | 96745064 |
t0002 | 0/0 | 1352 | 12 | 10 | 2 | 0 | 0 | 0 | LMAN2L_chr2_96700929_96745064 | LMAN2L | copy fasta | chr2 | 96700929 | 96745064 |
t0003 | 0/0 | 1352 | 1 | 0 | 0 | 0 | 1 | 0 | LMAN2L_chr2_96700929_96745064 | LMAN2L | copy fasta | chr2 | 96700929 | 96745064 |
t0004 | 0/0 | 1352 | 1 | 1 | 0 | 0 | 0 | 0 | LMAN2L_chr2_96700929_96745064 | LMAN2L | copy fasta | chr2 | 96700929 | 96745064 |
t0005 | 0/0 | 1352 | 1 | 1 | 0 | 0 | 0 | 0 | LMAN2L_chr2_96700929_96745064 | LMAN2L | copy fasta | chr2 | 96700929 | 96745064 |
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 | 1/1 | 34 | 1 | 5 | 19 | 2 | 5 | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
g0002 | 0/0 | 28 | 1 | 13 | 9 | 4 | 1 | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
g0003 | 0/0 | 9 | 9 | 0 | 0 | 0 | 0 | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
g0004 | 0/0 | 8 | 7 | 1 | 0 | 0 | 0 | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
g0005 | 0/0 | 6 | 0 | 0 | 5 | 0 | 1 | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
g0006 | 0/0 | 5 | 0 | 4 | 1 | 0 | 0 | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
g0007 | 0/0 | 5 | 2 | 0 | 0 | 2 | 1 | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
g0008 | 0/0 | 5 | 0 | 3 | 0 | 2 | 0 | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
g0009 | 0/0 | 4 | 1 | 0 | 3 | 0 | 0 | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
g0010 | 0/0 | 4 | 1 | 3 | 0 | 0 | 0 | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
g0011 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
g0012 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
g0013 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
g0014 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
g0015 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
g0016 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
g0018 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
g0020 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
g0023 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
g0024 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
g0025 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
g0027 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
g0039 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
g0095 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
g0115 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
g0117 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
g0118 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
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 | 1047 | 265 | 84 | 52 | 95 | 14 | 18 | LMAN2L_chr2_96700929_96745064 | LMAN2L | copy fasta | chr2 | 96700929 | 96745064 |
a0001c0003 | 0/0 | 1047 | 1 | 0 | 1 | 0 | 0 | 0 | LMAN2L_chr2_96700929_96745064 | LMAN2L | copy fasta | chr2 | 96700929 | 96745064 |
a0002c0002 | 0/0 | 1047 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN2L_chr2_96700929_96745064 | LMAN2L | copy fasta | chr2 | 96700929 | 96745064 |
a0003c0004 | 0/0 | 1047 | 1 | 0 | 1 | 0 | 0 | 0 | LMAN2L_chr2_96700929_96745064 | LMAN2L | copy fasta | chr2 | 96700929 | 96745064 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 1/1 | 2398 | 251 | 72 | 51 | 95 | 13 | 18 | LMAN2L_chr2_96700929_96745064 | LMAN2L | copy fasta | chr2 | 96700929 | 96745064 |
a0001c0001t0002 | 0/0 | 2398 | 11 | 10 | 1 | 0 | 0 | 0 | LMAN2L_chr2_96700929_96745064 | LMAN2L | copy fasta | chr2 | 96700929 | 96745064 |
a0001c0001t0003 | 0/0 | 2398 | 1 | 0 | 0 | 0 | 1 | 0 | LMAN2L_chr2_96700929_96745064 | LMAN2L | copy fasta | chr2 | 96700929 | 96745064 |
a0001c0001t0004 | 0/0 | 2398 | 1 | 1 | 0 | 0 | 0 | 0 | LMAN2L_chr2_96700929_96745064 | LMAN2L | copy fasta | chr2 | 96700929 | 96745064 |
a0001c0001t0005 | 0/0 | 2398 | 1 | 1 | 0 | 0 | 0 | 0 | LMAN2L_chr2_96700929_96745064 | LMAN2L | copy fasta | chr2 | 96700929 | 96745064 |
a0001c0003t0002 | 0/0 | 2398 | 1 | 0 | 1 | 0 | 0 | 0 | LMAN2L_chr2_96700929_96745064 | LMAN2L | copy fasta | chr2 | 96700929 | 96745064 |
a0002c0002t0001 | 0/0 | 2398 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN2L_chr2_96700929_96745064 | LMAN2L | copy fasta | chr2 | 96700929 | 96745064 |
a0003c0004t0001 | 0/0 | 2398 | 1 | 0 | 1 | 0 | 0 | 0 | LMAN2L_chr2_96700929_96745064 | LMAN2L | copy fasta | chr2 | 96700929 | 96745064 |
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 | 1/1 | 34 | 1 | 5 | 19 | 2 | 5 | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
a0001c0001t0001g0002 | 0/0 | 28 | 1 | 13 | 9 | 4 | 1 | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
a0001c0001t0001g0003 | 0/0 | 9 | 9 | 0 | 0 | 0 | 0 | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
a0001c0001t0001g0005 | 0/0 | 6 | 0 | 0 | 5 | 0 | 1 | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
a0001c0001t0001g0006 | 0/0 | 5 | 0 | 4 | 1 | 0 | 0 | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
a0001c0001t0001g0007 | 0/0 | 5 | 2 | 0 | 0 | 2 | 1 | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
a0001c0001t0001g0008 | 0/0 | 5 | 0 | 3 | 0 | 2 | 0 | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
a0001c0001t0001g0009 | 0/0 | 4 | 1 | 0 | 3 | 0 | 0 | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
a0001c0001t0001g0010 | 0/0 | 4 | 1 | 3 | 0 | 0 | 0 | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
a0001c0001t0001g0011 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
a0001c0001t0001g0012 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
a0001c0001t0001g0013 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
a0001c0001t0001g0014 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
a0001c0001t0001g0015 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
a0001c0001t0001g0016 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
a0001c0001t0001g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
a0001c0001t0001g0018 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
a0001c0001t0001g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
a0001c0001t0001g0020 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
a0001c0001t0001g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
a0001c0001t0001g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
a0001c0001t0001g0023 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
a0001c0001t0001g0024 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
a0001c0001t0001g0025 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
a0001c0001t0001g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
a0001c0001t0001g0027 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
a0001c0001t0001g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
a0001c0001t0001g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
a0001c0001t0001g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
a0001c0001t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
a0001c0001t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
a0001c0001t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
a0001c0001t0001g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
a0001c0001t0001g0039 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
a0001c0001t0001g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
a0001c0001t0001g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
a0001c0001t0001g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
a0001c0001t0001g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
a0001c0001t0001g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
a0001c0001t0001g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
a0001c0001t0001g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
a0001c0001t0001g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
a0001c0001t0001g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
a0001c0001t0001g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
a0001c0001t0001g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
a0001c0001t0001g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
a0001c0001t0001g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
a0001c0001t0001g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
a0001c0001t0001g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
a0001c0001t0001g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
a0001c0001t0001g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
a0001c0001t0001g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
a0001c0001t0001g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
a0001c0001t0001g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
a0001c0001t0001g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
a0001c0001t0001g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
a0001c0001t0001g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
a0001c0001t0001g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
a0001c0001t0001g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
a0001c0001t0001g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
a0001c0001t0001g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
a0001c0001t0001g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
a0001c0001t0001g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
a0001c0001t0001g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
a0001c0001t0001g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
a0001c0001t0001g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
a0001c0001t0001g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
a0001c0001t0001g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
a0001c0001t0001g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
a0001c0001t0001g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
a0001c0001t0001g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
a0001c0001t0001g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
a0001c0001t0001g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
a0001c0001t0001g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
a0001c0001t0001g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
a0001c0001t0001g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
a0001c0001t0001g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
a0001c0001t0001g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
a0001c0001t0001g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
a0001c0001t0001g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
a0001c0001t0001g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
a0001c0001t0001g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
a0001c0001t0001g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
a0001c0001t0001g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
a0001c0001t0001g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
a0001c0001t0001g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
a0001c0001t0001g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
a0001c0001t0002g0004 | 0/0 | 8 | 7 | 1 | 0 | 0 | 0 | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
a0001c0001t0002g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
a0001c0001t0002g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
a0001c0001t0002g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
a0001c0001t0003g0095 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
a0001c0001t0004g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
a0001c0001t0005g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
a0001c0003t0002g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
a0002c0002t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
a0003c0004t0001g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0001 | g0117 | EUR | GBR | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
HG00099 | hp2 | a0001 | c0001 | t0003 | g0095 | EUR | GBR | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
HG00280 | hp1 | a0001 | c0001 | t0001 | g0007 | EUR | FIN | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
HG00280 | hp2 | a0001 | c0001 | t0001 | g0002 | EUR | FIN | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
HG00323 | hp1 | a0001 | c0001 | t0001 | g0115 | EUR | FIN | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
HG00323 | hp2 | a0001 | c0001 | t0001 | g0002 | EUR | FIN | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
HG00408 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
HG00408 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | CHS | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
HG00544 | hp1 | a0001 | c0001 | t0001 | g0022 | EAS | CHS | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
HG00544 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
HG00558 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
HG00558 | hp2 | a0001 | c0001 | t0001 | g0133 | EAS | CHS | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
HG00609 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | CHS | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
HG00609 | hp2 | a0001 | c0001 | t0001 | g0089 | EAS | CHS | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
HG00639 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
HG00639 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
HG00642 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
HG00642 | hp2 | a0001 | c0001 | t0001 | g0018 | AMR | PUR | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
HG00673 | hp1 | a0001 | c0001 | t0001 | g0127 | EAS | CHS | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
HG00673 | hp2 | a0001 | c0001 | t0001 | g0125 | EAS | CHS | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
HG00733 | hp1 | a0001 | c0001 | t0001 | g0097 | AMR | PUR | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
HG00733 | hp2 | a0001 | c0001 | t0001 | g0008 | AMR | PUR | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
HG00741 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
HG00741 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
HG01069 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
HG01069 | hp2 | a0001 | c0001 | t0001 | g0116 | AMR | PUR | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
HG01070 | hp1 | a0001 | c0001 | t0001 | g0024 | AMR | PUR | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
HG01070 | hp2 | a0001 | c0001 | t0001 | g0049 | AMR | PUR | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
HG01071 | hp1 | a0001 | c0001 | t0001 | g0048 | AMR | PUR | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
HG01071 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
HG01081 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
HG01081 | hp2 | a0001 | c0001 | t0001 | g0063 | AMR | PUR | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
HG01099 | hp1 | a0001 | c0001 | t0001 | g0010 | AMR | PUR | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
HG01099 | hp2 | a0001 | c0001 | t0001 | g0008 | AMR | PUR | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
HG01168 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
HG01168 | hp2 | a0001 | c0001 | t0001 | g0010 | AMR | PUR | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
HG01169 | hp1 | a0001 | c0001 | t0001 | g0010 | AMR | PUR | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
HG01169 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
HG01175 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
HG01175 | hp2 | a0001 | c0001 | t0001 | g0091 | AMR | PUR | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
HG01192 | hp1 | a0001 | c0001 | t0001 | g0020 | AMR | PUR | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
HG01192 | hp2 | a0001 | c0001 | t0001 | g0008 | AMR | PUR | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
HG01243 | hp1 | a0003 | c0004 | t0001 | g0144 | AMR | PUR | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
HG01243 | hp2 | a0001 | c0001 | t0001 | g0126 | AMR | PUR | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
HG01255 | hp1 | a0001 | c0001 | t0001 | g0114 | AMR | CLM | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
HG01255 | hp2 | a0001 | c0001 | t0001 | g0128 | AMR | CLM | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
HG01256 | hp1 | a0001 | c0001 | t0001 | g0020 | AMR | CLM | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
HG01256 | hp2 | a0001 | c0001 | t0001 | g0046 | AMR | CLM | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
HG01261 | hp1 | a0001 | c0001 | t0001 | g0034 | AMR | CLM | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
HG01261 | hp2 | a0001 | c0001 | t0002 | g0004 | AMR | CLM | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
HG01346 | hp1 | a0001 | c0001 | t0001 | g0140 | AMR | CLM | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
HG01346 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
HG01358 | hp1 | a0001 | c0003 | t0002 | g0032 | AMR | CLM | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
HG01358 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
HG01361 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
HG01361 | hp2 | a0001 | c0001 | t0001 | g0141 | AMR | CLM | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
HG01496 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
HG01496 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
HG01515 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | IBS | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
HG01515 | hp2 | a0001 | c0001 | t0001 | g0008 | EUR | IBS | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
HG01517 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | IBS | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
HG01517 | hp2 | a0001 | c0001 | t0001 | g0008 | EUR | IBS | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
HG01884 | hp1 | a0001 | c0001 | t0001 | g0015 | AFR | ACB | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
HG01884 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | ACB | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
HG01891 | hp1 | a0001 | c0001 | t0001 | g0124 | AFR | ACB | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
HG01891 | hp2 | a0001 | c0001 | t0001 | g0070 | AFR | ACB | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
HG01943 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | PEL | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
HG01943 | hp2 | a0001 | c0001 | t0001 | g0134 | AMR | PEL | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
HG01975 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
HG01975 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
HG01981 | hp1 | a0001 | c0001 | t0001 | g0045 | AMR | PEL | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
HG01981 | hp2 | a0001 | c0001 | t0001 | g0098 | AMR | PEL | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
HG01993 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
HG01993 | hp2 | a0001 | c0001 | t0001 | g0090 | AMR | PEL | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
HG02004 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
HG02004 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
HG02040 | hp1 | a0001 | c0001 | t0001 | g0109 | EAS | KHV | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
HG02040 | hp2 | a0001 | c0001 | t0001 | g0092 | EAS | KHV | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
HG02055 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
HG02055 | hp2 | a0001 | c0001 | t0001 | g0050 | AFR | ACB | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
HG02056 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | KHV | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
HG02056 | hp2 | a0001 | c0001 | t0001 | g0143 | EAS | KHV | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
HG02071 | hp1 | a0001 | c0001 | t0001 | g0104 | EAS | KHV | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
HG02071 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
HG02145 | hp1 | a0001 | c0001 | t0001 | g0027 | AFR | ACB | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
HG02145 | hp2 | a0001 | c0001 | t0004 | g0074 | AFR | ACB | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
HG02155 | hp1 | a0001 | c0001 | t0001 | g0053 | EAS | CDX | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
HG02155 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | CDX | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
HG02165 | hp1 | a0001 | c0001 | t0001 | g0105 | EAS | CDX | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
HG02165 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | CDX | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
HG02257 | hp1 | a0001 | c0001 | t0001 | g0041 | AFR | ACB | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
HG02257 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | ACB | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
HG02258 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | ACB | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
HG02258 | hp2 | a0001 | c0001 | t0002 | g0004 | AFR | ACB | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
HG02615 | hp1 | a0001 | c0001 | t0001 | g0059 | AFR | GWD | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
HG02615 | hp2 | a0001 | c0001 | t0001 | g0009 | AFR | GWD | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
HG02622 | hp1 | a0001 | c0001 | t0001 | g0119 | AFR | GWD | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
HG02622 | hp2 | a0001 | c0001 | t0001 | g0064 | AFR | GWD | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
HG02630 | hp1 | a0001 | c0001 | t0001 | g0067 | AFR | GWD | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
HG02630 | hp2 | a0001 | c0001 | t0001 | g0082 | AFR | GWD | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
HG02698 | hp1 | a0001 | c0001 | t0001 | g0007 | SAS | PJL | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
HG02698 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
HG02717 | hp1 | a0001 | c0001 | t0001 | g0016 | AFR | GWD | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
HG02717 | hp2 | a0001 | c0001 | t0001 | g0013 | AFR | GWD | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
HG02723 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | GWD | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
HG02723 | hp2 | a0001 | c0001 | t0001 | g0016 | AFR | GWD | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
HG02735 | hp1 | a0001 | c0001 | t0001 | g0108 | SAS | PJL | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
HG02735 | hp2 | a0001 | c0001 | t0001 | g0139 | SAS | PJL | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
HG02809 | hp1 | a0001 | c0001 | t0001 | g0043 | AFR | GWD | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
HG02809 | hp2 | a0001 | c0001 | t0001 | g0014 | AFR | GWD | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
HG02886 | hp1 | a0001 | c0001 | t0001 | g0010 | AFR | GWD | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
HG02886 | hp2 | a0001 | c0001 | t0001 | g0007 | AFR | GWD | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
HG02895 | hp1 | a0001 | c0001 | t0001 | g0044 | AFR | GWD | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
HG02895 | hp2 | a0001 | c0001 | t0002 | g0029 | AFR | GWD | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
HG02896 | hp1 | a0001 | c0001 | t0001 | g0027 | AFR | GWD | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
HG02896 | hp2 | a0001 | c0001 | t0001 | g0079 | AFR | GWD | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
HG02897 | hp1 | a0001 | c0001 | t0002 | g0004 | AFR | GWD | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
HG02897 | hp2 | a0001 | c0001 | t0001 | g0113 | AFR | GWD | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
HG02922 | hp1 | a0001 | c0001 | t0002 | g0031 | AFR | ESN | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
HG02922 | hp2 | a0001 | c0001 | t0001 | g0081 | AFR | ESN | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
HG02965 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | ESN | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
HG02965 | hp2 | a0001 | c0001 | t0001 | g0018 | AFR | ESN | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
HG02970 | hp1 | a0001 | c0001 | t0001 | g0068 | AFR | ESN | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
HG02970 | hp2 | a0001 | c0001 | t0002 | g0004 | AFR | ESN | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
HG02976 | hp1 | a0001 | c0001 | t0001 | g0013 | AFR | ESN | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
HG02976 | hp2 | a0001 | c0001 | t0001 | g0069 | AFR | ESN | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
HG03017 | hp1 | a0001 | c0001 | t0001 | g0042 | SAS | PJL | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
HG03017 | hp2 | a0001 | c0001 | t0001 | g0121 | SAS | PJL | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
HG03041 | hp1 | a0001 | c0001 | t0002 | g0004 | AFR | GWD | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
HG03041 | hp2 | a0001 | c0001 | t0001 | g0015 | AFR | GWD | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
HG03098 | hp1 | a0001 | c0001 | t0001 | g0014 | AFR | MSL | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
HG03098 | hp2 | a0001 | c0001 | t0001 | g0058 | AFR | MSL | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
HG03130 | hp1 | a0001 | c0001 | t0001 | g0016 | AFR | ESN | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
HG03130 | hp2 | a0001 | c0001 | t0001 | g0072 | AFR | ESN | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
HG03139 | hp1 | a0001 | c0001 | t0002 | g0030 | AFR | ESN | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
HG03139 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | ESN | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
HG03195 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | ESN | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
HG03195 | hp2 | a0001 | c0001 | t0001 | g0100 | AFR | ESN | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
HG03209 | hp1 | a0001 | c0001 | t0001 | g0060 | AFR | MSL | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
HG03209 | hp2 | a0001 | c0001 | t0001 | g0071 | AFR | MSL | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
HG03225 | hp1 | a0001 | c0001 | t0001 | g0011 | AFR | MSL | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
HG03225 | hp2 | a0001 | c0001 | t0002 | g0004 | AFR | MSL | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
HG03453 | hp1 | a0001 | c0001 | t0001 | g0025 | AFR | MSL | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
HG03453 | hp2 | a0001 | c0001 | t0001 | g0083 | AFR | MSL | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
HG03486 | hp1 | a0001 | c0001 | t0001 | g0015 | AFR | MSL | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
HG03486 | hp2 | a0001 | c0001 | t0001 | g0073 | AFR | MSL | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
HG03516 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | ESN | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
HG03516 | hp2 | a0001 | c0001 | t0001 | g0066 | AFR | ESN | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
HG03579 | hp1 | a0001 | c0001 | t0002 | g0004 | AFR | MSL | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
HG03579 | hp2 | a0001 | c0001 | t0001 | g0065 | AFR | MSL | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
HG03669 | hp1 | a0001 | c0001 | t0001 | g0122 | SAS | PJL | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
HG03669 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
HG03710 | hp1 | a0001 | c0001 | t0001 | g0130 | SAS | PJL | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
HG03710 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
HG03834 | hp1 | a0001 | c0001 | t0001 | g0080 | SAS | BEB | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
HG03834 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
HG03927 | hp1 | a0001 | c0001 | t0001 | g0039 | SAS | BEB | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
HG03927 | hp2 | a0001 | c0001 | t0001 | g0023 | SAS | BEB | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
HG03942 | hp1 | a0001 | c0001 | t0001 | g0136 | SAS | BEB | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
HG03942 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
HG04204 | hp1 | a0001 | c0001 | t0001 | g0005 | SAS | STU | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
HG04204 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | STU | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
NA18522 | hp1 | a0001 | c0001 | t0001 | g0111 | AFR | YRI | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
NA18522 | hp2 | a0001 | c0001 | t0001 | g0123 | AFR | YRI | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
NA18747 | hp1 | a0001 | c0001 | t0001 | g0142 | EAS | CHB | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
NA18747 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHB | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
NA18906 | hp1 | a0001 | c0001 | t0001 | g0088 | AFR | YRI | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
NA18906 | hp2 | a0001 | c0001 | t0001 | g0013 | AFR | YRI | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
NA18939 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
NA18939 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
NA18943 | hp1 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
NA18943 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
NA18945 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
NA18945 | hp2 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
NA18947 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
NA18947 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
NA18950 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
NA18950 | hp2 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
NA18951 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
NA18951 | hp2 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
NA18953 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
NA18953 | hp2 | a0001 | c0001 | t0001 | g0077 | EAS | JPT | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
NA18956 | hp1 | a0001 | c0001 | t0001 | g0084 | EAS | JPT | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
NA18956 | hp2 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
NA18957 | hp1 | a0001 | c0001 | t0001 | g0102 | EAS | JPT | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
NA18957 | hp2 | a0001 | c0001 | t0001 | g0132 | EAS | JPT | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
NA18962 | hp1 | a0001 | c0001 | t0001 | g0055 | EAS | JPT | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
NA18962 | hp2 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
NA18966 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
NA18966 | hp2 | a0001 | c0001 | t0001 | g0086 | EAS | JPT | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
NA18970 | hp1 | a0001 | c0001 | t0001 | g0103 | EAS | JPT | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
NA18970 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
NA18972 | hp1 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
NA18972 | hp2 | a0001 | c0001 | t0001 | g0110 | EAS | JPT | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
NA18973 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
NA18973 | hp2 | a0001 | c0001 | t0001 | g0078 | EAS | JPT | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
NA18979 | hp1 | a0001 | c0001 | t0001 | g0087 | EAS | JPT | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
NA18979 | hp2 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
NA18981 | hp1 | a0002 | c0002 | t0001 | g0056 | EAS | JPT | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
NA18981 | hp2 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
NA18983 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
NA18983 | hp2 | a0001 | c0001 | t0001 | g0112 | EAS | JPT | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
NA18985 | hp1 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
NA18985 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
NA18986 | hp1 | a0001 | c0001 | t0001 | g0131 | EAS | JPT | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
NA18986 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
NA18998 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
NA18998 | hp2 | a0001 | c0001 | t0001 | g0135 | EAS | JPT | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
NA18999 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
NA18999 | hp2 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
NA19000 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
NA19000 | hp2 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
NA19004 | hp1 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
NA19004 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
NA19010 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
NA19010 | hp2 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
NA19011 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
NA19011 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
NA19030 | hp1 | a0001 | c0001 | t0001 | g0051 | AFR | LWK | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
NA19030 | hp2 | a0001 | c0001 | t0001 | g0099 | AFR | LWK | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
NA19043 | hp1 | a0001 | c0001 | t0001 | g0075 | AFR | LWK | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
NA19043 | hp2 | a0001 | c0001 | t0005 | g0057 | AFR | LWK | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
NA19054 | hp1 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
NA19054 | hp2 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
NA19055 | hp1 | a0001 | c0001 | t0001 | g0076 | EAS | JPT | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
NA19055 | hp2 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
NA19056 | hp1 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
NA19056 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
NA19058 | hp1 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
NA19058 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
NA19063 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
NA19063 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
NA19064 | hp1 | a0001 | c0001 | t0001 | g0054 | EAS | JPT | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
NA19064 | hp2 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
NA19070 | hp1 | a0001 | c0001 | t0001 | g0052 | EAS | JPT | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
NA19070 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
NA19074 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
NA19074 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
NA19077 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
NA19077 | hp2 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
NA19085 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
NA19085 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
NA19086 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
NA19086 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
NA19091 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
NA19091 | hp2 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
NA19240 | hp1 | a0001 | c0001 | t0001 | g0011 | AFR | YRI | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
NA19240 | hp2 | a0001 | c0001 | t0002 | g0004 | AFR | YRI | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
NA20129 | hp1 | a0001 | c0001 | t0001 | g0062 | AFR | ASW | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
NA20129 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | ASW | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
NA20752 | hp1 | a0001 | c0001 | t0001 | g0002 | EUR | TSI | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
NA20752 | hp2 | a0001 | c0001 | t0001 | g0007 | EUR | TSI | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
NA20805 | hp1 | a0001 | c0001 | t0001 | g0118 | EUR | TSI | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
NA20805 | hp2 | a0001 | c0001 | t0001 | g0002 | EUR | TSI | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
HG01123 | hp1 | a0001 | c0001 | t0001 | g0137 | AMR | CLM | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
HG01123 | hp2 | a0001 | c0001 | t0001 | g0047 | AMR | CLM | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
HG02109 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | ACB | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
HG02109 | hp2 | a0001 | c0001 | t0001 | g0120 | AFR | ACB | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
HG02486 | hp1 | a0001 | c0001 | t0001 | g0061 | AFR | ACB | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
HG02486 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | ACB | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
HG06807 | hp1 | a0001 | c0001 | t0001 | g0085 | AFR | USA | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
HG06807 | hp2 | a0001 | c0001 | t0001 | g0025 | AFR | USA | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
NA20300 | hp1 | a0001 | c0001 | t0001 | g0014 | AFR | USA | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
NA20300 | hp2 | a0001 | c0001 | t0001 | g0011 | AFR | USA | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
NA21309 | hp1 | a0001 | c0001 | t0001 | g0038 | AFR | LWK | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
NA21309 | hp2 | a0001 | c0001 | t0001 | g0011 | AFR | LWK | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0001 | REF | REF | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0001 | REF | REF | LMAN2L_chr2_96700929_96745064 | LMAN2L | chr2 | 96700929 | 96745064 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:96707267
|
G | A | 1 | a0002 | 1 | NA18981.hp1 | missense_variant | MODERATE | c.1036C>T | p.Arg346Cys | LMAN2L | ENSG00000114988.12 | transcript | ENST00000264963.9 | protein_coding | 8/8 | 1060/2398 | 1036/1047 | 346/348 | chr2 | 96707267 | ||
chr2:96739865
|
T | C | 1 | a0003 | 1 | HG01243.hp1 | missense_variant | MODERATE | c.176A>G | p.Lys59Arg | LMAN2L | ENSG00000114988.12 | transcript | ENST00000264963.9 | protein_coding | 1/8 | 200/2398 | 176/1047 | 59/348 | chr2 | 96739865 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:96734524
|
T | C | 1 | a0001c0003 | 1 | HG01358.hp1 | splice_region_variant&synonymous_variant | LOW | c.309A>G | p.Pro103Pro | LMAN2L | ENSG00000114988.12 | transcript | ENST00000264963.9 | protein_coding | 3/8 | 333/2398 | 309/1047 | 103/348 | chr2 | 96734524 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:96706642
|
C | T | 1 | a0001c0001t0004 | 1 | HG02145.hp2 | 3_prime_UTR_variant | MODIFIER | c.*614G>A | LMAN2L | ENSG00000114988.12 | transcript | ENST00000264963.9 | protein_coding | 8/8 | 614 | chr2 | 96706642 | |||||
chr2:96706922
|
C | T | 1 | a0001c0001t0003 | 1 | HG00099.hp2 | 3_prime_UTR_variant | MODIFIER | c.*334G>A | LMAN2L | ENSG00000114988.12 | transcript | ENST00000264963.9 | protein_coding | 8/8 | 334 | chr2 | 96706922 | |||||
chr2:96707077
|
T | C | 1 | a0001c0001t0005 | 1 | NA19043.hp2 | 3_prime_UTR_variant | MODIFIER | c.*179A>G | LMAN2L | ENSG00000114988.12 | transcript | ENST00000264963.9 | protein_coding | 8/8 | 179 | chr2 | 96707077 | |||||
chr2:96740061
|
C | T | 2 | a0001c0001t0002a0001c0003t0002 | 12 | HG01261.hp2 HG01358.hp1 HG02258.hp2 others(9): Show |
5_prime_UTR_variant | MODIFIER | c.-21G>A | LMAN2L | ENSG00000114988.12 | transcript | ENST00000264963.9 | protein_coding | 1/8 | 21 | chr2 | 96740061 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:96708027
|
G | A | 1 | a0001c0003t0002g0032 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.785-194C>T | LMAN2L | ENSG00000114988.12 | transcript | ENST00000264963.9 | protein_coding | 6/7 | chr2 | 96708027 | ||||||
chr2:96708042
|
C | T | 1 | a0001c0001t0001g0098 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.785-209G>A | LMAN2L | ENSG00000114988.12 | transcript | ENST00000264963.9 | protein_coding | 6/7 | chr2 | 96708042 | ||||||
chr2:96708080
|
G | A | 35 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0012others(32): Show | 72 | HG00280.hp2 HG00323.hp2 HG00544.hp2 others(69): Show |
intron_variant | MODIFIER | c.785-247C>T | LMAN2L | ENSG00000114988.12 | transcript | ENST00000264963.9 | protein_coding | 6/7 | chr2 | 96708080 | ||||||
chr2:96708182
|
G | A | 1 | a0001c0001t0001g0025 | 2 | HG03453.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.785-349C>T | LMAN2L | ENSG00000114988.12 | transcript | ENST00000264963.9 | protein_coding | 6/7 | chr2 | 96708182 | ||||||
chr2:96708282
|
C | T | 2 | a0001c0001t0001g0063a0001c0001t0001g0092 | 2 | HG01081.hp2 HG02040.hp2 |
intron_variant | MODIFIER | c.785-449G>A | LMAN2L | ENSG00000114988.12 | transcript | ENST00000264963.9 | protein_coding | 6/7 | chr2 | 96708282 | ||||||
chr2:96708587
|
G | A | 1 | a0001c0001t0001g0050 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.785-754C>T | LMAN2L | ENSG00000114988.12 | transcript | ENST00000264963.9 | protein_coding | 6/7 | chr2 | 96708587 | ||||||
chr2:96708621
|
G | A | 1 | a0001c0001t0001g0067 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.785-788C>T | LMAN2L | ENSG00000114988.12 | transcript | ENST00000264963.9 | protein_coding | 6/7 | chr2 | 96708621 | ||||||
chr2:96708685
|
G | A | 1 | a0001c0001t0001g0088 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.785-852C>T | LMAN2L | ENSG00000114988.12 | transcript | ENST00000264963.9 | protein_coding | 6/7 | chr2 | 96708685 | ||||||
chr2:96708885
|
T | C | 1 | a0001c0001t0001g0082 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.785-1052A>G | LMAN2L | ENSG00000114988.12 | transcript | ENST00000264963.9 | protein_coding | 6/7 | chr2 | 96708885 | ||||||
chr2:96708908
|
C | CT | 77 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(74): Show | 138 | HG00280.hp2 HG00323.hp2 HG00544.hp1 others(135): Show |
intron_variant | MODIFIER | c.785-1076dupA | LMAN2L | ENSG00000114988.12 | transcript | ENST00000264963.9 | protein_coding | 6/7 | chr2 | 96708908 | ||||||
chr2:96708908
|
CT | C | 6 | a0001c0001t0001g0055a0001c0001t0001g0069a0001c0001t0001g0096others(3): Show | 6 | HG00099.hp1 HG02976.hp2 NA18957.hp1 others(3): Show |
intron_variant | MODIFIER | c.785-1076delA | LMAN2L | ENSG00000114988.12 | transcript | ENST00000264963.9 | protein_coding | 6/7 | chr2 | 96708908 | ||||||
chr2:96708984
|
G | A | 1 | a0001c0001t0001g0100 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.785-1151C>T | LMAN2L | ENSG00000114988.12 | transcript | ENST00000264963.9 | protein_coding | 6/7 | chr2 | 96708984 | ||||||
chr2:96709075
|
C | T | 2 | a0001c0001t0001g0078a0001c0001t0001g0084 | 2 | NA18956.hp1 NA18973.hp2 |
intron_variant | MODIFIER | c.785-1242G>A | LMAN2L | ENSG00000114988.12 | transcript | ENST00000264963.9 | protein_coding | 6/7 | chr2 | 96709075 | ||||||
chr2:96709076
|
G | A | 22 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0013others(19): Show | 30 | HG01070.hp2 HG01071.hp1 HG01099.hp1 others(27): Show |
intron_variant | MODIFIER | c.785-1243C>T | LMAN2L | ENSG00000114988.12 | transcript | ENST00000264963.9 | protein_coding | 6/7 | chr2 | 96709076 | ||||||
chr2:96709126
|
G | A | 1 | a0001c0001t0001g0067 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.785-1293C>T | LMAN2L | ENSG00000114988.12 | transcript | ENST00000264963.9 | protein_coding | 6/7 | chr2 | 96709126 | ||||||
chr2:96709267
|
T | C | 4 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0018others(1): Show | 9 | HG00642.hp2 HG01884.hp1 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.785-1434A>G | LMAN2L | ENSG00000114988.12 | transcript | ENST00000264963.9 | protein_coding | 6/7 | chr2 | 96709267 | ||||||
chr2:96709688
|
G | C | 1 | a0001c0001t0001g0097 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.785-1855C>G | LMAN2L | ENSG00000114988.12 | transcript | ENST00000264963.9 | protein_coding | 6/7 | chr2 | 96709688 | ||||||
chr2:96709697
|
G | A | 1 | a0001c0001t0001g0012 | 4 | NA18939.hp1 NA18947.hp2 NA19010.hp1 others(1): Show |
intron_variant | MODIFIER | c.785-1864C>T | LMAN2L | ENSG00000114988.12 | transcript | ENST00000264963.9 | protein_coding | 6/7 | chr2 | 96709697 | ||||||
chr2:96709740
|
A | C | 1 | a0001c0001t0001g0123 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.785-1907T>G | LMAN2L | ENSG00000114988.12 | transcript | ENST00000264963.9 | protein_coding | 6/7 | chr2 | 96709740 | ||||||
chr2:96709812
|
C | T | 22 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0013others(19): Show | 30 | HG01070.hp2 HG01071.hp1 HG01099.hp1 others(27): Show |
intron_variant | MODIFIER | c.784+1844G>A | LMAN2L | ENSG00000114988.12 | transcript | ENST00000264963.9 | protein_coding | 6/7 | chr2 | 96709812 | ||||||
chr2:96709880
|
G | C | 3 | a0001c0001t0001g0003a0001c0001t0001g0065a0001c0001t0001g0072 | 11 | HG01884.hp2 HG02109.hp1 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.784+1776C>G | LMAN2L | ENSG00000114988.12 | transcript | ENST00000264963.9 | protein_coding | 6/7 | chr2 | 96709880 | ||||||
chr2:96710100
|
T | C | 1 | a0001c0001t0001g0073 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.784+1556A>G | LMAN2L | ENSG00000114988.12 | transcript | ENST00000264963.9 | protein_coding | 6/7 | chr2 | 96710100 | ||||||
chr2:96710176
|
C | G | 1 | a0001c0001t0001g0046 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.784+1480G>C | LMAN2L | ENSG00000114988.12 | transcript | ENST00000264963.9 | protein_coding | 6/7 | chr2 | 96710176 | ||||||
chr2:96710219
|
A | T | 1 | a0003c0004t0001g0144 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.784+1437T>A | LMAN2L | ENSG00000114988.12 | transcript | ENST00000264963.9 | protein_coding | 6/7 | chr2 | 96710219 | ||||||
chr2:96710223
|
C | A | 1 | a0003c0004t0001g0144 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.784+1433G>T | LMAN2L | ENSG00000114988.12 | transcript | ENST00000264963.9 | protein_coding | 6/7 | chr2 | 96710223 | ||||||
chr2:96710441
|
G | A | 1 | a0001c0001t0001g0067 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.784+1215C>T | LMAN2L | ENSG00000114988.12 | transcript | ENST00000264963.9 | protein_coding | 6/7 | chr2 | 96710441 | ||||||
chr2:96710444
|
C | T | 1 | a0001c0001t0001g0053 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.784+1212G>A | LMAN2L | ENSG00000114988.12 | transcript | ENST00000264963.9 | protein_coding | 6/7 | chr2 | 96710444 | ||||||
chr2:96710445
|
G | A | 1 | a0001c0001t0001g0085 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.784+1211C>T | LMAN2L | ENSG00000114988.12 | transcript | ENST00000264963.9 | protein_coding | 6/7 | chr2 | 96710445 | ||||||
chr2:96710579
|
G | A | 1 | a0003c0004t0001g0144 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.784+1077C>T | LMAN2L | ENSG00000114988.12 | transcript | ENST00000264963.9 | protein_coding | 6/7 | chr2 | 96710579 | ||||||
chr2:96710670
|
A | AT | 32 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0012others(29): Show | 69 | HG00280.hp2 HG00323.hp2 HG00544.hp2 others(66): Show |
intron_variant | MODIFIER | c.784+985_784+986ins others(1): Show |
LMAN2L | ENSG00000114988.12 | transcript | ENST00000264963.9 | protein_coding | 6/7 | chr2 | 96710670 | ||||||
chr2:96710671
|
A | T | 3 | a0001c0001t0001g0062a0001c0001t0001g0064a0001c0001t0001g0070 | 3 | HG01891.hp2 HG02622.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.784+985T>A | LMAN2L | ENSG00000114988.12 | transcript | ENST00000264963.9 | protein_coding | 6/7 | chr2 | 96710671 | ||||||
chr2:96710793
|
C | T | 7 | a0001c0001t0001g0003a0001c0001t0001g0014a0001c0001t0001g0015others(4): Show | 20 | HG00642.hp2 HG01884.hp1 HG01884.hp2 others(17): Show |
intron_variant | MODIFIER | c.784+863G>A | LMAN2L | ENSG00000114988.12 | transcript | ENST00000264963.9 | protein_coding | 6/7 | chr2 | 96710793 | ||||||
chr2:96711646
|
G | A | 4 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0018others(1): Show | 9 | HG00642.hp2 HG01884.hp1 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.784+10C>T | LMAN2L | ENSG00000114988.12 | transcript | ENST00000264963.9 | protein_coding | 6/7 | chr2 | 96711646 | ||||||
chr2:96712146
|
C | T | 22 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0013others(19): Show | 30 | HG01070.hp2 HG01071.hp1 HG01099.hp1 others(27): Show |
intron_variant | MODIFIER | c.508-121G>A | LMAN2L | ENSG00000114988.12 | transcript | ENST00000264963.9 | protein_coding | 4/7 | chr2 | 96712146 | ||||||
chr2:96712500
|
T | C | 1 | a0001c0001t0001g0067 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.508-475A>G | LMAN2L | ENSG00000114988.12 | transcript | ENST00000264963.9 | protein_coding | 4/7 | chr2 | 96712500 | ||||||
chr2:96712508
|
C | T | 2 | a0001c0001t0001g0130a0001c0001t0001g0140 | 2 | HG01346.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.508-483G>A | LMAN2L | ENSG00000114988.12 | transcript | ENST00000264963.9 | protein_coding | 4/7 | chr2 | 96712508 | ||||||
chr2:96712609
|
C | T | 1 | a0001c0001t0001g0110 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.508-584G>A | LMAN2L | ENSG00000114988.12 | transcript | ENST00000264963.9 | protein_coding | 4/7 | chr2 | 96712609 | ||||||
chr2:96713008
|
G | A | 1 | a0001c0001t0001g0064 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.508-983C>T | LMAN2L | ENSG00000114988.12 | transcript | ENST00000264963.9 | protein_coding | 4/7 | chr2 | 96713008 | ||||||
chr2:96713498
|
C | T | 1 | a0001c0001t0001g0050 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.508-1473G>A | LMAN2L | ENSG00000114988.12 | transcript | ENST00000264963.9 | protein_coding | 4/7 | chr2 | 96713498 | ||||||
chr2:96713550
|
G | A | 1 | a0001c0001t0001g0138 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.508-1525C>T | LMAN2L | ENSG00000114988.12 | transcript | ENST00000264963.9 | protein_coding | 4/7 | chr2 | 96713550 | ||||||
chr2:96714369
|
G | A | 1 | a0001c0001t0001g0143 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.508-2344C>T | LMAN2L | ENSG00000114988.12 | transcript | ENST00000264963.9 | protein_coding | 4/7 | chr2 | 96714369 | ||||||
chr2:96714492
|
T | G | 41 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0012others(38): Show | 85 | HG00280.hp2 HG00323.hp2 HG00544.hp2 others(82): Show |
intron_variant | MODIFIER | c.508-2467A>C | LMAN2L | ENSG00000114988.12 | transcript | ENST00000264963.9 | protein_coding | 4/7 | chr2 | 96714492 | ||||||
chr2:96714743
|
C | A | 1 | a0001c0001t0001g0050 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.508-2718G>T | LMAN2L | ENSG00000114988.12 | transcript | ENST00000264963.9 | protein_coding | 4/7 | chr2 | 96714743 | ||||||
chr2:96715165
|
C | T | 1 | a0001c0001t0001g0083 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.508-3140G>A | LMAN2L | ENSG00000114988.12 | transcript | ENST00000264963.9 | protein_coding | 4/7 | chr2 | 96715165 | ||||||
chr2:96715819
|
C | T | 2 | a0001c0001t0001g0008a0001c0001t0001g0118 | 6 | HG00733.hp2 HG01099.hp2 HG01192.hp2 others(3): Show |
intron_variant | MODIFIER | c.508-3794G>A | LMAN2L | ENSG00000114988.12 | transcript | ENST00000264963.9 | protein_coding | 4/7 | chr2 | 96715819 | ||||||
chr2:96716107
|
G | C | 24 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0013others(21): Show | 32 | HG01070.hp2 HG01071.hp1 HG01099.hp1 others(29): Show |
intron_variant | MODIFIER | c.508-4082C>G | LMAN2L | ENSG00000114988.12 | transcript | ENST00000264963.9 | protein_coding | 4/7 | chr2 | 96716107 | ||||||
chr2:96716485
|
T | C | 1 | a0001c0001t0001g0041 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.508-4460A>G | LMAN2L | ENSG00000114988.12 | transcript | ENST00000264963.9 | protein_coding | 4/7 | chr2 | 96716485 | ||||||
chr2:96716963
|
T | G | 1 | a0001c0001t0001g0083 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.508-4938A>C | LMAN2L | ENSG00000114988.12 | transcript | ENST00000264963.9 | protein_coding | 4/7 | chr2 | 96716963 | ||||||
chr2:96717217
|
A | G | 1 | a0003c0004t0001g0144 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.508-5192T>C | LMAN2L | ENSG00000114988.12 | transcript | ENST00000264963.9 | protein_coding | 4/7 | chr2 | 96717217 | ||||||
chr2:96717270
|
T | C | 43 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0012others(40): Show | 87 | HG00280.hp2 HG00323.hp2 HG00544.hp2 others(84): Show |
intron_variant | MODIFIER | c.508-5245A>G | LMAN2L | ENSG00000114988.12 | transcript | ENST00000264963.9 | protein_coding | 4/7 | chr2 | 96717270 | ||||||
chr2:96717526
|
T | G | 5 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0114others(2): Show | 13 | HG00099.hp1 HG00280.hp1 HG00733.hp2 others(10): Show |
intron_variant | MODIFIER | c.508-5501A>C | LMAN2L | ENSG00000114988.12 | transcript | ENST00000264963.9 | protein_coding | 4/7 | chr2 | 96717526 | ||||||
chr2:96717533
|
G | GA | 27 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0013others(24): Show | 36 | HG01070.hp2 HG01071.hp1 HG01099.hp1 others(33): Show |
intron_variant | MODIFIER | c.508-5509dupT | LMAN2L | ENSG00000114988.12 | transcript | ENST00000264963.9 | protein_coding | 4/7 | chr2 | 96717533 | ||||||
chr2:96717533
|
GA | G | 40 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0014others(37): Show | 66 | HG00609.hp1 HG00642.hp2 HG01261.hp2 others(63): Show |
intron_variant | MODIFIER | c.508-5509delT | LMAN2L | ENSG00000114988.12 | transcript | ENST00000264963.9 | protein_coding | 4/7 | chr2 | 96717533 | ||||||
chr2:96717533
|
GAA | G | 20 | a0001c0001t0001g0002a0001c0001t0001g0012a0001c0001t0001g0028others(17): Show | 51 | HG00280.hp2 HG00323.hp2 HG00544.hp2 others(48): Show |
intron_variant | MODIFIER | c.508-5510_508-5509d others(4): Show |
LMAN2L | ENSG00000114988.12 | transcript | ENST00000264963.9 | protein_coding | 4/7 | chr2 | 96717533 | ||||||
chr2:96717805
|
C | T | 1 | a0001c0001t0001g0080 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.508-5780G>A | LMAN2L | ENSG00000114988.12 | transcript | ENST00000264963.9 | protein_coding | 4/7 | chr2 | 96717805 | ||||||
chr2:96717835
|
G | A | 2 | a0001c0001t0001g0048a0001c0001t0001g0049 | 2 | HG01070.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.508-5810C>T | LMAN2L | ENSG00000114988.12 | transcript | ENST00000264963.9 | protein_coding | 4/7 | chr2 | 96717835 | ||||||
chr2:96717840
|
T | TAA | 22 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0013others(19): Show | 30 | HG01070.hp2 HG01071.hp1 HG01099.hp1 others(27): Show |
intron_variant | MODIFIER | c.508-5817_508-5816d others(4): Show |
LMAN2L | ENSG00000114988.12 | transcript | ENST00000264963.9 | protein_coding | 4/7 | chr2 | 96717840 | ||||||
chr2:96717949
|
A | G | 24 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0013others(21): Show | 32 | HG01070.hp2 HG01071.hp1 HG01099.hp1 others(29): Show |
intron_variant | MODIFIER | c.508-5924T>C | LMAN2L | ENSG00000114988.12 | transcript | ENST00000264963.9 | protein_coding | 4/7 | chr2 | 96717949 | ||||||
chr2:96718116
|
C | T | 4 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0018others(1): Show | 9 | HG00642.hp2 HG01884.hp1 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.508-6091G>A | LMAN2L | ENSG00000114988.12 | transcript | ENST00000264963.9 | protein_coding | 4/7 | chr2 | 96718116 | ||||||
chr2:96718594
|
G | A | 1 | a0001c0001t0001g0085 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.508-6569C>T | LMAN2L | ENSG00000114988.12 | transcript | ENST00000264963.9 | protein_coding | 4/7 | chr2 | 96718594 | ||||||
chr2:96718878
|
G | A | 1 | a0001c0001t0001g0121 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.508-6853C>T | LMAN2L | ENSG00000114988.12 | transcript | ENST00000264963.9 | protein_coding | 4/7 | chr2 | 96718878 | ||||||
chr2:96718940
|
C | T | 1 | a0001c0001t0001g0064 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.508-6915G>A | LMAN2L | ENSG00000114988.12 | transcript | ENST00000264963.9 | protein_coding | 4/7 | chr2 | 96718940 | ||||||
chr2:96718991
|
G | A | 24 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0013others(21): Show | 32 | HG01070.hp2 HG01071.hp1 HG01099.hp1 others(29): Show |
intron_variant | MODIFIER | c.508-6966C>T | LMAN2L | ENSG00000114988.12 | transcript | ENST00000264963.9 | protein_coding | 4/7 | chr2 | 96718991 | ||||||
chr2:96719333
|
G | A | 1 | a0001c0001t0001g0064 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.508-7308C>T | LMAN2L | ENSG00000114988.12 | transcript | ENST00000264963.9 | protein_coding | 4/7 | chr2 | 96719333 | ||||||
chr2:96719416
|
TAA | T | 43 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0012others(40): Show | 87 | HG00280.hp2 HG00323.hp2 HG00544.hp2 others(84): Show |
intron_variant | MODIFIER | c.508-7393_508-7392d others(4): Show |
LMAN2L | ENSG00000114988.12 | transcript | ENST00000264963.9 | protein_coding | 4/7 | chr2 | 96719416 | ||||||
chr2:96719584
|
CA | C | 3 | a0001c0001t0001g0003a0001c0001t0001g0065a0001c0001t0001g0072 | 11 | HG01884.hp2 HG02109.hp1 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.508-7560delT | LMAN2L | ENSG00000114988.12 | transcript | ENST00000264963.9 | protein_coding | 4/7 | chr2 | 96719584 | ||||||
chr2:96719848
|
T | C | 2 | a0001c0001t0001g0008a0001c0001t0001g0118 | 6 | HG00733.hp2 HG01099.hp2 HG01192.hp2 others(3): Show |
intron_variant | MODIFIER | c.508-7823A>G | LMAN2L | ENSG00000114988.12 | transcript | ENST00000264963.9 | protein_coding | 4/7 | chr2 | 96719848 | ||||||
chr2:96720272
|
C | T | 1 | a0001c0001t0001g0038 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.508-8247G>A | LMAN2L | ENSG00000114988.12 | transcript | ENST00000264963.9 | protein_coding | 4/7 | chr2 | 96720272 | ||||||
chr2:96720277
|
C | T | 1 | a0001c0001t0001g0079 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.508-8252G>A | LMAN2L | ENSG00000114988.12 | transcript | ENST00000264963.9 | protein_coding | 4/7 | chr2 | 96720277 | ||||||
chr2:96720503
|
G | C | 1 | a0001c0001t0001g0021 | 2 | NA18945.hp2 NA19064.hp2 |
intron_variant | MODIFIER | c.508-8478C>G | LMAN2L | ENSG00000114988.12 | transcript | ENST00000264963.9 | protein_coding | 4/7 | chr2 | 96720503 | ||||||
chr2:96720620
|
G | T | 1 | a0001c0001t0001g0143 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.508-8595C>A | LMAN2L | ENSG00000114988.12 | transcript | ENST00000264963.9 | protein_coding | 4/7 | chr2 | 96720620 | ||||||
chr2:96720712
|
G | A | 3 | a0001c0001t0001g0017a0001c0001t0001g0021a0001c0001t0001g0089 | 5 | HG00408.hp2 HG00609.hp2 HG02155.hp2 others(2): Show |
intron_variant | MODIFIER | c.508-8687C>T | LMAN2L | ENSG00000114988.12 | transcript | ENST00000264963.9 | protein_coding | 4/7 | chr2 | 96720712 | ||||||
chr2:96720737
|
G | A | 1 | a0001c0001t0001g0098 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.508-8712C>T | LMAN2L | ENSG00000114988.12 | transcript | ENST00000264963.9 | protein_coding | 4/7 | chr2 | 96720737 | ||||||
chr2:96720973
|
G | A | 3 | a0001c0001t0001g0003a0001c0001t0001g0065a0001c0001t0001g0072 | 11 | HG01884.hp2 HG02109.hp1 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.508-8948C>T | LMAN2L | ENSG00000114988.12 | transcript | ENST00000264963.9 | protein_coding | 4/7 | chr2 | 96720973 | ||||||
chr2:96721088
|
C | CA | 7 | a0001c0001t0001g0058a0001c0001t0001g0059a0001c0001t0001g0060others(4): Show | 7 | HG02109.hp2 HG02486.hp1 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.508-9064_508-9063i others(3): Show |
LMAN2L | ENSG00000114988.12 | transcript | ENST00000264963.9 | protein_coding | 4/7 | chr2 | 96721088 | ||||||
chr2:96721089
|
C | A | 106 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(103): Show | 186 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(183): Show |
intron_variant | MODIFIER | c.508-9064G>T | LMAN2L | ENSG00000114988.12 | transcript | ENST00000264963.9 | protein_coding | 4/7 | chr2 | 96721089 | ||||||
chr2:96721104
|
T | C | 1 | a0001c0001t0001g0059 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.508-9079A>G | LMAN2L | ENSG00000114988.12 | transcript | ENST00000264963.9 | protein_coding | 4/7 | chr2 | 96721104 | ||||||
chr2:96721326
|
CT | C | 63 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0012others(60): Show | 109 | HG00280.hp2 HG00323.hp2 HG00544.hp2 others(106): Show |
intron_variant | MODIFIER | c.508-9302delA | LMAN2L | ENSG00000114988.12 | transcript | ENST00000264963.9 | protein_coding | 4/7 | chr2 | 96721326 | ||||||
chr2:96721326
|
CTT | C | 2 | a0001c0001t0001g0003a0001c0001t0001g0065 | 10 | HG01884.hp2 HG02109.hp1 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.508-9303_508-9302d others(4): Show |
LMAN2L | ENSG00000114988.12 | transcript | ENST00000264963.9 | protein_coding | 4/7 | chr2 | 96721326 | ||||||
chr2:96721440
|
C | T | 1 | a0001c0001t0001g0081 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.508-9415G>A | LMAN2L | ENSG00000114988.12 | transcript | ENST00000264963.9 | protein_coding | 4/7 | chr2 | 96721440 | ||||||
chr2:96721552
|
C | T | 2 | a0001c0001t0001g0093a0001c0001t0001g0125 | 2 | HG00673.hp2 NA18956.hp2 |
intron_variant | MODIFIER | c.508-9527G>A | LMAN2L | ENSG00000114988.12 | transcript | ENST00000264963.9 | protein_coding | 4/7 | chr2 | 96721552 | ||||||
chr2:96721624
|
C | A | 2 | a0001c0001t0001g0115a0001c0001t0001g0116 | 2 | HG00323.hp1 HG01069.hp2 |
intron_variant | MODIFIER | c.508-9599G>T | LMAN2L | ENSG00000114988.12 | transcript | ENST00000264963.9 | protein_coding | 4/7 | chr2 | 96721624 | ||||||
chr2:96721994
|
G | A | 5 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0114others(2): Show | 13 | HG00099.hp1 HG00280.hp1 HG00733.hp2 others(10): Show |
intron_variant | MODIFIER | c.508-9969C>T | LMAN2L | ENSG00000114988.12 | transcript | ENST00000264963.9 | protein_coding | 4/7 | chr2 | 96721994 | ||||||
chr2:96722204
|
G | A | 1 | a0003c0004t0001g0144 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.508-10179C>T | LMAN2L | ENSG00000114988.12 | transcript | ENST00000264963.9 | protein_coding | 4/7 | chr2 | 96722204 | ||||||
chr2:96722258
|
G | A | 1 | a0001c0001t0001g0140 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.508-10233C>T | LMAN2L | ENSG00000114988.12 | transcript | ENST00000264963.9 | protein_coding | 4/7 | chr2 | 96722258 | ||||||
chr2:96722522
|
A | G | 1 | a0001c0001t0001g0135 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.508-10497T>C | LMAN2L | ENSG00000114988.12 | transcript | ENST00000264963.9 | protein_coding | 4/7 | chr2 | 96722522 | ||||||
chr2:96722528
|
C | T | 1 | a0001c0001t0001g0047 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.508-10503G>A | LMAN2L | ENSG00000114988.12 | transcript | ENST00000264963.9 | protein_coding | 4/7 | chr2 | 96722528 | ||||||
chr2:96723003
|
G | T | 2 | a0001c0001t0001g0035a0001c0001t0001g0037 | 2 | NA19054.hp1 NA19091.hp2 |
intron_variant | MODIFIER | c.507+10516C>A | LMAN2L | ENSG00000114988.12 | transcript | ENST00000264963.9 | protein_coding | 4/7 | chr2 | 96723003 | ||||||
chr2:96723090
|
T | A | 1 | a0001c0001t0001g0060 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.507+10429A>T | LMAN2L | ENSG00000114988.12 | transcript | ENST00000264963.9 | protein_coding | 4/7 | chr2 | 96723090 | ||||||
chr2:96723147
|
A | G | 36 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0010others(33): Show | 57 | HG00642.hp2 HG01070.hp2 HG01071.hp1 others(54): Show |
intron_variant | MODIFIER | c.507+10372T>C | LMAN2L | ENSG00000114988.12 | transcript | ENST00000264963.9 | protein_coding | 4/7 | chr2 | 96723147 | ||||||
chr2:96723196
|
A | G | 1 | a0001c0001t0001g0092 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.507+10323T>C | LMAN2L | ENSG00000114988.12 | transcript | ENST00000264963.9 | protein_coding | 4/7 | chr2 | 96723196 | ||||||
chr2:96723810
|
C | T | 1 | a0001c0001t0001g0046 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.507+9709G>A | LMAN2L | ENSG00000114988.12 | transcript | ENST00000264963.9 | protein_coding | 4/7 | chr2 | 96723810 | ||||||
chr2:96723816
|
C | T | 1 | a0001c0001t0001g0092 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.507+9703G>A | LMAN2L | ENSG00000114988.12 | transcript | ENST00000264963.9 | protein_coding | 4/7 | chr2 | 96723816 | ||||||
chr2:96723948
|
A | G | 4 | a0001c0001t0001g0058a0001c0001t0001g0059a0001c0001t0001g0061others(1): Show | 4 | HG02486.hp1 HG02615.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.507+9571T>C | LMAN2L | ENSG00000114988.12 | transcript | ENST00000264963.9 | protein_coding | 4/7 | chr2 | 96723948 | ||||||
chr2:96724008
|
A | G | 1 | a0001c0001t0001g0109 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.507+9511T>C | LMAN2L | ENSG00000114988.12 | transcript | ENST00000264963.9 | protein_coding | 4/7 | chr2 | 96724008 | ||||||
chr2:96724016
|
G | A | 1 | a0001c0001t0001g0025 | 2 | HG03453.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.507+9503C>T | LMAN2L | ENSG00000114988.12 | transcript | ENST00000264963.9 | protein_coding | 4/7 | chr2 | 96724016 | ||||||
chr2:96724047
|
C | A | 3 | a0001c0001t0001g0003a0001c0001t0001g0065a0001c0001t0001g0072 | 11 | HG01884.hp2 HG02109.hp1 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.507+9472G>T | LMAN2L | ENSG00000114988.12 | transcript | ENST00000264963.9 | protein_coding | 4/7 | chr2 | 96724047 | ||||||
chr2:96724054
|
G | A | 3 | a0001c0001t0001g0026a0001c0001t0001g0101a0001c0001t0001g0102 | 4 | NA18957.hp1 NA18972.hp1 NA18985.hp1 others(1): Show |
intron_variant | MODIFIER | c.507+9465C>T | LMAN2L | ENSG00000114988.12 | transcript | ENST00000264963.9 | protein_coding | 4/7 | chr2 | 96724054 | ||||||
chr2:96724130
|
T | C | 8 | a0001c0001t0001g0003a0001c0001t0001g0014a0001c0001t0001g0015others(5): Show | 21 | HG00642.hp2 HG01884.hp1 HG01884.hp2 others(18): Show |
intron_variant | MODIFIER | c.507+9389A>G | LMAN2L | ENSG00000114988.12 | transcript | ENST00000264963.9 | protein_coding | 4/7 | chr2 | 96724130 | ||||||
chr2:96724254
|
A | T | 1 | a0001c0001t0001g0134 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.507+9265T>A | LMAN2L | ENSG00000114988.12 | transcript | ENST00000264963.9 | protein_coding | 4/7 | chr2 | 96724254 | ||||||
chr2:96724321
|
C | T | 2 | a0001c0001t0001g0018a0001c0001t0001g0069 | 3 | HG00642.hp2 HG02965.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.507+9198G>A | LMAN2L | ENSG00000114988.12 | transcript | ENST00000264963.9 | protein_coding | 4/7 | chr2 | 96724321 | ||||||
chr2:96724452
|
T | C | 3 | a0001c0001t0001g0003a0001c0001t0001g0065a0001c0001t0001g0072 | 11 | HG01884.hp2 HG02109.hp1 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.507+9067A>G | LMAN2L | ENSG00000114988.12 | transcript | ENST00000264963.9 | protein_coding | 4/7 | chr2 | 96724452 | ||||||
chr2:96724569
|
G | A | 1 | a0001c0001t0001g0081 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.507+8950C>T | LMAN2L | ENSG00000114988.12 | transcript | ENST00000264963.9 | protein_coding | 4/7 | chr2 | 96724569 | ||||||
chr2:96724624
|
G | A | 3 | a0001c0001t0001g0062a0001c0001t0001g0064a0001c0001t0001g0070 | 3 | HG01891.hp2 HG02622.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.507+8895C>T | LMAN2L | ENSG00000114988.12 | transcript | ENST00000264963.9 | protein_coding | 4/7 | chr2 | 96724624 | ||||||
chr2:96724917
|
C | T | 1 | a0001c0001t0001g0073 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.507+8602G>A | LMAN2L | ENSG00000114988.12 | transcript | ENST00000264963.9 | protein_coding | 4/7 | chr2 | 96724917 | ||||||
chr2:96725017
|
G | A | 1 | a0001c0001t0001g0081 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.507+8502C>T | LMAN2L | ENSG00000114988.12 | transcript | ENST00000264963.9 | protein_coding | 4/7 | chr2 | 96725017 | ||||||
chr2:96725216
|
C | T | 20 | a0001c0001t0001g0002a0001c0001t0001g0012a0001c0001t0001g0028others(17): Show | 51 | HG00280.hp2 HG00323.hp2 HG00544.hp2 others(48): Show |
intron_variant | MODIFIER | c.507+8303G>A | LMAN2L | ENSG00000114988.12 | transcript | ENST00000264963.9 | protein_coding | 4/7 | chr2 | 96725216 | ||||||
chr2:96725444
|
C | CT | 7 | a0001c0001t0001g0019a0001c0001t0001g0033a0001c0001t0001g0078others(4): Show | 8 | HG00558.hp2 HG01175.hp2 NA18951.hp1 others(5): Show |
intron_variant | MODIFIER | c.507+8074dupA | LMAN2L | ENSG00000114988.12 | transcript | ENST00000264963.9 | protein_coding | 4/7 | chr2 | 96725444 | ||||||
chr2:96725514
|
C | A | 5 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0018others(2): Show | 10 | HG00642.hp2 HG01884.hp1 HG02809.hp2 others(7): Show |
intron_variant | MODIFIER | c.507+8005G>T | LMAN2L | ENSG00000114988.12 | transcript | ENST00000264963.9 | protein_coding | 4/7 | chr2 | 96725514 | ||||||
chr2:96726168
|
AAT | A | 4 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0018others(1): Show | 9 | HG00642.hp2 HG01884.hp1 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.507+7349_507+7350d others(4): Show |
LMAN2L | ENSG00000114988.12 | transcript | ENST00000264963.9 | protein_coding | 4/7 | chr2 | 96726168 | ||||||
chr2:96726256
|
T | C | 1 | a0001c0001t0001g0051 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.507+7263A>G | LMAN2L | ENSG00000114988.12 | transcript | ENST00000264963.9 | protein_coding | 4/7 | chr2 | 96726256 | ||||||
chr2:96726262
|
G | GTT | 3 | a0001c0001t0001g0006a0001c0001t0001g0090a0001c0001t0001g0126 | 7 | HG00639.hp2 HG00741.hp2 HG01169.hp2 others(4): Show |
intron_variant | MODIFIER | c.507+7255_507+7256d others(4): Show |
LMAN2L | ENSG00000114988.12 | transcript | ENST00000264963.9 | protein_coding | 4/7 | chr2 | 96726262 | ||||||
chr2:96726488
|
C | T | 3 | a0001c0001t0001g0003a0001c0001t0001g0065a0001c0001t0001g0072 | 11 | HG01884.hp2 HG02109.hp1 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.507+7031G>A | LMAN2L | ENSG00000114988.12 | transcript | ENST00000264963.9 | protein_coding | 4/7 | chr2 | 96726488 | ||||||
chr2:96726686
|
G | A | 35 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0010others(32): Show | 56 | HG00642.hp2 HG01070.hp2 HG01071.hp1 others(53): Show |
intron_variant | MODIFIER | c.507+6833C>T | LMAN2L | ENSG00000114988.12 | transcript | ENST00000264963.9 | protein_coding | 4/7 | chr2 | 96726686 | ||||||
chr2:96726957
|
G | A | 26 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0013others(23): Show | 34 | HG01070.hp2 HG01071.hp1 HG01099.hp1 others(31): Show |
intron_variant | MODIFIER | c.507+6562C>T | LMAN2L | ENSG00000114988.12 | transcript | ENST00000264963.9 | protein_coding | 4/7 | chr2 | 96726957 | ||||||
chr2:96726970
|
C | G | 89 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(86): Show | 154 | HG00280.hp2 HG00323.hp2 HG00544.hp2 others(151): Show |
intron_variant | MODIFIER | c.507+6549G>C | LMAN2L | ENSG00000114988.12 | transcript | ENST00000264963.9 | protein_coding | 4/7 | chr2 | 96726970 | ||||||
chr2:96727041
|
G | A | 35 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0012others(32): Show | 72 | HG00280.hp2 HG00323.hp2 HG00544.hp2 others(69): Show |
intron_variant | MODIFIER | c.507+6478C>T | LMAN2L | ENSG00000114988.12 | transcript | ENST00000264963.9 | protein_coding | 4/7 | chr2 | 96727041 | ||||||
chr2:96727131
|
C | CAT | 2 | a0001c0001t0001g0021a0001c0001t0001g0089 | 3 | HG00609.hp2 NA18945.hp2 NA19064.hp2 |
intron_variant | MODIFIER | c.507+6386_507+6387d others(4): Show |
LMAN2L | ENSG00000114988.12 | transcript | ENST00000264963.9 | protein_coding | 4/7 | chr2 | 96727131 | ||||||
chr2:96727133
|
T | C | 1 | a0001c0001t0001g0103 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.507+6386A>G | LMAN2L | ENSG00000114988.12 | transcript | ENST00000264963.9 | protein_coding | 4/7 | chr2 | 96727133 | ||||||
chr2:96727371
|
A | C | 35 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0010others(32): Show | 56 | HG00642.hp2 HG01070.hp2 HG01071.hp1 others(53): Show |
intron_variant | MODIFIER | c.507+6148T>G | LMAN2L | ENSG00000114988.12 | transcript | ENST00000264963.9 | protein_coding | 4/7 | chr2 | 96727371 | ||||||
chr2:96727468
|
C | T | 1 | a0001c0001t0001g0045 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.507+6051G>A | LMAN2L | ENSG00000114988.12 | transcript | ENST00000264963.9 | protein_coding | 4/7 | chr2 | 96727468 | ||||||
chr2:96727626
|
T | A | 1 | a0001c0001t0001g0051 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.507+5893A>T | LMAN2L | ENSG00000114988.12 | transcript | ENST00000264963.9 | protein_coding | 4/7 | chr2 | 96727626 | ||||||
chr2:96727775
|
C | G | 8 | a0001c0001t0001g0003a0001c0001t0001g0014a0001c0001t0001g0015others(5): Show | 21 | HG00642.hp2 HG01884.hp1 HG01884.hp2 others(18): Show |
intron_variant | MODIFIER | c.507+5744G>C | LMAN2L | ENSG00000114988.12 | transcript | ENST00000264963.9 | protein_coding | 4/7 | chr2 | 96727775 | ||||||
chr2:96727985
|
C | G | 2 | a0001c0001t0001g0123a0001c0001t0001g0124 | 2 | HG01891.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.507+5534G>C | LMAN2L | ENSG00000114988.12 | transcript | ENST00000264963.9 | protein_coding | 4/7 | chr2 | 96727985 | ||||||
chr2:96727999
|
A | T | 27 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0013others(24): Show | 35 | HG01070.hp2 HG01071.hp1 HG01099.hp1 others(32): Show |
intron_variant | MODIFIER | c.507+5520T>A | LMAN2L | ENSG00000114988.12 | transcript | ENST00000264963.9 | protein_coding | 4/7 | chr2 | 96727999 | ||||||
chr2:96728155
|
C | T | 2 | a0001c0001t0001g0028a0001c0001t0001g0132 | 3 | NA18957.hp2 NA18979.hp2 NA18999.hp2 |
intron_variant | MODIFIER | c.507+5364G>A | LMAN2L | ENSG00000114988.12 | transcript | ENST00000264963.9 | protein_coding | 4/7 | chr2 | 96728155 | ||||||
chr2:96728161
|
A | G | 1 | a0001c0001t0001g0107 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.507+5358T>C | LMAN2L | ENSG00000114988.12 | transcript | ENST00000264963.9 | protein_coding | 4/7 | chr2 | 96728161 | ||||||
chr2:96728214
|
G | A | 1 | a0002c0002t0001g0056 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.507+5305C>T | LMAN2L | ENSG00000114988.12 | transcript | ENST00000264963.9 | protein_coding | 4/7 | chr2 | 96728214 | ||||||
chr2:96728253
|
C | G | 1 | a0001c0001t0001g0076 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.507+5266G>C | LMAN2L | ENSG00000114988.12 | transcript | ENST00000264963.9 | protein_coding | 4/7 | chr2 | 96728253 | ||||||
chr2:96728316
|
G | A | 2 | a0001c0001t0001g0104a0001c0001t0001g0105 | 2 | HG02071.hp1 HG02165.hp1 |
intron_variant | MODIFIER | c.507+5203C>T | LMAN2L | ENSG00000114988.12 | transcript | ENST00000264963.9 | protein_coding | 4/7 | chr2 | 96728316 | ||||||
chr2:96728358
|
C | T | 1 | a0001c0001t0001g0119 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.507+5161G>A | LMAN2L | ENSG00000114988.12 | transcript | ENST00000264963.9 | protein_coding | 4/7 | chr2 | 96728358 | ||||||
chr2:96728505
|
C | CA | 42 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0012others(39): Show | 86 | HG00280.hp2 HG00323.hp2 HG00544.hp2 others(83): Show |
intron_variant | MODIFIER | c.507+5013dupT | LMAN2L | ENSG00000114988.12 | transcript | ENST00000264963.9 | protein_coding | 4/7 | chr2 | 96728505 | ||||||
chr2:96728505
|
C | CAA | 27 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0013others(24): Show | 35 | HG01070.hp2 HG01071.hp1 HG01099.hp1 others(32): Show |
intron_variant | MODIFIER | c.507+5012_507+5013d others(4): Show |
LMAN2L | ENSG00000114988.12 | transcript | ENST00000264963.9 | protein_coding | 4/7 | chr2 | 96728505 | ||||||
chr2:96728505
|
CA | C | 6 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0018others(3): Show | 11 | HG00642.hp2 HG01884.hp1 HG02735.hp1 others(8): Show |
intron_variant | MODIFIER | c.507+5013delT | LMAN2L | ENSG00000114988.12 | transcript | ENST00000264963.9 | protein_coding | 4/7 | chr2 | 96728505 | ||||||
chr2:96728609
|
G | A | 1 | a0001c0001t0001g0141 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.507+4910C>T | LMAN2L | ENSG00000114988.12 | transcript | ENST00000264963.9 | protein_coding | 4/7 | chr2 | 96728609 | ||||||
chr2:96728658
|
C | T | 1 | a0001c0001t0001g0050 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.507+4861G>A | LMAN2L | ENSG00000114988.12 | transcript | ENST00000264963.9 | protein_coding | 4/7 | chr2 | 96728658 | ||||||
chr2:96728668
|
C | G | 1 | a0001c0001t0005g0057 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.507+4851G>C | LMAN2L | ENSG00000114988.12 | transcript | ENST00000264963.9 | protein_coding | 4/7 | chr2 | 96728668 | ||||||
chr2:96728669
|
G | C | 35 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0010others(32): Show | 56 | HG00642.hp2 HG01070.hp2 HG01071.hp1 others(53): Show |
intron_variant | MODIFIER | c.507+4850C>G | LMAN2L | ENSG00000114988.12 | transcript | ENST00000264963.9 | protein_coding | 4/7 | chr2 | 96728669 | ||||||
chr2:96728737
|
G | C | 2 | a0001c0001t0001g0073a0001c0001t0004g0074 | 2 | HG02145.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.507+4782C>G | LMAN2L | ENSG00000114988.12 | transcript | ENST00000264963.9 | protein_coding | 4/7 | chr2 | 96728737 | ||||||
chr2:96728797
|
A | G | 1 | a0001c0001t0001g0051 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.507+4722T>C | LMAN2L | ENSG00000114988.12 | transcript | ENST00000264963.9 | protein_coding | 4/7 | chr2 | 96728797 | ||||||
chr2:96728875
|
A | C | 1 | a0001c0001t0001g0071 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.507+4644T>G | LMAN2L | ENSG00000114988.12 | transcript | ENST00000264963.9 | protein_coding | 4/7 | chr2 | 96728875 | ||||||
chr2:96729018
|
A | G | 1 | a0001c0001t0001g0020 | 2 | HG01192.hp1 HG01256.hp1 |
intron_variant | MODIFIER | c.507+4501T>C | LMAN2L | ENSG00000114988.12 | transcript | ENST00000264963.9 | protein_coding | 4/7 | chr2 | 96729018 | ||||||
chr2:96729199
|
A | T | 5 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0018others(2): Show | 10 | HG00642.hp2 HG01884.hp1 HG02809.hp2 others(7): Show |
intron_variant | MODIFIER | c.507+4320T>A | LMAN2L | ENSG00000114988.12 | transcript | ENST00000264963.9 | protein_coding | 4/7 | chr2 | 96729199 | ||||||
chr2:96729430
|
C | T | 5 | a0001c0001t0002g0004a0001c0001t0002g0029a0001c0001t0002g0030others(2): Show | 12 | HG01261.hp2 HG01358.hp1 HG02258.hp2 others(9): Show |
intron_variant | MODIFIER | c.507+4089G>A | LMAN2L | ENSG00000114988.12 | transcript | ENST00000264963.9 | protein_coding | 4/7 | chr2 | 96729430 | ||||||
chr2:96729548
|
G | A | 1 | a0001c0001t0001g0051 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.507+3971C>T | LMAN2L | ENSG00000114988.12 | transcript | ENST00000264963.9 | protein_coding | 4/7 | chr2 | 96729548 | ||||||
chr2:96729653
|
C | T | 1 | a0001c0001t0001g0052 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.507+3866G>A | LMAN2L | ENSG00000114988.12 | transcript | ENST00000264963.9 | protein_coding | 4/7 | chr2 | 96729653 | ||||||
chr2:96729675
|
A | AT | 27 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0013others(24): Show | 35 | HG01070.hp2 HG01071.hp1 HG01099.hp1 others(32): Show |
intron_variant | MODIFIER | c.507+3843dupA | LMAN2L | ENSG00000114988.12 | transcript | ENST00000264963.9 | protein_coding | 4/7 | chr2 | 96729675 | ||||||
chr2:96729709
|
T | C | 1 | a0001c0001t0001g0050 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.507+3810A>G | LMAN2L | ENSG00000114988.12 | transcript | ENST00000264963.9 | protein_coding | 4/7 | chr2 | 96729709 | ||||||
chr2:96729797
|
C | T | 1 | a0001c0001t0001g0076 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.507+3722G>A | LMAN2L | ENSG00000114988.12 | transcript | ENST00000264963.9 | protein_coding | 4/7 | chr2 | 96729797 | ||||||
chr2:96730222
|
T | TAAAACTC others(326): Show |
1 | a0001c0001t0002g0031 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.507+3296_507+3297i others(335): Show |
LMAN2L | ENSG00000114988.12 | transcript | ENST00000264963.9 | protein_coding | 4/7 | chr2 | 96730222 | ||||||
chr2:96730230
|
T | C | 3 | a0001c0001t0001g0003a0001c0001t0001g0065a0001c0001t0001g0072 | 11 | HG01884.hp2 HG02109.hp1 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.507+3289A>G | LMAN2L | ENSG00000114988.12 | transcript | ENST00000264963.9 | protein_coding | 4/7 | chr2 | 96730230 | ||||||
chr2:96730317
|
T | C | 2 | a0001c0001t0001g0043a0001c0001t0001g0044 | 2 | HG02809.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.507+3202A>G | LMAN2L | ENSG00000114988.12 | transcript | ENST00000264963.9 | protein_coding | 4/7 | chr2 | 96730317 | ||||||
chr2:96730666
|
T | C | 89 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(86): Show | 154 | HG00280.hp2 HG00323.hp2 HG00544.hp2 others(151): Show |
intron_variant | MODIFIER | c.507+2853A>G | LMAN2L | ENSG00000114988.12 | transcript | ENST00000264963.9 | protein_coding | 4/7 | chr2 | 96730666 | ||||||
chr2:96730671
|
C | CCTCT | 35 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0010others(32): Show | 56 | HG00642.hp2 HG01070.hp2 HG01071.hp1 others(53): Show |
intron_variant | MODIFIER | c.507+2844_507+2847d others(6): Show |
LMAN2L | ENSG00000114988.12 | transcript | ENST00000264963.9 | protein_coding | 4/7 | chr2 | 96730671 | ||||||
chr2:96730752
|
G | C | 1 | a0003c0004t0001g0144 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.507+2767C>G | LMAN2L | ENSG00000114988.12 | transcript | ENST00000264963.9 | protein_coding | 4/7 | chr2 | 96730752 | ||||||
chr2:96730895
|
G | A | 1 | a0001c0001t0001g0045 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.507+2624C>T | LMAN2L | ENSG00000114988.12 | transcript | ENST00000264963.9 | protein_coding | 4/7 | chr2 | 96730895 | ||||||
chr2:96730968
|
C | T | 5 | a0001c0001t0001g0066a0001c0001t0001g0067a0001c0001t0001g0071others(2): Show | 5 | HG02145.hp2 HG02630.hp1 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.507+2551G>A | LMAN2L | ENSG00000114988.12 | transcript | ENST00000264963.9 | protein_coding | 4/7 | chr2 | 96730968 | ||||||
chr2:96731030
|
G | A | 1 | a0001c0001t0001g0106 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.507+2489C>T | LMAN2L | ENSG00000114988.12 | transcript | ENST00000264963.9 | protein_coding | 4/7 | chr2 | 96731030 | ||||||
chr2:96731158
|
T | A | 8 | a0001c0001t0001g0003a0001c0001t0001g0014a0001c0001t0001g0015others(5): Show | 21 | HG00642.hp2 HG01884.hp1 HG01884.hp2 others(18): Show |
intron_variant | MODIFIER | c.507+2361A>T | LMAN2L | ENSG00000114988.12 | transcript | ENST00000264963.9 | protein_coding | 4/7 | chr2 | 96731158 | ||||||
chr2:96731312
|
C | T | 3 | a0001c0001t0001g0062a0001c0001t0001g0064a0001c0001t0001g0070 | 3 | HG01891.hp2 HG02622.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.507+2207G>A | LMAN2L | ENSG00000114988.12 | transcript | ENST00000264963.9 | protein_coding | 4/7 | chr2 | 96731312 | ||||||
chr2:96731367
|
C | A | 1 | a0001c0001t0001g0107 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.507+2152G>T | LMAN2L | ENSG00000114988.12 | transcript | ENST00000264963.9 | protein_coding | 4/7 | chr2 | 96731367 | ||||||
chr2:96731532
|
G | C | 1 | a0001c0001t0001g0108 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.507+1987C>G | LMAN2L | ENSG00000114988.12 | transcript | ENST00000264963.9 | protein_coding | 4/7 | chr2 | 96731532 | ||||||
chr2:96731553
|
G | A | 1 | a0001c0001t0001g0109 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.507+1966C>T | LMAN2L | ENSG00000114988.12 | transcript | ENST00000264963.9 | protein_coding | 4/7 | chr2 | 96731553 | ||||||
chr2:96731808
|
G | A | 1 | a0001c0001t0001g0085 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.507+1711C>T | LMAN2L | ENSG00000114988.12 | transcript | ENST00000264963.9 | protein_coding | 4/7 | chr2 | 96731808 | ||||||
chr2:96731911
|
G | A | 1 | a0001c0001t0001g0142 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.507+1608C>T | LMAN2L | ENSG00000114988.12 | transcript | ENST00000264963.9 | protein_coding | 4/7 | chr2 | 96731911 | ||||||
chr2:96732252
|
G | GTAT | 35 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0010others(32): Show | 56 | HG00642.hp2 HG01070.hp2 HG01071.hp1 others(53): Show |
intron_variant | MODIFIER | c.507+1266_507+1267i others(5): Show |
LMAN2L | ENSG00000114988.12 | transcript | ENST00000264963.9 | protein_coding | 4/7 | chr2 | 96732252 | ||||||
chr2:96732351
|
A | G | 1 | a0001c0001t0001g0071 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.507+1168T>C | LMAN2L | ENSG00000114988.12 | transcript | ENST00000264963.9 | protein_coding | 4/7 | chr2 | 96732351 | ||||||
chr2:96732367
|
C | T | 2 | a0001c0001t0001g0123a0001c0001t0001g0124 | 2 | HG01891.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.507+1152G>A | LMAN2L | ENSG00000114988.12 | transcript | ENST00000264963.9 | protein_coding | 4/7 | chr2 | 96732367 | ||||||
chr2:96732631
|
G | C | 2 | a0001c0001t0001g0123a0001c0001t0001g0124 | 2 | HG01891.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.507+888C>G | LMAN2L | ENSG00000114988.12 | transcript | ENST00000264963.9 | protein_coding | 4/7 | chr2 | 96732631 | ||||||
chr2:96732791
|
C | CT | 12 | a0001c0001t0001g0027a0001c0001t0001g0050a0001c0001t0001g0051others(9): Show | 13 | HG01243.hp1 HG01891.hp1 HG01891.hp2 others(10): Show |
intron_variant | MODIFIER | c.507+727dupA | LMAN2L | ENSG00000114988.12 | transcript | ENST00000264963.9 | protein_coding | 4/7 | chr2 | 96732791 | ||||||
chr2:96732791
|
C | CTT | 23 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0013others(20): Show | 31 | HG01070.hp2 HG01071.hp1 HG01099.hp1 others(28): Show |
intron_variant | MODIFIER | c.507+726_507+727dup others(2): Show |
LMAN2L | ENSG00000114988.12 | transcript | ENST00000264963.9 | protein_coding | 4/7 | chr2 | 96732791 | ||||||
chr2:96733000
|
C | T | 5 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0018others(2): Show | 10 | HG00642.hp2 HG01884.hp1 HG02809.hp2 others(7): Show |
intron_variant | MODIFIER | c.507+519G>A | LMAN2L | ENSG00000114988.12 | transcript | ENST00000264963.9 | protein_coding | 4/7 | chr2 | 96733000 | ||||||
chr2:96733020
|
C | T | 27 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0013others(24): Show | 35 | HG01070.hp2 HG01071.hp1 HG01099.hp1 others(32): Show |
intron_variant | MODIFIER | c.507+499G>A | LMAN2L | ENSG00000114988.12 | transcript | ENST00000264963.9 | protein_coding | 4/7 | chr2 | 96733020 | ||||||
chr2:96733267
|
C | G | 1 | a0001c0001t0001g0036 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.507+252G>C | LMAN2L | ENSG00000114988.12 | transcript | ENST00000264963.9 | protein_coding | 4/7 | chr2 | 96733267 | ||||||
chr2:96733312
|
C | G | 1 | a0001c0001t0001g0035 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.507+207G>C | LMAN2L | ENSG00000114988.12 | transcript | ENST00000264963.9 | protein_coding | 4/7 | chr2 | 96733312 | ||||||
chr2:96733359
|
C | T | 27 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0013others(24): Show | 35 | HG01070.hp2 HG01071.hp1 HG01099.hp1 others(32): Show |
intron_variant | MODIFIER | c.507+160G>A | LMAN2L | ENSG00000114988.12 | transcript | ENST00000264963.9 | protein_coding | 4/7 | chr2 | 96733359 | ||||||
chr2:96733363
|
T | C | 27 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0013others(24): Show | 35 | HG01070.hp2 HG01071.hp1 HG01099.hp1 others(32): Show |
intron_variant | MODIFIER | c.507+156A>G | LMAN2L | ENSG00000114988.12 | transcript | ENST00000264963.9 | protein_coding | 4/7 | chr2 | 96733363 | ||||||
chr2:96733711
|
T | C | 1 | a0001c0001t0001g0051 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.425-110A>G | LMAN2L | ENSG00000114988.12 | transcript | ENST00000264963.9 | protein_coding | 3/7 | chr2 | 96733711 | ||||||
chr2:96733842
|
T | G | 5 | a0001c0001t0002g0004a0001c0001t0002g0029a0001c0001t0002g0030others(2): Show | 12 | HG01261.hp2 HG01358.hp1 HG02258.hp2 others(9): Show |
intron_variant | MODIFIER | c.425-241A>C | LMAN2L | ENSG00000114988.12 | transcript | ENST00000264963.9 | protein_coding | 3/7 | chr2 | 96733842 | ||||||
chr2:96733848
|
A | T | 2 | a0001c0001t0001g0086a0001c0001t0001g0112 | 2 | NA18966.hp2 NA18983.hp2 |
intron_variant | MODIFIER | c.425-247T>A | LMAN2L | ENSG00000114988.12 | transcript | ENST00000264963.9 | protein_coding | 3/7 | chr2 | 96733848 | ||||||
chr2:96734224
|
A | T | 1 | a0001c0001t0001g0014 | 3 | HG02809.hp2 HG03098.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.424+185T>A | LMAN2L | ENSG00000114988.12 | transcript | ENST00000264963.9 | protein_coding | 3/7 | chr2 | 96734224 | ||||||
chr2:96734353
|
G | A | 1 | a0001c0001t0001g0085 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.424+56C>T | LMAN2L | ENSG00000114988.12 | transcript | ENST00000264963.9 | protein_coding | 3/7 | chr2 | 96734353 | ||||||
chr2:96734587
|
A | G | 90 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(87): Show | 155 | HG00280.hp2 HG00323.hp2 HG00544.hp2 others(152): Show |
intron_variant | MODIFIER | c.307-61T>C | LMAN2L | ENSG00000114988.12 | transcript | ENST00000264963.9 | protein_coding | 2/7 | chr2 | 96734587 | ||||||
chr2:96734683
|
A | C | 1 | a0001c0001t0001g0017 | 2 | HG00408.hp2 HG02155.hp2 |
intron_variant | MODIFIER | c.307-157T>G | LMAN2L | ENSG00000114988.12 | transcript | ENST00000264963.9 | protein_coding | 2/7 | chr2 | 96734683 | ||||||
chr2:96734856
|
C | T | 1 | a0001c0001t0001g0114 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.307-330G>A | LMAN2L | ENSG00000114988.12 | transcript | ENST00000264963.9 | protein_coding | 2/7 | chr2 | 96734856 | ||||||
chr2:96735001
|
T | G | 1 | a0001c0001t0001g0110 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.307-475A>C | LMAN2L | ENSG00000114988.12 | transcript | ENST00000264963.9 | protein_coding | 2/7 | chr2 | 96735001 | ||||||
chr2:96735016
|
GAAT | G | 27 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0013others(24): Show | 35 | HG01070.hp2 HG01071.hp1 HG01099.hp1 others(32): Show |
intron_variant | MODIFIER | c.307-493_307-491del others(3): Show |
LMAN2L | ENSG00000114988.12 | transcript | ENST00000264963.9 | protein_coding | 2/7 | chr2 | 96735016 | ||||||
chr2:96735060
|
G | A | 2 | a0001c0001t0001g0011a0001c0001t0001g0111 | 5 | HG03225.hp1 NA18522.hp1 NA19240.hp1 others(2): Show |
intron_variant | MODIFIER | c.307-534C>T | LMAN2L | ENSG00000114988.12 | transcript | ENST00000264963.9 | protein_coding | 2/7 | chr2 | 96735060 | ||||||
chr2:96735565
|
G | A | 1 | a0001c0001t0001g0112 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.307-1039C>T | LMAN2L | ENSG00000114988.12 | transcript | ENST00000264963.9 | protein_coding | 2/7 | chr2 | 96735565 | ||||||
chr2:96735635
|
G | A | 2 | a0001c0001t0001g0027a0001c0001t0001g0113 | 3 | HG02145.hp1 HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.307-1109C>T | LMAN2L | ENSG00000114988.12 | transcript | ENST00000264963.9 | protein_coding | 2/7 | chr2 | 96735635 | ||||||
chr2:96735937
|
A | G | 27 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0013others(24): Show | 35 | HG01070.hp2 HG01071.hp1 HG01099.hp1 others(32): Show |
intron_variant | MODIFIER | c.307-1411T>C | LMAN2L | ENSG00000114988.12 | transcript | ENST00000264963.9 | protein_coding | 2/7 | chr2 | 96735937 | ||||||
chr2:96735978
|
C | T | 1 | a0001c0001t0001g0130 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.307-1452G>A | LMAN2L | ENSG00000114988.12 | transcript | ENST00000264963.9 | protein_coding | 2/7 | chr2 | 96735978 | ||||||
chr2:96735990
|
C | T | 1 | a0003c0004t0001g0144 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.307-1464G>A | LMAN2L | ENSG00000114988.12 | transcript | ENST00000264963.9 | protein_coding | 2/7 | chr2 | 96735990 | ||||||
chr2:96736327
|
T | C | 7 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0114others(4): Show | 15 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(12): Show |
intron_variant | MODIFIER | c.306+1622A>G | LMAN2L | ENSG00000114988.12 | transcript | ENST00000264963.9 | protein_coding | 2/7 | chr2 | 96736327 | ||||||
chr2:96736473
|
G | C | 6 | a0001c0001t0001g0010a0001c0001t0001g0034a0001c0001t0001g0046others(3): Show | 9 | HG01070.hp2 HG01071.hp1 HG01099.hp1 others(6): Show |
intron_variant | MODIFIER | c.306+1476C>G | LMAN2L | ENSG00000114988.12 | transcript | ENST00000264963.9 | protein_coding | 2/7 | chr2 | 96736473 | ||||||
chr2:96736584
|
T | C | 7 | a0001c0001t0001g0058a0001c0001t0001g0059a0001c0001t0001g0060others(4): Show | 7 | HG02109.hp2 HG02486.hp1 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.306+1365A>G | LMAN2L | ENSG00000114988.12 | transcript | ENST00000264963.9 | protein_coding | 2/7 | chr2 | 96736584 | ||||||
chr2:96736816
|
C | T | 2 | a0001c0001t0001g0066a0001c0001t0001g0067 | 2 | HG02630.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.306+1133G>A | LMAN2L | ENSG00000114988.12 | transcript | ENST00000264963.9 | protein_coding | 2/7 | chr2 | 96736816 | ||||||
chr2:96736831
|
G | A | 1 | a0001c0001t0001g0050 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.306+1118C>T | LMAN2L | ENSG00000114988.12 | transcript | ENST00000264963.9 | protein_coding | 2/7 | chr2 | 96736831 | ||||||
chr2:96736902
|
T | C | 2 | a0001c0001t0001g0119a0001c0001t0001g0120 | 2 | HG02109.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.306+1047A>G | LMAN2L | ENSG00000114988.12 | transcript | ENST00000264963.9 | protein_coding | 2/7 | chr2 | 96736902 | ||||||
chr2:96737279
|
A | G | 1 | a0001c0001t0001g0065 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.306+670T>C | LMAN2L | ENSG00000114988.12 | transcript | ENST00000264963.9 | protein_coding | 2/7 | chr2 | 96737279 | ||||||
chr2:96737298
|
G | C | 1 | a0001c0003t0002g0032 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.306+651C>G | LMAN2L | ENSG00000114988.12 | transcript | ENST00000264963.9 | protein_coding | 2/7 | chr2 | 96737298 | ||||||
chr2:96737373
|
G | A | 20 | a0001c0001t0001g0002a0001c0001t0001g0012a0001c0001t0001g0028others(17): Show | 51 | HG00280.hp2 HG00323.hp2 HG00544.hp2 others(48): Show |
intron_variant | MODIFIER | c.306+576C>T | LMAN2L | ENSG00000114988.12 | transcript | ENST00000264963.9 | protein_coding | 2/7 | chr2 | 96737373 | ||||||
chr2:96737377
|
C | T | 1 | a0001c0001t0001g0064 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.306+572G>A | LMAN2L | ENSG00000114988.12 | transcript | ENST00000264963.9 | protein_coding | 2/7 | chr2 | 96737377 | ||||||
chr2:96737378
|
G | A | 1 | a0001c0001t0001g0051 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.306+571C>T | LMAN2L | ENSG00000114988.12 | transcript | ENST00000264963.9 | protein_coding | 2/7 | chr2 | 96737378 | ||||||
chr2:96737384
|
T | C | 1 | a0001c0001t0001g0061 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.306+565A>G | LMAN2L | ENSG00000114988.12 | transcript | ENST00000264963.9 | protein_coding | 2/7 | chr2 | 96737384 | ||||||
chr2:96737467
|
T | C | 1 | a0001c0001t0001g0121 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.306+482A>G | LMAN2L | ENSG00000114988.12 | transcript | ENST00000264963.9 | protein_coding | 2/7 | chr2 | 96737467 | ||||||
chr2:96737486
|
C | CA | 26 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0013others(23): Show | 34 | HG01070.hp2 HG01071.hp1 HG01099.hp1 others(31): Show |
intron_variant | MODIFIER | c.306+462dupT | LMAN2L | ENSG00000114988.12 | transcript | ENST00000264963.9 | protein_coding | 2/7 | chr2 | 96737486 | ||||||
chr2:96737729
|
A | G | 1 | a0001c0001t0001g0129 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.306+220T>C | LMAN2L | ENSG00000114988.12 | transcript | ENST00000264963.9 | protein_coding | 2/7 | chr2 | 96737729 | ||||||
chr2:96737872
|
A | C | 1 | a0001c0001t0001g0063 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.306+77T>G | LMAN2L | ENSG00000114988.12 | transcript | ENST00000264963.9 | protein_coding | 2/7 | chr2 | 96737872 | ||||||
chr2:96738147
|
C | T | 1 | a0001c0001t0001g0128 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.188-80G>A | LMAN2L | ENSG00000114988.12 | transcript | ENST00000264963.9 | protein_coding | 1/7 | chr2 | 96738147 | ||||||
chr2:96738323
|
G | A | 1 | a0001c0001t0001g0143 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.188-256C>T | LMAN2L | ENSG00000114988.12 | transcript | ENST00000264963.9 | protein_coding | 1/7 | chr2 | 96738323 | ||||||
chr2:96738535
|
G | A | 1 | a0001c0001t0001g0122 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.188-468C>T | LMAN2L | ENSG00000114988.12 | transcript | ENST00000264963.9 | protein_coding | 1/7 | chr2 | 96738535 | ||||||
chr2:96738560
|
T | C | 2 | a0001c0001t0001g0123a0001c0001t0001g0124 | 2 | HG01891.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.188-493A>G | LMAN2L | ENSG00000114988.12 | transcript | ENST00000264963.9 | protein_coding | 1/7 | chr2 | 96738560 | ||||||
chr2:96738595
|
G | A | 1 | a0001c0001t0001g0013 | 3 | HG02717.hp2 HG02976.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.188-528C>T | LMAN2L | ENSG00000114988.12 | transcript | ENST00000264963.9 | protein_coding | 1/7 | chr2 | 96738595 | ||||||
chr2:96738721
|
C | T | 1 | a0001c0001t0001g0062 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.188-654G>A | LMAN2L | ENSG00000114988.12 | transcript | ENST00000264963.9 | protein_coding | 1/7 | chr2 | 96738721 | ||||||
chr2:96738769
|
CT | C | 5 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0001t0001g0054others(2): Show | 5 | HG02155.hp1 NA18962.hp1 NA18981.hp1 others(2): Show |
intron_variant | MODIFIER | c.188-703delA | LMAN2L | ENSG00000114988.12 | transcript | ENST00000264963.9 | protein_coding | 1/7 | chr2 | 96738769 | ||||||
chr2:96739001
|
A | G | 5 | a0001c0001t0001g0058a0001c0001t0001g0059a0001c0001t0001g0060others(2): Show | 5 | HG02486.hp1 HG02615.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.187+853T>C | LMAN2L | ENSG00000114988.12 | transcript | ENST00000264963.9 | protein_coding | 1/7 | chr2 | 96739001 | ||||||
chr2:96739179
|
C | T | 1 | a0001c0001t0001g0127 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.187+675G>A | LMAN2L | ENSG00000114988.12 | transcript | ENST00000264963.9 | protein_coding | 1/7 | chr2 | 96739179 | ||||||
chr2:96739196
|
G | A | 1 | a0001c0001t0001g0125 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.187+658C>T | LMAN2L | ENSG00000114988.12 | transcript | ENST00000264963.9 | protein_coding | 1/7 | chr2 | 96739196 | ||||||
chr2:96739390
|
C | T | 27 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0013others(24): Show | 35 | HG01070.hp2 HG01071.hp1 HG01099.hp1 others(32): Show |
intron_variant | MODIFIER | c.187+464G>A | LMAN2L | ENSG00000114988.12 | transcript | ENST00000264963.9 | protein_coding | 1/7 | chr2 | 96739390 | ||||||
chr2:96739570
|
T | C | 1 | a0001c0001t0001g0126 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.187+284A>G | LMAN2L | ENSG00000114988.12 | transcript | ENST00000264963.9 | protein_coding | 1/7 | chr2 | 96739570 | ||||||
chr2:96739703
|
G | A | 20 | a0001c0001t0001g0002a0001c0001t0001g0012a0001c0001t0001g0028others(17): Show | 51 | HG00280.hp2 HG00323.hp2 HG00544.hp2 others(48): Show |
intron_variant | MODIFIER | c.187+151C>T | LMAN2L | ENSG00000114988.12 | transcript | ENST00000264963.9 | protein_coding | 1/7 | chr2 | 96739703 | ||||||
chr2:96739739
|
C | G | 1 | a0001c0001t0001g0033 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.187+115G>C | LMAN2L | ENSG00000114988.12 | transcript | ENST00000264963.9 | protein_coding | 1/7 | chr2 | 96739739 |