geneid | 51072 |
---|---|
ensemblid | ENSG00000162959.14 |
hgncid | 14014 |
symbol | MEMO1 |
name | mediator of cell motility 1 |
refseq_nuc | NM_001301833.4 |
refseq_prot | NP_001288762.1 |
ensembl_nuc | ENST00000404530.6 |
ensembl_prot | ENSP00000385557.1 |
mane_status | MANE Select |
chr | chr2 |
start | 31867823 |
end | 32011008 |
strand | - |
ver | v1.2 |
region | chr2:31867823-32011008 |
region5000 | chr2:31862823-32016008 |
regionname0 | MEMO1_chr2_31867823_32011008 |
regionname5000 | MEMO1_chr2_31862823_32016008 |
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 | 297 | 303 | 80 | 61 | 124 | 12 | 24 | 98 | MEMO1_chr2_31862823_32016008 | MEMO1 | copy fasta | chr2 | 31862823 | 32016008 |
a0002 | 0/0 | 297 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | copy fasta | chr2 | 31862823 | 32016008 |
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 | 894 | 303 | 80 | 61 | 124 | 12 | 24 | MEMO1_chr2_31862823_32016008 | MEMO1 | copy fasta | chr2 | 31862823 | 32016008 |
c0002 | 0/0 | 894 | 1 | 0 | 1 | 0 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | copy fasta | chr2 | 31862823 | 32016008 |
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 | 623 | 301 | 77 | 62 | 124 | 12 | 24 | MEMO1_chr2_31862823_32016008 | MEMO1 | copy fasta | chr2 | 31862823 | 32016008 |
t0002 | 0/0 | 623 | 3 | 3 | 0 | 0 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | copy fasta | chr2 | 31862823 | 32016008 |
ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
g0002 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
g0008 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
g0014 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
g0020 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
g0022 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
g0026 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
g0030 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
g0060 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
g0061 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
g0077 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
g0118 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
g0138 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
g0147 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
g0216 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
g0218 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
g0238 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
g0255 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
g0257 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
g0280 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
g0300 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
g0301 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
g0302 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
g0303 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
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 | 894 | 303 | 80 | 61 | 124 | 12 | 24 | MEMO1_chr2_31862823_32016008 | MEMO1 | copy fasta | chr2 | 31862823 | 32016008 |
a0002c0002 | 0/0 | 894 | 1 | 0 | 1 | 0 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | copy fasta | chr2 | 31862823 | 32016008 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 1/1 | 1516 | 300 | 77 | 61 | 124 | 12 | 24 | MEMO1_chr2_31862823_32016008 | MEMO1 | copy fasta | chr2 | 31862823 | 32016008 |
a0001c0001t0002 | 0/0 | 1516 | 3 | 3 | 0 | 0 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | copy fasta | chr2 | 31862823 | 32016008 |
a0002c0002t0001 | 0/0 | 1516 | 1 | 0 | 1 | 0 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | copy fasta | chr2 | 31862823 | 32016008 |
actghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
a0001c0001t0001g0002 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
a0001c0001t0001g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
a0001c0001t0001g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
a0001c0001t0001g0008 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
a0001c0001t0001g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
a0001c0001t0001g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
a0001c0001t0001g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
a0001c0001t0001g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
a0001c0001t0001g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
a0001c0001t0001g0014 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
a0001c0001t0001g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
a0001c0001t0001g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
a0001c0001t0001g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
a0001c0001t0001g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
a0001c0001t0001g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
a0001c0001t0001g0020 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
a0001c0001t0001g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
a0001c0001t0001g0022 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
a0001c0001t0001g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
a0001c0001t0001g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
a0001c0001t0001g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
a0001c0001t0001g0026 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
a0001c0001t0001g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
a0001c0001t0001g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
a0001c0001t0001g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
a0001c0001t0001g0030 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
a0001c0001t0001g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
a0001c0001t0001g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
a0001c0001t0001g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
a0001c0001t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
a0001c0001t0001g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
a0001c0001t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
a0001c0001t0001g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
a0001c0001t0001g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
a0001c0001t0001g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
a0001c0001t0001g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
a0001c0001t0001g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
a0001c0001t0001g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
a0001c0001t0001g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
a0001c0001t0001g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
a0001c0001t0001g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
a0001c0001t0001g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
a0001c0001t0001g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
a0001c0001t0001g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
a0001c0001t0001g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
a0001c0001t0001g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
a0001c0001t0001g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
a0001c0001t0001g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
a0001c0001t0001g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
a0001c0001t0001g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
a0001c0001t0001g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
a0001c0001t0001g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
a0001c0001t0001g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
a0001c0001t0001g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
a0001c0001t0001g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
a0001c0001t0001g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
a0001c0001t0001g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
a0001c0001t0001g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
a0001c0001t0001g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
a0001c0001t0001g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
a0001c0001t0001g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
a0001c0001t0001g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
a0001c0001t0001g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
a0001c0001t0001g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
a0001c0001t0001g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
a0001c0001t0001g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
a0001c0001t0001g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
a0001c0001t0001g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
a0001c0001t0001g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
a0001c0001t0001g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
a0001c0001t0001g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
a0001c0001t0001g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
a0001c0001t0001g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
a0001c0001t0001g0138 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
a0001c0001t0001g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
a0001c0001t0001g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
a0001c0001t0001g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
a0001c0001t0001g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
a0001c0001t0001g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
a0001c0001t0001g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
a0001c0001t0001g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
a0001c0001t0001g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
a0001c0001t0001g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
a0001c0001t0001g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
a0001c0001t0001g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
a0001c0001t0001g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
a0001c0001t0001g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
a0001c0001t0001g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
a0001c0001t0001g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
a0001c0001t0001g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
a0001c0001t0001g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
a0001c0001t0001g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
a0001c0001t0001g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
a0001c0001t0001g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
a0001c0001t0001g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
a0001c0001t0001g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
a0001c0001t0001g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
a0001c0001t0001g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
a0001c0001t0001g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
a0001c0001t0001g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
a0001c0001t0001g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
a0001c0001t0001g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
a0001c0001t0001g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
a0001c0001t0001g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
a0001c0001t0001g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
a0001c0001t0001g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
a0001c0001t0001g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
a0001c0001t0001g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
a0001c0001t0001g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
a0001c0001t0001g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
a0001c0001t0001g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
a0001c0001t0001g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
a0001c0001t0001g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
a0001c0001t0001g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
a0001c0001t0001g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
a0001c0001t0001g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
a0001c0001t0001g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
a0001c0001t0001g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
a0001c0001t0001g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
a0001c0001t0001g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
a0001c0001t0001g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
a0001c0001t0001g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
a0001c0001t0001g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
a0001c0001t0001g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
a0001c0001t0001g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
a0001c0001t0001g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
a0001c0001t0001g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
a0001c0001t0001g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
a0001c0001t0001g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
a0001c0001t0001g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
a0001c0001t0001g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
a0001c0001t0001g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
a0001c0001t0001g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
a0001c0001t0001g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
a0001c0001t0001g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
a0001c0001t0001g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
a0001c0001t0001g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
a0001c0001t0001g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
a0001c0001t0001g0257 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
a0001c0001t0001g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
a0001c0001t0001g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
a0001c0001t0001g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
a0001c0001t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
a0001c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
a0001c0001t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
a0001c0001t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
a0001c0001t0001g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
a0001c0001t0001g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
a0001c0001t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
a0001c0001t0001g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
a0001c0001t0001g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
a0001c0001t0001g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
a0001c0001t0001g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
a0001c0001t0001g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
a0001c0001t0001g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
a0001c0001t0001g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
a0001c0001t0001g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
a0001c0001t0001g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
a0001c0001t0001g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
a0001c0001t0001g0280 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
a0001c0001t0001g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
a0001c0001t0001g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
a0001c0001t0001g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
a0001c0001t0001g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
a0001c0001t0001g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
a0001c0001t0001g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
a0001c0001t0001g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
a0001c0001t0001g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
a0001c0001t0001g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
a0001c0001t0001g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
a0001c0001t0001g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
a0001c0001t0001g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
a0001c0001t0001g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
a0001c0001t0001g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
a0001c0001t0001g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
a0001c0001t0001g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
a0001c0001t0001g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
a0001c0001t0001g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
a0001c0001t0001g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
a0001c0001t0001g0300 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
a0001c0001t0001g0301 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
a0001c0001t0001g0302 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
a0001c0001t0001g0303 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
a0001c0001t0001g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
a0001c0001t0002g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
a0001c0001t0002g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
a0001c0001t0002g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
a0002c0002t0001g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0001 | g0014 | EUR | GBR | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
HG00099 | hp2 | a0001 | c0001 | t0001 | g0118 | EUR | GBR | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
HG00140 | hp1 | a0001 | c0001 | t0001 | g0077 | EUR | GBR | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
HG00140 | hp2 | a0001 | c0001 | t0001 | g0026 | EUR | GBR | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
HG00408 | hp1 | a0001 | c0001 | t0001 | g0230 | EAS | CHS | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
HG00408 | hp2 | a0001 | c0001 | t0001 | g0188 | EAS | CHS | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
HG00423 | hp1 | a0001 | c0001 | t0001 | g0168 | EAS | CHS | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
HG00423 | hp2 | a0001 | c0001 | t0001 | g0119 | EAS | CHS | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
HG00438 | hp1 | a0001 | c0001 | t0001 | g0109 | EAS | CHS | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
HG00438 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | CHS | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
HG00597 | hp1 | a0001 | c0001 | t0001 | g0021 | EAS | CHS | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
HG00597 | hp2 | a0001 | c0001 | t0001 | g0298 | EAS | CHS | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
HG00621 | hp1 | a0001 | c0001 | t0001 | g0066 | EAS | CHS | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
HG00621 | hp2 | a0001 | c0001 | t0001 | g0117 | EAS | CHS | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
HG00639 | hp1 | a0001 | c0001 | t0001 | g0153 | AMR | PUR | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
HG00639 | hp2 | a0001 | c0001 | t0001 | g0046 | AMR | PUR | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
HG00642 | hp1 | a0001 | c0001 | t0001 | g0143 | AMR | PUR | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
HG00642 | hp2 | a0001 | c0001 | t0001 | g0214 | AMR | PUR | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
HG00673 | hp1 | a0001 | c0001 | t0001 | g0042 | EAS | CHS | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
HG00673 | hp2 | a0001 | c0001 | t0001 | g0110 | EAS | CHS | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
HG00735 | hp1 | a0001 | c0001 | t0001 | g0088 | AMR | PUR | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
HG00735 | hp2 | a0001 | c0001 | t0001 | g0115 | AMR | PUR | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
HG00738 | hp1 | a0001 | c0001 | t0001 | g0058 | AMR | PUR | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
HG00738 | hp2 | a0001 | c0001 | t0001 | g0103 | AMR | PUR | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
HG00741 | hp1 | a0001 | c0001 | t0001 | g0033 | AMR | PUR | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
HG00741 | hp2 | a0001 | c0001 | t0001 | g0120 | AMR | PUR | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
HG01070 | hp1 | a0001 | c0001 | t0001 | g0217 | AMR | PUR | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
HG01070 | hp2 | a0001 | c0001 | t0001 | g0112 | AMR | PUR | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
HG01071 | hp1 | a0001 | c0001 | t0001 | g0106 | AMR | PUR | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
HG01071 | hp2 | a0001 | c0001 | t0001 | g0221 | AMR | PUR | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
HG01081 | hp1 | a0001 | c0001 | t0001 | g0180 | AMR | PUR | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
HG01081 | hp2 | a0001 | c0001 | t0001 | g0189 | AMR | PUR | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
HG01106 | hp1 | a0001 | c0001 | t0001 | g0215 | AMR | PUR | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
HG01106 | hp2 | a0001 | c0001 | t0001 | g0152 | AMR | PUR | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
HG01109 | hp1 | a0001 | c0001 | t0001 | g0076 | AMR | PUR | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
HG01109 | hp2 | a0001 | c0001 | t0001 | g0291 | AMR | PUR | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
HG01168 | hp1 | a0001 | c0001 | t0001 | g0258 | AMR | PUR | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
HG01168 | hp2 | a0002 | c0002 | t0001 | g0144 | AMR | PUR | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
HG01169 | hp1 | a0001 | c0001 | t0001 | g0113 | AMR | PUR | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
HG01169 | hp2 | a0001 | c0001 | t0001 | g0259 | AMR | PUR | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
HG01243 | hp1 | a0001 | c0001 | t0001 | g0150 | AMR | PUR | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
HG01243 | hp2 | a0001 | c0001 | t0001 | g0273 | AMR | PUR | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
HG01255 | hp1 | a0001 | c0001 | t0001 | g0135 | AMR | CLM | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
HG01255 | hp2 | a0001 | c0001 | t0001 | g0289 | AMR | CLM | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
HG01257 | hp1 | a0001 | c0001 | t0001 | g0145 | AMR | CLM | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
HG01257 | hp2 | a0001 | c0001 | t0001 | g0253 | AMR | CLM | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
HG01258 | hp1 | a0001 | c0001 | t0001 | g0256 | AMR | CLM | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
HG01258 | hp2 | a0001 | c0001 | t0001 | g0148 | AMR | CLM | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
HG01261 | hp1 | a0001 | c0001 | t0001 | g0166 | AMR | CLM | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
HG01261 | hp2 | a0001 | c0001 | t0001 | g0299 | AMR | CLM | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
HG01361 | hp1 | a0001 | c0001 | t0001 | g0232 | AMR | CLM | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
HG01361 | hp2 | a0001 | c0001 | t0001 | g0121 | AMR | CLM | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
HG01433 | hp1 | a0001 | c0001 | t0001 | g0032 | AMR | CLM | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
HG01433 | hp2 | a0001 | c0001 | t0001 | g0254 | AMR | CLM | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
HG01496 | hp1 | a0001 | c0001 | t0001 | g0102 | AMR | CLM | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
HG01496 | hp2 | a0001 | c0001 | t0001 | g0302 | AMR | CLM | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
HG01515 | hp1 | a0001 | c0001 | t0001 | g0060 | EUR | IBS | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
HG01515 | hp2 | a0001 | c0001 | t0001 | g0022 | EUR | IBS | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
HG01516 | hp1 | a0001 | c0001 | t0001 | g0147 | EUR | IBS | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
HG01516 | hp2 | a0001 | c0001 | t0001 | g0280 | EUR | IBS | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
HG01884 | hp1 | a0001 | c0001 | t0001 | g0210 | AFR | ACB | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
HG01884 | hp2 | a0001 | c0001 | t0001 | g0304 | AFR | ACB | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
HG01891 | hp1 | a0001 | c0001 | t0002 | g0003 | AFR | ACB | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
HG01891 | hp2 | a0001 | c0001 | t0001 | g0243 | AFR | ACB | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
HG01928 | hp1 | a0001 | c0001 | t0001 | g0044 | AMR | PEL | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
HG01928 | hp2 | a0001 | c0001 | t0001 | g0156 | AMR | PEL | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
HG01934 | hp1 | a0001 | c0001 | t0001 | g0183 | AMR | PEL | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
HG01934 | hp2 | a0001 | c0001 | t0001 | g0158 | AMR | PEL | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
HG01943 | hp1 | a0001 | c0001 | t0001 | g0160 | AMR | PEL | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
HG01943 | hp2 | a0001 | c0001 | t0001 | g0038 | AMR | PEL | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
HG01975 | hp1 | a0001 | c0001 | t0001 | g0028 | AMR | PEL | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
HG01975 | hp2 | a0001 | c0001 | t0001 | g0039 | AMR | PEL | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
HG01978 | hp1 | a0001 | c0001 | t0001 | g0176 | AMR | PEL | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
HG01978 | hp2 | a0001 | c0001 | t0001 | g0146 | AMR | PEL | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
HG01993 | hp1 | a0001 | c0001 | t0001 | g0179 | AMR | PEL | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
HG01993 | hp2 | a0001 | c0001 | t0001 | g0131 | AMR | PEL | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
HG02004 | hp1 | a0001 | c0001 | t0001 | g0056 | AMR | PEL | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
HG02004 | hp2 | a0001 | c0001 | t0001 | g0049 | AMR | PEL | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
HG02040 | hp1 | a0001 | c0001 | t0001 | g0053 | EAS | KHV | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
HG02040 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | KHV | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
HG02055 | hp1 | a0001 | c0001 | t0001 | g0276 | AFR | ACB | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
HG02055 | hp2 | a0001 | c0001 | t0001 | g0193 | AFR | ACB | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
HG02071 | hp1 | a0001 | c0001 | t0001 | g0155 | EAS | KHV | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
HG02071 | hp2 | a0001 | c0001 | t0001 | g0196 | EAS | KHV | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
HG02083 | hp1 | a0001 | c0001 | t0001 | g0231 | EAS | KHV | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
HG02083 | hp2 | a0001 | c0001 | t0001 | g0263 | EAS | KHV | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
HG02129 | hp1 | a0001 | c0001 | t0001 | g0288 | EAS | KHV | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
HG02129 | hp2 | a0001 | c0001 | t0001 | g0065 | EAS | KHV | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
HG02148 | hp1 | a0001 | c0001 | t0001 | g0167 | AMR | PEL | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
HG02148 | hp2 | a0001 | c0001 | t0001 | g0157 | AMR | PEL | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
HG02155 | hp1 | a0001 | c0001 | t0001 | g0285 | EAS | CDX | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
HG02155 | hp2 | a0001 | c0001 | t0001 | g0287 | EAS | CDX | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
HG02165 | hp1 | a0001 | c0001 | t0001 | g0128 | EAS | CDX | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
HG02165 | hp2 | a0001 | c0001 | t0001 | g0031 | EAS | CDX | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
HG02257 | hp1 | a0001 | c0001 | t0001 | g0139 | AFR | ACB | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
HG02257 | hp2 | a0001 | c0001 | t0001 | g0204 | AFR | ACB | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
HG02258 | hp1 | a0001 | c0001 | t0001 | g0293 | AFR | ACB | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
HG02258 | hp2 | a0001 | c0001 | t0001 | g0035 | AFR | ACB | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
HG02273 | hp1 | a0001 | c0001 | t0001 | g0130 | AMR | PEL | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
HG02273 | hp2 | a0001 | c0001 | t0001 | g0169 | AMR | PEL | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
HG02280 | hp1 | a0001 | c0001 | t0001 | g0208 | AFR | ACB | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
HG02280 | hp2 | a0001 | c0001 | t0001 | g0271 | AFR | ACB | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
HG02293 | hp1 | a0001 | c0001 | t0001 | g0159 | AMR | PEL | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
HG02293 | hp2 | a0001 | c0001 | t0001 | g0151 | AMR | PEL | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
HG02300 | hp1 | a0001 | c0001 | t0001 | g0283 | AMR | PEL | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
HG02300 | hp2 | a0001 | c0001 | t0001 | g0127 | AMR | PEL | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
HG02615 | hp1 | a0001 | c0001 | t0001 | g0207 | AFR | GWD | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
HG02615 | hp2 | a0001 | c0001 | t0001 | g0274 | AFR | GWD | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
HG02622 | hp1 | a0001 | c0001 | t0001 | g0290 | AFR | GWD | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
HG02622 | hp2 | a0001 | c0001 | t0001 | g0201 | AFR | GWD | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
HG02698 | hp1 | a0001 | c0001 | t0001 | g0030 | SAS | PJL | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
HG02698 | hp2 | a0001 | c0001 | t0001 | g0082 | SAS | PJL | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
HG02717 | hp1 | a0001 | c0001 | t0001 | g0072 | AFR | GWD | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
HG02717 | hp2 | a0001 | c0001 | t0001 | g0206 | AFR | GWD | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
HG02723 | hp1 | a0001 | c0001 | t0001 | g0241 | AFR | GWD | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
HG02723 | hp2 | a0001 | c0001 | t0001 | g0051 | AFR | GWD | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
HG02738 | hp1 | a0001 | c0001 | t0001 | g0301 | SAS | PJL | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
HG02738 | hp2 | a0001 | c0001 | t0001 | g0162 | SAS | PJL | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
HG02809 | hp1 | a0001 | c0001 | t0001 | g0209 | AFR | GWD | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
HG02809 | hp2 | a0001 | c0001 | t0001 | g0240 | AFR | GWD | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
HG02818 | hp1 | a0001 | c0001 | t0001 | g0047 | AFR | GWD | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
HG02818 | hp2 | a0001 | c0001 | t0001 | g0211 | AFR | GWD | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
HG02895 | hp1 | a0001 | c0001 | t0001 | g0205 | AFR | GWD | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
HG02895 | hp2 | a0001 | c0001 | t0001 | g0270 | AFR | GWD | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
HG02897 | hp1 | a0001 | c0001 | t0001 | g0239 | AFR | GWD | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
HG02897 | hp2 | a0001 | c0001 | t0002 | g0004 | AFR | GWD | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
HG02922 | hp1 | a0001 | c0001 | t0002 | g0005 | AFR | ESN | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
HG02922 | hp2 | a0001 | c0001 | t0001 | g0198 | AFR | ESN | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
HG02965 | hp1 | a0001 | c0001 | t0001 | g0272 | AFR | ESN | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
HG02965 | hp2 | a0001 | c0001 | t0001 | g0015 | AFR | ESN | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
HG02970 | hp1 | a0001 | c0001 | t0001 | g0099 | AFR | ESN | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
HG02970 | hp2 | a0001 | c0001 | t0001 | g0279 | AFR | ESN | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
HG03041 | hp1 | a0001 | c0001 | t0001 | g0067 | AFR | GWD | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
HG03041 | hp2 | a0001 | c0001 | t0001 | g0295 | AFR | GWD | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
HG03098 | hp1 | a0001 | c0001 | t0001 | g0202 | AFR | MSL | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
HG03098 | hp2 | a0001 | c0001 | t0001 | g0199 | AFR | MSL | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
HG03130 | hp1 | a0001 | c0001 | t0001 | g0197 | AFR | ESN | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
HG03130 | hp2 | a0001 | c0001 | t0001 | g0260 | AFR | ESN | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
HG03139 | hp1 | a0001 | c0001 | t0001 | g0084 | AFR | ESN | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
HG03139 | hp2 | a0001 | c0001 | t0001 | g0236 | AFR | ESN | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
HG03195 | hp1 | a0001 | c0001 | t0001 | g0071 | AFR | ESN | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
HG03195 | hp2 | a0001 | c0001 | t0001 | g0141 | AFR | ESN | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
HG03209 | hp1 | a0001 | c0001 | t0001 | g0100 | AFR | MSL | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
HG03209 | hp2 | a0001 | c0001 | t0001 | g0292 | AFR | MSL | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
HG03225 | hp1 | a0001 | c0001 | t0001 | g0136 | AFR | MSL | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
HG03225 | hp2 | a0001 | c0001 | t0001 | g0083 | AFR | MSL | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
HG03453 | hp1 | a0001 | c0001 | t0001 | g0242 | AFR | MSL | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
HG03453 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | MSL | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
HG03486 | hp1 | a0001 | c0001 | t0001 | g0268 | AFR | MSL | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
HG03486 | hp2 | a0001 | c0001 | t0001 | g0195 | AFR | MSL | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
HG03490 | hp1 | a0001 | c0001 | t0001 | g0129 | SAS | PJL | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
HG03490 | hp2 | a0001 | c0001 | t0001 | g0073 | SAS | PJL | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
HG03491 | hp1 | a0001 | c0001 | t0001 | g0020 | SAS | PJL | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
HG03491 | hp2 | a0001 | c0001 | t0001 | g0184 | SAS | PJL | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
HG03516 | hp1 | a0001 | c0001 | t0001 | g0192 | AFR | ESN | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
HG03516 | hp2 | a0001 | c0001 | t0001 | g0101 | AFR | ESN | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
HG03540 | hp1 | a0001 | c0001 | t0001 | g0219 | AFR | GWD | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
HG03540 | hp2 | a0001 | c0001 | t0001 | g0070 | AFR | GWD | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
HG03579 | hp1 | a0001 | c0001 | t0001 | g0220 | AFR | MSL | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
HG03579 | hp2 | a0001 | c0001 | t0001 | g0172 | AFR | MSL | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
HG03688 | hp1 | a0001 | c0001 | t0001 | g0134 | SAS | STU | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
HG03688 | hp2 | a0001 | c0001 | t0001 | g0174 | SAS | STU | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
HG03704 | hp1 | a0001 | c0001 | t0001 | g0123 | SAS | PJL | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
HG03704 | hp2 | a0001 | c0001 | t0001 | g0255 | SAS | PJL | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
HG03831 | hp1 | a0001 | c0001 | t0001 | g0300 | SAS | BEB | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
HG03831 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | BEB | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
HG03927 | hp1 | a0001 | c0001 | t0001 | g0233 | SAS | BEB | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
HG03927 | hp2 | a0001 | c0001 | t0001 | g0303 | SAS | BEB | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
HG04199 | hp1 | a0001 | c0001 | t0001 | g0133 | SAS | STU | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
HG04199 | hp2 | a0001 | c0001 | t0001 | g0040 | SAS | STU | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
HG04204 | hp1 | a0001 | c0001 | t0001 | g0222 | SAS | STU | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
HG04204 | hp2 | a0001 | c0001 | t0001 | g0080 | SAS | STU | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
HG04228 | hp1 | a0001 | c0001 | t0001 | g0116 | SAS | STU | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
HG04228 | hp2 | a0001 | c0001 | t0001 | g0234 | SAS | STU | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
NA18522 | hp1 | a0001 | c0001 | t0001 | g0194 | AFR | YRI | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
NA18522 | hp2 | a0001 | c0001 | t0001 | g0114 | AFR | YRI | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
NA18612 | hp1 | a0001 | c0001 | t0001 | g0029 | EAS | CHB | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
NA18612 | hp2 | a0001 | c0001 | t0001 | g0043 | EAS | CHB | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
NA18906 | hp1 | a0001 | c0001 | t0001 | g0037 | AFR | YRI | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
NA18906 | hp2 | a0001 | c0001 | t0001 | g0294 | AFR | YRI | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
NA18939 | hp1 | a0001 | c0001 | t0001 | g0286 | EAS | JPT | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
NA18939 | hp2 | a0001 | c0001 | t0001 | g0191 | EAS | JPT | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
NA18940 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
NA18940 | hp2 | a0001 | c0001 | t0001 | g0165 | EAS | JPT | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
NA18942 | hp1 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
NA18942 | hp2 | a0001 | c0001 | t0001 | g0068 | EAS | JPT | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
NA18943 | hp1 | a0001 | c0001 | t0001 | g0057 | EAS | JPT | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
NA18943 | hp2 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
NA18944 | hp1 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
NA18944 | hp2 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
NA18949 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
NA18949 | hp2 | a0001 | c0001 | t0001 | g0227 | EAS | JPT | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
NA18950 | hp1 | a0001 | c0001 | t0001 | g0091 | EAS | JPT | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
NA18950 | hp2 | a0001 | c0001 | t0001 | g0245 | EAS | JPT | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
NA18951 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
NA18951 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
NA18952 | hp1 | a0001 | c0001 | t0001 | g0246 | EAS | JPT | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
NA18952 | hp2 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
NA18953 | hp1 | a0001 | c0001 | t0001 | g0054 | EAS | JPT | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
NA18953 | hp2 | a0001 | c0001 | t0001 | g0269 | EAS | JPT | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
NA18956 | hp1 | a0001 | c0001 | t0001 | g0075 | EAS | JPT | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
NA18956 | hp2 | a0001 | c0001 | t0001 | g0226 | EAS | JPT | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
NA18960 | hp1 | a0001 | c0001 | t0001 | g0063 | EAS | JPT | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
NA18960 | hp2 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
NA18963 | hp1 | a0001 | c0001 | t0001 | g0161 | EAS | JPT | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
NA18963 | hp2 | a0001 | c0001 | t0001 | g0050 | EAS | JPT | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
NA18964 | hp1 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
NA18964 | hp2 | a0001 | c0001 | t0001 | g0264 | EAS | JPT | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
NA18968 | hp1 | a0001 | c0001 | t0001 | g0074 | EAS | JPT | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
NA18968 | hp2 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
NA18969 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
NA18969 | hp2 | a0001 | c0001 | t0001 | g0052 | EAS | JPT | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
NA18971 | hp1 | a0001 | c0001 | t0001 | g0281 | EAS | JPT | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
NA18971 | hp2 | a0001 | c0001 | t0001 | g0086 | EAS | JPT | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
NA18973 | hp1 | a0001 | c0001 | t0001 | g0081 | EAS | JPT | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
NA18973 | hp2 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
NA18974 | hp1 | a0001 | c0001 | t0001 | g0097 | EAS | JPT | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
NA18974 | hp2 | a0001 | c0001 | t0001 | g0251 | EAS | JPT | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
NA18975 | hp1 | a0001 | c0001 | t0001 | g0223 | EAS | JPT | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
NA18975 | hp2 | a0001 | c0001 | t0001 | g0122 | EAS | JPT | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
NA18977 | hp1 | a0001 | c0001 | t0001 | g0055 | EAS | JPT | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
NA18977 | hp2 | a0001 | c0001 | t0001 | g0297 | EAS | JPT | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
NA18978 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
NA18978 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
NA18980 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
NA18980 | hp2 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
NA18984 | hp1 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
NA18984 | hp2 | a0001 | c0001 | t0001 | g0190 | EAS | JPT | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
NA18986 | hp1 | a0001 | c0001 | t0001 | g0250 | EAS | JPT | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
NA18986 | hp2 | a0001 | c0001 | t0001 | g0212 | EAS | JPT | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
NA18998 | hp1 | a0001 | c0001 | t0001 | g0045 | EAS | JPT | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
NA18998 | hp2 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
NA19000 | hp1 | a0001 | c0001 | t0001 | g0062 | EAS | JPT | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
NA19000 | hp2 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
NA19003 | hp1 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
NA19003 | hp2 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
NA19004 | hp1 | a0001 | c0001 | t0001 | g0177 | EAS | JPT | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
NA19004 | hp2 | a0001 | c0001 | t0001 | g0149 | EAS | JPT | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
NA19009 | hp1 | a0001 | c0001 | t0001 | g0262 | EAS | JPT | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
NA19009 | hp2 | a0001 | c0001 | t0001 | g0178 | EAS | JPT | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
NA19010 | hp1 | a0001 | c0001 | t0001 | g0181 | EAS | JPT | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
NA19010 | hp2 | a0001 | c0001 | t0001 | g0163 | EAS | JPT | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
NA19011 | hp1 | a0001 | c0001 | t0001 | g0235 | EAS | JPT | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
NA19011 | hp2 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
NA19012 | hp1 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
NA19012 | hp2 | a0001 | c0001 | t0001 | g0266 | EAS | JPT | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
NA19030 | hp1 | a0001 | c0001 | t0001 | g0277 | AFR | LWK | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
NA19030 | hp2 | a0001 | c0001 | t0001 | g0213 | AFR | LWK | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
NA19043 | hp1 | a0001 | c0001 | t0001 | g0137 | AFR | LWK | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
NA19043 | hp2 | a0001 | c0001 | t0001 | g0278 | AFR | LWK | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
NA19056 | hp1 | a0001 | c0001 | t0001 | g0048 | EAS | JPT | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
NA19056 | hp2 | a0001 | c0001 | t0001 | g0267 | EAS | JPT | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
NA19057 | hp1 | a0001 | c0001 | t0001 | g0125 | EAS | JPT | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
NA19057 | hp2 | a0001 | c0001 | t0001 | g0079 | EAS | JPT | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
NA19063 | hp1 | a0001 | c0001 | t0001 | g0087 | EAS | JPT | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
NA19063 | hp2 | a0001 | c0001 | t0001 | g0249 | EAS | JPT | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
NA19064 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
NA19064 | hp2 | a0001 | c0001 | t0001 | g0224 | EAS | JPT | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
NA19068 | hp1 | a0001 | c0001 | t0001 | g0187 | EAS | JPT | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
NA19068 | hp2 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
NA19070 | hp1 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
NA19070 | hp2 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
NA19076 | hp1 | a0001 | c0001 | t0001 | g0252 | EAS | JPT | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
NA19076 | hp2 | a0001 | c0001 | t0001 | g0059 | EAS | JPT | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
NA19077 | hp1 | a0001 | c0001 | t0001 | g0284 | EAS | JPT | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
NA19077 | hp2 | a0001 | c0001 | t0001 | g0164 | EAS | JPT | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
NA19079 | hp1 | a0001 | c0001 | t0001 | g0282 | EAS | JPT | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
NA19079 | hp2 | a0001 | c0001 | t0001 | g0173 | EAS | JPT | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
NA19080 | hp1 | a0001 | c0001 | t0001 | g0261 | EAS | JPT | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
NA19080 | hp2 | a0001 | c0001 | t0001 | g0171 | EAS | JPT | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
NA19082 | hp1 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
NA19082 | hp2 | a0001 | c0001 | t0001 | g0170 | EAS | JPT | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
NA19084 | hp1 | a0001 | c0001 | t0001 | g0111 | EAS | JPT | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
NA19084 | hp2 | a0001 | c0001 | t0001 | g0248 | EAS | JPT | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
NA19085 | hp1 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
NA19085 | hp2 | a0001 | c0001 | t0001 | g0244 | EAS | JPT | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
NA19088 | hp1 | a0001 | c0001 | t0001 | g0182 | EAS | JPT | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
NA19088 | hp2 | a0001 | c0001 | t0001 | g0247 | EAS | JPT | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
NA19090 | hp1 | a0001 | c0001 | t0001 | g0186 | EAS | JPT | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
NA19090 | hp2 | a0001 | c0001 | t0001 | g0265 | EAS | JPT | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
NA19240 | hp1 | a0001 | c0001 | t0001 | g0228 | AFR | YRI | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
NA19240 | hp2 | a0001 | c0001 | t0001 | g0237 | AFR | YRI | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
NA20129 | hp1 | a0001 | c0001 | t0001 | g0098 | AFR | ASW | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
NA20129 | hp2 | a0001 | c0001 | t0001 | g0200 | AFR | ASW | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
NA20752 | hp1 | a0001 | c0001 | t0001 | g0008 | EUR | TSI | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
NA20752 | hp2 | a0001 | c0001 | t0001 | g0218 | EUR | TSI | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
NA20805 | hp1 | a0001 | c0001 | t0001 | g0061 | EUR | TSI | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
NA20805 | hp2 | a0001 | c0001 | t0001 | g0216 | EUR | TSI | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
NA20905 | hp1 | a0001 | c0001 | t0001 | g0238 | SAS | GIH | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
NA20905 | hp2 | a0001 | c0001 | t0001 | g0175 | SAS | GIH | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
HG02109 | hp1 | a0001 | c0001 | t0001 | g0064 | AFR | ACB | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
HG02109 | hp2 | a0001 | c0001 | t0001 | g0132 | AFR | ACB | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
HG03471 | hp1 | a0001 | c0001 | t0001 | g0275 | AFR | MSL | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
HG03471 | hp2 | a0001 | c0001 | t0001 | g0229 | AFR | MSL | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
HG06807 | hp1 | a0001 | c0001 | t0001 | g0069 | AFR | USA | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
HG06807 | hp2 | a0001 | c0001 | t0001 | g0296 | AFR | USA | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
NA18955 | hp1 | a0001 | c0001 | t0001 | g0225 | EAS | JPT | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
NA18955 | hp2 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
NA20300 | hp1 | a0001 | c0001 | t0001 | g0185 | AFR | USA | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
NA20300 | hp2 | a0001 | c0001 | t0001 | g0203 | AFR | USA | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
NA21309 | hp1 | a0001 | c0001 | t0001 | g0078 | AFR | LWK | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
NA21309 | hp2 | a0001 | c0001 | t0001 | g0023 | AFR | LWK | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0257 | REF | REF | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0138 | REF | REF | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:31932071
|
T | C | 1 | a0002 | 1 | HG01168.hp2 | missense_variant | MODERATE | c.208A>G | p.Ile70Val | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 4/10 | 292/1516 | 208/894 | 70/297 | chr2 | 31932071 |
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 |
---|
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:31868313
|
G | A | 1 | a0001c0001t0002 | 3 | HG01891.hp1 HG02897.hp2 HG02922.hp1 |
3_prime_UTR_variant | MODIFIER | c.*48C>T | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 10/10 | 48 | chr2 | 31868313 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:31868526
|
T | C | 1 | a0001c0001t0001g0211 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.763-34A>G | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 9/9 | chr2 | 31868526 | ||||||
chr2:31868604
|
T | C | 1 | a0001c0001t0001g0215 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.763-112A>G | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 9/9 | chr2 | 31868604 | ||||||
chr2:31868807
|
C | T | 1 | a0001c0001t0001g0017 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.763-315G>A | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 9/9 | chr2 | 31868807 | ||||||
chr2:31868935
|
T | C | 2 | a0001c0001t0001g0271a0001c0001t0001g0281 | 2 | HG02280.hp2 NA18971.hp1 |
intron_variant | MODIFIER | c.763-443A>G | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 9/9 | chr2 | 31868935 | ||||||
chr2:31869060
|
G | C | 1 | a0001c0001t0001g0296 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.763-568C>G | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 9/9 | chr2 | 31869060 | ||||||
chr2:31869221
|
T | C | 1 | a0001c0001t0001g0282 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.762+627A>G | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 9/9 | chr2 | 31869221 | ||||||
chr2:31869430
|
T | G | 6 | a0001c0001t0001g0178a0001c0001t0001g0181a0001c0001t0001g0182others(3): Show | 6 | HG00408.hp2 HG02071.hp2 NA19009.hp2 others(3): Show |
intron_variant | MODIFIER | c.762+418A>C | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 9/9 | chr2 | 31869430 | ||||||
chr2:31869464
|
G | A | 1 | a0001c0001t0001g0014 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.762+384C>T | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 9/9 | chr2 | 31869464 | ||||||
chr2:31869686
|
C | T | 1 | a0001c0001t0001g0297 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.762+162G>A | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 9/9 | chr2 | 31869686 | ||||||
chr2:31869741
|
T | C | 1 | a0001c0001t0001g0014 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.762+107A>G | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 9/9 | chr2 | 31869741 | ||||||
chr2:31869836
|
A | G | 1 | a0001c0001t0001g0191 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.762+12T>C | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 9/9 | chr2 | 31869836 | ||||||
chr2:31869954
|
T | TA | 6 | a0001c0001t0001g0051a0001c0001t0001g0064a0001c0001t0001g0184others(3): Show | 6 | HG01243.hp2 HG02109.hp1 HG02615.hp2 others(3): Show |
splice_region_variant&intron_variant | LOW | c.658-3dupT | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 8/9 | chr2 | 31869954 | ||||||
chr2:31869967
|
AAAG | A | 8 | a0001c0001t0001g0232a0001c0001t0001g0233a0001c0001t0001g0234others(5): Show | 8 | HG01361.hp1 HG02258.hp1 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.658-18_658-16delCT others(1): Show |
MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 8/9 | chr2 | 31869967 | ||||||
chr2:31870062
|
G | T | 48 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0011others(45): Show | 48 | HG01168.hp1 HG01169.hp2 HG01255.hp2 others(45): Show |
intron_variant | MODIFIER | c.658-110C>A | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 8/9 | chr2 | 31870062 | ||||||
chr2:31870126
|
T | C | 1 | a0001c0001t0001g0236 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.658-174A>G | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 8/9 | chr2 | 31870126 | ||||||
chr2:31870176
|
TTTA | T | 19 | a0001c0001t0001g0069a0001c0001t0001g0071a0001c0001t0001g0072others(16): Show | 19 | HG00408.hp2 HG00642.hp2 HG01081.hp1 others(16): Show |
intron_variant | MODIFIER | c.658-227_658-225del others(3): Show |
MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 8/9 | chr2 | 31870176 | ||||||
chr2:31870257
|
AATATT | A | 3 | a0001c0001t0002g0003a0001c0001t0002g0004a0001c0001t0002g0005 | 3 | HG01891.hp1 HG02897.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.658-310_658-306del others(5): Show |
MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 8/9 | chr2 | 31870257 | ||||||
chr2:31870483
|
T | C | 1 | a0001c0001t0001g0289 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.658-531A>G | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 8/9 | chr2 | 31870483 | ||||||
chr2:31870522
|
A | G | 7 | a0001c0001t0001g0028a0001c0001t0001g0118a0001c0001t0001g0145others(4): Show | 7 | HG00099.hp2 HG00639.hp1 HG01243.hp1 others(4): Show |
intron_variant | MODIFIER | c.658-570T>C | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 8/9 | chr2 | 31870522 | ||||||
chr2:31870638
|
G | A | 1 | a0001c0001t0001g0278 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.658-686C>T | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 8/9 | chr2 | 31870638 | ||||||
chr2:31870642
|
T | C | 2 | a0001c0001t0001g0083a0001c0001t0001g0084 | 2 | HG03139.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.658-690A>G | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 8/9 | chr2 | 31870642 | ||||||
chr2:31870887
|
G | C | 1 | a0001c0001t0001g0229 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.658-935C>G | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 8/9 | chr2 | 31870887 | ||||||
chr2:31871038
|
T | C | 4 | a0001c0001t0001g0239a0001c0001t0001g0240a0001c0001t0001g0241others(1): Show | 4 | HG02723.hp1 HG02809.hp2 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.658-1086A>G | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 8/9 | chr2 | 31871038 | ||||||
chr2:31871154
|
C | T | 3 | a0001c0001t0001g0199a0001c0001t0001g0200a0001c0001t0001g0201 | 3 | HG02622.hp2 HG03098.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.658-1202G>A | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 8/9 | chr2 | 31871154 | ||||||
chr2:31871282
|
T | C | 2 | a0001c0001t0001g0035a0001c0001t0001g0092 | 2 | HG02258.hp2 NA18980.hp2 |
intron_variant | MODIFIER | c.658-1330A>G | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 8/9 | chr2 | 31871282 | ||||||
chr2:31871381
|
C | T | 293 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(290): Show | 293 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(290): Show |
intron_variant | MODIFIER | c.658-1429G>A | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 8/9 | chr2 | 31871381 | ||||||
chr2:31871411
|
C | T | 1 | a0001c0001t0001g0146 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.658-1459G>A | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 8/9 | chr2 | 31871411 | ||||||
chr2:31871492
|
CAT | C | 3 | a0001c0001t0001g0283a0001c0001t0001g0289a0001c0001t0001g0302 | 3 | HG01255.hp2 HG01496.hp2 HG02300.hp1 |
intron_variant | MODIFIER | c.658-1542_658-1541d others(4): Show |
MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 8/9 | chr2 | 31871492 | ||||||
chr2:31871496
|
T | TAC | 4 | a0001c0001t0001g0292a0001c0001t0001g0293a0001c0001t0001g0294others(1): Show | 4 | HG02258.hp1 HG03041.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.658-1545_658-1544i others(4): Show |
MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 8/9 | chr2 | 31871496 | ||||||
chr2:31871496
|
TATAC | T | 3 | a0001c0001t0002g0003a0001c0001t0002g0004a0001c0001t0002g0005 | 3 | HG01891.hp1 HG02897.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.658-1548_658-1545d others(6): Show |
MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 8/9 | chr2 | 31871496 | ||||||
chr2:31871498
|
T | C | 7 | a0001c0001t0001g0275a0001c0001t0001g0276a0001c0001t0001g0277others(4): Show | 7 | HG02055.hp1 HG02258.hp1 HG03041.hp2 others(4): Show |
intron_variant | MODIFIER | c.658-1546A>G | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 8/9 | chr2 | 31871498 | ||||||
chr2:31871498
|
T | TAC | 8 | a0001c0001t0001g0098a0001c0001t0001g0101a0001c0001t0001g0114others(5): Show | 8 | HG01361.hp1 HG02055.hp2 HG03486.hp2 others(5): Show |
intron_variant | MODIFIER | c.658-1548_658-1547d others(4): Show |
MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 8/9 | chr2 | 31871498 | ||||||
chr2:31871498
|
TAC | T | 152 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0010others(149): Show | 152 | HG00140.hp2 HG00423.hp2 HG00438.hp1 others(149): Show |
intron_variant | MODIFIER | c.658-1548_658-1547d others(4): Show |
MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 8/9 | chr2 | 31871498 | ||||||
chr2:31871500
|
C | T | 108 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(105): Show | 108 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(105): Show |
intron_variant | MODIFIER | c.658-1548G>A | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 8/9 | chr2 | 31871500 | ||||||
chr2:31871502
|
C | T | 1 | a0001c0001t0001g0284 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.658-1550G>A | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 8/9 | chr2 | 31871502 | ||||||
chr2:31871516
|
CACAT | C | 9 | a0001c0001t0001g0007a0001c0001t0001g0009a0001c0001t0001g0036others(6): Show | 9 | HG00621.hp2 HG02622.hp2 HG02922.hp2 others(6): Show |
intron_variant | MODIFIER | c.658-1568_658-1565d others(6): Show |
MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 8/9 | chr2 | 31871516 | ||||||
chr2:31871516
|
CACATAT | C | 4 | a0001c0001t0001g0197a0001c0001t0001g0272a0001c0001t0001g0273others(1): Show | 4 | HG01243.hp2 HG02615.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.658-1570_658-1565d others(8): Show |
MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 8/9 | chr2 | 31871516 | ||||||
chr2:31871518
|
CAT | C | 111 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0014others(108): Show | 111 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(108): Show |
intron_variant | MODIFIER | c.658-1568_658-1567d others(4): Show |
MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 8/9 | chr2 | 31871518 | ||||||
chr2:31871520
|
T | C | 7 | a0001c0001t0001g0292a0001c0001t0001g0293a0001c0001t0001g0294others(4): Show | 7 | HG01891.hp1 HG02258.hp1 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.658-1568A>G | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 8/9 | chr2 | 31871520 | ||||||
chr2:31871604
|
C | T | 1 | a0001c0001t0001g0060 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.658-1652G>A | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 8/9 | chr2 | 31871604 | ||||||
chr2:31871633
|
T | G | 3 | a0001c0001t0001g0117a0001c0001t0001g0128a0001c0001t0001g0187 | 3 | HG00621.hp2 HG02165.hp1 NA19068.hp1 |
intron_variant | MODIFIER | c.658-1681A>C | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 8/9 | chr2 | 31871633 | ||||||
chr2:31871676
|
C | T | 4 | a0001c0001t0001g0239a0001c0001t0001g0240a0001c0001t0001g0241others(1): Show | 4 | HG02723.hp1 HG02809.hp2 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.658-1724G>A | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 8/9 | chr2 | 31871676 | ||||||
chr2:31872016
|
A | AACACACA others(1): Show |
43 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0010others(40): Show | 43 | HG01168.hp1 HG01169.hp2 HG01255.hp2 others(40): Show |
intron_variant | MODIFIER | c.658-2072_658-2065d others(10): Show |
MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 8/9 | chr2 | 31872016 | ||||||
chr2:31872016
|
A | AACACACA others(3): Show |
179 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(176): Show | 179 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(176): Show |
intron_variant | MODIFIER | c.658-2074_658-2065d others(12): Show |
MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 8/9 | chr2 | 31872016 | ||||||
chr2:31872016
|
A | AACACACA others(5): Show |
33 | a0001c0001t0001g0015a0001c0001t0001g0017a0001c0001t0001g0028others(30): Show | 33 | HG00099.hp2 HG00639.hp1 HG00642.hp2 others(30): Show |
intron_variant | MODIFIER | c.658-2076_658-2065d others(14): Show |
MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 8/9 | chr2 | 31872016 | ||||||
chr2:31872016
|
A | AACACACA others(7): Show |
15 | a0001c0001t0001g0085a0001c0001t0001g0086a0001c0001t0001g0129others(12): Show | 15 | HG00423.hp1 HG01081.hp2 HG01106.hp1 others(12): Show |
intron_variant | MODIFIER | c.658-2078_658-2065d others(16): Show |
MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 8/9 | chr2 | 31872016 | ||||||
chr2:31872016
|
A | AACACACA others(9): Show |
14 | a0001c0001t0001g0071a0001c0001t0001g0197a0001c0001t0001g0198others(11): Show | 14 | HG01257.hp2 HG01258.hp1 HG02280.hp2 others(11): Show |
intron_variant | MODIFIER | c.658-2080_658-2065d others(18): Show |
MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 8/9 | chr2 | 31872016 | ||||||
chr2:31872016
|
A | AACACACA others(11): Show |
4 | a0001c0001t0001g0185a0001c0001t0001g0199a0001c0001t0001g0293others(1): Show | 4 | HG02258.hp1 HG03041.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.658-2082_658-2065d others(20): Show |
MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 8/9 | chr2 | 31872016 | ||||||
chr2:31872016
|
A | AACACACA others(13): Show |
4 | a0001c0001t0001g0277a0001c0001t0001g0292a0001c0001t0001g0294others(1): Show | 4 | HG01891.hp1 HG03209.hp2 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.658-2084_658-2065d others(22): Show |
MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 8/9 | chr2 | 31872016 | ||||||
chr2:31872016
|
A | AACACACA others(15): Show |
2 | a0001c0001t0001g0275a0001c0001t0001g0276 | 2 | HG02055.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.658-2086_658-2065d others(24): Show |
MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 8/9 | chr2 | 31872016 | ||||||
chr2:31872016
|
A | AACACACA others(21): Show |
1 | a0001c0001t0001g0274 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.658-2092_658-2065d others(30): Show |
MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 8/9 | chr2 | 31872016 | ||||||
chr2:31872016
|
A | AACACACA others(23): Show |
2 | a0001c0001t0001g0272a0001c0001t0001g0273 | 2 | HG01243.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.658-2065_658-2064i others(32): Show |
MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 8/9 | chr2 | 31872016 | ||||||
chr2:31872123
|
G | A | 1 | a0001c0001t0001g0019 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.658-2171C>T | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 8/9 | chr2 | 31872123 | ||||||
chr2:31872194
|
G | A | 1 | a0001c0001t0001g0140 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.658-2242C>T | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 8/9 | chr2 | 31872194 | ||||||
chr2:31872303
|
C | T | 12 | a0001c0001t0001g0032a0001c0001t0001g0033a0001c0001t0001g0041others(9): Show | 12 | HG00741.hp1 HG01433.hp1 HG02040.hp1 others(9): Show |
intron_variant | MODIFIER | c.658-2351G>A | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 8/9 | chr2 | 31872303 | ||||||
chr2:31872442
|
C | T | 3 | a0001c0001t0001g0275a0001c0001t0001g0276a0001c0001t0001g0277 | 3 | HG02055.hp1 HG03471.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.658-2490G>A | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 8/9 | chr2 | 31872442 | ||||||
chr2:31872621
|
A | C | 1 | a0001c0001t0001g0279 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.658-2669T>G | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 8/9 | chr2 | 31872621 | ||||||
chr2:31873071
|
G | GA | 6 | a0001c0001t0001g0272a0001c0001t0001g0273a0001c0001t0001g0274others(3): Show | 6 | HG01243.hp2 HG01891.hp1 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.658-3120dupT | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 8/9 | chr2 | 31873071 | ||||||
chr2:31873185
|
T | C | 2 | a0001c0001t0001g0290a0001c0001t0001g0291 | 2 | HG01109.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.658-3233A>G | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 8/9 | chr2 | 31873185 | ||||||
chr2:31873230
|
G | A | 1 | a0001c0001t0001g0191 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.658-3278C>T | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 8/9 | chr2 | 31873230 | ||||||
chr2:31873264
|
G | A | 1 | a0001c0001t0001g0078 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.658-3312C>T | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 8/9 | chr2 | 31873264 | ||||||
chr2:31873271
|
T | C | 1 | a0001c0001t0001g0215 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.658-3319A>G | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 8/9 | chr2 | 31873271 | ||||||
chr2:31873677
|
T | A | 1 | a0001c0001t0001g0190 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.658-3725A>T | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 8/9 | chr2 | 31873677 | ||||||
chr2:31874061
|
A | T | 3 | a0001c0001t0001g0028a0001c0001t0001g0118a0001c0001t0001g0153 | 3 | HG00099.hp2 HG00639.hp1 HG01975.hp1 |
intron_variant | MODIFIER | c.658-4109T>A | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 8/9 | chr2 | 31874061 | ||||||
chr2:31874126
|
T | C | 1 | a0001c0001t0001g0184 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.658-4174A>G | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 8/9 | chr2 | 31874126 | ||||||
chr2:31874136
|
A | G | 1 | a0001c0001t0001g0184 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.658-4184T>C | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 8/9 | chr2 | 31874136 | ||||||
chr2:31874214
|
T | C | 7 | a0001c0001t0001g0034a0001c0001t0001g0178a0001c0001t0001g0181others(4): Show | 7 | HG00408.hp2 HG02071.hp2 NA18955.hp2 others(4): Show |
intron_variant | MODIFIER | c.658-4262A>G | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 8/9 | chr2 | 31874214 | ||||||
chr2:31874329
|
C | T | 3 | a0001c0001t0001g0232a0001c0001t0001g0233a0001c0001t0001g0234 | 3 | HG01361.hp1 HG03927.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.658-4377G>A | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 8/9 | chr2 | 31874329 | ||||||
chr2:31874467
|
T | C | 1 | a0001c0001t0001g0140 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.658-4515A>G | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 8/9 | chr2 | 31874467 | ||||||
chr2:31874809
|
T | C | 2 | a0001c0001t0001g0238a0001c0001t0001g0300 | 2 | HG03831.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.658-4857A>G | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 8/9 | chr2 | 31874809 | ||||||
chr2:31874824
|
A | T | 2 | a0001c0001t0001g0236a0001c0001t0001g0237 | 2 | HG03139.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.658-4872T>A | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 8/9 | chr2 | 31874824 | ||||||
chr2:31874918
|
C | CAT | 111 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(108): Show | 111 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(108): Show |
intron_variant | MODIFIER | c.658-4968_658-4967d others(4): Show |
MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 8/9 | chr2 | 31874918 | ||||||
chr2:31875241
|
A | T | 59 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0011others(56): Show | 59 | HG01168.hp1 HG01169.hp2 HG01243.hp2 others(56): Show |
intron_variant | MODIFIER | c.658-5289T>A | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 8/9 | chr2 | 31875241 | ||||||
chr2:31875827
|
C | A | 3 | a0001c0001t0001g0232a0001c0001t0001g0233a0001c0001t0001g0234 | 3 | HG01361.hp1 HG03927.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.658-5875G>T | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 8/9 | chr2 | 31875827 | ||||||
chr2:31875863
|
T | G | 3 | a0001c0001t0001g0272a0001c0001t0001g0273a0001c0001t0001g0274 | 3 | HG01243.hp2 HG02615.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.658-5911A>C | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 8/9 | chr2 | 31875863 | ||||||
chr2:31875940
|
G | T | 8 | a0001c0001t0001g0134a0001c0001t0001g0152a0001c0001t0001g0156others(5): Show | 8 | HG01106.hp2 HG01261.hp1 HG01928.hp2 others(5): Show |
intron_variant | MODIFIER | c.658-5988C>A | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 8/9 | chr2 | 31875940 | ||||||
chr2:31875941
|
C | A | 8 | a0001c0001t0001g0134a0001c0001t0001g0152a0001c0001t0001g0156others(5): Show | 8 | HG01106.hp2 HG01261.hp1 HG01928.hp2 others(5): Show |
intron_variant | MODIFIER | c.658-5989G>T | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 8/9 | chr2 | 31875941 | ||||||
chr2:31875990
|
T | C | 118 | a0001c0001t0001g0001a0001c0001t0001g0015a0001c0001t0001g0017others(115): Show | 118 | HG00099.hp2 HG00140.hp2 HG00423.hp2 others(115): Show |
intron_variant | MODIFIER | c.658-6038A>G | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 8/9 | chr2 | 31875990 | ||||||
chr2:31876094
|
T | C | 1 | a0001c0001t0001g0060 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.658-6142A>G | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 8/9 | chr2 | 31876094 | ||||||
chr2:31876107
|
C | A | 1 | a0001c0001t0001g0022 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.658-6155G>T | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 8/9 | chr2 | 31876107 | ||||||
chr2:31876383
|
C | G | 3 | a0001c0001t0001g0136a0001c0001t0001g0137a0001c0001t0001g0228 | 3 | HG03225.hp1 NA19043.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.658-6431G>C | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 8/9 | chr2 | 31876383 | ||||||
chr2:31876525
|
C | T | 73 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0011others(70): Show | 73 | HG01106.hp1 HG01109.hp2 HG01168.hp1 others(70): Show |
intron_variant | MODIFIER | c.658-6573G>A | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 8/9 | chr2 | 31876525 | ||||||
chr2:31876632
|
T | C | 2 | a0001c0001t0001g0290a0001c0001t0001g0291 | 2 | HG01109.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.658-6680A>G | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 8/9 | chr2 | 31876632 | ||||||
chr2:31876678
|
C | A | 1 | a0001c0001t0001g0002 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.657+6708G>T | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 8/9 | chr2 | 31876678 | ||||||
chr2:31876911
|
C | G | 3 | a0001c0001t0001g0078a0001c0001t0001g0185a0001c0001t0001g0215 | 3 | HG01106.hp1 NA20300.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.657+6475G>C | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 8/9 | chr2 | 31876911 | ||||||
chr2:31876918
|
T | C | 1 | a0001c0001t0001g0232 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.657+6468A>G | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 8/9 | chr2 | 31876918 | ||||||
chr2:31877237
|
A | G | 1 | a0001c0001t0001g0189 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.657+6149T>C | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 8/9 | chr2 | 31877237 | ||||||
chr2:31877554
|
G | A | 3 | a0001c0001t0001g0286a0001c0001t0001g0287a0001c0001t0001g0288 | 3 | HG02129.hp1 HG02155.hp2 NA18939.hp1 |
intron_variant | MODIFIER | c.657+5832C>T | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 8/9 | chr2 | 31877554 | ||||||
chr2:31877620
|
G | A | 1 | a0001c0001t0001g0002 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.657+5766C>T | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 8/9 | chr2 | 31877620 | ||||||
chr2:31877686
|
G | A | 1 | a0001c0001t0001g0301 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.657+5700C>T | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 8/9 | chr2 | 31877686 | ||||||
chr2:31877731
|
T | A | 222 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(219): Show | 222 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(219): Show |
intron_variant | MODIFIER | c.657+5655A>T | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 8/9 | chr2 | 31877731 | ||||||
chr2:31877869
|
C | T | 1 | a0001c0001t0001g0018 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.657+5517G>A | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 8/9 | chr2 | 31877869 | ||||||
chr2:31877898
|
T | C | 1 | a0001c0001t0001g0296 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.657+5488A>G | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 8/9 | chr2 | 31877898 | ||||||
chr2:31877991
|
T | C | 2 | a0001c0001t0001g0290a0001c0001t0001g0291 | 2 | HG01109.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.657+5395A>G | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 8/9 | chr2 | 31877991 | ||||||
chr2:31878431
|
C | T | 3 | a0001c0001t0001g0275a0001c0001t0001g0276a0001c0001t0001g0277 | 3 | HG02055.hp1 HG03471.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.657+4955G>A | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 8/9 | chr2 | 31878431 | ||||||
chr2:31878613
|
G | A | 2 | a0001c0001t0001g0236a0001c0001t0001g0237 | 2 | HG03139.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.657+4773C>T | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 8/9 | chr2 | 31878613 | ||||||
chr2:31878620
|
G | A | 69 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(66): Show | 69 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(66): Show |
intron_variant | MODIFIER | c.657+4766C>T | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 8/9 | chr2 | 31878620 | ||||||
chr2:31878812
|
C | CAG | 291 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(288): Show | 291 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(288): Show |
intron_variant | MODIFIER | c.657+4573_657+4574i others(4): Show |
MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 8/9 | chr2 | 31878812 | ||||||
chr2:31878830
|
T | C | 1 | a0001c0001t0001g0107 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.657+4556A>G | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 8/9 | chr2 | 31878830 | ||||||
chr2:31878941
|
CAT | C | 3 | a0001c0001t0001g0078a0001c0001t0001g0185a0001c0001t0001g0215 | 3 | HG01106.hp1 NA20300.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.657+4443_657+4444d others(4): Show |
MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 8/9 | chr2 | 31878941 | ||||||
chr2:31879142
|
T | C | 3 | a0001c0001t0001g0292a0001c0001t0001g0293a0001c0001t0001g0294 | 3 | HG02258.hp1 HG03209.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.657+4244A>G | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 8/9 | chr2 | 31879142 | ||||||
chr2:31879244
|
A | G | 1 | a0001c0001t0001g0229 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.657+4142T>C | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 8/9 | chr2 | 31879244 | ||||||
chr2:31879309
|
A | T | 1 | a0001c0001t0001g0050 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.657+4077T>A | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 8/9 | chr2 | 31879309 | ||||||
chr2:31879618
|
A | T | 17 | a0001c0001t0001g0034a0001c0001t0001g0063a0001c0001t0001g0169others(14): Show | 17 | HG00408.hp2 HG00642.hp2 HG01081.hp1 others(14): Show |
intron_variant | MODIFIER | c.657+3768T>A | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 8/9 | chr2 | 31879618 | ||||||
chr2:31879632
|
A | G | 3 | a0001c0001t0001g0232a0001c0001t0001g0233a0001c0001t0001g0234 | 3 | HG01361.hp1 HG03927.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.657+3754T>C | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 8/9 | chr2 | 31879632 | ||||||
chr2:31879685
|
A | T | 113 | a0001c0001t0001g0001a0001c0001t0001g0017a0001c0001t0001g0018others(110): Show | 113 | HG00099.hp2 HG00140.hp2 HG00423.hp2 others(110): Show |
intron_variant | MODIFIER | c.657+3701T>A | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 8/9 | chr2 | 31879685 | ||||||
chr2:31880080
|
A | G | 6 | a0001c0001t0001g0156a0001c0001t0001g0157a0001c0001t0001g0158others(3): Show | 6 | HG01261.hp1 HG01928.hp2 HG01934.hp2 others(3): Show |
intron_variant | MODIFIER | c.657+3306T>C | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 8/9 | chr2 | 31880080 | ||||||
chr2:31880259
|
A | G | 1 | a0001c0001t0001g0040 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.657+3127T>C | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 8/9 | chr2 | 31880259 | ||||||
chr2:31880317
|
A | G | 224 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(221): Show | 224 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(221): Show |
intron_variant | MODIFIER | c.657+3069T>C | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 8/9 | chr2 | 31880317 | ||||||
chr2:31880436
|
A | T | 2 | a0001c0001t0001g0236a0001c0001t0001g0237 | 2 | HG03139.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.657+2950T>A | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 8/9 | chr2 | 31880436 | ||||||
chr2:31880735
|
G | C | 1 | a0001c0001t0001g0209 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.657+2651C>G | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 8/9 | chr2 | 31880735 | ||||||
chr2:31880880
|
C | T | 1 | a0001c0001t0001g0025 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.657+2506G>A | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 8/9 | chr2 | 31880880 | ||||||
chr2:31880971
|
C | A | 100 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(97): Show | 100 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(97): Show |
intron_variant | MODIFIER | c.657+2415G>T | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 8/9 | chr2 | 31880971 | ||||||
chr2:31881033
|
T | TA | 6 | a0001c0001t0001g0099a0001c0001t0001g0102a0001c0001t0001g0208others(3): Show | 6 | HG01109.hp2 HG01496.hp1 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.657+2352dupT | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 8/9 | chr2 | 31881033 | ||||||
chr2:31881495
|
T | TA | 91 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0019others(88): Show | 91 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(88): Show |
intron_variant | MODIFIER | c.657+1890dupT | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 8/9 | chr2 | 31881495 | ||||||
chr2:31881495
|
T | TAA | 13 | a0001c0001t0001g0021a0001c0001t0001g0026a0001c0001t0001g0118others(10): Show | 13 | HG00099.hp2 HG00140.hp2 HG00597.hp1 others(10): Show |
intron_variant | MODIFIER | c.657+1889_657+1890d others(4): Show |
MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 8/9 | chr2 | 31881495 | ||||||
chr2:31881495
|
TA | T | 32 | a0001c0001t0001g0034a0001c0001t0001g0069a0001c0001t0001g0071others(29): Show | 32 | HG00642.hp2 HG01070.hp1 HG01071.hp2 others(29): Show |
intron_variant | MODIFIER | c.657+1890delT | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 8/9 | chr2 | 31881495 | ||||||
chr2:31881495
|
TAA | T | 10 | a0001c0001t0001g0191a0001c0001t0001g0252a0001c0001t0001g0272others(7): Show | 10 | HG01243.hp2 HG02155.hp2 HG02615.hp2 others(7): Show |
intron_variant | MODIFIER | c.657+1889_657+1890d others(4): Show |
MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 8/9 | chr2 | 31881495 | ||||||
chr2:31881495
|
TAAA | T | 43 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0011others(40): Show | 43 | HG01168.hp1 HG01169.hp2 HG01255.hp2 others(40): Show |
intron_variant | MODIFIER | c.657+1888_657+1890d others(5): Show |
MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 8/9 | chr2 | 31881495 | ||||||
chr2:31881846
|
G | C | 2 | a0001c0001t0001g0236a0001c0001t0001g0237 | 2 | HG03139.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.657+1540C>G | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 8/9 | chr2 | 31881846 | ||||||
chr2:31881872
|
G | A | 6 | a0001c0001t0001g0272a0001c0001t0001g0273a0001c0001t0001g0274others(3): Show | 6 | HG01243.hp2 HG01891.hp1 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.657+1514C>T | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 8/9 | chr2 | 31881872 | ||||||
chr2:31881974
|
G | A | 1 | a0001c0001t0001g0008 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.657+1412C>T | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 8/9 | chr2 | 31881974 | ||||||
chr2:31882059
|
G | A | 2 | a0001c0001t0001g0049a0001c0001t0001g0070 | 2 | HG02004.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.657+1327C>T | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 8/9 | chr2 | 31882059 | ||||||
chr2:31882143
|
C | CTAAA | 3 | a0001c0001t0001g0272a0001c0001t0001g0273a0001c0001t0001g0274 | 3 | HG01243.hp2 HG02615.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.657+1239_657+1242d others(6): Show |
MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 8/9 | chr2 | 31882143 | ||||||
chr2:31882332
|
A | C | 4 | a0001c0001t0001g0292a0001c0001t0001g0293a0001c0001t0001g0294others(1): Show | 4 | HG02258.hp1 HG03041.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.657+1054T>G | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 8/9 | chr2 | 31882332 | ||||||
chr2:31882481
|
C | T | 299 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(296): Show | 299 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(296): Show |
intron_variant | MODIFIER | c.657+905G>A | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 8/9 | chr2 | 31882481 | ||||||
chr2:31882485
|
A | G | 6 | a0001c0001t0001g0099a0001c0001t0001g0102a0001c0001t0001g0208others(3): Show | 6 | HG01109.hp2 HG01496.hp1 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.657+901T>C | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 8/9 | chr2 | 31882485 | ||||||
chr2:31882717
|
C | T | 62 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0011others(59): Show | 62 | HG01168.hp1 HG01169.hp2 HG01243.hp2 others(59): Show |
intron_variant | MODIFIER | c.657+669G>A | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 8/9 | chr2 | 31882717 | ||||||
chr2:31882736
|
TATG | T | 3 | a0001c0001t0002g0003a0001c0001t0002g0004a0001c0001t0002g0005 | 3 | HG01891.hp1 HG02897.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.657+647_657+649del others(3): Show |
MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 8/9 | chr2 | 31882736 | ||||||
chr2:31882924
|
T | C | 48 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0011others(45): Show | 48 | HG01168.hp1 HG01169.hp2 HG01255.hp2 others(45): Show |
intron_variant | MODIFIER | c.657+462A>G | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 8/9 | chr2 | 31882924 | ||||||
chr2:31883204
|
G | A | 1 | a0001c0001t0001g0189 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.657+182C>T | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 8/9 | chr2 | 31883204 | ||||||
chr2:31883723
|
T | C | 1 | a0001c0001t0001g0115 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.581-261A>G | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 7/9 | chr2 | 31883723 | ||||||
chr2:31883839
|
T | G | 1 | a0001c0001t0001g0129 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.581-377A>C | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 7/9 | chr2 | 31883839 | ||||||
chr2:31883903
|
G | A | 13 | a0001c0001t0001g0078a0001c0001t0001g0099a0001c0001t0001g0102others(10): Show | 13 | HG01106.hp1 HG01109.hp2 HG01361.hp1 others(10): Show |
intron_variant | MODIFIER | c.581-441C>T | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 7/9 | chr2 | 31883903 | ||||||
chr2:31883903
|
GA | G | 6 | a0001c0001t0001g0216a0001c0001t0001g0217a0001c0001t0001g0218others(3): Show | 6 | HG01070.hp1 HG01071.hp2 HG01261.hp2 others(3): Show |
intron_variant | MODIFIER | c.581-442delT | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 7/9 | chr2 | 31883903 | ||||||
chr2:31884029
|
G | A | 1 | a0001c0001t0001g0284 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.581-567C>T | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 7/9 | chr2 | 31884029 | ||||||
chr2:31884234
|
A | C | 4 | a0001c0001t0001g0292a0001c0001t0001g0293a0001c0001t0001g0294others(1): Show | 4 | HG02258.hp1 HG03041.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.581-772T>G | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 7/9 | chr2 | 31884234 | ||||||
chr2:31884234
|
A | G | 3 | a0001c0001t0001g0272a0001c0001t0001g0273a0001c0001t0001g0274 | 3 | HG01243.hp2 HG02615.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.581-772T>C | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 7/9 | chr2 | 31884234 | ||||||
chr2:31884296
|
C | T | 2 | a0001c0001t0001g0271a0001c0001t0001g0296 | 2 | HG02280.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.581-834G>A | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 7/9 | chr2 | 31884296 | ||||||
chr2:31884326
|
A | C | 3 | a0001c0001t0001g0232a0001c0001t0001g0233a0001c0001t0001g0234 | 3 | HG01361.hp1 HG03927.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.581-864T>G | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 7/9 | chr2 | 31884326 | ||||||
chr2:31884346
|
T | A | 1 | a0001c0001t0001g0278 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.581-884A>T | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 7/9 | chr2 | 31884346 | ||||||
chr2:31884359
|
A | G | 1 | a0001c0001t0001g0200 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.581-897T>C | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 7/9 | chr2 | 31884359 | ||||||
chr2:31884364
|
CTTAATG | C | 48 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0011others(45): Show | 48 | HG01168.hp1 HG01169.hp2 HG01255.hp2 others(45): Show |
intron_variant | MODIFIER | c.581-908_581-903del others(6): Show |
MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 7/9 | chr2 | 31884364 | ||||||
chr2:31884463
|
G | A | 17 | a0001c0001t0001g0078a0001c0001t0001g0099a0001c0001t0001g0102others(14): Show | 17 | HG01106.hp1 HG01109.hp2 HG01361.hp1 others(14): Show |
intron_variant | MODIFIER | c.581-1001C>T | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 7/9 | chr2 | 31884463 | ||||||
chr2:31884519
|
T | C | 1 | a0001c0001t0001g0088 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.581-1057A>G | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 7/9 | chr2 | 31884519 | ||||||
chr2:31884706
|
T | G | 3 | a0001c0001t0001g0232a0001c0001t0001g0233a0001c0001t0001g0234 | 3 | HG01361.hp1 HG03927.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.581-1244A>C | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 7/9 | chr2 | 31884706 | ||||||
chr2:31884733
|
G | A | 1 | a0001c0001t0001g0296 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.581-1271C>T | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 7/9 | chr2 | 31884733 | ||||||
chr2:31884827
|
T | C | 1 | a0001c0001t0001g0136 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.581-1365A>G | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 7/9 | chr2 | 31884827 | ||||||
chr2:31884935
|
TAAAAA | T | 48 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0011others(45): Show | 48 | HG01168.hp1 HG01169.hp2 HG01255.hp2 others(45): Show |
intron_variant | MODIFIER | c.581-1478_581-1474d others(7): Show |
MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 7/9 | chr2 | 31884935 | ||||||
chr2:31885245
|
G | A | 1 | a0001c0001t0001g0242 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.581-1783C>T | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 7/9 | chr2 | 31885245 | ||||||
chr2:31885257
|
C | G | 4 | a0001c0001t0001g0236a0001c0001t0001g0237a0001c0001t0001g0271others(1): Show | 4 | HG02280.hp2 HG03139.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.581-1795G>C | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 7/9 | chr2 | 31885257 | ||||||
chr2:31885346
|
C | A | 1 | a0001c0001t0001g0123 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.581-1884G>T | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 7/9 | chr2 | 31885346 | ||||||
chr2:31885426
|
T | C | 5 | a0001c0001t0001g0197a0001c0001t0001g0198a0001c0001t0001g0199others(2): Show | 5 | HG02622.hp2 HG02922.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.581-1964A>G | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 7/9 | chr2 | 31885426 | ||||||
chr2:31885656
|
T | C | 18 | a0001c0001t0001g0015a0001c0001t0001g0078a0001c0001t0001g0099others(15): Show | 18 | HG01106.hp1 HG01109.hp2 HG01361.hp1 others(15): Show |
intron_variant | MODIFIER | c.581-2194A>G | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 7/9 | chr2 | 31885656 | ||||||
chr2:31885751
|
T | C | 2 | a0001c0001t0001g0104a0001c0001t0001g0105 | 2 | NA18984.hp1 NA19070.hp2 |
intron_variant | MODIFIER | c.581-2289A>G | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 7/9 | chr2 | 31885751 | ||||||
chr2:31885820
|
A | T | 80 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0011others(77): Show | 80 | HG01106.hp1 HG01109.hp2 HG01168.hp1 others(77): Show |
intron_variant | MODIFIER | c.581-2358T>A | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 7/9 | chr2 | 31885820 | ||||||
chr2:31885929
|
G | C | 5 | a0001c0001t0001g0038a0001c0001t0001g0039a0001c0001t0001g0052others(2): Show | 5 | HG01943.hp2 HG01975.hp2 HG02148.hp1 others(2): Show |
intron_variant | MODIFIER | c.581-2467C>G | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 7/9 | chr2 | 31885929 | ||||||
chr2:31886198
|
G | A | 2 | a0001c0001t0001g0243a0001c0001t0001g0268 | 2 | HG01891.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.581-2736C>T | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 7/9 | chr2 | 31886198 | ||||||
chr2:31886401
|
T | C | 3 | a0001c0001t0001g0275a0001c0001t0001g0276a0001c0001t0001g0277 | 3 | HG02055.hp1 HG03471.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.581-2939A>G | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 7/9 | chr2 | 31886401 | ||||||
chr2:31886569
|
C | T | 3 | a0001c0001t0001g0254a0001c0001t0001g0258a0001c0001t0001g0259 | 3 | HG01168.hp1 HG01169.hp2 HG01433.hp2 |
intron_variant | MODIFIER | c.581-3107G>A | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 7/9 | chr2 | 31886569 | ||||||
chr2:31886736
|
T | A | 13 | a0001c0001t0001g0244a0001c0001t0001g0249a0001c0001t0001g0250others(10): Show | 13 | HG02083.hp2 NA18953.hp2 NA18964.hp2 others(10): Show |
intron_variant | MODIFIER | c.581-3274A>T | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 7/9 | chr2 | 31886736 | ||||||
chr2:31886882
|
T | C | 3 | a0001c0001t0002g0003a0001c0001t0002g0004a0001c0001t0002g0005 | 3 | HG01891.hp1 HG02897.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.581-3420A>G | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 7/9 | chr2 | 31886882 | ||||||
chr2:31887173
|
T | C | 1 | a0001c0001t0001g0191 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.581-3711A>G | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 7/9 | chr2 | 31887173 | ||||||
chr2:31887204
|
C | G | 3 | a0001c0001t0001g0069a0001c0001t0001g0071a0001c0001t0001g0072 | 3 | HG02717.hp1 HG03195.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.581-3742G>C | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 7/9 | chr2 | 31887204 | ||||||
chr2:31887291
|
C | G | 2 | a0001c0001t0001g0011a0001c0001t0001g0013 | 2 | NA18940.hp1 NA19064.hp1 |
intron_variant | MODIFIER | c.581-3829G>C | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 7/9 | chr2 | 31887291 | ||||||
chr2:31887362
|
T | C | 1 | a0001c0001t0001g0193 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.581-3900A>G | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 7/9 | chr2 | 31887362 | ||||||
chr2:31887397
|
T | A | 111 | a0001c0001t0001g0001a0001c0001t0001g0015a0001c0001t0001g0017others(108): Show | 111 | HG00140.hp2 HG00423.hp2 HG00438.hp1 others(108): Show |
intron_variant | MODIFIER | c.581-3935A>T | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 7/9 | chr2 | 31887397 | ||||||
chr2:31887583
|
T | C | 50 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0011others(47): Show | 50 | HG01168.hp1 HG01169.hp2 HG01255.hp2 others(47): Show |
intron_variant | MODIFIER | c.581-4121A>G | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 7/9 | chr2 | 31887583 | ||||||
chr2:31887657
|
G | C | 56 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0011others(53): Show | 56 | HG01168.hp1 HG01169.hp2 HG01255.hp2 others(53): Show |
intron_variant | MODIFIER | c.581-4195C>G | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 7/9 | chr2 | 31887657 | ||||||
chr2:31887726
|
A | G | 3 | a0001c0001t0001g0232a0001c0001t0001g0233a0001c0001t0001g0234 | 3 | HG01361.hp1 HG03927.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.581-4264T>C | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 7/9 | chr2 | 31887726 | ||||||
chr2:31887787
|
C | T | 71 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0011others(68): Show | 71 | HG01106.hp1 HG01109.hp2 HG01168.hp1 others(68): Show |
intron_variant | MODIFIER | c.580+4205G>A | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 7/9 | chr2 | 31887787 | ||||||
chr2:31888166
|
A | T | 3 | a0001c0001t0001g0232a0001c0001t0001g0233a0001c0001t0001g0234 | 3 | HG01361.hp1 HG03927.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.580+3826T>A | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 7/9 | chr2 | 31888166 | ||||||
chr2:31888269
|
A | AG | 3 | a0001c0001t0001g0232a0001c0001t0001g0233a0001c0001t0001g0234 | 3 | HG01361.hp1 HG03927.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.580+3722dupC | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 7/9 | chr2 | 31888269 | ||||||
chr2:31889386
|
T | C | 1 | a0001c0001t0001g0232 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.580+2606A>G | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 7/9 | chr2 | 31889386 | ||||||
chr2:31889430
|
A | T | 1 | a0001c0001t0001g0296 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.580+2562T>A | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 7/9 | chr2 | 31889430 | ||||||
chr2:31889500
|
C | T | 1 | a0001c0001t0001g0066 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.580+2492G>A | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 7/9 | chr2 | 31889500 | ||||||
chr2:31889614
|
C | T | 1 | a0001c0001t0001g0133 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.580+2378G>A | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 7/9 | chr2 | 31889614 | ||||||
chr2:31889788
|
G | A | 1 | a0001c0001t0001g0282 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.580+2204C>T | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 7/9 | chr2 | 31889788 | ||||||
chr2:31890474
|
C | A | 1 | a0001c0001t0001g0185 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.580+1518G>T | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 7/9 | chr2 | 31890474 | ||||||
chr2:31890620
|
G | T | 1 | a0001c0001t0001g0027 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.580+1372C>A | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 7/9 | chr2 | 31890620 | ||||||
chr2:31890762
|
G | A | 1 | a0001c0001t0001g0030 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.580+1230C>T | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 7/9 | chr2 | 31890762 | ||||||
chr2:31890835
|
T | C | 3 | a0001c0001t0002g0003a0001c0001t0002g0004a0001c0001t0002g0005 | 3 | HG01891.hp1 HG02897.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.580+1157A>G | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 7/9 | chr2 | 31890835 | ||||||
chr2:31891312
|
G | A | 1 | a0001c0001t0001g0295 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.580+680C>T | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 7/9 | chr2 | 31891312 | ||||||
chr2:31891345
|
A | G | 4 | a0001c0001t0001g0216a0001c0001t0001g0217a0001c0001t0001g0218others(1): Show | 4 | HG01070.hp1 HG01261.hp2 NA20752.hp2 others(1): Show |
intron_variant | MODIFIER | c.580+647T>C | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 7/9 | chr2 | 31891345 | ||||||
chr2:31891895
|
A | C | 9 | a0001c0001t0001g0018a0001c0001t0001g0093a0001c0001t0001g0094others(6): Show | 9 | NA18942.hp1 NA18943.hp2 NA18944.hp1 others(6): Show |
intron_variant | MODIFIER | c.580+97T>G | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 7/9 | chr2 | 31891895 | ||||||
chr2:31891928
|
GAA | G | 5 | a0001c0001t0001g0197a0001c0001t0001g0198a0001c0001t0001g0199others(2): Show | 5 | HG02622.hp2 HG02922.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.580+62_580+63delTT | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 7/9 | chr2 | 31891928 | ||||||
chr2:31892529
|
T | C | 1 | a0001c0001t0001g0301 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.438-395A>G | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 6/9 | chr2 | 31892529 | ||||||
chr2:31892592
|
C | T | 1 | a0001c0001t0001g0296 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.438-458G>A | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 6/9 | chr2 | 31892592 | ||||||
chr2:31892667
|
T | G | 1 | a0001c0001t0001g0194 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.438-533A>C | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 6/9 | chr2 | 31892667 | ||||||
chr2:31892846
|
G | C | 1 | a0001c0001t0001g0203 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.438-712C>G | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 6/9 | chr2 | 31892846 | ||||||
chr2:31892929
|
T | A | 3 | a0001c0001t0002g0003a0001c0001t0002g0004a0001c0001t0002g0005 | 3 | HG01891.hp1 HG02897.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.438-795A>T | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 6/9 | chr2 | 31892929 | ||||||
chr2:31893137
|
G | T | 3 | a0001c0001t0001g0029a0001c0001t0001g0154a0001c0001t0001g0155 | 3 | HG02071.hp1 NA18612.hp1 NA19003.hp2 |
intron_variant | MODIFIER | c.438-1003C>A | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 6/9 | chr2 | 31893137 | ||||||
chr2:31893177
|
G | A | 1 | a0001c0001t0001g0023 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.438-1043C>T | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 6/9 | chr2 | 31893177 | ||||||
chr2:31893487
|
A | T | 61 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0011others(58): Show | 61 | HG01081.hp2 HG01168.hp1 HG01169.hp2 others(58): Show |
intron_variant | MODIFIER | c.438-1353T>A | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 6/9 | chr2 | 31893487 | ||||||
chr2:31893756
|
C | T | 3 | a0001c0001t0002g0003a0001c0001t0002g0004a0001c0001t0002g0005 | 3 | HG01891.hp1 HG02897.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.438-1622G>A | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 6/9 | chr2 | 31893756 | ||||||
chr2:31893791
|
CAT | C | 14 | a0001c0001t0001g0032a0001c0001t0001g0033a0001c0001t0001g0040others(11): Show | 14 | HG00741.hp1 HG01433.hp1 HG02004.hp1 others(11): Show |
intron_variant | MODIFIER | c.438-1659_438-1658d others(4): Show |
MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 6/9 | chr2 | 31893791 | ||||||
chr2:31893867
|
G | A | 1 | a0001c0001t0001g0207 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.438-1733C>T | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 6/9 | chr2 | 31893867 | ||||||
chr2:31893924
|
C | A | 1 | a0001c0001t0001g0118 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.438-1790G>T | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 6/9 | chr2 | 31893924 | ||||||
chr2:31894050
|
G | A | 1 | a0001c0001t0001g0078 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.438-1916C>T | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 6/9 | chr2 | 31894050 | ||||||
chr2:31894523
|
C | T | 1 | a0001c0001t0001g0278 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.438-2389G>A | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 6/9 | chr2 | 31894523 | ||||||
chr2:31894649
|
C | T | 1 | a0001c0001t0001g0042 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.438-2515G>A | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 6/9 | chr2 | 31894649 | ||||||
chr2:31895073
|
T | C | 1 | a0001c0001t0001g0291 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.438-2939A>G | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 6/9 | chr2 | 31895073 | ||||||
chr2:31895257
|
T | A | 2 | a0001c0001t0001g0074a0001c0001t0001g0075 | 2 | NA18956.hp1 NA18968.hp1 |
intron_variant | MODIFIER | c.438-3123A>T | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 6/9 | chr2 | 31895257 | ||||||
chr2:31895354
|
A | G | 289 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(286): Show | 289 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(286): Show |
intron_variant | MODIFIER | c.438-3220T>C | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 6/9 | chr2 | 31895354 | ||||||
chr2:31895675
|
A | G | 2 | a0001c0001t0001g0236a0001c0001t0001g0237 | 2 | HG03139.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.438-3541T>C | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 6/9 | chr2 | 31895675 | ||||||
chr2:31895837
|
C | CT | 84 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0008others(81): Show | 84 | HG00408.hp2 HG00438.hp1 HG00438.hp2 others(81): Show |
intron_variant | MODIFIER | c.438-3704dupA | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 6/9 | chr2 | 31895837 | ||||||
chr2:31895837
|
C | CTT | 10 | a0001c0001t0001g0240a0001c0001t0001g0245a0001c0001t0001g0248others(7): Show | 10 | HG01243.hp2 HG02055.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.438-3705_438-3704d others(4): Show |
MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 6/9 | chr2 | 31895837 | ||||||
chr2:31895837
|
CTT | C | 7 | a0001c0001t0001g0078a0001c0001t0001g0185a0001c0001t0001g0215others(4): Show | 7 | HG01106.hp1 HG01891.hp1 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.438-3705_438-3704d others(4): Show |
MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 6/9 | chr2 | 31895837 | ||||||
chr2:31895867
|
C | T | 4 | a0001c0001t0001g0239a0001c0001t0001g0240a0001c0001t0001g0241others(1): Show | 4 | HG02723.hp1 HG02809.hp2 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.438-3733G>A | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 6/9 | chr2 | 31895867 | ||||||
chr2:31895882
|
G | A | 1 | a0001c0001t0001g0229 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.438-3748C>T | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 6/9 | chr2 | 31895882 | ||||||
chr2:31895921
|
T | C | 3 | a0001c0001t0001g0275a0001c0001t0001g0276a0001c0001t0001g0277 | 3 | HG02055.hp1 HG03471.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.438-3787A>G | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 6/9 | chr2 | 31895921 | ||||||
chr2:31896090
|
G | A | 2 | a0001c0001t0001g0185a0001c0001t0001g0215 | 2 | HG01106.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.438-3956C>T | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 6/9 | chr2 | 31896090 | ||||||
chr2:31896187
|
T | C | 4 | a0001c0001t0001g0292a0001c0001t0001g0293a0001c0001t0001g0294others(1): Show | 4 | HG02258.hp1 HG03041.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.438-4053A>G | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 6/9 | chr2 | 31896187 | ||||||
chr2:31896215
|
A | G | 1 | a0001c0001t0001g0038 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.438-4081T>C | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 6/9 | chr2 | 31896215 | ||||||
chr2:31896421
|
C | A | 1 | a0001c0001t0001g0284 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.438-4287G>T | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 6/9 | chr2 | 31896421 | ||||||
chr2:31896680
|
A | G | 2 | a0001c0001t0001g0100a0001c0001t0001g0192 | 2 | HG03209.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.438-4546T>C | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 6/9 | chr2 | 31896680 | ||||||
chr2:31896695
|
T | A | 1 | a0001c0001t0001g0186 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.438-4561A>T | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 6/9 | chr2 | 31896695 | ||||||
chr2:31896745
|
T | TATTTGTA others(62): Show |
1 | a0001c0001t0001g0161 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.438-4680_438-4612d others(71): Show |
MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 6/9 | chr2 | 31896745 | ||||||
chr2:31896875
|
C | A | 4 | a0001c0001t0001g0292a0001c0001t0001g0293a0001c0001t0001g0294others(1): Show | 4 | HG02258.hp1 HG03041.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.438-4741G>T | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 6/9 | chr2 | 31896875 | ||||||
chr2:31897131
|
T | C | 64 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0011others(61): Show | 64 | HG01168.hp1 HG01169.hp2 HG01243.hp2 others(61): Show |
intron_variant | MODIFIER | c.438-4997A>G | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 6/9 | chr2 | 31897131 | ||||||
chr2:31897233
|
C | T | 1 | a0001c0001t0001g0058 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.438-5099G>A | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 6/9 | chr2 | 31897233 | ||||||
chr2:31897350
|
G | T | 3 | a0001c0001t0002g0003a0001c0001t0002g0004a0001c0001t0002g0005 | 3 | HG01891.hp1 HG02897.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.438-5216C>A | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 6/9 | chr2 | 31897350 | ||||||
chr2:31897517
|
A | G | 61 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0011others(58): Show | 61 | HG01168.hp1 HG01169.hp2 HG01255.hp2 others(58): Show |
intron_variant | MODIFIER | c.438-5383T>C | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 6/9 | chr2 | 31897517 | ||||||
chr2:31897585
|
T | C | 2 | a0001c0001t0001g0185a0001c0001t0001g0215 | 2 | HG01106.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.438-5451A>G | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 6/9 | chr2 | 31897585 | ||||||
chr2:31897597
|
T | C | 1 | a0001c0001t0001g0221 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.438-5463A>G | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 6/9 | chr2 | 31897597 | ||||||
chr2:31897663
|
T | C | 1 | a0001c0001t0001g0215 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.438-5529A>G | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 6/9 | chr2 | 31897663 | ||||||
chr2:31897826
|
A | G | 4 | a0001c0001t0001g0253a0001c0001t0001g0255a0001c0001t0001g0256others(1): Show | 4 | HG01257.hp2 HG01258.hp1 HG03704.hp2 others(1): Show |
intron_variant | MODIFIER | c.438-5692T>C | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 6/9 | chr2 | 31897826 | ||||||
chr2:31897830
|
A | G | 4 | a0001c0001t0001g0253a0001c0001t0001g0255a0001c0001t0001g0256others(1): Show | 4 | HG01257.hp2 HG01258.hp1 HG03704.hp2 others(1): Show |
intron_variant | MODIFIER | c.438-5696T>C | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 6/9 | chr2 | 31897830 | ||||||
chr2:31897836
|
G | T | 4 | a0001c0001t0001g0253a0001c0001t0001g0255a0001c0001t0001g0256others(1): Show | 4 | HG01257.hp2 HG01258.hp1 HG03704.hp2 others(1): Show |
intron_variant | MODIFIER | c.438-5702C>A | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 6/9 | chr2 | 31897836 | ||||||
chr2:31897838
|
A | G | 4 | a0001c0001t0001g0253a0001c0001t0001g0255a0001c0001t0001g0256others(1): Show | 4 | HG01257.hp2 HG01258.hp1 HG03704.hp2 others(1): Show |
intron_variant | MODIFIER | c.438-5704T>C | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 6/9 | chr2 | 31897838 | ||||||
chr2:31897847
|
T | C | 4 | a0001c0001t0001g0253a0001c0001t0001g0255a0001c0001t0001g0256others(1): Show | 4 | HG01257.hp2 HG01258.hp1 HG03704.hp2 others(1): Show |
intron_variant | MODIFIER | c.438-5713A>G | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 6/9 | chr2 | 31897847 | ||||||
chr2:31897850
|
G | A | 4 | a0001c0001t0001g0253a0001c0001t0001g0255a0001c0001t0001g0256others(1): Show | 4 | HG01257.hp2 HG01258.hp1 HG03704.hp2 others(1): Show |
intron_variant | MODIFIER | c.438-5716C>T | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 6/9 | chr2 | 31897850 | ||||||
chr2:31897851
|
C | CTT | 4 | a0001c0001t0001g0253a0001c0001t0001g0255a0001c0001t0001g0256others(1): Show | 4 | HG01257.hp2 HG01258.hp1 HG03704.hp2 others(1): Show |
intron_variant | MODIFIER | c.438-5719_438-5718d others(4): Show |
MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 6/9 | chr2 | 31897851 | ||||||
chr2:31897869
|
A | C | 4 | a0001c0001t0001g0253a0001c0001t0001g0255a0001c0001t0001g0256others(1): Show | 4 | HG01257.hp2 HG01258.hp1 HG03704.hp2 others(1): Show |
intron_variant | MODIFIER | c.438-5735T>G | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 6/9 | chr2 | 31897869 | ||||||
chr2:31897875
|
T | C | 2 | a0001c0001t0001g0083a0001c0001t0001g0084 | 2 | HG03139.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.438-5741A>G | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 6/9 | chr2 | 31897875 | ||||||
chr2:31897877
|
C | T | 4 | a0001c0001t0001g0253a0001c0001t0001g0255a0001c0001t0001g0256others(1): Show | 4 | HG01257.hp2 HG01258.hp1 HG03704.hp2 others(1): Show |
intron_variant | MODIFIER | c.438-5743G>A | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 6/9 | chr2 | 31897877 | ||||||
chr2:31897879
|
C | G | 4 | a0001c0001t0001g0253a0001c0001t0001g0255a0001c0001t0001g0256others(1): Show | 4 | HG01257.hp2 HG01258.hp1 HG03704.hp2 others(1): Show |
intron_variant | MODIFIER | c.438-5745G>C | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 6/9 | chr2 | 31897879 | ||||||
chr2:31897889
|
T | C | 4 | a0001c0001t0001g0253a0001c0001t0001g0255a0001c0001t0001g0256others(1): Show | 4 | HG01257.hp2 HG01258.hp1 HG03704.hp2 others(1): Show |
intron_variant | MODIFIER | c.438-5755A>G | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 6/9 | chr2 | 31897889 | ||||||
chr2:31897893
|
A | G | 4 | a0001c0001t0001g0253a0001c0001t0001g0255a0001c0001t0001g0256others(1): Show | 4 | HG01257.hp2 HG01258.hp1 HG03704.hp2 others(1): Show |
intron_variant | MODIFIER | c.438-5759T>C | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 6/9 | chr2 | 31897893 | ||||||
chr2:31897895
|
T | C | 4 | a0001c0001t0001g0253a0001c0001t0001g0255a0001c0001t0001g0256others(1): Show | 4 | HG01257.hp2 HG01258.hp1 HG03704.hp2 others(1): Show |
intron_variant | MODIFIER | c.438-5761A>G | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 6/9 | chr2 | 31897895 | ||||||
chr2:31897896
|
G | T | 4 | a0001c0001t0001g0253a0001c0001t0001g0255a0001c0001t0001g0256others(1): Show | 4 | HG01257.hp2 HG01258.hp1 HG03704.hp2 others(1): Show |
intron_variant | MODIFIER | c.438-5762C>A | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 6/9 | chr2 | 31897896 | ||||||
chr2:31897908
|
T | A | 4 | a0001c0001t0001g0253a0001c0001t0001g0255a0001c0001t0001g0256others(1): Show | 4 | HG01257.hp2 HG01258.hp1 HG03704.hp2 others(1): Show |
intron_variant | MODIFIER | c.438-5774A>T | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 6/9 | chr2 | 31897908 | ||||||
chr2:31897914
|
G | A | 4 | a0001c0001t0001g0253a0001c0001t0001g0255a0001c0001t0001g0256others(1): Show | 4 | HG01257.hp2 HG01258.hp1 HG03704.hp2 others(1): Show |
intron_variant | MODIFIER | c.438-5780C>T | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 6/9 | chr2 | 31897914 | ||||||
chr2:31897919
|
T | C | 4 | a0001c0001t0001g0253a0001c0001t0001g0255a0001c0001t0001g0256others(1): Show | 4 | HG01257.hp2 HG01258.hp1 HG03704.hp2 others(1): Show |
intron_variant | MODIFIER | c.438-5785A>G | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 6/9 | chr2 | 31897919 | ||||||
chr2:31897920
|
G | A | 4 | a0001c0001t0001g0253a0001c0001t0001g0255a0001c0001t0001g0256others(1): Show | 4 | HG01257.hp2 HG01258.hp1 HG03704.hp2 others(1): Show |
intron_variant | MODIFIER | c.438-5786C>T | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 6/9 | chr2 | 31897920 | ||||||
chr2:31897940
|
T | C | 4 | a0001c0001t0001g0253a0001c0001t0001g0255a0001c0001t0001g0256others(1): Show | 4 | HG01257.hp2 HG01258.hp1 HG03704.hp2 others(1): Show |
intron_variant | MODIFIER | c.438-5806A>G | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 6/9 | chr2 | 31897940 | ||||||
chr2:31897948
|
G | T | 4 | a0001c0001t0001g0253a0001c0001t0001g0255a0001c0001t0001g0256others(1): Show | 4 | HG01257.hp2 HG01258.hp1 HG03704.hp2 others(1): Show |
intron_variant | MODIFIER | c.438-5814C>A | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 6/9 | chr2 | 31897948 | ||||||
chr2:31897959
|
C | G | 4 | a0001c0001t0001g0253a0001c0001t0001g0255a0001c0001t0001g0256others(1): Show | 4 | HG01257.hp2 HG01258.hp1 HG03704.hp2 others(1): Show |
intron_variant | MODIFIER | c.438-5825G>C | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 6/9 | chr2 | 31897959 | ||||||
chr2:31897969
|
T | C | 4 | a0001c0001t0001g0253a0001c0001t0001g0255a0001c0001t0001g0256others(1): Show | 4 | HG01257.hp2 HG01258.hp1 HG03704.hp2 others(1): Show |
intron_variant | MODIFIER | c.438-5835A>G | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 6/9 | chr2 | 31897969 | ||||||
chr2:31897982
|
A | G | 4 | a0001c0001t0001g0253a0001c0001t0001g0255a0001c0001t0001g0256others(1): Show | 4 | HG01257.hp2 HG01258.hp1 HG03704.hp2 others(1): Show |
intron_variant | MODIFIER | c.438-5848T>C | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 6/9 | chr2 | 31897982 | ||||||
chr2:31897994
|
T | C | 1 | a0001c0001t0001g0275 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.438-5860A>G | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 6/9 | chr2 | 31897994 | ||||||
chr2:31898000
|
C | A | 4 | a0001c0001t0001g0253a0001c0001t0001g0255a0001c0001t0001g0256others(1): Show | 4 | HG01257.hp2 HG01258.hp1 HG03704.hp2 others(1): Show |
intron_variant | MODIFIER | c.438-5866G>T | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 6/9 | chr2 | 31898000 | ||||||
chr2:31898001
|
A | G | 4 | a0001c0001t0001g0253a0001c0001t0001g0255a0001c0001t0001g0256others(1): Show | 4 | HG01257.hp2 HG01258.hp1 HG03704.hp2 others(1): Show |
intron_variant | MODIFIER | c.438-5867T>C | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 6/9 | chr2 | 31898001 | ||||||
chr2:31898022
|
C | T | 4 | a0001c0001t0001g0253a0001c0001t0001g0255a0001c0001t0001g0256others(1): Show | 4 | HG01257.hp2 HG01258.hp1 HG03704.hp2 others(1): Show |
intron_variant | MODIFIER | c.438-5888G>A | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 6/9 | chr2 | 31898022 | ||||||
chr2:31898025
|
G | GA | 4 | a0001c0001t0001g0253a0001c0001t0001g0255a0001c0001t0001g0256others(1): Show | 4 | HG01257.hp2 HG01258.hp1 HG03704.hp2 others(1): Show |
intron_variant | MODIFIER | c.438-5892_438-5891i others(3): Show |
MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 6/9 | chr2 | 31898025 | ||||||
chr2:31898029
|
C | T | 4 | a0001c0001t0001g0253a0001c0001t0001g0255a0001c0001t0001g0256others(1): Show | 4 | HG01257.hp2 HG01258.hp1 HG03704.hp2 others(1): Show |
intron_variant | MODIFIER | c.438-5895G>A | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 6/9 | chr2 | 31898029 | ||||||
chr2:31898051
|
A | G | 4 | a0001c0001t0001g0253a0001c0001t0001g0255a0001c0001t0001g0256others(1): Show | 4 | HG01257.hp2 HG01258.hp1 HG03704.hp2 others(1): Show |
intron_variant | MODIFIER | c.438-5917T>C | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 6/9 | chr2 | 31898051 | ||||||
chr2:31898064
|
T | C | 4 | a0001c0001t0001g0253a0001c0001t0001g0255a0001c0001t0001g0256others(1): Show | 4 | HG01257.hp2 HG01258.hp1 HG03704.hp2 others(1): Show |
intron_variant | MODIFIER | c.438-5930A>G | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 6/9 | chr2 | 31898064 | ||||||
chr2:31898080
|
C | T | 4 | a0001c0001t0001g0253a0001c0001t0001g0255a0001c0001t0001g0256others(1): Show | 4 | HG01257.hp2 HG01258.hp1 HG03704.hp2 others(1): Show |
intron_variant | MODIFIER | c.438-5946G>A | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 6/9 | chr2 | 31898080 | ||||||
chr2:31898083
|
T | C | 4 | a0001c0001t0001g0253a0001c0001t0001g0255a0001c0001t0001g0256others(1): Show | 4 | HG01257.hp2 HG01258.hp1 HG03704.hp2 others(1): Show |
intron_variant | MODIFIER | c.438-5949A>G | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 6/9 | chr2 | 31898083 | ||||||
chr2:31898084
|
G | A | 4 | a0001c0001t0001g0253a0001c0001t0001g0255a0001c0001t0001g0256others(1): Show | 4 | HG01257.hp2 HG01258.hp1 HG03704.hp2 others(1): Show |
intron_variant | MODIFIER | c.438-5950C>T | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 6/9 | chr2 | 31898084 | ||||||
chr2:31898088
|
C | A | 4 | a0001c0001t0001g0253a0001c0001t0001g0255a0001c0001t0001g0256others(1): Show | 4 | HG01257.hp2 HG01258.hp1 HG03704.hp2 others(1): Show |
intron_variant | MODIFIER | c.438-5954G>T | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 6/9 | chr2 | 31898088 | ||||||
chr2:31898123
|
G | T | 4 | a0001c0001t0001g0253a0001c0001t0001g0255a0001c0001t0001g0256others(1): Show | 4 | HG01257.hp2 HG01258.hp1 HG03704.hp2 others(1): Show |
intron_variant | MODIFIER | c.438-5989C>A | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 6/9 | chr2 | 31898123 | ||||||
chr2:31898129
|
T | C | 4 | a0001c0001t0001g0253a0001c0001t0001g0255a0001c0001t0001g0256others(1): Show | 4 | HG01257.hp2 HG01258.hp1 HG03704.hp2 others(1): Show |
intron_variant | MODIFIER | c.438-5995A>G | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 6/9 | chr2 | 31898129 | ||||||
chr2:31898130
|
G | A | 4 | a0001c0001t0001g0253a0001c0001t0001g0255a0001c0001t0001g0256others(1): Show | 4 | HG01257.hp2 HG01258.hp1 HG03704.hp2 others(1): Show |
intron_variant | MODIFIER | c.438-5996C>T | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 6/9 | chr2 | 31898130 | ||||||
chr2:31898138
|
T | A | 4 | a0001c0001t0001g0253a0001c0001t0001g0255a0001c0001t0001g0256others(1): Show | 4 | HG01257.hp2 HG01258.hp1 HG03704.hp2 others(1): Show |
intron_variant | MODIFIER | c.438-6004A>T | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 6/9 | chr2 | 31898138 | ||||||
chr2:31898139
|
G | A | 4 | a0001c0001t0001g0253a0001c0001t0001g0255a0001c0001t0001g0256others(1): Show | 4 | HG01257.hp2 HG01258.hp1 HG03704.hp2 others(1): Show |
intron_variant | MODIFIER | c.438-6005C>T | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 6/9 | chr2 | 31898139 | ||||||
chr2:31898143
|
C | T | 4 | a0001c0001t0001g0253a0001c0001t0001g0255a0001c0001t0001g0256others(1): Show | 4 | HG01257.hp2 HG01258.hp1 HG03704.hp2 others(1): Show |
intron_variant | MODIFIER | c.438-6009G>A | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 6/9 | chr2 | 31898143 | ||||||
chr2:31898147
|
A | G | 4 | a0001c0001t0001g0253a0001c0001t0001g0255a0001c0001t0001g0256others(1): Show | 4 | HG01257.hp2 HG01258.hp1 HG03704.hp2 others(1): Show |
intron_variant | MODIFIER | c.438-6013T>C | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 6/9 | chr2 | 31898147 | ||||||
chr2:31898155
|
G | C | 4 | a0001c0001t0001g0253a0001c0001t0001g0255a0001c0001t0001g0256others(1): Show | 4 | HG01257.hp2 HG01258.hp1 HG03704.hp2 others(1): Show |
intron_variant | MODIFIER | c.438-6021C>G | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 6/9 | chr2 | 31898155 | ||||||
chr2:31898156
|
A | C | 4 | a0001c0001t0001g0253a0001c0001t0001g0255a0001c0001t0001g0256others(1): Show | 4 | HG01257.hp2 HG01258.hp1 HG03704.hp2 others(1): Show |
intron_variant | MODIFIER | c.438-6022T>G | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 6/9 | chr2 | 31898156 | ||||||
chr2:31898178
|
A | T | 4 | a0001c0001t0001g0253a0001c0001t0001g0255a0001c0001t0001g0256others(1): Show | 4 | HG01257.hp2 HG01258.hp1 HG03704.hp2 others(1): Show |
intron_variant | MODIFIER | c.438-6044T>A | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 6/9 | chr2 | 31898178 | ||||||
chr2:31898181
|
AT | A | 4 | a0001c0001t0001g0253a0001c0001t0001g0255a0001c0001t0001g0256others(1): Show | 4 | HG01257.hp2 HG01258.hp1 HG03704.hp2 others(1): Show |
intron_variant | MODIFIER | c.438-6048delA | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 6/9 | chr2 | 31898181 | ||||||
chr2:31898195
|
T | A | 4 | a0001c0001t0001g0253a0001c0001t0001g0255a0001c0001t0001g0256others(1): Show | 4 | HG01257.hp2 HG01258.hp1 HG03704.hp2 others(1): Show |
intron_variant | MODIFIER | c.438-6061A>T | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 6/9 | chr2 | 31898195 | ||||||
chr2:31898200
|
C | T | 8 | a0001c0001t0001g0236a0001c0001t0001g0237a0001c0001t0001g0253others(5): Show | 8 | HG01257.hp2 HG01258.hp1 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.438-6066G>A | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 6/9 | chr2 | 31898200 | ||||||
chr2:31898316
|
G | A | 1 | a0001c0001t0001g0101 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.438-6182C>T | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 6/9 | chr2 | 31898316 | ||||||
chr2:31898516
|
T | C | 1 | a0001c0001t0001g0271 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.438-6382A>G | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 6/9 | chr2 | 31898516 | ||||||
chr2:31898519
|
T | C | 3 | a0001c0001t0001g0275a0001c0001t0001g0276a0001c0001t0001g0277 | 3 | HG02055.hp1 HG03471.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.438-6385A>G | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 6/9 | chr2 | 31898519 | ||||||
chr2:31898521
|
C | T | 3 | a0001c0001t0002g0003a0001c0001t0002g0004a0001c0001t0002g0005 | 3 | HG01891.hp1 HG02897.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.438-6387G>A | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 6/9 | chr2 | 31898521 | ||||||
chr2:31898832
|
T | C | 1 | a0001c0001t0001g0030 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.438-6698A>G | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 6/9 | chr2 | 31898832 | ||||||
chr2:31898911
|
T | C | 1 | a0001c0001t0001g0145 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.438-6777A>G | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 6/9 | chr2 | 31898911 | ||||||
chr2:31899130
|
A | T | 1 | a0001c0001t0001g0080 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.438-6996T>A | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 6/9 | chr2 | 31899130 | ||||||
chr2:31899506
|
C | A | 2 | a0001c0001t0001g0049a0001c0001t0001g0070 | 2 | HG02004.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.438-7372G>T | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 6/9 | chr2 | 31899506 | ||||||
chr2:31899768
|
T | C | 1 | a0001c0001t0001g0278 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.438-7634A>G | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 6/9 | chr2 | 31899768 | ||||||
chr2:31899799
|
A | G | 64 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0011others(61): Show | 64 | HG01168.hp1 HG01169.hp2 HG01243.hp2 others(61): Show |
intron_variant | MODIFIER | c.438-7665T>C | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 6/9 | chr2 | 31899799 | ||||||
chr2:31899871
|
A | G | 2 | a0001c0001t0001g0243a0001c0001t0001g0268 | 2 | HG01891.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.438-7737T>C | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 6/9 | chr2 | 31899871 | ||||||
chr2:31899871
|
A | T | 3 | a0001c0001t0001g0283a0001c0001t0001g0289a0001c0001t0001g0302 | 3 | HG01255.hp2 HG01496.hp2 HG02300.hp1 |
intron_variant | MODIFIER | c.438-7737T>A | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 6/9 | chr2 | 31899871 | ||||||
chr2:31899928
|
G | A | 75 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0011others(72): Show | 75 | HG01106.hp1 HG01109.hp2 HG01168.hp1 others(72): Show |
intron_variant | MODIFIER | c.438-7794C>T | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 6/9 | chr2 | 31899928 | ||||||
chr2:31899947
|
C | A | 4 | a0001c0001t0001g0038a0001c0001t0001g0039a0001c0001t0001g0052others(1): Show | 4 | HG01943.hp2 HG01975.hp2 NA18969.hp2 others(1): Show |
intron_variant | MODIFIER | c.438-7813G>T | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 6/9 | chr2 | 31899947 | ||||||
chr2:31900037
|
C | G | 3 | a0001c0001t0001g0275a0001c0001t0001g0276a0001c0001t0001g0277 | 3 | HG02055.hp1 HG03471.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.438-7903G>C | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 6/9 | chr2 | 31900037 | ||||||
chr2:31900122
|
C | T | 1 | a0001c0001t0001g0122 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.438-7988G>A | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 6/9 | chr2 | 31900122 | ||||||
chr2:31900185
|
T | C | 3 | a0001c0001t0001g0275a0001c0001t0001g0276a0001c0001t0001g0277 | 3 | HG02055.hp1 HG03471.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.438-8051A>G | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 6/9 | chr2 | 31900185 | ||||||
chr2:31900480
|
G | A | 2 | a0001c0001t0001g0034a0001c0001t0001g0050 | 2 | NA18955.hp2 NA18963.hp2 |
intron_variant | MODIFIER | c.438-8346C>T | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 6/9 | chr2 | 31900480 | ||||||
chr2:31900818
|
G | A | 3 | a0001c0001t0001g0232a0001c0001t0001g0233a0001c0001t0001g0234 | 3 | HG01361.hp1 HG03927.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.438-8684C>T | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 6/9 | chr2 | 31900818 | ||||||
chr2:31900867
|
C | T | 8 | a0001c0001t0001g0025a0001c0001t0001g0029a0001c0001t0001g0081others(5): Show | 8 | HG02071.hp1 NA18612.hp1 NA18964.hp1 others(5): Show |
intron_variant | MODIFIER | c.438-8733G>A | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 6/9 | chr2 | 31900867 | ||||||
chr2:31900882
|
A | T | 3 | a0001c0001t0001g0272a0001c0001t0001g0273a0001c0001t0001g0274 | 3 | HG01243.hp2 HG02615.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.438-8748T>A | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 6/9 | chr2 | 31900882 | ||||||
chr2:31900985
|
A | G | 59 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0011others(56): Show | 59 | HG01168.hp1 HG01169.hp2 HG01255.hp2 others(56): Show |
intron_variant | MODIFIER | c.438-8851T>C | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 6/9 | chr2 | 31900985 | ||||||
chr2:31901246
|
G | A | 15 | a0001c0001t0001g0078a0001c0001t0001g0185a0001c0001t0001g0215others(12): Show | 15 | HG01106.hp1 HG01109.hp2 HG01243.hp2 others(12): Show |
intron_variant | MODIFIER | c.438-9112C>T | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 6/9 | chr2 | 31901246 | ||||||
chr2:31901351
|
C | T | 1 | a0001c0001t0001g0114 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.438-9217G>A | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 6/9 | chr2 | 31901351 | ||||||
chr2:31901374
|
C | CA | 63 | a0001c0001t0001g0021a0001c0001t0001g0030a0001c0001t0001g0034others(60): Show | 63 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(60): Show |
intron_variant | MODIFIER | c.438-9241dupT | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 6/9 | chr2 | 31901374 | ||||||
chr2:31901374
|
CA | C | 19 | a0001c0001t0001g0010a0001c0001t0001g0023a0001c0001t0001g0024others(16): Show | 19 | HG01106.hp1 HG02055.hp1 HG02258.hp1 others(16): Show |
intron_variant | MODIFIER | c.438-9241delT | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 6/9 | chr2 | 31901374 | ||||||
chr2:31901374
|
CAA | C | 49 | a0001c0001t0001g0008a0001c0001t0001g0011a0001c0001t0001g0012others(46): Show | 49 | HG01168.hp1 HG01169.hp2 HG01255.hp2 others(46): Show |
intron_variant | MODIFIER | c.438-9242_438-9241d others(4): Show |
MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 6/9 | chr2 | 31901374 | ||||||
chr2:31901374
|
CAAAAAAA others(5): Show |
C | 3 | a0001c0001t0001g0049a0001c0001t0001g0089a0001c0001t0001g0090 | 3 | HG02004.hp2 NA18944.hp2 NA19003.hp1 |
intron_variant | MODIFIER | c.438-9252_438-9241d others(14): Show |
MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 6/9 | chr2 | 31901374 | ||||||
chr2:31901956
|
C | T | 62 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0011others(59): Show | 62 | HG01168.hp1 HG01169.hp2 HG01243.hp2 others(59): Show |
intron_variant | MODIFIER | c.438-9822G>A | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 6/9 | chr2 | 31901956 | ||||||
chr2:31901970
|
TA | T | 53 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0011others(50): Show | 53 | HG01168.hp1 HG01169.hp2 HG01255.hp2 others(50): Show |
intron_variant | MODIFIER | c.438-9837delT | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 6/9 | chr2 | 31901970 | ||||||
chr2:31902101
|
G | C | 6 | a0001c0001t0001g0290a0001c0001t0001g0291a0001c0001t0001g0292others(3): Show | 6 | HG01109.hp2 HG02258.hp1 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.438-9967C>G | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 6/9 | chr2 | 31902101 | ||||||
chr2:31902170
|
A | G | 2 | a0001c0001t0001g0074a0001c0001t0001g0075 | 2 | NA18956.hp1 NA18968.hp1 |
intron_variant | MODIFIER | c.438-10036T>C | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 6/9 | chr2 | 31902170 | ||||||
chr2:31902203
|
G | A | 53 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0011others(50): Show | 53 | HG01168.hp1 HG01169.hp2 HG01255.hp2 others(50): Show |
intron_variant | MODIFIER | c.438-10069C>T | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 6/9 | chr2 | 31902203 | ||||||
chr2:31902220
|
C | G | 3 | a0001c0001t0002g0003a0001c0001t0002g0004a0001c0001t0002g0005 | 3 | HG01891.hp1 HG02897.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.438-10086G>C | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 6/9 | chr2 | 31902220 | ||||||
chr2:31902340
|
C | T | 1 | a0001c0001t0001g0278 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.438-10206G>A | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 6/9 | chr2 | 31902340 | ||||||
chr2:31902419
|
T | C | 1 | a0001c0001t0001g0288 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.438-10285A>G | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 6/9 | chr2 | 31902419 | ||||||
chr2:31902659
|
A | G | 1 | a0001c0001t0001g0279 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.438-10525T>C | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 6/9 | chr2 | 31902659 | ||||||
chr2:31902718
|
G | A | 3 | a0001c0001t0001g0069a0001c0001t0001g0071a0001c0001t0001g0072 | 3 | HG02717.hp1 HG03195.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.438-10584C>T | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 6/9 | chr2 | 31902718 | ||||||
chr2:31902760
|
T | G | 1 | a0001c0001t0001g0026 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.438-10626A>C | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 6/9 | chr2 | 31902760 | ||||||
chr2:31903021
|
T | C | 5 | a0001c0001t0001g0197a0001c0001t0001g0198a0001c0001t0001g0199others(2): Show | 5 | HG02622.hp2 HG02922.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.438-10887A>G | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 6/9 | chr2 | 31903021 | ||||||
chr2:31903043
|
A | T | 14 | a0001c0001t0001g0032a0001c0001t0001g0033a0001c0001t0001g0034others(11): Show | 14 | HG00741.hp1 HG01433.hp1 HG02040.hp1 others(11): Show |
intron_variant | MODIFIER | c.438-10909T>A | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 6/9 | chr2 | 31903043 | ||||||
chr2:31903270
|
A | G | 1 | a0001c0001t0001g0075 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.438-11136T>C | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 6/9 | chr2 | 31903270 | ||||||
chr2:31903298
|
T | C | 3 | a0001c0001t0001g0069a0001c0001t0001g0071a0001c0001t0001g0072 | 3 | HG02717.hp1 HG03195.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.438-11164A>G | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 6/9 | chr2 | 31903298 | ||||||
chr2:31903327
|
C | T | 46 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0011others(43): Show | 46 | HG01255.hp2 HG01257.hp2 HG01258.hp1 others(43): Show |
intron_variant | MODIFIER | c.438-11193G>A | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 6/9 | chr2 | 31903327 | ||||||
chr2:31903384
|
C | T | 8 | a0001c0001t0001g0032a0001c0001t0001g0033a0001c0001t0001g0034others(5): Show | 8 | HG00741.hp1 HG01433.hp1 NA18955.hp2 others(5): Show |
intron_variant | MODIFIER | c.438-11250G>A | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 6/9 | chr2 | 31903384 | ||||||
chr2:31903433
|
G | A | 3 | a0001c0001t0001g0069a0001c0001t0001g0071a0001c0001t0001g0072 | 3 | HG02717.hp1 HG03195.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.438-11299C>T | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 6/9 | chr2 | 31903433 | ||||||
chr2:31903489
|
A | C | 89 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(86): Show | 89 | HG00639.hp2 HG00738.hp1 HG00741.hp1 others(86): Show |
intron_variant | MODIFIER | c.438-11355T>G | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 6/9 | chr2 | 31903489 | ||||||
chr2:31903532
|
G | A | 97 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(94): Show | 97 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(94): Show |
intron_variant | MODIFIER | c.438-11398C>T | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 6/9 | chr2 | 31903532 | ||||||
chr2:31903580
|
T | G | 6 | a0001c0001t0001g0290a0001c0001t0001g0291a0001c0001t0001g0292others(3): Show | 6 | HG01109.hp2 HG02258.hp1 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.438-11446A>C | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 6/9 | chr2 | 31903580 | ||||||
chr2:31903646
|
T | C | 1 | a0001c0001t0001g0129 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.438-11512A>G | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 6/9 | chr2 | 31903646 | ||||||
chr2:31903797
|
A | C | 1 | a0001c0001t0001g0136 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.438-11663T>G | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 6/9 | chr2 | 31903797 | ||||||
chr2:31904008
|
A | T | 1 | a0001c0001t0001g0221 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.438-11874T>A | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 6/9 | chr2 | 31904008 | ||||||
chr2:31904100
|
T | C | 2 | a0001c0001t0001g0074a0001c0001t0001g0075 | 2 | NA18956.hp1 NA18968.hp1 |
intron_variant | MODIFIER | c.438-11966A>G | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 6/9 | chr2 | 31904100 | ||||||
chr2:31904308
|
T | G | 1 | a0001c0001t0001g0271 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.438-12174A>C | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 6/9 | chr2 | 31904308 | ||||||
chr2:31904361
|
G | A | 3 | a0001c0001t0001g0232a0001c0001t0001g0233a0001c0001t0001g0234 | 3 | HG01361.hp1 HG03927.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.438-12227C>T | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 6/9 | chr2 | 31904361 | ||||||
chr2:31904418
|
A | G | 1 | a0001c0001t0001g0036 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.438-12284T>C | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 6/9 | chr2 | 31904418 | ||||||
chr2:31904540
|
A | G | 1 | a0001c0001t0001g0284 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.438-12406T>C | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 6/9 | chr2 | 31904540 | ||||||
chr2:31904610
|
A | G | 303 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(300): Show | 303 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(300): Show |
intron_variant | MODIFIER | c.438-12476T>C | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 6/9 | chr2 | 31904610 | ||||||
chr2:31904628
|
G | A | 7 | a0001c0001t0001g0278a0001c0001t0001g0290a0001c0001t0001g0291others(4): Show | 7 | HG01109.hp2 HG02258.hp1 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.438-12494C>T | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 6/9 | chr2 | 31904628 | ||||||
chr2:31904649
|
C | T | 72 | a0001c0001t0001g0007a0001c0001t0001g0017a0001c0001t0001g0018others(69): Show | 72 | HG00099.hp2 HG00140.hp2 HG00423.hp2 others(69): Show |
intron_variant | MODIFIER | c.438-12515G>A | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 6/9 | chr2 | 31904649 | ||||||
chr2:31904661
|
G | A | 1 | a0001c0001t0001g0221 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.438-12527C>T | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 6/9 | chr2 | 31904661 | ||||||
chr2:31904701
|
G | A | 1 | a0001c0001t0001g0178 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.438-12567C>T | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 6/9 | chr2 | 31904701 | ||||||
chr2:31904963
|
A | G | 64 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0011others(61): Show | 64 | HG01168.hp1 HG01169.hp2 HG01243.hp2 others(61): Show |
intron_variant | MODIFIER | c.438-12829T>C | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 6/9 | chr2 | 31904963 | ||||||
chr2:31905054
|
T | C | 73 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0011others(70): Show | 73 | HG01109.hp2 HG01168.hp1 HG01169.hp2 others(70): Show |
intron_variant | MODIFIER | c.437+12872A>G | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 6/9 | chr2 | 31905054 | ||||||
chr2:31905239
|
A | C | 1 | a0001c0001t0001g0115 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.437+12687T>G | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 6/9 | chr2 | 31905239 | ||||||
chr2:31905525
|
A | G | 1 | a0001c0001t0001g0087 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.437+12401T>C | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 6/9 | chr2 | 31905525 | ||||||
chr2:31905747
|
G | C | 1 | a0001c0001t0001g0273 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.437+12179C>G | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 6/9 | chr2 | 31905747 | ||||||
chr2:31905782
|
C | T | 2 | a0001c0001t0002g0003a0001c0001t0002g0005 | 2 | HG01891.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.437+12144G>A | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 6/9 | chr2 | 31905782 | ||||||
chr2:31905934
|
T | C | 3 | a0001c0001t0002g0003a0001c0001t0002g0004a0001c0001t0002g0005 | 3 | HG01891.hp1 HG02897.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.437+11992A>G | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 6/9 | chr2 | 31905934 | ||||||
chr2:31905975
|
A | AT | 6 | a0001c0001t0001g0026a0001c0001t0001g0087a0001c0001t0001g0095others(3): Show | 6 | HG00140.hp2 HG01109.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.437+11950dupA | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 6/9 | chr2 | 31905975 | ||||||
chr2:31906027
|
G | A | 61 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0011others(58): Show | 61 | HG01168.hp1 HG01169.hp2 HG01243.hp2 others(58): Show |
intron_variant | MODIFIER | c.437+11899C>T | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 6/9 | chr2 | 31906027 | ||||||
chr2:31906090
|
A | T | 112 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0015others(109): Show | 112 | HG00099.hp2 HG00140.hp2 HG00423.hp2 others(109): Show |
intron_variant | MODIFIER | c.437+11836T>A | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 6/9 | chr2 | 31906090 | ||||||
chr2:31906118
|
C | G | 9 | a0001c0001t0001g0232a0001c0001t0001g0233a0001c0001t0001g0234others(6): Show | 9 | HG01109.hp2 HG01361.hp1 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.437+11808G>C | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 6/9 | chr2 | 31906118 | ||||||
chr2:31906243
|
T | A | 3 | a0001c0001t0002g0003a0001c0001t0002g0004a0001c0001t0002g0005 | 3 | HG01891.hp1 HG02897.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.437+11683A>T | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 6/9 | chr2 | 31906243 | ||||||
chr2:31906249
|
C | T | 1 | a0001c0001t0001g0278 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.437+11677G>A | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 6/9 | chr2 | 31906249 | ||||||
chr2:31906288
|
G | T | 69 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0011others(66): Show | 69 | HG01109.hp2 HG01168.hp1 HG01169.hp2 others(66): Show |
intron_variant | MODIFIER | c.437+11638C>A | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 6/9 | chr2 | 31906288 | ||||||
chr2:31906317
|
GTTTGTT | G | 3 | a0001c0001t0001g0272a0001c0001t0001g0273a0001c0001t0001g0274 | 3 | HG01243.hp2 HG02615.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.437+11603_437+1160 others(10): Show |
MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 6/9 | chr2 | 31906317 | ||||||
chr2:31906332
|
T | C | 2 | a0001c0001t0001g0233a0001c0001t0001g0234 | 2 | HG03927.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.437+11594A>G | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 6/9 | chr2 | 31906332 | ||||||
chr2:31906355
|
G | A | 3 | a0001c0001t0001g0272a0001c0001t0001g0273a0001c0001t0001g0274 | 3 | HG01243.hp2 HG02615.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.437+11571C>T | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 6/9 | chr2 | 31906355 | ||||||
chr2:31906409
|
C | T | 1 | a0001c0001t0001g0145 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.437+11517G>A | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 6/9 | chr2 | 31906409 | ||||||
chr2:31906411
|
C | T | 61 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0011others(58): Show | 61 | HG01168.hp1 HG01169.hp2 HG01243.hp2 others(58): Show |
intron_variant | MODIFIER | c.437+11515G>A | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 6/9 | chr2 | 31906411 | ||||||
chr2:31906491
|
T | C | 61 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0011others(58): Show | 61 | HG01168.hp1 HG01169.hp2 HG01243.hp2 others(58): Show |
intron_variant | MODIFIER | c.437+11435A>G | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 6/9 | chr2 | 31906491 | ||||||
chr2:31906514
|
G | T | 1 | a0001c0001t0001g0260 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.437+11412C>A | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 6/9 | chr2 | 31906514 | ||||||
chr2:31906529
|
T | G | 1 | a0001c0001t0001g0058 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.437+11397A>C | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 6/9 | chr2 | 31906529 | ||||||
chr2:31906566
|
G | A | 2 | a0001c0001t0001g0290a0001c0001t0001g0291 | 2 | HG01109.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.437+11360C>T | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 6/9 | chr2 | 31906566 | ||||||
chr2:31906614
|
C | T | 61 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0011others(58): Show | 61 | HG01168.hp1 HG01169.hp2 HG01243.hp2 others(58): Show |
intron_variant | MODIFIER | c.437+11312G>A | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 6/9 | chr2 | 31906614 | ||||||
chr2:31906633
|
A | G | 1 | a0001c0001t0001g0184 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.437+11293T>C | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 6/9 | chr2 | 31906633 | ||||||
chr2:31906661
|
T | C | 1 | a0001c0001t0001g0242 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.437+11265A>G | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 6/9 | chr2 | 31906661 | ||||||
chr2:31906686
|
C | T | 2 | a0001c0001t0001g0243a0001c0001t0001g0268 | 2 | HG01891.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.437+11240G>A | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 6/9 | chr2 | 31906686 | ||||||
chr2:31906726
|
C | T | 3 | a0001c0001t0001g0117a0001c0001t0001g0128a0001c0001t0001g0187 | 3 | HG00621.hp2 HG02165.hp1 NA19068.hp1 |
intron_variant | MODIFIER | c.437+11200G>A | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 6/9 | chr2 | 31906726 | ||||||
chr2:31906729
|
C | G | 2 | a0001c0001t0001g0122a0001c0001t0001g0142 | 2 | NA18975.hp2 NA19000.hp2 |
intron_variant | MODIFIER | c.437+11197G>C | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 6/9 | chr2 | 31906729 | ||||||
chr2:31906750
|
T | C | 1 | a0001c0001t0001g0134 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.437+11176A>G | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 6/9 | chr2 | 31906750 | ||||||
chr2:31906846
|
T | A | 6 | a0001c0001t0001g0290a0001c0001t0001g0291a0001c0001t0001g0292others(3): Show | 6 | HG01109.hp2 HG02258.hp1 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.437+11080A>T | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 6/9 | chr2 | 31906846 | ||||||
chr2:31906932
|
T | A | 294 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(291): Show | 294 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(291): Show |
intron_variant | MODIFIER | c.437+10994A>T | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 6/9 | chr2 | 31906932 | ||||||
chr2:31907363
|
T | C | 2 | a0001c0001t0001g0233a0001c0001t0001g0234 | 2 | HG03927.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.437+10563A>G | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 6/9 | chr2 | 31907363 | ||||||
chr2:31907367
|
C | T | 1 | a0001c0001t0001g0164 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.437+10559G>A | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 6/9 | chr2 | 31907367 | ||||||
chr2:31907435
|
A | G | 3 | a0001c0001t0001g0292a0001c0001t0001g0293a0001c0001t0001g0294 | 3 | HG02258.hp1 HG03209.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.437+10491T>C | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 6/9 | chr2 | 31907435 | ||||||
chr2:31907502
|
A | G | 5 | a0001c0001t0001g0098a0001c0001t0001g0101a0001c0001t0001g0114others(2): Show | 5 | HG02055.hp2 HG03486.hp2 HG03516.hp2 others(2): Show |
intron_variant | MODIFIER | c.437+10424T>C | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 6/9 | chr2 | 31907502 | ||||||
chr2:31907550
|
T | A | 3 | a0001c0001t0001g0292a0001c0001t0001g0293a0001c0001t0001g0294 | 3 | HG02258.hp1 HG03209.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.437+10376A>T | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 6/9 | chr2 | 31907550 | ||||||
chr2:31907728
|
A | G | 64 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0011others(61): Show | 64 | HG01168.hp1 HG01169.hp2 HG01243.hp2 others(61): Show |
intron_variant | MODIFIER | c.437+10198T>C | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 6/9 | chr2 | 31907728 | ||||||
chr2:31907741
|
C | G | 3 | a0001c0001t0001g0232a0001c0001t0001g0233a0001c0001t0001g0234 | 3 | HG01361.hp1 HG03927.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.437+10185G>C | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 6/9 | chr2 | 31907741 | ||||||
chr2:31907786
|
A | AAC | 119 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0014others(116): Show | 119 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(116): Show |
intron_variant | MODIFIER | c.437+10138_437+1013 others(6): Show |
MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 6/9 | chr2 | 31907786 | ||||||
chr2:31907786
|
A | AACAC | 26 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0018others(23): Show | 26 | HG00738.hp2 HG01071.hp2 HG01169.hp1 others(23): Show |
intron_variant | MODIFIER | c.437+10136_437+1013 others(8): Show |
MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 6/9 | chr2 | 31907786 | ||||||
chr2:31907786
|
A | AACACAC | 9 | a0001c0001t0001g0078a0001c0001t0001g0098a0001c0001t0001g0106others(6): Show | 9 | HG01070.hp2 HG01071.hp1 HG01168.hp2 others(6): Show |
intron_variant | MODIFIER | c.437+10134_437+1013 others(10): Show |
MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 6/9 | chr2 | 31907786 | ||||||
chr2:31907786
|
A | C | 1 | a0001c0001t0001g0235 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.437+10140T>G | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 6/9 | chr2 | 31907786 | ||||||
chr2:31907786
|
AAC | A | 9 | a0001c0001t0001g0040a0001c0001t0001g0092a0001c0001t0001g0232others(6): Show | 9 | HG01361.hp1 HG01891.hp2 HG02129.hp1 others(6): Show |
intron_variant | MODIFIER | c.437+10138_437+1013 others(6): Show |
MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 6/9 | chr2 | 31907786 | ||||||
chr2:31907786
|
AACAC | A | 49 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0011others(46): Show | 49 | HG01168.hp1 HG01169.hp2 HG01255.hp2 others(46): Show |
intron_variant | MODIFIER | c.437+10136_437+1013 others(8): Show |
MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 6/9 | chr2 | 31907786 | ||||||
chr2:31907818
|
CACAT | C | 3 | a0001c0001t0002g0003a0001c0001t0002g0004a0001c0001t0002g0005 | 3 | HG01891.hp1 HG02897.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.437+10104_437+1010 others(8): Show |
MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 6/9 | chr2 | 31907818 | ||||||
chr2:31907822
|
T | C | 1 | a0001c0001t0001g0273 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.437+10104A>G | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 6/9 | chr2 | 31907822 | ||||||
chr2:31907898
|
CTTAT | C | 4 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0012others(1): Show | 4 | NA18940.hp1 NA18978.hp2 NA18980.hp1 others(1): Show |
intron_variant | MODIFIER | c.437+10024_437+1002 others(8): Show |
MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 6/9 | chr2 | 31907898 | ||||||
chr2:31907932
|
T | C | 4 | a0001c0001t0001g0275a0001c0001t0001g0276a0001c0001t0001g0277others(1): Show | 4 | HG02055.hp1 HG03471.hp1 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.437+9994A>G | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 6/9 | chr2 | 31907932 | ||||||
chr2:31907996
|
G | A | 1 | a0001c0001t0001g0206 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.437+9930C>T | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 6/9 | chr2 | 31907996 | ||||||
chr2:31908187
|
T | C | 1 | a0001c0001t0001g0139 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.437+9739A>G | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 6/9 | chr2 | 31908187 | ||||||
chr2:31908229
|
G | C | 4 | a0001c0001t0001g0292a0001c0001t0001g0293a0001c0001t0001g0294others(1): Show | 4 | HG02258.hp1 HG03041.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.437+9697C>G | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 6/9 | chr2 | 31908229 | ||||||
chr2:31908329
|
T | A | 3 | a0001c0001t0001g0199a0001c0001t0001g0200a0001c0001t0001g0201 | 3 | HG02622.hp2 HG03098.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.437+9597A>T | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 6/9 | chr2 | 31908329 | ||||||
chr2:31908394
|
T | C | 1 | a0001c0001t0001g0295 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.437+9532A>G | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 6/9 | chr2 | 31908394 | ||||||
chr2:31908408
|
T | C | 1 | a0001c0001t0001g0015 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.437+9518A>G | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 6/9 | chr2 | 31908408 | ||||||
chr2:31908542
|
T | C | 1 | a0001c0001t0001g0295 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.437+9384A>G | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 6/9 | chr2 | 31908542 | ||||||
chr2:31908683
|
C | T | 64 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0011others(61): Show | 64 | HG01168.hp1 HG01169.hp2 HG01243.hp2 others(61): Show |
intron_variant | MODIFIER | c.437+9243G>A | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 6/9 | chr2 | 31908683 | ||||||
chr2:31908881
|
A | G | 64 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0011others(61): Show | 64 | HG01168.hp1 HG01169.hp2 HG01243.hp2 others(61): Show |
intron_variant | MODIFIER | c.437+9045T>C | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 6/9 | chr2 | 31908881 | ||||||
chr2:31909279
|
G | A | 1 | a0001c0001t0001g0260 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.437+8647C>T | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 6/9 | chr2 | 31909279 | ||||||
chr2:31909515
|
C | T | 1 | a0001c0001t0001g0260 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.437+8411G>A | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 6/9 | chr2 | 31909515 | ||||||
chr2:31909686
|
C | G | 1 | a0001c0001t0001g0162 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.437+8240G>C | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 6/9 | chr2 | 31909686 | ||||||
chr2:31909776
|
G | C | 1 | a0001c0001t0002g0004 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.437+8150C>G | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 6/9 | chr2 | 31909776 | ||||||
chr2:31909911
|
C | T | 1 | a0001c0001t0001g0149 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.437+8015G>A | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 6/9 | chr2 | 31909911 | ||||||
chr2:31909989
|
A | G | 1 | a0001c0001t0001g0296 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.437+7937T>C | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 6/9 | chr2 | 31909989 | ||||||
chr2:31910048
|
T | C | 3 | a0001c0001t0001g0048a0001c0001t0001g0054a0001c0001t0001g0055 | 3 | NA18953.hp1 NA18977.hp1 NA19056.hp1 |
intron_variant | MODIFIER | c.437+7878A>G | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 6/9 | chr2 | 31910048 | ||||||
chr2:31910116
|
G | A | 1 | a0001c0001t0001g0182 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.437+7810C>T | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 6/9 | chr2 | 31910116 | ||||||
chr2:31910309
|
T | C | 1 | a0001c0001t0001g0046 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.437+7617A>G | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 6/9 | chr2 | 31910309 | ||||||
chr2:31910370
|
T | C | 3 | a0001c0001t0001g0136a0001c0001t0001g0137a0001c0001t0001g0228 | 3 | HG03225.hp1 NA19043.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.437+7556A>G | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 6/9 | chr2 | 31910370 | ||||||
chr2:31910588
|
C | T | 1 | a0001c0001t0001g0278 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.437+7338G>A | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 6/9 | chr2 | 31910588 | ||||||
chr2:31910598
|
T | C | 2 | a0001c0001t0001g0290a0001c0001t0001g0291 | 2 | HG01109.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.437+7328A>G | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 6/9 | chr2 | 31910598 | ||||||
chr2:31910637
|
A | T | 1 | a0001c0001t0002g0003 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.437+7289T>A | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 6/9 | chr2 | 31910637 | ||||||
chr2:31910646
|
G | A | 1 | a0001c0001t0001g0181 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.437+7280C>T | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 6/9 | chr2 | 31910646 | ||||||
chr2:31910685
|
C | A | 1 | a0001c0001t0001g0070 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.437+7241G>T | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 6/9 | chr2 | 31910685 | ||||||
chr2:31910700
|
A | G | 3 | a0001c0001t0001g0232a0001c0001t0001g0233a0001c0001t0001g0234 | 3 | HG01361.hp1 HG03927.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.437+7226T>C | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 6/9 | chr2 | 31910700 | ||||||
chr2:31910872
|
A | C | 1 | a0001c0001t0001g0278 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.437+7054T>G | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 6/9 | chr2 | 31910872 | ||||||
chr2:31910888
|
A | C | 102 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0017others(99): Show | 102 | HG00099.hp2 HG00140.hp2 HG00423.hp2 others(99): Show |
intron_variant | MODIFIER | c.437+7038T>G | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 6/9 | chr2 | 31910888 | ||||||
chr2:31911048
|
A | G | 2 | a0001c0001t0001g0290a0001c0001t0001g0291 | 2 | HG01109.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.437+6878T>C | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 6/9 | chr2 | 31911048 | ||||||
chr2:31911083
|
G | C | 1 | a0001c0001t0001g0165 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.437+6843C>G | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 6/9 | chr2 | 31911083 | ||||||
chr2:31911136
|
T | C | 8 | a0001c0001t0001g0032a0001c0001t0001g0033a0001c0001t0001g0034others(5): Show | 8 | HG00741.hp1 HG01433.hp1 NA18955.hp2 others(5): Show |
intron_variant | MODIFIER | c.437+6790A>G | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 6/9 | chr2 | 31911136 | ||||||
chr2:31911153
|
G | C | 1 | a0001c0001t0001g0034 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.437+6773C>G | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 6/9 | chr2 | 31911153 | ||||||
chr2:31911250
|
C | T | 303 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(300): Show | 303 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(300): Show |
intron_variant | MODIFIER | c.437+6676G>A | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 6/9 | chr2 | 31911250 | ||||||
chr2:31911305
|
A | T | 64 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0011others(61): Show | 64 | HG01168.hp1 HG01169.hp2 HG01243.hp2 others(61): Show |
intron_variant | MODIFIER | c.437+6621T>A | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 6/9 | chr2 | 31911305 | ||||||
chr2:31911336
|
G | A | 1 | a0001c0001t0001g0152 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.437+6590C>T | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 6/9 | chr2 | 31911336 | ||||||
chr2:31911547
|
G | A | 1 | a0001c0001t0001g0015 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.437+6379C>T | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 6/9 | chr2 | 31911547 | ||||||
chr2:31911620
|
T | G | 3 | a0001c0001t0001g0203a0001c0001t0001g0208a0001c0001t0001g0209 | 3 | HG02280.hp1 HG02809.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.437+6306A>C | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 6/9 | chr2 | 31911620 | ||||||
chr2:31912067
|
G | A | 3 | a0001c0001t0001g0292a0001c0001t0001g0293a0001c0001t0001g0294 | 3 | HG02258.hp1 HG03209.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.437+5859C>T | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 6/9 | chr2 | 31912067 | ||||||
chr2:31912172
|
T | C | 2 | a0001c0001t0001g0290a0001c0001t0001g0291 | 2 | HG01109.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.437+5754A>G | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 6/9 | chr2 | 31912172 | ||||||
chr2:31912251
|
G | A | 2 | a0001c0001t0001g0271a0001c0001t0001g0296 | 2 | HG02280.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.437+5675C>T | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 6/9 | chr2 | 31912251 | ||||||
chr2:31912317
|
G | A | 1 | a0001c0001t0001g0232 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.437+5609C>T | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 6/9 | chr2 | 31912317 | ||||||
chr2:31912374
|
A | G | 3 | a0001c0001t0001g0272a0001c0001t0001g0273a0001c0001t0001g0274 | 3 | HG01243.hp2 HG02615.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.437+5552T>C | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 6/9 | chr2 | 31912374 | ||||||
chr2:31912466
|
T | A | 1 | a0001c0001t0001g0226 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.437+5460A>T | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 6/9 | chr2 | 31912466 | ||||||
chr2:31912513
|
C | CA | 18 | a0001c0001t0001g0062a0001c0001t0001g0088a0001c0001t0001g0097others(15): Show | 18 | HG00735.hp1 HG01070.hp2 HG01071.hp1 others(15): Show |
intron_variant | MODIFIER | c.437+5412dupT | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 6/9 | chr2 | 31912513 | ||||||
chr2:31912521
|
A | G | 5 | a0001c0001t0001g0098a0001c0001t0001g0101a0001c0001t0001g0114others(2): Show | 5 | HG02055.hp2 HG03486.hp2 HG03516.hp2 others(2): Show |
intron_variant | MODIFIER | c.437+5405T>C | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 6/9 | chr2 | 31912521 | ||||||
chr2:31912664
|
T | C | 1 | a0001c0001t0001g0260 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.437+5262A>G | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 6/9 | chr2 | 31912664 | ||||||
chr2:31913043
|
C | G | 1 | a0001c0001t0001g0030 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.437+4883G>C | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 6/9 | chr2 | 31913043 | ||||||
chr2:31913108
|
T | C | 1 | a0001c0001t0001g0279 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.437+4818A>G | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 6/9 | chr2 | 31913108 | ||||||
chr2:31913217
|
T | A | 1 | a0001c0001t0001g0078 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.437+4709A>T | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 6/9 | chr2 | 31913217 | ||||||
chr2:31913243
|
C | T | 111 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0017others(108): Show | 111 | HG00099.hp2 HG00140.hp2 HG00423.hp2 others(108): Show |
intron_variant | MODIFIER | c.437+4683G>A | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 6/9 | chr2 | 31913243 | ||||||
chr2:31913244
|
G | A | 1 | a0001c0001t0001g0242 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.437+4682C>T | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 6/9 | chr2 | 31913244 | ||||||
chr2:31913248
|
C | CA | 38 | a0001c0001t0001g0022a0001c0001t0001g0032a0001c0001t0001g0033others(35): Show | 38 | HG00621.hp1 HG00673.hp2 HG00738.hp1 others(35): Show |
intron_variant | MODIFIER | c.437+4677dupT | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 6/9 | chr2 | 31913248 | ||||||
chr2:31913248
|
C | CAAA | 40 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0011others(37): Show | 40 | HG01168.hp1 HG01169.hp2 HG01255.hp2 others(37): Show |
intron_variant | MODIFIER | c.437+4675_437+4677d others(5): Show |
MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 6/9 | chr2 | 31913248 | ||||||
chr2:31913248
|
C | CAAAA | 8 | a0001c0001t0001g0012a0001c0001t0001g0250a0001c0001t0001g0268others(5): Show | 8 | HG01516.hp2 HG02129.hp1 HG02738.hp1 others(5): Show |
intron_variant | MODIFIER | c.437+4674_437+4677d others(6): Show |
MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 6/9 | chr2 | 31913248 | ||||||
chr2:31913428
|
A | G | 6 | a0001c0001t0001g0272a0001c0001t0001g0273a0001c0001t0001g0274others(3): Show | 6 | HG01243.hp2 HG01891.hp1 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.437+4498T>C | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 6/9 | chr2 | 31913428 | ||||||
chr2:31913498
|
T | C | 1 | a0001c0001t0001g0232 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.437+4428A>G | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 6/9 | chr2 | 31913498 | ||||||
chr2:31913517
|
GT | G | 65 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0011others(62): Show | 65 | HG01070.hp2 HG01071.hp1 HG01168.hp1 others(62): Show |
intron_variant | MODIFIER | c.437+4408delA | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 6/9 | chr2 | 31913517 | ||||||
chr2:31913517
|
GTT | G | 7 | a0001c0001t0001g0275a0001c0001t0001g0276a0001c0001t0001g0277others(4): Show | 7 | HG01891.hp1 HG02055.hp1 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.437+4407_437+4408d others(4): Show |
MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 6/9 | chr2 | 31913517 | ||||||
chr2:31913518
|
T | G | 2 | a0001c0001t0001g0089a0001c0001t0001g0090 | 2 | NA18944.hp2 NA19003.hp1 |
intron_variant | MODIFIER | c.437+4408A>C | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 6/9 | chr2 | 31913518 | ||||||
chr2:31913522
|
T | G | 4 | a0001c0001t0001g0292a0001c0001t0001g0293a0001c0001t0001g0294others(1): Show | 4 | HG02258.hp1 HG03041.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.437+4404A>C | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 6/9 | chr2 | 31913522 | ||||||
chr2:31913530
|
T | A | 5 | a0001c0001t0001g0208a0001c0001t0001g0209a0001c0001t0001g0232others(2): Show | 5 | HG01361.hp1 HG02280.hp1 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.437+4396A>T | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 6/9 | chr2 | 31913530 | ||||||
chr2:31913533
|
A | T | 4 | a0001c0001t0001g0015a0001c0001t0001g0093a0001c0001t0001g0094others(1): Show | 4 | HG02965.hp2 NA18942.hp1 NA18943.hp2 others(1): Show |
intron_variant | MODIFIER | c.437+4393T>A | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 6/9 | chr2 | 31913533 | ||||||
chr2:31913696
|
T | G | 3 | a0001c0001t0001g0232a0001c0001t0001g0233a0001c0001t0001g0234 | 3 | HG01361.hp1 HG03927.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.437+4230A>C | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 6/9 | chr2 | 31913696 | ||||||
chr2:31913706
|
G | A | 50 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0011others(47): Show | 50 | HG01168.hp1 HG01169.hp2 HG01255.hp2 others(47): Show |
intron_variant | MODIFIER | c.437+4220C>T | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 6/9 | chr2 | 31913706 | ||||||
chr2:31913853
|
G | A | 1 | a0001c0001t0001g0152 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.437+4073C>T | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 6/9 | chr2 | 31913853 | ||||||
chr2:31913873
|
T | C | 1 | a0001c0001t0001g0296 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.437+4053A>G | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 6/9 | chr2 | 31913873 | ||||||
chr2:31913922
|
A | G | 1 | a0001c0001t0001g0179 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.437+4004T>C | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 6/9 | chr2 | 31913922 | ||||||
chr2:31914580
|
G | A | 1 | a0001c0001t0001g0153 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.437+3346C>T | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 6/9 | chr2 | 31914580 | ||||||
chr2:31914723
|
G | A | 8 | a0001c0001t0001g0134a0001c0001t0001g0152a0001c0001t0001g0156others(5): Show | 8 | HG01106.hp2 HG01261.hp1 HG01928.hp2 others(5): Show |
intron_variant | MODIFIER | c.437+3203C>T | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 6/9 | chr2 | 31914723 | ||||||
chr2:31914961
|
T | TA | 91 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0009others(88): Show | 91 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(88): Show |
intron_variant | MODIFIER | c.437+2964dupT | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 6/9 | chr2 | 31914961 | ||||||
chr2:31914961
|
TA | T | 61 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0011others(58): Show | 61 | HG01168.hp1 HG01168.hp2 HG01169.hp1 others(58): Show |
intron_variant | MODIFIER | c.437+2964delT | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 6/9 | chr2 | 31914961 | ||||||
chr2:31914961
|
TAA | T | 9 | a0001c0001t0001g0239a0001c0001t0001g0244a0001c0001t0001g0250others(6): Show | 9 | HG01516.hp2 HG02083.hp2 HG02895.hp2 others(6): Show |
intron_variant | MODIFIER | c.437+2963_437+2964d others(4): Show |
MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 6/9 | chr2 | 31914961 | ||||||
chr2:31914963
|
A | T | 1 | a0001c0001t0001g0278 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.437+2963T>A | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 6/9 | chr2 | 31914963 | ||||||
chr2:31914964
|
A | T | 2 | a0001c0001t0001g0239a0001c0001t0001g0270 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.437+2962T>A | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 6/9 | chr2 | 31914964 | ||||||
chr2:31915270
|
C | T | 1 | a0001c0001t0001g0129 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.437+2656G>A | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 6/9 | chr2 | 31915270 | ||||||
chr2:31915570
|
AAAG | A | 58 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0011others(55): Show | 58 | HG01168.hp1 HG01169.hp2 HG01255.hp2 others(55): Show |
intron_variant | MODIFIER | c.437+2353_437+2355d others(5): Show |
MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 6/9 | chr2 | 31915570 | ||||||
chr2:31915582
|
G | A | 1 | a0001c0001t0001g0014 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.437+2344C>T | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 6/9 | chr2 | 31915582 | ||||||
chr2:31915778
|
G | C | 1 | a0001c0001t0001g0171 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.437+2148C>G | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 6/9 | chr2 | 31915778 | ||||||
chr2:31916180
|
T | C | 1 | a0001c0001t0001g0282 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.437+1746A>G | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 6/9 | chr2 | 31916180 | ||||||
chr2:31916263
|
C | T | 1 | a0001c0001t0001g0115 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.437+1663G>A | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 6/9 | chr2 | 31916263 | ||||||
chr2:31916365
|
A | T | 2 | a0001c0001t0001g0236a0001c0001t0001g0237 | 2 | HG03139.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.437+1561T>A | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 6/9 | chr2 | 31916365 | ||||||
chr2:31916377
|
C | T | 2 | a0001c0001t0001g0243a0001c0001t0001g0268 | 2 | HG01891.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.437+1549G>A | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 6/9 | chr2 | 31916377 | ||||||
chr2:31916382
|
C | A | 1 | a0001c0001t0001g0040 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.437+1544G>T | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 6/9 | chr2 | 31916382 | ||||||
chr2:31916562
|
T | C | 3 | a0001c0001t0001g0178a0001c0001t0001g0186a0001c0001t0001g0188 | 3 | HG00408.hp2 NA19009.hp2 NA19090.hp1 |
intron_variant | MODIFIER | c.437+1364A>G | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 6/9 | chr2 | 31916562 | ||||||
chr2:31916564
|
A | T | 2 | a0001c0001t0001g0236a0001c0001t0001g0237 | 2 | HG03139.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.437+1362T>A | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 6/9 | chr2 | 31916564 | ||||||
chr2:31916839
|
G | C | 6 | a0001c0001t0001g0272a0001c0001t0001g0273a0001c0001t0001g0274others(3): Show | 6 | HG01243.hp2 HG01891.hp1 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.437+1087C>G | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 6/9 | chr2 | 31916839 | ||||||
chr2:31917245
|
T | C | 4 | a0001c0001t0001g0236a0001c0001t0001g0237a0001c0001t0001g0271others(1): Show | 4 | HG02280.hp2 HG03139.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.437+681A>G | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 6/9 | chr2 | 31917245 | ||||||
chr2:31917322
|
T | C | 3 | a0001c0001t0002g0003a0001c0001t0002g0004a0001c0001t0002g0005 | 3 | HG01891.hp1 HG02897.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.437+604A>G | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 6/9 | chr2 | 31917322 | ||||||
chr2:31917362
|
C | T | 1 | a0001c0001t0001g0260 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.437+564G>A | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 6/9 | chr2 | 31917362 | ||||||
chr2:31917420
|
T | C | 3 | a0001c0001t0001g0272a0001c0001t0001g0273a0001c0001t0001g0274 | 3 | HG01243.hp2 HG02615.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.437+506A>G | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 6/9 | chr2 | 31917420 | ||||||
chr2:31917451
|
C | A | 98 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0009others(95): Show | 98 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(95): Show |
intron_variant | MODIFIER | c.437+475G>T | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 6/9 | chr2 | 31917451 | ||||||
chr2:31917559
|
A | G | 1 | a0001c0001t0001g0271 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.437+367T>C | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 6/9 | chr2 | 31917559 | ||||||
chr2:31917683
|
C | A | 1 | a0001c0001t0001g0193 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.437+243G>T | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 6/9 | chr2 | 31917683 | ||||||
chr2:31918304
|
A | G | 2 | a0001c0001t0001g0146a0001c0001t0001g0151 | 2 | HG01978.hp2 HG02293.hp2 |
intron_variant | MODIFIER | c.326-267T>C | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 5/9 | chr2 | 31918304 | ||||||
chr2:31918322
|
A | G | 3 | a0001c0001t0001g0106a0001c0001t0001g0112a0002c0002t0001g0144 | 3 | HG01070.hp2 HG01071.hp1 HG01168.hp2 |
intron_variant | MODIFIER | c.326-285T>C | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 5/9 | chr2 | 31918322 | ||||||
chr2:31918507
|
G | A | 1 | a0001c0001t0001g0294 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.326-470C>T | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 5/9 | chr2 | 31918507 | ||||||
chr2:31918752
|
A | T | 1 | a0001c0001t0001g0094 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.326-715T>A | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 5/9 | chr2 | 31918752 | ||||||
chr2:31918762
|
G | A | 1 | a0001c0001t0001g0076 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.326-725C>T | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 5/9 | chr2 | 31918762 | ||||||
chr2:31918764
|
A | G | 4 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0012others(1): Show | 4 | NA18940.hp1 NA18978.hp2 NA18980.hp1 others(1): Show |
intron_variant | MODIFIER | c.326-727T>C | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 5/9 | chr2 | 31918764 | ||||||
chr2:31919060
|
T | C | 4 | a0001c0001t0001g0292a0001c0001t0001g0293a0001c0001t0001g0294others(1): Show | 4 | HG02258.hp1 HG03041.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.326-1023A>G | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 5/9 | chr2 | 31919060 | ||||||
chr2:31919426
|
T | C | 1 | a0001c0001t0001g0271 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.325+1372A>G | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 5/9 | chr2 | 31919426 | ||||||
chr2:31919624
|
G | A | 3 | a0001c0001t0002g0003a0001c0001t0002g0004a0001c0001t0002g0005 | 3 | HG01891.hp1 HG02897.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.325+1174C>T | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 5/9 | chr2 | 31919624 | ||||||
chr2:31919639
|
C | G | 1 | a0001c0001t0001g0102 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.325+1159G>C | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 5/9 | chr2 | 31919639 | ||||||
chr2:31919665
|
T | C | 1 | a0001c0001t0001g0023 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.325+1133A>G | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 5/9 | chr2 | 31919665 | ||||||
chr2:31919684
|
T | G | 73 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0011others(70): Show | 73 | HG01109.hp2 HG01168.hp1 HG01169.hp2 others(70): Show |
intron_variant | MODIFIER | c.325+1114A>C | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 5/9 | chr2 | 31919684 | ||||||
chr2:31919804
|
C | T | 9 | a0001c0001t0001g0189a0001c0001t0001g0216a0001c0001t0001g0217others(6): Show | 9 | HG01070.hp1 HG01071.hp2 HG01081.hp2 others(6): Show |
intron_variant | MODIFIER | c.325+994G>A | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 5/9 | chr2 | 31919804 | ||||||
chr2:31919868
|
G | A | 1 | a0001c0001t0001g0272 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.325+930C>T | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 5/9 | chr2 | 31919868 | ||||||
chr2:31919915
|
C | T | 1 | a0001c0001t0001g0182 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.325+883G>A | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 5/9 | chr2 | 31919915 | ||||||
chr2:31919949
|
C | CGT | 40 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0011others(37): Show | 40 | HG01168.hp1 HG01169.hp2 HG01255.hp2 others(37): Show |
intron_variant | MODIFIER | c.325+847_325+848dup others(2): Show |
MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 5/9 | chr2 | 31919949 | ||||||
chr2:31919949
|
C | CGTGT | 5 | a0001c0001t0001g0239a0001c0001t0001g0240a0001c0001t0001g0241others(2): Show | 5 | HG02723.hp1 HG02809.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.325+845_325+848dup others(4): Show |
MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 5/9 | chr2 | 31919949 | ||||||
chr2:31919949
|
CGT | C | 217 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(214): Show | 217 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(214): Show |
intron_variant | MODIFIER | c.325+847_325+848del others(2): Show |
MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 5/9 | chr2 | 31919949 | ||||||
chr2:31919949
|
CGTGT | C | 9 | a0001c0001t0001g0204a0001c0001t0001g0229a0001c0001t0001g0236others(6): Show | 9 | HG01243.hp2 HG01891.hp1 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.325+845_325+848del others(4): Show |
MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 5/9 | chr2 | 31919949 | ||||||
chr2:31919949
|
CGTGTGT | C | 5 | a0001c0001t0001g0026a0001c0001t0001g0084a0001c0001t0001g0147others(2): Show | 5 | HG00140.hp2 HG01258.hp2 HG01516.hp1 others(2): Show |
intron_variant | MODIFIER | c.325+843_325+848del others(6): Show |
MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 5/9 | chr2 | 31919949 | ||||||
chr2:31919952
|
G | A | 1 | a0001c0001t0001g0103 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.325+846C>T | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 5/9 | chr2 | 31919952 | ||||||
chr2:31919953
|
T | C | 1 | a0001c0001t0001g0103 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.325+845A>G | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 5/9 | chr2 | 31919953 | ||||||
chr2:31920163
|
TC | T | 20 | a0001c0001t0001g0069a0001c0001t0001g0071a0001c0001t0001g0072others(17): Show | 20 | HG00408.hp2 HG00642.hp2 HG01081.hp1 others(17): Show |
intron_variant | MODIFIER | c.325+634delG | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 5/9 | chr2 | 31920163 | ||||||
chr2:31920169
|
C | A | 1 | a0001c0001t0001g0296 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.325+629G>T | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 5/9 | chr2 | 31920169 | ||||||
chr2:31920186
|
C | A | 2 | a0001c0001t0001g0290a0001c0001t0001g0291 | 2 | HG01109.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.325+612G>T | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 5/9 | chr2 | 31920186 | ||||||
chr2:31920249
|
C | T | 11 | a0001c0001t0001g0032a0001c0001t0001g0033a0001c0001t0001g0034others(8): Show | 11 | HG00741.hp1 HG01433.hp1 HG02040.hp1 others(8): Show |
intron_variant | MODIFIER | c.325+549G>A | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 5/9 | chr2 | 31920249 | ||||||
chr2:31920327
|
T | A | 2 | a0001c0001t0001g0290a0001c0001t0001g0291 | 2 | HG01109.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.325+471A>T | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 5/9 | chr2 | 31920327 | ||||||
chr2:31920345
|
T | C | 5 | a0001c0001t0001g0232a0001c0001t0001g0233a0001c0001t0001g0234others(2): Show | 5 | HG01109.hp2 HG01361.hp1 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.325+453A>G | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 5/9 | chr2 | 31920345 | ||||||
chr2:31920445
|
G | A | 1 | a0001c0001t0001g0228 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.325+353C>T | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 5/9 | chr2 | 31920445 | ||||||
chr2:31920509
|
G | C | 1 | a0001c0001t0001g0242 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.325+289C>G | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 5/9 | chr2 | 31920509 | ||||||
chr2:31920638
|
A | G | 1 | a0001c0001t0001g0053 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.325+160T>C | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 5/9 | chr2 | 31920638 | ||||||
chr2:31920674
|
A | G | 3 | a0001c0001t0001g0232a0001c0001t0001g0233a0001c0001t0001g0234 | 3 | HG01361.hp1 HG03927.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.325+124T>C | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 5/9 | chr2 | 31920674 | ||||||
chr2:31920783
|
T | C | 1 | a0001c0001t0001g0009 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.325+15A>G | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 5/9 | chr2 | 31920783 | ||||||
chr2:31921091
|
C | T | 4 | a0001c0001t0001g0216a0001c0001t0001g0217a0001c0001t0001g0218others(1): Show | 4 | HG01070.hp1 HG01261.hp2 NA20752.hp2 others(1): Show |
intron_variant | MODIFIER | c.213-181G>A | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 4/9 | chr2 | 31921091 | ||||||
chr2:31921406
|
A | G | 1 | a0001c0001t0001g0172 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.213-496T>C | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 4/9 | chr2 | 31921406 | ||||||
chr2:31921459
|
T | C | 2 | a0001c0001t0001g0290a0001c0001t0001g0291 | 2 | HG01109.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.213-549A>G | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 4/9 | chr2 | 31921459 | ||||||
chr2:31921500
|
C | T | 1 | a0001c0001t0001g0002 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.213-590G>A | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 4/9 | chr2 | 31921500 | ||||||
chr2:31921523
|
C | T | 64 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0011others(61): Show | 64 | HG01168.hp1 HG01169.hp2 HG01243.hp2 others(61): Show |
intron_variant | MODIFIER | c.213-613G>A | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 4/9 | chr2 | 31921523 | ||||||
chr2:31921534
|
A | G | 3 | a0001c0001t0001g0292a0001c0001t0001g0293a0001c0001t0001g0294 | 3 | HG02258.hp1 HG03209.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.213-624T>C | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 4/9 | chr2 | 31921534 | ||||||
chr2:31921694
|
C | T | 1 | a0001c0001t0001g0078 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.213-784G>A | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 4/9 | chr2 | 31921694 | ||||||
chr2:31922041
|
A | C | 3 | a0001c0001t0001g0232a0001c0001t0001g0233a0001c0001t0001g0234 | 3 | HG01361.hp1 HG03927.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.213-1131T>G | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 4/9 | chr2 | 31922041 | ||||||
chr2:31922057
|
A | G | 1 | a0001c0001t0001g0278 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.213-1147T>C | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 4/9 | chr2 | 31922057 | ||||||
chr2:31922133
|
T | G | 1 | a0001c0001t0001g0279 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.213-1223A>C | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 4/9 | chr2 | 31922133 | ||||||
chr2:31922136
|
T | C | 4 | a0001c0001t0001g0292a0001c0001t0001g0293a0001c0001t0001g0294others(1): Show | 4 | HG02258.hp1 HG03041.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.213-1226A>G | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 4/9 | chr2 | 31922136 | ||||||
chr2:31922315
|
A | G | 1 | a0001c0001t0001g0185 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.213-1405T>C | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 4/9 | chr2 | 31922315 | ||||||
chr2:31922343
|
G | GA | 7 | a0001c0001t0001g0117a0001c0001t0001g0128a0001c0001t0001g0235others(4): Show | 7 | HG00621.hp2 HG02165.hp1 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.213-1434dupT | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 4/9 | chr2 | 31922343 | ||||||
chr2:31922543
|
T | A | 1 | a0001c0001t0001g0078 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.213-1633A>T | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 4/9 | chr2 | 31922543 | ||||||
chr2:31922746
|
G | A | 1 | a0001c0001t0001g0274 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.213-1836C>T | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 4/9 | chr2 | 31922746 | ||||||
chr2:31922791
|
G | A | 60 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0011others(57): Show | 60 | HG01168.hp1 HG01169.hp2 HG01243.hp2 others(57): Show |
intron_variant | MODIFIER | c.213-1881C>T | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 4/9 | chr2 | 31922791 | ||||||
chr2:31922898
|
T | A | 73 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0011others(70): Show | 73 | HG01109.hp2 HG01168.hp1 HG01169.hp2 others(70): Show |
intron_variant | MODIFIER | c.213-1988A>T | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 4/9 | chr2 | 31922898 | ||||||
chr2:31922962
|
C | A | 2 | a0001c0001t0001g0243a0001c0001t0001g0268 | 2 | HG01891.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.213-2052G>T | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 4/9 | chr2 | 31922962 | ||||||
chr2:31923100
|
A | G | 2 | a0001c0001t0001g0095a0001c0001t0001g0096 | 2 | NA18944.hp1 NA19011.hp2 |
intron_variant | MODIFIER | c.213-2190T>C | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 4/9 | chr2 | 31923100 | ||||||
chr2:31923308
|
C | T | 64 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0011others(61): Show | 64 | HG01168.hp1 HG01169.hp2 HG01243.hp2 others(61): Show |
intron_variant | MODIFIER | c.213-2398G>A | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 4/9 | chr2 | 31923308 | ||||||
chr2:31923536
|
T | C | 1 | a0001c0001t0001g0091 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.213-2626A>G | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 4/9 | chr2 | 31923536 | ||||||
chr2:31923550
|
G | T | 58 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0011others(55): Show | 58 | HG01168.hp1 HG01169.hp2 HG01255.hp2 others(55): Show |
intron_variant | MODIFIER | c.213-2640C>A | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 4/9 | chr2 | 31923550 | ||||||
chr2:31923567
|
T | A | 64 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0011others(61): Show | 64 | HG01168.hp1 HG01169.hp2 HG01243.hp2 others(61): Show |
intron_variant | MODIFIER | c.213-2657A>T | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 4/9 | chr2 | 31923567 | ||||||
chr2:31923787
|
C | A | 1 | a0001c0001t0001g0237 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.213-2877G>T | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 4/9 | chr2 | 31923787 | ||||||
chr2:31923989
|
C | G | 73 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0011others(70): Show | 73 | HG01109.hp2 HG01168.hp1 HG01169.hp2 others(70): Show |
intron_variant | MODIFIER | c.213-3079G>C | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 4/9 | chr2 | 31923989 | ||||||
chr2:31924028
|
A | G | 58 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0011others(55): Show | 58 | HG01168.hp1 HG01169.hp2 HG01255.hp2 others(55): Show |
intron_variant | MODIFIER | c.213-3118T>C | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 4/9 | chr2 | 31924028 | ||||||
chr2:31924053
|
T | C | 1 | a0001c0001t0001g0196 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.213-3143A>G | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 4/9 | chr2 | 31924053 | ||||||
chr2:31924090
|
TCC | T | 58 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0011others(55): Show | 58 | HG01168.hp1 HG01169.hp2 HG01255.hp2 others(55): Show |
intron_variant | MODIFIER | c.213-3182_213-3181d others(4): Show |
MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 4/9 | chr2 | 31924090 | ||||||
chr2:31924107
|
C | A | 3 | a0001c0001t0001g0021a0001c0001t0001g0027a0001c0001t0001g0149 | 3 | HG00597.hp1 NA19004.hp2 NA19085.hp1 |
intron_variant | MODIFIER | c.213-3197G>T | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 4/9 | chr2 | 31924107 | ||||||
chr2:31924180
|
T | C | 1 | a0001c0001t0001g0234 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.213-3270A>G | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 4/9 | chr2 | 31924180 | ||||||
chr2:31924306
|
C | T | 1 | a0001c0001t0001g0015 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.213-3396G>A | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 4/9 | chr2 | 31924306 | ||||||
chr2:31924404
|
C | A | 50 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0011others(47): Show | 50 | HG01168.hp1 HG01169.hp2 HG01255.hp2 others(47): Show |
intron_variant | MODIFIER | c.213-3494G>T | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 4/9 | chr2 | 31924404 | ||||||
chr2:31924446
|
T | TA | 50 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0011others(47): Show | 50 | HG01168.hp1 HG01169.hp2 HG01255.hp2 others(47): Show |
intron_variant | MODIFIER | c.213-3537dupT | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 4/9 | chr2 | 31924446 | ||||||
chr2:31924446
|
T | TAA | 8 | a0001c0001t0001g0236a0001c0001t0001g0237a0001c0001t0001g0271others(5): Show | 8 | HG01243.hp2 HG02280.hp2 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.213-3538_213-3537d others(4): Show |
MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 4/9 | chr2 | 31924446 | ||||||
chr2:31924830
|
T | A | 2 | a0001c0001t0001g0271a0001c0001t0001g0296 | 2 | HG02280.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.213-3920A>T | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 4/9 | chr2 | 31924830 | ||||||
chr2:31924930
|
T | C | 2 | a0001c0001t0001g0289a0001c0001t0001g0302 | 2 | HG01255.hp2 HG01496.hp2 |
intron_variant | MODIFIER | c.213-4020A>G | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 4/9 | chr2 | 31924930 | ||||||
chr2:31925274
|
G | A | 11 | a0001c0001t0001g0035a0001c0001t0001g0058a0001c0001t0001g0060others(8): Show | 11 | HG00597.hp2 HG00735.hp1 HG00738.hp1 others(8): Show |
intron_variant | MODIFIER | c.213-4364C>T | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 4/9 | chr2 | 31925274 | ||||||
chr2:31925469
|
C | T | 1 | a0001c0001t0001g0213 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.213-4559G>A | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 4/9 | chr2 | 31925469 | ||||||
chr2:31925475
|
C | CA | 20 | a0001c0001t0001g0014a0001c0001t0001g0064a0001c0001t0001g0072others(17): Show | 20 | HG00099.hp1 HG01106.hp1 HG01261.hp2 others(17): Show |
intron_variant | MODIFIER | c.213-4566dupT | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 4/9 | chr2 | 31925475 | ||||||
chr2:31925475
|
C | CAAAAA | 49 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0011others(46): Show | 49 | HG01169.hp2 HG01255.hp2 HG01257.hp2 others(46): Show |
intron_variant | MODIFIER | c.213-4570_213-4566d others(7): Show |
MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 4/9 | chr2 | 31925475 | ||||||
chr2:31925475
|
C | CAAAAAA | 10 | a0001c0001t0001g0013a0001c0001t0001g0019a0001c0001t0001g0245others(7): Show | 10 | HG01243.hp2 HG02055.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.213-4571_213-4566d others(8): Show |
MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 4/9 | chr2 | 31925475 | ||||||
chr2:31925475
|
C | CAAAAAAA others(1): Show |
10 | a0001c0001t0001g0104a0001c0001t0001g0118a0001c0001t0001g0122others(7): Show | 10 | HG00099.hp2 HG02273.hp1 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.213-4573_213-4566d others(10): Show |
MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 4/9 | chr2 | 31925475 | ||||||
chr2:31925475
|
C | CAAAAAAA others(2): Show |
43 | a0001c0001t0001g0018a0001c0001t0001g0021a0001c0001t0001g0024others(40): Show | 43 | HG00423.hp2 HG00438.hp1 HG00597.hp1 others(40): Show |
intron_variant | MODIFIER | c.213-4574_213-4566d others(11): Show |
MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 4/9 | chr2 | 31925475 | ||||||
chr2:31925475
|
C | CAAAAAAA others(3): Show |
38 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0015others(35): Show | 38 | HG00735.hp2 HG00741.hp2 HG01070.hp2 others(35): Show |
intron_variant | MODIFIER | c.213-4575_213-4566d others(12): Show |
MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 4/9 | chr2 | 31925475 | ||||||
chr2:31925475
|
C | CAAAAAAA others(4): Show |
14 | a0001c0001t0001g0075a0001c0001t0001g0136a0001c0001t0001g0141others(11): Show | 14 | HG01928.hp2 HG01934.hp2 HG01943.hp1 others(11): Show |
intron_variant | MODIFIER | c.213-4576_213-4566d others(13): Show |
MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 4/9 | chr2 | 31925475 | ||||||
chr2:31925475
|
C | CAAAAAAA others(5): Show |
4 | a0001c0001t0001g0023a0001c0001t0001g0157a0001c0001t0001g0166others(1): Show | 4 | HG01261.hp1 HG02148.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.213-4577_213-4566d others(14): Show |
MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 4/9 | chr2 | 31925475 | ||||||
chr2:31925475
|
C | CAAAAAAA others(6): Show |
1 | a0001c0001t0001g0026 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.213-4578_213-4566d others(15): Show |
MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 4/9 | chr2 | 31925475 | ||||||
chr2:31925475
|
C | CAAAAAAA others(7): Show |
2 | a0001c0001t0001g0103a0001c0001t0001g0153 | 2 | HG00639.hp1 HG00738.hp2 |
intron_variant | MODIFIER | c.213-4579_213-4566d others(16): Show |
MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 4/9 | chr2 | 31925475 | ||||||
chr2:31925475
|
C | CAAACAAA others(7): Show |
1 | a0001c0001t0001g0294 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.213-4566_213-4565i others(16): Show |
MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 4/9 | chr2 | 31925475 | ||||||
chr2:31925475
|
C | CAAACAAA others(35): Show |
1 | a0001c0001t0001g0292 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.213-4566_213-4565i others(44): Show |
MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 4/9 | chr2 | 31925475 | ||||||
chr2:31925475
|
C | CAAACAAA others(39): Show |
1 | a0001c0001t0001g0293 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.213-4566_213-4565i others(48): Show |
MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 4/9 | chr2 | 31925475 | ||||||
chr2:31925475
|
CAAAAAAA others(4): Show |
C | 1 | a0001c0001t0001g0055 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.213-4576_213-4566d others(13): Show |
MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 4/9 | chr2 | 31925475 | ||||||
chr2:31925475
|
CAAAAAAA others(5): Show |
C | 66 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0009others(63): Show | 66 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(63): Show |
intron_variant | MODIFIER | c.213-4577_213-4566d others(14): Show |
MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 4/9 | chr2 | 31925475 | ||||||
chr2:31925492
|
A | AAAAAAAG others(4): Show |
1 | a0001c0001t0001g0295 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.213-4583_213-4582i others(13): Show |
MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 4/9 | chr2 | 31925492 | ||||||
chr2:31925492
|
A | G | 3 | a0001c0001t0001g0292a0001c0001t0001g0293a0001c0001t0001g0294 | 3 | HG02258.hp1 HG03209.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.213-4582T>C | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 4/9 | chr2 | 31925492 | ||||||
chr2:31925574
|
A | G | 1 | a0001c0001t0001g0028 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.213-4664T>C | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 4/9 | chr2 | 31925574 | ||||||
chr2:31925900
|
G | C | 3 | a0001c0001t0001g0089a0001c0001t0001g0090a0001c0001t0001g0091 | 3 | NA18944.hp2 NA18950.hp1 NA19003.hp1 |
intron_variant | MODIFIER | c.213-4990C>G | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 4/9 | chr2 | 31925900 | ||||||
chr2:31926066
|
T | C | 3 | a0001c0001t0002g0003a0001c0001t0002g0004a0001c0001t0002g0005 | 3 | HG01891.hp1 HG02897.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.213-5156A>G | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 4/9 | chr2 | 31926066 | ||||||
chr2:31926241
|
A | C | 2 | a0001c0001t0001g0290a0001c0001t0001g0291 | 2 | HG01109.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.213-5331T>G | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 4/9 | chr2 | 31926241 | ||||||
chr2:31926313
|
G | A | 3 | a0001c0001t0001g0007a0001c0001t0001g0290a0001c0001t0001g0291 | 3 | HG01109.hp2 HG02622.hp1 NA18978.hp1 |
intron_variant | MODIFIER | c.213-5403C>T | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 4/9 | chr2 | 31926313 | ||||||
chr2:31926376
|
G | GA | 8 | a0001c0001t0001g0010a0001c0001t0001g0012a0001c0001t0001g0245others(5): Show | 8 | HG01496.hp2 HG02280.hp2 HG03486.hp1 others(5): Show |
intron_variant | MODIFIER | c.213-5467dupT | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 4/9 | chr2 | 31926376 | ||||||
chr2:31926376
|
GA | G | 214 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(211): Show | 214 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(211): Show |
intron_variant | MODIFIER | c.213-5467delT | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 4/9 | chr2 | 31926376 | ||||||
chr2:31926376
|
GAA | G | 10 | a0001c0001t0001g0051a0001c0001t0001g0232a0001c0001t0001g0233others(7): Show | 10 | HG01109.hp2 HG01361.hp1 HG02258.hp1 others(7): Show |
intron_variant | MODIFIER | c.213-5468_213-5467d others(4): Show |
MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 4/9 | chr2 | 31926376 | ||||||
chr2:31926466
|
G | A | 73 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0011others(70): Show | 73 | HG01109.hp2 HG01168.hp1 HG01169.hp2 others(70): Show |
intron_variant | MODIFIER | c.213-5556C>T | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 4/9 | chr2 | 31926466 | ||||||
chr2:31926519
|
T | C | 10 | a0001c0001t0001g0280a0001c0001t0001g0281a0001c0001t0001g0282others(7): Show | 10 | HG01255.hp2 HG01496.hp2 HG01516.hp2 others(7): Show |
intron_variant | MODIFIER | c.212+5548A>G | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 4/9 | chr2 | 31926519 | ||||||
chr2:31926577
|
A | T | 1 | a0001c0001t0001g0062 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.212+5490T>A | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 4/9 | chr2 | 31926577 | ||||||
chr2:31926677
|
T | C | 1 | a0001c0001t0001g0284 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.212+5390A>G | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 4/9 | chr2 | 31926677 | ||||||
chr2:31926882
|
CAAAAA | C | 9 | a0001c0001t0001g0189a0001c0001t0001g0216a0001c0001t0001g0217others(6): Show | 9 | HG01070.hp1 HG01071.hp2 HG01081.hp2 others(6): Show |
intron_variant | MODIFIER | c.212+5180_212+5184d others(7): Show |
MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 4/9 | chr2 | 31926882 | ||||||
chr2:31927017
|
A | G | 1 | a0001c0001t0001g0189 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.212+5050T>C | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 4/9 | chr2 | 31927017 | ||||||
chr2:31927052
|
T | C | 1 | a0001c0001t0001g0131 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.212+5015A>G | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 4/9 | chr2 | 31927052 | ||||||
chr2:31927094
|
G | A | 61 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0011others(58): Show | 61 | HG01168.hp1 HG01169.hp2 HG01243.hp2 others(58): Show |
intron_variant | MODIFIER | c.212+4973C>T | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 4/9 | chr2 | 31927094 | ||||||
chr2:31927330
|
T | C | 1 | a0001c0001t0001g0088 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.212+4737A>G | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 4/9 | chr2 | 31927330 | ||||||
chr2:31927361
|
T | C | 1 | a0001c0001t0001g0083 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.212+4706A>G | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 4/9 | chr2 | 31927361 | ||||||
chr2:31927566
|
T | C | 1 | a0001c0001t0001g0018 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.212+4501A>G | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 4/9 | chr2 | 31927566 | ||||||
chr2:31927580
|
G | C | 1 | a0001c0001t0001g0018 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.212+4487C>G | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 4/9 | chr2 | 31927580 | ||||||
chr2:31927639
|
T | TA | 114 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(111): Show | 114 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(111): Show |
intron_variant | MODIFIER | c.212+4427dupT | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 4/9 | chr2 | 31927639 | ||||||
chr2:31927674
|
T | C | 1 | a0001c0001t0001g0008 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.212+4393A>G | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 4/9 | chr2 | 31927674 | ||||||
chr2:31927792
|
A | C | 2 | a0001c0001t0001g0061a0001c0001t0001g0088 | 2 | HG00735.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.212+4275T>G | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 4/9 | chr2 | 31927792 | ||||||
chr2:31927882
|
T | G | 62 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0011others(59): Show | 62 | HG01168.hp1 HG01169.hp2 HG01243.hp2 others(59): Show |
intron_variant | MODIFIER | c.212+4185A>C | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 4/9 | chr2 | 31927882 | ||||||
chr2:31927925
|
A | G | 3 | a0001c0001t0001g0001a0001c0001t0001g0204a0001c0001t0001g0211 | 3 | HG02257.hp2 HG02818.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.212+4142T>C | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 4/9 | chr2 | 31927925 | ||||||
chr2:31927936
|
C | T | 2 | a0001c0001t0001g0238a0001c0001t0001g0300 | 2 | HG03831.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.212+4131G>A | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 4/9 | chr2 | 31927936 | ||||||
chr2:31927992
|
A | G | 2 | a0001c0001t0001g0290a0001c0001t0001g0291 | 2 | HG01109.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.212+4075T>C | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 4/9 | chr2 | 31927992 | ||||||
chr2:31928117
|
A | C | 4 | a0001c0001t0001g0292a0001c0001t0001g0293a0001c0001t0001g0294others(1): Show | 4 | HG02258.hp1 HG03041.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.212+3950T>G | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 4/9 | chr2 | 31928117 | ||||||
chr2:31928416
|
A | G | 1 | a0001c0001t0001g0232 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.212+3651T>C | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 4/9 | chr2 | 31928416 | ||||||
chr2:31928424
|
G | A | 3 | a0001c0001t0001g0106a0001c0001t0001g0112a0002c0002t0001g0144 | 3 | HG01070.hp2 HG01071.hp1 HG01168.hp2 |
intron_variant | MODIFIER | c.212+3643C>T | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 4/9 | chr2 | 31928424 | ||||||
chr2:31928474
|
G | A | 4 | a0001c0001t0001g0280a0001c0001t0001g0283a0001c0001t0001g0289others(1): Show | 4 | HG01255.hp2 HG01496.hp2 HG01516.hp2 others(1): Show |
intron_variant | MODIFIER | c.212+3593C>T | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 4/9 | chr2 | 31928474 | ||||||
chr2:31928476
|
G | A | 1 | a0001c0001t0001g0132 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.212+3591C>T | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 4/9 | chr2 | 31928476 | ||||||
chr2:31928503
|
C | T | 1 | a0001c0001t0001g0078 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.212+3564G>A | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 4/9 | chr2 | 31928503 | ||||||
chr2:31928540
|
C | G | 1 | a0001c0001t0001g0078 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.212+3527G>C | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 4/9 | chr2 | 31928540 | ||||||
chr2:31928546
|
CA | C | 285 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(282): Show | 285 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(282): Show |
intron_variant | MODIFIER | c.212+3520delT | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 4/9 | chr2 | 31928546 | ||||||
chr2:31928552
|
A | G | 4 | a0001c0001t0001g0275a0001c0001t0001g0276a0001c0001t0001g0277others(1): Show | 4 | HG02055.hp1 HG03471.hp1 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.212+3515T>C | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 4/9 | chr2 | 31928552 | ||||||
chr2:31928654
|
A | G | 1 | a0001c0001t0001g0278 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.212+3413T>C | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 4/9 | chr2 | 31928654 | ||||||
chr2:31928814
|
C | T | 1 | a0001c0001t0001g0210 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.212+3253G>A | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 4/9 | chr2 | 31928814 | ||||||
chr2:31929056
|
AT | A | 3 | a0001c0001t0001g0015a0001c0001t0001g0049a0001c0001t0001g0070 | 3 | HG02004.hp2 HG02965.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.212+3010delA | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 4/9 | chr2 | 31929056 | ||||||
chr2:31929266
|
T | A | 4 | a0001c0001t0001g0239a0001c0001t0001g0240a0001c0001t0001g0241others(1): Show | 4 | HG02723.hp1 HG02809.hp2 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.212+2801A>T | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 4/9 | chr2 | 31929266 | ||||||
chr2:31929391
|
TA | T | 50 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0011others(47): Show | 50 | HG01168.hp1 HG01169.hp2 HG01255.hp2 others(47): Show |
intron_variant | MODIFIER | c.212+2675delT | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 4/9 | chr2 | 31929391 | ||||||
chr2:31929457
|
T | C | 3 | a0001c0001t0001g0044a0001c0001t0001g0066a0001c0001t0001g0171 | 3 | HG00621.hp1 HG01928.hp1 NA19080.hp2 |
intron_variant | MODIFIER | c.212+2610A>G | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 4/9 | chr2 | 31929457 | ||||||
chr2:31929501
|
G | A | 1 | a0001c0001t0001g0018 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.212+2566C>T | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 4/9 | chr2 | 31929501 | ||||||
chr2:31929554
|
T | C | 1 | a0001c0001t0001g0279 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.212+2513A>G | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 4/9 | chr2 | 31929554 | ||||||
chr2:31929628
|
T | C | 3 | a0001c0001t0001g0006a0001c0001t0001g0031a0001c0001t0001g0190 | 3 | HG00438.hp2 HG02165.hp2 NA18984.hp2 |
intron_variant | MODIFIER | c.212+2439A>G | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 4/9 | chr2 | 31929628 | ||||||
chr2:31930062
|
C | T | 1 | a0001c0001t0001g0107 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.212+2005G>A | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 4/9 | chr2 | 31930062 | ||||||
chr2:31930106
|
A | G | 69 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0009others(66): Show | 69 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(66): Show |
intron_variant | MODIFIER | c.212+1961T>C | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 4/9 | chr2 | 31930106 | ||||||
chr2:31930315
|
A | G | 1 | a0001c0001t0001g0193 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.212+1752T>C | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 4/9 | chr2 | 31930315 | ||||||
chr2:31930377
|
A | G | 10 | a0001c0001t0001g0280a0001c0001t0001g0281a0001c0001t0001g0282others(7): Show | 10 | HG01255.hp2 HG01496.hp2 HG01516.hp2 others(7): Show |
intron_variant | MODIFIER | c.212+1690T>C | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 4/9 | chr2 | 31930377 | ||||||
chr2:31930447
|
T | C | 4 | a0001c0001t0001g0216a0001c0001t0001g0217a0001c0001t0001g0218others(1): Show | 4 | HG01070.hp1 HG01261.hp2 NA20752.hp2 others(1): Show |
intron_variant | MODIFIER | c.212+1620A>G | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 4/9 | chr2 | 31930447 | ||||||
chr2:31930557
|
G | A | 1 | a0001c0001t0001g0060 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.212+1510C>T | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 4/9 | chr2 | 31930557 | ||||||
chr2:31930658
|
T | A | 302 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(299): Show | 302 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(299): Show |
intron_variant | MODIFIER | c.212+1409A>T | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 4/9 | chr2 | 31930658 | ||||||
chr2:31930660
|
T | A | 3 | a0001c0001t0002g0003a0001c0001t0002g0004a0001c0001t0002g0005 | 3 | HG01891.hp1 HG02897.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.212+1407A>T | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 4/9 | chr2 | 31930660 | ||||||
chr2:31930707
|
G | A | 3 | a0001c0001t0001g0085a0001c0001t0001g0086a0001c0001t0001g0235 | 3 | NA18971.hp2 NA19011.hp1 NA19070.hp1 |
intron_variant | MODIFIER | c.212+1360C>T | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 4/9 | chr2 | 31930707 | ||||||
chr2:31930739
|
G | A | 1 | a0001c0001t0001g0188 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.212+1328C>T | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 4/9 | chr2 | 31930739 | ||||||
chr2:31930806
|
T | C | 1 | a0001c0001t0001g0060 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.212+1261A>G | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 4/9 | chr2 | 31930806 | ||||||
chr2:31930811
|
A | AT | 14 | a0001c0001t0001g0009a0001c0001t0001g0012a0001c0001t0001g0068others(11): Show | 14 | HG01928.hp2 HG02055.hp1 HG02300.hp1 others(11): Show |
intron_variant | MODIFIER | c.212+1255dupA | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 4/9 | chr2 | 31930811 | ||||||
chr2:31930811
|
A | ATTTTTTT others(3): Show |
8 | a0001c0001t0001g0232a0001c0001t0001g0272a0001c0001t0001g0273others(5): Show | 8 | HG01109.hp2 HG01243.hp2 HG01361.hp1 others(5): Show |
intron_variant | MODIFIER | c.212+1246_212+1255d others(12): Show |
MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 4/9 | chr2 | 31930811 | ||||||
chr2:31930811
|
A | ATTTTTTT others(4): Show |
5 | a0001c0001t0001g0233a0001c0001t0001g0234a0001c0001t0001g0271others(2): Show | 5 | HG01891.hp1 HG02280.hp2 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.212+1245_212+1255d others(13): Show |
MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 4/9 | chr2 | 31930811 | ||||||
chr2:31930811
|
A | ATTTTTTT others(5): Show |
4 | a0001c0001t0001g0292a0001c0001t0001g0293a0001c0001t0001g0294others(1): Show | 4 | HG02258.hp1 HG03209.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.212+1244_212+1255d others(14): Show |
MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 4/9 | chr2 | 31930811 | ||||||
chr2:31930811
|
A | ATTTTTTT others(6): Show |
3 | a0001c0001t0001g0236a0001c0001t0001g0237a0001c0001t0001g0278 | 3 | HG03139.hp2 NA19043.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.212+1243_212+1255d others(15): Show |
MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 4/9 | chr2 | 31930811 | ||||||
chr2:31931006
|
T | C | 1 | a0001c0001t0001g0279 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.212+1061A>G | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 4/9 | chr2 | 31931006 | ||||||
chr2:31931046
|
G | C | 2 | a0001c0001t0001g0290a0001c0001t0001g0291 | 2 | HG01109.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.212+1021C>G | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 4/9 | chr2 | 31931046 | ||||||
chr2:31931325
|
C | T | 57 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0011others(54): Show | 57 | HG01168.hp1 HG01169.hp2 HG01255.hp2 others(54): Show |
intron_variant | MODIFIER | c.212+742G>A | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 4/9 | chr2 | 31931325 | ||||||
chr2:31931450
|
T | G | 3 | a0001c0001t0001g0021a0001c0001t0001g0027a0001c0001t0001g0149 | 3 | HG00597.hp1 NA19004.hp2 NA19085.hp1 |
intron_variant | MODIFIER | c.212+617A>C | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 4/9 | chr2 | 31931450 | ||||||
chr2:31931550
|
GT | G | 50 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0011others(47): Show | 50 | HG01168.hp1 HG01169.hp2 HG01255.hp2 others(47): Show |
intron_variant | MODIFIER | c.212+516delA | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 4/9 | chr2 | 31931550 | ||||||
chr2:31931557
|
T | G | 1 | a0001c0001t0001g0189 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.212+510A>C | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 4/9 | chr2 | 31931557 | ||||||
chr2:31931620
|
T | C | 3 | a0001c0001t0001g0199a0001c0001t0001g0200a0001c0001t0001g0201 | 3 | HG02622.hp2 HG03098.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.212+447A>G | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 4/9 | chr2 | 31931620 | ||||||
chr2:31932444
|
G | GT | 14 | a0001c0001t0001g0082a0001c0001t0001g0232a0001c0001t0001g0233others(11): Show | 14 | HG01109.hp2 HG01361.hp1 HG02055.hp1 others(11): Show |
intron_variant | MODIFIER | c.144-310dupA | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 3/9 | chr2 | 31932444 | ||||||
chr2:31932445
|
T | A | 1 | a0001c0001t0001g0197 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.144-310A>T | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 3/9 | chr2 | 31932445 | ||||||
chr2:31932579
|
T | C | 1 | a0001c0001t0001g0234 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.144-444A>G | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 3/9 | chr2 | 31932579 | ||||||
chr2:31932806
|
G | A | 1 | a0001c0001t0001g0108 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.144-671C>T | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 3/9 | chr2 | 31932806 | ||||||
chr2:31933071
|
T | C | 2 | a0001c0001t0001g0290a0001c0001t0001g0291 | 2 | HG01109.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.144-936A>G | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 3/9 | chr2 | 31933071 | ||||||
chr2:31933185
|
T | C | 1 | a0001c0001t0001g0008 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.144-1050A>G | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 3/9 | chr2 | 31933185 | ||||||
chr2:31933242
|
C | A | 1 | a0001c0001t0001g0056 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.144-1107G>T | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 3/9 | chr2 | 31933242 | ||||||
chr2:31933251
|
A | G | 1 | a0001c0001t0001g0130 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.144-1116T>C | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 3/9 | chr2 | 31933251 | ||||||
chr2:31933252
|
TATTACAG others(20): Show |
T | 3 | a0001c0001t0001g0232a0001c0001t0001g0233a0001c0001t0001g0234 | 3 | HG01361.hp1 HG03927.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.144-1144_144-1118d others(29): Show |
MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 3/9 | chr2 | 31933252 | ||||||
chr2:31933290
|
G | A | 3 | a0001c0001t0002g0003a0001c0001t0002g0004a0001c0001t0002g0005 | 3 | HG01891.hp1 HG02897.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.144-1155C>T | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 3/9 | chr2 | 31933290 | ||||||
chr2:31933293
|
T | C | 4 | a0001c0001t0001g0236a0001c0001t0001g0237a0001c0001t0001g0271others(1): Show | 4 | HG02280.hp2 HG03139.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.144-1158A>G | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 3/9 | chr2 | 31933293 | ||||||
chr2:31933317
|
T | TA | 25 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0023others(22): Show | 25 | HG00099.hp2 HG00423.hp2 HG00597.hp1 others(22): Show |
intron_variant | MODIFIER | c.144-1183dupT | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 3/9 | chr2 | 31933317 | ||||||
chr2:31933317
|
T | TAA | 9 | a0001c0001t0001g0007a0001c0001t0001g0029a0001c0001t0001g0122others(6): Show | 9 | HG01106.hp2 HG01261.hp1 HG01928.hp2 others(6): Show |
intron_variant | MODIFIER | c.144-1184_144-1183d others(4): Show |
MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 3/9 | chr2 | 31933317 | ||||||
chr2:31933317
|
T | TAAA | 8 | a0001c0001t0001g0113a0001c0001t0001g0134a0001c0001t0001g0142others(5): Show | 8 | HG01169.hp1 HG01943.hp1 HG02148.hp2 others(5): Show |
intron_variant | MODIFIER | c.144-1185_144-1183d others(5): Show |
MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 3/9 | chr2 | 31933317 | ||||||
chr2:31933317
|
TA | T | 16 | a0001c0001t0001g0020a0001c0001t0001g0026a0001c0001t0001g0086others(13): Show | 16 | HG00140.hp2 HG00597.hp2 HG01070.hp1 others(13): Show |
intron_variant | MODIFIER | c.144-1183delT | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 3/9 | chr2 | 31933317 | ||||||
chr2:31933317
|
TAA | T | 22 | a0001c0001t0001g0009a0001c0001t0001g0034a0001c0001t0001g0035others(19): Show | 22 | HG01928.hp1 HG01934.hp1 HG01943.hp2 others(19): Show |
intron_variant | MODIFIER | c.144-1184_144-1183d others(4): Show |
MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 3/9 | chr2 | 31933317 | ||||||
chr2:31933317
|
TAAA | T | 64 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0016others(61): Show | 64 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(61): Show |
intron_variant | MODIFIER | c.144-1185_144-1183d others(5): Show |
MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 3/9 | chr2 | 31933317 | ||||||
chr2:31933317
|
TAAAA | T | 11 | a0001c0001t0001g0014a0001c0001t0001g0031a0001c0001t0001g0042others(8): Show | 11 | HG00099.hp1 HG00140.hp1 HG00673.hp1 others(8): Show |
intron_variant | MODIFIER | c.144-1186_144-1183d others(6): Show |
MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 3/9 | chr2 | 31933317 | ||||||
chr2:31933317
|
TAAAAAAA others(4): Show |
T | 1 | a0001c0001t0001g0303 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.144-1193_144-1183d others(13): Show |
MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 3/9 | chr2 | 31933317 | ||||||
chr2:31933331
|
AAAAAAAA others(18): Show |
A | 1 | a0001c0001t0001g0238 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.144-1221_144-1197d others(27): Show |
MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 3/9 | chr2 | 31933331 | ||||||
chr2:31933331
|
AAAAAAAA others(30): Show |
A | 2 | a0001c0001t0001g0232a0001c0001t0001g0234 | 2 | HG01361.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.144-1233_144-1197d others(39): Show |
MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 3/9 | chr2 | 31933331 | ||||||
chr2:31933332
|
AAAAAAAA others(29): Show |
A | 1 | a0001c0001t0001g0233 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.144-1233_144-1198d others(38): Show |
MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 3/9 | chr2 | 31933332 | ||||||
chr2:31933334
|
A | T | 2 | a0001c0001t0002g0004a0001c0001t0002g0005 | 2 | HG02897.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.144-1199T>A | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 3/9 | chr2 | 31933334 | ||||||
chr2:31933335
|
AAAAAAAA others(9): Show |
A | 1 | a0001c0001t0001g0291 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.144-1216_144-1201d others(18): Show |
MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 3/9 | chr2 | 31933335 | ||||||
chr2:31933336
|
A | T | 2 | a0001c0001t0002g0004a0001c0001t0002g0005 | 2 | HG02897.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.144-1201T>A | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 3/9 | chr2 | 31933336 | ||||||
chr2:31933338
|
A | T | 2 | a0001c0001t0002g0004a0001c0001t0002g0005 | 2 | HG02897.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.144-1203T>A | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 3/9 | chr2 | 31933338 | ||||||
chr2:31933339
|
AAAAAAAA others(6): Show |
A | 2 | a0001c0001t0001g0276a0001c0001t0001g0277 | 2 | HG02055.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.144-1217_144-1205d others(15): Show |
MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 3/9 | chr2 | 31933339 | ||||||
chr2:31933340
|
A | T | 5 | a0001c0001t0001g0206a0001c0001t0001g0290a0001c0001t0002g0003others(2): Show | 5 | HG01891.hp1 HG02622.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.144-1205T>A | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 3/9 | chr2 | 31933340 | ||||||
chr2:31933340
|
AAAAAAAA others(5): Show |
A | 1 | a0001c0001t0001g0278 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.144-1217_144-1206d others(14): Show |
MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 3/9 | chr2 | 31933340 | ||||||
chr2:31933341
|
AAAAAAAA others(6): Show |
A | 1 | a0001c0001t0001g0275 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.144-1219_144-1207d others(15): Show |
MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 3/9 | chr2 | 31933341 | ||||||
chr2:31933342
|
A | T | 6 | a0001c0001t0001g0206a0001c0001t0001g0271a0001c0001t0001g0290others(3): Show | 6 | HG01891.hp1 HG02280.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.144-1207T>A | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 3/9 | chr2 | 31933342 | ||||||
chr2:31933343
|
AAAAAAAT others(6): Show |
A | 1 | a0001c0001t0001g0237 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.144-1221_144-1209d others(15): Show |
MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 3/9 | chr2 | 31933343 | ||||||
chr2:31933344
|
A | AATATATA others(7): Show |
1 | a0001c0001t0001g0163 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.144-1210_144-1209i others(16): Show |
MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 3/9 | chr2 | 31933344 | ||||||
chr2:31933344
|
A | ATATATAT others(6): Show |
1 | a0001c0001t0001g0141 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.144-1210_144-1209i others(15): Show |
MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 3/9 | chr2 | 31933344 | ||||||
chr2:31933344
|
A | ATATTTAT others(6): Show |
1 | a0001c0001t0001g0058 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.144-1210_144-1209i others(15): Show |
MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 3/9 | chr2 | 31933344 | ||||||
chr2:31933344
|
A | ATTATATA others(13): Show |
1 | a0001c0001t0001g0190 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.144-1210_144-1209i others(22): Show |
MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 3/9 | chr2 | 31933344 | ||||||
chr2:31933344
|
A | T | 6 | a0001c0001t0001g0206a0001c0001t0001g0271a0001c0001t0001g0290others(3): Show | 6 | HG01891.hp1 HG02280.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.144-1209T>A | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 3/9 | chr2 | 31933344 | ||||||
chr2:31933344
|
AAAAAATT others(5): Show |
A | 1 | a0001c0001t0001g0236 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.144-1221_144-1210d others(14): Show |
MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 3/9 | chr2 | 31933344 | ||||||
chr2:31933346
|
A | ATTATATA others(5): Show |
1 | a0001c0001t0001g0054 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.144-1212_144-1211i others(14): Show |
MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 3/9 | chr2 | 31933346 | ||||||
chr2:31933346
|
A | ATTATATA others(7): Show |
1 | a0001c0001t0001g0172 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.144-1212_144-1211i others(16): Show |
MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 3/9 | chr2 | 31933346 | ||||||
chr2:31933346
|
A | T | 16 | a0001c0001t0001g0058a0001c0001t0001g0072a0001c0001t0001g0141others(13): Show | 16 | HG00738.hp1 HG01243.hp2 HG01891.hp1 others(13): Show |
intron_variant | MODIFIER | c.144-1211T>A | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 3/9 | chr2 | 31933346 | ||||||
chr2:31933348
|
A | T | 20 | a0001c0001t0001g0054a0001c0001t0001g0058a0001c0001t0001g0072others(17): Show | 20 | HG00738.hp1 HG01243.hp2 HG01891.hp1 others(17): Show |
intron_variant | MODIFIER | c.144-1213T>A | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 3/9 | chr2 | 31933348 | ||||||
chr2:31933348
|
AATTT | A | 20 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0012others(17): Show | 20 | HG01168.hp1 HG02083.hp2 HG02738.hp1 others(17): Show |
intron_variant | MODIFIER | c.144-1217_144-1214d others(6): Show |
MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 3/9 | chr2 | 31933348 | ||||||
chr2:31933348
|
AATTTAT | A | 6 | a0001c0001t0001g0094a0001c0001t0001g0282a0001c0001t0001g0284others(3): Show | 6 | HG01255.hp2 HG01496.hp2 HG02155.hp2 others(3): Show |
intron_variant | MODIFIER | c.144-1219_144-1214d others(8): Show |
MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 3/9 | chr2 | 31933348 | ||||||
chr2:31933349
|
ATTTAT | A | 11 | a0001c0001t0001g0008a0001c0001t0001g0243a0001c0001t0001g0246others(8): Show | 11 | HG01169.hp2 HG01433.hp2 HG01891.hp2 others(8): Show |
intron_variant | MODIFIER | c.144-1219_144-1215d others(7): Show |
MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 3/9 | chr2 | 31933349 | ||||||
chr2:31933350
|
T | A | 2 | a0001c0001t0001g0101a0001c0001t0001g0257 | 2 | HG03516.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.144-1215A>T | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 3/9 | chr2 | 31933350 | ||||||
chr2:31933351
|
T | A | 28 | a0001c0001t0001g0054a0001c0001t0001g0058a0001c0001t0001g0072others(25): Show | 28 | HG00738.hp1 HG01243.hp2 HG01257.hp2 others(25): Show |
intron_variant | MODIFIER | c.144-1216A>T | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 3/9 | chr2 | 31933351 | ||||||
chr2:31933351
|
T | TTATATA | 4 | a0001c0001t0001g0046a0001c0001t0001g0047a0001c0001t0001g0169others(1): Show | 4 | HG00639.hp2 HG01934.hp1 HG02273.hp2 others(1): Show |
intron_variant | MODIFIER | c.144-1222_144-1217d others(8): Show |
MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 3/9 | chr2 | 31933351 | ||||||
chr2:31933351
|
T | TTATATAT others(1): Show |
3 | a0001c0001t0001g0083a0001c0001t0001g0084a0001c0001t0001g0088 | 3 | HG00735.hp1 HG03139.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.144-1224_144-1217d others(10): Show |
MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 3/9 | chr2 | 31933351 | ||||||
chr2:31933351
|
T | TTATATAT others(3): Show |
1 | a0001c0001t0001g0085 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.144-1226_144-1217d others(12): Show |
MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 3/9 | chr2 | 31933351 | ||||||
chr2:31933351
|
T | TTATATAT others(5): Show |
6 | a0001c0001t0001g0006a0001c0001t0001g0055a0001c0001t0001g0065others(3): Show | 6 | HG00438.hp2 HG00597.hp2 HG02129.hp2 others(3): Show |
intron_variant | MODIFIER | c.144-1228_144-1217d others(14): Show |
MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 3/9 | chr2 | 31933351 | ||||||
chr2:31933351
|
T | TTATATAT others(7): Show |
6 | a0001c0001t0001g0033a0001c0001t0001g0043a0001c0001t0001g0057others(3): Show | 6 | HG00741.hp1 NA18612.hp2 NA18943.hp1 others(3): Show |
intron_variant | MODIFIER | c.144-1230_144-1217d others(16): Show |
MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 3/9 | chr2 | 31933351 | ||||||
chr2:31933351
|
T | TTATATAT others(9): Show |
11 | a0001c0001t0001g0014a0001c0001t0001g0030a0001c0001t0001g0031others(8): Show | 11 | HG00099.hp1 HG00642.hp2 HG01433.hp1 others(8): Show |
intron_variant | MODIFIER | c.144-1232_144-1217d others(18): Show |
MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 3/9 | chr2 | 31933351 | ||||||
chr2:31933351
|
T | TTATATAT others(11): Show |
13 | a0001c0001t0001g0009a0001c0001t0001g0036a0001c0001t0001g0045others(10): Show | 13 | HG02004.hp1 HG02040.hp1 HG02148.hp1 others(10): Show |
intron_variant | MODIFIER | c.144-1234_144-1217d others(20): Show |
MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 3/9 | chr2 | 31933351 | ||||||
chr2:31933351
|
T | TTATATAT others(13): Show |
12 | a0001c0001t0001g0037a0001c0001t0001g0048a0001c0001t0001g0064others(9): Show | 12 | HG01884.hp2 HG01993.hp1 HG02071.hp2 others(9): Show |
intron_variant | MODIFIER | c.144-1236_144-1217d others(22): Show |
MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 3/9 | chr2 | 31933351 | ||||||
chr2:31933351
|
T | TTATATAT others(15): Show |
8 | a0001c0001t0001g0016a0001c0001t0001g0040a0001c0001t0001g0069others(5): Show | 8 | HG00408.hp2 HG03195.hp1 HG04199.hp2 others(5): Show |
intron_variant | MODIFIER | c.144-1238_144-1217d others(24): Show |
MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 3/9 | chr2 | 31933351 | ||||||
chr2:31933351
|
T | TTATATAT others(17): Show |
5 | a0001c0001t0001g0039a0001c0001t0001g0051a0001c0001t0001g0062others(2): Show | 5 | HG00423.hp1 HG01975.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.144-1240_144-1217d others(26): Show |
MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 3/9 | chr2 | 31933351 | ||||||
chr2:31933351
|
T | TTATATAT others(19): Show |
2 | a0001c0001t0001g0042a0001c0001t0001g0191 | 2 | HG00673.hp1 NA18939.hp2 |
intron_variant | MODIFIER | c.144-1242_144-1217d others(28): Show |
MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 3/9 | chr2 | 31933351 | ||||||
chr2:31933351
|
T | TTATATAT others(21): Show |
1 | a0001c0001t0001g0035 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.144-1244_144-1217d others(30): Show |
MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 3/9 | chr2 | 31933351 | ||||||
chr2:31933351
|
T | TTATATAT others(23): Show |
1 | a0001c0001t0001g0038 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.144-1246_144-1217d others(32): Show |
MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 3/9 | chr2 | 31933351 | ||||||
chr2:31933351
|
TTA | T | 11 | a0001c0001t0001g0020a0001c0001t0001g0098a0001c0001t0001g0100others(8): Show | 11 | HG01071.hp2 HG01081.hp2 HG02055.hp2 others(8): Show |
intron_variant | MODIFIER | c.144-1218_144-1217d others(4): Show |
MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 3/9 | chr2 | 31933351 | ||||||
chr2:31933351
|
TTATA | T | 11 | a0001c0001t0001g0061a0001c0001t0001g0106a0001c0001t0001g0112others(8): Show | 11 | HG01070.hp1 HG01070.hp2 HG01071.hp1 others(8): Show |
intron_variant | MODIFIER | c.144-1220_144-1217d others(6): Show |
MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 3/9 | chr2 | 31933351 | ||||||
chr2:31933351
|
TTATATA | T | 26 | a0001c0001t0001g0007a0001c0001t0001g0022a0001c0001t0001g0026others(23): Show | 26 | HG00099.hp2 HG00140.hp2 HG00621.hp1 others(23): Show |
intron_variant | MODIFIER | c.144-1222_144-1217d others(8): Show |
MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 3/9 | chr2 | 31933351 | ||||||
chr2:31933351
|
TTATATAT others(1): Show |
T | 83 | a0001c0001t0001g0001a0001c0001t0001g0015a0001c0001t0001g0017others(80): Show | 83 | HG00423.hp2 HG00438.hp1 HG00597.hp1 others(80): Show |
intron_variant | MODIFIER | c.144-1224_144-1217d others(10): Show |
MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 3/9 | chr2 | 31933351 | ||||||
chr2:31933351
|
TTATATAT others(3): Show |
T | 3 | a0001c0001t0001g0041a0001c0001t0001g0049a0001c0001t0001g0070 | 3 | HG02004.hp2 HG03540.hp2 NA19068.hp2 |
intron_variant | MODIFIER | c.144-1226_144-1217d others(12): Show |
MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 3/9 | chr2 | 31933351 | ||||||
chr2:31933351
|
TTATATAT others(5): Show |
T | 1 | a0001c0001t0001g0175 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.144-1228_144-1217d others(14): Show |
MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 3/9 | chr2 | 31933351 | ||||||
chr2:31933354
|
T | A | 18 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0012others(15): Show | 18 | HG01168.hp1 HG02083.hp2 HG03831.hp1 others(15): Show |
intron_variant | MODIFIER | c.144-1219A>T | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 3/9 | chr2 | 31933354 | ||||||
chr2:31933356
|
T | A | 23 | a0001c0001t0001g0008a0001c0001t0001g0244a0001c0001t0001g0245others(20): Show | 23 | HG01255.hp2 HG01433.hp2 HG01496.hp2 others(20): Show |
intron_variant | MODIFIER | c.144-1221A>T | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 3/9 | chr2 | 31933356 | ||||||
chr2:31933357
|
A | T | 1 | a0001c0001t0001g0155 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.144-1222T>A | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 3/9 | chr2 | 31933357 | ||||||
chr2:31933358
|
T | A | 2 | a0001c0001t0001g0245a0001c0001t0001g0267 | 2 | NA18950.hp2 NA19056.hp2 |
intron_variant | MODIFIER | c.144-1223A>T | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 3/9 | chr2 | 31933358 | ||||||
chr2:31933359
|
A | T | 1 | a0001c0001t0001g0129 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.144-1224T>A | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 3/9 | chr2 | 31933359 | ||||||
chr2:31933360
|
T | A | 1 | a0001c0001t0001g0267 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.144-1225A>T | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 3/9 | chr2 | 31933360 | ||||||
chr2:31933384
|
G | T | 3 | a0001c0001t0001g0232a0001c0001t0001g0233a0001c0001t0001g0234 | 3 | HG01361.hp1 HG03927.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.144-1249C>A | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 3/9 | chr2 | 31933384 | ||||||
chr2:31933451
|
A | C | 1 | a0001c0001t0001g0080 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.144-1316T>G | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 3/9 | chr2 | 31933451 | ||||||
chr2:31933880
|
T | G | 2 | a0001c0001t0001g0253a0001c0001t0001g0256 | 2 | HG01257.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.144-1745A>C | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 3/9 | chr2 | 31933880 | ||||||
chr2:31934059
|
T | C | 3 | a0001c0001t0001g0232a0001c0001t0001g0233a0001c0001t0001g0234 | 3 | HG01361.hp1 HG03927.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.144-1924A>G | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 3/9 | chr2 | 31934059 | ||||||
chr2:31934469
|
T | TA | 9 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0012others(6): Show | 9 | HG01106.hp1 HG01109.hp2 HG01361.hp1 others(6): Show |
intron_variant | MODIFIER | c.144-2335dupT | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 3/9 | chr2 | 31934469 | ||||||
chr2:31934469
|
TA | T | 9 | a0001c0001t0001g0102a0001c0001t0001g0156a0001c0001t0001g0157others(6): Show | 9 | HG01261.hp1 HG01496.hp1 HG01928.hp2 others(6): Show |
intron_variant | MODIFIER | c.144-2335delT | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 3/9 | chr2 | 31934469 | ||||||
chr2:31934629
|
A | G | 3 | a0001c0001t0001g0232a0001c0001t0001g0233a0001c0001t0001g0234 | 3 | HG01361.hp1 HG03927.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.144-2494T>C | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 3/9 | chr2 | 31934629 | ||||||
chr2:31934751
|
T | C | 1 | a0001c0001t0001g0279 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.144-2616A>G | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 3/9 | chr2 | 31934751 | ||||||
chr2:31934805
|
G | A | 4 | a0001c0001t0001g0106a0001c0001t0001g0112a0001c0001t0001g0215others(1): Show | 4 | HG01070.hp2 HG01071.hp1 HG01106.hp1 others(1): Show |
intron_variant | MODIFIER | c.144-2670C>T | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 3/9 | chr2 | 31934805 | ||||||
chr2:31934913
|
A | G | 2 | a0001c0001t0001g0047a0001c0001t0001g0067 | 2 | HG02818.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.144-2778T>C | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 3/9 | chr2 | 31934913 | ||||||
chr2:31934914
|
G | C | 1 | a0001c0001t0001g0184 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.144-2779C>G | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 3/9 | chr2 | 31934914 | ||||||
chr2:31935070
|
T | G | 3 | a0001c0001t0001g0232a0001c0001t0001g0233a0001c0001t0001g0234 | 3 | HG01361.hp1 HG03927.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.144-2935A>C | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 3/9 | chr2 | 31935070 | ||||||
chr2:31935210
|
C | T | 1 | a0001c0001t0001g0232 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.144-3075G>A | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 3/9 | chr2 | 31935210 | ||||||
chr2:31935314
|
C | T | 3 | a0001c0001t0002g0003a0001c0001t0002g0004a0001c0001t0002g0005 | 3 | HG01891.hp1 HG02897.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.144-3179G>A | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 3/9 | chr2 | 31935314 | ||||||
chr2:31935332
|
ATATACCC others(8): Show |
A | 1 | a0001c0001t0001g0075 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.144-3212_144-3198d others(17): Show |
MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 3/9 | chr2 | 31935332 | ||||||
chr2:31935344
|
A | C | 4 | a0001c0001t0001g0292a0001c0001t0001g0293a0001c0001t0001g0294others(1): Show | 4 | HG02258.hp1 HG03041.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.144-3209T>G | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 3/9 | chr2 | 31935344 | ||||||
chr2:31935354
|
A | G | 3 | a0001c0001t0001g0292a0001c0001t0001g0293a0001c0001t0001g0294 | 3 | HG02258.hp1 HG03209.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.144-3219T>C | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 3/9 | chr2 | 31935354 | ||||||
chr2:31935411
|
A | C | 3 | a0001c0001t0001g0089a0001c0001t0001g0090a0001c0001t0001g0091 | 3 | NA18944.hp2 NA18950.hp1 NA19003.hp1 |
intron_variant | MODIFIER | c.144-3276T>G | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 3/9 | chr2 | 31935411 | ||||||
chr2:31935462
|
T | C | 3 | a0001c0001t0001g0232a0001c0001t0001g0233a0001c0001t0001g0234 | 3 | HG01361.hp1 HG03927.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.144-3327A>G | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 3/9 | chr2 | 31935462 | ||||||
chr2:31935475
|
G | C | 1 | a0001c0001t0001g0215 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.144-3340C>G | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 3/9 | chr2 | 31935475 | ||||||
chr2:31935499
|
G | A | 1 | a0001c0001t0001g0232 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.144-3364C>T | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 3/9 | chr2 | 31935499 | ||||||
chr2:31935747
|
T | C | 299 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(296): Show | 299 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(296): Show |
intron_variant | MODIFIER | c.144-3612A>G | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 3/9 | chr2 | 31935747 | ||||||
chr2:31935795
|
G | A | 2 | a0001c0001t0001g0100a0001c0001t0001g0101 | 2 | HG03209.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.144-3660C>T | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 3/9 | chr2 | 31935795 | ||||||
chr2:31935842
|
CG | C | 3 | a0001c0001t0001g0275a0001c0001t0001g0276a0001c0001t0001g0277 | 3 | HG02055.hp1 HG03471.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.144-3708delC | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 3/9 | chr2 | 31935842 | ||||||
chr2:31935866
|
A | G | 9 | a0001c0001t0001g0118a0001c0001t0001g0120a0001c0001t0001g0121others(6): Show | 9 | HG00099.hp2 HG00642.hp1 HG00741.hp2 others(6): Show |
intron_variant | MODIFIER | c.144-3731T>C | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 3/9 | chr2 | 31935866 | ||||||
chr2:31936172
|
C | G | 2 | a0001c0001t0001g0100a0001c0001t0001g0101 | 2 | HG03209.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.144-4037G>C | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 3/9 | chr2 | 31936172 | ||||||
chr2:31936290
|
A | G | 1 | a0001c0001t0001g0070 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.144-4155T>C | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 3/9 | chr2 | 31936290 | ||||||
chr2:31936309
|
G | A | 1 | a0001c0001t0001g0232 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.144-4174C>T | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 3/9 | chr2 | 31936309 | ||||||
chr2:31936481
|
C | G | 1 | a0001c0001t0001g0189 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.144-4346G>C | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 3/9 | chr2 | 31936481 | ||||||
chr2:31936602
|
T | C | 1 | a0001c0001t0001g0271 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.144-4467A>G | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 3/9 | chr2 | 31936602 | ||||||
chr2:31936686
|
A | G | 2 | a0001c0001t0001g0271a0001c0001t0001g0296 | 2 | HG02280.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.144-4551T>C | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 3/9 | chr2 | 31936686 | ||||||
chr2:31936955
|
T | C | 1 | a0001c0001t0001g0079 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.144-4820A>G | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 3/9 | chr2 | 31936955 | ||||||
chr2:31937023
|
T | G | 4 | a0001c0001t0001g0216a0001c0001t0001g0217a0001c0001t0001g0218others(1): Show | 4 | HG01070.hp1 HG01261.hp2 NA20752.hp2 others(1): Show |
intron_variant | MODIFIER | c.144-4888A>C | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 3/9 | chr2 | 31937023 | ||||||
chr2:31937226
|
G | A | 1 | a0001c0001t0001g0215 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.144-5091C>T | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 3/9 | chr2 | 31937226 | ||||||
chr2:31937293
|
G | C | 1 | a0001c0001t0001g0016 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.144-5158C>G | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 3/9 | chr2 | 31937293 | ||||||
chr2:31938173
|
T | C | 2 | a0001c0001t0001g0290a0001c0001t0001g0291 | 2 | HG01109.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.143+5129A>G | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 3/9 | chr2 | 31938173 | ||||||
chr2:31938198
|
C | G | 1 | a0001c0001t0001g0232 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.143+5104G>C | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 3/9 | chr2 | 31938198 | ||||||
chr2:31938345
|
TA | T | 6 | a0001c0001t0001g0290a0001c0001t0001g0291a0001c0001t0001g0292others(3): Show | 6 | HG01109.hp2 HG02258.hp1 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.143+4956delT | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 3/9 | chr2 | 31938345 | ||||||
chr2:31938422
|
G | A | 5 | a0001c0001t0001g0145a0001c0001t0001g0146a0001c0001t0001g0150others(2): Show | 5 | HG01243.hp1 HG01257.hp1 HG01978.hp2 others(2): Show |
intron_variant | MODIFIER | c.143+4880C>T | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 3/9 | chr2 | 31938422 | ||||||
chr2:31938442
|
C | T | 4 | a0001c0001t0001g0236a0001c0001t0001g0237a0001c0001t0001g0271others(1): Show | 4 | HG02280.hp2 HG03139.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.143+4860G>A | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 3/9 | chr2 | 31938442 | ||||||
chr2:31938786
|
A | AT | 94 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0009others(91): Show | 94 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(91): Show |
intron_variant | MODIFIER | c.143+4515dupA | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 3/9 | chr2 | 31938786 | ||||||
chr2:31938786
|
AT | A | 13 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0112others(10): Show | 13 | HG01070.hp2 HG01109.hp2 HG01243.hp2 others(10): Show |
intron_variant | MODIFIER | c.143+4515delA | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 3/9 | chr2 | 31938786 | ||||||
chr2:31938786
|
ATT | A | 55 | a0001c0001t0001g0008a0001c0001t0001g0012a0001c0001t0001g0013others(52): Show | 55 | HG01168.hp1 HG01169.hp2 HG01255.hp2 others(52): Show |
intron_variant | MODIFIER | c.143+4514_143+4515d others(4): Show |
MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 3/9 | chr2 | 31938786 | ||||||
chr2:31938913
|
A | G | 1 | a0001c0001t0001g0008 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.143+4389T>C | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 3/9 | chr2 | 31938913 | ||||||
chr2:31939109
|
CA | C | 288 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(285): Show | 288 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(285): Show |
intron_variant | MODIFIER | c.143+4192delT | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 3/9 | chr2 | 31939109 | ||||||
chr2:31939308
|
C | T | 4 | a0001c0001t0001g0239a0001c0001t0001g0240a0001c0001t0001g0241others(1): Show | 4 | HG02723.hp1 HG02809.hp2 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.143+3994G>A | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 3/9 | chr2 | 31939308 | ||||||
chr2:31939454
|
T | C | 6 | a0001c0001t0001g0156a0001c0001t0001g0157a0001c0001t0001g0158others(3): Show | 6 | HG01261.hp1 HG01928.hp2 HG01934.hp2 others(3): Show |
intron_variant | MODIFIER | c.143+3848A>G | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 3/9 | chr2 | 31939454 | ||||||
chr2:31939612
|
T | C | 2 | a0001c0001t0001g0233a0001c0001t0001g0234 | 2 | HG03927.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.143+3690A>G | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 3/9 | chr2 | 31939612 | ||||||
chr2:31939878
|
G | A | 1 | a0001c0001t0001g0300 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.143+3424C>T | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 3/9 | chr2 | 31939878 | ||||||
chr2:31940130
|
T | C | 1 | a0001c0001t0001g0215 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.143+3172A>G | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 3/9 | chr2 | 31940130 | ||||||
chr2:31940288
|
C | G | 10 | a0001c0001t0001g0280a0001c0001t0001g0281a0001c0001t0001g0282others(7): Show | 10 | HG01255.hp2 HG01496.hp2 HG01516.hp2 others(7): Show |
intron_variant | MODIFIER | c.143+3014G>C | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 3/9 | chr2 | 31940288 | ||||||
chr2:31940356
|
G | C | 3 | a0001c0001t0001g0272a0001c0001t0001g0273a0001c0001t0001g0274 | 3 | HG01243.hp2 HG02615.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.143+2946C>G | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 3/9 | chr2 | 31940356 | ||||||
chr2:31940505
|
A | T | 72 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0011others(69): Show | 72 | HG01109.hp2 HG01168.hp1 HG01169.hp2 others(69): Show |
intron_variant | MODIFIER | c.143+2797T>A | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 3/9 | chr2 | 31940505 | ||||||
chr2:31940525
|
A | T | 1 | a0001c0001t0001g0182 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.143+2777T>A | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 3/9 | chr2 | 31940525 | ||||||
chr2:31940603
|
A | C | 1 | a0001c0001t0001g0008 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.143+2699T>G | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 3/9 | chr2 | 31940603 | ||||||
chr2:31940708
|
A | T | 2 | a0001c0001t0001g0290a0001c0001t0001g0291 | 2 | HG01109.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.143+2594T>A | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 3/9 | chr2 | 31940708 | ||||||
chr2:31940813
|
G | A | 2 | a0001c0001t0001g0085a0001c0001t0001g0235 | 2 | NA19011.hp1 NA19070.hp1 |
intron_variant | MODIFIER | c.143+2489C>T | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 3/9 | chr2 | 31940813 | ||||||
chr2:31940857
|
T | G | 1 | a0001c0001t0001g0053 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.143+2445A>C | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 3/9 | chr2 | 31940857 | ||||||
chr2:31940979
|
T | C | 6 | a0001c0001t0001g0290a0001c0001t0001g0291a0001c0001t0001g0292others(3): Show | 6 | HG01109.hp2 HG02258.hp1 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.143+2323A>G | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 3/9 | chr2 | 31940979 | ||||||
chr2:31941123
|
C | A | 6 | a0001c0001t0001g0290a0001c0001t0001g0291a0001c0001t0001g0292others(3): Show | 6 | HG01109.hp2 HG02258.hp1 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.143+2179G>T | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 3/9 | chr2 | 31941123 | ||||||
chr2:31941375
|
C | T | 3 | a0001c0001t0001g0232a0001c0001t0001g0233a0001c0001t0001g0234 | 3 | HG01361.hp1 HG03927.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.143+1927G>A | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 3/9 | chr2 | 31941375 | ||||||
chr2:31941526
|
T | C | 3 | a0001c0001t0001g0106a0001c0001t0001g0112a0002c0002t0001g0144 | 3 | HG01070.hp2 HG01071.hp1 HG01168.hp2 |
intron_variant | MODIFIER | c.143+1776A>G | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 3/9 | chr2 | 31941526 | ||||||
chr2:31941659
|
A | G | 1 | a0001c0001t0001g0115 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.143+1643T>C | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 3/9 | chr2 | 31941659 | ||||||
chr2:31941826
|
T | C | 3 | a0001c0001t0001g0109a0001c0001t0001g0110a0001c0001t0001g0111 | 3 | HG00438.hp1 HG00673.hp2 NA19084.hp1 |
intron_variant | MODIFIER | c.143+1476A>G | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 3/9 | chr2 | 31941826 | ||||||
chr2:31941984
|
A | T | 2 | a0001c0001t0001g0103a0001c0001t0001g0213 | 2 | HG00738.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.143+1318T>A | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 3/9 | chr2 | 31941984 | ||||||
chr2:31942163
|
G | A | 1 | a0001c0001t0001g0069 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.143+1139C>T | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 3/9 | chr2 | 31942163 | ||||||
chr2:31942472
|
C | T | 81 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0011others(78): Show | 81 | HG01070.hp1 HG01071.hp2 HG01081.hp2 others(78): Show |
intron_variant | MODIFIER | c.143+830G>A | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 3/9 | chr2 | 31942472 | ||||||
chr2:31942772
|
T | C | 69 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0009others(66): Show | 69 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(66): Show |
intron_variant | MODIFIER | c.143+530A>G | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 3/9 | chr2 | 31942772 | ||||||
chr2:31943011
|
G | A | 1 | a0001c0001t0001g0059 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.143+291C>T | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 3/9 | chr2 | 31943011 | ||||||
chr2:31943054
|
C | T | 112 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0017others(109): Show | 112 | HG00099.hp2 HG00140.hp2 HG00423.hp2 others(109): Show |
intron_variant | MODIFIER | c.143+248G>A | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 3/9 | chr2 | 31943054 | ||||||
chr2:31943202
|
T | C | 1 | a0001c0001t0001g0083 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.143+100A>G | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 3/9 | chr2 | 31943202 | ||||||
chr2:31943478
|
T | A | 4 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0012others(1): Show | 4 | NA18940.hp1 NA18978.hp2 NA18980.hp1 others(1): Show |
intron_variant | MODIFIER | c.62-95A>T | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31943478 | ||||||
chr2:31943482
|
C | A | 4 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0012others(1): Show | 4 | NA18940.hp1 NA18978.hp2 NA18980.hp1 others(1): Show |
intron_variant | MODIFIER | c.62-99G>T | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31943482 | ||||||
chr2:31943624
|
C | G | 2 | a0001c0001t0001g0243a0001c0001t0001g0268 | 2 | HG01891.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.62-241G>C | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31943624 | ||||||
chr2:31943658
|
T | C | 3 | a0001c0001t0002g0003a0001c0001t0002g0004a0001c0001t0002g0005 | 3 | HG01891.hp1 HG02897.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.62-275A>G | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31943658 | ||||||
chr2:31943766
|
C | T | 2 | a0001c0001t0001g0051a0001c0001t0001g0064 | 2 | HG02109.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.62-383G>A | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31943766 | ||||||
chr2:31943939
|
G | A | 72 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0011others(69): Show | 72 | HG01109.hp2 HG01168.hp1 HG01169.hp2 others(69): Show |
intron_variant | MODIFIER | c.62-556C>T | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31943939 | ||||||
chr2:31944047
|
A | C | 1 | a0001c0001t0001g0227 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.62-664T>G | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31944047 | ||||||
chr2:31944362
|
G | A | 64 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0011others(61): Show | 64 | HG01168.hp1 HG01169.hp2 HG01243.hp2 others(61): Show |
intron_variant | MODIFIER | c.62-979C>T | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31944362 | ||||||
chr2:31944496
|
T | C | 73 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0011others(70): Show | 73 | HG01070.hp1 HG01071.hp2 HG01081.hp2 others(70): Show |
intron_variant | MODIFIER | c.62-1113A>G | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31944496 | ||||||
chr2:31944846
|
T | A | 1 | a0001c0001t0001g0065 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.62-1463A>T | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31944846 | ||||||
chr2:31944854
|
T | C | 3 | a0001c0001t0001g0232a0001c0001t0001g0233a0001c0001t0001g0234 | 3 | HG01361.hp1 HG03927.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.62-1471A>G | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31944854 | ||||||
chr2:31945036
|
T | G | 64 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0011others(61): Show | 64 | HG01168.hp1 HG01169.hp2 HG01243.hp2 others(61): Show |
intron_variant | MODIFIER | c.62-1653A>C | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31945036 | ||||||
chr2:31945105
|
G | T | 2 | a0001c0001t0001g0243a0001c0001t0001g0268 | 2 | HG01891.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.62-1722C>A | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31945105 | ||||||
chr2:31945153
|
C | T | 1 | a0001c0001t0001g0232 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.62-1770G>A | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31945153 | ||||||
chr2:31945333
|
C | T | 1 | a0001c0001t0001g0061 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.62-1950G>A | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31945333 | ||||||
chr2:31945452
|
G | A | 1 | a0001c0001t0001g0040 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.62-2069C>T | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31945452 | ||||||
chr2:31945520
|
C | T | 1 | a0001c0001t0001g0289 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.62-2137G>A | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31945520 | ||||||
chr2:31945595
|
T | A | 1 | a0001c0001t0001g0263 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.62-2212A>T | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31945595 | ||||||
chr2:31945853
|
T | C | 3 | a0001c0001t0001g0275a0001c0001t0001g0276a0001c0001t0001g0277 | 3 | HG02055.hp1 HG03471.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.62-2470A>G | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31945853 | ||||||
chr2:31945855
|
T | G | 76 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0011others(73): Show | 76 | HG01070.hp1 HG01071.hp2 HG01081.hp2 others(73): Show |
intron_variant | MODIFIER | c.62-2472A>C | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31945855 | ||||||
chr2:31946003
|
G | A | 1 | a0001c0001t0001g0181 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.62-2620C>T | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31946003 | ||||||
chr2:31946022
|
C | T | 2 | a0001c0001t0001g0197a0001c0001t0001g0198 | 2 | HG02922.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.62-2639G>A | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31946022 | ||||||
chr2:31946048
|
A | C | 69 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0011others(66): Show | 69 | HG01070.hp1 HG01071.hp2 HG01081.hp2 others(66): Show |
intron_variant | MODIFIER | c.62-2665T>G | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31946048 | ||||||
chr2:31946102
|
G | A | 6 | a0001c0001t0001g0025a0001c0001t0001g0081a0001c0001t0001g0223others(3): Show | 6 | HG01243.hp2 HG02615.hp2 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.62-2719C>T | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31946102 | ||||||
chr2:31946360
|
A | G | 1 | a0001c0001t0001g0137 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.62-2977T>C | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31946360 | ||||||
chr2:31946405
|
G | C | 1 | a0001c0001t0001g0079 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.62-3022C>G | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31946405 | ||||||
chr2:31946406
|
T | C | 2 | a0001c0001t0001g0271a0001c0001t0001g0296 | 2 | HG02280.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.62-3023A>G | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31946406 | ||||||
chr2:31946728
|
T | C | 1 | a0001c0001t0001g0295 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.62-3345A>G | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31946728 | ||||||
chr2:31947393
|
A | G | 1 | a0001c0001t0001g0175 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.62-4010T>C | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31947393 | ||||||
chr2:31947548
|
A | T | 1 | a0001c0001t0001g0193 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.62-4165T>A | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31947548 | ||||||
chr2:31947598
|
T | A | 8 | a0001c0001t0001g0134a0001c0001t0001g0152a0001c0001t0001g0156others(5): Show | 8 | HG01106.hp2 HG01261.hp1 HG01928.hp2 others(5): Show |
intron_variant | MODIFIER | c.62-4215A>T | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31947598 | ||||||
chr2:31947642
|
C | A | 72 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0011others(69): Show | 72 | HG01109.hp2 HG01168.hp1 HG01169.hp2 others(69): Show |
intron_variant | MODIFIER | c.62-4259G>T | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31947642 | ||||||
chr2:31947815
|
G | GCA | 3 | a0001c0001t0001g0272a0001c0001t0001g0273a0001c0001t0001g0274 | 3 | HG01243.hp2 HG02615.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.62-4434_62-4433dup others(2): Show |
MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31947815 | ||||||
chr2:31947896
|
C | T | 1 | a0001c0001t0001g0174 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.62-4513G>A | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31947896 | ||||||
chr2:31948072
|
T | C | 1 | a0001c0001t0001g0278 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.62-4689A>G | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31948072 | ||||||
chr2:31948105
|
T | C | 5 | a0001c0001t0001g0098a0001c0001t0001g0192a0001c0001t0001g0193others(2): Show | 5 | HG02055.hp2 HG03486.hp2 HG03516.hp1 others(2): Show |
intron_variant | MODIFIER | c.62-4722A>G | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31948105 | ||||||
chr2:31948173
|
A | G | 1 | a0001c0001t0001g0019 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.62-4790T>C | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31948173 | ||||||
chr2:31948232
|
A | G | 1 | a0001c0001t0001g0232 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.62-4849T>C | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31948232 | ||||||
chr2:31948241
|
T | C | 1 | a0001c0001t0001g0116 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.62-4858A>G | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31948241 | ||||||
chr2:31948715
|
G | A | 1 | a0001c0001t0001g0214 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.62-5332C>T | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31948715 | ||||||
chr2:31948844
|
T | C | 1 | a0001c0001t0001g0216 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.62-5461A>G | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31948844 | ||||||
chr2:31948950
|
A | C | 3 | a0001c0001t0001g0292a0001c0001t0001g0293a0001c0001t0001g0294 | 3 | HG02258.hp1 HG03209.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.62-5567T>G | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31948950 | ||||||
chr2:31949240
|
T | G | 3 | a0001c0001t0001g0272a0001c0001t0001g0273a0001c0001t0001g0274 | 3 | HG01243.hp2 HG02615.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.62-5857A>C | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31949240 | ||||||
chr2:31949446
|
T | C | 82 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0011others(79): Show | 82 | HG01070.hp1 HG01071.hp2 HG01081.hp2 others(79): Show |
intron_variant | MODIFIER | c.62-6063A>G | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31949446 | ||||||
chr2:31949492
|
G | C | 1 | a0001c0001t0001g0174 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.62-6109C>G | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31949492 | ||||||
chr2:31949523
|
A | G | 2 | a0001c0001t0001g0290a0001c0001t0001g0291 | 2 | HG01109.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.62-6140T>C | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31949523 | ||||||
chr2:31949570
|
T | C | 2 | a0001c0001t0001g0289a0001c0001t0001g0302 | 2 | HG01255.hp2 HG01496.hp2 |
intron_variant | MODIFIER | c.62-6187A>G | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31949570 | ||||||
chr2:31949585
|
C | T | 20 | a0001c0001t0001g0069a0001c0001t0001g0071a0001c0001t0001g0072others(17): Show | 20 | HG00408.hp2 HG00642.hp2 HG01081.hp1 others(17): Show |
intron_variant | MODIFIER | c.62-6202G>A | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31949585 | ||||||
chr2:31949597
|
A | G | 1 | a0001c0001t0001g0176 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.62-6214T>C | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31949597 | ||||||
chr2:31949642
|
C | CA | 134 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0015others(131): Show | 134 | HG00099.hp2 HG00140.hp2 HG00423.hp2 others(131): Show |
intron_variant | MODIFIER | c.62-6260dupT | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31949642 | ||||||
chr2:31949642
|
C | CAA | 100 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(97): Show | 100 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(97): Show |
intron_variant | MODIFIER | c.62-6261_62-6260dup others(2): Show |
MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31949642 | ||||||
chr2:31949642
|
C | CAAA | 16 | a0001c0001t0001g0009a0001c0001t0001g0080a0001c0001t0001g0178others(13): Show | 16 | HG00408.hp2 HG01081.hp1 HG02071.hp2 others(13): Show |
intron_variant | MODIFIER | c.62-6262_62-6260dup others(3): Show |
MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31949642 | ||||||
chr2:31949663
|
C | A | 2 | a0001c0001t0001g0182a0001c0001t0001g0217 | 2 | HG01070.hp1 NA19088.hp1 |
intron_variant | MODIFIER | c.62-6280G>T | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31949663 | ||||||
chr2:31949892
|
A | AAT | 60 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0011others(57): Show | 60 | HG01168.hp1 HG01169.hp2 HG01243.hp2 others(57): Show |
intron_variant | MODIFIER | c.62-6511_62-6510dup others(2): Show |
MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31949892 | ||||||
chr2:31949905
|
G | A | 63 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0011others(60): Show | 63 | HG01168.hp1 HG01169.hp2 HG01243.hp2 others(60): Show |
intron_variant | MODIFIER | c.62-6522C>T | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31949905 | ||||||
chr2:31950138
|
T | C | 2 | a0001c0001t0001g0047a0001c0001t0001g0067 | 2 | HG02818.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.62-6755A>G | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31950138 | ||||||
chr2:31950255
|
C | T | 1 | a0001c0001t0001g0061 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.62-6872G>A | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31950255 | ||||||
chr2:31950338
|
A | G | 5 | a0001c0001t0001g0098a0001c0001t0001g0192a0001c0001t0001g0193others(2): Show | 5 | HG02055.hp2 HG03486.hp2 HG03516.hp1 others(2): Show |
intron_variant | MODIFIER | c.62-6955T>C | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31950338 | ||||||
chr2:31950376
|
G | A | 3 | a0001c0001t0001g0275a0001c0001t0001g0276a0001c0001t0001g0277 | 3 | HG02055.hp1 HG03471.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.62-6993C>T | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31950376 | ||||||
chr2:31951330
|
A | G | 3 | a0001c0001t0001g0275a0001c0001t0001g0276a0001c0001t0001g0277 | 3 | HG02055.hp1 HG03471.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.62-7947T>C | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31951330 | ||||||
chr2:31951381
|
T | C | 2 | a0001c0001t0001g0019a0001c0001t0001g0163 | 2 | NA18969.hp1 NA19010.hp2 |
intron_variant | MODIFIER | c.62-7998A>G | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31951381 | ||||||
chr2:31951386
|
T | A | 5 | a0001c0001t0001g0236a0001c0001t0001g0292a0001c0001t0001g0293others(2): Show | 5 | HG02258.hp1 HG03041.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.62-8003A>T | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31951386 | ||||||
chr2:31951516
|
G | C | 1 | a0001c0001t0001g0015 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.62-8133C>G | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31951516 | ||||||
chr2:31951517
|
G | GT | 60 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0011others(57): Show | 60 | HG01168.hp1 HG01169.hp2 HG01255.hp2 others(57): Show |
intron_variant | MODIFIER | c.62-8135dupA | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31951517 | ||||||
chr2:31951517
|
G | T | 1 | a0001c0001t0001g0078 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.62-8134C>A | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31951517 | ||||||
chr2:31951553
|
G | A | 1 | a0001c0001t0001g0103 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.62-8170C>T | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31951553 | ||||||
chr2:31951658
|
G | A | 1 | a0001c0001t0001g0014 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.62-8275C>T | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31951658 | ||||||
chr2:31951737
|
G | A | 1 | a0001c0001t0001g0014 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.62-8354C>T | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31951737 | ||||||
chr2:31951929
|
G | T | 3 | a0001c0001t0002g0003a0001c0001t0002g0004a0001c0001t0002g0005 | 3 | HG01891.hp1 HG02897.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.62-8546C>A | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31951929 | ||||||
chr2:31952099
|
G | A | 1 | a0001c0001t0001g0298 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.62-8716C>T | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31952099 | ||||||
chr2:31952243
|
A | G | 1 | a0001c0001t0001g0161 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.62-8860T>C | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31952243 | ||||||
chr2:31952664
|
G | A | 2 | a0001c0001t0001g0074a0001c0001t0001g0075 | 2 | NA18956.hp1 NA18968.hp1 |
intron_variant | MODIFIER | c.62-9281C>T | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31952664 | ||||||
chr2:31952706
|
T | C | 3 | a0001c0001t0001g0232a0001c0001t0001g0233a0001c0001t0001g0234 | 3 | HG01361.hp1 HG03927.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.62-9323A>G | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31952706 | ||||||
chr2:31953092
|
G | A | 1 | a0001c0001t0001g0068 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.62-9709C>T | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31953092 | ||||||
chr2:31953366
|
C | CA | 10 | a0001c0001t0001g0032a0001c0001t0001g0058a0001c0001t0001g0119others(7): Show | 10 | HG00423.hp2 HG00738.hp1 HG01106.hp1 others(7): Show |
intron_variant | MODIFIER | c.62-9984dupT | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31953366 | ||||||
chr2:31953366
|
CA | C | 53 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0011others(50): Show | 53 | HG01168.hp1 HG01169.hp2 HG01255.hp2 others(50): Show |
intron_variant | MODIFIER | c.62-9984delT | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31953366 | ||||||
chr2:31953366
|
CAA | C | 15 | a0001c0001t0001g0232a0001c0001t0001g0233a0001c0001t0001g0234others(12): Show | 15 | HG01109.hp2 HG01361.hp1 HG01891.hp1 others(12): Show |
intron_variant | MODIFIER | c.62-9985_62-9984del others(2): Show |
MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31953366 | ||||||
chr2:31953384
|
A | C | 19 | a0001c0001t0001g0069a0001c0001t0001g0071a0001c0001t0001g0072others(16): Show | 19 | HG00408.hp2 HG00642.hp2 HG01081.hp1 others(16): Show |
intron_variant | MODIFIER | c.62-10001T>G | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31953384 | ||||||
chr2:31953449
|
A | G | 3 | a0001c0001t0001g0275a0001c0001t0001g0276a0001c0001t0001g0277 | 3 | HG02055.hp1 HG03471.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.62-10066T>C | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31953449 | ||||||
chr2:31953454
|
A | AT | 112 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0015others(109): Show | 112 | HG00099.hp2 HG00140.hp2 HG00423.hp2 others(109): Show |
intron_variant | MODIFIER | c.62-10072dupA | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31953454 | ||||||
chr2:31953500
|
G | A | 303 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(300): Show | 303 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(300): Show |
intron_variant | MODIFIER | c.62-10117C>T | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31953500 | ||||||
chr2:31953519
|
G | A | 1 | a0001c0001t0001g0260 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.62-10136C>T | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31953519 | ||||||
chr2:31953683
|
C | T | 108 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0017others(105): Show | 108 | HG00099.hp2 HG00140.hp2 HG00423.hp2 others(105): Show |
intron_variant | MODIFIER | c.62-10300G>A | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31953683 | ||||||
chr2:31954009
|
G | C | 1 | a0001c0001t0001g0237 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.62-10626C>G | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31954009 | ||||||
chr2:31954036
|
C | G | 3 | a0001c0001t0002g0003a0001c0001t0002g0004a0001c0001t0002g0005 | 3 | HG01891.hp1 HG02897.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.62-10653G>C | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31954036 | ||||||
chr2:31954120
|
G | A | 1 | a0001c0001t0001g0290 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.62-10737C>T | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31954120 | ||||||
chr2:31954463
|
T | A | 49 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0011others(46): Show | 49 | HG01168.hp1 HG01169.hp2 HG01255.hp2 others(46): Show |
intron_variant | MODIFIER | c.62-11080A>T | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31954463 | ||||||
chr2:31954510
|
C | T | 3 | a0001c0001t0002g0003a0001c0001t0002g0004a0001c0001t0002g0005 | 3 | HG01891.hp1 HG02897.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.62-11127G>A | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31954510 | ||||||
chr2:31954524
|
G | A | 1 | a0001c0001t0001g0202 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.62-11141C>T | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31954524 | ||||||
chr2:31954664
|
C | T | 1 | a0001c0001t0001g0207 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.62-11281G>A | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31954664 | ||||||
chr2:31954724
|
C | T | 12 | a0001c0001t0001g0189a0001c0001t0001g0216a0001c0001t0001g0217others(9): Show | 12 | HG01070.hp1 HG01071.hp2 HG01081.hp2 others(9): Show |
intron_variant | MODIFIER | c.62-11341G>A | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31954724 | ||||||
chr2:31954766
|
G | A | 1 | a0001c0001t0001g0098 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.62-11383C>T | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31954766 | ||||||
chr2:31954822
|
G | A | 1 | a0001c0001t0001g0077 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.62-11439C>T | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31954822 | ||||||
chr2:31954922
|
A | G | 1 | a0001c0001t0001g0260 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.62-11539T>C | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31954922 | ||||||
chr2:31955143
|
A | G | 3 | a0001c0001t0001g0083a0001c0001t0001g0084a0001c0001t0001g0228 | 3 | HG03139.hp1 HG03225.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.62-11760T>C | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31955143 | ||||||
chr2:31955324
|
T | G | 2 | a0001c0001t0001g0233a0001c0001t0001g0234 | 2 | HG03927.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.62-11941A>C | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31955324 | ||||||
chr2:31955566
|
T | C | 1 | a0001c0001t0001g0272 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.62-12183A>G | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31955566 | ||||||
chr2:31955772
|
C | T | 1 | a0001c0001t0001g0301 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.62-12389G>A | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31955772 | ||||||
chr2:31955823
|
G | C | 3 | a0001c0001t0001g0272a0001c0001t0001g0273a0001c0001t0001g0274 | 3 | HG01243.hp2 HG02615.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.62-12440C>G | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31955823 | ||||||
chr2:31955914
|
G | A | 1 | a0001c0001t0001g0058 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.62-12531C>T | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31955914 | ||||||
chr2:31955995
|
T | C | 1 | a0001c0001t0001g0303 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.62-12612A>G | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31955995 | ||||||
chr2:31956083
|
T | C | 1 | a0001c0001t0001g0295 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.62-12700A>G | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31956083 | ||||||
chr2:31956090
|
G | A | 7 | a0001c0001t0001g0210a0001c0001t0001g0290a0001c0001t0001g0291others(4): Show | 7 | HG01109.hp2 HG01884.hp1 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.62-12707C>T | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31956090 | ||||||
chr2:31956145
|
A | G | 3 | a0001c0001t0001g0232a0001c0001t0001g0233a0001c0001t0001g0234 | 3 | HG01361.hp1 HG03927.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.62-12762T>C | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31956145 | ||||||
chr2:31956154
|
A | C | 1 | a0001c0001t0001g0119 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.62-12771T>G | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31956154 | ||||||
chr2:31956163
|
T | C | 1 | a0001c0001t0001g0233 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.62-12780A>G | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31956163 | ||||||
chr2:31956200
|
G | A | 1 | a0001c0001t0001g0153 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.62-12817C>T | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31956200 | ||||||
chr2:31956340
|
G | GA | 17 | a0001c0001t0001g0236a0001c0001t0001g0237a0001c0001t0001g0252others(14): Show | 17 | HG01243.hp2 HG01891.hp1 HG02055.hp1 others(14): Show |
intron_variant | MODIFIER | c.62-12958dupT | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31956340 | ||||||
chr2:31956355
|
G | A | 63 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0011others(60): Show | 63 | HG01168.hp1 HG01169.hp2 HG01243.hp2 others(60): Show |
intron_variant | MODIFIER | c.62-12972C>T | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31956355 | ||||||
chr2:31956400
|
A | G | 3 | a0001c0001t0001g0272a0001c0001t0001g0273a0001c0001t0001g0274 | 3 | HG01243.hp2 HG02615.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.62-13017T>C | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31956400 | ||||||
chr2:31956401
|
T | C | 2 | a0001c0001t0001g0236a0001c0001t0001g0237 | 2 | HG03139.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.62-13018A>G | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31956401 | ||||||
chr2:31956462
|
A | C | 1 | a0001c0001t0001g0020 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.62-13079T>G | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31956462 | ||||||
chr2:31956672
|
C | T | 1 | a0001c0001t0001g0189 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.62-13289G>A | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31956672 | ||||||
chr2:31956740
|
G | A | 1 | a0001c0001t0001g0222 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.62-13357C>T | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31956740 | ||||||
chr2:31956798
|
T | C | 1 | a0001c0001t0001g0208 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.62-13415A>G | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31956798 | ||||||
chr2:31956812
|
T | G | 1 | a0001c0001t0001g0234 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.62-13429A>C | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31956812 | ||||||
chr2:31956882
|
G | A | 3 | a0001c0001t0002g0003a0001c0001t0002g0004a0001c0001t0002g0005 | 3 | HG01891.hp1 HG02897.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.62-13499C>T | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31956882 | ||||||
chr2:31956939
|
G | T | 303 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(300): Show | 303 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(300): Show |
intron_variant | MODIFIER | c.62-13556C>A | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31956939 | ||||||
chr2:31957142
|
CA | C | 15 | a0001c0001t0001g0020a0001c0001t0001g0022a0001c0001t0001g0028others(12): Show | 15 | HG00642.hp1 HG00735.hp2 HG00741.hp2 others(12): Show |
intron_variant | MODIFIER | c.62-13760delT | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31957142 | ||||||
chr2:31957288
|
A | C | 1 | a0001c0001t0001g0232 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.62-13905T>G | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31957288 | ||||||
chr2:31957459
|
T | C | 100 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0015others(97): Show | 100 | HG00099.hp2 HG00140.hp2 HG00423.hp2 others(97): Show |
intron_variant | MODIFIER | c.62-14076A>G | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31957459 | ||||||
chr2:31957643
|
A | C | 1 | a0001c0001t0001g0137 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.62-14260T>G | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31957643 | ||||||
chr2:31957715
|
C | A | 2 | a0001c0001t0001g0103a0001c0001t0001g0213 | 2 | HG00738.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.62-14332G>T | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31957715 | ||||||
chr2:31957820
|
A | G | 1 | a0001c0001t0001g0077 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.62-14437T>C | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31957820 | ||||||
chr2:31957828
|
T | C | 1 | a0001c0001t0001g0296 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.62-14445A>G | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31957828 | ||||||
chr2:31957960
|
T | C | 2 | a0001c0001t0001g0243a0001c0001t0001g0268 | 2 | HG01891.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.62-14577A>G | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31957960 | ||||||
chr2:31958179
|
A | C | 1 | a0001c0001t0001g0059 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.62-14796T>G | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31958179 | ||||||
chr2:31958355
|
G | A | 1 | a0001c0001t0001g0296 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.62-14972C>T | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31958355 | ||||||
chr2:31958542
|
T | C | 73 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0011others(70): Show | 73 | HG01109.hp2 HG01168.hp1 HG01169.hp2 others(70): Show |
intron_variant | MODIFIER | c.62-15159A>G | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31958542 | ||||||
chr2:31958692
|
C | A | 3 | a0001c0001t0001g0290a0001c0001t0001g0291a0001c0001t0002g0003 | 3 | HG01109.hp2 HG01891.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.62-15309G>T | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31958692 | ||||||
chr2:31958698
|
C | T | 112 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0017others(109): Show | 112 | HG00099.hp2 HG00140.hp2 HG00423.hp2 others(109): Show |
intron_variant | MODIFIER | c.62-15315G>A | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31958698 | ||||||
chr2:31958738
|
G | A | 1 | a0001c0001t0001g0141 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.62-15355C>T | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31958738 | ||||||
chr2:31959003
|
G | A | 1 | a0001c0001t0001g0272 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.62-15620C>T | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31959003 | ||||||
chr2:31959008
|
T | G | 1 | a0001c0001t0001g0210 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.62-15625A>C | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31959008 | ||||||
chr2:31959186
|
T | C | 3 | a0001c0001t0001g0272a0001c0001t0001g0273a0001c0001t0001g0274 | 3 | HG01243.hp2 HG02615.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.62-15803A>G | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31959186 | ||||||
chr2:31959499
|
C | T | 61 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0011others(58): Show | 61 | HG01168.hp1 HG01169.hp2 HG01243.hp2 others(58): Show |
intron_variant | MODIFIER | c.62-16116G>A | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31959499 | ||||||
chr2:31959501
|
G | GA | 61 | a0001c0001t0001g0008a0001c0001t0001g0011a0001c0001t0001g0012others(58): Show | 61 | HG01168.hp1 HG01169.hp2 HG01243.hp2 others(58): Show |
intron_variant | MODIFIER | c.62-16119dupT | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31959501 | ||||||
chr2:31959744
|
C | T | 2 | a0001c0001t0001g0219a0001c0001t0001g0220 | 2 | HG03540.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.62-16361G>A | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31959744 | ||||||
chr2:31959764
|
A | G | 1 | a0001c0001t0001g0096 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.62-16381T>C | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31959764 | ||||||
chr2:31959785
|
AT | A | 292 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(289): Show | 292 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(289): Show |
intron_variant | MODIFIER | c.62-16403delA | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31959785 | ||||||
chr2:31959828
|
C | T | 2 | a0001c0001t0001g0272a0001c0001t0001g0274 | 2 | HG02615.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.62-16445G>A | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31959828 | ||||||
chr2:31959864
|
T | A | 9 | a0001c0001t0001g0189a0001c0001t0001g0216a0001c0001t0001g0217others(6): Show | 9 | HG01070.hp1 HG01071.hp2 HG01081.hp2 others(6): Show |
intron_variant | MODIFIER | c.62-16481A>T | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31959864 | ||||||
chr2:31959887
|
A | G | 1 | a0001c0001t0001g0090 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.62-16504T>C | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31959887 | ||||||
chr2:31959961
|
C | T | 5 | a0001c0001t0001g0107a0001c0001t0001g0108a0001c0001t0001g0109others(2): Show | 5 | HG00438.hp1 HG00673.hp2 NA18952.hp2 others(2): Show |
intron_variant | MODIFIER | c.62-16578G>A | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31959961 | ||||||
chr2:31960054
|
G | A | 36 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0011others(33): Show | 36 | HG01168.hp1 HG01169.hp2 HG01257.hp2 others(33): Show |
intron_variant | MODIFIER | c.62-16671C>T | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31960054 | ||||||
chr2:31960126
|
G | T | 1 | a0001c0001t0001g0232 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.62-16743C>A | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31960126 | ||||||
chr2:31960130
|
G | T | 3 | a0001c0001t0002g0003a0001c0001t0002g0004a0001c0001t0002g0005 | 3 | HG01891.hp1 HG02897.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.62-16747C>A | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31960130 | ||||||
chr2:31960131
|
A | T | 3 | a0001c0001t0002g0003a0001c0001t0002g0004a0001c0001t0002g0005 | 3 | HG01891.hp1 HG02897.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.62-16748T>A | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31960131 | ||||||
chr2:31960276
|
T | G | 3 | a0001c0001t0001g0185a0001c0001t0001g0215a0001c0001t0001g0279 | 3 | HG01106.hp1 HG02970.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.62-16893A>C | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31960276 | ||||||
chr2:31960335
|
A | G | 9 | a0001c0001t0001g0290a0001c0001t0001g0291a0001c0001t0001g0292others(6): Show | 9 | HG01109.hp2 HG01891.hp1 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.62-16952T>C | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31960335 | ||||||
chr2:31960374
|
A | C | 3 | a0001c0001t0001g0232a0001c0001t0001g0233a0001c0001t0001g0234 | 3 | HG01361.hp1 HG03927.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.62-16991T>G | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31960374 | ||||||
chr2:31960446
|
G | T | 2 | a0001c0001t0001g0272a0001c0001t0001g0274 | 2 | HG02615.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.62-17063C>A | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31960446 | ||||||
chr2:31960582
|
A | C | 7 | a0001c0001t0001g0014a0001c0001t0001g0049a0001c0001t0001g0070others(4): Show | 7 | HG00099.hp1 HG02004.hp2 HG02698.hp2 others(4): Show |
intron_variant | MODIFIER | c.62-17199T>G | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31960582 | ||||||
chr2:31960822
|
G | C | 3 | a0001c0001t0002g0003a0001c0001t0002g0004a0001c0001t0002g0005 | 3 | HG01891.hp1 HG02897.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.62-17439C>G | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31960822 | ||||||
chr2:31960829
|
G | A | 4 | a0001c0001t0001g0292a0001c0001t0001g0293a0001c0001t0001g0294others(1): Show | 4 | HG02258.hp1 HG03041.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.62-17446C>T | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31960829 | ||||||
chr2:31960833
|
G | A | 1 | a0001c0001t0001g0215 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.62-17450C>T | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31960833 | ||||||
chr2:31960851
|
G | T | 1 | a0001c0001t0001g0078 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.62-17468C>A | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31960851 | ||||||
chr2:31961141
|
C | T | 1 | a0001c0001t0001g0243 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.62-17758G>A | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31961141 | ||||||
chr2:31961236
|
T | C | 2 | a0001c0001t0001g0236a0001c0001t0001g0237 | 2 | HG03139.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.62-17853A>G | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31961236 | ||||||
chr2:31961280
|
C | A | 3 | a0001c0001t0001g0292a0001c0001t0001g0293a0001c0001t0001g0294 | 3 | HG02258.hp1 HG03209.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.62-17897G>T | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31961280 | ||||||
chr2:31961370
|
A | G | 3 | a0001c0001t0002g0003a0001c0001t0002g0004a0001c0001t0002g0005 | 3 | HG01891.hp1 HG02897.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.62-17987T>C | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31961370 | ||||||
chr2:31961389
|
T | G | 3 | a0001c0001t0001g0093a0001c0001t0001g0094a0001c0001t0001g0097 | 3 | NA18942.hp1 NA18943.hp2 NA18974.hp1 |
intron_variant | MODIFIER | c.62-18006A>C | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31961389 | ||||||
chr2:31961508
|
A | T | 2 | a0001c0001t0001g0290a0001c0001t0001g0291 | 2 | HG01109.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.62-18125T>A | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31961508 | ||||||
chr2:31961618
|
C | A | 1 | a0001c0001t0001g0301 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.62-18235G>T | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31961618 | ||||||
chr2:31961618
|
CA | C | 54 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0011others(51): Show | 54 | HG01168.hp1 HG01169.hp2 HG01255.hp2 others(51): Show |
intron_variant | MODIFIER | c.62-18236delT | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31961618 | ||||||
chr2:31961619
|
A | C | 1 | a0001c0001t0001g0301 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.62-18236T>G | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31961619 | ||||||
chr2:31961627
|
A | C | 1 | a0001c0001t0001g0260 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.62-18244T>G | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31961627 | ||||||
chr2:31961638
|
C | T | 1 | a0001c0001t0001g0271 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.62-18255G>A | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31961638 | ||||||
chr2:31961760
|
A | G | 1 | a0001c0001t0001g0271 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.62-18377T>C | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31961760 | ||||||
chr2:31961777
|
C | CA | 9 | a0001c0001t0001g0018a0001c0001t0001g0093a0001c0001t0001g0094others(6): Show | 9 | NA18942.hp1 NA18943.hp2 NA18944.hp1 others(6): Show |
intron_variant | MODIFIER | c.62-18395dupT | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31961777 | ||||||
chr2:31962016
|
T | TA | 56 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0011others(53): Show | 56 | HG01168.hp1 HG01169.hp2 HG01255.hp2 others(53): Show |
intron_variant | MODIFIER | c.62-18634dupT | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31962016 | ||||||
chr2:31962118
|
G | A | 3 | a0001c0001t0001g0232a0001c0001t0001g0233a0001c0001t0001g0234 | 3 | HG01361.hp1 HG03927.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.62-18735C>T | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31962118 | ||||||
chr2:31962194
|
G | C | 1 | a0001c0001t0001g0300 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.62-18811C>G | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31962194 | ||||||
chr2:31962200
|
C | T | 1 | a0001c0001t0001g0298 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.62-18817G>A | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31962200 | ||||||
chr2:31962239
|
C | A | 62 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0011others(59): Show | 62 | HG01168.hp1 HG01169.hp2 HG01255.hp2 others(59): Show |
intron_variant | MODIFIER | c.62-18856G>T | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31962239 | ||||||
chr2:31962279
|
T | C | 4 | a0001c0001t0001g0292a0001c0001t0001g0293a0001c0001t0001g0294others(1): Show | 4 | HG02258.hp1 HG03041.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.62-18896A>G | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31962279 | ||||||
chr2:31962330
|
C | T | 2 | a0001c0001t0001g0271a0001c0001t0001g0296 | 2 | HG02280.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.62-18947G>A | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31962330 | ||||||
chr2:31962530
|
G | GACACTGA others(8): Show |
1 | a0001c0001t0001g0233 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.62-19162_62-19148d others(17): Show |
MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31962530 | ||||||
chr2:31962583
|
T | C | 3 | a0001c0001t0002g0003a0001c0001t0002g0004a0001c0001t0002g0005 | 3 | HG01891.hp1 HG02897.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.62-19200A>G | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31962583 | ||||||
chr2:31962856
|
G | A | 1 | a0001c0001t0001g0232 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.62-19473C>T | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31962856 | ||||||
chr2:31962863
|
T | C | 1 | a0001c0001t0001g0129 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.62-19480A>G | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31962863 | ||||||
chr2:31963069
|
C | T | 71 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0011others(68): Show | 71 | HG01109.hp2 HG01168.hp1 HG01169.hp2 others(68): Show |
intron_variant | MODIFIER | c.62-19686G>A | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31963069 | ||||||
chr2:31963170
|
A | G | 1 | a0001c0001t0001g0133 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.62-19787T>C | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31963170 | ||||||
chr2:31963548
|
T | C | 2 | a0001c0001t0001g0290a0001c0001t0001g0291 | 2 | HG01109.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.62-20165A>G | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31963548 | ||||||
chr2:31963748
|
C | T | 3 | a0001c0001t0001g0106a0001c0001t0001g0112a0002c0002t0001g0144 | 3 | HG01070.hp2 HG01071.hp1 HG01168.hp2 |
intron_variant | MODIFIER | c.62-20365G>A | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31963748 | ||||||
chr2:31963846
|
T | C | 2 | a0001c0001t0001g0290a0001c0001t0001g0291 | 2 | HG01109.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.62-20463A>G | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31963846 | ||||||
chr2:31963875
|
A | G | 2 | a0001c0001t0001g0219a0001c0001t0001g0220 | 2 | HG03540.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.62-20492T>C | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31963875 | ||||||
chr2:31963911
|
T | C | 4 | a0001c0001t0001g0292a0001c0001t0001g0293a0001c0001t0001g0294others(1): Show | 4 | HG02258.hp1 HG03041.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.62-20528A>G | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31963911 | ||||||
chr2:31963916
|
A | T | 49 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0011others(46): Show | 49 | HG01168.hp1 HG01169.hp2 HG01255.hp2 others(46): Show |
intron_variant | MODIFIER | c.62-20533T>A | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31963916 | ||||||
chr2:31964094
|
C | T | 55 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0011others(52): Show | 55 | HG01168.hp1 HG01169.hp2 HG01255.hp2 others(52): Show |
intron_variant | MODIFIER | c.62-20711G>A | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31964094 | ||||||
chr2:31964175
|
G | A | 55 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0011others(52): Show | 55 | HG01168.hp1 HG01169.hp2 HG01255.hp2 others(52): Show |
intron_variant | MODIFIER | c.62-20792C>T | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31964175 | ||||||
chr2:31964239
|
C | T | 1 | a0001c0001t0001g0043 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.62-20856G>A | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31964239 | ||||||
chr2:31964525
|
C | T | 2 | a0001c0001t0001g0271a0001c0001t0001g0296 | 2 | HG02280.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.62-21142G>A | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31964525 | ||||||
chr2:31964544
|
A | C | 4 | a0001c0001t0001g0239a0001c0001t0001g0240a0001c0001t0001g0241others(1): Show | 4 | HG02723.hp1 HG02809.hp2 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.62-21161T>G | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31964544 | ||||||
chr2:31964729
|
A | T | 60 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0011others(57): Show | 60 | HG01168.hp1 HG01169.hp2 HG01243.hp2 others(57): Show |
intron_variant | MODIFIER | c.62-21346T>A | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31964729 | ||||||
chr2:31964945
|
G | A | 3 | a0001c0001t0001g0232a0001c0001t0001g0233a0001c0001t0001g0234 | 3 | HG01361.hp1 HG03927.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.62-21562C>T | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31964945 | ||||||
chr2:31965050
|
C | G | 6 | a0001c0001t0001g0219a0001c0001t0001g0220a0001c0001t0001g0236others(3): Show | 6 | HG02280.hp2 HG03139.hp2 HG03540.hp1 others(3): Show |
intron_variant | MODIFIER | c.62-21667G>C | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31965050 | ||||||
chr2:31965293
|
AAGGGAAG others(1): Show |
A | 4 | a0001c0001t0001g0292a0001c0001t0001g0293a0001c0001t0001g0294others(1): Show | 4 | HG02258.hp1 HG03041.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.62-21918_62-21911d others(10): Show |
MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31965293 | ||||||
chr2:31965299
|
A | AGGAGGGA others(13): Show |
98 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0009others(95): Show | 98 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(95): Show |
intron_variant | MODIFIER | c.62-21936_62-21917d others(22): Show |
MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31965299 | ||||||
chr2:31965352
|
T | C | 3 | a0001c0001t0001g0272a0001c0001t0001g0273a0001c0001t0001g0274 | 3 | HG01243.hp2 HG02615.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.62-21969A>G | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31965352 | ||||||
chr2:31965434
|
A | C | 6 | a0001c0001t0001g0290a0001c0001t0001g0291a0001c0001t0001g0292others(3): Show | 6 | HG01109.hp2 HG02258.hp1 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.62-22051T>G | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31965434 | ||||||
chr2:31965435
|
T | C | 73 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0011others(70): Show | 73 | HG01109.hp2 HG01168.hp1 HG01169.hp2 others(70): Show |
intron_variant | MODIFIER | c.62-22052A>G | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31965435 | ||||||
chr2:31965828
|
G | C | 4 | a0001c0001t0001g0292a0001c0001t0001g0293a0001c0001t0001g0294others(1): Show | 4 | HG02258.hp1 HG03041.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.62-22445C>G | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31965828 | ||||||
chr2:31966146
|
G | C | 1 | a0001c0001t0001g0252 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.62-22763C>G | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31966146 | ||||||
chr2:31966193
|
C | G | 2 | a0001c0001t0001g0236a0001c0001t0001g0237 | 2 | HG03139.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.62-22810G>C | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31966193 | ||||||
chr2:31966268
|
T | A | 2 | a0001c0001t0001g0059a0001c0001t0002g0003 | 2 | HG01891.hp1 NA19076.hp2 |
intron_variant | MODIFIER | c.62-22885A>T | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31966268 | ||||||
chr2:31966278
|
T | C | 1 | a0001c0001t0001g0040 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.62-22895A>G | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31966278 | ||||||
chr2:31966333
|
C | T | 2 | a0001c0001t0001g0103a0001c0001t0001g0213 | 2 | HG00738.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.62-22950G>A | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31966333 | ||||||
chr2:31966596
|
T | C | 17 | a0001c0001t0001g0232a0001c0001t0001g0233a0001c0001t0001g0234others(14): Show | 17 | HG01109.hp2 HG01243.hp2 HG01361.hp1 others(14): Show |
intron_variant | MODIFIER | c.62-23213A>G | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31966596 | ||||||
chr2:31966610
|
G | C | 1 | a0001c0001t0001g0200 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.62-23227C>G | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31966610 | ||||||
chr2:31966657
|
G | A | 1 | a0001c0001t0001g0068 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.62-23274C>T | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31966657 | ||||||
chr2:31966668
|
G | C | 3 | a0001c0001t0001g0232a0001c0001t0001g0233a0001c0001t0001g0234 | 3 | HG01361.hp1 HG03927.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.62-23285C>G | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31966668 | ||||||
chr2:31966718
|
G | C | 1 | a0001c0001t0001g0279 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.62-23335C>G | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31966718 | ||||||
chr2:31966720
|
A | G | 109 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0015others(106): Show | 109 | HG00099.hp2 HG00140.hp2 HG00423.hp2 others(106): Show |
intron_variant | MODIFIER | c.62-23337T>C | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31966720 | ||||||
chr2:31966727
|
T | C | 105 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0017others(102): Show | 105 | HG00099.hp2 HG00140.hp2 HG00423.hp2 others(102): Show |
intron_variant | MODIFIER | c.62-23344A>G | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31966727 | ||||||
chr2:31966732
|
C | CA | 6 | a0001c0001t0001g0014a0001c0001t0001g0049a0001c0001t0001g0070others(3): Show | 6 | HG00099.hp1 HG02004.hp2 HG02698.hp2 others(3): Show |
intron_variant | MODIFIER | c.62-23350dupT | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31966732 | ||||||
chr2:31966732
|
C | CAAAAAAA others(4): Show |
81 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0017others(78): Show | 81 | HG00099.hp2 HG00140.hp2 HG00423.hp2 others(78): Show |
intron_variant | MODIFIER | c.62-23360_62-23350d others(13): Show |
MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31966732 | ||||||
chr2:31966732
|
C | CAAAAAAA others(5): Show |
16 | a0001c0001t0001g0021a0001c0001t0001g0024a0001c0001t0001g0025others(13): Show | 16 | HG00438.hp1 HG00597.hp1 HG01361.hp2 others(13): Show |
intron_variant | MODIFIER | c.62-23361_62-23350d others(14): Show |
MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31966732 | ||||||
chr2:31966732
|
C | CAAAAAAA others(8): Show |
1 | a0001c0001t0001g0157 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.62-23350_62-23349i others(17): Show |
MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31966732 | ||||||
chr2:31966732
|
C | CAAAAAAA others(9): Show |
2 | a0001c0001t0001g0100a0001c0001t0001g0134 | 2 | HG03209.hp1 HG03688.hp1 |
intron_variant | MODIFIER | c.62-23350_62-23349i others(18): Show |
MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31966732 | ||||||
chr2:31966732
|
C | CAAAAAAA others(10): Show |
1 | a0001c0001t0001g0101 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.62-23350_62-23349i others(19): Show |
MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31966732 | ||||||
chr2:31966732
|
C | CAAAAAAA others(24): Show |
2 | a0001c0001t0001g0159a0001c0001t0001g0166 | 2 | HG01261.hp1 HG02293.hp1 |
intron_variant | MODIFIER | c.62-23350_62-23349i others(33): Show |
MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31966732 | ||||||
chr2:31966732
|
C | CAAAAAAA others(28): Show |
1 | a0001c0001t0001g0160 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.62-23350_62-23349i others(37): Show |
MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31966732 | ||||||
chr2:31966732
|
C | CAAAAAAA others(29): Show |
2 | a0001c0001t0001g0152a0001c0001t0001g0156 | 2 | HG01106.hp2 HG01928.hp2 |
intron_variant | MODIFIER | c.62-23350_62-23349i others(38): Show |
MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31966732 | ||||||
chr2:31966732
|
C | CAAAAAAA others(30): Show |
1 | a0001c0001t0001g0158 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.62-23350_62-23349i others(39): Show |
MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31966732 | ||||||
chr2:31966757
|
A | G | 4 | a0001c0001t0001g0292a0001c0001t0001g0293a0001c0001t0001g0294others(1): Show | 4 | HG02258.hp1 HG03041.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.62-23374T>C | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31966757 | ||||||
chr2:31966971
|
T | C | 1 | a0001c0001t0001g0184 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.62-23588A>G | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31966971 | ||||||
chr2:31967027
|
T | C | 3 | a0001c0001t0001g0272a0001c0001t0001g0273a0001c0001t0001g0274 | 3 | HG01243.hp2 HG02615.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.62-23644A>G | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31967027 | ||||||
chr2:31967031
|
T | C | 2 | a0001c0001t0001g0233a0001c0001t0001g0234 | 2 | HG03927.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.62-23648A>G | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31967031 | ||||||
chr2:31967070
|
G | A | 4 | a0001c0001t0001g0219a0001c0001t0001g0220a0001c0001t0001g0271others(1): Show | 4 | HG02280.hp2 HG03540.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.62-23687C>T | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31967070 | ||||||
chr2:31967072
|
G | C | 57 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0011others(54): Show | 57 | HG01168.hp1 HG01169.hp2 HG01255.hp2 others(54): Show |
intron_variant | MODIFIER | c.62-23689C>G | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31967072 | ||||||
chr2:31967124
|
AT | A | 288 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(285): Show | 288 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(285): Show |
intron_variant | MODIFIER | c.62-23742delA | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31967124 | ||||||
chr2:31967146
|
C | T | 1 | a0001c0001t0001g0303 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.62-23763G>A | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31967146 | ||||||
chr2:31967181
|
C | T | 53 | a0001c0001t0001g0008a0001c0001t0001g0219a0001c0001t0001g0220others(50): Show | 53 | HG01168.hp1 HG01169.hp2 HG01255.hp2 others(50): Show |
intron_variant | MODIFIER | c.62-23798G>A | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31967181 | ||||||
chr2:31967284
|
C | T | 1 | a0001c0001t0001g0260 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.62-23901G>A | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31967284 | ||||||
chr2:31967289
|
A | T | 1 | a0001c0001t0001g0269 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.62-23906T>A | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31967289 | ||||||
chr2:31967329
|
G | A | 4 | a0001c0001t0001g0292a0001c0001t0001g0293a0001c0001t0001g0294others(1): Show | 4 | HG02258.hp1 HG03041.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.62-23946C>T | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31967329 | ||||||
chr2:31967404
|
G | A | 53 | a0001c0001t0001g0008a0001c0001t0001g0219a0001c0001t0001g0220others(50): Show | 53 | HG01168.hp1 HG01169.hp2 HG01255.hp2 others(50): Show |
intron_variant | MODIFIER | c.62-24021C>T | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31967404 | ||||||
chr2:31967420
|
G | A | 1 | a0001c0001t0001g0021 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.62-24037C>T | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31967420 | ||||||
chr2:31967456
|
A | G | 6 | a0001c0001t0001g0219a0001c0001t0001g0220a0001c0001t0001g0236others(3): Show | 6 | HG02280.hp2 HG03139.hp2 HG03540.hp1 others(3): Show |
intron_variant | MODIFIER | c.62-24073T>C | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31967456 | ||||||
chr2:31967540
|
C | T | 4 | a0001c0001t0001g0239a0001c0001t0001g0240a0001c0001t0001g0241others(1): Show | 4 | HG02723.hp1 HG02809.hp2 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.62-24157G>A | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31967540 | ||||||
chr2:31967556
|
T | C | 1 | a0001c0001t0001g0215 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.62-24173A>G | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31967556 | ||||||
chr2:31967643
|
G | A | 6 | a0001c0001t0001g0216a0001c0001t0001g0217a0001c0001t0001g0218others(3): Show | 6 | HG01070.hp1 HG01071.hp2 HG01261.hp2 others(3): Show |
intron_variant | MODIFIER | c.62-24260C>T | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31967643 | ||||||
chr2:31967672
|
G | A | 1 | a0001c0001t0001g0107 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.62-24289C>T | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31967672 | ||||||
chr2:31967823
|
C | G | 1 | a0002c0002t0001g0144 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.62-24440G>C | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31967823 | ||||||
chr2:31967854
|
T | C | 5 | a0001c0001t0001g0236a0001c0001t0001g0237a0001c0001t0002g0003others(2): Show | 5 | HG01891.hp1 HG02897.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.62-24471A>G | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31967854 | ||||||
chr2:31968034
|
G | A | 9 | a0001c0001t0001g0290a0001c0001t0001g0291a0001c0001t0001g0292others(6): Show | 9 | HG01109.hp2 HG01891.hp1 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.62-24651C>T | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31968034 | ||||||
chr2:31968305
|
G | A | 2 | a0001c0001t0001g0290a0001c0001t0001g0291 | 2 | HG01109.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.62-24922C>T | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31968305 | ||||||
chr2:31969104
|
T | C | 1 | a0001c0001t0002g0005 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.62-25721A>G | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31969104 | ||||||
chr2:31969125
|
T | C | 3 | a0001c0001t0001g0057a0001c0001t0001g0230a0001c0001t0001g0231 | 3 | HG00408.hp1 HG02083.hp1 NA18943.hp1 |
intron_variant | MODIFIER | c.62-25742A>G | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31969125 | ||||||
chr2:31969263
|
C | CTA | 4 | a0001c0001t0001g0042a0001c0001t0001g0143a0001c0001t0001g0168others(1): Show | 4 | HG00423.hp1 HG00642.hp1 HG00673.hp1 others(1): Show |
intron_variant | MODIFIER | c.62-25882_62-25881d others(4): Show |
MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31969263 | ||||||
chr2:31969316
|
A | G | 1 | a0001c0001t0001g0065 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.62-25933T>C | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31969316 | ||||||
chr2:31969359
|
T | TGA | 70 | a0001c0001t0001g0008a0001c0001t0001g0219a0001c0001t0001g0220others(67): Show | 70 | HG01109.hp2 HG01168.hp1 HG01169.hp2 others(67): Show |
intron_variant | MODIFIER | c.62-25977_62-25976i others(4): Show |
MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31969359 | ||||||
chr2:31969359
|
T | TTACGTGT others(25): Show |
1 | a0001c0001t0001g0070 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.62-26008_62-25977d others(34): Show |
MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31969359 | ||||||
chr2:31969362
|
C | T | 8 | a0001c0001t0001g0134a0001c0001t0001g0152a0001c0001t0001g0156others(5): Show | 8 | HG01106.hp2 HG01261.hp1 HG01928.hp2 others(5): Show |
intron_variant | MODIFIER | c.62-25979G>A | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31969362 | ||||||
chr2:31969392
|
T | TAC | 3 | a0001c0001t0001g0216a0001c0001t0001g0217a0001c0001t0001g0299 | 3 | HG01070.hp1 HG01261.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.62-26011_62-26010d others(4): Show |
MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31969392 | ||||||
chr2:31969423
|
AC | A | 3 | a0001c0001t0001g0275a0001c0001t0001g0276a0001c0001t0001g0277 | 3 | HG02055.hp1 HG03471.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.62-26041delG | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31969423 | ||||||
chr2:31969424
|
CAT | C | 109 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0015others(106): Show | 109 | HG00099.hp2 HG00140.hp2 HG00423.hp2 others(106): Show |
intron_variant | MODIFIER | c.62-26043_62-26042d others(4): Show |
MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31969424 | ||||||
chr2:31969437
|
G | A | 1 | a0001c0001t0001g0291 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.62-26054C>T | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31969437 | ||||||
chr2:31969443
|
G | T | 1 | a0001c0001t0002g0003 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.62-26060C>A | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31969443 | ||||||
chr2:31969464
|
G | A | 1 | a0001c0001t0001g0039 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.62-26081C>T | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31969464 | ||||||
chr2:31969570
|
TGG | T | 8 | a0001c0001t0001g0238a0001c0001t0001g0240a0001c0001t0001g0241others(5): Show | 8 | HG01433.hp2 HG02723.hp1 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.62-26189_62-26188d others(4): Show |
MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31969570 | ||||||
chr2:31969572
|
GGGGT | G | 10 | a0001c0001t0001g0239a0001c0001t0001g0247a0001c0001t0001g0251others(7): Show | 10 | HG01255.hp2 HG01496.hp2 HG02083.hp2 others(7): Show |
intron_variant | MODIFIER | c.62-26193_62-26190d others(6): Show |
MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31969572 | ||||||
chr2:31969572
|
GGGGTGT | G | 21 | a0001c0001t0001g0008a0001c0001t0001g0237a0001c0001t0001g0244others(18): Show | 21 | HG01168.hp1 HG01169.hp2 HG01516.hp2 others(18): Show |
intron_variant | MODIFIER | c.62-26195_62-26190d others(8): Show |
MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31969572 | ||||||
chr2:31969572
|
GGGGTGTG others(1): Show |
G | 9 | a0001c0001t0001g0236a0001c0001t0001g0243a0001c0001t0001g0265others(6): Show | 9 | HG01109.hp2 HG01891.hp2 HG02300.hp1 others(6): Show |
intron_variant | MODIFIER | c.62-26197_62-26190d others(10): Show |
MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31969572 | ||||||
chr2:31969572
|
GGGGTGTG others(3): Show |
G | 2 | a0001c0001t0001g0260a0001c0001t0001g0284 | 2 | HG03130.hp2 NA19077.hp1 |
intron_variant | MODIFIER | c.62-26199_62-26190d others(12): Show |
MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31969572 | ||||||
chr2:31969572
|
GGGGTGTG others(5): Show |
G | 3 | a0001c0001t0001g0275a0001c0001t0001g0276a0001c0001t0001g0277 | 3 | HG02055.hp1 HG03471.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.62-26201_62-26190d others(14): Show |
MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31969572 | ||||||
chr2:31969572
|
GGGGTGTG others(11): Show |
G | 3 | a0001c0001t0001g0232a0001c0001t0001g0233a0001c0001t0001g0234 | 3 | HG01361.hp1 HG03927.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.62-26207_62-26190d others(20): Show |
MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31969572 | ||||||
chr2:31969574
|
G | T | 14 | a0001c0001t0001g0219a0001c0001t0001g0220a0001c0001t0001g0253others(11): Show | 14 | HG01243.hp2 HG01257.hp2 HG01258.hp1 others(11): Show |
intron_variant | MODIFIER | c.62-26191C>A | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31969574 | ||||||
chr2:31969582
|
T | TGTGG | 3 | a0001c0001t0001g0043a0001c0001t0001g0045a0001c0001t0001g0190 | 3 | NA18612.hp2 NA18984.hp2 NA18998.hp1 |
intron_variant | MODIFIER | c.62-26203_62-26200d others(6): Show |
MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31969582 | ||||||
chr2:31969586
|
G | GGT | 24 | a0001c0001t0001g0006a0001c0001t0001g0009a0001c0001t0001g0021others(21): Show | 24 | HG00438.hp1 HG00438.hp2 HG00597.hp1 others(21): Show |
intron_variant | MODIFIER | c.62-26205_62-26204d others(4): Show |
MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31969586 | ||||||
chr2:31969586
|
G | GGTGT | 7 | a0001c0001t0001g0001a0001c0001t0001g0015a0001c0001t0001g0023others(4): Show | 7 | HG00673.hp2 HG02965.hp2 HG03453.hp2 others(4): Show |
intron_variant | MODIFIER | c.62-26207_62-26204d others(6): Show |
MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31969586 | ||||||
chr2:31969586
|
G | GGTGTGT | 3 | a0001c0001t0001g0062a0001c0001t0001g0063a0001c0001t0001g0065 | 3 | HG02129.hp2 NA18960.hp1 NA19000.hp1 |
intron_variant | MODIFIER | c.62-26209_62-26204d others(8): Show |
MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31969586 | ||||||
chr2:31969586
|
G | GGTGTGTG others(5): Show |
1 | a0001c0001t0001g0116 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.62-26215_62-26204d others(14): Show |
MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31969586 | ||||||
chr2:31969586
|
G | T | 58 | a0001c0001t0001g0008a0001c0001t0001g0067a0001c0001t0001g0071others(55): Show | 58 | HG00597.hp2 HG01109.hp2 HG01168.hp1 others(55): Show |
intron_variant | MODIFIER | c.62-26203C>A | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31969586 | ||||||
chr2:31969586
|
GGT | G | 29 | a0001c0001t0001g0007a0001c0001t0001g0029a0001c0001t0001g0038others(26): Show | 29 | HG00735.hp1 HG00738.hp1 HG00738.hp2 others(26): Show |
intron_variant | MODIFIER | c.62-26205_62-26204d others(4): Show |
MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31969586 | ||||||
chr2:31969586
|
GGTGT | G | 55 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0012others(52): Show | 55 | HG00099.hp1 HG00423.hp2 HG00621.hp2 others(52): Show |
intron_variant | MODIFIER | c.62-26207_62-26204d others(6): Show |
MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31969586 | ||||||
chr2:31969586
|
GGTGTGT | G | 32 | a0001c0001t0001g0013a0001c0001t0001g0020a0001c0001t0001g0026others(29): Show | 32 | HG00140.hp2 HG00642.hp1 HG00735.hp2 others(29): Show |
intron_variant | MODIFIER | c.62-26209_62-26204d others(8): Show |
MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31969586 | ||||||
chr2:31969586
|
GGTGTGTG others(1): Show |
G | 18 | a0001c0001t0001g0070a0001c0001t0001g0073a0001c0001t0001g0118others(15): Show | 18 | HG00099.hp2 HG00408.hp1 HG01106.hp2 others(15): Show |
intron_variant | MODIFIER | c.62-26211_62-26204d others(10): Show |
MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31969586 | ||||||
chr2:31969586
|
GGTGTGTG others(3): Show |
G | 2 | a0001c0001t0001g0079a0001c0001t0001g0114 | 2 | NA18522.hp2 NA19057.hp2 |
intron_variant | MODIFIER | c.62-26213_62-26204d others(12): Show |
MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31969586 | ||||||
chr2:31969586
|
GGTGTGTG others(5): Show |
G | 4 | a0001c0001t0001g0295a0001c0001t0002g0003a0001c0001t0002g0004others(1): Show | 4 | HG01891.hp1 HG02897.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.62-26215_62-26204d others(14): Show |
MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31969586 | ||||||
chr2:31969588
|
T | G | 4 | a0001c0001t0001g0049a0001c0001t0001g0220a0001c0001t0001g0253others(1): Show | 4 | HG01257.hp2 HG01258.hp1 HG02004.hp2 others(1): Show |
intron_variant | MODIFIER | c.62-26205A>C | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31969588 | ||||||
chr2:31969590
|
T | G | 9 | a0001c0001t0001g0016a0001c0001t0001g0238a0001c0001t0001g0240others(6): Show | 9 | HG01433.hp2 HG02723.hp1 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.62-26207A>C | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31969590 | ||||||
chr2:31969592
|
T | G | 12 | a0001c0001t0001g0218a0001c0001t0001g0239a0001c0001t0001g0247others(9): Show | 12 | HG01255.hp2 HG01261.hp2 HG01496.hp2 others(9): Show |
intron_variant | MODIFIER | c.62-26209A>C | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31969592 | ||||||
chr2:31969594
|
T | G | 25 | a0001c0001t0001g0008a0001c0001t0001g0135a0001c0001t0001g0216others(22): Show | 25 | HG01070.hp1 HG01071.hp2 HG01168.hp1 others(22): Show |
intron_variant | MODIFIER | c.62-26211A>C | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31969594 | ||||||
chr2:31969596
|
T | G | 10 | a0001c0001t0001g0236a0001c0001t0001g0237a0001c0001t0001g0243others(7): Show | 10 | HG01109.hp2 HG01891.hp2 HG02300.hp1 others(7): Show |
intron_variant | MODIFIER | c.62-26213A>C | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31969596 | ||||||
chr2:31969598
|
T | G | 4 | a0001c0001t0001g0236a0001c0001t0001g0260a0001c0001t0001g0272others(1): Show | 4 | HG02965.hp1 HG03130.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.62-26215A>C | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31969598 | ||||||
chr2:31969600
|
T | G | 8 | a0001c0001t0001g0273a0001c0001t0001g0274a0001c0001t0001g0275others(5): Show | 8 | HG01243.hp2 HG01891.hp1 HG02055.hp1 others(5): Show |
intron_variant | MODIFIER | c.62-26217A>C | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31969600 | ||||||
chr2:31969604
|
T | G | 3 | a0001c0001t0001g0232a0001c0001t0001g0233a0001c0001t0001g0234 | 3 | HG01361.hp1 HG03927.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.62-26221A>C | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31969604 | ||||||
chr2:31969635
|
T | G | 1 | a0001c0001t0001g0260 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.62-26252A>C | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31969635 | ||||||
chr2:31969649
|
C | G | 3 | a0001c0001t0001g0232a0001c0001t0001g0233a0001c0001t0001g0234 | 3 | HG01361.hp1 HG03927.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.62-26266G>C | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31969649 | ||||||
chr2:31969681
|
A | G | 2 | a0001c0001t0001g0290a0001c0001t0001g0291 | 2 | HG01109.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.62-26298T>C | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31969681 | ||||||
chr2:31969715
|
C | T | 1 | a0001c0001t0001g0152 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.62-26332G>A | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31969715 | ||||||
chr2:31969738
|
C | T | 64 | a0001c0001t0001g0008a0001c0001t0001g0219a0001c0001t0001g0220others(61): Show | 64 | HG01109.hp2 HG01168.hp1 HG01169.hp2 others(61): Show |
intron_variant | MODIFIER | c.62-26355G>A | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31969738 | ||||||
chr2:31969777
|
C | CT | 9 | a0001c0001t0001g0290a0001c0001t0001g0291a0001c0001t0001g0292others(6): Show | 9 | HG01109.hp2 HG01891.hp1 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.62-26395dupA | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31969777 | ||||||
chr2:31969777
|
CT | C | 56 | a0001c0001t0001g0008a0001c0001t0001g0039a0001c0001t0001g0219others(53): Show | 56 | HG01168.hp1 HG01169.hp2 HG01255.hp2 others(53): Show |
intron_variant | MODIFIER | c.62-26395delA | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31969777 | ||||||
chr2:31969827
|
C | G | 1 | a0001c0001t0001g0271 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.62-26444G>C | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31969827 | ||||||
chr2:31970009
|
T | C | 1 | a0001c0001t0001g0284 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.62-26626A>G | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31970009 | ||||||
chr2:31970048
|
T | C | 2 | a0001c0001t0001g0290a0001c0001t0001g0291 | 2 | HG01109.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.62-26665A>G | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31970048 | ||||||
chr2:31970219
|
C | G | 6 | a0001c0001t0001g0290a0001c0001t0001g0291a0001c0001t0001g0292others(3): Show | 6 | HG01109.hp2 HG02258.hp1 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.62-26836G>C | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31970219 | ||||||
chr2:31970229
|
C | G | 3 | a0001c0001t0001g0232a0001c0001t0001g0233a0001c0001t0001g0234 | 3 | HG01361.hp1 HG03927.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.62-26846G>C | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31970229 | ||||||
chr2:31970278
|
G | T | 1 | a0001c0001t0001g0030 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.62-26895C>A | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31970278 | ||||||
chr2:31970425
|
C | T | 1 | a0001c0001t0001g0188 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.62-27042G>A | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31970425 | ||||||
chr2:31970450
|
A | G | 1 | a0001c0001t0001g0160 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.62-27067T>C | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31970450 | ||||||
chr2:31970600
|
C | G | 1 | a0001c0001t0001g0035 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.62-27217G>C | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31970600 | ||||||
chr2:31970634
|
C | CA | 7 | a0001c0001t0001g0185a0001c0001t0001g0290a0001c0001t0001g0291others(4): Show | 7 | HG01109.hp2 HG02258.hp1 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.62-27252dupT | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31970634 | ||||||
chr2:31970788
|
G | C | 5 | a0001c0001t0001g0216a0001c0001t0001g0217a0001c0001t0001g0218others(2): Show | 5 | HG01070.hp1 HG01071.hp2 HG01261.hp2 others(2): Show |
intron_variant | MODIFIER | c.62-27405C>G | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31970788 | ||||||
chr2:31971188
|
T | C | 1 | a0001c0001t0001g0213 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.62-27805A>G | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31971188 | ||||||
chr2:31971342
|
G | A | 1 | a0001c0001t0001g0067 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.62-27959C>T | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31971342 | ||||||
chr2:31971399
|
C | T | 1 | a0001c0001t0001g0022 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.62-28016G>A | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31971399 | ||||||
chr2:31971480
|
G | A | 2 | a0001c0001t0001g0236a0001c0001t0001g0237 | 2 | HG03139.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.62-28097C>T | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31971480 | ||||||
chr2:31971529
|
C | A | 1 | a0001c0001t0001g0043 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.62-28146G>T | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31971529 | ||||||
chr2:31971614
|
A | C | 58 | a0001c0001t0001g0008a0001c0001t0001g0219a0001c0001t0001g0220others(55): Show | 58 | HG01168.hp1 HG01169.hp2 HG01243.hp2 others(55): Show |
intron_variant | MODIFIER | c.62-28231T>G | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31971614 | ||||||
chr2:31971724
|
T | C | 62 | a0001c0001t0001g0008a0001c0001t0001g0219a0001c0001t0001g0220others(59): Show | 62 | HG01109.hp2 HG01168.hp1 HG01169.hp2 others(59): Show |
intron_variant | MODIFIER | c.62-28341A>G | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31971724 | ||||||
chr2:31971735
|
C | T | 1 | a0001c0001t0002g0004 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.62-28352G>A | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31971735 | ||||||
chr2:31971941
|
T | A | 68 | a0001c0001t0001g0008a0001c0001t0001g0219a0001c0001t0001g0220others(65): Show | 68 | HG01109.hp2 HG01168.hp1 HG01169.hp2 others(65): Show |
intron_variant | MODIFIER | c.62-28558A>T | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31971941 | ||||||
chr2:31972079
|
C | T | 1 | a0001c0001t0001g0296 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.62-28696G>A | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31972079 | ||||||
chr2:31972136
|
C | G | 6 | a0001c0001t0001g0290a0001c0001t0001g0291a0001c0001t0001g0292others(3): Show | 6 | HG01109.hp2 HG02258.hp1 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.62-28753G>C | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31972136 | ||||||
chr2:31972264
|
C | T | 43 | a0001c0001t0001g0238a0001c0001t0001g0239a0001c0001t0001g0240others(40): Show | 43 | HG01168.hp1 HG01169.hp2 HG01255.hp2 others(40): Show |
intron_variant | MODIFIER | c.62-28881G>A | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31972264 | ||||||
chr2:31972335
|
A | G | 5 | a0001c0001t0001g0169a0001c0001t0001g0176a0001c0001t0001g0177others(2): Show | 5 | HG01934.hp1 HG01978.hp1 HG01993.hp1 others(2): Show |
intron_variant | MODIFIER | c.62-28952T>C | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31972335 | ||||||
chr2:31972517
|
C | T | 1 | a0001c0001t0001g0236 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.62-29134G>A | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31972517 | ||||||
chr2:31972630
|
G | A | 1 | a0001c0001t0001g0232 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.62-29247C>T | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31972630 | ||||||
chr2:31972949
|
A | G | 3 | a0001c0001t0001g0275a0001c0001t0001g0276a0001c0001t0001g0277 | 3 | HG02055.hp1 HG03471.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.62-29566T>C | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31972949 | ||||||
chr2:31972972
|
T | C | 1 | a0001c0001t0001g0110 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.62-29589A>G | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31972972 | ||||||
chr2:31973151
|
T | C | 3 | a0001c0001t0001g0275a0001c0001t0001g0276a0001c0001t0001g0277 | 3 | HG02055.hp1 HG03471.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.62-29768A>G | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31973151 | ||||||
chr2:31973453
|
C | T | 9 | a0001c0001t0001g0290a0001c0001t0001g0291a0001c0001t0001g0292others(6): Show | 9 | HG01109.hp2 HG01891.hp1 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.62-30070G>A | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31973453 | ||||||
chr2:31973523
|
G | T | 2 | a0001c0001t0001g0271a0001c0001t0001g0296 | 2 | HG02280.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.62-30140C>A | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31973523 | ||||||
chr2:31973583
|
A | G | 3 | a0001c0001t0001g0275a0001c0001t0001g0276a0001c0001t0001g0277 | 3 | HG02055.hp1 HG03471.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.62-30200T>C | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31973583 | ||||||
chr2:31973774
|
T | C | 57 | a0001c0001t0001g0008a0001c0001t0001g0236a0001c0001t0001g0237others(54): Show | 57 | HG01168.hp1 HG01169.hp2 HG01243.hp2 others(54): Show |
intron_variant | MODIFIER | c.62-30391A>G | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31973774 | ||||||
chr2:31973778
|
A | G | 65 | a0001c0001t0001g0008a0001c0001t0001g0219a0001c0001t0001g0220others(62): Show | 65 | HG01109.hp2 HG01168.hp1 HG01169.hp2 others(62): Show |
intron_variant | MODIFIER | c.62-30395T>C | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31973778 | ||||||
chr2:31973938
|
C | T | 1 | a0001c0001t0001g0185 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.62-30555G>A | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31973938 | ||||||
chr2:31974160
|
T | C | 2 | a0001c0001t0001g0243a0001c0001t0001g0268 | 2 | HG01891.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.62-30777A>G | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31974160 | ||||||
chr2:31974243
|
A | T | 1 | a0001c0001t0001g0233 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.62-30860T>A | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31974243 | ||||||
chr2:31974485
|
G | A | 1 | a0001c0001t0001g0189 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.62-31102C>T | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31974485 | ||||||
chr2:31974505
|
G | C | 1 | a0001c0001t0001g0222 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.62-31122C>G | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31974505 | ||||||
chr2:31974506
|
G | C | 2 | a0001c0001t0001g0236a0001c0001t0001g0237 | 2 | HG03139.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.62-31123C>G | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31974506 | ||||||
chr2:31974687
|
G | A | 3 | a0001c0001t0001g0048a0001c0001t0001g0054a0001c0001t0001g0055 | 3 | NA18953.hp1 NA18977.hp1 NA19056.hp1 |
intron_variant | MODIFIER | c.62-31304C>T | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31974687 | ||||||
chr2:31975086
|
C | T | 1 | a0001c0001t0001g0296 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.62-31703G>A | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31975086 | ||||||
chr2:31975102
|
G | A | 2 | a0001c0001t0001g0239a0001c0001t0001g0270 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.62-31719C>T | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31975102 | ||||||
chr2:31975199
|
C | T | 1 | a0001c0001t0001g0268 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.62-31816G>A | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31975199 | ||||||
chr2:31975761
|
G | A | 2 | a0001c0001t0001g0024a0001c0001t0001g0165 | 2 | NA18940.hp2 NA18968.hp2 |
intron_variant | MODIFIER | c.62-32378C>T | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31975761 | ||||||
chr2:31975854
|
T | C | 1 | a0001c0001t0001g0296 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.62-32471A>G | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31975854 | ||||||
chr2:31975971
|
C | T | 3 | a0001c0001t0001g0232a0001c0001t0001g0233a0001c0001t0001g0234 | 3 | HG01361.hp1 HG03927.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.62-32588G>A | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31975971 | ||||||
chr2:31976001
|
C | A | 4 | a0001c0001t0001g0292a0001c0001t0001g0293a0001c0001t0001g0294others(1): Show | 4 | HG02258.hp1 HG03041.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.62-32618G>T | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31976001 | ||||||
chr2:31976570
|
T | A | 58 | a0001c0001t0001g0008a0001c0001t0001g0219a0001c0001t0001g0220others(55): Show | 58 | HG01168.hp1 HG01169.hp2 HG01243.hp2 others(55): Show |
intron_variant | MODIFIER | c.62-33187A>T | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31976570 | ||||||
chr2:31977219
|
G | A | 1 | a0001c0001t0001g0301 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.61+32968C>T | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31977219 | ||||||
chr2:31977296
|
G | A | 1 | a0001c0001t0001g0092 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.61+32891C>T | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31977296 | ||||||
chr2:31977404
|
C | G | 2 | a0001c0001t0001g0233a0001c0001t0001g0234 | 2 | HG03927.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.61+32783G>C | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31977404 | ||||||
chr2:31977422
|
A | G | 4 | a0001c0001t0001g0016a0001c0001t0001g0043a0001c0001t0001g0045others(1): Show | 4 | NA18612.hp2 NA18951.hp2 NA18984.hp2 others(1): Show |
intron_variant | MODIFIER | c.61+32765T>C | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31977422 | ||||||
chr2:31977514
|
A | T | 1 | a0001c0001t0001g0152 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.61+32673T>A | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31977514 | ||||||
chr2:31977805
|
T | C | 2 | a0001c0001t0001g0236a0001c0001t0001g0237 | 2 | HG03139.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.61+32382A>G | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31977805 | ||||||
chr2:31977944
|
C | T | 3 | a0001c0001t0001g0275a0001c0001t0001g0276a0001c0001t0001g0277 | 3 | HG02055.hp1 HG03471.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.61+32243G>A | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31977944 | ||||||
chr2:31977958
|
A | G | 1 | a0001c0001t0001g0081 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.61+32229T>C | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31977958 | ||||||
chr2:31978091
|
T | G | 4 | a0001c0001t0001g0292a0001c0001t0001g0293a0001c0001t0001g0294others(1): Show | 4 | HG02258.hp1 HG03041.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.61+32096A>C | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31978091 | ||||||
chr2:31978139
|
C | T | 1 | a0001c0001t0001g0232 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.61+32048G>A | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31978139 | ||||||
chr2:31978309
|
C | T | 1 | a0001c0001t0001g0060 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.61+31878G>A | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31978309 | ||||||
chr2:31978417
|
G | C | 1 | a0001c0001t0001g0183 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.61+31770C>G | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31978417 | ||||||
chr2:31978539
|
C | T | 1 | a0001c0001t0002g0004 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.61+31648G>A | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31978539 | ||||||
chr2:31978558
|
G | A | 1 | a0001c0001t0001g0295 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.61+31629C>T | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31978558 | ||||||
chr2:31978650
|
C | T | 2 | a0001c0001t0001g0239a0001c0001t0001g0270 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.61+31537G>A | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31978650 | ||||||
chr2:31978710
|
G | A | 1 | a0001c0001t0001g0058 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.61+31477C>T | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31978710 | ||||||
chr2:31978957
|
C | T | 3 | a0001c0001t0001g0275a0001c0001t0001g0276a0001c0001t0001g0277 | 3 | HG02055.hp1 HG03471.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.61+31230G>A | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31978957 | ||||||
chr2:31978967
|
C | G | 63 | a0001c0001t0001g0008a0001c0001t0001g0236a0001c0001t0001g0237others(60): Show | 63 | HG01109.hp2 HG01168.hp1 HG01169.hp2 others(60): Show |
intron_variant | MODIFIER | c.61+31220G>C | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31978967 | ||||||
chr2:31978968
|
CA | C | 4 | a0001c0001t0001g0292a0001c0001t0001g0293a0001c0001t0001g0294others(1): Show | 4 | HG02258.hp1 HG03041.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.61+31218delT | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31978968 | ||||||
chr2:31979052
|
AC | A | 3 | a0001c0001t0001g0232a0001c0001t0001g0233a0001c0001t0001g0234 | 3 | HG01361.hp1 HG03927.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.61+31134delG | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31979052 | ||||||
chr2:31979069
|
G | T | 57 | a0001c0001t0001g0008a0001c0001t0001g0236a0001c0001t0001g0237others(54): Show | 57 | HG01168.hp1 HG01169.hp2 HG01243.hp2 others(54): Show |
intron_variant | MODIFIER | c.61+31118C>A | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31979069 | ||||||
chr2:31979093
|
G | A | 46 | a0001c0001t0001g0008a0001c0001t0001g0238a0001c0001t0001g0239others(43): Show | 46 | HG01168.hp1 HG01169.hp2 HG01255.hp2 others(43): Show |
intron_variant | MODIFIER | c.61+31094C>T | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31979093 | ||||||
chr2:31979200
|
G | A | 1 | a0001c0001t0001g0056 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.61+30987C>T | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31979200 | ||||||
chr2:31979358
|
T | C | 1 | a0001c0001t0001g0271 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.61+30829A>G | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31979358 | ||||||
chr2:31979401
|
T | A | 3 | a0001c0001t0001g0048a0001c0001t0001g0054a0001c0001t0001g0055 | 3 | NA18953.hp1 NA18977.hp1 NA19056.hp1 |
intron_variant | MODIFIER | c.61+30786A>T | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31979401 | ||||||
chr2:31979796
|
T | C | 1 | a0001c0001t0001g0165 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.61+30391A>G | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31979796 | ||||||
chr2:31979920
|
T | G | 3 | a0001c0001t0001g0292a0001c0001t0001g0293a0001c0001t0001g0294 | 3 | HG02258.hp1 HG03209.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.61+30267A>C | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31979920 | ||||||
chr2:31979979
|
T | C | 2 | a0001c0001t0001g0054a0001c0001t0001g0055 | 2 | NA18953.hp1 NA18977.hp1 |
intron_variant | MODIFIER | c.61+30208A>G | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31979979 | ||||||
chr2:31980009
|
TA | T | 64 | a0001c0001t0001g0008a0001c0001t0001g0052a0001c0001t0001g0063others(61): Show | 64 | HG01070.hp1 HG01109.hp2 HG01168.hp1 others(61): Show |
intron_variant | MODIFIER | c.61+30177delT | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31980009 | ||||||
chr2:31980032
|
A | G | 3 | a0001c0001t0001g0069a0001c0001t0001g0071a0001c0001t0001g0072 | 3 | HG02717.hp1 HG03195.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.61+30155T>C | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31980032 | ||||||
chr2:31980098
|
C | T | 68 | a0001c0001t0001g0008a0001c0001t0001g0232a0001c0001t0001g0233others(65): Show | 68 | HG01109.hp2 HG01168.hp1 HG01169.hp2 others(65): Show |
intron_variant | MODIFIER | c.61+30089G>A | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31980098 | ||||||
chr2:31980151
|
G | C | 3 | a0001c0001t0002g0003a0001c0001t0002g0004a0001c0001t0002g0005 | 3 | HG01891.hp1 HG02897.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.61+30036C>G | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31980151 | ||||||
chr2:31980261
|
C | T | 1 | a0001c0001t0001g0123 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.61+29926G>A | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31980261 | ||||||
chr2:31980292
|
G | C | 1 | a0001c0001t0001g0155 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.61+29895C>G | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31980292 | ||||||
chr2:31980327
|
G | A | 1 | a0001c0001t0001g0070 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.61+29860C>T | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31980327 | ||||||
chr2:31980402
|
C | A | 1 | a0001c0001t0001g0119 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.61+29785G>T | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31980402 | ||||||
chr2:31980902
|
A | G | 1 | a0001c0001t0001g0298 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.61+29285T>C | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31980902 | ||||||
chr2:31980960
|
T | G | 185 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(182): Show | 185 | HG00099.hp2 HG00140.hp2 HG00423.hp2 others(182): Show |
intron_variant | MODIFIER | c.61+29227A>C | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31980960 | ||||||
chr2:31981252
|
G | C | 6 | a0001c0001t0001g0232a0001c0001t0001g0233a0001c0001t0001g0234others(3): Show | 6 | HG01243.hp2 HG01361.hp1 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.61+28935C>G | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31981252 | ||||||
chr2:31981438
|
T | C | 2 | a0001c0001t0001g0271a0001c0001t0001g0296 | 2 | HG02280.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.61+28749A>G | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31981438 | ||||||
chr2:31981565
|
T | C | 1 | a0001c0001t0001g0290 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.61+28622A>G | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31981565 | ||||||
chr2:31981911
|
G | A | 1 | a0001c0001t0001g0233 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.61+28276C>T | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31981911 | ||||||
chr2:31981943
|
C | T | 69 | a0001c0001t0001g0008a0001c0001t0001g0232a0001c0001t0001g0233others(66): Show | 69 | HG01109.hp2 HG01168.hp1 HG01169.hp2 others(66): Show |
intron_variant | MODIFIER | c.61+28244G>A | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31981943 | ||||||
chr2:31982015
|
C | A | 8 | a0001c0001t0001g0216a0001c0001t0001g0217a0001c0001t0001g0218others(5): Show | 8 | HG01070.hp1 HG01071.hp2 HG01261.hp2 others(5): Show |
intron_variant | MODIFIER | c.61+28172G>T | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31982015 | ||||||
chr2:31982050
|
A | G | 2 | a0001c0001t0001g0122a0001c0001t0001g0142 | 2 | NA18975.hp2 NA19000.hp2 |
intron_variant | MODIFIER | c.61+28137T>C | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31982050 | ||||||
chr2:31982189
|
C | T | 1 | a0001c0001t0001g0103 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.61+27998G>A | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31982189 | ||||||
chr2:31982277
|
C | G | 2 | a0001c0001t0001g0233a0001c0001t0001g0234 | 2 | HG03927.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.61+27910G>C | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31982277 | ||||||
chr2:31982296
|
C | T | 1 | a0001c0001t0001g0195 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.61+27891G>A | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31982296 | ||||||
chr2:31982320
|
G | A | 2 | a0001c0001t0001g0290a0001c0001t0001g0291 | 2 | HG01109.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.61+27867C>T | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31982320 | ||||||
chr2:31982588
|
C | CA | 29 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0012others(26): Show | 29 | HG00408.hp2 HG00642.hp2 HG00673.hp1 others(26): Show |
intron_variant | MODIFIER | c.61+27598dupT | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31982588 | ||||||
chr2:31982588
|
CA | C | 58 | a0001c0001t0001g0008a0001c0001t0001g0038a0001c0001t0001g0059others(55): Show | 58 | HG01109.hp2 HG01168.hp1 HG01169.hp2 others(55): Show |
intron_variant | MODIFIER | c.61+27598delT | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31982588 | ||||||
chr2:31982658
|
G | A | 1 | a0001c0001t0001g0030 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.61+27529C>T | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31982658 | ||||||
chr2:31982719
|
A | G | 61 | a0001c0001t0001g0008a0001c0001t0001g0219a0001c0001t0001g0220others(58): Show | 61 | HG01109.hp2 HG01168.hp1 HG01169.hp2 others(58): Show |
intron_variant | MODIFIER | c.61+27468T>C | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31982719 | ||||||
chr2:31982991
|
C | A | 1 | a0001c0001t0001g0008 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.61+27196G>T | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31982991 | ||||||
chr2:31983028
|
C | T | 1 | a0001c0001t0001g0232 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.61+27159G>A | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31983028 | ||||||
chr2:31983084
|
A | G | 3 | a0001c0001t0001g0232a0001c0001t0001g0233a0001c0001t0001g0234 | 3 | HG01361.hp1 HG03927.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.61+27103T>C | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31983084 | ||||||
chr2:31983128
|
A | C | 58 | a0001c0001t0001g0008a0001c0001t0001g0219a0001c0001t0001g0220others(55): Show | 58 | HG01168.hp1 HG01169.hp2 HG01243.hp2 others(55): Show |
intron_variant | MODIFIER | c.61+27059T>G | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31983128 | ||||||
chr2:31983134
|
G | A | 1 | a0001c0001t0001g0065 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.61+27053C>T | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31983134 | ||||||
chr2:31983201
|
T | C | 69 | a0001c0001t0001g0008a0001c0001t0001g0232a0001c0001t0001g0233others(66): Show | 69 | HG01109.hp2 HG01168.hp1 HG01169.hp2 others(66): Show |
intron_variant | MODIFIER | c.61+26986A>G | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31983201 | ||||||
chr2:31983380
|
G | C | 113 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0017others(110): Show | 113 | HG00099.hp2 HG00140.hp2 HG00423.hp2 others(110): Show |
intron_variant | MODIFIER | c.61+26807C>G | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31983380 | ||||||
chr2:31983417
|
G | A | 1 | a0001c0001t0001g0186 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.61+26770C>T | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31983417 | ||||||
chr2:31983485
|
G | A | 102 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0009others(99): Show | 102 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(99): Show |
intron_variant | MODIFIER | c.61+26702C>T | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31983485 | ||||||
chr2:31983487
|
G | A | 1 | a0001c0001t0001g0120 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.61+26700C>T | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31983487 | ||||||
chr2:31983503
|
C | T | 1 | a0001c0001t0001g0134 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.61+26684G>A | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31983503 | ||||||
chr2:31983537
|
C | T | 60 | a0001c0001t0001g0008a0001c0001t0001g0236a0001c0001t0001g0237others(57): Show | 60 | HG01168.hp1 HG01169.hp2 HG01243.hp2 others(57): Show |
intron_variant | MODIFIER | c.61+26650G>A | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31983537 | ||||||
chr2:31983596
|
G | A | 4 | a0001c0001t0001g0239a0001c0001t0001g0240a0001c0001t0001g0241others(1): Show | 4 | HG02723.hp1 HG02809.hp2 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.61+26591C>T | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31983596 | ||||||
chr2:31983637
|
T | C | 1 | a0001c0001t0001g0274 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.61+26550A>G | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31983637 | ||||||
chr2:31983712
|
G | A | 2 | a0001c0001t0001g0233a0001c0001t0001g0234 | 2 | HG03927.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.61+26475C>T | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31983712 | ||||||
chr2:31983725
|
C | T | 1 | a0001c0001t0001g0201 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.61+26462G>A | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31983725 | ||||||
chr2:31983780
|
G | C | 1 | a0001c0001t0001g0200 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.61+26407C>G | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31983780 | ||||||
chr2:31984082
|
T | C | 3 | a0001c0001t0001g0272a0001c0001t0001g0273a0001c0001t0001g0274 | 3 | HG01243.hp2 HG02615.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.61+26105A>G | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31984082 | ||||||
chr2:31984128
|
A | G | 2 | a0001c0001t0001g0243a0001c0001t0001g0268 | 2 | HG01891.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.61+26059T>C | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31984128 | ||||||
chr2:31984377
|
A | G | 2 | a0001c0001t0001g0236a0001c0001t0001g0237 | 2 | HG03139.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.61+25810T>C | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31984377 | ||||||
chr2:31984581
|
G | A | 2 | a0001c0001t0001g0290a0001c0001t0001g0291 | 2 | HG01109.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.61+25606C>T | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31984581 | ||||||
chr2:31984661
|
C | T | 2 | a0001c0001t0001g0290a0001c0001t0001g0291 | 2 | HG01109.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.61+25526G>A | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31984661 | ||||||
chr2:31984740
|
A | T | 1 | a0001c0001t0001g0221 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.61+25447T>A | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31984740 | ||||||
chr2:31984801
|
G | A | 1 | a0001c0001t0001g0111 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.61+25386C>T | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31984801 | ||||||
chr2:31984884
|
T | C | 1 | a0001c0001t0001g0007 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.61+25303A>G | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31984884 | ||||||
chr2:31984922
|
T | C | 1 | a0001c0001t0001g0022 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.61+25265A>G | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31984922 | ||||||
chr2:31984934
|
G | A | 1 | a0001c0001t0001g0175 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.61+25253C>T | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31984934 | ||||||
chr2:31984992
|
A | C | 56 | a0001c0001t0001g0008a0001c0001t0001g0236a0001c0001t0001g0237others(53): Show | 56 | HG01168.hp1 HG01169.hp2 HG01243.hp2 others(53): Show |
intron_variant | MODIFIER | c.61+25195T>G | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31984992 | ||||||
chr2:31985241
|
G | A | 2 | a0001c0001t0001g0290a0001c0001t0001g0291 | 2 | HG01109.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.61+24946C>T | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31985241 | ||||||
chr2:31985360
|
T | C | 3 | a0001c0001t0001g0001a0001c0001t0001g0139a0001c0001t0001g0211 | 3 | HG02257.hp1 HG02818.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.61+24827A>G | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31985360 | ||||||
chr2:31985406
|
A | C | 1 | a0001c0001t0001g0210 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.61+24781T>G | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31985406 | ||||||
chr2:31985453
|
G | A | 5 | a0001c0001t0001g0271a0001c0001t0001g0272a0001c0001t0001g0273others(2): Show | 5 | HG01243.hp2 HG02280.hp2 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.61+24734C>T | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31985453 | ||||||
chr2:31985535
|
A | G | 1 | a0001c0001t0001g0182 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.61+24652T>C | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31985535 | ||||||
chr2:31985611
|
A | C | 296 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(293): Show | 296 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(293): Show |
intron_variant | MODIFIER | c.61+24576T>G | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31985611 | ||||||
chr2:31985869
|
C | A | 4 | a0001c0001t0001g0239a0001c0001t0001g0240a0001c0001t0001g0241others(1): Show | 4 | HG02723.hp1 HG02809.hp2 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.61+24318G>T | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31985869 | ||||||
chr2:31985990
|
T | C | 56 | a0001c0001t0001g0008a0001c0001t0001g0236a0001c0001t0001g0237others(53): Show | 56 | HG01168.hp1 HG01169.hp2 HG01243.hp2 others(53): Show |
intron_variant | MODIFIER | c.61+24197A>G | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31985990 | ||||||
chr2:31986121
|
G | A | 2 | a0001c0001t0001g0219a0001c0001t0001g0220 | 2 | HG03540.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.61+24066C>T | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31986121 | ||||||
chr2:31986163
|
G | A | 53 | a0001c0001t0001g0008a0001c0001t0001g0236a0001c0001t0001g0237others(50): Show | 53 | HG01168.hp1 HG01169.hp2 HG01255.hp2 others(50): Show |
intron_variant | MODIFIER | c.61+24024C>T | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31986163 | ||||||
chr2:31986213
|
T | C | 1 | a0001c0001t0001g0171 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.61+23974A>G | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31986213 | ||||||
chr2:31986293
|
G | A | 1 | a0001c0001t0001g0067 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.61+23894C>T | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31986293 | ||||||
chr2:31986333
|
G | A | 1 | a0001c0001t0001g0210 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.61+23854C>T | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31986333 | ||||||
chr2:31986345
|
G | A | 1 | a0001c0001t0001g0139 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.61+23842C>T | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31986345 | ||||||
chr2:31986354
|
C | A | 3 | a0001c0001t0001g0232a0001c0001t0001g0233a0001c0001t0001g0234 | 3 | HG01361.hp1 HG03927.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.61+23833G>T | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31986354 | ||||||
chr2:31986365
|
G | A | 2 | a0001c0001t0001g0236a0001c0001t0001g0237 | 2 | HG03139.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.61+23822C>T | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31986365 | ||||||
chr2:31986481
|
T | A | 1 | a0001c0001t0001g0234 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.61+23706A>T | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31986481 | ||||||
chr2:31986495
|
T | A | 1 | a0001c0001t0001g0078 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.61+23692A>T | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31986495 | ||||||
chr2:31986694
|
T | C | 1 | a0001c0001t0001g0201 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.61+23493A>G | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31986694 | ||||||
chr2:31986831
|
A | C | 1 | a0001c0001t0001g0089 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.61+23356T>G | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31986831 | ||||||
chr2:31986832
|
A | T | 1 | a0001c0001t0001g0089 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.61+23355T>A | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31986832 | ||||||
chr2:31986842
|
G | A | 3 | a0001c0001t0002g0003a0001c0001t0002g0004a0001c0001t0002g0005 | 3 | HG01891.hp1 HG02897.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.61+23345C>T | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31986842 | ||||||
chr2:31986855
|
C | T | 3 | a0001c0001t0001g0232a0001c0001t0001g0233a0001c0001t0001g0234 | 3 | HG01361.hp1 HG03927.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.61+23332G>A | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31986855 | ||||||
chr2:31986901
|
G | C | 8 | a0001c0001t0001g0134a0001c0001t0001g0152a0001c0001t0001g0156others(5): Show | 8 | HG01106.hp2 HG01261.hp1 HG01928.hp2 others(5): Show |
intron_variant | MODIFIER | c.61+23286C>G | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31986901 | ||||||
chr2:31986905
|
T | C | 2 | a0001c0001t0001g0029a0001c0001t0001g0155 | 2 | HG02071.hp1 NA18612.hp1 |
intron_variant | MODIFIER | c.61+23282A>G | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31986905 | ||||||
chr2:31987026
|
T | C | 2 | a0001c0001t0001g0271a0001c0001t0001g0296 | 2 | HG02280.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.61+23161A>G | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31987026 | ||||||
chr2:31987229
|
C | T | 7 | a0001c0001t0001g0236a0001c0001t0001g0237a0001c0001t0001g0271others(4): Show | 7 | HG01243.hp2 HG02280.hp2 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.61+22958G>A | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31987229 | ||||||
chr2:31987342
|
A | G | 1 | a0001c0001t0001g0278 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.61+22845T>C | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31987342 | ||||||
chr2:31987378
|
C | T | 2 | a0001c0001t0001g0104a0001c0001t0001g0105 | 2 | NA18984.hp1 NA19070.hp2 |
intron_variant | MODIFIER | c.61+22809G>A | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31987378 | ||||||
chr2:31987589
|
T | C | 1 | a0001c0001t0001g0172 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.61+22598A>G | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31987589 | ||||||
chr2:31987685
|
C | A | 1 | a0001c0001t0001g0082 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.61+22502G>T | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31987685 | ||||||
chr2:31987866
|
T | G | 53 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0009others(50): Show | 53 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(50): Show |
intron_variant | MODIFIER | c.61+22321A>C | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31987866 | ||||||
chr2:31988070
|
A | G | 1 | a0001c0001t0001g0070 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.61+22117T>C | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31988070 | ||||||
chr2:31988279
|
G | T | 53 | a0001c0001t0001g0008a0001c0001t0001g0236a0001c0001t0001g0237others(50): Show | 53 | HG01168.hp1 HG01169.hp2 HG01255.hp2 others(50): Show |
intron_variant | MODIFIER | c.61+21908C>A | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31988279 | ||||||
chr2:31988313
|
G | A | 3 | a0001c0001t0001g0178a0001c0001t0001g0186a0001c0001t0001g0188 | 3 | HG00408.hp2 NA19009.hp2 NA19090.hp1 |
intron_variant | MODIFIER | c.61+21874C>T | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31988313 | ||||||
chr2:31988546
|
G | A | 3 | a0001c0001t0002g0003a0001c0001t0002g0004a0001c0001t0002g0005 | 3 | HG01891.hp1 HG02897.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.61+21641C>T | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31988546 | ||||||
chr2:31988577
|
T | C | 6 | a0001c0001t0001g0216a0001c0001t0001g0217a0001c0001t0001g0218others(3): Show | 6 | HG01070.hp1 HG01071.hp2 HG01261.hp2 others(3): Show |
intron_variant | MODIFIER | c.61+21610A>G | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31988577 | ||||||
chr2:31988590
|
C | G | 1 | a0001c0001t0001g0279 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.61+21597G>C | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31988590 | ||||||
chr2:31988841
|
T | C | 46 | a0001c0001t0001g0008a0001c0001t0001g0238a0001c0001t0001g0239others(43): Show | 46 | HG01168.hp1 HG01169.hp2 HG01255.hp2 others(43): Show |
intron_variant | MODIFIER | c.61+21346A>G | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31988841 | ||||||
chr2:31988868
|
A | G | 2 | a0001c0001t0001g0258a0001c0001t0001g0259 | 2 | HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.61+21319T>C | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31988868 | ||||||
chr2:31988919
|
G | A | 3 | a0001c0001t0001g0216a0001c0001t0001g0217a0001c0001t0001g0299 | 3 | HG01070.hp1 HG01261.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.61+21268C>T | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31988919 | ||||||
chr2:31989078
|
T | C | 1 | a0001c0001t0001g0202 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.61+21109A>G | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31989078 | ||||||
chr2:31989139
|
G | C | 1 | a0001c0001t0001g0149 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.61+21048C>G | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31989139 | ||||||
chr2:31989159
|
C | T | 8 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0012others(5): Show | 8 | HG00408.hp2 NA18940.hp1 NA18978.hp2 others(5): Show |
intron_variant | MODIFIER | c.61+21028G>A | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31989159 | ||||||
chr2:31989228
|
CA | C | 7 | a0001c0001t0001g0052a0001c0001t0001g0145a0001c0001t0001g0258others(4): Show | 7 | HG01168.hp1 HG01257.hp1 HG01891.hp1 others(4): Show |
intron_variant | MODIFIER | c.61+20958delT | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31989228 | ||||||
chr2:31989323
|
G | A | 5 | a0001c0001t0001g0197a0001c0001t0001g0198a0001c0001t0001g0199others(2): Show | 5 | HG02622.hp2 HG02922.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.61+20864C>T | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31989323 | ||||||
chr2:31989556
|
G | A | 3 | a0001c0001t0001g0275a0001c0001t0001g0276a0001c0001t0001g0277 | 3 | HG02055.hp1 HG03471.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.61+20631C>T | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31989556 | ||||||
chr2:31989692
|
T | C | 3 | a0001c0001t0001g0272a0001c0001t0001g0273a0001c0001t0001g0274 | 3 | HG01243.hp2 HG02615.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.61+20495A>G | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31989692 | ||||||
chr2:31989887
|
T | C | 3 | a0001c0001t0001g0286a0001c0001t0001g0287a0001c0001t0001g0288 | 3 | HG02129.hp1 HG02155.hp2 NA18939.hp1 |
intron_variant | MODIFIER | c.61+20300A>G | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31989887 | ||||||
chr2:31990342
|
T | C | 2 | a0001c0001t0001g0236a0001c0001t0001g0237 | 2 | HG03139.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.61+19845A>G | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31990342 | ||||||
chr2:31990448
|
G | T | 292 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(289): Show | 292 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(289): Show |
intron_variant | MODIFIER | c.61+19739C>A | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31990448 | ||||||
chr2:31990504
|
T | C | 69 | a0001c0001t0001g0008a0001c0001t0001g0232a0001c0001t0001g0233others(66): Show | 69 | HG01109.hp2 HG01168.hp1 HG01169.hp2 others(66): Show |
intron_variant | MODIFIER | c.61+19683A>G | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31990504 | ||||||
chr2:31990571
|
C | CA | 9 | a0001c0001t0001g0189a0001c0001t0001g0216a0001c0001t0001g0217others(6): Show | 9 | HG01070.hp1 HG01071.hp2 HG01081.hp2 others(6): Show |
intron_variant | MODIFIER | c.61+19615_61+19616i others(3): Show |
MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31990571 | ||||||
chr2:31990571
|
C | CT | 8 | a0001c0001t0001g0059a0001c0001t0001g0097a0001c0001t0001g0103others(5): Show | 8 | HG00738.hp2 HG01361.hp1 HG03453.hp1 others(5): Show |
intron_variant | MODIFIER | c.61+19615dupA | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31990571 | ||||||
chr2:31990598
|
C | G | 1 | a0001c0001t0001g0061 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.61+19589G>C | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31990598 | ||||||
chr2:31990699
|
G | A | 13 | a0001c0001t0001g0244a0001c0001t0001g0249a0001c0001t0001g0250others(10): Show | 13 | HG02083.hp2 NA18953.hp2 NA18964.hp2 others(10): Show |
intron_variant | MODIFIER | c.61+19488C>T | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31990699 | ||||||
chr2:31990753
|
A | G | 1 | a0001c0001t0001g0175 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.61+19434T>C | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31990753 | ||||||
chr2:31990801
|
A | G | 3 | a0001c0001t0001g0232a0001c0001t0001g0233a0001c0001t0001g0234 | 3 | HG01361.hp1 HG03927.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.61+19386T>C | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31990801 | ||||||
chr2:31991299
|
G | A | 2 | a0001c0001t0001g0228a0001c0001t0001g0290 | 2 | HG02622.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.61+18888C>T | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31991299 | ||||||
chr2:31991571
|
CA | C | 280 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(277): Show | 280 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(277): Show |
intron_variant | MODIFIER | c.61+18615delT | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31991571 | ||||||
chr2:31991686
|
C | CAT | 303 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(300): Show | 303 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(300): Show |
intron_variant | MODIFIER | c.61+18499_61+18500d others(4): Show |
MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31991686 | ||||||
chr2:31992258
|
T | C | 1 | a0001c0001t0001g0188 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.61+17929A>G | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31992258 | ||||||
chr2:31992300
|
G | A | 1 | a0001c0001t0001g0169 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.61+17887C>T | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31992300 | ||||||
chr2:31992337
|
A | G | 293 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(290): Show | 293 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(290): Show |
intron_variant | MODIFIER | c.61+17850T>C | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31992337 | ||||||
chr2:31992362
|
G | A | 3 | a0001c0001t0001g0136a0001c0001t0001g0137a0001c0001t0001g0228 | 3 | HG03225.hp1 NA19043.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.61+17825C>T | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31992362 | ||||||
chr2:31992372
|
T | C | 3 | a0001c0001t0001g0232a0001c0001t0001g0233a0001c0001t0001g0234 | 3 | HG01361.hp1 HG03927.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.61+17815A>G | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31992372 | ||||||
chr2:31992581
|
C | T | 1 | a0001c0001t0001g0224 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.61+17606G>A | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31992581 | ||||||
chr2:31992667
|
C | A | 1 | a0001c0001t0001g0068 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.61+17520G>T | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31992667 | ||||||
chr2:31992703
|
G | A | 3 | a0001c0001t0002g0003a0001c0001t0002g0004a0001c0001t0002g0005 | 3 | HG01891.hp1 HG02897.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.61+17484C>T | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31992703 | ||||||
chr2:31992721
|
G | T | 297 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(294): Show | 297 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(294): Show |
intron_variant | MODIFIER | c.61+17466C>A | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31992721 | ||||||
chr2:31992899
|
A | G | 1 | a0001c0001t0001g0215 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.61+17288T>C | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31992899 | ||||||
chr2:31993067
|
G | A | 1 | a0001c0001t0001g0205 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.61+17120C>T | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31993067 | ||||||
chr2:31993135
|
C | T | 72 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0011others(69): Show | 72 | HG01109.hp2 HG01168.hp1 HG01169.hp2 others(69): Show |
intron_variant | MODIFIER | c.61+17052G>A | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31993135 | ||||||
chr2:31993611
|
T | C | 3 | a0001c0001t0001g0232a0001c0001t0001g0233a0001c0001t0001g0234 | 3 | HG01361.hp1 HG03927.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.61+16576A>G | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31993611 | ||||||
chr2:31993657
|
T | G | 2 | a0001c0001t0001g0049a0001c0001t0001g0070 | 2 | HG02004.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.61+16530A>C | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31993657 | ||||||
chr2:31993836
|
C | T | 2 | a0001c0001t0001g0290a0001c0001t0001g0291 | 2 | HG01109.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.61+16351G>A | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31993836 | ||||||
chr2:31993844
|
T | C | 1 | a0001c0001t0001g0232 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.61+16343A>G | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31993844 | ||||||
chr2:31993945
|
C | T | 2 | a0001c0001t0001g0014a0001c0001t0001g0082 | 2 | HG00099.hp1 HG02698.hp2 |
intron_variant | MODIFIER | c.61+16242G>A | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31993945 | ||||||
chr2:31993949
|
C | CT | 44 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0021others(41): Show | 44 | HG00140.hp2 HG00438.hp1 HG00597.hp1 others(41): Show |
intron_variant | MODIFIER | c.61+16237dupA | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31993949 | ||||||
chr2:31993949
|
C | CTT | 6 | a0001c0001t0001g0095a0001c0001t0001g0208a0001c0001t0001g0212others(3): Show | 6 | HG01891.hp2 HG02280.hp1 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.61+16236_61+16237d others(4): Show |
MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31993949 | ||||||
chr2:31993949
|
C | CTTTTTTT others(3): Show |
3 | a0001c0001t0001g0272a0001c0001t0001g0273a0001c0001t0001g0274 | 3 | HG01243.hp2 HG02615.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.61+16228_61+16237d others(12): Show |
MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31993949 | ||||||
chr2:31993949
|
C | T | 2 | a0001c0001t0001g0290a0001c0001t0001g0291 | 2 | HG01109.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.61+16238G>A | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31993949 | ||||||
chr2:31993949
|
CT | C | 53 | a0001c0001t0001g0006a0001c0001t0001g0009a0001c0001t0001g0016others(50): Show | 53 | HG00140.hp1 HG00423.hp1 HG00438.hp2 others(50): Show |
intron_variant | MODIFIER | c.61+16237delA | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31993949 | ||||||
chr2:31993949
|
CTT | C | 6 | a0001c0001t0001g0036a0001c0001t0001g0046a0001c0001t0001g0073others(3): Show | 6 | HG00639.hp2 HG01891.hp1 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.61+16236_61+16237d others(4): Show |
MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31993949 | ||||||
chr2:31993949
|
CTTTTTTT others(4): Show |
C | 1 | a0001c0001t0001g0268 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.61+16227_61+16237d others(13): Show |
MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31993949 | ||||||
chr2:31993949
|
CTTTTTTT others(6): Show |
C | 1 | a0001c0001t0001g0279 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.61+16225_61+16237d others(15): Show |
MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31993949 | ||||||
chr2:31993949
|
CTTTTTTT others(11): Show |
C | 4 | a0001c0001t0001g0292a0001c0001t0001g0293a0001c0001t0001g0294others(1): Show | 4 | HG02258.hp1 HG03041.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.61+16220_61+16237d others(20): Show |
MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31993949 | ||||||
chr2:31994153
|
G | T | 3 | a0001c0001t0001g0292a0001c0001t0001g0293a0001c0001t0001g0294 | 3 | HG02258.hp1 HG03209.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.61+16034C>A | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31994153 | ||||||
chr2:31994231
|
A | C | 61 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0011others(58): Show | 61 | HG01168.hp1 HG01169.hp2 HG01243.hp2 others(58): Show |
intron_variant | MODIFIER | c.61+15956T>G | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31994231 | ||||||
chr2:31994256
|
C | T | 61 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0011others(58): Show | 61 | HG01168.hp1 HG01169.hp2 HG01243.hp2 others(58): Show |
intron_variant | MODIFIER | c.61+15931G>A | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31994256 | ||||||
chr2:31994333
|
A | G | 1 | a0001c0001t0001g0191 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.61+15854T>C | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31994333 | ||||||
chr2:31994504
|
T | C | 98 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0009others(95): Show | 98 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(95): Show |
intron_variant | MODIFIER | c.61+15683A>G | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31994504 | ||||||
chr2:31994526
|
A | G | 3 | a0001c0001t0001g0048a0001c0001t0001g0054a0001c0001t0001g0055 | 3 | NA18953.hp1 NA18977.hp1 NA19056.hp1 |
intron_variant | MODIFIER | c.61+15661T>C | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31994526 | ||||||
chr2:31994579
|
C | A | 1 | a0001c0001t0001g0207 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.61+15608G>T | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31994579 | ||||||
chr2:31994624
|
T | C | 73 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0011others(70): Show | 73 | HG01109.hp2 HG01168.hp1 HG01169.hp2 others(70): Show |
intron_variant | MODIFIER | c.61+15563A>G | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31994624 | ||||||
chr2:31994637
|
A | T | 4 | a0001c0001t0001g0100a0001c0001t0001g0101a0001c0001t0001g0232others(1): Show | 4 | HG01361.hp1 HG03209.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.61+15550T>A | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31994637 | ||||||
chr2:31994640
|
T | A | 59 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0011others(56): Show | 59 | HG01081.hp2 HG01168.hp1 HG01169.hp2 others(56): Show |
intron_variant | MODIFIER | c.61+15547A>T | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31994640 | ||||||
chr2:31994756
|
T | G | 1 | a0001c0001t0001g0039 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.61+15431A>C | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31994756 | ||||||
chr2:31994805
|
G | A | 1 | a0001c0001t0001g0271 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.61+15382C>T | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31994805 | ||||||
chr2:31994916
|
C | T | 1 | a0001c0001t0001g0145 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.61+15271G>A | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31994916 | ||||||
chr2:31995028
|
G | A | 6 | a0001c0001t0001g0216a0001c0001t0001g0217a0001c0001t0001g0218others(3): Show | 6 | HG01070.hp1 HG01071.hp2 HG01261.hp2 others(3): Show |
intron_variant | MODIFIER | c.61+15159C>T | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31995028 | ||||||
chr2:31995033
|
A | G | 1 | a0001c0001t0001g0076 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.61+15154T>C | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31995033 | ||||||
chr2:31995193
|
T | C | 2 | a0001c0001t0001g0253a0001c0001t0001g0256 | 2 | HG01257.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.61+14994A>G | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31995193 | ||||||
chr2:31995622
|
G | C | 1 | a0001c0001t0001g0159 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.61+14565C>G | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31995622 | ||||||
chr2:31996185
|
A | AGGGAGAG others(13): Show |
1 | a0001c0001t0001g0082 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.61+13982_61+14001d others(22): Show |
MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31996185 | ||||||
chr2:31996275
|
C | T | 1 | a0001c0001t0001g0042 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.61+13912G>A | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31996275 | ||||||
chr2:31996276
|
G | A | 1 | a0001c0001t0001g0010 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.61+13911C>T | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31996276 | ||||||
chr2:31996280
|
G | A | 1 | a0001c0001t0001g0045 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.61+13907C>T | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31996280 | ||||||
chr2:31996348
|
GACAA | G | 3 | a0001c0001t0001g0275a0001c0001t0001g0276a0001c0001t0001g0277 | 3 | HG02055.hp1 HG03471.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.61+13835_61+13838d others(6): Show |
MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31996348 | ||||||
chr2:31996403
|
G | C | 57 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0011others(54): Show | 57 | HG01168.hp1 HG01169.hp2 HG01255.hp2 others(54): Show |
intron_variant | MODIFIER | c.61+13784C>G | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31996403 | ||||||
chr2:31996422
|
C | A | 9 | a0001c0001t0001g0001a0001c0001t0001g0114a0001c0001t0001g0141others(6): Show | 9 | HG02257.hp2 HG02717.hp2 HG02818.hp2 others(6): Show |
intron_variant | MODIFIER | c.61+13765G>T | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31996422 | ||||||
chr2:31996493
|
G | C | 3 | a0001c0001t0001g0275a0001c0001t0001g0276a0001c0001t0001g0277 | 3 | HG02055.hp1 HG03471.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.61+13694C>G | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31996493 | ||||||
chr2:31996583
|
C | T | 55 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0011others(52): Show | 55 | HG01168.hp1 HG01169.hp2 HG01255.hp2 others(52): Show |
intron_variant | MODIFIER | c.61+13604G>A | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31996583 | ||||||
chr2:31996630
|
A | G | 2 | a0001c0001t0001g0239a0001c0001t0001g0270 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.61+13557T>C | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31996630 | ||||||
chr2:31996694
|
T | C | 2 | a0001c0001t0001g0061a0001c0001t0001g0088 | 2 | HG00735.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.61+13493A>G | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31996694 | ||||||
chr2:31996710
|
T | C | 1 | a0001c0001t0001g0176 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.61+13477A>G | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31996710 | ||||||
chr2:31996801
|
G | A | 2 | a0001c0001t0001g0099a0001c0001t0001g0102 | 2 | HG01496.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.61+13386C>T | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31996801 | ||||||
chr2:31996907
|
T | C | 3 | a0001c0001t0001g0185a0001c0001t0001g0215a0001c0001t0001g0279 | 3 | HG01106.hp1 HG02970.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.61+13280A>G | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31996907 | ||||||
chr2:31997015
|
G | C | 1 | a0001c0001t0001g0046 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.61+13172C>G | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31997015 | ||||||
chr2:31997248
|
T | A | 1 | a0001c0001t0001g0290 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.61+12939A>T | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31997248 | ||||||
chr2:31997421
|
G | C | 1 | a0001c0001t0001g0059 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.61+12766C>G | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31997421 | ||||||
chr2:31997605
|
T | G | 3 | a0001c0001t0002g0003a0001c0001t0002g0004a0001c0001t0002g0005 | 3 | HG01891.hp1 HG02897.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.61+12582A>C | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31997605 | ||||||
chr2:31997743
|
C | T | 3 | a0001c0001t0001g0272a0001c0001t0001g0273a0001c0001t0001g0274 | 3 | HG01243.hp2 HG02615.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.61+12444G>A | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31997743 | ||||||
chr2:31997766
|
T | A | 3 | a0001c0001t0001g0272a0001c0001t0001g0273a0001c0001t0001g0274 | 3 | HG01243.hp2 HG02615.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.61+12421A>T | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31997766 | ||||||
chr2:31997920
|
G | C | 3 | a0001c0001t0001g0024a0001c0001t0001g0164a0001c0001t0001g0165 | 3 | NA18940.hp2 NA18968.hp2 NA19077.hp2 |
intron_variant | MODIFIER | c.61+12267C>G | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31997920 | ||||||
chr2:31997977
|
C | T | 1 | a0001c0001t0001g0295 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.61+12210G>A | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31997977 | ||||||
chr2:31998069
|
T | C | 5 | a0001c0001t0001g0202a0001c0001t0001g0203a0001c0001t0001g0204others(2): Show | 5 | HG02257.hp2 HG02717.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.61+12118A>G | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31998069 | ||||||
chr2:31998182
|
A | G | 3 | a0001c0001t0001g0185a0001c0001t0001g0215a0001c0001t0001g0279 | 3 | HG01106.hp1 HG02970.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.61+12005T>C | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31998182 | ||||||
chr2:31998387
|
T | C | 12 | a0001c0001t0001g0221a0001c0001t0001g0280a0001c0001t0001g0281others(9): Show | 12 | HG01071.hp2 HG01255.hp2 HG01496.hp2 others(9): Show |
intron_variant | MODIFIER | c.61+11800A>G | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31998387 | ||||||
chr2:31998544
|
T | C | 1 | a0001c0001t0001g0090 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.61+11643A>G | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31998544 | ||||||
chr2:31998616
|
T | C | 3 | a0001c0001t0001g0232a0001c0001t0001g0233a0001c0001t0001g0234 | 3 | HG01361.hp1 HG03927.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.61+11571A>G | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31998616 | ||||||
chr2:31998666
|
G | C | 1 | a0001c0001t0001g0078 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.61+11521C>G | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31998666 | ||||||
chr2:31998731
|
C | T | 1 | a0001c0001t0001g0093 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.61+11456G>A | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31998731 | ||||||
chr2:31998737
|
T | C | 3 | a0001c0001t0001g0199a0001c0001t0001g0200a0001c0001t0001g0201 | 3 | HG02622.hp2 HG03098.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.61+11450A>G | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31998737 | ||||||
chr2:31998779
|
G | A | 3 | a0001c0001t0001g0037a0001c0001t0001g0172a0001c0001t0001g0304 | 3 | HG01884.hp2 HG03579.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.61+11408C>T | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31998779 | ||||||
chr2:31998799
|
CA | C | 9 | a0001c0001t0001g0020a0001c0001t0001g0034a0001c0001t0001g0050others(6): Show | 9 | HG01070.hp2 HG01169.hp1 HG03486.hp2 others(6): Show |
intron_variant | MODIFIER | c.61+11387delT | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31998799 | ||||||
chr2:31999148
|
A | C | 3 | a0001c0001t0001g0034a0001c0001t0001g0050a0001c0001t0001g0063 | 3 | NA18955.hp2 NA18960.hp1 NA18963.hp2 |
intron_variant | MODIFIER | c.61+11039T>G | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31999148 | ||||||
chr2:31999433
|
T | C | 3 | a0001c0001t0001g0232a0001c0001t0001g0233a0001c0001t0001g0234 | 3 | HG01361.hp1 HG03927.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.61+10754A>G | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31999433 | ||||||
chr2:31999532
|
C | T | 3 | a0001c0001t0001g0272a0001c0001t0001g0273a0001c0001t0001g0274 | 3 | HG01243.hp2 HG02615.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.61+10655G>A | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31999532 | ||||||
chr2:31999569
|
T | C | 3 | a0001c0001t0001g0232a0001c0001t0001g0233a0001c0001t0001g0234 | 3 | HG01361.hp1 HG03927.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.61+10618A>G | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31999569 | ||||||
chr2:31999611
|
A | T | 1 | a0001c0001t0001g0221 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.61+10576T>A | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31999611 | ||||||
chr2:31999706
|
T | C | 1 | a0001c0001t0001g0189 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.61+10481A>G | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31999706 | ||||||
chr2:31999804
|
T | C | 1 | a0001c0001t0001g0284 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.61+10383A>G | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31999804 | ||||||
chr2:31999882
|
A | AT | 21 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0037others(18): Show | 21 | HG00438.hp2 HG01243.hp2 HG01261.hp1 others(18): Show |
intron_variant | MODIFIER | c.61+10304dupA | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31999882 | ||||||
chr2:31999882
|
AT | A | 75 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0010others(72): Show | 75 | HG01070.hp1 HG01071.hp2 HG01081.hp2 others(72): Show |
intron_variant | MODIFIER | c.61+10304delA | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31999882 | ||||||
chr2:31999937
|
G | C | 11 | a0001c0001t0001g0280a0001c0001t0001g0281a0001c0001t0001g0282others(8): Show | 11 | HG01255.hp2 HG01496.hp2 HG01516.hp2 others(8): Show |
intron_variant | MODIFIER | c.61+10250C>G | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31999937 | ||||||
chr2:32000031
|
C | T | 1 | a0001c0001t0001g0279 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.61+10156G>A | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 32000031 | ||||||
chr2:32000252
|
G | A | 1 | a0001c0001t0001g0160 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.61+9935C>T | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 32000252 | ||||||
chr2:32000510
|
G | A | 3 | a0001c0001t0001g0232a0001c0001t0001g0290a0001c0001t0001g0291 | 3 | HG01109.hp2 HG01361.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.61+9677C>T | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 32000510 | ||||||
chr2:32000519
|
C | T | 1 | a0001c0001t0001g0285 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.61+9668G>A | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 32000519 | ||||||
chr2:32000520
|
G | A | 3 | a0001c0001t0001g0010a0001c0001t0001g0290a0001c0001t0001g0291 | 3 | HG01109.hp2 HG02622.hp1 NA18978.hp2 |
intron_variant | MODIFIER | c.61+9667C>T | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 32000520 | ||||||
chr2:32000572
|
G | A | 1 | a0001c0001t0001g0099 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.61+9615C>T | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 32000572 | ||||||
chr2:32000790
|
A | AT | 28 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0012others(25): Show | 28 | HG01109.hp2 HG01243.hp2 HG02083.hp2 others(25): Show |
intron_variant | MODIFIER | c.61+9396dupA | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 32000790 | ||||||
chr2:32000790
|
A | ATT | 31 | a0001c0001t0001g0008a0001c0001t0001g0236a0001c0001t0001g0237others(28): Show | 31 | HG01168.hp1 HG01169.hp2 HG01255.hp2 others(28): Show |
intron_variant | MODIFIER | c.61+9395_61+9396dup others(2): Show |
MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 32000790 | ||||||
chr2:32000790
|
AT | A | 8 | a0001c0001t0001g0023a0001c0001t0001g0072a0001c0001t0001g0082others(5): Show | 8 | HG00642.hp2 HG01081.hp1 HG01891.hp1 others(5): Show |
intron_variant | MODIFIER | c.61+9396delA | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 32000790 | ||||||
chr2:32000796
|
T | C | 6 | a0001c0001t0001g0093a0001c0001t0001g0094a0001c0001t0001g0095others(3): Show | 6 | NA18942.hp1 NA18943.hp2 NA18944.hp1 others(3): Show |
intron_variant | MODIFIER | c.61+9391A>G | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 32000796 | ||||||
chr2:32001032
|
A | AT | 82 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(79): Show | 82 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(79): Show |
intron_variant | MODIFIER | c.61+9154dupA | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 32001032 | ||||||
chr2:32001032
|
A | ATT | 20 | a0001c0001t0001g0034a0001c0001t0001g0037a0001c0001t0001g0038others(17): Show | 20 | HG01109.hp1 HG01884.hp2 HG01943.hp2 others(17): Show |
intron_variant | MODIFIER | c.61+9153_61+9154dup others(2): Show |
MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 32001032 | ||||||
chr2:32001032
|
AT | A | 64 | a0001c0001t0001g0008a0001c0001t0001g0011a0001c0001t0001g0012others(61): Show | 64 | HG00408.hp2 HG00642.hp2 HG01081.hp1 others(61): Show |
intron_variant | MODIFIER | c.61+9154delA | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 32001032 | ||||||
chr2:32001056
|
G | C | 1 | a0001c0001t0001g0227 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.61+9131C>G | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 32001056 | ||||||
chr2:32001066
|
T | G | 62 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0011others(59): Show | 62 | HG01168.hp1 HG01169.hp2 HG01243.hp2 others(59): Show |
intron_variant | MODIFIER | c.61+9121A>C | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 32001066 | ||||||
chr2:32001093
|
C | T | 2 | a0001c0001t0001g0014a0001c0001t0001g0082 | 2 | HG00099.hp1 HG02698.hp2 |
intron_variant | MODIFIER | c.61+9094G>A | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 32001093 | ||||||
chr2:32001197
|
G | C | 74 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0011others(71): Show | 74 | HG01109.hp2 HG01168.hp1 HG01169.hp2 others(71): Show |
intron_variant | MODIFIER | c.61+8990C>G | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 32001197 | ||||||
chr2:32001220
|
T | C | 51 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0011others(48): Show | 51 | HG01168.hp1 HG01169.hp2 HG01255.hp2 others(48): Show |
intron_variant | MODIFIER | c.61+8967A>G | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 32001220 | ||||||
chr2:32001238
|
A | G | 7 | a0001c0001t0001g0099a0001c0001t0001g0100a0001c0001t0001g0101others(4): Show | 7 | HG01496.hp1 HG02280.hp1 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.61+8949T>C | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 32001238 | ||||||
chr2:32001286
|
G | A | 3 | a0001c0001t0001g0232a0001c0001t0001g0233a0001c0001t0001g0234 | 3 | HG01361.hp1 HG03927.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.61+8901C>T | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 32001286 | ||||||
chr2:32001383
|
A | C | 4 | a0001c0001t0001g0038a0001c0001t0001g0039a0001c0001t0001g0052others(1): Show | 4 | HG01943.hp2 HG01975.hp2 NA18969.hp2 others(1): Show |
intron_variant | MODIFIER | c.61+8804T>G | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 32001383 | ||||||
chr2:32001447
|
C | T | 5 | a0001c0001t0001g0037a0001c0001t0001g0051a0001c0001t0001g0064others(2): Show | 5 | HG01884.hp2 HG02109.hp1 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.61+8740G>A | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 32001447 | ||||||
chr2:32001459
|
G | C | 1 | a0001c0001t0001g0033 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.61+8728C>G | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 32001459 | ||||||
chr2:32001529
|
T | A | 1 | a0001c0001t0001g0140 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.61+8658A>T | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 32001529 | ||||||
chr2:32001601
|
T | C | 3 | a0001c0001t0001g0292a0001c0001t0001g0293a0001c0001t0001g0294 | 3 | HG02258.hp1 HG03209.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.61+8586A>G | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 32001601 | ||||||
chr2:32001638
|
G | A | 2 | a0001c0001t0001g0290a0001c0001t0001g0291 | 2 | HG01109.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.61+8549C>T | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 32001638 | ||||||
chr2:32001656
|
T | C | 51 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0011others(48): Show | 51 | HG01168.hp1 HG01169.hp2 HG01255.hp2 others(48): Show |
intron_variant | MODIFIER | c.61+8531A>G | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 32001656 | ||||||
chr2:32001695
|
G | C | 1 | a0001c0001t0001g0221 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.61+8492C>G | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 32001695 | ||||||
chr2:32001835
|
C | A | 4 | a0001c0001t0001g0108a0001c0001t0001g0109a0001c0001t0001g0110others(1): Show | 4 | HG00438.hp1 HG00673.hp2 NA18952.hp2 others(1): Show |
intron_variant | MODIFIER | c.61+8352G>T | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 32001835 | ||||||
chr2:32001898
|
AGCGCCTT others(3): Show |
A | 2 | a0001c0001t0001g0290a0001c0001t0001g0291 | 2 | HG01109.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.61+8279_61+8288del others(10): Show |
MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 32001898 | ||||||
chr2:32001917
|
G | A | 97 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0009others(94): Show | 97 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(94): Show |
intron_variant | MODIFIER | c.61+8270C>T | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 32001917 | ||||||
chr2:32001918
|
A | G | 2 | a0001c0001t0001g0290a0001c0001t0001g0291 | 2 | HG01109.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.61+8269T>C | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 32001918 | ||||||
chr2:32002060
|
C | A | 3 | a0001c0001t0002g0003a0001c0001t0002g0004a0001c0001t0002g0005 | 3 | HG01891.hp1 HG02897.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.61+8127G>T | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 32002060 | ||||||
chr2:32002123
|
C | A | 1 | a0001c0001t0001g0141 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.61+8064G>T | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 32002123 | ||||||
chr2:32002144
|
C | CA | 22 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0014others(19): Show | 22 | HG00099.hp1 HG00140.hp1 HG00639.hp1 others(19): Show |
intron_variant | MODIFIER | c.61+8042dupT | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 32002144 | ||||||
chr2:32002144
|
CA | C | 17 | a0001c0001t0001g0017a0001c0001t0001g0093a0001c0001t0001g0115others(14): Show | 17 | HG00408.hp1 HG00735.hp2 HG01081.hp1 others(14): Show |
intron_variant | MODIFIER | c.61+8042delT | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 32002144 | ||||||
chr2:32002158
|
A | T | 1 | a0001c0001t0001g0275 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.61+8029T>A | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 32002158 | ||||||
chr2:32002160
|
A | T | 3 | a0001c0001t0001g0275a0001c0001t0001g0276a0001c0001t0001g0277 | 3 | HG02055.hp1 HG03471.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.61+8027T>A | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 32002160 | ||||||
chr2:32002162
|
A | T | 6 | a0001c0001t0001g0015a0001c0001t0001g0239a0001c0001t0001g0270others(3): Show | 6 | HG02055.hp1 HG02895.hp2 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.61+8025T>A | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 32002162 | ||||||
chr2:32002164
|
A | ATAT | 5 | a0001c0001t0001g0192a0001c0001t0001g0193a0001c0001t0001g0194others(2): Show | 5 | HG01109.hp2 HG02055.hp2 HG03516.hp1 others(2): Show |
intron_variant | MODIFIER | c.61+8022_61+8023ins others(3): Show |
MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 32002164 | ||||||
chr2:32002164
|
A | T | 36 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0012others(33): Show | 36 | HG01106.hp1 HG02055.hp1 HG02083.hp2 others(33): Show |
intron_variant | MODIFIER | c.61+8023T>A | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 32002164 | ||||||
chr2:32002166
|
A | AT | 18 | a0001c0001t0001g0009a0001c0001t0001g0037a0001c0001t0001g0038others(15): Show | 18 | HG00423.hp1 HG00597.hp2 HG00639.hp2 others(15): Show |
intron_variant | MODIFIER | c.61+8020_61+8021ins others(1): Show |
MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 32002166 | ||||||
chr2:32002166
|
A | ATAT | 3 | a0001c0001t0001g0258a0001c0001t0001g0259a0001c0001t0001g0290 | 3 | HG01168.hp1 HG01169.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.61+8020_61+8021ins others(3): Show |
MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 32002166 | ||||||
chr2:32002166
|
A | T | 74 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0011others(71): Show | 74 | HG01106.hp1 HG01109.hp2 HG01255.hp2 others(71): Show |
intron_variant | MODIFIER | c.61+8021T>A | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 32002166 | ||||||
chr2:32002168
|
A | AAT | 8 | a0001c0001t0001g0019a0001c0001t0001g0062a0001c0001t0001g0063others(5): Show | 8 | HG00735.hp1 HG01169.hp1 HG01928.hp2 others(5): Show |
intron_variant | MODIFIER | c.61+8017_61+8018dup others(2): Show |
MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 32002168 | ||||||
chr2:32002168
|
A | AT | 33 | a0001c0001t0001g0006a0001c0001t0001g0016a0001c0001t0001g0030others(30): Show | 33 | HG00438.hp2 HG00738.hp1 HG00741.hp1 others(30): Show |
intron_variant | MODIFIER | c.61+8018_61+8019ins others(1): Show |
MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 32002168 | ||||||
chr2:32002168
|
A | T | 135 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(132): Show | 135 | HG00423.hp1 HG00438.hp1 HG00597.hp2 others(132): Show |
intron_variant | MODIFIER | c.61+8019T>A | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 32002168 | ||||||
chr2:32002169
|
AT | A | 4 | a0001c0001t0001g0164a0001c0001t0001g0184a0001c0001t0001g0207others(1): Show | 4 | HG01168.hp2 HG02615.hp1 HG03491.hp2 others(1): Show |
intron_variant | MODIFIER | c.61+8017delA | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 32002169 | ||||||
chr2:32002170
|
T | A | 20 | a0001c0001t0001g0002a0001c0001t0001g0026a0001c0001t0001g0027others(17): Show | 20 | HG00140.hp1 HG00140.hp2 HG00639.hp1 others(17): Show |
intron_variant | MODIFIER | c.61+8017A>T | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 32002170 | ||||||
chr2:32002172
|
T | A | 1 | a0001c0001t0001g0153 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.61+8015A>T | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 32002172 | ||||||
chr2:32002178
|
T | C | 1 | a0001c0001t0001g0234 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.61+8009A>G | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 32002178 | ||||||
chr2:32002180
|
T | C | 1 | a0001c0001t0001g0234 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.61+8007A>G | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 32002180 | ||||||
chr2:32002180
|
T | TAC | 3 | a0001c0001t0001g0261a0001c0001t0001g0265a0001c0001t0001g0266 | 3 | NA19012.hp2 NA19080.hp1 NA19090.hp2 |
intron_variant | MODIFIER | c.61+8006_61+8007ins others(2): Show |
MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 32002180 | ||||||
chr2:32002180
|
T | TACACACA others(3): Show |
1 | a0001c0001t0001g0232 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.61+8006_61+8007ins others(10): Show |
MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 32002180 | ||||||
chr2:32002180
|
T | TACACACA others(7): Show |
3 | a0001c0001t0001g0292a0001c0001t0001g0293a0001c0001t0001g0294 | 3 | HG02258.hp1 HG03209.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.61+8006_61+8007ins others(14): Show |
MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 32002180 | ||||||
chr2:32002182
|
T | C | 15 | a0001c0001t0001g0232a0001c0001t0001g0233a0001c0001t0001g0234others(12): Show | 15 | HG01168.hp1 HG01169.hp2 HG01361.hp1 others(12): Show |
intron_variant | MODIFIER | c.61+8005A>G | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 32002182 | ||||||
chr2:32002182
|
T | TAC | 35 | a0001c0001t0001g0008a0001c0001t0001g0011a0001c0001t0001g0012others(32): Show | 35 | HG01255.hp2 HG01257.hp2 HG01258.hp1 others(32): Show |
intron_variant | MODIFIER | c.61+8004_61+8005ins others(2): Show |
MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 32002182 | ||||||
chr2:32002184
|
T | C | 53 | a0001c0001t0001g0008a0001c0001t0001g0011a0001c0001t0001g0012others(50): Show | 53 | HG01168.hp1 HG01169.hp2 HG01255.hp2 others(50): Show |
intron_variant | MODIFIER | c.61+8003A>G | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 32002184 | ||||||
chr2:32002184
|
T | TACACAC | 3 | a0001c0001t0001g0286a0001c0001t0001g0287a0001c0001t0001g0288 | 3 | HG02129.hp1 HG02155.hp2 NA18939.hp1 |
intron_variant | MODIFIER | c.61+8002_61+8003ins others(6): Show |
MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 32002184 | ||||||
chr2:32002186
|
T | C | 77 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0010others(74): Show | 77 | HG01071.hp2 HG01081.hp2 HG01109.hp2 others(74): Show |
intron_variant | MODIFIER | c.61+8001A>G | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 32002186 | ||||||
chr2:32002186
|
T | TAC | 7 | a0001c0001t0001g0217a0001c0001t0001g0218a0001c0001t0001g0222others(4): Show | 7 | HG01070.hp1 HG01243.hp2 HG01261.hp2 others(4): Show |
intron_variant | MODIFIER | c.61+7999_61+8000dup others(2): Show |
MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 32002186 | ||||||
chr2:32002186
|
T | TATACACA others(13): Show |
1 | a0001c0001t0001g0295 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.61+8000_61+8001ins others(20): Show |
MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 32002186 | ||||||
chr2:32002188
|
C | T | 99 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0014others(96): Show | 99 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(96): Show |
intron_variant | MODIFIER | c.61+7999G>A | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 32002188 | ||||||
chr2:32002204
|
T | C | 17 | a0001c0001t0001g0156a0001c0001t0001g0157a0001c0001t0001g0158others(14): Show | 17 | HG01261.hp1 HG01361.hp1 HG01891.hp1 others(14): Show |
intron_variant | MODIFIER | c.61+7983A>G | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 32002204 | ||||||
chr2:32002206
|
T | TATATACG others(25): Show |
1 | a0001c0001t0002g0003 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.61+7949_61+7980dup others(32): Show |
MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 32002206 | ||||||
chr2:32002206
|
T | TATATACG others(57): Show |
1 | a0001c0001t0002g0005 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.61+7980_61+7981ins others(64): Show |
MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 32002206 | ||||||
chr2:32002226
|
T | C | 1 | a0001c0001t0001g0289 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.61+7961A>G | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 32002226 | ||||||
chr2:32002226
|
T | TGTGTATA others(19): Show |
3 | a0001c0001t0001g0292a0001c0001t0001g0293a0001c0001t0001g0294 | 3 | HG02258.hp1 HG03209.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.61+7935_61+7960dup others(26): Show |
MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 32002226 | ||||||
chr2:32002227
|
G | A | 4 | a0001c0001t0001g0014a0001c0001t0001g0082a0001c0001t0001g0083others(1): Show | 4 | HG00099.hp1 HG02698.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.61+7960C>T | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 32002227 | ||||||
chr2:32002245
|
A | G | 3 | a0001c0001t0002g0003a0001c0001t0002g0004a0001c0001t0002g0005 | 3 | HG01891.hp1 HG02897.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.61+7942T>C | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 32002245 | ||||||
chr2:32002252
|
C | CGTATATG others(31): Show |
2 | a0001c0001t0002g0003a0001c0001t0002g0004 | 2 | HG01891.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.61+7934_61+7935ins others(38): Show |
MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 32002252 | ||||||
chr2:32002268
|
C | T | 3 | a0001c0001t0002g0003a0001c0001t0002g0004a0001c0001t0002g0005 | 3 | HG01891.hp1 HG02897.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.61+7919G>A | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 32002268 | ||||||
chr2:32002286
|
T | TATATAC | 4 | a0001c0001t0001g0292a0001c0001t0001g0293a0001c0001t0001g0294others(1): Show | 4 | HG02258.hp1 HG03041.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.61+7895_61+7900dup others(6): Show |
MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 32002286 | ||||||
chr2:32002313
|
A | C | 62 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0011others(59): Show | 62 | HG01168.hp1 HG01169.hp2 HG01243.hp2 others(59): Show |
intron_variant | MODIFIER | c.61+7874T>G | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 32002313 | ||||||
chr2:32002363
|
G | A | 7 | a0001c0001t0001g0262a0001c0001t0001g0263a0001c0001t0001g0264others(4): Show | 7 | HG02083.hp2 NA18953.hp2 NA18964.hp2 others(4): Show |
intron_variant | MODIFIER | c.61+7824C>T | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 32002363 | ||||||
chr2:32002385
|
A | C | 2 | a0001c0001t0001g0290a0001c0001t0001g0291 | 2 | HG01109.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.61+7802T>G | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 32002385 | ||||||
chr2:32002444
|
ATACATAT others(26): Show |
A | 2 | a0001c0001t0001g0290a0001c0001t0001g0291 | 2 | HG01109.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.61+7710_61+7742del others(33): Show |
MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 32002444 | ||||||
chr2:32002520
|
C | G | 4 | a0001c0001t0001g0239a0001c0001t0001g0240a0001c0001t0001g0241others(1): Show | 4 | HG02723.hp1 HG02809.hp2 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.61+7667G>C | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 32002520 | ||||||
chr2:32002575
|
A | G | 3 | a0001c0001t0001g0032a0001c0001t0001g0033a0001c0001t0001g0087 | 3 | HG00741.hp1 HG01433.hp1 NA19063.hp1 |
intron_variant | MODIFIER | c.61+7612T>C | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 32002575 | ||||||
chr2:32002722
|
T | A | 1 | a0001c0001t0001g0015 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.61+7465A>T | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 32002722 | ||||||
chr2:32002738
|
A | G | 3 | a0001c0001t0001g0093a0001c0001t0001g0094a0001c0001t0001g0097 | 3 | NA18942.hp1 NA18943.hp2 NA18974.hp1 |
intron_variant | MODIFIER | c.61+7449T>C | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 32002738 | ||||||
chr2:32002788
|
A | G | 2 | a0001c0001t0001g0006a0001c0001t0001g0031 | 2 | HG00438.hp2 HG02165.hp2 |
intron_variant | MODIFIER | c.61+7399T>C | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 32002788 | ||||||
chr2:32002892
|
C | G | 1 | a0001c0001t0001g0030 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.61+7295G>C | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 32002892 | ||||||
chr2:32003247
|
ATAG | A | 3 | a0001c0001t0002g0003a0001c0001t0002g0004a0001c0001t0002g0005 | 3 | HG01891.hp1 HG02897.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.61+6937_61+6939del others(3): Show |
MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 32003247 | ||||||
chr2:32003410
|
A | G | 3 | a0001c0001t0001g0292a0001c0001t0001g0293a0001c0001t0001g0294 | 3 | HG02258.hp1 HG03209.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.61+6777T>C | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 32003410 | ||||||
chr2:32003415
|
A | G | 3 | a0001c0001t0001g0232a0001c0001t0001g0233a0001c0001t0001g0234 | 3 | HG01361.hp1 HG03927.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.61+6772T>C | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 32003415 | ||||||
chr2:32003912
|
G | C | 1 | a0001c0001t0001g0206 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.61+6275C>G | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 32003912 | ||||||
chr2:32003919
|
G | A | 3 | a0001c0001t0001g0085a0001c0001t0001g0086a0001c0001t0001g0235 | 3 | NA18971.hp2 NA19011.hp1 NA19070.hp1 |
intron_variant | MODIFIER | c.61+6268C>T | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 32003919 | ||||||
chr2:32003937
|
G | A | 3 | a0001c0001t0001g0232a0001c0001t0001g0233a0001c0001t0001g0234 | 3 | HG01361.hp1 HG03927.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.61+6250C>T | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 32003937 | ||||||
chr2:32003964
|
T | C | 1 | a0001c0001t0001g0190 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.61+6223A>G | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 32003964 | ||||||
chr2:32004116
|
G | A | 1 | a0001c0001t0001g0191 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.61+6071C>T | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 32004116 | ||||||
chr2:32004208
|
T | C | 2 | a0001c0001t0001g0290a0001c0001t0001g0291 | 2 | HG01109.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.61+5979A>G | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 32004208 | ||||||
chr2:32004381
|
A | G | 51 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0011others(48): Show | 51 | HG01168.hp1 HG01169.hp2 HG01255.hp2 others(48): Show |
intron_variant | MODIFIER | c.61+5806T>C | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 32004381 | ||||||
chr2:32004461
|
A | C | 2 | a0001c0001t0001g0238a0001c0001t0001g0300 | 2 | HG03831.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.61+5726T>G | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 32004461 | ||||||
chr2:32004645
|
G | A | 3 | a0001c0001t0002g0003a0001c0001t0002g0004a0001c0001t0002g0005 | 3 | HG01891.hp1 HG02897.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.61+5542C>T | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 32004645 | ||||||
chr2:32004657
|
T | G | 1 | a0001c0001t0001g0161 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.61+5530A>C | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 32004657 | ||||||
chr2:32004675
|
T | G | 5 | a0001c0001t0001g0098a0001c0001t0001g0192a0001c0001t0001g0193others(2): Show | 5 | HG02055.hp2 HG03486.hp2 HG03516.hp1 others(2): Show |
intron_variant | MODIFIER | c.61+5512A>C | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 32004675 | ||||||
chr2:32004689
|
G | A | 1 | a0001c0001t0001g0196 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.61+5498C>T | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 32004689 | ||||||
chr2:32004926
|
C | CA | 13 | a0001c0001t0001g0002a0001c0001t0001g0162a0001c0001t0001g0229others(10): Show | 13 | HG01109.hp2 HG02258.hp1 HG02280.hp2 others(10): Show |
intron_variant | MODIFIER | c.61+5260dupT | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 32004926 | ||||||
chr2:32005014
|
T | C | 3 | a0001c0001t0002g0003a0001c0001t0002g0004a0001c0001t0002g0005 | 3 | HG01891.hp1 HG02897.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.61+5173A>G | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 32005014 | ||||||
chr2:32005158
|
G | C | 1 | a0001c0001t0001g0008 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.61+5029C>G | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 32005158 | ||||||
chr2:32005318
|
C | CA | 19 | a0001c0001t0001g0007a0001c0001t0001g0087a0001c0001t0001g0088others(16): Show | 19 | HG00735.hp1 HG01109.hp2 HG01261.hp1 others(16): Show |
intron_variant | MODIFIER | c.61+4868dupT | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 32005318 | ||||||
chr2:32005359
|
T | C | 3 | a0001c0001t0001g0089a0001c0001t0001g0090a0001c0001t0001g0091 | 3 | NA18944.hp2 NA18950.hp1 NA19003.hp1 |
intron_variant | MODIFIER | c.61+4828A>G | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 32005359 | ||||||
chr2:32005402
|
C | CTA | 192 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0008others(189): Show | 192 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(189): Show |
intron_variant | MODIFIER | c.61+4784_61+4785ins others(2): Show |
MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 32005402 | ||||||
chr2:32005667
|
C | T | 1 | a0001c0001t0001g0098 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.61+4520G>A | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 32005667 | ||||||
chr2:32005674
|
G | A | 1 | a0001c0001t0001g0092 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.61+4513C>T | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 32005674 | ||||||
chr2:32005713
|
T | C | 3 | a0001c0001t0001g0275a0001c0001t0001g0276a0001c0001t0001g0277 | 3 | HG02055.hp1 HG03471.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.61+4474A>G | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 32005713 | ||||||
chr2:32005767
|
T | A | 5 | a0001c0001t0001g0275a0001c0001t0001g0276a0001c0001t0001g0277others(2): Show | 5 | HG02055.hp1 HG02970.hp2 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.61+4420A>T | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 32005767 | ||||||
chr2:32005896
|
T | C | 5 | a0001c0001t0001g0197a0001c0001t0001g0198a0001c0001t0001g0199others(2): Show | 5 | HG02622.hp2 HG02922.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.61+4291A>G | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 32005896 | ||||||
chr2:32005951
|
C | T | 6 | a0001c0001t0001g0093a0001c0001t0001g0094a0001c0001t0001g0095others(3): Show | 6 | NA18942.hp1 NA18943.hp2 NA18944.hp1 others(3): Show |
intron_variant | MODIFIER | c.61+4236G>A | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 32005951 | ||||||
chr2:32006084
|
G | C | 3 | a0001c0001t0002g0003a0001c0001t0002g0004a0001c0001t0002g0005 | 3 | HG01891.hp1 HG02897.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.61+4103C>G | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 32006084 | ||||||
chr2:32006206
|
G | A | 5 | a0001c0001t0001g0202a0001c0001t0001g0203a0001c0001t0001g0204others(2): Show | 5 | HG02257.hp2 HG02717.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.61+3981C>T | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 32006206 | ||||||
chr2:32006530
|
T | C | 2 | a0001c0001t0001g0236a0001c0001t0001g0237 | 2 | HG03139.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.61+3657A>G | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 32006530 | ||||||
chr2:32006549
|
C | A | 1 | a0001c0001t0001g0207 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.61+3638G>T | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 32006549 | ||||||
chr2:32006591
|
C | A | 1 | a0001c0001t0001g0278 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.61+3596G>T | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 32006591 | ||||||
chr2:32006591
|
C | CA | 15 | a0001c0001t0001g0208a0001c0001t0001g0209a0001c0001t0001g0210others(12): Show | 15 | HG01243.hp2 HG01884.hp1 HG02055.hp1 others(12): Show |
intron_variant | MODIFIER | c.61+3595dupT | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 32006591 | ||||||
chr2:32006606
|
A | G | 1 | a0001c0001t0001g0280 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.61+3581T>C | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 32006606 | ||||||
chr2:32006833
|
C | T | 2 | a0001c0001t0001g0290a0001c0001t0001g0291 | 2 | HG01109.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.61+3354G>A | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 32006833 | ||||||
chr2:32006964
|
C | CA | 13 | a0001c0001t0001g0007a0001c0001t0001g0212a0001c0001t0001g0213others(10): Show | 13 | HG00642.hp2 HG01070.hp1 HG01071.hp2 others(10): Show |
intron_variant | MODIFIER | c.61+3222dupT | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 32006964 | ||||||
chr2:32006964
|
CA | C | 92 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0009others(89): Show | 92 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(89): Show |
intron_variant | MODIFIER | c.61+3222delT | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 32006964 | ||||||
chr2:32006964
|
CAA | C | 46 | a0001c0001t0001g0008a0001c0001t0001g0016a0001c0001t0001g0238others(43): Show | 46 | HG01168.hp1 HG01169.hp2 HG01255.hp2 others(43): Show |
intron_variant | MODIFIER | c.61+3221_61+3222del others(2): Show |
MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 32006964 | ||||||
chr2:32006964
|
CAAAA | C | 12 | a0001c0001t0001g0232a0001c0001t0001g0233a0001c0001t0001g0236others(9): Show | 12 | HG01243.hp2 HG01361.hp1 HG02055.hp1 others(9): Show |
intron_variant | MODIFIER | c.61+3219_61+3222del others(4): Show |
MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 32006964 | ||||||
chr2:32007036
|
T | C | 1 | a0001c0001t0001g0223 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.61+3151A>G | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 32007036 | ||||||
chr2:32007087
|
A | G | 3 | a0001c0001t0001g0232a0001c0001t0001g0233a0001c0001t0001g0234 | 3 | HG01361.hp1 HG03927.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.61+3100T>C | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 32007087 | ||||||
chr2:32007374
|
C | T | 1 | a0001c0001t0002g0003 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.61+2813G>A | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 32007374 | ||||||
chr2:32007549
|
C | CA | 70 | a0001c0001t0001g0008a0001c0001t0001g0232a0001c0001t0001g0233others(67): Show | 70 | HG01109.hp2 HG01168.hp1 HG01169.hp2 others(67): Show |
intron_variant | MODIFIER | c.61+2637_61+2638ins others(1): Show |
MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 32007549 | ||||||
chr2:32007605
|
G | C | 4 | a0001c0001t0001g0224a0001c0001t0001g0225a0001c0001t0001g0226others(1): Show | 4 | NA18949.hp2 NA18955.hp1 NA18956.hp2 others(1): Show |
intron_variant | MODIFIER | c.61+2582C>G | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 32007605 | ||||||
chr2:32007677
|
A | G | 1 | a0001c0001t0001g0015 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.61+2510T>C | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 32007677 | ||||||
chr2:32007767
|
A | C | 1 | a0001c0001t0001g0014 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.61+2420T>G | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 32007767 | ||||||
chr2:32007782
|
G | A | 1 | a0001c0001t0001g0274 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.61+2405C>T | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 32007782 | ||||||
chr2:32007808
|
T | C | 75 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0011others(72): Show | 75 | HG01109.hp2 HG01168.hp1 HG01169.hp2 others(72): Show |
intron_variant | MODIFIER | c.61+2379A>G | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 32007808 | ||||||
chr2:32007809
|
G | A | 1 | a0001c0001t0001g0228 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.61+2378C>T | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 32007809 | ||||||
chr2:32007985
|
G | C | 1 | a0001c0001t0001g0229 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.61+2202C>G | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 32007985 | ||||||
chr2:32007993
|
T | A | 6 | a0001c0001t0001g0290a0001c0001t0001g0291a0001c0001t0001g0292others(3): Show | 6 | HG01109.hp2 HG02258.hp1 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.61+2194A>T | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 32007993 | ||||||
chr2:32008129
|
G | C | 1 | a0001c0001t0001g0279 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.61+2058C>G | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 32008129 | ||||||
chr2:32008174
|
CA | C | 3 | a0001c0001t0001g0232a0001c0001t0001g0233a0001c0001t0001g0234 | 3 | HG01361.hp1 HG03927.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.61+2012delT | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 32008174 | ||||||
chr2:32008179
|
C | T | 3 | a0001c0001t0001g0232a0001c0001t0001g0233a0001c0001t0001g0234 | 3 | HG01361.hp1 HG03927.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.61+2008G>A | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 32008179 | ||||||
chr2:32008199
|
A | G | 60 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0011others(57): Show | 60 | HG01168.hp1 HG01169.hp2 HG01255.hp2 others(57): Show |
intron_variant | MODIFIER | c.61+1988T>C | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 32008199 | ||||||
chr2:32008294
|
T | C | 3 | a0001c0001t0001g0229a0001c0001t0001g0230a0001c0001t0001g0231 | 3 | HG00408.hp1 HG02083.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.61+1893A>G | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 32008294 | ||||||
chr2:32008323
|
C | G | 1 | a0001c0001t0001g0232 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.61+1864G>C | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 32008323 | ||||||
chr2:32008355
|
G | A | 4 | a0001c0001t0001g0292a0001c0001t0001g0293a0001c0001t0001g0294others(1): Show | 4 | HG02258.hp1 HG03041.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.61+1832C>T | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 32008355 | ||||||
chr2:32008525
|
A | T | 3 | a0001c0001t0002g0003a0001c0001t0002g0004a0001c0001t0002g0005 | 3 | HG01891.hp1 HG02897.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.61+1662T>A | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 32008525 | ||||||
chr2:32008623
|
T | A | 6 | a0001c0001t0001g0290a0001c0001t0001g0291a0001c0001t0001g0292others(3): Show | 6 | HG01109.hp2 HG02258.hp1 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.61+1564A>T | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 32008623 | ||||||
chr2:32008872
|
G | C | 2 | a0001c0001t0001g0230a0001c0001t0001g0231 | 2 | HG00408.hp1 HG02083.hp1 |
intron_variant | MODIFIER | c.61+1315C>G | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 32008872 | ||||||
chr2:32009181
|
G | C | 3 | a0001c0001t0001g0232a0001c0001t0001g0233a0001c0001t0001g0234 | 3 | HG01361.hp1 HG03927.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.61+1006C>G | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 32009181 | ||||||
chr2:32009199
|
A | C | 1 | a0001c0001t0001g0009 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.61+988T>G | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 32009199 | ||||||
chr2:32009471
|
G | A | 1 | a0001c0001t0001g0235 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.61+716C>T | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 32009471 | ||||||
chr2:32009579
|
G | C | 5 | a0001c0001t0001g0275a0001c0001t0001g0276a0001c0001t0001g0277others(2): Show | 5 | HG02055.hp1 HG02970.hp2 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.61+608C>G | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 32009579 | ||||||
chr2:32009587
|
G | A | 59 | a0001c0001t0001g0008a0001c0001t0001g0236a0001c0001t0001g0237others(56): Show | 59 | HG01168.hp1 HG01169.hp2 HG01243.hp2 others(56): Show |
intron_variant | MODIFIER | c.61+600C>T | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 32009587 | ||||||
chr2:32009721
|
C | T | 1 | a0001c0001t0001g0008 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.61+466G>A | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 32009721 | ||||||
chr2:32009877
|
T | C | 11 | a0001c0001t0001g0280a0001c0001t0001g0281a0001c0001t0001g0282others(8): Show | 11 | HG01255.hp2 HG01496.hp2 HG01516.hp2 others(8): Show |
intron_variant | MODIFIER | c.61+310A>G | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 32009877 | ||||||
chr2:32010082
|
C | G | 1 | a0001c0001t0001g0007 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.61+105G>C | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 32010082 | ||||||
chr2:32010411
|
A | C | 1 | a0001c0001t0001g0006 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.-17-147T>G | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 1/9 | chr2 | 32010411 | ||||||
chr2:32010417
|
C | T | 3 | a0001c0001t0002g0003a0001c0001t0002g0004a0001c0001t0002g0005 | 3 | HG01891.hp1 HG02897.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.-17-153G>A | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 1/9 | chr2 | 32010417 | ||||||
chr2:32010544
|
G | GC | 6 | a0001c0001t0001g0290a0001c0001t0001g0291a0001c0001t0001g0292others(3): Show | 6 | HG01109.hp2 HG02258.hp1 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.-17-281dupG | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 1/9 | chr2 | 32010544 | ||||||
chr2:32010610
|
C | G | 1 | a0001c0001t0001g0002 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.-18+332G>C | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 1/9 | chr2 | 32010610 | ||||||
chr2:32010646
|
C | CCCCACCC others(13): Show |
1 | a0001c0001t0001g0001 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-18+276_-18+295dup others(20): Show |
MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 1/9 | chr2 | 32010646 | ||||||
chr2:32010653
|
C | A | 1 | a0001c0001t0001g0296 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-18+289G>T | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 1/9 | chr2 | 32010653 | ||||||
chr2:32010676
|
G | GC | 7 | a0001c0001t0001g0297a0001c0001t0001g0298a0001c0001t0001g0299others(4): Show | 7 | HG00597.hp2 HG01261.hp2 HG01496.hp2 others(4): Show |
intron_variant | MODIFIER | c.-18+265dupG | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 1/9 | chr2 | 32010676 | ||||||
chr2:32010726
|
G | A | 1 | a0001c0001t0001g0303 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.-18+216C>T | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 1/9 | chr2 | 32010726 | ||||||
chr2:32010918
|
G | A | 1 | a0001c0001t0001g0304 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.-18+24C>T | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 1/9 | chr2 | 32010918 |