Item | Value |
---|---|
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 | 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 | MSNRV others(292): Show |
chr2 | 31862823 | 32016008 |
a0002 | 0/0 | 297 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | MSNRV others(292): Show |
chr2 | 31862823 | 32016008 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 891 | 303 | 80 | 61 | 124 | 12 | 24 | MEMO1_chr2_31862823_32016008 | MEMO1 | ATGTC others(886): Show |
chr2 | 31862823 | 32016008 | ||
a0002c0002 | 0/0 | 891 | 1 | 0 | 1 | 0 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | ATGTC others(886): Show |
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 | GAGAT others(1511): Show |
chr2 | 31862823 | 32016008 |
a0001c0001t0002 | 0/0 | 1516 | 3 | 3 | 0 | 0 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | GAGAT others(1511): Show |
chr2 | 31862823 | 32016008 |
a0002c0002t0001 | 0/0 | 1516 | 1 | 0 | 1 | 0 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | GAGAT others(1511): Show |
chr2 | 31862823 | 32016008 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
a0001c0001t0001g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
a0001c0001t0001g0003 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | 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 | 1 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
a0001c0001t0001g0009 | 0/0 | 1 | 0 | 0 | 0 | 1 | 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 | 1 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
a0001c0001t0001g0015 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
a0001c0001t0001g0016 | 0/0 | 1 | 1 | 0 | 0 | 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 | 0 | 0 | 1 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
a0001c0001t0001g0020 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | 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 | 1 | 0 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
a0001c0001t0001g0023 | 0/0 | 1 | 0 | 0 | 1 | 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 | 1 | 0 | 0 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
a0001c0001t0001g0028 | 0/0 | 1 | 0 | 0 | 1 | 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 | 1 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
a0001c0001t0001g0031 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
a0001c0001t0001g0032 | 0/0 | 1 | 0 | 0 | 1 | 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 | 1 | 0 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
a0001c0001t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
a0001c0001t0001g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
a0001c0001t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
a0001c0001t0001g0038 | 0/0 | 1 | 1 | 0 | 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 | 1 | 0 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | 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 | 0 | 1 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
a0001c0001t0001g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
a0001c0001t0001g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
a0001c0001t0001g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
a0001c0001t0001g0049 | 0/0 | 1 | 1 | 0 | 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 | 0 | 1 | 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 | 0 | 1 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
a0001c0001t0001g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
a0001c0001t0001g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 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 | 1 | 0 | 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 | 0 | 0 | 0 | 1 | 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 | 0 | 0 | 0 | 1 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
a0001c0001t0001g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
a0001c0001t0001g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
a0001c0001t0001g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | 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 | 0 | 0 | 1 | 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 | 0 | 1 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
a0001c0001t0001g0089 | 0/0 | 1 | 0 | 1 | 0 | 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 | 0 | 0 | 1 | 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 | 0 | 1 | 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 | 1 | 0 | 0 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
a0001c0001t0001g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
a0001c0001t0001g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 0 | 1 | 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 | 1 | 0 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
a0001c0001t0001g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
a0001c0001t0001g0111 | 0/0 | 1 | 0 | 1 | 0 | 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 | 0 | 1 | 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 | 1 | 0 | 0 | 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 | 1 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 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 | 1 | 0 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
a0001c0001t0001g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
a0001c0001t0001g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
a0001c0001t0001g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
a0001c0001t0001g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
a0001c0001t0001g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | 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 | 0 | 1 | 0 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
a0001c0001t0001g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
a0001c0001t0001g0138 | 0/0 | 1 | 1 | 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 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
a0001c0001t0001g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
a0001c0001t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
a0001c0001t0001g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
a0001c0001t0001g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 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 | 1 | 0 | 0 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 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 | 1 | 0 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
a0001c0001t0001g0155 | 0/0 | 1 | 0 | 1 | 0 | 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 | 0 | 1 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
a0001c0001t0001g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | 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 | 0 | 1 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
a0001c0001t0001g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 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 | 1 | 0 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
a0001c0001t0001g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
a0001c0001t0001g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
a0001c0001t0001g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | 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 | 0 | 0 | 1 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 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 | 0 | 0 | 1 | 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 | 1 | 0 | 0 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 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 | 1 | 0 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 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 | 1 | 0 | 0 | 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 | 0 | 0 | 1 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
a0001c0001t0001g0196 | 0/0 | 1 | 1 | 0 | 0 | 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 | 0 | 1 | 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 | 0 | 0 | 1 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
a0001c0001t0001g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
a0001c0001t0001g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 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 | 0 | 1 | 0 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | 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 | 1 | 0 | 0 | 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 | 0 | 0 | 1 | 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 | 1 | 0 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | 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 | 1 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
a0001c0001t0001g0235 | 0/0 | 1 | 1 | 0 | 0 | 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 | 0 | 0 | 0 | 0 | 1 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
a0001c0001t0001g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | 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 | 0/1 | 1 | 0 | 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 | 1 | 0 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
a0001c0001t0001g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | 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 | 1 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
a0001c0001t0001g0257 | 0/0 | 1 | 0 | 1 | 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 | 1 | 0 | 0 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 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 | 1 | 0 | 0 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
a0001c0001t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
a0001c0001t0001g0269 | 0/0 | 1 | 1 | 0 | 0 | 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 | 0 | 1 | 0 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
a0001c0001t0001g0273 | 0/0 | 1 | 1 | 0 | 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 | 0 | 0 | 0 | 1 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
a0001c0001t0001g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 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 | 1 | 0 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
a0001c0001t0001g0283 | 0/0 | 1 | 0 | 0 | 1 | 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 | 1 | 0 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
a0001c0001t0001g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
a0001c0001t0001g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
a0001c0001t0001g0291 | 0/0 | 1 | 1 | 0 | 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 | 0 | 0 | 1 | 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 | 1 | 0 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
a0001c0001t0001g0299 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | 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 | 1 | 0 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
a0001c0001t0001g0302 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
a0001c0001t0001g0303 | 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 |
a0001c0001t0002g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
a0002c0002t0001g0121 | 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 | g0015 | EUR | GBR | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
HG00099 | hp2 | a0001 | c0001 | t0001 | g0107 | EUR | GBR | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
HG00140 | hp1 | a0001 | c0001 | t0001 | g0076 | EUR | GBR | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
HG00140 | hp2 | a0001 | c0001 | t0001 | g0020 | EUR | GBR | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
HG00408 | hp1 | a0001 | c0001 | t0001 | g0229 | EAS | CHS | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
HG00408 | hp2 | a0001 | c0001 | t0001 | g0187 | EAS | CHS | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
HG00423 | hp1 | a0001 | c0001 | t0001 | g0167 | EAS | CHS | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
HG00423 | hp2 | a0001 | c0001 | t0001 | g0108 | EAS | CHS | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
HG00438 | hp1 | a0001 | c0001 | t0001 | g0147 | EAS | CHS | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
HG00438 | hp2 | a0001 | c0001 | t0001 | g0007 | 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 | g0297 | EAS | CHS | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
HG00621 | hp1 | a0001 | c0001 | t0001 | g0061 | EAS | CHS | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
HG00621 | hp2 | a0001 | c0001 | t0001 | g0106 | EAS | CHS | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
HG00639 | hp1 | a0001 | c0001 | t0001 | g0155 | AMR | PUR | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
HG00639 | hp2 | a0001 | c0001 | t0001 | g0047 | AMR | PUR | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
HG00642 | hp1 | a0001 | c0001 | t0001 | g0156 | AMR | PUR | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
HG00642 | hp2 | a0001 | c0001 | t0001 | g0213 | AMR | PUR | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
HG00673 | hp1 | a0001 | c0001 | t0001 | g0043 | EAS | CHS | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
HG00673 | hp2 | a0001 | c0001 | t0001 | g0148 | EAS | CHS | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
HG00735 | hp1 | a0001 | c0001 | t0001 | g0089 | AMR | PUR | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
HG00735 | hp2 | a0001 | c0001 | t0001 | g0100 | AMR | PUR | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
HG00738 | hp1 | a0001 | c0001 | t0001 | g0063 | AMR | PUR | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
HG00738 | hp2 | a0001 | c0001 | t0001 | g0115 | AMR | PUR | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
HG00741 | hp1 | a0001 | c0001 | t0001 | g0034 | AMR | PUR | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
HG00741 | hp2 | a0001 | c0001 | t0001 | g0109 | AMR | PUR | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
HG01070 | hp1 | a0001 | c0001 | t0001 | g0216 | AMR | PUR | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
HG01070 | hp2 | a0001 | c0001 | t0001 | g0113 | AMR | PUR | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
HG01071 | hp1 | a0001 | c0001 | t0001 | g0123 | AMR | PUR | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
HG01071 | hp2 | a0001 | c0001 | t0001 | g0220 | AMR | PUR | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
HG01081 | hp1 | a0001 | c0001 | t0001 | g0173 | AMR | PUR | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
HG01081 | hp2 | a0001 | c0001 | t0001 | g0188 | AMR | PUR | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
HG01106 | hp1 | a0001 | c0001 | t0001 | g0214 | AMR | PUR | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
HG01106 | hp2 | a0001 | c0001 | t0001 | g0157 | AMR | PUR | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
HG01109 | hp1 | a0001 | c0001 | t0001 | g0074 | AMR | PUR | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
HG01109 | hp2 | a0001 | c0001 | t0001 | g0290 | AMR | PUR | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
HG01168 | hp1 | a0001 | c0001 | t0001 | g0257 | AMR | PUR | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
HG01168 | hp2 | a0002 | c0002 | t0001 | g0121 | AMR | PUR | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
HG01169 | hp1 | a0001 | c0001 | t0001 | g0112 | AMR | PUR | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
HG01169 | hp2 | a0001 | c0001 | t0001 | g0258 | AMR | PUR | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
HG01243 | hp1 | a0001 | c0001 | t0001 | g0153 | AMR | PUR | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
HG01243 | hp2 | a0001 | c0001 | t0001 | g0272 | AMR | PUR | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
HG01255 | hp1 | a0001 | c0001 | t0001 | g0137 | AMR | CLM | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
HG01255 | hp2 | a0001 | c0001 | t0001 | g0288 | AMR | CLM | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
HG01257 | hp1 | a0001 | c0001 | t0001 | g0114 | AMR | CLM | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
HG01257 | hp2 | a0001 | c0001 | t0001 | g0251 | AMR | CLM | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
HG01258 | hp1 | a0001 | c0001 | t0001 | g0254 | AMR | CLM | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
HG01258 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
HG01261 | hp1 | a0001 | c0001 | t0001 | g0162 | AMR | CLM | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
HG01261 | hp2 | a0001 | c0001 | t0001 | g0298 | AMR | CLM | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
HG01361 | hp1 | a0001 | c0001 | t0001 | g0231 | AMR | CLM | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
HG01361 | hp2 | a0001 | c0001 | t0001 | g0111 | AMR | CLM | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
HG01433 | hp1 | a0001 | c0001 | t0001 | g0033 | AMR | CLM | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
HG01433 | hp2 | a0001 | c0001 | t0001 | g0252 | AMR | CLM | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
HG01496 | hp1 | a0001 | c0001 | t0001 | g0104 | AMR | CLM | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
HG01496 | hp2 | a0001 | c0001 | t0001 | g0301 | AMR | CLM | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
HG01515 | hp1 | a0001 | c0001 | t0001 | g0067 | EUR | IBS | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
HG01515 | hp2 | a0001 | c0001 | t0001 | g0026 | EUR | IBS | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
HG01516 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | IBS | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
HG01516 | hp2 | a0001 | c0001 | t0001 | g0279 | EUR | IBS | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
HG01884 | hp1 | a0001 | c0001 | t0001 | g0209 | AFR | ACB | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
HG01884 | hp2 | a0001 | c0001 | t0001 | g0303 | AFR | ACB | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
HG01891 | hp1 | a0001 | c0001 | t0002 | g0004 | AFR | ACB | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
HG01891 | hp2 | a0001 | c0001 | t0001 | g0242 | AFR | ACB | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
HG01928 | hp1 | a0001 | c0001 | t0001 | g0045 | AMR | PEL | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
HG01928 | hp2 | a0001 | c0001 | t0001 | g0110 | 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 | g0136 | AMR | PEL | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
HG01943 | hp1 | a0001 | c0001 | t0001 | g0144 | AMR | PEL | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
HG01943 | hp2 | a0001 | c0001 | t0001 | g0039 | AMR | PEL | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
HG01975 | hp1 | a0001 | c0001 | t0001 | g0022 | AMR | PEL | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
HG01975 | hp2 | a0001 | c0001 | t0001 | g0040 | AMR | PEL | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
HG01978 | hp1 | a0001 | c0001 | t0001 | g0168 | AMR | PEL | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
HG01978 | hp2 | a0001 | c0001 | t0001 | g0128 | AMR | PEL | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
HG01993 | hp1 | a0001 | c0001 | t0001 | g0171 | AMR | PEL | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
HG01993 | hp2 | a0001 | c0001 | t0001 | g0125 | AMR | PEL | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
HG02004 | hp1 | a0001 | c0001 | t0001 | g0060 | AMR | PEL | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
HG02004 | hp2 | a0001 | c0001 | t0001 | g0059 | 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 | g0018 | EAS | KHV | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
HG02055 | hp1 | a0001 | c0001 | t0001 | g0275 | AFR | ACB | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
HG02055 | hp2 | a0001 | c0001 | t0001 | g0192 | AFR | ACB | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
HG02071 | hp1 | a0001 | c0001 | t0001 | g0159 | EAS | KHV | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
HG02071 | hp2 | a0001 | c0001 | t0001 | g0195 | EAS | KHV | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
HG02083 | hp1 | a0001 | c0001 | t0001 | g0230 | EAS | KHV | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
HG02083 | hp2 | a0001 | c0001 | t0001 | g0262 | EAS | KHV | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
HG02129 | hp1 | a0001 | c0001 | t0001 | g0287 | EAS | KHV | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
HG02129 | hp2 | a0001 | c0001 | t0001 | g0054 | EAS | KHV | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
HG02148 | hp1 | a0001 | c0001 | t0001 | g0166 | AMR | PEL | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
HG02148 | hp2 | a0001 | c0001 | t0001 | g0135 | AMR | PEL | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
HG02155 | hp1 | a0001 | c0001 | t0001 | g0284 | EAS | CDX | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
HG02155 | hp2 | a0001 | c0001 | t0001 | g0286 | EAS | CDX | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
HG02165 | hp1 | a0001 | c0001 | t0001 | g0122 | EAS | CDX | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
HG02165 | hp2 | a0001 | c0001 | t0001 | g0032 | EAS | CDX | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
HG02257 | hp1 | a0001 | c0001 | t0001 | g0143 | AFR | ACB | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
HG02257 | hp2 | a0001 | c0001 | t0001 | g0203 | AFR | ACB | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
HG02258 | hp1 | a0001 | c0001 | t0001 | g0292 | AFR | ACB | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
HG02258 | hp2 | a0001 | c0001 | t0001 | g0036 | AFR | ACB | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
HG02273 | hp1 | a0001 | c0001 | t0001 | g0124 | AMR | PEL | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
HG02273 | hp2 | a0001 | c0001 | t0001 | g0172 | AMR | PEL | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
HG02280 | hp1 | a0001 | c0001 | t0001 | g0207 | AFR | ACB | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
HG02280 | hp2 | a0001 | c0001 | t0001 | g0270 | AFR | ACB | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
HG02293 | hp1 | a0001 | c0001 | t0001 | g0141 | AMR | PEL | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
HG02293 | hp2 | a0001 | c0001 | t0001 | g0154 | AMR | PEL | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
HG02300 | hp1 | a0001 | c0001 | t0001 | g0282 | AMR | PEL | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
HG02300 | hp2 | a0001 | c0001 | t0001 | g0132 | AMR | PEL | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
HG02615 | hp1 | a0001 | c0001 | t0001 | g0206 | AFR | GWD | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
HG02615 | hp2 | a0001 | c0001 | t0001 | g0273 | AFR | GWD | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
HG02622 | hp1 | a0001 | c0001 | t0001 | g0289 | AFR | GWD | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
HG02622 | hp2 | a0001 | c0001 | t0001 | g0200 | AFR | GWD | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
HG02698 | hp1 | a0001 | c0001 | t0001 | g0031 | SAS | PJL | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
HG02698 | hp2 | a0001 | c0001 | t0001 | g0085 | SAS | PJL | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
HG02717 | hp1 | a0001 | c0001 | t0001 | g0073 | AFR | GWD | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
HG02717 | hp2 | a0001 | c0001 | t0001 | g0205 | AFR | GWD | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
HG02723 | hp1 | a0001 | c0001 | t0001 | g0240 | AFR | GWD | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
HG02723 | hp2 | a0001 | c0001 | t0001 | g0048 | AFR | GWD | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
HG02738 | hp1 | a0001 | c0001 | t0001 | g0300 | SAS | PJL | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
HG02738 | hp2 | a0001 | c0001 | t0001 | g0161 | SAS | PJL | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
HG02809 | hp1 | a0001 | c0001 | t0001 | g0208 | AFR | GWD | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
HG02809 | hp2 | a0001 | c0001 | t0001 | g0239 | AFR | GWD | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
HG02818 | hp1 | a0001 | c0001 | t0001 | g0051 | AFR | GWD | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
HG02818 | hp2 | a0001 | c0001 | t0001 | g0210 | AFR | GWD | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
HG02895 | hp1 | a0001 | c0001 | t0001 | g0204 | AFR | GWD | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
HG02895 | hp2 | a0001 | c0001 | t0001 | g0269 | AFR | GWD | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
HG02897 | hp1 | a0001 | c0001 | t0001 | g0238 | AFR | GWD | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
HG02897 | hp2 | a0001 | c0001 | t0002 | g0005 | AFR | GWD | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
HG02922 | hp1 | a0001 | c0001 | t0002 | g0006 | AFR | ESN | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
HG02922 | hp2 | a0001 | c0001 | t0001 | g0196 | AFR | ESN | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
HG02965 | hp1 | a0001 | c0001 | t0001 | g0271 | AFR | ESN | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
HG02965 | hp2 | a0001 | c0001 | t0001 | g0016 | AFR | ESN | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
HG02970 | hp1 | a0001 | c0001 | t0001 | g0101 | AFR | ESN | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
HG02970 | hp2 | a0001 | c0001 | t0001 | g0278 | AFR | ESN | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
HG03041 | hp1 | a0001 | c0001 | t0001 | g0064 | AFR | GWD | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
HG03041 | hp2 | a0001 | c0001 | t0001 | g0294 | AFR | GWD | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
HG03098 | hp1 | a0001 | c0001 | t0001 | g0201 | AFR | MSL | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
HG03098 | hp2 | a0001 | c0001 | t0001 | g0197 | AFR | MSL | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
HG03130 | hp1 | a0001 | c0001 | t0001 | g0198 | AFR | ESN | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
HG03130 | hp2 | a0001 | c0001 | t0001 | g0259 | 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 | g0235 | 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 | g0150 | AFR | ESN | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
HG03209 | hp1 | a0001 | c0001 | t0001 | g0102 | AFR | MSL | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
HG03209 | hp2 | a0001 | c0001 | t0001 | g0291 | AFR | MSL | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
HG03225 | hp1 | a0001 | c0001 | t0001 | g0138 | 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 | g0241 | AFR | MSL | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
HG03453 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | MSL | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
HG03486 | hp1 | a0001 | c0001 | t0001 | g0267 | AFR | MSL | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
HG03486 | hp2 | a0001 | c0001 | t0001 | g0194 | AFR | MSL | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
HG03490 | hp1 | a0001 | c0001 | t0001 | g0130 | SAS | PJL | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
HG03490 | hp2 | a0001 | c0001 | t0001 | g0075 | SAS | PJL | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
HG03491 | hp1 | a0001 | c0001 | t0001 | g0019 | SAS | PJL | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
HG03491 | hp2 | a0001 | c0001 | t0001 | g0182 | SAS | PJL | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
HG03516 | hp1 | a0001 | c0001 | t0001 | g0191 | AFR | ESN | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
HG03516 | hp2 | a0001 | c0001 | t0001 | g0103 | AFR | ESN | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
HG03540 | hp1 | a0001 | c0001 | t0001 | g0218 | 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 | g0219 | AFR | MSL | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
HG03579 | hp2 | a0001 | c0001 | t0001 | g0174 | 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 | g0176 | SAS | STU | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
HG03704 | hp1 | a0001 | c0001 | t0001 | g0119 | SAS | PJL | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
HG03704 | hp2 | a0001 | c0001 | t0001 | g0253 | SAS | PJL | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
HG03831 | hp1 | a0001 | c0001 | t0001 | g0299 | SAS | BEB | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
HG03831 | hp2 | a0001 | c0001 | t0001 | g0003 | SAS | BEB | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
HG03927 | hp1 | a0001 | c0001 | t0001 | g0232 | SAS | BEB | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
HG03927 | hp2 | a0001 | c0001 | t0001 | g0302 | SAS | BEB | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
HG04199 | hp1 | a0001 | c0001 | t0001 | g0131 | SAS | STU | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
HG04199 | hp2 | a0001 | c0001 | t0001 | g0041 | SAS | STU | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
HG04204 | hp1 | a0001 | c0001 | t0001 | g0221 | SAS | STU | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
HG04204 | hp2 | a0001 | c0001 | t0001 | g0081 | SAS | STU | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
HG04228 | hp1 | a0001 | c0001 | t0001 | g0105 | SAS | STU | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
HG04228 | hp2 | a0001 | c0001 | t0001 | g0233 | SAS | STU | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
NA18522 | hp1 | a0001 | c0001 | t0001 | g0193 | AFR | YRI | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
NA18522 | hp2 | a0001 | c0001 | t0001 | g0142 | AFR | YRI | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
NA18612 | hp1 | a0001 | c0001 | t0001 | g0030 | EAS | CHB | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
NA18612 | hp2 | a0001 | c0001 | t0001 | g0044 | EAS | CHB | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
NA18906 | hp1 | a0001 | c0001 | t0001 | g0038 | AFR | YRI | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
NA18906 | hp2 | a0001 | c0001 | t0001 | g0293 | AFR | YRI | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
NA18939 | hp1 | a0001 | c0001 | t0001 | g0285 | EAS | JPT | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
NA18939 | hp2 | a0001 | c0001 | t0001 | g0190 | EAS | JPT | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
NA18940 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
NA18940 | hp2 | a0001 | c0001 | t0001 | g0164 | EAS | JPT | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
NA18942 | hp1 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
NA18942 | hp2 | a0001 | c0001 | t0001 | g0065 | EAS | JPT | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
NA18943 | hp1 | a0001 | c0001 | t0001 | g0062 | EAS | JPT | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
NA18943 | hp2 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
NA18944 | hp1 | a0001 | c0001 | t0001 | g0097 | EAS | JPT | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
NA18944 | hp2 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
NA18949 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
NA18949 | hp2 | a0001 | c0001 | t0001 | g0226 | 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 | g0025 | EAS | JPT | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
NA18951 | hp2 | a0001 | c0001 | t0001 | g0017 | 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 | g0146 | EAS | JPT | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
NA18953 | hp1 | a0001 | c0001 | t0001 | g0056 | EAS | JPT | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
NA18953 | hp2 | a0001 | c0001 | t0001 | g0268 | EAS | JPT | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
NA18956 | hp1 | a0001 | c0001 | t0001 | g0078 | EAS | JPT | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
NA18956 | hp2 | a0001 | c0001 | t0001 | g0224 | EAS | JPT | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
NA18960 | hp1 | a0001 | c0001 | t0001 | g0055 | EAS | JPT | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
NA18960 | hp2 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
NA18963 | hp1 | a0001 | c0001 | t0001 | g0160 | EAS | JPT | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
NA18963 | hp2 | a0001 | c0001 | t0001 | g0068 | EAS | JPT | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
NA18964 | hp1 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
NA18964 | hp2 | a0001 | c0001 | t0001 | g0263 | EAS | JPT | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
NA18968 | hp1 | a0001 | c0001 | t0001 | g0077 | EAS | JPT | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
NA18968 | hp2 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
NA18969 | hp1 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
NA18969 | hp2 | a0001 | c0001 | t0001 | g0050 | EAS | JPT | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
NA18971 | hp1 | a0001 | c0001 | t0001 | g0280 | EAS | JPT | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
NA18971 | hp2 | a0001 | c0001 | t0001 | g0087 | EAS | JPT | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
NA18973 | hp1 | a0001 | c0001 | t0001 | g0082 | EAS | JPT | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
NA18973 | hp2 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
NA18974 | hp1 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
NA18974 | hp2 | a0001 | c0001 | t0001 | g0255 | EAS | JPT | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
NA18975 | hp1 | a0001 | c0001 | t0001 | g0222 | EAS | JPT | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
NA18975 | hp2 | a0001 | c0001 | t0001 | g0116 | EAS | JPT | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
NA18977 | hp1 | a0001 | c0001 | t0001 | g0058 | EAS | JPT | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
NA18977 | hp2 | a0001 | c0001 | t0001 | g0296 | EAS | JPT | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
NA18978 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
NA18978 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
NA18980 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
NA18980 | hp2 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
NA18984 | hp1 | a0001 | c0001 | t0001 | g0117 | EAS | JPT | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
NA18984 | hp2 | a0001 | c0001 | t0001 | g0189 | 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 | g0046 | EAS | JPT | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
NA18998 | hp2 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
NA19000 | hp1 | a0001 | c0001 | t0001 | g0052 | EAS | JPT | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
NA19000 | hp2 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
NA19003 | hp1 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
NA19003 | hp2 | a0001 | c0001 | t0001 | g0158 | EAS | JPT | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
NA19004 | hp1 | a0001 | c0001 | t0001 | g0169 | EAS | JPT | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
NA19004 | hp2 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
NA19009 | hp1 | a0001 | c0001 | t0001 | g0261 | EAS | JPT | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
NA19009 | hp2 | a0001 | c0001 | t0001 | g0170 | EAS | JPT | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
NA19010 | hp1 | a0001 | c0001 | t0001 | g0180 | 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 | g0234 | EAS | JPT | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
NA19011 | hp2 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
NA19012 | hp1 | a0001 | c0001 | t0001 | g0145 | EAS | JPT | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
NA19012 | hp2 | a0001 | c0001 | t0001 | g0265 | EAS | JPT | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
NA19030 | hp1 | a0001 | c0001 | t0001 | g0276 | AFR | LWK | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
NA19030 | hp2 | a0001 | c0001 | t0001 | g0211 | AFR | LWK | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
NA19043 | hp1 | a0001 | c0001 | t0001 | g0139 | AFR | LWK | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
NA19043 | hp2 | a0001 | c0001 | t0001 | g0277 | AFR | LWK | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
NA19056 | hp1 | a0001 | c0001 | t0001 | g0057 | EAS | JPT | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
NA19056 | hp2 | a0001 | c0001 | t0001 | g0266 | EAS | JPT | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
NA19057 | hp1 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
NA19057 | hp2 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
NA19063 | hp1 | a0001 | c0001 | t0001 | g0088 | 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 | g0012 | EAS | JPT | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
NA19064 | hp2 | a0001 | c0001 | t0001 | g0223 | EAS | JPT | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
NA19068 | hp1 | a0001 | c0001 | t0001 | g0186 | EAS | JPT | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
NA19068 | hp2 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
NA19070 | hp1 | a0001 | c0001 | t0001 | g0086 | EAS | JPT | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
NA19070 | hp2 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
NA19076 | hp1 | a0001 | c0001 | t0001 | g0256 | EAS | JPT | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
NA19076 | hp2 | a0001 | c0001 | t0001 | g0066 | EAS | JPT | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
NA19077 | hp1 | a0001 | c0001 | t0001 | g0283 | EAS | JPT | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
NA19077 | hp2 | a0001 | c0001 | t0001 | g0165 | EAS | JPT | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
NA19079 | hp1 | a0001 | c0001 | t0001 | g0281 | EAS | JPT | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
NA19079 | hp2 | a0001 | c0001 | t0001 | g0175 | EAS | JPT | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
NA19080 | hp1 | a0001 | c0001 | t0001 | g0260 | EAS | JPT | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
NA19080 | hp2 | a0001 | c0001 | t0001 | g0179 | EAS | JPT | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
NA19082 | hp1 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
NA19082 | hp2 | a0001 | c0001 | t0001 | g0177 | EAS | JPT | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
NA19084 | hp1 | a0001 | c0001 | t0001 | g0149 | EAS | JPT | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
NA19084 | hp2 | a0001 | c0001 | t0001 | g0247 | EAS | JPT | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
NA19085 | hp1 | a0001 | c0001 | t0001 | g0023 | 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 | g0181 | EAS | JPT | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
NA19088 | hp2 | a0001 | c0001 | t0001 | g0248 | EAS | JPT | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
NA19090 | hp1 | a0001 | c0001 | t0001 | g0185 | EAS | JPT | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
NA19090 | hp2 | a0001 | c0001 | t0001 | g0264 | EAS | JPT | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
NA19240 | hp1 | a0001 | c0001 | t0001 | g0227 | AFR | YRI | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
NA19240 | hp2 | a0001 | c0001 | t0001 | g0236 | AFR | YRI | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
NA20129 | hp1 | a0001 | c0001 | t0001 | g0099 | AFR | ASW | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
NA20129 | hp2 | a0001 | c0001 | t0001 | g0199 | AFR | ASW | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
NA20752 | hp1 | a0001 | c0001 | t0001 | g0009 | EUR | TSI | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
NA20752 | hp2 | a0001 | c0001 | t0001 | g0217 | EUR | TSI | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
NA20805 | hp1 | a0001 | c0001 | t0001 | g0072 | EUR | TSI | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
NA20805 | hp2 | a0001 | c0001 | t0001 | g0215 | EUR | TSI | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
NA20905 | hp1 | a0001 | c0001 | t0001 | g0237 | SAS | GIH | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
NA20905 | hp2 | a0001 | c0001 | t0001 | g0178 | SAS | GIH | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
HG02109 | hp1 | a0001 | c0001 | t0001 | g0049 | AFR | ACB | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
HG02109 | hp2 | a0001 | c0001 | t0001 | g0126 | AFR | ACB | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
HG03471 | hp1 | a0001 | c0001 | t0001 | g0274 | AFR | MSL | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
HG03471 | hp2 | a0001 | c0001 | t0001 | g0228 | 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 | g0295 | 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 | g0035 | EAS | JPT | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
NA20300 | hp1 | a0001 | c0001 | t0001 | g0184 | AFR | USA | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
NA20300 | hp2 | a0001 | c0001 | t0001 | g0202 | AFR | USA | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
NA21309 | hp1 | a0001 | c0001 | t0001 | g0079 | AFR | LWK | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
NA21309 | hp2 | a0001 | c0001 | t0001 | g0027 | AFR | LWK | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0243 | REF | REF | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0140 | REF | REF | MEMO1_chr2_31862823_32016008 | MEMO1 | chr2 | 31862823 | 32016008 |
view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
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 |
view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|
view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
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 |
view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:31868526 | T | C | 1 | a0001c0001t0001g0210 | 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 | a0001c0001t0001g0214 | 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 | a0001c0001t0001g0018 | 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 | a0001c0001t0001g0270 a0001c0001t0001g0280 |
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 | a0001c0001t0001g0295 | 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 | a0001c0001t0001g0281 | 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 | a0001c0001t0001g0170 a0001c0001t0001g0180 a0001c0001t0001g0181 others(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 | a0001c0001t0001g0015 | 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 | a0001c0001t0001g0296 | 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 | a0001c0001t0001g0015 | 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 | a0001c0001t0001g0190 | 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 | a0001c0001t0001g0048 a0001c0001t0001g0049 a0001c0001t0001g0182 others(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 | a0001c0001t0001g0231 a0001c0001t0001g0232 a0001c0001t0001g0233 others(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 | 47 | a0001c0001t0001g0009 a0001c0001t0001g0011 a0001c0001t0001g0012 others(44): Show |
47 | HG01168.hp1 HG01169.hp2 HG01255.hp2 others(44): 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 | a0001c0001t0001g0235 | 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 | a0001c0001t0001g0069 a0001c0001t0001g0071 a0001c0001t0001g0073 others(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 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0006 |
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 | a0001c0001t0001g0288 | 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 | a0001c0001t0001g0022 a0001c0001t0001g0107 a0001c0001t0001g0114 others(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 | a0001c0001t0001g0277 | 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 | a0001c0001t0001g0083 a0001c0001t0001g0084 |
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 | a0001c0001t0001g0228 | 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 | a0001c0001t0001g0238 a0001c0001t0001g0239 a0001c0001t0001g0240 others(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 | a0001c0001t0001g0197 a0001c0001t0001g0199 a0001c0001t0001g0200 |
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 | a0001c0001t0001g0036 a0001c0001t0001g0093 |
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 | 291 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(288): Show |
292 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(289): 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 | a0001c0001t0001g0128 | 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 | a0001c0001t0001g0282 a0001c0001t0001g0288 a0001c0001t0001g0301 |
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 | a0001c0001t0001g0291 a0001c0001t0001g0292 a0001c0001t0001g0293 others(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 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0006 |
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 | a0001c0001t0001g0274 a0001c0001t0001g0275 a0001c0001t0001g0276 others(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 | a0001c0001t0001g0099 a0001c0001t0001g0103 a0001c0001t0001g0142 others(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 | 150 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0009 others(147): Show |
151 | HG00140.hp2 HG00423.hp2 HG00438.hp1 others(148): 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 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(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 | a0001c0001t0001g0283 | 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 | a0001c0001t0001g0008 a0001c0001t0001g0010 a0001c0001t0001g0037 others(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 | a0001c0001t0001g0198 a0001c0001t0001g0271 a0001c0001t0001g0272 others(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 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0015 others(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 | a0001c0001t0001g0291 a0001c0001t0001g0292 a0001c0001t0001g0293 others(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 | a0001c0001t0001g0067 | 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 | a0001c0001t0001g0106 a0001c0001t0001g0122 a0001c0001t0001g0186 |
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 | a0001c0001t0001g0238 a0001c0001t0001g0239 a0001c0001t0001g0240 others(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 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0011 others(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 |
178 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(175): 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 | a0001c0001t0001g0016 a0001c0001t0001g0018 a0001c0001t0001g0022 others(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 | a0001c0001t0001g0086 a0001c0001t0001g0087 a0001c0001t0001g0110 others(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 |
13 | a0001c0001t0001g0071 a0001c0001t0001g0196 a0001c0001t0001g0198 others(10): Show |
13 | HG01257.hp2 HG01258.hp1 HG02280.hp2 others(10): 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 | a0001c0001t0001g0184 a0001c0001t0001g0197 a0001c0001t0001g0292 others(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 | a0001c0001t0001g0276 a0001c0001t0001g0291 a0001c0001t0001g0293 others(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 | a0001c0001t0001g0274 a0001c0001t0001g0275 |
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 | a0001c0001t0001g0273 | 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 | a0001c0001t0001g0271 a0001c0001t0001g0272 |
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 | a0001c0001t0001g0024 | 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 | a0001c0001t0001g0145 | 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 | a0001c0001t0001g0033 a0001c0001t0001g0034 a0001c0001t0001g0042 others(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 | a0001c0001t0001g0274 a0001c0001t0001g0275 a0001c0001t0001g0276 |
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 | a0001c0001t0001g0278 | 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 | a0001c0001t0001g0271 a0001c0001t0001g0272 a0001c0001t0001g0273 others(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 | a0001c0001t0001g0289 a0001c0001t0001g0290 |
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 | a0001c0001t0001g0190 | 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 | a0001c0001t0001g0079 | 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 | a0001c0001t0001g0214 | 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 | a0001c0001t0001g0189 | 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 | a0001c0001t0001g0022 a0001c0001t0001g0107 a0001c0001t0001g0155 |
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 | a0001c0001t0001g0182 | 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 | a0001c0001t0001g0182 | 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 | a0001c0001t0001g0035 a0001c0001t0001g0170 a0001c0001t0001g0180 others(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 | a0001c0001t0001g0231 a0001c0001t0001g0232 a0001c0001t0001g0233 |
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 | a0001c0001t0001g0145 | 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 | a0001c0001t0001g0237 a0001c0001t0001g0299 |
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 | a0001c0001t0001g0235 a0001c0001t0001g0236 |
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 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(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 | 58 | a0001c0001t0001g0009 a0001c0001t0001g0011 a0001c0001t0001g0012 others(55): Show |
58 | HG01168.hp1 HG01169.hp2 HG01243.hp2 others(55): 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 | a0001c0001t0001g0231 a0001c0001t0001g0232 a0001c0001t0001g0233 |
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 | a0001c0001t0001g0271 a0001c0001t0001g0272 a0001c0001t0001g0273 |
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 | a0001c0001t0001g0110 a0001c0001t0001g0134 a0001c0001t0001g0135 others(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 | a0001c0001t0001g0110 a0001c0001t0001g0134 a0001c0001t0001g0135 others(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 | 117 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0016 others(114): 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 | a0001c0001t0001g0067 | 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 | a0001c0001t0001g0026 | 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 | a0001c0001t0001g0138 a0001c0001t0001g0139 a0001c0001t0001g0227 |
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 | 72 | a0001c0001t0001g0009 a0001c0001t0001g0011 a0001c0001t0001g0012 others(69): Show |
72 | HG01106.hp1 HG01109.hp2 HG01168.hp1 others(69): 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 | a0001c0001t0001g0289 a0001c0001t0001g0290 |
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 | a0001c0001t0001g0003 | 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 | a0001c0001t0001g0079 a0001c0001t0001g0184 a0001c0001t0001g0214 |
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 | a0001c0001t0001g0231 | 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 | a0001c0001t0001g0188 | 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 | a0001c0001t0001g0285 a0001c0001t0001g0286 a0001c0001t0001g0287 |
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 | a0001c0001t0001g0003 | 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 | a0001c0001t0001g0300 | 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 | 221 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(218): 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 | a0001c0001t0001g0025 | 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 | a0001c0001t0001g0295 | 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 | a0001c0001t0001g0289 a0001c0001t0001g0290 |
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 | a0001c0001t0001g0274 a0001c0001t0001g0275 a0001c0001t0001g0276 |
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 | a0001c0001t0001g0235 a0001c0001t0001g0236 |
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 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(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 | 289 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(286): Show |
290 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(287): 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 | a0001c0001t0001g0133 | 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 | a0001c0001t0001g0079 a0001c0001t0001g0184 a0001c0001t0001g0214 |
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 | a0001c0001t0001g0291 a0001c0001t0001g0292 a0001c0001t0001g0293 |
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 | a0001c0001t0001g0228 | 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 | a0001c0001t0001g0068 | 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 | a0001c0001t0001g0035 a0001c0001t0001g0055 a0001c0001t0001g0168 others(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 | a0001c0001t0001g0231 a0001c0001t0001g0232 a0001c0001t0001g0233 |
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 | 112 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0018 others(109): 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 | a0001c0001t0001g0110 a0001c0001t0001g0135 a0001c0001t0001g0136 others(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 | a0001c0001t0001g0041 | 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 | 223 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(220): 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 | a0001c0001t0001g0235 a0001c0001t0001g0236 |
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 | a0001c0001t0001g0208 | 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 | a0001c0001t0001g0029 | 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 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(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 | a0001c0001t0001g0101 a0001c0001t0001g0104 a0001c0001t0001g0207 others(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 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0022 others(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 | 12 | a0001c0001t0001g0001 a0001c0001t0001g0020 a0001c0001t0001g0021 others(9): 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 | a0001c0001t0001g0035 a0001c0001t0001g0069 a0001c0001t0001g0071 others(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 | a0001c0001t0001g0190 a0001c0001t0001g0256 a0001c0001t0001g0271 others(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 | 42 | a0001c0001t0001g0009 a0001c0001t0001g0011 a0001c0001t0001g0012 others(39): Show |
42 | HG01168.hp1 HG01169.hp2 HG01255.hp2 others(39): 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 | a0001c0001t0001g0235 a0001c0001t0001g0236 |
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 | a0001c0001t0001g0271 a0001c0001t0001g0272 a0001c0001t0001g0273 others(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 | a0001c0001t0001g0009 | 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 | a0001c0001t0001g0059 a0001c0001t0001g0070 |
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 | a0001c0001t0001g0271 a0001c0001t0001g0272 a0001c0001t0001g0273 |
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 | a0001c0001t0001g0291 a0001c0001t0001g0292 a0001c0001t0001g0293 others(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 | 297 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(294): Show |
298 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(295): 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 | a0001c0001t0001g0101 a0001c0001t0001g0104 a0001c0001t0001g0207 others(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 | 61 | a0001c0001t0001g0009 a0001c0001t0001g0011 a0001c0001t0001g0012 others(58): Show |
61 | HG01168.hp1 HG01169.hp2 HG01243.hp2 others(58): 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 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0006 |
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 | 47 | a0001c0001t0001g0009 a0001c0001t0001g0011 a0001c0001t0001g0012 others(44): Show |
47 | HG01168.hp1 HG01169.hp2 HG01255.hp2 others(44): 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 | a0001c0001t0001g0188 | 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 | a0001c0001t0001g0100 | 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 | a0001c0001t0001g0130 | 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 | a0001c0001t0001g0079 a0001c0001t0001g0101 a0001c0001t0001g0104 others(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 | a0001c0001t0001g0215 a0001c0001t0001g0216 a0001c0001t0001g0217 others(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 | a0001c0001t0001g0283 | 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 | a0001c0001t0001g0291 a0001c0001t0001g0292 a0001c0001t0001g0293 others(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 | a0001c0001t0001g0271 a0001c0001t0001g0272 a0001c0001t0001g0273 |
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 | a0001c0001t0001g0270 a0001c0001t0001g0295 |
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 | a0001c0001t0001g0231 a0001c0001t0001g0232 a0001c0001t0001g0233 |
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 | a0001c0001t0001g0277 | 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 | a0001c0001t0001g0199 | 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 | 47 | a0001c0001t0001g0009 a0001c0001t0001g0011 a0001c0001t0001g0012 others(44): Show |
47 | HG01168.hp1 HG01169.hp2 HG01255.hp2 others(44): 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 | a0001c0001t0001g0079 a0001c0001t0001g0101 a0001c0001t0001g0104 others(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 | a0001c0001t0001g0089 | 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 | a0001c0001t0001g0231 a0001c0001t0001g0232 a0001c0001t0001g0233 |
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 | a0001c0001t0001g0295 | 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 | a0001c0001t0001g0138 | 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 | 47 | a0001c0001t0001g0009 a0001c0001t0001g0011 a0001c0001t0001g0012 others(44): Show |
47 | HG01168.hp1 HG01169.hp2 HG01255.hp2 others(44): 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 | a0001c0001t0001g0241 | 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 | a0001c0001t0001g0235 a0001c0001t0001g0236 a0001c0001t0001g0270 others(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 | a0001c0001t0001g0119 | 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 | a0001c0001t0001g0196 a0001c0001t0001g0197 a0001c0001t0001g0198 others(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 | a0001c0001t0001g0016 a0001c0001t0001g0079 a0001c0001t0001g0101 others(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 | a0001c0001t0001g0117 a0001c0001t0001g0118 |
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 | 79 | a0001c0001t0001g0009 a0001c0001t0001g0011 a0001c0001t0001g0012 others(76): Show |
79 | HG01106.hp1 HG01109.hp2 HG01168.hp1 others(76): 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 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0001g0050 others(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 | a0001c0001t0001g0242 a0001c0001t0001g0267 |
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 | a0001c0001t0001g0274 a0001c0001t0001g0275 a0001c0001t0001g0276 |
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 | a0001c0001t0001g0252 a0001c0001t0001g0257 a0001c0001t0001g0258 |
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 | a0001c0001t0001g0244 a0001c0001t0001g0249 a0001c0001t0001g0250 others(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 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0006 |
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 | a0001c0001t0001g0190 | 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 | a0001c0001t0001g0069 a0001c0001t0001g0071 a0001c0001t0001g0073 |
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 | a0001c0001t0001g0012 a0001c0001t0001g0014 |
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 | a0001c0001t0001g0192 | 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 | 110 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0016 others(107): 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 | 49 | a0001c0001t0001g0009 a0001c0001t0001g0011 a0001c0001t0001g0012 others(46): Show |
49 | HG01168.hp1 HG01169.hp2 HG01255.hp2 others(46): Show |
intron_variant | MODIFIER | c.581-4121A>G | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 7/9 | chr2 | 31887583 | |||||||
chr2:31887657 | G | C | 55 | a0001c0001t0001g0009 a0001c0001t0001g0011 a0001c0001t0001g0012 others(52): Show |
55 | HG01168.hp1 HG01169.hp2 HG01255.hp2 others(52): 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 | a0001c0001t0001g0231 a0001c0001t0001g0232 a0001c0001t0001g0233 |
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 | 70 | a0001c0001t0001g0009 a0001c0001t0001g0011 a0001c0001t0001g0012 others(67): Show |
70 | HG01106.hp1 HG01109.hp2 HG01168.hp1 others(67): 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 | a0001c0001t0001g0231 a0001c0001t0001g0232 a0001c0001t0001g0233 |
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 | a0001c0001t0001g0231 a0001c0001t0001g0232 a0001c0001t0001g0233 |
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 | a0001c0001t0001g0231 | 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 | a0001c0001t0001g0295 | 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 | a0001c0001t0001g0061 | 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 | a0001c0001t0001g0131 | 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 | a0001c0001t0001g0281 | 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 | a0001c0001t0001g0184 | 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 | a0001c0001t0001g0023 | 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 | a0001c0001t0001g0031 | 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 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0006 |
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 | a0001c0001t0001g0294 | 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 | a0001c0001t0001g0215 a0001c0001t0001g0216 a0001c0001t0001g0217 others(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 | a0001c0001t0001g0025 a0001c0001t0001g0094 a0001c0001t0001g0095 others(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 | a0001c0001t0001g0196 a0001c0001t0001g0197 a0001c0001t0001g0198 others(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 | a0001c0001t0001g0300 | 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 | a0001c0001t0001g0295 | 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 | a0001c0001t0001g0193 | 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 | a0001c0001t0001g0202 | 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 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0006 |
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 | a0001c0001t0001g0030 a0001c0001t0001g0158 a0001c0001t0001g0159 |
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 | a0001c0001t0001g0027 | 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 | 60 | a0001c0001t0001g0009 a0001c0001t0001g0011 a0001c0001t0001g0012 others(57): Show |
60 | HG01081.hp2 HG01168.hp1 HG01169.hp2 others(57): 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 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0006 |
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 | a0001c0001t0001g0033 a0001c0001t0001g0034 a0001c0001t0001g0041 others(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 | a0001c0001t0001g0206 | 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 | a0001c0001t0001g0107 | 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 | a0001c0001t0001g0079 | 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 | a0001c0001t0001g0277 | 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 | a0001c0001t0001g0043 | 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 | a0001c0001t0001g0290 | 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 | a0001c0001t0001g0077 a0001c0001t0001g0078 |
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 | 287 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(284): Show |
288 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(285): 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 | a0001c0001t0001g0235 a0001c0001t0001g0236 |
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 | 83 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0009 others(80): Show |
83 | HG00408.hp2 HG00438.hp1 HG00438.hp2 others(80): Show |
intron_variant | MODIFIER | c.438-3704dupA | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 6/9 | chr2 | 31895837 | |||||||
chr2:31895837 | C | CTT | 10 | a0001c0001t0001g0239 a0001c0001t0001g0245 a0001c0001t0001g0247 others(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 | a0001c0001t0001g0079 a0001c0001t0001g0184 a0001c0001t0001g0214 others(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 | a0001c0001t0001g0238 a0001c0001t0001g0239 a0001c0001t0001g0240 others(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 | a0001c0001t0001g0228 | 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 | a0001c0001t0001g0274 a0001c0001t0001g0275 a0001c0001t0001g0276 |
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 | a0001c0001t0001g0184 a0001c0001t0001g0214 |
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 | a0001c0001t0001g0291 a0001c0001t0001g0292 a0001c0001t0001g0293 others(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 | a0001c0001t0001g0039 | 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 | a0001c0001t0001g0283 | 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 | a0001c0001t0001g0102 a0001c0001t0001g0191 |
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 | a0001c0001t0001g0185 | 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 | a0001c0001t0001g0160 | 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 | a0001c0001t0001g0291 a0001c0001t0001g0292 a0001c0001t0001g0293 others(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 | 63 | a0001c0001t0001g0009 a0001c0001t0001g0011 a0001c0001t0001g0012 others(60): Show |
63 | HG01168.hp1 HG01169.hp2 HG01243.hp2 others(60): 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 | a0001c0001t0001g0063 | 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 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0006 |
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 | 60 | a0001c0001t0001g0009 a0001c0001t0001g0011 a0001c0001t0001g0012 others(57): Show |
60 | HG01168.hp1 HG01169.hp2 HG01255.hp2 others(57): 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 | a0001c0001t0001g0184 a0001c0001t0001g0214 |
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 | a0001c0001t0001g0220 | 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 | a0001c0001t0001g0214 | 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 | 3 | a0001c0001t0001g0251 a0001c0001t0001g0253 a0001c0001t0001g0254 |
3 | HG01257.hp2 HG01258.hp1 HG03704.hp2 |
intron_variant | MODIFIER | c.438-5692T>C | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 6/9 | chr2 | 31897826 | |||||||
chr2:31897830 | A | G | 3 | a0001c0001t0001g0251 a0001c0001t0001g0253 a0001c0001t0001g0254 |
3 | HG01257.hp2 HG01258.hp1 HG03704.hp2 |
intron_variant | MODIFIER | c.438-5696T>C | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 6/9 | chr2 | 31897830 | |||||||
chr2:31897836 | G | T | 3 | a0001c0001t0001g0251 a0001c0001t0001g0253 a0001c0001t0001g0254 |
3 | HG01257.hp2 HG01258.hp1 HG03704.hp2 |
intron_variant | MODIFIER | c.438-5702C>A | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 6/9 | chr2 | 31897836 | |||||||
chr2:31897838 | A | G | 3 | a0001c0001t0001g0251 a0001c0001t0001g0253 a0001c0001t0001g0254 |
3 | HG01257.hp2 HG01258.hp1 HG03704.hp2 |
intron_variant | MODIFIER | c.438-5704T>C | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 6/9 | chr2 | 31897838 | |||||||
chr2:31897847 | T | C | 3 | a0001c0001t0001g0251 a0001c0001t0001g0253 a0001c0001t0001g0254 |
3 | HG01257.hp2 HG01258.hp1 HG03704.hp2 |
intron_variant | MODIFIER | c.438-5713A>G | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 6/9 | chr2 | 31897847 | |||||||
chr2:31897850 | G | A | 3 | a0001c0001t0001g0251 a0001c0001t0001g0253 a0001c0001t0001g0254 |
3 | HG01257.hp2 HG01258.hp1 HG03704.hp2 |
intron_variant | MODIFIER | c.438-5716C>T | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 6/9 | chr2 | 31897850 | |||||||
chr2:31897851 | C | CTT | 3 | a0001c0001t0001g0251 a0001c0001t0001g0253 a0001c0001t0001g0254 |
3 | HG01257.hp2 HG01258.hp1 HG03704.hp2 |
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 | 3 | a0001c0001t0001g0251 a0001c0001t0001g0253 a0001c0001t0001g0254 |
3 | HG01257.hp2 HG01258.hp1 HG03704.hp2 |
intron_variant | MODIFIER | c.438-5735T>G | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 6/9 | chr2 | 31897869 | |||||||
chr2:31897875 | T | C | 2 | a0001c0001t0001g0083 a0001c0001t0001g0084 |
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 | 3 | a0001c0001t0001g0251 a0001c0001t0001g0253 a0001c0001t0001g0254 |
3 | HG01257.hp2 HG01258.hp1 HG03704.hp2 |
intron_variant | MODIFIER | c.438-5743G>A | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 6/9 | chr2 | 31897877 | |||||||
chr2:31897879 | C | G | 3 | a0001c0001t0001g0251 a0001c0001t0001g0253 a0001c0001t0001g0254 |
3 | HG01257.hp2 HG01258.hp1 HG03704.hp2 |
intron_variant | MODIFIER | c.438-5745G>C | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 6/9 | chr2 | 31897879 | |||||||
chr2:31897889 | T | C | 3 | a0001c0001t0001g0251 a0001c0001t0001g0253 a0001c0001t0001g0254 |
3 | HG01257.hp2 HG01258.hp1 HG03704.hp2 |
intron_variant | MODIFIER | c.438-5755A>G | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 6/9 | chr2 | 31897889 | |||||||
chr2:31897893 | A | G | 3 | a0001c0001t0001g0251 a0001c0001t0001g0253 a0001c0001t0001g0254 |
3 | HG01257.hp2 HG01258.hp1 HG03704.hp2 |
intron_variant | MODIFIER | c.438-5759T>C | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 6/9 | chr2 | 31897893 | |||||||
chr2:31897895 | T | C | 3 | a0001c0001t0001g0251 a0001c0001t0001g0253 a0001c0001t0001g0254 |
3 | HG01257.hp2 HG01258.hp1 HG03704.hp2 |
intron_variant | MODIFIER | c.438-5761A>G | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 6/9 | chr2 | 31897895 | |||||||
chr2:31897896 | G | T | 3 | a0001c0001t0001g0251 a0001c0001t0001g0253 a0001c0001t0001g0254 |
3 | HG01257.hp2 HG01258.hp1 HG03704.hp2 |
intron_variant | MODIFIER | c.438-5762C>A | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 6/9 | chr2 | 31897896 | |||||||
chr2:31897908 | T | A | 3 | a0001c0001t0001g0251 a0001c0001t0001g0253 a0001c0001t0001g0254 |
3 | HG01257.hp2 HG01258.hp1 HG03704.hp2 |
intron_variant | MODIFIER | c.438-5774A>T | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 6/9 | chr2 | 31897908 | |||||||
chr2:31897914 | G | A | 3 | a0001c0001t0001g0251 a0001c0001t0001g0253 a0001c0001t0001g0254 |
3 | HG01257.hp2 HG01258.hp1 HG03704.hp2 |
intron_variant | MODIFIER | c.438-5780C>T | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 6/9 | chr2 | 31897914 | |||||||
chr2:31897919 | T | C | 3 | a0001c0001t0001g0251 a0001c0001t0001g0253 a0001c0001t0001g0254 |
3 | HG01257.hp2 HG01258.hp1 HG03704.hp2 |
intron_variant | MODIFIER | c.438-5785A>G | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 6/9 | chr2 | 31897919 | |||||||
chr2:31897920 | G | A | 3 | a0001c0001t0001g0251 a0001c0001t0001g0253 a0001c0001t0001g0254 |
3 | HG01257.hp2 HG01258.hp1 HG03704.hp2 |
intron_variant | MODIFIER | c.438-5786C>T | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 6/9 | chr2 | 31897920 | |||||||
chr2:31897940 | T | C | 3 | a0001c0001t0001g0251 a0001c0001t0001g0253 a0001c0001t0001g0254 |
3 | HG01257.hp2 HG01258.hp1 HG03704.hp2 |
intron_variant | MODIFIER | c.438-5806A>G | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 6/9 | chr2 | 31897940 | |||||||
chr2:31897948 | G | T | 3 | a0001c0001t0001g0251 a0001c0001t0001g0253 a0001c0001t0001g0254 |
3 | HG01257.hp2 HG01258.hp1 HG03704.hp2 |
intron_variant | MODIFIER | c.438-5814C>A | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 6/9 | chr2 | 31897948 | |||||||
chr2:31897959 | C | G | 3 | a0001c0001t0001g0251 a0001c0001t0001g0253 a0001c0001t0001g0254 |
3 | HG01257.hp2 HG01258.hp1 HG03704.hp2 |
intron_variant | MODIFIER | c.438-5825G>C | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 6/9 | chr2 | 31897959 | |||||||
chr2:31897969 | T | C | 3 | a0001c0001t0001g0251 a0001c0001t0001g0253 a0001c0001t0001g0254 |
3 | HG01257.hp2 HG01258.hp1 HG03704.hp2 |
intron_variant | MODIFIER | c.438-5835A>G | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 6/9 | chr2 | 31897969 | |||||||
chr2:31897982 | A | G | 3 | a0001c0001t0001g0251 a0001c0001t0001g0253 a0001c0001t0001g0254 |
3 | HG01257.hp2 HG01258.hp1 HG03704.hp2 |
intron_variant | MODIFIER | c.438-5848T>C | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 6/9 | chr2 | 31897982 | |||||||
chr2:31897994 | T | C | 1 | a0001c0001t0001g0274 | 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 | 3 | a0001c0001t0001g0251 a0001c0001t0001g0253 a0001c0001t0001g0254 |
3 | HG01257.hp2 HG01258.hp1 HG03704.hp2 |
intron_variant | MODIFIER | c.438-5866G>T | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 6/9 | chr2 | 31898000 | |||||||
chr2:31898001 | A | G | 3 | a0001c0001t0001g0251 a0001c0001t0001g0253 a0001c0001t0001g0254 |
3 | HG01257.hp2 HG01258.hp1 HG03704.hp2 |
intron_variant | MODIFIER | c.438-5867T>C | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 6/9 | chr2 | 31898001 | |||||||
chr2:31898022 | C | T | 3 | a0001c0001t0001g0251 a0001c0001t0001g0253 a0001c0001t0001g0254 |
3 | HG01257.hp2 HG01258.hp1 HG03704.hp2 |
intron_variant | MODIFIER | c.438-5888G>A | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 6/9 | chr2 | 31898022 | |||||||
chr2:31898025 | G | GA | 3 | a0001c0001t0001g0251 a0001c0001t0001g0253 a0001c0001t0001g0254 |
3 | HG01257.hp2 HG01258.hp1 HG03704.hp2 |
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 | 3 | a0001c0001t0001g0251 a0001c0001t0001g0253 a0001c0001t0001g0254 |
3 | HG01257.hp2 HG01258.hp1 HG03704.hp2 |
intron_variant | MODIFIER | c.438-5895G>A | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 6/9 | chr2 | 31898029 | |||||||
chr2:31898051 | A | G | 3 | a0001c0001t0001g0251 a0001c0001t0001g0253 a0001c0001t0001g0254 |
3 | HG01257.hp2 HG01258.hp1 HG03704.hp2 |
intron_variant | MODIFIER | c.438-5917T>C | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 6/9 | chr2 | 31898051 | |||||||
chr2:31898064 | T | C | 3 | a0001c0001t0001g0251 a0001c0001t0001g0253 a0001c0001t0001g0254 |
3 | HG01257.hp2 HG01258.hp1 HG03704.hp2 |
intron_variant | MODIFIER | c.438-5930A>G | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 6/9 | chr2 | 31898064 | |||||||
chr2:31898080 | C | T | 3 | a0001c0001t0001g0251 a0001c0001t0001g0253 a0001c0001t0001g0254 |
3 | HG01257.hp2 HG01258.hp1 HG03704.hp2 |
intron_variant | MODIFIER | c.438-5946G>A | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 6/9 | chr2 | 31898080 | |||||||
chr2:31898083 | T | C | 3 | a0001c0001t0001g0251 a0001c0001t0001g0253 a0001c0001t0001g0254 |
3 | HG01257.hp2 HG01258.hp1 HG03704.hp2 |
intron_variant | MODIFIER | c.438-5949A>G | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 6/9 | chr2 | 31898083 | |||||||
chr2:31898084 | G | A | 3 | a0001c0001t0001g0251 a0001c0001t0001g0253 a0001c0001t0001g0254 |
3 | HG01257.hp2 HG01258.hp1 HG03704.hp2 |
intron_variant | MODIFIER | c.438-5950C>T | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 6/9 | chr2 | 31898084 | |||||||
chr2:31898088 | C | A | 3 | a0001c0001t0001g0251 a0001c0001t0001g0253 a0001c0001t0001g0254 |
3 | HG01257.hp2 HG01258.hp1 HG03704.hp2 |
intron_variant | MODIFIER | c.438-5954G>T | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 6/9 | chr2 | 31898088 | |||||||
chr2:31898123 | G | T | 3 | a0001c0001t0001g0251 a0001c0001t0001g0253 a0001c0001t0001g0254 |
3 | HG01257.hp2 HG01258.hp1 HG03704.hp2 |
intron_variant | MODIFIER | c.438-5989C>A | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 6/9 | chr2 | 31898123 | |||||||
chr2:31898129 | T | C | 3 | a0001c0001t0001g0251 a0001c0001t0001g0253 a0001c0001t0001g0254 |
3 | HG01257.hp2 HG01258.hp1 HG03704.hp2 |
intron_variant | MODIFIER | c.438-5995A>G | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 6/9 | chr2 | 31898129 | |||||||
chr2:31898130 | G | A | 3 | a0001c0001t0001g0251 a0001c0001t0001g0253 a0001c0001t0001g0254 |
3 | HG01257.hp2 HG01258.hp1 HG03704.hp2 |
intron_variant | MODIFIER | c.438-5996C>T | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 6/9 | chr2 | 31898130 | |||||||
chr2:31898138 | T | A | 3 | a0001c0001t0001g0251 a0001c0001t0001g0253 a0001c0001t0001g0254 |
3 | HG01257.hp2 HG01258.hp1 HG03704.hp2 |
intron_variant | MODIFIER | c.438-6004A>T | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 6/9 | chr2 | 31898138 | |||||||
chr2:31898139 | G | A | 3 | a0001c0001t0001g0251 a0001c0001t0001g0253 a0001c0001t0001g0254 |
3 | HG01257.hp2 HG01258.hp1 HG03704.hp2 |
intron_variant | MODIFIER | c.438-6005C>T | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 6/9 | chr2 | 31898139 | |||||||
chr2:31898143 | C | T | 3 | a0001c0001t0001g0251 a0001c0001t0001g0253 a0001c0001t0001g0254 |
3 | HG01257.hp2 HG01258.hp1 HG03704.hp2 |
intron_variant | MODIFIER | c.438-6009G>A | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 6/9 | chr2 | 31898143 | |||||||
chr2:31898147 | A | G | 3 | a0001c0001t0001g0251 a0001c0001t0001g0253 a0001c0001t0001g0254 |
3 | HG01257.hp2 HG01258.hp1 HG03704.hp2 |
intron_variant | MODIFIER | c.438-6013T>C | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 6/9 | chr2 | 31898147 | |||||||
chr2:31898155 | G | C | 3 | a0001c0001t0001g0251 a0001c0001t0001g0253 a0001c0001t0001g0254 |
3 | HG01257.hp2 HG01258.hp1 HG03704.hp2 |
intron_variant | MODIFIER | c.438-6021C>G | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 6/9 | chr2 | 31898155 | |||||||
chr2:31898156 | A | C | 3 | a0001c0001t0001g0251 a0001c0001t0001g0253 a0001c0001t0001g0254 |
3 | HG01257.hp2 HG01258.hp1 HG03704.hp2 |
intron_variant | MODIFIER | c.438-6022T>G | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 6/9 | chr2 | 31898156 | |||||||
chr2:31898178 | A | T | 3 | a0001c0001t0001g0251 a0001c0001t0001g0253 a0001c0001t0001g0254 |
3 | HG01257.hp2 HG01258.hp1 HG03704.hp2 |
intron_variant | MODIFIER | c.438-6044T>A | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 6/9 | chr2 | 31898178 | |||||||
chr2:31898181 | AT | A | 3 | a0001c0001t0001g0251 a0001c0001t0001g0253 a0001c0001t0001g0254 |
3 | HG01257.hp2 HG01258.hp1 HG03704.hp2 |
intron_variant | MODIFIER | c.438-6048delA | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 6/9 | chr2 | 31898181 | |||||||
chr2:31898195 | T | A | 3 | a0001c0001t0001g0251 a0001c0001t0001g0253 a0001c0001t0001g0254 |
3 | HG01257.hp2 HG01258.hp1 HG03704.hp2 |
intron_variant | MODIFIER | c.438-6061A>T | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 6/9 | chr2 | 31898195 | |||||||
chr2:31898200 | C | T | 7 | a0001c0001t0001g0235 a0001c0001t0001g0236 a0001c0001t0001g0251 others(4): Show |
7 | HG01257.hp2 HG01258.hp1 HG02280.hp2 others(4): 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 | a0001c0001t0001g0103 | 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 | a0001c0001t0001g0270 | 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 | a0001c0001t0001g0274 a0001c0001t0001g0275 a0001c0001t0001g0276 |
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 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0006 |
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 | a0001c0001t0001g0031 | 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 | a0001c0001t0001g0114 | 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 | a0001c0001t0001g0081 | 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 | a0001c0001t0001g0059 a0001c0001t0001g0070 |
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 | a0001c0001t0001g0277 | 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 | 63 | a0001c0001t0001g0009 a0001c0001t0001g0011 a0001c0001t0001g0012 others(60): Show |
63 | HG01168.hp1 HG01169.hp2 HG01243.hp2 others(60): 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 | a0001c0001t0001g0242 a0001c0001t0001g0267 |
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 | a0001c0001t0001g0282 a0001c0001t0001g0288 a0001c0001t0001g0301 |
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 | 74 | a0001c0001t0001g0009 a0001c0001t0001g0011 a0001c0001t0001g0012 others(71): Show |
74 | HG01106.hp1 HG01109.hp2 HG01168.hp1 others(71): 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 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0001g0050 others(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 | a0001c0001t0001g0274 a0001c0001t0001g0275 a0001c0001t0001g0276 |
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 | a0001c0001t0001g0116 | 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 | a0001c0001t0001g0274 a0001c0001t0001g0275 a0001c0001t0001g0276 |
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 | a0001c0001t0001g0035 a0001c0001t0001g0068 |
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 | a0001c0001t0001g0231 a0001c0001t0001g0232 a0001c0001t0001g0233 |
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 | a0001c0001t0001g0029 a0001c0001t0001g0030 a0001c0001t0001g0082 others(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 | a0001c0001t0001g0271 a0001c0001t0001g0272 a0001c0001t0001g0273 |
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 | 58 | a0001c0001t0001g0009 a0001c0001t0001g0011 a0001c0001t0001g0012 others(55): Show |
58 | HG01168.hp1 HG01169.hp2 HG01255.hp2 others(55): 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 | a0001c0001t0001g0079 a0001c0001t0001g0184 a0001c0001t0001g0214 others(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 | a0001c0001t0001g0142 | 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 | a0001c0001t0001g0021 a0001c0001t0001g0031 a0001c0001t0001g0035 others(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 | a0001c0001t0001g0011 a0001c0001t0001g0027 a0001c0001t0001g0028 others(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 | 48 | a0001c0001t0001g0009 a0001c0001t0001g0012 a0001c0001t0001g0013 others(45): Show |
48 | HG01168.hp1 HG01169.hp2 HG01255.hp2 others(45): 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 | a0001c0001t0001g0059 a0001c0001t0001g0090 a0001c0001t0001g0092 |
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 | 61 | a0001c0001t0001g0009 a0001c0001t0001g0011 a0001c0001t0001g0012 others(58): Show |
61 | HG01168.hp1 HG01169.hp2 HG01243.hp2 others(58): Show |
intron_variant | MODIFIER | c.438-9822G>A | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 6/9 | chr2 | 31901956 | |||||||
chr2:31901970 | TA | T | 52 | a0001c0001t0001g0009 a0001c0001t0001g0011 a0001c0001t0001g0012 others(49): Show |
52 | HG01168.hp1 HG01169.hp2 HG01255.hp2 others(49): Show |
intron_variant | MODIFIER | c.438-9837delT | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 6/9 | chr2 | 31901970 | |||||||
chr2:31902101 | G | C | 6 | a0001c0001t0001g0289 a0001c0001t0001g0290 a0001c0001t0001g0291 others(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 | a0001c0001t0001g0077 a0001c0001t0001g0078 |
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 | 52 | a0001c0001t0001g0009 a0001c0001t0001g0011 a0001c0001t0001g0012 others(49): Show |
52 | HG01168.hp1 HG01169.hp2 HG01255.hp2 others(49): 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 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0006 |
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 | a0001c0001t0001g0277 | 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 | a0001c0001t0001g0287 | 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 | a0001c0001t0001g0278 | 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 | a0001c0001t0001g0069 a0001c0001t0001g0071 a0001c0001t0001g0073 |
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 | a0001c0001t0001g0020 | 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 | a0001c0001t0001g0196 a0001c0001t0001g0197 a0001c0001t0001g0198 others(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 | a0001c0001t0001g0033 a0001c0001t0001g0034 a0001c0001t0001g0035 others(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 | a0001c0001t0001g0078 | 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 | a0001c0001t0001g0069 a0001c0001t0001g0071 a0001c0001t0001g0073 |
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 | 45 | a0001c0001t0001g0009 a0001c0001t0001g0011 a0001c0001t0001g0012 others(42): Show |
45 | HG01255.hp2 HG01257.hp2 HG01258.hp1 others(42): 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 | a0001c0001t0001g0033 a0001c0001t0001g0034 a0001c0001t0001g0035 others(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 | a0001c0001t0001g0069 a0001c0001t0001g0071 a0001c0001t0001g0073 |
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 | 88 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0009 others(85): Show |
88 | HG00639.hp2 HG00738.hp1 HG00741.hp1 others(85): 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 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(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 | a0001c0001t0001g0289 a0001c0001t0001g0290 a0001c0001t0001g0291 others(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 | a0001c0001t0001g0130 | 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 | a0001c0001t0001g0138 | 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 | a0001c0001t0001g0220 | 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 | a0001c0001t0001g0077 a0001c0001t0001g0078 |
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 | a0001c0001t0001g0270 | 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 | a0001c0001t0001g0231 a0001c0001t0001g0232 a0001c0001t0001g0233 |
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 | a0001c0001t0001g0037 | 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 | a0001c0001t0001g0283 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.438-12406T>C | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 6/9 | chr2 | 31904540 | |||||||
chr2:31904628 | G | A | 7 | a0001c0001t0001g0277 a0001c0001t0001g0289 a0001c0001t0001g0290 others(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 | 71 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0018 others(68): 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 | a0001c0001t0001g0220 | 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 | a0001c0001t0001g0170 | 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 | 63 | a0001c0001t0001g0009 a0001c0001t0001g0011 a0001c0001t0001g0012 others(60): Show |
63 | HG01168.hp1 HG01169.hp2 HG01243.hp2 others(60): Show |
intron_variant | MODIFIER | c.438-12829T>C | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 6/9 | chr2 | 31904963 | |||||||
chr2:31905054 | T | C | 72 | a0001c0001t0001g0009 a0001c0001t0001g0011 a0001c0001t0001g0012 others(69): Show |
72 | HG01109.hp2 HG01168.hp1 HG01169.hp2 others(69): 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 | a0001c0001t0001g0100 | 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 | a0001c0001t0001g0088 | 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 | a0001c0001t0001g0272 | 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 | a0001c0001t0002g0004 a0001c0001t0002g0006 |
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 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0006 |
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 | a0001c0001t0001g0020 a0001c0001t0001g0088 a0001c0001t0001g0096 others(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 | 60 | a0001c0001t0001g0009 a0001c0001t0001g0011 a0001c0001t0001g0012 others(57): Show |
60 | HG01168.hp1 HG01169.hp2 HG01243.hp2 others(57): Show |
intron_variant | MODIFIER | c.437+11899C>T | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 6/9 | chr2 | 31906027 | |||||||
chr2:31906090 | A | T | 111 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0008 others(108): 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 | a0001c0001t0001g0231 a0001c0001t0001g0232 a0001c0001t0001g0233 others(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 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0006 |
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 | a0001c0001t0001g0277 | 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 | 68 | a0001c0001t0001g0009 a0001c0001t0001g0011 a0001c0001t0001g0012 others(65): Show |
68 | HG01109.hp2 HG01168.hp1 HG01169.hp2 others(65): 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 | a0001c0001t0001g0271 a0001c0001t0001g0272 a0001c0001t0001g0273 |
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 | a0001c0001t0001g0232 a0001c0001t0001g0233 |
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 | a0001c0001t0001g0271 a0001c0001t0001g0272 a0001c0001t0001g0273 |
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 | a0001c0001t0001g0114 | 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 | 60 | a0001c0001t0001g0009 a0001c0001t0001g0011 a0001c0001t0001g0012 others(57): Show |
60 | HG01168.hp1 HG01169.hp2 HG01243.hp2 others(57): Show |
intron_variant | MODIFIER | c.437+11515G>A | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 6/9 | chr2 | 31906411 | |||||||
chr2:31906491 | T | C | 60 | a0001c0001t0001g0009 a0001c0001t0001g0011 a0001c0001t0001g0012 others(57): Show |
60 | HG01168.hp1 HG01169.hp2 HG01243.hp2 others(57): 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 | a0001c0001t0001g0259 | 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 | a0001c0001t0001g0063 | 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 | a0001c0001t0001g0289 a0001c0001t0001g0290 |
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 | 60 | a0001c0001t0001g0009 a0001c0001t0001g0011 a0001c0001t0001g0012 others(57): Show |
60 | HG01168.hp1 HG01169.hp2 HG01243.hp2 others(57): 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 | a0001c0001t0001g0182 | 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 | a0001c0001t0001g0241 | 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 | a0001c0001t0001g0242 a0001c0001t0001g0267 |
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 | a0001c0001t0001g0106 a0001c0001t0001g0122 a0001c0001t0001g0186 |
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 | a0001c0001t0001g0116 a0001c0001t0001g0151 |
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 | a0001c0001t0001g0289 a0001c0001t0001g0290 a0001c0001t0001g0291 others(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 | 292 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(289): Show |
293 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(290): 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 | a0001c0001t0001g0232 a0001c0001t0001g0233 |
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 | a0001c0001t0001g0165 | 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 | a0001c0001t0001g0291 a0001c0001t0001g0292 a0001c0001t0001g0293 |
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 | a0001c0001t0001g0099 a0001c0001t0001g0103 a0001c0001t0001g0142 others(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 | a0001c0001t0001g0291 a0001c0001t0001g0292 a0001c0001t0001g0293 |
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 | 63 | a0001c0001t0001g0009 a0001c0001t0001g0011 a0001c0001t0001g0012 others(60): Show |
63 | HG01168.hp1 HG01169.hp2 HG01243.hp2 others(60): 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 | a0001c0001t0001g0231 a0001c0001t0001g0232 a0001c0001t0001g0233 |
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 | 118 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(115): 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 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0025 others(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 | a0001c0001t0001g0079 a0001c0001t0001g0099 a0001c0001t0001g0113 others(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 | a0001c0001t0001g0234 | 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 | a0001c0001t0001g0041 a0001c0001t0001g0093 a0001c0001t0001g0231 others(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 | 48 | a0001c0001t0001g0009 a0001c0001t0001g0011 a0001c0001t0001g0012 others(45): Show |
48 | HG01168.hp1 HG01169.hp2 HG01255.hp2 others(45): 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 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0006 |
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 | a0001c0001t0001g0272 | 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 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(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 | a0001c0001t0001g0274 a0001c0001t0001g0275 a0001c0001t0001g0276 others(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 | a0001c0001t0001g0205 | 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 | a0001c0001t0001g0143 | 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 | a0001c0001t0001g0291 a0001c0001t0001g0292 a0001c0001t0001g0293 others(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 | a0001c0001t0001g0197 a0001c0001t0001g0199 a0001c0001t0001g0200 |
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 | a0001c0001t0001g0294 | 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 | a0001c0001t0001g0016 | 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 | a0001c0001t0001g0294 | 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 | 63 | a0001c0001t0001g0009 a0001c0001t0001g0011 a0001c0001t0001g0012 others(60): Show |
63 | HG01168.hp1 HG01169.hp2 HG01243.hp2 others(60): Show |
intron_variant | MODIFIER | c.437+9243G>A | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 6/9 | chr2 | 31908683 | |||||||
chr2:31908881 | A | G | 63 | a0001c0001t0001g0009 a0001c0001t0001g0011 a0001c0001t0001g0012 others(60): Show |
63 | HG01168.hp1 HG01169.hp2 HG01243.hp2 others(60): 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 | a0001c0001t0001g0259 | 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 | a0001c0001t0001g0259 | 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 | a0001c0001t0001g0161 | 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 | a0001c0001t0002g0005 | 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 | a0001c0001t0001g0152 | 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 | a0001c0001t0001g0295 | 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 | a0001c0001t0001g0056 a0001c0001t0001g0057 a0001c0001t0001g0058 |
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 | a0001c0001t0001g0181 | 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 | a0001c0001t0001g0047 | 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 | a0001c0001t0001g0138 a0001c0001t0001g0139 a0001c0001t0001g0227 |
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 | a0001c0001t0001g0277 | 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 | a0001c0001t0001g0289 a0001c0001t0001g0290 |
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 | a0001c0001t0002g0004 | 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 | a0001c0001t0001g0180 | 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 | a0001c0001t0001g0231 a0001c0001t0001g0232 a0001c0001t0001g0233 |
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 | a0001c0001t0001g0277 | 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 | 101 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0008 others(98): 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 | a0001c0001t0001g0289 a0001c0001t0001g0290 |
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 | a0001c0001t0001g0164 | 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 | a0001c0001t0001g0033 a0001c0001t0001g0034 a0001c0001t0001g0035 others(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 | a0001c0001t0001g0035 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.437+6773C>G | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 6/9 | chr2 | 31911153 | |||||||
chr2:31911305 | A | T | 63 | a0001c0001t0001g0009 a0001c0001t0001g0011 a0001c0001t0001g0012 others(60): Show |
63 | HG01168.hp1 HG01169.hp2 HG01243.hp2 others(60): 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 | a0001c0001t0001g0157 | 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 | a0001c0001t0001g0016 | 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 | a0001c0001t0001g0202 a0001c0001t0001g0207 a0001c0001t0001g0208 |
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 | a0001c0001t0001g0291 a0001c0001t0001g0292 a0001c0001t0001g0293 |
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 | a0001c0001t0001g0289 a0001c0001t0001g0290 |
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 | a0001c0001t0001g0270 a0001c0001t0001g0295 |
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 | a0001c0001t0001g0231 | 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 | a0001c0001t0001g0271 a0001c0001t0001g0272 a0001c0001t0001g0273 |
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 | a0001c0001t0001g0224 | 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 | a0001c0001t0001g0052 a0001c0001t0001g0089 a0001c0001t0001g0098 others(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 | a0001c0001t0001g0099 a0001c0001t0001g0103 a0001c0001t0001g0142 others(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 | a0001c0001t0001g0259 | 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 | a0001c0001t0001g0031 | 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 | a0001c0001t0001g0278 | 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 | a0001c0001t0001g0079 | 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 | 110 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0008 others(107): 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 | a0001c0001t0001g0241 | 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 | a0001c0001t0001g0026 a0001c0001t0001g0033 a0001c0001t0001g0034 others(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 | 39 | a0001c0001t0001g0009 a0001c0001t0001g0011 a0001c0001t0001g0012 others(36): Show |
39 | HG01168.hp1 HG01169.hp2 HG01255.hp2 others(36): 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 | a0001c0001t0001g0013 a0001c0001t0001g0250 a0001c0001t0001g0267 others(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 | a0001c0001t0001g0271 a0001c0001t0001g0272 a0001c0001t0001g0273 others(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 | a0001c0001t0001g0231 | 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 | 64 | a0001c0001t0001g0009 a0001c0001t0001g0011 a0001c0001t0001g0012 others(61): Show |
64 | HG01070.hp2 HG01071.hp1 HG01168.hp1 others(61): Show |
intron_variant | MODIFIER | c.437+4408delA | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 6/9 | chr2 | 31913517 | |||||||
chr2:31913517 | GTT | G | 7 | a0001c0001t0001g0274 a0001c0001t0001g0275 a0001c0001t0001g0276 others(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 | a0001c0001t0001g0090 a0001c0001t0001g0092 |
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 | a0001c0001t0001g0291 a0001c0001t0001g0292 a0001c0001t0001g0293 others(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 | a0001c0001t0001g0207 a0001c0001t0001g0208 a0001c0001t0001g0231 others(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 | a0001c0001t0001g0016 a0001c0001t0001g0094 a0001c0001t0001g0095 others(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 | a0001c0001t0001g0231 a0001c0001t0001g0232 a0001c0001t0001g0233 |
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 | 49 | a0001c0001t0001g0009 a0001c0001t0001g0011 a0001c0001t0001g0012 others(46): Show |
49 | HG01168.hp1 HG01169.hp2 HG01255.hp2 others(46): 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 | a0001c0001t0001g0157 | 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 | a0001c0001t0001g0295 | 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 | a0001c0001t0001g0171 | 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 | a0001c0001t0001g0155 | 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 | a0001c0001t0001g0110 a0001c0001t0001g0134 a0001c0001t0001g0135 others(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 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0010 others(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 | 60 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0011 others(57): Show |
60 | HG01168.hp1 HG01168.hp2 HG01169.hp1 others(57): Show |
intron_variant | MODIFIER | c.437+2964delT | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 6/9 | chr2 | 31914961 | |||||||
chr2:31914961 | TAA | T | 9 | a0001c0001t0001g0238 a0001c0001t0001g0244 a0001c0001t0001g0250 others(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 | a0001c0001t0001g0277 | 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 | a0001c0001t0001g0238 a0001c0001t0001g0269 |
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 | a0001c0001t0001g0130 | 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 | 57 | a0001c0001t0001g0009 a0001c0001t0001g0011 a0001c0001t0001g0012 others(54): Show |
57 | HG01168.hp1 HG01169.hp2 HG01255.hp2 others(54): 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 | a0001c0001t0001g0015 | 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 | a0001c0001t0001g0179 | 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 | a0001c0001t0001g0281 | 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 | a0001c0001t0001g0100 | 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 | a0001c0001t0001g0235 a0001c0001t0001g0236 |
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 | a0001c0001t0001g0242 a0001c0001t0001g0267 |
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 | a0001c0001t0001g0041 | 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 | a0001c0001t0001g0170 a0001c0001t0001g0185 a0001c0001t0001g0187 |
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 | a0001c0001t0001g0235 a0001c0001t0001g0236 |
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 | a0001c0001t0001g0271 a0001c0001t0001g0272 a0001c0001t0001g0273 others(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 | a0001c0001t0001g0235 a0001c0001t0001g0236 a0001c0001t0001g0270 others(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 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0006 |
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 | a0001c0001t0001g0259 | 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 | a0001c0001t0001g0271 a0001c0001t0001g0272 a0001c0001t0001g0273 |
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 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0010 others(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 | a0001c0001t0001g0270 | 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 | a0001c0001t0001g0192 | 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 | a0001c0001t0001g0128 a0001c0001t0001g0154 |
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 | a0001c0001t0001g0113 a0001c0001t0001g0123 a0002c0002t0001g0121 |
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 | a0001c0001t0001g0293 | 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 | a0001c0001t0001g0095 | 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 | a0001c0001t0001g0074 | 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 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(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 | a0001c0001t0001g0291 a0001c0001t0001g0292 a0001c0001t0001g0293 others(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 | a0001c0001t0001g0270 | 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 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0006 |
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 | a0001c0001t0001g0104 | 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 | a0001c0001t0001g0027 | 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 | 72 | a0001c0001t0001g0009 a0001c0001t0001g0011 a0001c0001t0001g0012 others(69): Show |
72 | HG01109.hp2 HG01168.hp1 HG01169.hp2 others(69): 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 | a0001c0001t0001g0188 a0001c0001t0001g0215 a0001c0001t0001g0216 others(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 | a0001c0001t0001g0271 | 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 | a0001c0001t0001g0181 | 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 | 39 | a0001c0001t0001g0009 a0001c0001t0001g0011 a0001c0001t0001g0012 others(36): Show |
39 | HG01168.hp1 HG01169.hp2 HG01255.hp2 others(36): 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 | a0001c0001t0001g0238 a0001c0001t0001g0239 a0001c0001t0001g0240 others(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 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0007 others(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 | a0001c0001t0001g0203 a0001c0001t0001g0228 a0001c0001t0001g0235 others(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 | 4 | a0001c0001t0001g0001 a0001c0001t0001g0020 a0001c0001t0001g0084 others(1): 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 | a0001c0001t0001g0115 | 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 | a0001c0001t0001g0115 | 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 | a0001c0001t0001g0069 a0001c0001t0001g0071 a0001c0001t0001g0073 others(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 | a0001c0001t0001g0295 | 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 | a0001c0001t0001g0289 a0001c0001t0001g0290 |
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 | a0001c0001t0001g0033 a0001c0001t0001g0034 a0001c0001t0001g0035 others(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 | a0001c0001t0001g0289 a0001c0001t0001g0290 |
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 | a0001c0001t0001g0231 a0001c0001t0001g0232 a0001c0001t0001g0233 others(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 | a0001c0001t0001g0227 | 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 | a0001c0001t0001g0241 | 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 | a0001c0001t0001g0231 a0001c0001t0001g0232 a0001c0001t0001g0233 |
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 | a0001c0001t0001g0010 | 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 | a0001c0001t0001g0215 a0001c0001t0001g0216 a0001c0001t0001g0217 others(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 | a0001c0001t0001g0174 | 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 | a0001c0001t0001g0289 a0001c0001t0001g0290 |
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 | a0001c0001t0001g0003 | 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 | 63 | a0001c0001t0001g0009 a0001c0001t0001g0011 a0001c0001t0001g0012 others(60): Show |
63 | HG01168.hp1 HG01169.hp2 HG01243.hp2 others(60): 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 | a0001c0001t0001g0291 a0001c0001t0001g0292 a0001c0001t0001g0293 |
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 | a0001c0001t0001g0079 | 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 | a0001c0001t0001g0231 a0001c0001t0001g0232 a0001c0001t0001g0233 |
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 | a0001c0001t0001g0277 | 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 | a0001c0001t0001g0278 | 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 | a0001c0001t0001g0291 a0001c0001t0001g0292 a0001c0001t0001g0293 others(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 | a0001c0001t0001g0184 | 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 | a0001c0001t0001g0106 a0001c0001t0001g0122 a0001c0001t0001g0234 others(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 | a0001c0001t0001g0079 | 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 | a0001c0001t0001g0273 | 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 | 59 | a0001c0001t0001g0009 a0001c0001t0001g0011 a0001c0001t0001g0012 others(56): Show |
59 | HG01168.hp1 HG01169.hp2 HG01243.hp2 others(56): Show |
intron_variant | MODIFIER | c.213-1881C>T | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 4/9 | chr2 | 31922791 | |||||||
chr2:31922898 | T | A | 72 | a0001c0001t0001g0009 a0001c0001t0001g0011 a0001c0001t0001g0012 others(69): Show |
72 | HG01109.hp2 HG01168.hp1 HG01169.hp2 others(69): 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 | a0001c0001t0001g0242 a0001c0001t0001g0267 |
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 | a0001c0001t0001g0096 a0001c0001t0001g0097 |
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 | 63 | a0001c0001t0001g0009 a0001c0001t0001g0011 a0001c0001t0001g0012 others(60): Show |
63 | HG01168.hp1 HG01169.hp2 HG01243.hp2 others(60): 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 | 57 | a0001c0001t0001g0009 a0001c0001t0001g0011 a0001c0001t0001g0012 others(54): Show |
57 | HG01168.hp1 HG01169.hp2 HG01255.hp2 others(54): Show |
intron_variant | MODIFIER | c.213-2640C>A | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 4/9 | chr2 | 31923550 | |||||||
chr2:31923567 | T | A | 63 | a0001c0001t0001g0009 a0001c0001t0001g0011 a0001c0001t0001g0012 others(60): Show |
63 | HG01168.hp1 HG01169.hp2 HG01243.hp2 others(60): 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 | a0001c0001t0001g0236 | 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 | 72 | a0001c0001t0001g0009 a0001c0001t0001g0011 a0001c0001t0001g0012 others(69): Show |
72 | HG01109.hp2 HG01168.hp1 HG01169.hp2 others(69): Show |
intron_variant | MODIFIER | c.213-3079G>C | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 4/9 | chr2 | 31923989 | |||||||
chr2:31924028 | A | G | 57 | a0001c0001t0001g0009 a0001c0001t0001g0011 a0001c0001t0001g0012 others(54): Show |
57 | HG01168.hp1 HG01169.hp2 HG01255.hp2 others(54): 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 | a0001c0001t0001g0195 | 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 | 57 | a0001c0001t0001g0009 a0001c0001t0001g0011 a0001c0001t0001g0012 others(54): Show |
57 | HG01168.hp1 HG01169.hp2 HG01255.hp2 others(54): 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 | a0001c0001t0001g0021 a0001c0001t0001g0023 a0001c0001t0001g0152 |
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 | a0001c0001t0001g0233 | 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 | a0001c0001t0001g0016 | 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 | 49 | a0001c0001t0001g0009 a0001c0001t0001g0011 a0001c0001t0001g0012 others(46): Show |
49 | HG01168.hp1 HG01169.hp2 HG01255.hp2 others(46): Show |
intron_variant | MODIFIER | c.213-3494G>T | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 4/9 | chr2 | 31924404 | |||||||
chr2:31924446 | T | TA | 49 | a0001c0001t0001g0009 a0001c0001t0001g0011 a0001c0001t0001g0012 others(46): Show |
49 | HG01168.hp1 HG01169.hp2 HG01255.hp2 others(46): Show |
intron_variant | MODIFIER | c.213-3537dupT | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 4/9 | chr2 | 31924446 | |||||||
chr2:31924446 | T | TAA | 8 | a0001c0001t0001g0235 a0001c0001t0001g0236 a0001c0001t0001g0270 others(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 | a0001c0001t0001g0270 a0001c0001t0001g0295 |
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 | a0001c0001t0001g0288 a0001c0001t0001g0301 |
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 | a0001c0001t0001g0036 a0001c0001t0001g0063 a0001c0001t0001g0067 others(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 | a0001c0001t0001g0211 | 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 | a0001c0001t0001g0015 a0001c0001t0001g0049 a0001c0001t0001g0073 others(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 | 48 | a0001c0001t0001g0009 a0001c0001t0001g0011 a0001c0001t0001g0012 others(45): Show |
48 | HG01169.hp2 HG01255.hp2 HG01257.hp2 others(45): 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 | a0001c0001t0001g0014 a0001c0001t0001g0024 a0001c0001t0001g0245 others(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 | a0001c0001t0001g0107 a0001c0001t0001g0116 a0001c0001t0001g0117 others(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 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0023 others(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 |
37 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0008 others(34): 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 | a0001c0001t0001g0078 a0001c0001t0001g0110 a0001c0001t0001g0136 others(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 | a0001c0001t0001g0027 a0001c0001t0001g0135 a0001c0001t0001g0162 others(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 | a0001c0001t0001g0020 | 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 | a0001c0001t0001g0115 a0001c0001t0001g0155 |
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 | a0001c0001t0001g0293 | 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 | a0001c0001t0001g0291 | 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 | a0001c0001t0001g0292 | 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 | a0001c0001t0001g0058 | 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 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0010 others(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 | a0001c0001t0001g0294 | 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 | a0001c0001t0001g0291 a0001c0001t0001g0292 a0001c0001t0001g0293 |
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 | a0001c0001t0001g0022 | 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 | a0001c0001t0001g0090 a0001c0001t0001g0091 a0001c0001t0001g0092 |
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 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0006 |
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 | a0001c0001t0001g0289 a0001c0001t0001g0290 |
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 | a0001c0001t0001g0008 a0001c0001t0001g0289 a0001c0001t0001g0290 |
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 | a0001c0001t0001g0011 a0001c0001t0001g0013 a0001c0001t0001g0245 others(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 | 213 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(210): 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 | a0001c0001t0001g0048 a0001c0001t0001g0231 a0001c0001t0001g0232 others(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 | 72 | a0001c0001t0001g0009 a0001c0001t0001g0011 a0001c0001t0001g0012 others(69): Show |
72 | HG01109.hp2 HG01168.hp1 HG01169.hp2 others(69): 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 | a0001c0001t0001g0279 a0001c0001t0001g0280 a0001c0001t0001g0281 others(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 | a0001c0001t0001g0052 | 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 | a0001c0001t0001g0283 | 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 | a0001c0001t0001g0188 a0001c0001t0001g0215 a0001c0001t0001g0216 others(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 | a0001c0001t0001g0188 | 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 | a0001c0001t0001g0125 | 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 | 60 | a0001c0001t0001g0009 a0001c0001t0001g0011 a0001c0001t0001g0012 others(57): Show |
60 | HG01168.hp1 HG01169.hp2 HG01243.hp2 others(57): 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 | a0001c0001t0001g0089 | 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 | a0001c0001t0001g0025 | 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 | a0001c0001t0001g0025 | 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 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0007 others(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 | a0001c0001t0001g0009 | 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 | a0001c0001t0001g0072 a0001c0001t0001g0089 |
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 | 61 | a0001c0001t0001g0009 a0001c0001t0001g0011 a0001c0001t0001g0012 others(58): Show |
61 | HG01168.hp1 HG01169.hp2 HG01243.hp2 others(58): 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 | a0001c0001t0001g0002 a0001c0001t0001g0203 a0001c0001t0001g0210 |
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 | a0001c0001t0001g0237 a0001c0001t0001g0299 |
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 | a0001c0001t0001g0289 a0001c0001t0001g0290 |
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 | a0001c0001t0001g0291 a0001c0001t0001g0292 a0001c0001t0001g0293 others(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 | a0001c0001t0001g0231 | 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 | a0001c0001t0001g0113 a0001c0001t0001g0123 a0002c0002t0001g0121 |
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 | a0001c0001t0001g0279 a0001c0001t0001g0282 a0001c0001t0001g0288 others(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 | a0001c0001t0001g0126 | 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 | a0001c0001t0001g0079 | 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 | a0001c0001t0001g0079 | 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 | 283 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(280): Show |
284 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(281): Show |
intron_variant | MODIFIER | c.212+3520delT | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 4/9 | chr2 | 31928546 | |||||||
chr2:31928552 | A | G | 4 | a0001c0001t0001g0274 a0001c0001t0001g0275 a0001c0001t0001g0276 others(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 | a0001c0001t0001g0277 | 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 | a0001c0001t0001g0209 | 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 | a0001c0001t0001g0016 a0001c0001t0001g0059 a0001c0001t0001g0070 |
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 | a0001c0001t0001g0238 a0001c0001t0001g0239 a0001c0001t0001g0240 others(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 | 49 | a0001c0001t0001g0009 a0001c0001t0001g0011 a0001c0001t0001g0012 others(46): Show |
49 | HG01168.hp1 HG01169.hp2 HG01255.hp2 others(46): Show |
intron_variant | MODIFIER | c.212+2675delT | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 4/9 | chr2 | 31929391 | |||||||
chr2:31929457 | T | C | 3 | a0001c0001t0001g0045 a0001c0001t0001g0061 a0001c0001t0001g0179 |
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 | a0001c0001t0001g0025 | 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 | a0001c0001t0001g0278 | 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 | a0001c0001t0001g0007 a0001c0001t0001g0032 a0001c0001t0001g0189 |
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 | a0001c0001t0001g0133 | 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 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0010 others(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 | a0001c0001t0001g0192 | 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 | a0001c0001t0001g0279 a0001c0001t0001g0280 a0001c0001t0001g0281 others(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 | a0001c0001t0001g0215 a0001c0001t0001g0216 a0001c0001t0001g0217 others(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 | a0001c0001t0001g0067 | 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 | 300 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(297): Show |
301 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(298): 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 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0006 |
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 | a0001c0001t0001g0086 a0001c0001t0001g0087 a0001c0001t0001g0234 |
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 | a0001c0001t0001g0187 | 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 | a0001c0001t0001g0067 | 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 | a0001c0001t0001g0010 a0001c0001t0001g0013 a0001c0001t0001g0065 others(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 | a0001c0001t0001g0231 a0001c0001t0001g0271 a0001c0001t0001g0272 others(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 | a0001c0001t0001g0232 a0001c0001t0001g0233 a0001c0001t0001g0270 others(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 | a0001c0001t0001g0291 a0001c0001t0001g0292 a0001c0001t0001g0293 others(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 | a0001c0001t0001g0235 a0001c0001t0001g0236 a0001c0001t0001g0277 |
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 | a0001c0001t0001g0278 | 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 | a0001c0001t0001g0289 a0001c0001t0001g0290 |
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 | 56 | a0001c0001t0001g0009 a0001c0001t0001g0011 a0001c0001t0001g0012 others(53): Show |
56 | HG01168.hp1 HG01169.hp2 HG01255.hp2 others(53): 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 | a0001c0001t0001g0021 a0001c0001t0001g0023 a0001c0001t0001g0152 |
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 | 49 | a0001c0001t0001g0009 a0001c0001t0001g0011 a0001c0001t0001g0012 others(46): Show |
49 | HG01168.hp1 HG01169.hp2 HG01255.hp2 others(46): Show |
intron_variant | MODIFIER | c.212+516delA | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 4/9 | chr2 | 31931550 | |||||||
chr2:31931557 | T | G | 1 | a0001c0001t0001g0188 | 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 | a0001c0001t0001g0197 a0001c0001t0001g0199 a0001c0001t0001g0200 |
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 | a0001c0001t0001g0085 a0001c0001t0001g0231 a0001c0001t0001g0232 others(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 | a0001c0001t0001g0198 | 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 | a0001c0001t0001g0233 | 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 | a0001c0001t0001g0146 | 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 | a0001c0001t0001g0289 a0001c0001t0001g0290 |
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 | a0001c0001t0001g0009 | 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 | a0001c0001t0001g0060 | 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 | a0001c0001t0001g0124 | 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 | a0001c0001t0001g0231 a0001c0001t0001g0232 a0001c0001t0001g0233 |
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 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0006 |
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 | a0001c0001t0001g0235 a0001c0001t0001g0236 a0001c0001t0001g0270 others(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 | a0001c0001t0001g0021 a0001c0001t0001g0026 a0001c0001t0001g0027 others(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 | a0001c0001t0001g0008 a0001c0001t0001g0030 a0001c0001t0001g0110 others(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 | 7 | a0001c0001t0001g0112 a0001c0001t0001g0134 a0001c0001t0001g0135 others(4): Show |
7 | HG01169.hp1 HG01943.hp1 HG02148.hp2 others(4): 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 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0087 others(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 | a0001c0001t0001g0010 a0001c0001t0001g0035 a0001c0001t0001g0036 others(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 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0017 others(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 | a0001c0001t0001g0015 a0001c0001t0001g0032 a0001c0001t0001g0043 others(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 | a0001c0001t0001g0302 | 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 | a0001c0001t0001g0237 | 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 | a0001c0001t0001g0231 a0001c0001t0001g0233 |
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 | a0001c0001t0001g0232 | 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 | a0001c0001t0002g0005 a0001c0001t0002g0006 |
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 | a0001c0001t0001g0290 | 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 | a0001c0001t0002g0005 a0001c0001t0002g0006 |
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 | a0001c0001t0002g0005 a0001c0001t0002g0006 |
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 | a0001c0001t0001g0275 a0001c0001t0001g0276 |
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 | a0001c0001t0001g0205 a0001c0001t0001g0289 a0001c0001t0002g0004 others(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 | a0001c0001t0001g0277 | 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 | a0001c0001t0001g0274 | 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 | a0001c0001t0001g0205 a0001c0001t0001g0270 a0001c0001t0001g0289 others(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 | a0001c0001t0001g0236 | 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 | a0001c0001t0001g0150 | 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 | a0001c0001t0001g0063 | 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 | a0001c0001t0001g0189 | 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 | a0001c0001t0001g0205 a0001c0001t0001g0270 a0001c0001t0001g0289 others(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 | a0001c0001t0001g0235 | 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 | a0001c0001t0001g0056 | 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 | a0001c0001t0001g0174 | 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 | a0001c0001t0001g0063 a0001c0001t0001g0073 a0001c0001t0001g0150 others(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 | a0001c0001t0001g0056 a0001c0001t0001g0063 a0001c0001t0001g0073 others(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 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(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 | a0001c0001t0001g0095 a0001c0001t0001g0281 a0001c0001t0001g0283 others(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 | a0001c0001t0001g0009 a0001c0001t0001g0242 a0001c0001t0001g0246 others(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 | 1 | a0001c0001t0001g0103 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.144-1215A>T | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 3/9 | chr2 | 31933350 | |||||||
chr2:31933351 | T | A | 27 | a0001c0001t0001g0056 a0001c0001t0001g0063 a0001c0001t0001g0073 others(24): Show |
27 | HG00738.hp1 HG01243.hp2 HG01257.hp2 others(24): 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 | a0001c0001t0001g0047 a0001c0001t0001g0051 a0001c0001t0001g0172 others(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 | a0001c0001t0001g0083 a0001c0001t0001g0084 a0001c0001t0001g0089 |
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 | a0001c0001t0001g0086 | 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 | a0001c0001t0001g0007 a0001c0001t0001g0054 a0001c0001t0001g0058 others(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 | a0001c0001t0001g0034 a0001c0001t0001g0044 a0001c0001t0001g0055 others(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 | a0001c0001t0001g0015 a0001c0001t0001g0031 a0001c0001t0001g0032 others(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 | a0001c0001t0001g0010 a0001c0001t0001g0037 a0001c0001t0001g0046 others(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 | a0001c0001t0001g0038 a0001c0001t0001g0049 a0001c0001t0001g0057 others(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 | a0001c0001t0001g0017 a0001c0001t0001g0041 a0001c0001t0001g0069 others(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 | a0001c0001t0001g0040 a0001c0001t0001g0048 a0001c0001t0001g0052 others(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 | a0001c0001t0001g0043 a0001c0001t0001g0190 |
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 | a0001c0001t0001g0036 | 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 | a0001c0001t0001g0039 | 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 | a0001c0001t0001g0019 a0001c0001t0001g0099 a0001c0001t0001g0102 others(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 | a0001c0001t0001g0072 a0001c0001t0001g0113 a0001c0001t0001g0123 others(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 | 25 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0020 others(22): 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 | a0001c0001t0001g0002 a0001c0001t0001g0016 a0001c0001t0001g0018 others(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 | a0001c0001t0001g0042 a0001c0001t0001g0059 a0001c0001t0001g0070 |
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 | a0001c0001t0001g0178 | 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 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(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 | a0001c0001t0001g0009 a0001c0001t0001g0244 a0001c0001t0001g0245 others(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 | a0001c0001t0001g0159 | 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 | a0001c0001t0001g0245 a0001c0001t0001g0266 |
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 | a0001c0001t0001g0130 | 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 | a0001c0001t0001g0266 | 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 | a0001c0001t0001g0231 a0001c0001t0001g0232 a0001c0001t0001g0233 |
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 | a0001c0001t0001g0081 | 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 | a0001c0001t0001g0251 a0001c0001t0001g0254 |
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 | a0001c0001t0001g0231 a0001c0001t0001g0232 a0001c0001t0001g0233 |
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 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(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 | a0001c0001t0001g0104 a0001c0001t0001g0110 a0001c0001t0001g0135 others(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 | a0001c0001t0001g0231 a0001c0001t0001g0232 a0001c0001t0001g0233 |
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 | a0001c0001t0001g0278 | 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 | a0001c0001t0001g0113 a0001c0001t0001g0123 a0001c0001t0001g0214 others(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 | a0001c0001t0001g0051 a0001c0001t0001g0064 |
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 | a0001c0001t0001g0182 | 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 | a0001c0001t0001g0231 a0001c0001t0001g0232 a0001c0001t0001g0233 |
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 | a0001c0001t0001g0231 | 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 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0006 |
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 | a0001c0001t0001g0078 | 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 | a0001c0001t0001g0291 a0001c0001t0001g0292 a0001c0001t0001g0293 others(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 | a0001c0001t0001g0291 a0001c0001t0001g0292 a0001c0001t0001g0293 |
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 | a0001c0001t0001g0090 a0001c0001t0001g0091 a0001c0001t0001g0092 |
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 | a0001c0001t0001g0231 a0001c0001t0001g0232 a0001c0001t0001g0233 |
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 | a0001c0001t0001g0214 | 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 | a0001c0001t0001g0231 | 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 | 297 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(294): Show |
298 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(295): 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 | a0001c0001t0001g0102 a0001c0001t0001g0103 |
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 | a0001c0001t0001g0274 a0001c0001t0001g0275 a0001c0001t0001g0276 |
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 | a0001c0001t0001g0107 a0001c0001t0001g0109 a0001c0001t0001g0111 others(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 | a0001c0001t0001g0102 a0001c0001t0001g0103 |
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 | a0001c0001t0001g0231 | 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 | a0001c0001t0001g0188 | 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 | a0001c0001t0001g0270 | 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 | a0001c0001t0001g0270 a0001c0001t0001g0295 |
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 | a0001c0001t0001g0080 | 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 | a0001c0001t0001g0215 a0001c0001t0001g0216 a0001c0001t0001g0217 others(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 | a0001c0001t0001g0214 | 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 | a0001c0001t0001g0017 | 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 | a0001c0001t0001g0289 a0001c0001t0001g0290 |
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 | a0001c0001t0001g0231 | 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 | a0001c0001t0001g0289 a0001c0001t0001g0290 a0001c0001t0001g0291 others(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 | a0001c0001t0001g0114 a0001c0001t0001g0128 a0001c0001t0001g0153 others(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 | a0001c0001t0001g0235 a0001c0001t0001g0236 a0001c0001t0001g0270 others(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 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0010 others(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 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0113 others(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 | 54 | a0001c0001t0001g0009 a0001c0001t0001g0013 a0001c0001t0001g0014 others(51): Show |
54 | HG01168.hp1 HG01169.hp2 HG01255.hp2 others(51): 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 | a0001c0001t0001g0009 | 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 | 286 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(283): Show |
287 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(284): Show |
intron_variant | MODIFIER | c.143+4192delT | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 3/9 | chr2 | 31939109 | |||||||
chr2:31939308 | C | T | 4 | a0001c0001t0001g0238 a0001c0001t0001g0239 a0001c0001t0001g0240 others(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 | a0001c0001t0001g0110 a0001c0001t0001g0135 a0001c0001t0001g0136 others(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 | a0001c0001t0001g0232 a0001c0001t0001g0233 |
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 | a0001c0001t0001g0299 | 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 | a0001c0001t0001g0214 | 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 | a0001c0001t0001g0279 a0001c0001t0001g0280 a0001c0001t0001g0281 others(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 | a0001c0001t0001g0271 a0001c0001t0001g0272 a0001c0001t0001g0273 |
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 | 71 | a0001c0001t0001g0009 a0001c0001t0001g0011 a0001c0001t0001g0012 others(68): Show |
71 | HG01109.hp2 HG01168.hp1 HG01169.hp2 others(68): 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 | a0001c0001t0001g0181 | 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 | a0001c0001t0001g0009 | 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 | a0001c0001t0001g0289 a0001c0001t0001g0290 |
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 | a0001c0001t0001g0086 a0001c0001t0001g0234 |
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 | a0001c0001t0001g0289 a0001c0001t0001g0290 a0001c0001t0001g0291 others(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 | a0001c0001t0001g0289 a0001c0001t0001g0290 a0001c0001t0001g0291 others(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 | a0001c0001t0001g0231 a0001c0001t0001g0232 a0001c0001t0001g0233 |
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 | a0001c0001t0001g0113 a0001c0001t0001g0123 a0002c0002t0001g0121 |
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 | a0001c0001t0001g0100 | 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 | a0001c0001t0001g0147 a0001c0001t0001g0148 a0001c0001t0001g0149 |
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 | a0001c0001t0001g0115 a0001c0001t0001g0211 |
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 | 80 | a0001c0001t0001g0009 a0001c0001t0001g0011 a0001c0001t0001g0012 others(77): Show |
80 | HG01070.hp1 HG01071.hp2 HG01081.hp2 others(77): 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 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0010 others(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 | a0001c0001t0001g0066 | 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 | 111 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0008 others(108): 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 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(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 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(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 | a0001c0001t0001g0242 a0001c0001t0001g0267 |
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 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0006 |
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 | a0001c0001t0001g0048 a0001c0001t0001g0049 |
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 | 71 | a0001c0001t0001g0009 a0001c0001t0001g0011 a0001c0001t0001g0012 others(68): Show |
71 | HG01109.hp2 HG01168.hp1 HG01169.hp2 others(68): 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 | a0001c0001t0001g0226 | 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 | 63 | a0001c0001t0001g0009 a0001c0001t0001g0011 a0001c0001t0001g0012 others(60): Show |
63 | HG01168.hp1 HG01169.hp2 HG01243.hp2 others(60): Show |
intron_variant | MODIFIER | c.62-979C>T | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31944362 | |||||||
chr2:31944496 | T | C | 72 | a0001c0001t0001g0009 a0001c0001t0001g0011 a0001c0001t0001g0012 others(69): Show |
72 | HG01070.hp1 HG01071.hp2 HG01081.hp2 others(69): 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 | a0001c0001t0001g0054 | 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 | a0001c0001t0001g0231 a0001c0001t0001g0232 a0001c0001t0001g0233 |
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 | 63 | a0001c0001t0001g0009 a0001c0001t0001g0011 a0001c0001t0001g0012 others(60): Show |
63 | HG01168.hp1 HG01169.hp2 HG01243.hp2 others(60): 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 | a0001c0001t0001g0242 a0001c0001t0001g0267 |
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 | a0001c0001t0001g0231 | 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 | a0001c0001t0001g0072 | 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 | a0001c0001t0001g0041 | 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 | a0001c0001t0001g0288 | 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 | a0001c0001t0001g0262 | 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 | a0001c0001t0001g0274 a0001c0001t0001g0275 a0001c0001t0001g0276 |
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 | 75 | a0001c0001t0001g0009 a0001c0001t0001g0011 a0001c0001t0001g0012 others(72): Show |
75 | HG01070.hp1 HG01071.hp2 HG01081.hp2 others(72): 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 | a0001c0001t0001g0180 | 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 | a0001c0001t0001g0196 a0001c0001t0001g0198 |
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 | 68 | a0001c0001t0001g0009 a0001c0001t0001g0011 a0001c0001t0001g0012 others(65): Show |
68 | HG01070.hp1 HG01071.hp2 HG01081.hp2 others(65): 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 | a0001c0001t0001g0029 a0001c0001t0001g0082 a0001c0001t0001g0222 others(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 | a0001c0001t0001g0139 | 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 | a0001c0001t0001g0080 | 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 | a0001c0001t0001g0270 a0001c0001t0001g0295 |
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 | a0001c0001t0001g0294 | 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 | a0001c0001t0001g0178 | 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 | a0001c0001t0001g0192 | 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 | a0001c0001t0001g0110 a0001c0001t0001g0134 a0001c0001t0001g0135 others(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 | 71 | a0001c0001t0001g0009 a0001c0001t0001g0011 a0001c0001t0001g0012 others(68): Show |
71 | HG01109.hp2 HG01168.hp1 HG01169.hp2 others(68): 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 | a0001c0001t0001g0271 a0001c0001t0001g0272 a0001c0001t0001g0273 |
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 | a0001c0001t0001g0176 | 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 | a0001c0001t0001g0277 | 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 | a0001c0001t0001g0099 a0001c0001t0001g0191 a0001c0001t0001g0192 others(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 | a0001c0001t0001g0024 | 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 | a0001c0001t0001g0231 | 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 | a0001c0001t0001g0105 | 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 | a0001c0001t0001g0213 | 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 | a0001c0001t0001g0215 | 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 | a0001c0001t0001g0291 a0001c0001t0001g0292 a0001c0001t0001g0293 |
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 | a0001c0001t0001g0271 a0001c0001t0001g0272 a0001c0001t0001g0273 |
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 | 81 | a0001c0001t0001g0009 a0001c0001t0001g0011 a0001c0001t0001g0012 others(78): Show |
81 | HG01070.hp1 HG01071.hp2 HG01081.hp2 others(78): 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 | a0001c0001t0001g0176 | 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 | a0001c0001t0001g0289 a0001c0001t0001g0290 |
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 | a0001c0001t0001g0288 a0001c0001t0001g0301 |
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 | a0001c0001t0001g0069 a0001c0001t0001g0071 a0001c0001t0001g0073 others(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 | a0001c0001t0001g0168 | 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 | 133 | a0001c0001t0001g0001 a0001c0001t0001g0013 a0001c0001t0001g0014 others(130): 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 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0007 others(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 | a0001c0001t0001g0010 a0001c0001t0001g0081 a0001c0001t0001g0170 others(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 | a0001c0001t0001g0181 a0001c0001t0001g0216 |
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 | 59 | a0001c0001t0001g0009 a0001c0001t0001g0011 a0001c0001t0001g0012 others(56): Show |
59 | HG01168.hp1 HG01169.hp2 HG01243.hp2 others(56): 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 | 62 | a0001c0001t0001g0009 a0001c0001t0001g0011 a0001c0001t0001g0012 others(59): Show |
62 | HG01168.hp1 HG01169.hp2 HG01243.hp2 others(59): 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 | a0001c0001t0001g0051 a0001c0001t0001g0064 |
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 | a0001c0001t0001g0072 | 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 | a0001c0001t0001g0099 a0001c0001t0001g0191 a0001c0001t0001g0192 others(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 | a0001c0001t0001g0274 a0001c0001t0001g0275 a0001c0001t0001g0276 |
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 | a0001c0001t0001g0274 a0001c0001t0001g0275 a0001c0001t0001g0276 |
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 | a0001c0001t0001g0024 a0001c0001t0001g0163 |
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 | a0001c0001t0001g0235 a0001c0001t0001g0291 a0001c0001t0001g0292 others(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 | a0001c0001t0001g0016 | 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 | 59 | a0001c0001t0001g0009 a0001c0001t0001g0011 a0001c0001t0001g0012 others(56): Show |
59 | HG01168.hp1 HG01169.hp2 HG01255.hp2 others(56): Show |
intron_variant | MODIFIER | c.62-8135dupA | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31951517 | |||||||
chr2:31951517 | G | T | 1 | a0001c0001t0001g0079 | 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 | a0001c0001t0001g0115 | 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 | a0001c0001t0001g0015 | 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 | a0001c0001t0001g0015 | 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 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0006 |
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 | a0001c0001t0001g0297 | 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 | a0001c0001t0001g0160 | 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 | a0001c0001t0001g0077 a0001c0001t0001g0078 |
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 | a0001c0001t0001g0231 a0001c0001t0001g0232 a0001c0001t0001g0233 |
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 | a0001c0001t0001g0065 | 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 | a0001c0001t0001g0033 a0001c0001t0001g0063 a0001c0001t0001g0108 others(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 | 52 | a0001c0001t0001g0009 a0001c0001t0001g0011 a0001c0001t0001g0012 others(49): Show |
52 | HG01168.hp1 HG01169.hp2 HG01255.hp2 others(49): Show |
intron_variant | MODIFIER | c.62-9984delT | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31953366 | |||||||
chr2:31953366 | CAA | C | 15 | a0001c0001t0001g0231 a0001c0001t0001g0232 a0001c0001t0001g0233 others(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 | a0001c0001t0001g0069 a0001c0001t0001g0071 a0001c0001t0001g0073 others(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 | a0001c0001t0001g0274 a0001c0001t0001g0275 a0001c0001t0001g0276 |
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 | 111 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0008 others(108): 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 | |||||||
chr2:31953519 | G | A | 1 | a0001c0001t0001g0259 | 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 | 107 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0008 others(104): 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 | a0001c0001t0001g0236 | 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 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0006 |
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 | a0001c0001t0001g0289 | 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 | 48 | a0001c0001t0001g0009 a0001c0001t0001g0011 a0001c0001t0001g0012 others(45): Show |
48 | HG01168.hp1 HG01169.hp2 HG01255.hp2 others(45): 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 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0006 |
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 | a0001c0001t0001g0201 | 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 | a0001c0001t0001g0206 | 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 | a0001c0001t0001g0188 a0001c0001t0001g0215 a0001c0001t0001g0216 others(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 | a0001c0001t0001g0099 | 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 | a0001c0001t0001g0076 | 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 | a0001c0001t0001g0259 | 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 | a0001c0001t0001g0083 a0001c0001t0001g0084 a0001c0001t0001g0227 |
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 | a0001c0001t0001g0232 a0001c0001t0001g0233 |
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 | a0001c0001t0001g0271 | 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 | a0001c0001t0001g0300 | 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 | a0001c0001t0001g0271 a0001c0001t0001g0272 a0001c0001t0001g0273 |
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 | a0001c0001t0001g0063 | 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 | a0001c0001t0001g0302 | 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 | a0001c0001t0001g0294 | 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 | a0001c0001t0001g0209 a0001c0001t0001g0289 a0001c0001t0001g0290 others(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 | a0001c0001t0001g0231 a0001c0001t0001g0232 a0001c0001t0001g0233 |
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 | a0001c0001t0001g0108 | 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 | a0001c0001t0001g0232 | 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 | a0001c0001t0001g0155 | 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 | a0001c0001t0001g0235 a0001c0001t0001g0236 a0001c0001t0001g0256 others(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 | 62 | a0001c0001t0001g0009 a0001c0001t0001g0011 a0001c0001t0001g0012 others(59): Show |
62 | HG01168.hp1 HG01169.hp2 HG01243.hp2 others(59): 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 | a0001c0001t0001g0271 a0001c0001t0001g0272 a0001c0001t0001g0273 |
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 | a0001c0001t0001g0235 a0001c0001t0001g0236 |
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 | a0001c0001t0001g0019 | 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 | a0001c0001t0001g0188 | 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 | a0001c0001t0001g0221 | 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 | a0001c0001t0001g0207 | 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 | a0001c0001t0001g0233 | 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 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0006 |
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 | |||||||
chr2:31957142 | CA | C | 15 | a0001c0001t0001g0019 a0001c0001t0001g0022 a0001c0001t0001g0026 others(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 | a0001c0001t0001g0231 | 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 | 99 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0008 others(96): 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 | a0001c0001t0001g0139 | 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 | a0001c0001t0001g0115 a0001c0001t0001g0211 |
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 | a0001c0001t0001g0076 | 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 | a0001c0001t0001g0295 | 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 | a0001c0001t0001g0242 a0001c0001t0001g0267 |
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 | a0001c0001t0001g0066 | 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 | a0001c0001t0001g0295 | 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 | 72 | a0001c0001t0001g0009 a0001c0001t0001g0011 a0001c0001t0001g0012 others(69): Show |
72 | HG01109.hp2 HG01168.hp1 HG01169.hp2 others(69): 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 | a0001c0001t0001g0289 a0001c0001t0001g0290 a0001c0001t0002g0004 |
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 | 111 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0008 others(108): 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 | a0001c0001t0001g0150 | 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 | a0001c0001t0001g0271 | 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 | a0001c0001t0001g0209 | 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 | a0001c0001t0001g0271 a0001c0001t0001g0272 a0001c0001t0001g0273 |
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 | 60 | a0001c0001t0001g0009 a0001c0001t0001g0011 a0001c0001t0001g0012 others(57): Show |
60 | HG01168.hp1 HG01169.hp2 HG01243.hp2 others(57): Show |
intron_variant | MODIFIER | c.62-16116G>A | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31959499 | |||||||
chr2:31959501 | G | GA | 60 | a0001c0001t0001g0009 a0001c0001t0001g0012 a0001c0001t0001g0013 others(57): Show |
60 | HG01168.hp1 HG01169.hp2 HG01243.hp2 others(57): Show |
intron_variant | MODIFIER | c.62-16119dupT | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31959501 | |||||||
chr2:31959744 | C | T | 2 | a0001c0001t0001g0218 a0001c0001t0001g0219 |
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 | a0001c0001t0001g0097 | 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 | 290 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(287): Show |
291 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(288): Show |
intron_variant | MODIFIER | c.62-16403delA | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31959785 | |||||||
chr2:31959828 | C | T | 2 | a0001c0001t0001g0271 a0001c0001t0001g0273 |
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 | a0001c0001t0001g0188 a0001c0001t0001g0215 a0001c0001t0001g0216 others(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 | a0001c0001t0001g0092 | 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 | a0001c0001t0001g0133 a0001c0001t0001g0146 a0001c0001t0001g0147 others(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 | 35 | a0001c0001t0001g0009 a0001c0001t0001g0011 a0001c0001t0001g0012 others(32): Show |
35 | HG01168.hp1 HG01169.hp2 HG01257.hp2 others(32): 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 | a0001c0001t0001g0231 | 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 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0006 |
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 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0006 |
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 | a0001c0001t0001g0184 a0001c0001t0001g0214 a0001c0001t0001g0278 |
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 | a0001c0001t0001g0289 a0001c0001t0001g0290 a0001c0001t0001g0291 others(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 | a0001c0001t0001g0231 a0001c0001t0001g0232 a0001c0001t0001g0233 |
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 | a0001c0001t0001g0271 a0001c0001t0001g0273 |
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 | a0001c0001t0001g0015 a0001c0001t0001g0059 a0001c0001t0001g0070 others(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 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0006 |
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 | a0001c0001t0001g0291 a0001c0001t0001g0292 a0001c0001t0001g0293 others(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 | a0001c0001t0001g0214 | 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 | a0001c0001t0001g0079 | 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 | a0001c0001t0001g0242 | 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 | a0001c0001t0001g0235 a0001c0001t0001g0236 |
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 | a0001c0001t0001g0291 a0001c0001t0001g0292 a0001c0001t0001g0293 |
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 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0006 |
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 | a0001c0001t0001g0094 a0001c0001t0001g0095 a0001c0001t0001g0098 |
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 | a0001c0001t0001g0289 a0001c0001t0001g0290 |
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 | a0001c0001t0001g0300 | 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 | 53 | a0001c0001t0001g0009 a0001c0001t0001g0011 a0001c0001t0001g0012 others(50): Show |
53 | HG01168.hp1 HG01169.hp2 HG01255.hp2 others(50): Show |
intron_variant | MODIFIER | c.62-18236delT | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31961618 | |||||||
chr2:31961619 | A | C | 1 | a0001c0001t0001g0300 | 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 | a0001c0001t0001g0259 | 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 | a0001c0001t0001g0270 | 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 | a0001c0001t0001g0270 | 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 | a0001c0001t0001g0025 a0001c0001t0001g0094 a0001c0001t0001g0095 others(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 | 55 | a0001c0001t0001g0009 a0001c0001t0001g0011 a0001c0001t0001g0012 others(52): Show |
55 | HG01168.hp1 HG01169.hp2 HG01255.hp2 others(52): Show |
intron_variant | MODIFIER | c.62-18634dupT | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31962016 | |||||||
chr2:31962118 | G | A | 3 | a0001c0001t0001g0231 a0001c0001t0001g0232 a0001c0001t0001g0233 |
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 | a0001c0001t0001g0299 | 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 | a0001c0001t0001g0297 | 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 | 61 | a0001c0001t0001g0009 a0001c0001t0001g0011 a0001c0001t0001g0012 others(58): Show |
61 | HG01168.hp1 HG01169.hp2 HG01255.hp2 others(58): 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 | a0001c0001t0001g0291 a0001c0001t0001g0292 a0001c0001t0001g0293 others(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 | a0001c0001t0001g0270 a0001c0001t0001g0295 |
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 | a0001c0001t0001g0232 | 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 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0006 |
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 | a0001c0001t0001g0231 | 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 | a0001c0001t0001g0130 | 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 | 70 | a0001c0001t0001g0009 a0001c0001t0001g0011 a0001c0001t0001g0012 others(67): Show |
70 | HG01109.hp2 HG01168.hp1 HG01169.hp2 others(67): 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 | a0001c0001t0001g0131 | 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 | a0001c0001t0001g0289 a0001c0001t0001g0290 |
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 | a0001c0001t0001g0113 a0001c0001t0001g0123 a0002c0002t0001g0121 |
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 | a0001c0001t0001g0289 a0001c0001t0001g0290 |
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 | a0001c0001t0001g0218 a0001c0001t0001g0219 |
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 | a0001c0001t0001g0291 a0001c0001t0001g0292 a0001c0001t0001g0293 others(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 | 48 | a0001c0001t0001g0009 a0001c0001t0001g0011 a0001c0001t0001g0012 others(45): Show |
48 | HG01168.hp1 HG01169.hp2 HG01255.hp2 others(45): Show |
intron_variant | MODIFIER | c.62-20533T>A | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31963916 | |||||||
chr2:31964094 | C | T | 54 | a0001c0001t0001g0009 a0001c0001t0001g0011 a0001c0001t0001g0012 others(51): Show |
54 | HG01168.hp1 HG01169.hp2 HG01255.hp2 others(51): Show |
intron_variant | MODIFIER | c.62-20711G>A | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31964094 | |||||||
chr2:31964175 | G | A | 54 | a0001c0001t0001g0009 a0001c0001t0001g0011 a0001c0001t0001g0012 others(51): Show |
54 | HG01168.hp1 HG01169.hp2 HG01255.hp2 others(51): 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 | a0001c0001t0001g0044 | 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 | a0001c0001t0001g0270 a0001c0001t0001g0295 |
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 | a0001c0001t0001g0238 a0001c0001t0001g0239 a0001c0001t0001g0240 others(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 | 59 | a0001c0001t0001g0009 a0001c0001t0001g0011 a0001c0001t0001g0012 others(56): Show |
59 | HG01168.hp1 HG01169.hp2 HG01243.hp2 others(56): 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 | a0001c0001t0001g0231 a0001c0001t0001g0232 a0001c0001t0001g0233 |
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 | a0001c0001t0001g0218 a0001c0001t0001g0219 a0001c0001t0001g0235 others(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 | a0001c0001t0001g0291 a0001c0001t0001g0292 a0001c0001t0001g0293 others(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 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0010 others(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 | a0001c0001t0001g0271 a0001c0001t0001g0272 a0001c0001t0001g0273 |
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 | a0001c0001t0001g0289 a0001c0001t0001g0290 a0001c0001t0001g0291 others(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 | 72 | a0001c0001t0001g0009 a0001c0001t0001g0011 a0001c0001t0001g0012 others(69): Show |
72 | HG01109.hp2 HG01168.hp1 HG01169.hp2 others(69): 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 | a0001c0001t0001g0291 a0001c0001t0001g0292 a0001c0001t0001g0293 others(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 | a0001c0001t0001g0256 | 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 | a0001c0001t0001g0235 a0001c0001t0001g0236 |
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 | a0001c0001t0001g0066 a0001c0001t0002g0004 |
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 | a0001c0001t0001g0041 | 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 | a0001c0001t0001g0115 a0001c0001t0001g0211 |
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 | a0001c0001t0001g0231 a0001c0001t0001g0232 a0001c0001t0001g0233 others(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 | a0001c0001t0001g0199 | 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 | a0001c0001t0001g0065 | 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 | a0001c0001t0001g0231 a0001c0001t0001g0232 a0001c0001t0001g0233 |
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 | a0001c0001t0001g0278 | 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 | 108 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0008 others(105): 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 | 104 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0008 others(101): 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 | a0001c0001t0001g0015 a0001c0001t0001g0059 a0001c0001t0001g0070 others(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 |
80 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0008 others(77): 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 | a0001c0001t0001g0021 a0001c0001t0001g0028 a0001c0001t0001g0029 others(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 | a0001c0001t0001g0135 | 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 | a0001c0001t0001g0102 a0001c0001t0001g0134 |
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 | a0001c0001t0001g0103 | 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 | a0001c0001t0001g0141 a0001c0001t0001g0162 |
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 | a0001c0001t0001g0144 | 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 | a0001c0001t0001g0110 a0001c0001t0001g0157 |
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 | a0001c0001t0001g0136 | 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 | a0001c0001t0001g0291 a0001c0001t0001g0292 a0001c0001t0001g0293 others(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 | a0001c0001t0001g0182 | 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 | a0001c0001t0001g0271 a0001c0001t0001g0272 a0001c0001t0001g0273 |
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 | a0001c0001t0001g0232 a0001c0001t0001g0233 |
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 | a0001c0001t0001g0218 a0001c0001t0001g0219 a0001c0001t0001g0270 others(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 | 56 | a0001c0001t0001g0009 a0001c0001t0001g0011 a0001c0001t0001g0012 others(53): Show |
56 | HG01168.hp1 HG01169.hp2 HG01255.hp2 others(53): Show |
intron_variant | MODIFIER | c.62-23689C>G | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31967072 | |||||||
chr2:31967124 | AT | A | 286 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(283): Show |
287 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(284): Show |
intron_variant | MODIFIER | c.62-23742delA | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31967124 | |||||||
chr2:31967146 | C | T | 1 | a0001c0001t0001g0302 | 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 | 52 | a0001c0001t0001g0009 a0001c0001t0001g0218 a0001c0001t0001g0219 others(49): Show |
52 | HG01168.hp1 HG01169.hp2 HG01255.hp2 others(49): 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 | a0001c0001t0001g0259 | 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 | a0001c0001t0001g0268 | 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 | a0001c0001t0001g0291 a0001c0001t0001g0292 a0001c0001t0001g0293 others(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 | 52 | a0001c0001t0001g0009 a0001c0001t0001g0218 a0001c0001t0001g0219 others(49): Show |
52 | HG01168.hp1 HG01169.hp2 HG01255.hp2 others(49): 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 | a0001c0001t0001g0218 a0001c0001t0001g0219 a0001c0001t0001g0235 others(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 | a0001c0001t0001g0238 a0001c0001t0001g0239 a0001c0001t0001g0240 others(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 | a0001c0001t0001g0214 | 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 | a0001c0001t0001g0215 a0001c0001t0001g0216 a0001c0001t0001g0217 others(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 | a0001c0001t0001g0133 | 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 | a0002c0002t0001g0121 | 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 | a0001c0001t0001g0235 a0001c0001t0001g0236 a0001c0001t0002g0004 others(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 | a0001c0001t0001g0289 a0001c0001t0001g0290 a0001c0001t0001g0291 others(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 | a0001c0001t0001g0289 a0001c0001t0001g0290 |
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 | a0001c0001t0002g0006 | 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 | a0001c0001t0001g0062 a0001c0001t0001g0229 a0001c0001t0001g0230 |
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 | a0001c0001t0001g0043 a0001c0001t0001g0156 a0001c0001t0001g0167 others(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 | a0001c0001t0001g0054 | 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 | 69 | a0001c0001t0001g0009 a0001c0001t0001g0218 a0001c0001t0001g0219 others(66): Show |
69 | HG01109.hp2 HG01168.hp1 HG01169.hp2 others(66): 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 | a0001c0001t0001g0110 a0001c0001t0001g0134 a0001c0001t0001g0135 others(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 | a0001c0001t0001g0215 a0001c0001t0001g0216 a0001c0001t0001g0298 |
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 | a0001c0001t0001g0274 a0001c0001t0001g0275 a0001c0001t0001g0276 |
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 | 108 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0008 others(105): 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 | a0001c0001t0001g0290 | 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 | a0001c0001t0002g0004 | 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 | a0001c0001t0001g0040 | 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 | 7 | a0001c0001t0001g0237 a0001c0001t0001g0239 a0001c0001t0001g0240 others(4): Show |
7 | HG01433.hp2 HG02723.hp1 HG02809.hp2 others(4): 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 | a0001c0001t0001g0238 a0001c0001t0001g0248 a0001c0001t0001g0255 others(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 | a0001c0001t0001g0009 a0001c0001t0001g0236 a0001c0001t0001g0244 others(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 | a0001c0001t0001g0235 a0001c0001t0001g0242 a0001c0001t0001g0264 others(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 | a0001c0001t0001g0259 a0001c0001t0001g0283 |
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 | a0001c0001t0001g0274 a0001c0001t0001g0275 a0001c0001t0001g0276 |
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 | a0001c0001t0001g0231 a0001c0001t0001g0232 a0001c0001t0001g0233 |
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 | a0001c0001t0001g0218 a0001c0001t0001g0219 a0001c0001t0001g0251 others(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 | a0001c0001t0001g0044 a0001c0001t0001g0046 a0001c0001t0001g0189 |
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 | a0001c0001t0001g0007 a0001c0001t0001g0010 a0001c0001t0001g0021 others(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 | a0001c0001t0001g0002 a0001c0001t0001g0016 a0001c0001t0001g0027 others(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 | a0001c0001t0001g0052 a0001c0001t0001g0054 a0001c0001t0001g0055 |
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 | a0001c0001t0001g0105 | 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 | 57 | a0001c0001t0001g0009 a0001c0001t0001g0064 a0001c0001t0001g0071 others(54): Show |
57 | HG00597.hp2 HG01109.hp2 HG01168.hp1 others(54): 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 | a0001c0001t0001g0008 a0001c0001t0001g0030 a0001c0001t0001g0039 others(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 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(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 | 31 | a0001c0001t0001g0001 a0001c0001t0001g0014 a0001c0001t0001g0019 others(28): 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 | a0001c0001t0001g0070 a0001c0001t0001g0075 a0001c0001t0001g0107 others(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 | a0001c0001t0001g0080 a0001c0001t0001g0142 |
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 | a0001c0001t0001g0294 a0001c0001t0002g0004 a0001c0001t0002g0005 others(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 | a0001c0001t0001g0059 a0001c0001t0001g0219 a0001c0001t0001g0251 others(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 | 8 | a0001c0001t0001g0017 a0001c0001t0001g0237 a0001c0001t0001g0239 others(5): Show |
8 | HG01433.hp2 HG02723.hp1 HG02809.hp2 others(5): 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 | a0001c0001t0001g0217 a0001c0001t0001g0238 a0001c0001t0001g0248 others(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 | a0001c0001t0001g0009 a0001c0001t0001g0137 a0001c0001t0001g0215 others(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 | a0001c0001t0001g0235 a0001c0001t0001g0236 a0001c0001t0001g0242 others(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 | a0001c0001t0001g0235 a0001c0001t0001g0259 a0001c0001t0001g0271 others(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 | a0001c0001t0001g0272 a0001c0001t0001g0273 a0001c0001t0001g0274 others(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 | a0001c0001t0001g0231 a0001c0001t0001g0232 a0001c0001t0001g0233 |
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 | a0001c0001t0001g0259 | 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 | a0001c0001t0001g0231 a0001c0001t0001g0232 a0001c0001t0001g0233 |
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 | a0001c0001t0001g0289 a0001c0001t0001g0290 |
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 | a0001c0001t0001g0157 | 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 | 63 | a0001c0001t0001g0009 a0001c0001t0001g0218 a0001c0001t0001g0219 others(60): Show |
63 | HG01109.hp2 HG01168.hp1 HG01169.hp2 others(60): 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 | a0001c0001t0001g0289 a0001c0001t0001g0290 a0001c0001t0001g0291 others(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 | 55 | a0001c0001t0001g0009 a0001c0001t0001g0040 a0001c0001t0001g0218 others(52): Show |
55 | HG01168.hp1 HG01169.hp2 HG01255.hp2 others(52): Show |
intron_variant | MODIFIER | c.62-26395delA | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31969777 | |||||||
chr2:31969827 | C | G | 1 | a0001c0001t0001g0270 | 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 | a0001c0001t0001g0283 | 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 | a0001c0001t0001g0289 a0001c0001t0001g0290 |
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 | a0001c0001t0001g0289 a0001c0001t0001g0290 a0001c0001t0001g0291 others(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 | a0001c0001t0001g0231 a0001c0001t0001g0232 a0001c0001t0001g0233 |
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 | a0001c0001t0001g0031 | 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 | a0001c0001t0001g0187 | 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 | a0001c0001t0001g0144 | 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 | a0001c0001t0001g0036 | 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 | a0001c0001t0001g0184 a0001c0001t0001g0289 a0001c0001t0001g0290 others(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 | a0001c0001t0001g0215 a0001c0001t0001g0216 a0001c0001t0001g0217 others(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 | a0001c0001t0001g0211 | 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 | a0001c0001t0001g0064 | 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 | a0001c0001t0001g0026 | 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 | a0001c0001t0001g0235 a0001c0001t0001g0236 |
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 | a0001c0001t0001g0044 | 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 | 57 | a0001c0001t0001g0009 a0001c0001t0001g0218 a0001c0001t0001g0219 others(54): Show |
57 | HG01168.hp1 HG01169.hp2 HG01243.hp2 others(54): Show |
intron_variant | MODIFIER | c.62-28231T>G | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31971614 | |||||||
chr2:31971724 | T | C | 61 | a0001c0001t0001g0009 a0001c0001t0001g0218 a0001c0001t0001g0219 others(58): Show |
61 | HG01109.hp2 HG01168.hp1 HG01169.hp2 others(58): 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 | a0001c0001t0002g0005 | 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 | 67 | a0001c0001t0001g0009 a0001c0001t0001g0218 a0001c0001t0001g0219 others(64): Show |
67 | HG01109.hp2 HG01168.hp1 HG01169.hp2 others(64): 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 | a0001c0001t0001g0295 | 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 | a0001c0001t0001g0289 a0001c0001t0001g0290 a0001c0001t0001g0291 others(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 | 42 | a0001c0001t0001g0237 a0001c0001t0001g0238 a0001c0001t0001g0239 others(39): Show |
42 | HG01168.hp1 HG01169.hp2 HG01255.hp2 others(39): 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 | a0001c0001t0001g0168 a0001c0001t0001g0169 a0001c0001t0001g0171 others(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 | a0001c0001t0001g0235 | 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 | a0001c0001t0001g0231 | 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 | a0001c0001t0001g0274 a0001c0001t0001g0275 a0001c0001t0001g0276 |
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 | a0001c0001t0001g0148 | 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 | a0001c0001t0001g0274 a0001c0001t0001g0275 a0001c0001t0001g0276 |
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 | a0001c0001t0001g0289 a0001c0001t0001g0290 a0001c0001t0001g0291 others(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 | a0001c0001t0001g0270 a0001c0001t0001g0295 |
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 | a0001c0001t0001g0274 a0001c0001t0001g0275 a0001c0001t0001g0276 |
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 | 56 | a0001c0001t0001g0009 a0001c0001t0001g0235 a0001c0001t0001g0236 others(53): Show |
56 | HG01168.hp1 HG01169.hp2 HG01243.hp2 others(53): Show |
intron_variant | MODIFIER | c.62-30391A>G | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31973774 | |||||||
chr2:31973778 | A | G | 64 | a0001c0001t0001g0009 a0001c0001t0001g0218 a0001c0001t0001g0219 others(61): Show |
64 | HG01109.hp2 HG01168.hp1 HG01169.hp2 others(61): 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 | a0001c0001t0001g0184 | 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 | a0001c0001t0001g0242 a0001c0001t0001g0267 |
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 | a0001c0001t0001g0232 | 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 | a0001c0001t0001g0188 | 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 | a0001c0001t0001g0221 | 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 | a0001c0001t0001g0235 a0001c0001t0001g0236 |
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 | a0001c0001t0001g0056 a0001c0001t0001g0057 a0001c0001t0001g0058 |
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 | a0001c0001t0001g0295 | 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 | a0001c0001t0001g0238 a0001c0001t0001g0269 |
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 | a0001c0001t0001g0267 | 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 | a0001c0001t0001g0028 a0001c0001t0001g0164 |
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 | a0001c0001t0001g0295 | 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 | a0001c0001t0001g0231 a0001c0001t0001g0232 a0001c0001t0001g0233 |
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 | a0001c0001t0001g0291 a0001c0001t0001g0292 a0001c0001t0001g0293 others(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 | 57 | a0001c0001t0001g0009 a0001c0001t0001g0218 a0001c0001t0001g0219 others(54): Show |
57 | HG01168.hp1 HG01169.hp2 HG01243.hp2 others(54): 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 | a0001c0001t0001g0300 | 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 | a0001c0001t0001g0093 | 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 | a0001c0001t0001g0232 a0001c0001t0001g0233 |
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 | a0001c0001t0001g0017 a0001c0001t0001g0044 a0001c0001t0001g0046 others(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 | a0001c0001t0001g0157 | 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 | a0001c0001t0001g0235 a0001c0001t0001g0236 |
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 | a0001c0001t0001g0274 a0001c0001t0001g0275 a0001c0001t0001g0276 |
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 | a0001c0001t0001g0082 | 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 | a0001c0001t0001g0291 a0001c0001t0001g0292 a0001c0001t0001g0293 others(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 | a0001c0001t0001g0231 | 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 | a0001c0001t0001g0067 | 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 | a0001c0001t0002g0005 | 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 | a0001c0001t0001g0294 | 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 | a0001c0001t0001g0238 a0001c0001t0001g0269 |
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 | a0001c0001t0001g0063 | 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 | a0001c0001t0001g0274 a0001c0001t0001g0275 a0001c0001t0001g0276 |
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 | 62 | a0001c0001t0001g0009 a0001c0001t0001g0235 a0001c0001t0001g0236 others(59): Show |
62 | HG01109.hp2 HG01168.hp1 HG01169.hp2 others(59): 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 | a0001c0001t0001g0291 a0001c0001t0001g0292 a0001c0001t0001g0293 others(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 | a0001c0001t0001g0231 a0001c0001t0001g0232 a0001c0001t0001g0233 |
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 | 56 | a0001c0001t0001g0009 a0001c0001t0001g0235 a0001c0001t0001g0236 others(53): Show |
56 | HG01168.hp1 HG01169.hp2 HG01243.hp2 others(53): Show |
intron_variant | MODIFIER | c.61+31118C>A | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31979069 | |||||||
chr2:31979093 | G | A | 45 | a0001c0001t0001g0009 a0001c0001t0001g0237 a0001c0001t0001g0238 others(42): Show |
45 | HG01168.hp1 HG01169.hp2 HG01255.hp2 others(42): 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 | a0001c0001t0001g0060 | 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 | a0001c0001t0001g0270 | 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 | a0001c0001t0001g0056 a0001c0001t0001g0057 a0001c0001t0001g0058 |
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 | a0001c0001t0001g0164 | 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 | a0001c0001t0001g0291 a0001c0001t0001g0292 a0001c0001t0001g0293 |
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 | a0001c0001t0001g0056 a0001c0001t0001g0058 |
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 | 63 | a0001c0001t0001g0009 a0001c0001t0001g0050 a0001c0001t0001g0055 others(60): Show |
63 | HG01070.hp1 HG01109.hp2 HG01168.hp1 others(60): Show |
intron_variant | MODIFIER | c.61+30177delT | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31980009 | |||||||
chr2:31980032 | A | G | 3 | a0001c0001t0001g0069 a0001c0001t0001g0071 a0001c0001t0001g0073 |
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 | 67 | a0001c0001t0001g0009 a0001c0001t0001g0231 a0001c0001t0001g0232 others(64): Show |
67 | HG01109.hp2 HG01168.hp1 HG01169.hp2 others(64): 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 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0006 |
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 | a0001c0001t0001g0119 | 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 | a0001c0001t0001g0159 | 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 | a0001c0001t0001g0108 | 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 | a0001c0001t0001g0297 | 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 | 183 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0008 others(180): Show |
184 | HG00099.hp2 HG00140.hp2 HG00423.hp2 others(181): 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 | a0001c0001t0001g0231 a0001c0001t0001g0232 a0001c0001t0001g0233 others(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 | a0001c0001t0001g0270 a0001c0001t0001g0295 |
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 | a0001c0001t0001g0289 | 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 | a0001c0001t0001g0232 | 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 | 68 | a0001c0001t0001g0009 a0001c0001t0001g0231 a0001c0001t0001g0232 others(65): Show |
68 | HG01109.hp2 HG01168.hp1 HG01169.hp2 others(65): 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 | a0001c0001t0001g0215 a0001c0001t0001g0216 a0001c0001t0001g0217 others(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 | a0001c0001t0001g0116 a0001c0001t0001g0151 |
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 | a0001c0001t0001g0115 | 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 | a0001c0001t0001g0232 a0001c0001t0001g0233 |
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 | a0001c0001t0001g0194 | 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 | a0001c0001t0001g0289 a0001c0001t0001g0290 |
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 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(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 | 57 | a0001c0001t0001g0009 a0001c0001t0001g0039 a0001c0001t0001g0066 others(54): Show |
57 | HG01109.hp2 HG01168.hp1 HG01169.hp2 others(54): Show |
intron_variant | MODIFIER | c.61+27598delT | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31982588 | |||||||
chr2:31982658 | G | A | 1 | a0001c0001t0001g0031 | 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 | 60 | a0001c0001t0001g0009 a0001c0001t0001g0218 a0001c0001t0001g0219 others(57): Show |
60 | HG01109.hp2 HG01168.hp1 HG01169.hp2 others(57): 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 | a0001c0001t0001g0009 | 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 | a0001c0001t0001g0231 | 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 | a0001c0001t0001g0231 a0001c0001t0001g0232 a0001c0001t0001g0233 |
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 | 57 | a0001c0001t0001g0009 a0001c0001t0001g0218 a0001c0001t0001g0219 others(54): Show |
57 | HG01168.hp1 HG01169.hp2 HG01243.hp2 others(54): 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 | a0001c0001t0001g0054 | 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 | 68 | a0001c0001t0001g0009 a0001c0001t0001g0231 a0001c0001t0001g0232 others(65): Show |
68 | HG01109.hp2 HG01168.hp1 HG01169.hp2 others(65): Show |
intron_variant | MODIFIER | c.61+26986A>G | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31983201 | |||||||
chr2:31983380 | G | C | 112 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0008 others(109): 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 | a0001c0001t0001g0185 | 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 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0010 others(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 | a0001c0001t0001g0109 | 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 | 59 | a0001c0001t0001g0009 a0001c0001t0001g0235 a0001c0001t0001g0236 others(56): Show |
59 | HG01168.hp1 HG01169.hp2 HG01243.hp2 others(56): 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 | a0001c0001t0001g0238 a0001c0001t0001g0239 a0001c0001t0001g0240 others(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 | a0001c0001t0001g0273 | 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 | a0001c0001t0001g0232 a0001c0001t0001g0233 |
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 | a0001c0001t0001g0200 | 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 | a0001c0001t0001g0199 | 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 | a0001c0001t0001g0271 a0001c0001t0001g0272 a0001c0001t0001g0273 |
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 | a0001c0001t0001g0242 a0001c0001t0001g0267 |
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 | a0001c0001t0001g0235 a0001c0001t0001g0236 |
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 | a0001c0001t0001g0289 a0001c0001t0001g0290 |
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 | a0001c0001t0001g0289 a0001c0001t0001g0290 |
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 | a0001c0001t0001g0220 | 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 | a0001c0001t0001g0149 | 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 | a0001c0001t0001g0008 | 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 | a0001c0001t0001g0026 | 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 | a0001c0001t0001g0178 | 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 | 55 | a0001c0001t0001g0009 a0001c0001t0001g0235 a0001c0001t0001g0236 others(52): Show |
55 | HG01168.hp1 HG01169.hp2 HG01243.hp2 others(52): 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 | a0001c0001t0001g0289 a0001c0001t0001g0290 |
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 | a0001c0001t0001g0002 a0001c0001t0001g0143 a0001c0001t0001g0210 |
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 | a0001c0001t0001g0209 | 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 | a0001c0001t0001g0270 a0001c0001t0001g0271 a0001c0001t0001g0272 others(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 | a0001c0001t0001g0181 | 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 | 294 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(291): Show |
295 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(292): 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 | a0001c0001t0001g0238 a0001c0001t0001g0239 a0001c0001t0001g0240 others(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 | 55 | a0001c0001t0001g0009 a0001c0001t0001g0235 a0001c0001t0001g0236 others(52): Show |
55 | HG01168.hp1 HG01169.hp2 HG01243.hp2 others(52): 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 | a0001c0001t0001g0218 a0001c0001t0001g0219 |
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 | 52 | a0001c0001t0001g0009 a0001c0001t0001g0235 a0001c0001t0001g0236 others(49): Show |
52 | HG01168.hp1 HG01169.hp2 HG01255.hp2 others(49): 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 | a0001c0001t0001g0179 | 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 | a0001c0001t0001g0064 | 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 | a0001c0001t0001g0209 | 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 | a0001c0001t0001g0143 | 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 | a0001c0001t0001g0231 a0001c0001t0001g0232 a0001c0001t0001g0233 |
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 | a0001c0001t0001g0235 a0001c0001t0001g0236 |
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 | a0001c0001t0001g0233 | 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 | a0001c0001t0001g0079 | 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 | a0001c0001t0001g0200 | 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 | a0001c0001t0001g0090 | 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 | a0001c0001t0001g0090 | 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 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0006 |
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 | a0001c0001t0001g0231 a0001c0001t0001g0232 a0001c0001t0001g0233 |
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 | a0001c0001t0001g0110 a0001c0001t0001g0134 a0001c0001t0001g0135 others(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 | a0001c0001t0001g0030 a0001c0001t0001g0159 |
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 | a0001c0001t0001g0270 a0001c0001t0001g0295 |
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 | a0001c0001t0001g0235 a0001c0001t0001g0236 a0001c0001t0001g0270 others(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 | a0001c0001t0001g0277 | 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 | a0001c0001t0001g0117 a0001c0001t0001g0118 |
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 | a0001c0001t0001g0174 | 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 | a0001c0001t0001g0085 | 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 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0010 others(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 | 52 | a0001c0001t0001g0009 a0001c0001t0001g0235 a0001c0001t0001g0236 others(49): Show |
52 | HG01168.hp1 HG01169.hp2 HG01255.hp2 others(49): 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 | a0001c0001t0001g0170 a0001c0001t0001g0185 a0001c0001t0001g0187 |
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 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0006 |
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 | a0001c0001t0001g0215 a0001c0001t0001g0216 a0001c0001t0001g0217 others(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 | a0001c0001t0001g0278 | 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 | 45 | a0001c0001t0001g0009 a0001c0001t0001g0237 a0001c0001t0001g0238 others(42): Show |
45 | HG01168.hp1 HG01169.hp2 HG01255.hp2 others(42): 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 | a0001c0001t0001g0257 a0001c0001t0001g0258 |
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 | a0001c0001t0001g0215 a0001c0001t0001g0216 a0001c0001t0001g0298 |
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 | a0001c0001t0001g0201 | 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 | a0001c0001t0001g0152 | 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 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(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 | a0001c0001t0001g0050 a0001c0001t0001g0114 a0001c0001t0001g0257 others(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 | a0001c0001t0001g0196 a0001c0001t0001g0197 a0001c0001t0001g0198 others(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 | a0001c0001t0001g0274 a0001c0001t0001g0275 a0001c0001t0001g0276 |
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 | a0001c0001t0001g0271 a0001c0001t0001g0272 a0001c0001t0001g0273 |
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 | a0001c0001t0001g0285 a0001c0001t0001g0286 a0001c0001t0001g0287 |
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 | a0001c0001t0001g0235 a0001c0001t0001g0236 |
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 | 290 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(287): Show |
291 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(288): Show |
intron_variant | MODIFIER | c.61+19739C>A | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31990448 | |||||||
chr2:31990504 | T | C | 68 | a0001c0001t0001g0009 a0001c0001t0001g0231 a0001c0001t0001g0232 others(65): Show |
68 | HG01109.hp2 HG01168.hp1 HG01169.hp2 others(65): 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 | a0001c0001t0001g0188 a0001c0001t0001g0215 a0001c0001t0001g0216 others(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 | a0001c0001t0001g0066 a0001c0001t0001g0098 a0001c0001t0001g0115 others(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 | a0001c0001t0001g0072 | 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 | a0001c0001t0001g0244 a0001c0001t0001g0249 a0001c0001t0001g0250 others(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 | a0001c0001t0001g0178 | 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 | a0001c0001t0001g0231 a0001c0001t0001g0232 a0001c0001t0001g0233 |
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 | a0001c0001t0001g0227 a0001c0001t0001g0289 |
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 | 278 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(275): Show |
279 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(276): Show |
intron_variant | MODIFIER | c.61+18615delT | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31991571 | |||||||
chr2:31992258 | T | C | 1 | a0001c0001t0001g0187 | 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 | a0001c0001t0001g0172 | 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 | 291 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(288): Show |
292 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(289): 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 | a0001c0001t0001g0138 a0001c0001t0001g0139 a0001c0001t0001g0227 |
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 | a0001c0001t0001g0231 a0001c0001t0001g0232 a0001c0001t0001g0233 |
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 | a0001c0001t0001g0223 | 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 | a0001c0001t0001g0065 | 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 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0006 |
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 | 295 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(292): Show |
296 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(293): 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 | a0001c0001t0001g0214 | 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 | a0001c0001t0001g0204 | 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 | 71 | a0001c0001t0001g0009 a0001c0001t0001g0011 a0001c0001t0001g0012 others(68): Show |
71 | HG01109.hp2 HG01168.hp1 HG01169.hp2 others(68): 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 | a0001c0001t0001g0231 a0001c0001t0001g0232 a0001c0001t0001g0233 |
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 | a0001c0001t0001g0059 a0001c0001t0001g0070 |
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 | a0001c0001t0001g0289 a0001c0001t0001g0290 |
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 | a0001c0001t0001g0231 | 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 | a0001c0001t0001g0015 a0001c0001t0001g0085 |
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 | a0001c0001t0001g0008 a0001c0001t0001g0011 a0001c0001t0001g0020 others(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 | a0001c0001t0001g0096 a0001c0001t0001g0207 a0001c0001t0001g0212 others(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 | a0001c0001t0001g0271 a0001c0001t0001g0272 a0001c0001t0001g0273 |
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 | a0001c0001t0001g0289 a0001c0001t0001g0290 |
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 | a0001c0001t0001g0007 a0001c0001t0001g0010 a0001c0001t0001g0017 others(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 | a0001c0001t0001g0037 a0001c0001t0001g0047 a0001c0001t0001g0075 others(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 | a0001c0001t0001g0267 | 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 | a0001c0001t0001g0278 | 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 | a0001c0001t0001g0291 a0001c0001t0001g0292 a0001c0001t0001g0293 others(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 | a0001c0001t0001g0291 a0001c0001t0001g0292 a0001c0001t0001g0293 |
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 | 60 | a0001c0001t0001g0009 a0001c0001t0001g0011 a0001c0001t0001g0012 others(57): Show |
60 | HG01168.hp1 HG01169.hp2 HG01243.hp2 others(57): Show |
intron_variant | MODIFIER | c.61+15956T>G | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31994231 | |||||||
chr2:31994256 | C | T | 60 | a0001c0001t0001g0009 a0001c0001t0001g0011 a0001c0001t0001g0012 others(57): Show |
60 | HG01168.hp1 HG01169.hp2 HG01243.hp2 others(57): 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 | a0001c0001t0001g0190 | 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 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0010 others(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 | a0001c0001t0001g0056 a0001c0001t0001g0057 a0001c0001t0001g0058 |
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 | a0001c0001t0001g0206 | 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 | 72 | a0001c0001t0001g0009 a0001c0001t0001g0011 a0001c0001t0001g0012 others(69): Show |
72 | HG01109.hp2 HG01168.hp1 HG01169.hp2 others(69): 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 | a0001c0001t0001g0102 a0001c0001t0001g0103 a0001c0001t0001g0231 others(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 | 58 | a0001c0001t0001g0009 a0001c0001t0001g0011 a0001c0001t0001g0012 others(55): Show |
58 | HG01081.hp2 HG01168.hp1 HG01169.hp2 others(55): 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 | a0001c0001t0001g0040 | 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 | a0001c0001t0001g0270 | 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 | a0001c0001t0001g0114 | 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 | a0001c0001t0001g0215 a0001c0001t0001g0216 a0001c0001t0001g0217 others(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 | a0001c0001t0001g0074 | 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 | a0001c0001t0001g0251 a0001c0001t0001g0254 |
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 | a0001c0001t0001g0141 | 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 | a0001c0001t0001g0085 | 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 | a0001c0001t0001g0043 | 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 | a0001c0001t0001g0011 | 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 | a0001c0001t0001g0046 | 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 | a0001c0001t0001g0274 a0001c0001t0001g0275 a0001c0001t0001g0276 |
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 | 56 | a0001c0001t0001g0009 a0001c0001t0001g0011 a0001c0001t0001g0012 others(53): Show |
56 | HG01168.hp1 HG01169.hp2 HG01255.hp2 others(53): 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 | a0001c0001t0001g0002 a0001c0001t0001g0142 a0001c0001t0001g0150 others(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 | a0001c0001t0001g0274 a0001c0001t0001g0275 a0001c0001t0001g0276 |
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 | 54 | a0001c0001t0001g0009 a0001c0001t0001g0011 a0001c0001t0001g0012 others(51): Show |
54 | HG01168.hp1 HG01169.hp2 HG01255.hp2 others(51): 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 | a0001c0001t0001g0238 a0001c0001t0001g0269 |
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 | a0001c0001t0001g0072 a0001c0001t0001g0089 |
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 | a0001c0001t0001g0168 | 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 | a0001c0001t0001g0101 a0001c0001t0001g0104 |
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 | a0001c0001t0001g0184 a0001c0001t0001g0214 a0001c0001t0001g0278 |
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 | a0001c0001t0001g0047 | 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 | a0001c0001t0001g0289 | 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 | a0001c0001t0001g0066 | 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 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0006 |
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 | a0001c0001t0001g0271 a0001c0001t0001g0272 a0001c0001t0001g0273 |
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 | a0001c0001t0001g0271 a0001c0001t0001g0272 a0001c0001t0001g0273 |
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 | a0001c0001t0001g0028 a0001c0001t0001g0164 a0001c0001t0001g0165 |
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 | a0001c0001t0001g0294 | 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 | a0001c0001t0001g0201 a0001c0001t0001g0202 a0001c0001t0001g0203 others(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 | a0001c0001t0001g0184 a0001c0001t0001g0214 a0001c0001t0001g0278 |
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 | a0001c0001t0001g0220 a0001c0001t0001g0279 a0001c0001t0001g0280 others(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 | a0001c0001t0001g0092 | 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 | a0001c0001t0001g0231 a0001c0001t0001g0232 a0001c0001t0001g0233 |
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 | a0001c0001t0001g0079 | 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 | a0001c0001t0001g0094 | 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 | a0001c0001t0001g0197 a0001c0001t0001g0199 a0001c0001t0001g0200 |
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 | a0001c0001t0001g0038 a0001c0001t0001g0174 a0001c0001t0001g0303 |
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 | a0001c0001t0001g0019 a0001c0001t0001g0035 a0001c0001t0001g0068 others(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 | a0001c0001t0001g0035 a0001c0001t0001g0055 a0001c0001t0001g0068 |
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 | a0001c0001t0001g0231 a0001c0001t0001g0232 a0001c0001t0001g0233 |
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 | a0001c0001t0001g0271 a0001c0001t0001g0272 a0001c0001t0001g0273 |
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 | a0001c0001t0001g0231 a0001c0001t0001g0232 a0001c0001t0001g0233 |
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 | a0001c0001t0001g0220 | 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 | a0001c0001t0001g0188 | 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 | a0001c0001t0001g0283 | 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 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0038 others(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 | 74 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0011 others(71): Show |
74 | HG01070.hp1 HG01071.hp2 HG01081.hp2 others(71): Show |
intron_variant | MODIFIER | c.61+10304delA | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 31999882 | |||||||
chr2:31999937 | G | C | 11 | a0001c0001t0001g0279 a0001c0001t0001g0280 a0001c0001t0001g0281 others(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 | a0001c0001t0001g0278 | 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 | a0001c0001t0001g0144 | 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 | a0001c0001t0001g0231 a0001c0001t0001g0289 a0001c0001t0001g0290 |
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 | a0001c0001t0001g0284 | 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 | a0001c0001t0001g0011 a0001c0001t0001g0289 a0001c0001t0001g0290 |
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 | a0001c0001t0001g0101 | 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 | 27 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(24): Show |
27 | HG01109.hp2 HG01243.hp2 HG02083.hp2 others(24): Show |
intron_variant | MODIFIER | c.61+9396dupA | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 32000790 | |||||||
chr2:32000790 | A | ATT | 31 | a0001c0001t0001g0009 a0001c0001t0001g0235 a0001c0001t0001g0236 others(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 | a0001c0001t0001g0027 a0001c0001t0001g0073 a0001c0001t0001g0085 others(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 | a0001c0001t0001g0094 a0001c0001t0001g0095 a0001c0001t0001g0096 others(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 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0007 others(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 | a0001c0001t0001g0035 a0001c0001t0001g0038 a0001c0001t0001g0039 others(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 | 63 | a0001c0001t0001g0009 a0001c0001t0001g0012 a0001c0001t0001g0013 others(60): Show |
63 | HG00408.hp2 HG00642.hp2 HG01081.hp1 others(60): Show |
intron_variant | MODIFIER | c.61+9154delA | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 32001032 | |||||||
chr2:32001056 | G | C | 1 | a0001c0001t0001g0226 | 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 | 61 | a0001c0001t0001g0009 a0001c0001t0001g0011 a0001c0001t0001g0012 others(58): Show |
61 | HG01168.hp1 HG01169.hp2 HG01243.hp2 others(58): 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 | a0001c0001t0001g0015 a0001c0001t0001g0085 |
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 | 73 | a0001c0001t0001g0009 a0001c0001t0001g0011 a0001c0001t0001g0012 others(70): Show |
73 | HG01109.hp2 HG01168.hp1 HG01169.hp2 others(70): Show |
intron_variant | MODIFIER | c.61+8990C>G | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | 32001197 | |||||||
chr2:32001220 | T | C | 50 | a0001c0001t0001g0009 a0001c0001t0001g0011 a0001c0001t0001g0012 others(47): Show |
50 | HG01168.hp1 HG01169.hp2 HG01255.hp2 others(47): 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 | a0001c0001t0001g0101 a0001c0001t0001g0102 a0001c0001t0001g0103 others(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 | a0001c0001t0001g0231 a0001c0001t0001g0232 a0001c0001t0001g0233 |
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 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0001g0050 others(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 | a0001c0001t0001g0038 a0001c0001t0001g0048 a0001c0001t0001g0049 others(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 | a0001c0001t0001g0034 | 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 | a0001c0001t0001g0145 | 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 | a0001c0001t0001g0291 a0001c0001t0001g0292 a0001c0001t0001g0293 |
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 | a0001c0001t0001g0289 a0001c0001t0001g0290 |
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 | 50 | a0001c0001t0001g0009 a0001c0001t0001g0011 a0001c0001t0001g0012 others(47): Show |
50 | HG01168.hp1 HG01169.hp2 HG01255.hp2 others(47): 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 | a0001c0001t0001g0220 | 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 | a0001c0001t0001g0146 a0001c0001t0001g0147 a0001c0001t0001g0148 others(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 | a0001c0001t0001g0289 a0001c0001t0001g0290 |
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 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0010 others(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 | a0001c0001t0001g0289 a0001c0001t0001g0290 |
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 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0006 |
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 | a0001c0001t0001g0150 | 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 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0015 others(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 | a0001c0001t0001g0018 a0001c0001t0001g0094 a0001c0001t0001g0100 others(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 | a0001c0001t0001g0274 | 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 | a0001c0001t0001g0274 a0001c0001t0001g0275 a0001c0001t0001g0276 |
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 | a0001c0001t0001g0016 a0001c0001t0001g0238 a0001c0001t0001g0269 others(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 | a0001c0001t0001g0191 a0001c0001t0001g0192 a0001c0001t0001g0193 others(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 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(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 | a0001c0001t0001g0010 a0001c0001t0001g0038 a0001c0001t0001g0039 others(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 | a0001c0001t0001g0257 a0001c0001t0001g0258 a0001c0001t0001g0289 |
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 | 73 | a0001c0001t0001g0009 a0001c0001t0001g0011 a0001c0001t0001g0012 others(70): Show |
73 | HG01106.hp1 HG01109.hp2 HG01255.hp2 others(70): 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 | a0001c0001t0001g0024 a0001c0001t0001g0052 a0001c0001t0001g0055 others(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 | a0001c0001t0001g0007 a0001c0001t0001g0017 a0001c0001t0001g0031 others(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 | 134 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0010 others(131): Show |
134 | HG00423.hp1 HG00438.hp1 HG00597.hp2 others(131): 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 | a0001c0001t0001g0165 a0001c0001t0001g0182 a0001c0001t0001g0206 others(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 | 19 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0020 others(16): 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 | a0001c0001t0001g0155 | 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 | a0001c0001t0001g0233 | 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 | a0001c0001t0001g0233 | 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 | a0001c0001t0001g0260 a0001c0001t0001g0264 a0001c0001t0001g0265 |
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 | a0001c0001t0001g0231 | 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 | a0001c0001t0001g0291 a0001c0001t0001g0292 a0001c0001t0001g0293 |
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 | a0001c0001t0001g0231 a0001c0001t0001g0232 a0001c0001t0001g0233 others(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 | 34 | a0001c0001t0001g0009 a0001c0001t0001g0012 a0001c0001t0001g0013 others(31): Show |
34 | HG01255.hp2 HG01257.hp2 HG01258.hp1 others(31): 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 | 52 | a0001c0001t0001g0009 a0001c0001t0001g0012 a0001c0001t0001g0013 others(49): Show |
52 | HG01168.hp1 HG01169.hp2 HG01255.hp2 others(49): 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 | a0001c0001t0001g0285 a0001c0001t0001g0286 a0001c0001t0001g0287 |
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 | 76 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0011 others(73): Show |
76 | HG01071.hp2 HG01081.hp2 HG01109.hp2 others(73): 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 | a0001c0001t0001g0216 a0001c0001t0001g0217 a0001c0001t0001g0221 others(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 | a0001c0001t0001g0294 | 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 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0015 others(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 | a0001c0001t0001g0110 a0001c0001t0001g0135 a0001c0001t0001g0136 others(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 | a0001c0001t0002g0004 | 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 | a0001c0001t0002g0006 | 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 | a0001c0001t0001g0288 | 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 | a0001c0001t0001g0291 a0001c0001t0001g0292 a0001c0001t0001g0293 |
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 | a0001c0001t0001g0015 a0001c0001t0001g0083 a0001c0001t0001g0084 others(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 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0006 |
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 | a0001c0001t0002g0004 a0001c0001t0002g0005 |
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 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0006 |
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 | a0001c0001t0001g0291 a0001c0001t0001g0292 a0001c0001t0001g0293 others(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 | 61 | a0001c0001t0001g0009 a0001c0001t0001g0011 a0001c0001t0001g0012 others(58): Show |
61 | HG01168.hp1 HG01169.hp2 HG01243.hp2 others(58): 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 | a0001c0001t0001g0261 a0001c0001t0001g0262 a0001c0001t0001g0263 others(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 | a0001c0001t0001g0289 a0001c0001t0001g0290 |
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 | a0001c0001t0001g0289 a0001c0001t0001g0290 |
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 | a0001c0001t0001g0238 a0001c0001t0001g0239 a0001c0001t0001g0240 others(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 | a0001c0001t0001g0033 a0001c0001t0001g0034 a0001c0001t0001g0088 |
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 | a0001c0001t0001g0016 | 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 | a0001c0001t0001g0094 a0001c0001t0001g0095 a0001c0001t0001g0098 |
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 | a0001c0001t0001g0007 a0001c0001t0001g0032 |
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 | a0001c0001t0001g0031 | 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 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0006 |
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 | a0001c0001t0001g0291 a0001c0001t0001g0292 a0001c0001t0001g0293 |
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 | a0001c0001t0001g0231 a0001c0001t0001g0232 a0001c0001t0001g0233 |
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 | a0001c0001t0001g0205 | 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 | a0001c0001t0001g0086 a0001c0001t0001g0087 a0001c0001t0001g0234 |
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 | a0001c0001t0001g0231 a0001c0001t0001g0232 a0001c0001t0001g0233 |
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 | a0001c0001t0001g0189 | 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 | a0001c0001t0001g0190 | 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 | a0001c0001t0001g0289 a0001c0001t0001g0290 |
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 | 50 | a0001c0001t0001g0009 a0001c0001t0001g0011 a0001c0001t0001g0012 others(47): Show |
50 | HG01168.hp1 HG01169.hp2 HG01255.hp2 others(47): 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 | a0001c0001t0001g0237 a0001c0001t0001g0299 |
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 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0006 |
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 | a0001c0001t0001g0160 | 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 | a0001c0001t0001g0099 a0001c0001t0001g0191 a0001c0001t0001g0192 others(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 | a0001c0001t0001g0195 | 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 | a0001c0001t0001g0003 a0001c0001t0001g0161 a0001c0001t0001g0228 others(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 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0006 |
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 | a0001c0001t0001g0009 | 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 | a0001c0001t0001g0008 a0001c0001t0001g0088 a0001c0001t0001g0089 others(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 | a0001c0001t0001g0090 a0001c0001t0001g0091 a0001c0001t0001g0092 |
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 | 191 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0009 others(188): Show |
191 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(188): 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 | a0001c0001t0001g0099 | 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 | a0001c0001t0001g0093 | 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 | a0001c0001t0001g0274 a0001c0001t0001g0275 a0001c0001t0001g0276 |
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 | a0001c0001t0001g0274 a0001c0001t0001g0275 a0001c0001t0001g0276 others(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 | a0001c0001t0001g0196 a0001c0001t0001g0197 a0001c0001t0001g0198 others(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 | a0001c0001t0001g0094 a0001c0001t0001g0095 a0001c0001t0001g0096 others(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 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0006 |
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 | a0001c0001t0001g0201 a0001c0001t0001g0202 a0001c0001t0001g0203 others(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 | a0001c0001t0001g0235 a0001c0001t0001g0236 |
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 | a0001c0001t0001g0206 | 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 | a0001c0001t0001g0277 | 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 | a0001c0001t0001g0207 a0001c0001t0001g0208 a0001c0001t0001g0209 others(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 | a0001c0001t0001g0279 | 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 | a0001c0001t0001g0289 a0001c0001t0001g0290 |
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 | a0001c0001t0001g0008 a0001c0001t0001g0211 a0001c0001t0001g0212 others(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 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0010 others(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 | 45 | a0001c0001t0001g0009 a0001c0001t0001g0017 a0001c0001t0001g0237 others(42): Show |
45 | HG01168.hp1 HG01169.hp2 HG01255.hp2 others(42): 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 | a0001c0001t0001g0231 a0001c0001t0001g0232 a0001c0001t0001g0235 others(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 | a0001c0001t0001g0222 | 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 | a0001c0001t0001g0231 a0001c0001t0001g0232 a0001c0001t0001g0233 |
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 | a0001c0001t0002g0004 | 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 | 69 | a0001c0001t0001g0009 a0001c0001t0001g0231 a0001c0001t0001g0232 others(66): Show |
69 | HG01109.hp2 HG01168.hp1 HG01169.hp2 others(66): 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 | a0001c0001t0001g0223 a0001c0001t0001g0224 a0001c0001t0001g0225 others(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 | a0001c0001t0001g0016 | 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 | a0001c0001t0001g0015 | 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 | a0001c0001t0001g0273 | 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 | 74 | a0001c0001t0001g0009 a0001c0001t0001g0011 a0001c0001t0001g0012 others(71): Show |
74 | HG01109.hp2 HG01168.hp1 HG01169.hp2 others(71): 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 | a0001c0001t0001g0227 | 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 | a0001c0001t0001g0228 | 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 | a0001c0001t0001g0289 a0001c0001t0001g0290 a0001c0001t0001g0291 others(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 | a0001c0001t0001g0278 | 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 | a0001c0001t0001g0231 a0001c0001t0001g0232 a0001c0001t0001g0233 |
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 | a0001c0001t0001g0231 a0001c0001t0001g0232 a0001c0001t0001g0233 |
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 | 59 | a0001c0001t0001g0009 a0001c0001t0001g0011 a0001c0001t0001g0012 others(56): Show |
59 | HG01168.hp1 HG01169.hp2 HG01255.hp2 others(56): 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 | a0001c0001t0001g0228 a0001c0001t0001g0229 a0001c0001t0001g0230 |
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 | a0001c0001t0001g0231 | 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 | a0001c0001t0001g0291 a0001c0001t0001g0292 a0001c0001t0001g0293 others(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 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0006 |
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 | a0001c0001t0001g0289 a0001c0001t0001g0290 a0001c0001t0001g0291 others(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 | a0001c0001t0001g0229 a0001c0001t0001g0230 |
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 | a0001c0001t0001g0231 a0001c0001t0001g0232 a0001c0001t0001g0233 |
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 | a0001c0001t0001g0010 | 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 | a0001c0001t0001g0234 | 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 | a0001c0001t0001g0274 a0001c0001t0001g0275 a0001c0001t0001g0276 others(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 | 58 | a0001c0001t0001g0009 a0001c0001t0001g0235 a0001c0001t0001g0236 others(55): Show |
58 | HG01168.hp1 HG01169.hp2 HG01243.hp2 others(55): 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 | a0001c0001t0001g0009 | 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 | a0001c0001t0001g0279 a0001c0001t0001g0280 a0001c0001t0001g0281 others(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 | a0001c0001t0001g0008 | 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 | a0001c0001t0001g0007 | 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 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0006 |
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 | a0001c0001t0001g0289 a0001c0001t0001g0290 a0001c0001t0001g0291 others(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 | a0001c0001t0001g0003 | 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 | a0001c0001t0001g0002 | 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 | a0001c0001t0001g0295 | 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 | a0001c0001t0001g0296 a0001c0001t0001g0297 a0001c0001t0001g0298 others(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 | a0001c0001t0001g0302 | 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 | a0001c0001t0001g0303 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.-18+24C>T | MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 1/9 | chr2 | 32010918 |