Item | Value |
---|---|
geneid | 254956 |
ensemblid | ENSG00000185681.13 |
hgncid | 17841 |
symbol | MORN5 |
name | MORN repeat containing 5 |
refseq_nuc | NM_198469.4 |
refseq_prot | NP_940871.2 |
ensembl_nuc | ENST00000373764.8 |
ensembl_prot | ENSP00000362869.3 |
mane_status | MANE Select |
chr | chr9 |
start | 122159908 |
end | 122200083 |
strand | + |
ver | v1.2 |
region | chr9:122159908-122200083 |
region5000 | chr9:122154908-122205083 |
regionname0 | MORN5_chr9_122159908_122200083 |
regionname5000 | MORN5_chr9_122154908_122205083 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 161 | 385 | 92 | 72 | 162 | 14 | 43 | 124 | MORN5_chr9_122154908_122205083 | MORN5 | MEYTG others(156): Show |
chr9 | 122154908 | 122205083 |
a0002 | 0/0 | 161 | 3 | 0 | 0 | 0 | 2 | 1 | 0 | MORN5_chr9_122154908_122205083 | MORN5 | MEYTG others(156): Show |
chr9 | 122154908 | 122205083 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 483 | 347 | 65 | 66 | 162 | 13 | 39 | MORN5_chr9_122154908_122205083 | MORN5 | ATGGA others(478): Show |
chr9 | 122154908 | 122205083 | ||
a0001c0002 | 0/0 | 483 | 19 | 12 | 3 | 0 | 0 | 4 | MORN5_chr9_122154908_122205083 | MORN5 | ATGGA others(478): Show |
chr9 | 122154908 | 122205083 | ||
a0001c0003 | 0/0 | 483 | 16 | 15 | 1 | 0 | 0 | 0 | MORN5_chr9_122154908_122205083 | MORN5 | ATGGA others(478): Show |
chr9 | 122154908 | 122205083 | ||
a0001c0005 | 0/0 | 483 | 3 | 0 | 2 | 0 | 1 | 0 | MORN5_chr9_122154908_122205083 | MORN5 | ATGGA others(478): Show |
chr9 | 122154908 | 122205083 | ||
a0002c0004 | 0/0 | 483 | 3 | 0 | 0 | 0 | 2 | 1 | MORN5_chr9_122154908_122205083 | MORN5 | ATGGA others(478): Show |
chr9 | 122154908 | 122205083 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 1/1 | 703 | 338 | 56 | 66 | 162 | 13 | 39 | MORN5_chr9_122154908_122205083 | MORN5 | GTCAT others(698): Show |
chr9 | 122154908 | 122205083 |
a0001c0001t0002 | 0/0 | 703 | 4 | 4 | 0 | 0 | 0 | 0 | MORN5_chr9_122154908_122205083 | MORN5 | GTCAT others(698): Show |
chr9 | 122154908 | 122205083 |
a0001c0001t0003 | 0/0 | 703 | 3 | 3 | 0 | 0 | 0 | 0 | MORN5_chr9_122154908_122205083 | MORN5 | GTCAT others(698): Show |
chr9 | 122154908 | 122205083 |
a0001c0001t0004 | 0/0 | 703 | 1 | 1 | 0 | 0 | 0 | 0 | MORN5_chr9_122154908_122205083 | MORN5 | GTCAT others(698): Show |
chr9 | 122154908 | 122205083 |
a0001c0001t0006 | 0/0 | 703 | 1 | 1 | 0 | 0 | 0 | 0 | MORN5_chr9_122154908_122205083 | MORN5 | GTCAT others(698): Show |
chr9 | 122154908 | 122205083 |
a0001c0002t0001 | 0/0 | 703 | 14 | 7 | 3 | 0 | 0 | 4 | MORN5_chr9_122154908_122205083 | MORN5 | GTCAT others(698): Show |
chr9 | 122154908 | 122205083 |
a0001c0002t0002 | 0/0 | 703 | 3 | 3 | 0 | 0 | 0 | 0 | MORN5_chr9_122154908_122205083 | MORN5 | GTCAT others(698): Show |
chr9 | 122154908 | 122205083 |
a0001c0002t0004 | 0/0 | 703 | 1 | 1 | 0 | 0 | 0 | 0 | MORN5_chr9_122154908_122205083 | MORN5 | GTCAT others(698): Show |
chr9 | 122154908 | 122205083 |
a0001c0002t0005 | 0/0 | 703 | 1 | 1 | 0 | 0 | 0 | 0 | MORN5_chr9_122154908_122205083 | MORN5 | GTCAT others(698): Show |
chr9 | 122154908 | 122205083 |
a0001c0003t0001 | 0/0 | 703 | 16 | 15 | 1 | 0 | 0 | 0 | MORN5_chr9_122154908_122205083 | MORN5 | GTCAT others(698): Show |
chr9 | 122154908 | 122205083 |
a0001c0005t0001 | 0/0 | 703 | 3 | 0 | 2 | 0 | 1 | 0 | MORN5_chr9_122154908_122205083 | MORN5 | GTCAT others(698): Show |
chr9 | 122154908 | 122205083 |
a0002c0004t0001 | 0/0 | 703 | 3 | 0 | 0 | 0 | 2 | 1 | MORN5_chr9_122154908_122205083 | MORN5 | GTCAT others(698): Show |
chr9 | 122154908 | 122205083 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 8 | 0 | 0 | 6 | 2 | 0 | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
a0001c0001t0001g0002 | 0/0 | 5 | 1 | 1 | 2 | 1 | 0 | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
a0001c0001t0001g0003 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
a0001c0001t0001g0004 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
a0001c0001t0001g0005 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
a0001c0001t0001g0006 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
a0001c0001t0001g0007 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
a0001c0001t0001g0008 | 0/0 | 3 | 0 | 2 | 1 | 0 | 0 | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
a0001c0001t0001g0010 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
a0001c0001t0001g0011 | 0/0 | 3 | 0 | 0 | 0 | 0 | 3 | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
a0001c0001t0001g0012 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
a0001c0001t0001g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
a0001c0001t0001g0014 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
a0001c0001t0001g0015 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
a0001c0001t0001g0016 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
a0001c0001t0001g0017 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
a0001c0001t0001g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
a0001c0001t0001g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
a0001c0001t0001g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
a0001c0001t0001g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
a0001c0001t0001g0022 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
a0001c0001t0001g0023 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
a0001c0001t0001g0024 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
a0001c0001t0001g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
a0001c0001t0001g0026 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
a0001c0001t0001g0027 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
a0001c0001t0001g0029 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
a0001c0001t0001g0031 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
a0001c0001t0001g0032 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
a0001c0001t0001g0033 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
a0001c0001t0001g0034 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
a0001c0001t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
a0001c0001t0001g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
a0001c0001t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
a0001c0001t0001g0039 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
a0001c0001t0001g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
a0001c0001t0001g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
a0001c0001t0001g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
a0001c0001t0001g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
a0001c0001t0001g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
a0001c0001t0001g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
a0001c0001t0001g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
a0001c0001t0001g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
a0001c0001t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
a0001c0001t0001g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
a0001c0001t0001g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
a0001c0001t0001g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
a0001c0001t0001g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
a0001c0001t0001g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
a0001c0001t0001g0112 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
a0001c0001t0001g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
a0001c0001t0001g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
a0001c0001t0001g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
a0001c0001t0001g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
a0001c0001t0001g0133 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
a0001c0001t0001g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
a0001c0001t0001g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
a0001c0001t0001g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
a0001c0001t0001g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
a0001c0001t0001g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
a0001c0001t0001g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
a0001c0001t0001g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
a0001c0001t0001g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
a0001c0001t0001g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
a0001c0001t0001g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
a0001c0001t0001g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
a0001c0001t0001g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
a0001c0001t0001g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
a0001c0001t0001g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
a0001c0001t0001g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
a0001c0001t0001g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
a0001c0001t0001g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
a0001c0001t0001g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
a0001c0001t0001g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
a0001c0001t0001g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
a0001c0001t0001g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
a0001c0001t0001g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
a0001c0001t0001g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
a0001c0001t0001g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
a0001c0001t0001g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
a0001c0001t0001g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
a0001c0001t0001g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
a0001c0001t0001g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
a0001c0001t0001g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
a0001c0001t0001g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
a0001c0001t0001g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
a0001c0001t0001g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
a0001c0001t0001g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
a0001c0001t0001g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
a0001c0001t0001g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
a0001c0001t0001g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
a0001c0001t0001g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
a0001c0001t0001g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
a0001c0001t0001g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
a0001c0001t0001g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
a0001c0001t0001g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
a0001c0001t0001g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
a0001c0001t0001g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
a0001c0001t0001g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
a0001c0001t0001g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
a0001c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
a0001c0001t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
a0001c0001t0001g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
a0001c0001t0001g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
a0001c0001t0001g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
a0001c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
a0001c0001t0001g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
a0001c0001t0001g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
a0001c0001t0001g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
a0001c0001t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
a0001c0001t0001g0269 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
a0001c0001t0001g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
a0001c0001t0001g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
a0001c0001t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
a0001c0001t0001g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
a0001c0001t0001g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
a0001c0001t0001g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
a0001c0001t0001g0276 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
a0001c0001t0001g0277 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
a0001c0001t0001g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
a0001c0001t0001g0279 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
a0001c0001t0001g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
a0001c0001t0001g0281 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
a0001c0001t0001g0282 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
a0001c0001t0001g0283 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
a0001c0001t0001g0284 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
a0001c0001t0001g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
a0001c0001t0001g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
a0001c0001t0001g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
a0001c0001t0001g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
a0001c0001t0001g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
a0001c0001t0001g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
a0001c0001t0001g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
a0001c0001t0001g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
a0001c0001t0001g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
a0001c0001t0001g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
a0001c0001t0001g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
a0001c0001t0001g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
a0001c0001t0001g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
a0001c0001t0001g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
a0001c0001t0001g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
a0001c0001t0001g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
a0001c0001t0001g0304 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
a0001c0001t0001g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
a0001c0001t0001g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
a0001c0001t0001g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
a0001c0001t0001g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
a0001c0001t0002g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
a0001c0001t0002g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
a0001c0001t0002g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
a0001c0001t0002g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
a0001c0001t0003g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
a0001c0001t0003g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
a0001c0001t0003g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
a0001c0001t0004g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
a0001c0001t0006g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
a0001c0002t0001g0028 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
a0001c0002t0001g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
a0001c0002t0001g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
a0001c0002t0001g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
a0001c0002t0001g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
a0001c0002t0001g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
a0001c0002t0001g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
a0001c0002t0001g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
a0001c0002t0001g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
a0001c0002t0001g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
a0001c0002t0001g0327 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
a0001c0002t0001g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
a0001c0002t0001g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
a0001c0002t0002g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
a0001c0002t0002g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
a0001c0002t0002g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
a0001c0002t0004g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
a0001c0002t0005g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
a0001c0003t0001g0035 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
a0001c0003t0001g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
a0001c0003t0001g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
a0001c0003t0001g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
a0001c0003t0001g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
a0001c0003t0001g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
a0001c0003t0001g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
a0001c0003t0001g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
a0001c0003t0001g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
a0001c0003t0001g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
a0001c0003t0001g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
a0001c0003t0001g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
a0001c0003t0001g0320 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
a0001c0003t0001g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
a0001c0003t0001g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
a0001c0005t0001g0009 | 0/0 | 3 | 0 | 2 | 0 | 1 | 0 | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
a0002c0004t0001g0030 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
a0002c0004t0001g0253 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0001 | g0002 | EUR | GBR | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
HG00099 | hp2 | a0001 | c0001 | t0001 | g0125 | EUR | GBR | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
HG00140 | hp1 | a0001 | c0001 | t0001 | g0127 | EUR | GBR | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
HG00140 | hp2 | a0001 | c0001 | t0001 | g0111 | EUR | GBR | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
HG00280 | hp1 | a0001 | c0005 | t0001 | g0009 | EUR | FIN | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
HG00280 | hp2 | a0001 | c0001 | t0001 | g0027 | EUR | FIN | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
HG00408 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | CHS | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
HG00408 | hp2 | a0001 | c0001 | t0001 | g0213 | EAS | CHS | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
HG00423 | hp1 | a0001 | c0001 | t0001 | g0056 | EAS | CHS | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
HG00423 | hp2 | a0001 | c0001 | t0001 | g0202 | EAS | CHS | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
HG00438 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | CHS | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
HG00438 | hp2 | a0001 | c0001 | t0001 | g0038 | EAS | CHS | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
HG00544 | hp1 | a0001 | c0001 | t0001 | g0020 | EAS | CHS | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
HG00544 | hp2 | a0001 | c0001 | t0001 | g0232 | EAS | CHS | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
HG00558 | hp1 | a0001 | c0001 | t0001 | g0172 | EAS | CHS | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
HG00558 | hp2 | a0001 | c0001 | t0001 | g0165 | EAS | CHS | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
HG00597 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
HG00597 | hp2 | a0001 | c0001 | t0001 | g0217 | EAS | CHS | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
HG00621 | hp1 | a0001 | c0001 | t0001 | g0228 | EAS | CHS | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
HG00621 | hp2 | a0001 | c0001 | t0001 | g0159 | EAS | CHS | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
HG00639 | hp1 | a0001 | c0001 | t0001 | g0304 | AMR | PUR | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
HG00639 | hp2 | a0001 | c0001 | t0001 | g0029 | AMR | PUR | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
HG00642 | hp1 | a0001 | c0001 | t0001 | g0177 | AMR | PUR | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
HG00642 | hp2 | a0001 | c0001 | t0001 | g0027 | AMR | PUR | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
HG00735 | hp1 | a0001 | c0001 | t0001 | g0086 | AMR | PUR | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
HG00735 | hp2 | a0001 | c0001 | t0001 | g0029 | AMR | PUR | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
HG00738 | hp1 | a0001 | c0001 | t0001 | g0256 | AMR | PUR | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
HG00738 | hp2 | a0001 | c0001 | t0001 | g0235 | AMR | PUR | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
HG00741 | hp1 | a0001 | c0001 | t0001 | g0262 | AMR | PUR | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
HG00741 | hp2 | a0001 | c0001 | t0001 | g0226 | AMR | PUR | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
HG01069 | hp1 | a0001 | c0001 | t0001 | g0259 | AMR | PUR | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
HG01069 | hp2 | a0001 | c0001 | t0001 | g0121 | AMR | PUR | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
HG01070 | hp1 | a0001 | c0001 | t0001 | g0083 | AMR | PUR | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
HG01070 | hp2 | a0001 | c0001 | t0001 | g0185 | AMR | PUR | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
HG01071 | hp1 | a0001 | c0001 | t0001 | g0024 | AMR | PUR | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
HG01071 | hp2 | a0001 | c0001 | t0001 | g0270 | AMR | PUR | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
HG01074 | hp1 | a0001 | c0001 | t0001 | g0264 | AMR | PUR | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
HG01074 | hp2 | a0001 | c0001 | t0001 | g0203 | AMR | PUR | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
HG01081 | hp1 | a0001 | c0001 | t0001 | g0243 | AMR | PUR | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
HG01081 | hp2 | a0001 | c0001 | t0001 | g0178 | AMR | PUR | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
HG01106 | hp1 | a0001 | c0001 | t0001 | g0100 | AMR | PUR | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
HG01106 | hp2 | a0001 | c0001 | t0001 | g0199 | AMR | PUR | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
HG01109 | hp1 | a0001 | c0001 | t0001 | g0090 | AMR | PUR | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
HG01109 | hp2 | a0001 | c0001 | t0001 | g0209 | AMR | PUR | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
HG01167 | hp1 | a0001 | c0001 | t0001 | g0212 | AMR | PUR | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
HG01167 | hp2 | a0001 | c0001 | t0001 | g0278 | AMR | PUR | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
HG01168 | hp1 | a0001 | c0001 | t0001 | g0174 | AMR | PUR | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
HG01168 | hp2 | a0001 | c0005 | t0001 | g0009 | AMR | PUR | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
HG01169 | hp1 | a0001 | c0005 | t0001 | g0009 | AMR | PUR | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
HG01169 | hp2 | a0001 | c0001 | t0001 | g0224 | AMR | PUR | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
HG01175 | hp1 | a0001 | c0001 | t0001 | g0223 | AMR | PUR | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
HG01175 | hp2 | a0001 | c0001 | t0001 | g0114 | AMR | PUR | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
HG01192 | hp1 | a0001 | c0001 | t0001 | g0031 | AMR | PUR | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
HG01192 | hp2 | a0001 | c0001 | t0001 | g0024 | AMR | PUR | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
HG01243 | hp1 | a0001 | c0002 | t0001 | g0327 | AMR | PUR | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
HG01243 | hp2 | a0001 | c0001 | t0001 | g0260 | AMR | PUR | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
HG01255 | hp1 | a0001 | c0001 | t0001 | g0032 | AMR | CLM | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
HG01255 | hp2 | a0001 | c0001 | t0001 | g0244 | AMR | CLM | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
HG01256 | hp1 | a0001 | c0001 | t0001 | g0015 | AMR | CLM | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
HG01256 | hp2 | a0001 | c0001 | t0001 | g0126 | AMR | CLM | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
HG01258 | hp1 | a0001 | c0002 | t0001 | g0106 | AMR | CLM | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
HG01258 | hp2 | a0001 | c0001 | t0001 | g0015 | AMR | CLM | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
HG01261 | hp1 | a0001 | c0001 | t0001 | g0266 | AMR | CLM | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
HG01261 | hp2 | a0001 | c0001 | t0001 | g0034 | AMR | CLM | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
HG01346 | hp1 | a0001 | c0001 | t0001 | g0147 | AMR | CLM | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
HG01346 | hp2 | a0001 | c0001 | t0001 | g0204 | AMR | CLM | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
HG01358 | hp1 | a0001 | c0001 | t0001 | g0031 | AMR | CLM | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
HG01358 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
HG01361 | hp1 | a0001 | c0001 | t0001 | g0017 | AMR | CLM | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
HG01361 | hp2 | a0001 | c0001 | t0001 | g0023 | AMR | CLM | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
HG01433 | hp1 | a0001 | c0001 | t0001 | g0234 | AMR | CLM | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
HG01433 | hp2 | a0001 | c0001 | t0001 | g0008 | AMR | CLM | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
HG01496 | hp1 | a0001 | c0001 | t0001 | g0242 | AMR | CLM | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
HG01496 | hp2 | a0001 | c0003 | t0001 | g0320 | AMR | CLM | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
HG01515 | hp1 | a0002 | c0004 | t0001 | g0030 | EUR | IBS | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
HG01515 | hp2 | a0001 | c0001 | t0001 | g0084 | EUR | IBS | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
HG01516 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | IBS | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
HG01516 | hp2 | a0001 | c0001 | t0001 | g0283 | EUR | IBS | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
HG01517 | hp1 | a0002 | c0004 | t0001 | g0253 | EUR | IBS | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
HG01517 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | IBS | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
HG01891 | hp1 | a0001 | c0001 | t0002 | g0323 | AFR | ACB | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
HG01891 | hp2 | a0001 | c0001 | t0001 | g0034 | AFR | ACB | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
HG01928 | hp1 | a0001 | c0001 | t0001 | g0099 | AMR | PEL | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
HG01928 | hp2 | a0001 | c0001 | t0001 | g0287 | AMR | PEL | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
HG01934 | hp1 | a0001 | c0002 | t0001 | g0105 | AMR | PEL | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
HG01934 | hp2 | a0001 | c0001 | t0001 | g0145 | AMR | PEL | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
HG01975 | hp1 | a0001 | c0001 | t0001 | g0146 | AMR | PEL | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
HG01975 | hp2 | a0001 | c0001 | t0001 | g0274 | AMR | PEL | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
HG01978 | hp1 | a0001 | c0001 | t0001 | g0275 | AMR | PEL | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
HG01978 | hp2 | a0001 | c0001 | t0001 | g0096 | AMR | PEL | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
HG01981 | hp1 | a0001 | c0001 | t0001 | g0016 | AMR | PEL | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
HG01981 | hp2 | a0001 | c0001 | t0001 | g0097 | AMR | PEL | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
HG01993 | hp1 | a0001 | c0001 | t0001 | g0017 | AMR | PEL | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
HG01993 | hp2 | a0001 | c0001 | t0001 | g0191 | AMR | PEL | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
HG02004 | hp1 | a0001 | c0001 | t0001 | g0058 | AMR | PEL | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
HG02004 | hp2 | a0001 | c0001 | t0001 | g0143 | AMR | PEL | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
HG02015 | hp1 | a0001 | c0001 | t0001 | g0149 | EAS | KHV | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
HG02015 | hp2 | a0001 | c0001 | t0001 | g0331 | EAS | KHV | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
HG02027 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | KHV | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
HG02027 | hp2 | a0001 | c0001 | t0001 | g0218 | EAS | KHV | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
HG02055 | hp1 | a0001 | c0001 | t0002 | g0317 | AFR | ACB | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
HG02055 | hp2 | a0001 | c0003 | t0001 | g0314 | AFR | ACB | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
HG02056 | hp1 | a0001 | c0001 | t0001 | g0180 | EAS | KHV | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
HG02056 | hp2 | a0001 | c0001 | t0001 | g0210 | EAS | KHV | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
HG02071 | hp1 | a0001 | c0001 | t0001 | g0129 | EAS | KHV | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
HG02071 | hp2 | a0001 | c0001 | t0001 | g0020 | EAS | KHV | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
HG02080 | hp1 | a0001 | c0001 | t0001 | g0118 | EAS | KHV | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
HG02080 | hp2 | a0001 | c0001 | t0001 | g0119 | EAS | KHV | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
HG02083 | hp1 | a0001 | c0001 | t0001 | g0051 | EAS | KHV | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
HG02083 | hp2 | a0001 | c0001 | t0001 | g0240 | EAS | KHV | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
HG02132 | hp1 | a0001 | c0001 | t0001 | g0057 | EAS | KHV | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
HG02132 | hp2 | a0001 | c0001 | t0001 | g0272 | EAS | KHV | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
HG02135 | hp1 | a0001 | c0001 | t0001 | g0215 | EAS | KHV | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
HG02135 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
HG02145 | hp1 | a0001 | c0001 | t0001 | g0201 | AFR | ACB | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
HG02145 | hp2 | a0001 | c0001 | t0001 | g0247 | AFR | ACB | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
HG02155 | hp1 | a0001 | c0001 | t0001 | g0128 | EAS | CDX | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
HG02155 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CDX | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
HG02165 | hp1 | a0001 | c0001 | t0001 | g0221 | EAS | CDX | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
HG02165 | hp2 | a0001 | c0001 | t0001 | g0183 | EAS | CDX | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
HG02257 | hp1 | a0001 | c0001 | t0001 | g0296 | AFR | ACB | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
HG02257 | hp2 | a0001 | c0001 | t0001 | g0082 | AFR | ACB | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
HG02258 | hp1 | a0001 | c0001 | t0001 | g0251 | AFR | ACB | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
HG02258 | hp2 | a0001 | c0001 | t0001 | g0301 | AFR | ACB | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
HG02273 | hp1 | a0001 | c0001 | t0001 | g0008 | AMR | PEL | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
HG02273 | hp2 | a0001 | c0001 | t0001 | g0098 | AMR | PEL | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
HG02280 | hp1 | a0001 | c0003 | t0001 | g0035 | AFR | ACB | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
HG02280 | hp2 | a0001 | c0001 | t0001 | g0091 | AFR | ACB | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
HG02451 | hp1 | a0001 | c0001 | t0001 | g0182 | AFR | ACB | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
HG02451 | hp2 | a0001 | c0001 | t0001 | g0158 | AFR | ACB | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
HG02523 | hp1 | a0001 | c0001 | t0001 | g0131 | EAS | KHV | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
HG02523 | hp2 | a0001 | c0001 | t0001 | g0219 | EAS | KHV | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
HG02572 | hp1 | a0001 | c0001 | t0001 | g0298 | AFR | GWD | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
HG02572 | hp2 | a0001 | c0003 | t0001 | g0308 | AFR | GWD | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
HG02602 | hp1 | a0001 | c0001 | t0001 | g0207 | SAS | PJL | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
HG02602 | hp2 | a0001 | c0001 | t0001 | g0022 | SAS | PJL | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
HG02615 | hp1 | a0001 | c0001 | t0001 | g0157 | AFR | GWD | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
HG02615 | hp2 | a0001 | c0002 | t0002 | g0088 | AFR | GWD | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
HG02622 | hp1 | a0001 | c0001 | t0001 | g0290 | AFR | GWD | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
HG02622 | hp2 | a0001 | c0002 | t0001 | g0092 | AFR | GWD | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
HG02630 | hp1 | a0001 | c0002 | t0005 | g0087 | AFR | GWD | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
HG02630 | hp2 | a0001 | c0003 | t0001 | g0319 | AFR | GWD | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
HG02683 | hp1 | a0001 | c0001 | t0001 | g0281 | SAS | PJL | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
HG02683 | hp2 | a0001 | c0001 | t0001 | g0124 | SAS | PJL | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
HG02698 | hp1 | a0001 | c0001 | t0001 | g0161 | SAS | PJL | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
HG02698 | hp2 | a0001 | c0001 | t0001 | g0110 | SAS | PJL | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
HG02717 | hp1 | a0001 | c0001 | t0001 | g0208 | AFR | GWD | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
HG02717 | hp2 | a0001 | c0001 | t0001 | g0245 | AFR | GWD | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
HG02723 | hp1 | a0001 | c0003 | t0001 | g0321 | AFR | GWD | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
HG02723 | hp2 | a0001 | c0001 | t0004 | g0326 | AFR | GWD | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
HG02735 | hp1 | a0001 | c0001 | t0001 | g0039 | SAS | PJL | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
HG02735 | hp2 | a0001 | c0001 | t0001 | g0236 | SAS | PJL | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
HG02738 | hp1 | a0001 | c0001 | t0001 | g0045 | SAS | PJL | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
HG02738 | hp2 | a0001 | c0001 | t0001 | g0196 | SAS | PJL | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
HG02809 | hp1 | a0001 | c0001 | t0001 | g0303 | AFR | GWD | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
HG02809 | hp2 | a0001 | c0003 | t0001 | g0035 | AFR | GWD | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
HG02818 | hp1 | a0001 | c0003 | t0001 | g0309 | AFR | GWD | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
HG02818 | hp2 | a0001 | c0001 | t0001 | g0246 | AFR | GWD | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
HG02886 | hp1 | a0001 | c0001 | t0003 | g0289 | AFR | GWD | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
HG02886 | hp2 | a0001 | c0001 | t0001 | g0295 | AFR | GWD | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
HG02895 | hp1 | a0001 | c0001 | t0001 | g0186 | AFR | GWD | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
HG02895 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | GWD | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
HG02896 | hp1 | a0001 | c0003 | t0001 | g0315 | AFR | GWD | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
HG02896 | hp2 | a0001 | c0001 | t0006 | g0288 | AFR | GWD | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
HG02897 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | GWD | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
HG02897 | hp2 | a0001 | c0003 | t0001 | g0310 | AFR | GWD | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
HG02922 | hp1 | a0001 | c0001 | t0001 | g0033 | AFR | ESN | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
HG02922 | hp2 | a0001 | c0001 | t0001 | g0249 | AFR | ESN | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
HG02965 | hp1 | a0001 | c0002 | t0001 | g0329 | AFR | ESN | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
HG02965 | hp2 | a0001 | c0001 | t0001 | g0033 | AFR | ESN | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
HG02970 | hp1 | a0001 | c0003 | t0001 | g0316 | AFR | ESN | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
HG02970 | hp2 | a0001 | c0001 | t0001 | g0300 | AFR | ESN | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
HG02976 | hp1 | a0001 | c0001 | t0001 | g0294 | AFR | ESN | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
HG02976 | hp2 | a0001 | c0001 | t0001 | g0297 | AFR | ESN | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
HG03017 | hp1 | a0001 | c0001 | t0001 | g0062 | SAS | PJL | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
HG03017 | hp2 | a0001 | c0002 | t0001 | g0028 | SAS | PJL | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
HG03041 | hp1 | a0001 | c0001 | t0003 | g0291 | AFR | GWD | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
HG03041 | hp2 | a0001 | c0002 | t0001 | g0328 | AFR | GWD | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
HG03098 | hp1 | a0001 | c0001 | t0001 | g0037 | AFR | MSL | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
HG03098 | hp2 | a0001 | c0001 | t0001 | g0238 | AFR | MSL | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
HG03130 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | ESN | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
HG03130 | hp2 | a0001 | c0001 | t0001 | g0225 | AFR | ESN | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
HG03139 | hp1 | a0001 | c0001 | t0001 | g0010 | AFR | ESN | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
HG03139 | hp2 | a0001 | c0001 | t0002 | g0322 | AFR | ESN | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
HG03209 | hp1 | a0001 | c0001 | t0001 | g0115 | AFR | MSL | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
HG03209 | hp2 | a0001 | c0003 | t0001 | g0311 | AFR | MSL | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
HG03225 | hp1 | a0001 | c0001 | t0001 | g0198 | AFR | MSL | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
HG03225 | hp2 | a0001 | c0001 | t0003 | g0075 | AFR | MSL | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
HG03239 | hp1 | a0001 | c0001 | t0001 | g0220 | SAS | PJL | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
HG03239 | hp2 | a0001 | c0001 | t0001 | g0263 | SAS | PJL | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
HG03453 | hp1 | a0001 | c0001 | t0001 | g0061 | AFR | MSL | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
HG03453 | hp2 | a0001 | c0001 | t0002 | g0324 | AFR | MSL | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
HG03486 | hp1 | a0001 | c0001 | t0001 | g0292 | AFR | MSL | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
HG03486 | hp2 | a0001 | c0001 | t0001 | g0305 | AFR | MSL | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
HG03490 | hp1 | a0001 | c0001 | t0001 | g0014 | SAS | PJL | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
HG03490 | hp2 | a0001 | c0001 | t0001 | g0200 | SAS | PJL | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
HG03491 | hp1 | a0001 | c0001 | t0001 | g0026 | SAS | PJL | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
HG03491 | hp2 | a0001 | c0002 | t0001 | g0102 | SAS | PJL | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
HG03492 | hp1 | a0001 | c0001 | t0001 | g0026 | SAS | PJL | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
HG03492 | hp2 | a0001 | c0001 | t0001 | g0014 | SAS | PJL | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
HG03516 | hp1 | a0001 | c0001 | t0001 | g0195 | AFR | ESN | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
HG03516 | hp2 | a0001 | c0002 | t0002 | g0094 | AFR | ESN | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
HG03540 | hp1 | a0001 | c0003 | t0001 | g0318 | AFR | GWD | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
HG03540 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | GWD | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
HG03579 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | MSL | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
HG03579 | hp2 | a0001 | c0001 | t0001 | g0299 | AFR | MSL | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
HG03654 | hp1 | a0001 | c0001 | t0001 | g0284 | SAS | PJL | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
HG03654 | hp2 | a0001 | c0001 | t0001 | g0269 | SAS | PJL | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
HG03688 | hp1 | a0001 | c0002 | t0001 | g0108 | SAS | STU | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
HG03688 | hp2 | a0001 | c0001 | t0001 | g0167 | SAS | STU | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
HG03704 | hp1 | a0001 | c0001 | t0001 | g0282 | SAS | PJL | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
HG03704 | hp2 | a0001 | c0001 | t0001 | g0150 | SAS | PJL | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
HG03710 | hp1 | a0001 | c0001 | t0001 | g0276 | SAS | PJL | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
HG03710 | hp2 | a0002 | c0004 | t0001 | g0030 | SAS | PJL | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
HG03831 | hp1 | a0001 | c0001 | t0001 | g0254 | SAS | BEB | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
HG03831 | hp2 | a0001 | c0001 | t0001 | g0237 | SAS | BEB | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
HG03834 | hp1 | a0001 | c0001 | t0001 | g0193 | SAS | BEB | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
HG03834 | hp2 | a0001 | c0001 | t0001 | g0059 | SAS | BEB | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
HG03927 | hp1 | a0001 | c0001 | t0001 | g0022 | SAS | BEB | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
HG03927 | hp2 | a0001 | c0001 | t0001 | g0152 | SAS | BEB | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
HG03942 | hp1 | a0001 | c0001 | t0001 | g0109 | SAS | BEB | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
HG03942 | hp2 | a0001 | c0002 | t0001 | g0028 | SAS | BEB | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
HG04115 | hp1 | a0001 | c0001 | t0001 | g0011 | SAS | STU | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
HG04115 | hp2 | a0001 | c0001 | t0001 | g0095 | SAS | STU | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
HG04184 | hp1 | a0001 | c0001 | t0001 | g0011 | SAS | BEB | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
HG04184 | hp2 | a0001 | c0001 | t0001 | g0176 | SAS | BEB | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
HG04228 | hp1 | a0001 | c0001 | t0001 | g0060 | SAS | STU | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
HG04228 | hp2 | a0001 | c0001 | t0001 | g0279 | SAS | STU | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
NA18522 | hp1 | a0001 | c0001 | t0001 | g0010 | AFR | YRI | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
NA18522 | hp2 | a0001 | c0001 | t0001 | g0089 | AFR | YRI | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
NA18747 | hp1 | a0001 | c0001 | t0001 | g0048 | EAS | CHB | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
NA18747 | hp2 | a0001 | c0001 | t0001 | g0148 | EAS | CHB | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
NA18906 | hp1 | a0001 | c0001 | t0001 | g0179 | AFR | YRI | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
NA18906 | hp2 | a0001 | c0002 | t0001 | g0103 | AFR | YRI | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
NA18939 | hp1 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
NA18939 | hp2 | a0001 | c0001 | t0001 | g0155 | EAS | JPT | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
NA18940 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
NA18940 | hp2 | a0001 | c0001 | t0001 | g0216 | EAS | JPT | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
NA18941 | hp1 | a0001 | c0001 | t0001 | g0077 | EAS | JPT | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
NA18941 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
NA18942 | hp1 | a0001 | c0001 | t0001 | g0169 | EAS | JPT | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
NA18942 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
NA18943 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
NA18943 | hp2 | a0001 | c0001 | t0001 | g0211 | EAS | JPT | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
NA18944 | hp1 | a0001 | c0001 | t0001 | g0135 | EAS | JPT | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
NA18944 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
NA18948 | hp1 | a0001 | c0001 | t0001 | g0268 | EAS | JPT | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
NA18948 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
NA18949 | hp1 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
NA18949 | hp2 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
NA18952 | hp1 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
NA18952 | hp2 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
NA18953 | hp1 | a0001 | c0001 | t0001 | g0214 | EAS | JPT | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
NA18953 | hp2 | a0001 | c0001 | t0001 | g0132 | EAS | JPT | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
NA18954 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
NA18954 | hp2 | a0001 | c0001 | t0001 | g0231 | EAS | JPT | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
NA18957 | hp1 | a0001 | c0001 | t0001 | g0229 | EAS | JPT | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
NA18957 | hp2 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
NA18960 | hp1 | a0001 | c0001 | t0001 | g0230 | EAS | JPT | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
NA18960 | hp2 | a0001 | c0001 | t0001 | g0257 | EAS | JPT | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
NA18961 | hp1 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
NA18961 | hp2 | a0001 | c0001 | t0001 | g0190 | EAS | JPT | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
NA18964 | hp1 | a0001 | c0001 | t0001 | g0189 | EAS | JPT | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
NA18964 | hp2 | a0001 | c0001 | t0001 | g0197 | EAS | JPT | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
NA18966 | hp1 | a0001 | c0001 | t0001 | g0227 | EAS | JPT | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
NA18966 | hp2 | a0001 | c0001 | t0001 | g0073 | EAS | JPT | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
NA18968 | hp1 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
NA18968 | hp2 | a0001 | c0001 | t0001 | g0071 | EAS | JPT | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
NA18971 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
NA18971 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
NA18972 | hp1 | a0001 | c0001 | t0001 | g0067 | EAS | JPT | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
NA18972 | hp2 | a0001 | c0001 | t0001 | g0188 | EAS | JPT | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
NA18973 | hp1 | a0001 | c0001 | t0001 | g0175 | EAS | JPT | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
NA18973 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
NA18974 | hp1 | a0001 | c0001 | t0001 | g0047 | EAS | JPT | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
NA18974 | hp2 | a0001 | c0001 | t0001 | g0184 | EAS | JPT | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
NA18975 | hp1 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
NA18975 | hp2 | a0001 | c0001 | t0001 | g0205 | EAS | JPT | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
NA18979 | hp1 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
NA18979 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
NA18980 | hp1 | a0001 | c0001 | t0001 | g0280 | EAS | JPT | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
NA18980 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
NA18981 | hp1 | a0001 | c0001 | t0001 | g0153 | EAS | JPT | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
NA18981 | hp2 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
NA18982 | hp1 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
NA18982 | hp2 | a0001 | c0001 | t0001 | g0050 | EAS | JPT | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
NA18983 | hp1 | a0001 | c0001 | t0001 | g0068 | EAS | JPT | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
NA18983 | hp2 | a0001 | c0001 | t0001 | g0081 | EAS | JPT | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
NA18984 | hp1 | a0001 | c0001 | t0001 | g0122 | EAS | JPT | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
NA18984 | hp2 | a0001 | c0001 | t0001 | g0261 | EAS | JPT | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
NA18986 | hp1 | a0001 | c0001 | t0001 | g0307 | EAS | JPT | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
NA18986 | hp2 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
NA18992 | hp1 | a0001 | c0001 | t0001 | g0043 | EAS | JPT | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
NA18992 | hp2 | a0001 | c0001 | t0001 | g0160 | EAS | JPT | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
NA18993 | hp1 | a0001 | c0001 | t0001 | g0054 | EAS | JPT | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
NA18993 | hp2 | a0001 | c0001 | t0001 | g0137 | EAS | JPT | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
NA18994 | hp1 | a0001 | c0001 | t0001 | g0306 | EAS | JPT | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
NA18994 | hp2 | a0001 | c0001 | t0001 | g0052 | EAS | JPT | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
NA18995 | hp1 | a0001 | c0001 | t0001 | g0072 | EAS | JPT | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
NA18995 | hp2 | a0001 | c0001 | t0001 | g0194 | EAS | JPT | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
NA18997 | hp1 | a0001 | c0001 | t0001 | g0181 | EAS | JPT | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
NA18997 | hp2 | a0001 | c0001 | t0001 | g0064 | EAS | JPT | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
NA18998 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
NA18998 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
NA18999 | hp1 | a0001 | c0001 | t0001 | g0222 | EAS | JPT | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
NA18999 | hp2 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
NA19001 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
NA19001 | hp2 | a0001 | c0001 | t0001 | g0265 | EAS | JPT | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
NA19003 | hp1 | a0001 | c0001 | t0001 | g0116 | EAS | JPT | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
NA19003 | hp2 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
NA19005 | hp1 | a0001 | c0001 | t0001 | g0273 | EAS | JPT | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
NA19005 | hp2 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
NA19009 | hp1 | a0001 | c0001 | t0001 | g0044 | EAS | JPT | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
NA19009 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
NA19012 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
NA19012 | hp2 | a0001 | c0001 | t0001 | g0066 | EAS | JPT | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
NA19030 | hp1 | a0001 | c0001 | t0001 | g0285 | AFR | LWK | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
NA19030 | hp2 | a0001 | c0001 | t0001 | g0293 | AFR | LWK | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
NA19054 | hp1 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
NA19054 | hp2 | a0001 | c0001 | t0001 | g0187 | EAS | JPT | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
NA19056 | hp1 | a0001 | c0001 | t0001 | g0162 | EAS | JPT | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
NA19056 | hp2 | a0001 | c0001 | t0001 | g0123 | EAS | JPT | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
NA19057 | hp1 | a0001 | c0001 | t0001 | g0233 | EAS | JPT | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
NA19057 | hp2 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
NA19058 | hp1 | a0001 | c0001 | t0001 | g0049 | EAS | JPT | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
NA19058 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
NA19060 | hp1 | a0001 | c0001 | t0001 | g0076 | EAS | JPT | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
NA19060 | hp2 | a0001 | c0001 | t0001 | g0164 | EAS | JPT | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
NA19063 | hp1 | a0001 | c0001 | t0001 | g0255 | EAS | JPT | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
NA19063 | hp2 | a0001 | c0001 | t0001 | g0078 | EAS | JPT | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
NA19064 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
NA19064 | hp2 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
NA19065 | hp1 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
NA19065 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
NA19068 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
NA19068 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
NA19070 | hp1 | a0001 | c0001 | t0001 | g0070 | EAS | JPT | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
NA19070 | hp2 | a0001 | c0001 | t0001 | g0117 | EAS | JPT | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
NA19074 | hp1 | a0001 | c0001 | t0001 | g0063 | EAS | JPT | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
NA19074 | hp2 | a0001 | c0001 | t0001 | g0053 | EAS | JPT | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
NA19076 | hp1 | a0001 | c0001 | t0001 | g0074 | EAS | JPT | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
NA19076 | hp2 | a0001 | c0001 | t0001 | g0271 | EAS | JPT | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
NA19079 | hp1 | a0001 | c0001 | t0001 | g0267 | EAS | JPT | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
NA19079 | hp2 | a0001 | c0001 | t0001 | g0055 | EAS | JPT | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
NA19084 | hp1 | a0001 | c0001 | t0001 | g0258 | EAS | JPT | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
NA19084 | hp2 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
NA19085 | hp1 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
NA19085 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
NA19086 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
NA19086 | hp2 | a0001 | c0001 | t0001 | g0241 | EAS | JPT | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
NA19087 | hp1 | a0001 | c0001 | t0001 | g0170 | EAS | JPT | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
NA19087 | hp2 | a0001 | c0001 | t0001 | g0046 | EAS | JPT | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
NA19088 | hp1 | a0001 | c0001 | t0001 | g0173 | EAS | JPT | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
NA19088 | hp2 | a0001 | c0001 | t0001 | g0069 | EAS | JPT | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
NA19090 | hp1 | a0001 | c0001 | t0001 | g0163 | EAS | JPT | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
NA19090 | hp2 | a0001 | c0001 | t0001 | g0192 | EAS | JPT | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
NA19091 | hp1 | a0001 | c0001 | t0001 | g0130 | EAS | JPT | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
NA19091 | hp2 | a0001 | c0001 | t0001 | g0079 | EAS | JPT | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
NA19240 | hp1 | a0001 | c0003 | t0001 | g0312 | AFR | YRI | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
NA19240 | hp2 | a0001 | c0001 | t0001 | g0151 | AFR | YRI | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
NA20129 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | ASW | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
NA20129 | hp2 | a0001 | c0003 | t0001 | g0325 | AFR | ASW | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
NA20752 | hp1 | a0001 | c0001 | t0001 | g0016 | EUR | TSI | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
NA20752 | hp2 | a0001 | c0001 | t0001 | g0277 | EUR | TSI | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
NA20805 | hp1 | a0001 | c0001 | t0001 | g0085 | EUR | TSI | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
NA20805 | hp2 | a0001 | c0001 | t0001 | g0141 | EUR | TSI | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
NA20905 | hp1 | a0001 | c0001 | t0001 | g0011 | SAS | GIH | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
NA20905 | hp2 | a0001 | c0001 | t0001 | g0206 | SAS | GIH | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
HG01123 | hp1 | a0001 | c0001 | t0001 | g0171 | AMR | CLM | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
HG01123 | hp2 | a0001 | c0001 | t0001 | g0065 | AMR | CLM | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
HG02109 | hp1 | a0001 | c0002 | t0001 | g0093 | AFR | ACB | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
HG02109 | hp2 | a0001 | c0001 | t0001 | g0252 | AFR | ACB | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
HG02486 | hp1 | a0001 | c0001 | t0001 | g0286 | AFR | ACB | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
HG02486 | hp2 | a0001 | c0002 | t0002 | g0101 | AFR | ACB | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
HG02559 | hp1 | a0001 | c0003 | t0001 | g0313 | AFR | ACB | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
HG02559 | hp2 | a0001 | c0001 | t0001 | g0010 | AFR | ACB | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
HG03471 | hp1 | a0001 | c0002 | t0004 | g0330 | AFR | MSL | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
HG03471 | hp2 | a0001 | c0001 | t0001 | g0250 | AFR | MSL | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
HG06807 | hp1 | a0001 | c0001 | t0001 | g0302 | AFR | USA | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
HG06807 | hp2 | a0001 | c0001 | t0001 | g0239 | AFR | USA | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
NA18955 | hp1 | a0001 | c0001 | t0001 | g0113 | EAS | JPT | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
NA18955 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
NA20300 | hp1 | a0001 | c0002 | t0001 | g0107 | AFR | USA | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
NA20300 | hp2 | a0001 | c0001 | t0001 | g0248 | AFR | USA | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
NA21309 | hp1 | a0001 | c0001 | t0001 | g0032 | AFR | LWK | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
NA21309 | hp2 | a0001 | c0002 | t0001 | g0104 | AFR | LWK | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0133 | REF | REF | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0112 | REF | REF | MORN5_chr9_122154908_122205083 | MORN5 | chr9 | 122154908 | 122205083 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr9:122169678 | G | T | 1 | a0002 | 3 | HG01515.hp1 HG01517.hp1 HG03710.hp2 |
missense_variant | MODERATE | c.229G>T | p.Asp77Tyr | MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 3/5 | 294/703 | 229/486 | 77/161 | chr9 | 122169678 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr9:122166801 | C | T | 1 | a0001c0003 | 16 | HG01496.hp2 HG02055.hp2 HG02280.hp1 others(13): Show |
synonymous_variant | LOW | c.81C>T | p.Thr27Thr | MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 2/5 | 146/703 | 81/486 | 27/161 | chr9 | 122166801 | |||
chr9:122166846 | C | T | 1 | a0001c0005 | 3 | HG00280.hp1 HG01168.hp2 HG01169.hp1 |
synonymous_variant | LOW | c.126C>T | p.Gly42Gly | MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 2/5 | 191/703 | 126/486 | 42/161 | chr9 | 122166846 | |||
chr9:122166882 | C | T | 1 | a0001c0002 | 19 | HG01243.hp1 HG01258.hp1 HG01934.hp1 others(16): Show |
synonymous_variant | LOW | c.162C>T | p.Tyr54Tyr | MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 2/5 | 227/703 | 162/486 | 54/161 | chr9 | 122166882 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr9:122159928 | A | G | 1 | a0001c0001t0006 | 1 | HG02896.hp2 | 5_prime_UTR_variant | MODIFIER | c.-45A>G | MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 1/5 | 45 | chr9 | 122159928 | ||||||
chr9:122199999 | G | A | 2 | a0001c0001t0002 a0001c0002t0002 |
7 | HG01891.hp1 HG02055.hp1 HG02486.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*68G>A | MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 5/5 | 68 | chr9 | 122199999 | ||||||
chr9:122200030 | G | A | 1 | a0001c0002t0005 | 1 | HG02630.hp1 | 3_prime_UTR_variant | MODIFIER | c.*99G>A | MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 5/5 | 99 | chr9 | 122200030 | ||||||
chr9:122200078 | C | T | 1 | a0001c0001t0003 | 3 | HG02886.hp1 HG03041.hp1 HG03225.hp2 |
3_prime_UTR_variant | MODIFIER | c.*147C>T | MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 5/5 | 147 | chr9 | 122200078 | ||||||
chr9:122200079 | G | T | 2 | a0001c0001t0004 a0001c0002t0004 |
2 | HG02723.hp2 HG03471.hp1 |
3_prime_UTR_variant | MODIFIER | c.*148G>T | MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 5/5 | 148 | chr9 | 122200079 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr9:122160101 | C | T | 1 | a0001c0001t0001g0331 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.47+82C>T | MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 1/4 | chr9 | 122160101 | |||||||
chr9:122160124 | C | T | 5 | a0001c0001t0004g0326 a0001c0002t0001g0327 a0001c0002t0001g0328 others(2): Show |
5 | HG01243.hp1 HG02723.hp2 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.47+105C>T | MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 1/4 | chr9 | 122160124 | |||||||
chr9:122160542 | TTTCC | T | 19 | a0001c0001t0002g0317 a0001c0001t0002g0322 a0001c0001t0002g0323 others(16): Show |
20 | HG01496.hp2 HG01891.hp1 HG02055.hp1 others(17): Show |
intron_variant | MODIFIER | c.47+542_47+545delCC others(2): Show |
MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr9 | 122160542 | ||||||
chr9:122160586 | C | T | 2 | a0001c0001t0001g0306 a0001c0001t0001g0307 |
2 | NA18986.hp1 NA18994.hp1 |
intron_variant | MODIFIER | c.47+567C>T | MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 1/4 | chr9 | 122160586 | |||||||
chr9:122160975 | A | G | 2 | a0001c0001t0001g0304 a0001c0001t0001g0305 |
2 | HG00639.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.47+956A>G | MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 1/4 | chr9 | 122160975 | |||||||
chr9:122161129 | G | C | 59 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0013 others(56): Show |
68 | HG00408.hp1 HG00423.hp1 HG00438.hp2 others(65): Show |
intron_variant | MODIFIER | c.47+1110G>C | MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 1/4 | chr9 | 122161129 | |||||||
chr9:122161171 | C | T | 39 | a0001c0001t0001g0033 a0001c0001t0001g0034 a0001c0001t0001g0290 others(36): Show |
42 | HG00639.hp1 HG01261.hp2 HG01496.hp2 others(39): Show |
intron_variant | MODIFIER | c.47+1152C>T | MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 1/4 | chr9 | 122161171 | |||||||
chr9:122161394 | T | C | 8 | a0001c0001t0001g0089 a0001c0001t0001g0090 a0001c0001t0001g0091 others(5): Show |
8 | HG01109.hp1 HG02109.hp1 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.47+1375T>C | MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 1/4 | chr9 | 122161394 | |||||||
chr9:122161551 | C | T | 19 | a0001c0001t0001g0033 a0001c0001t0001g0034 a0001c0001t0001g0290 others(16): Show |
21 | HG00639.hp1 HG01261.hp2 HG01891.hp2 others(18): Show |
intron_variant | MODIFIER | c.47+1532C>T | MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 1/4 | chr9 | 122161551 | |||||||
chr9:122161687 | C | T | 1 | a0001c0001t0001g0287 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.47+1668C>T | MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 1/4 | chr9 | 122161687 | |||||||
chr9:122161723 | G | A | 1 | a0001c0001t0001g0095 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.47+1704G>A | MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 1/4 | chr9 | 122161723 | |||||||
chr9:122161766 | C | T | 52 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0029 others(49): Show |
60 | HG00639.hp2 HG00735.hp2 HG00738.hp1 others(57): Show |
intron_variant | MODIFIER | c.47+1747C>T | MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 1/4 | chr9 | 122161766 | |||||||
chr9:122162255 | TACTC | T | 6 | a0001c0001t0001g0017 a0001c0001t0001g0096 a0001c0001t0001g0097 others(3): Show |
7 | HG01106.hp1 HG01361.hp1 HG01928.hp1 others(4): Show |
intron_variant | MODIFIER | c.47+2238_47+2241del others(4): Show |
MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr9 | 122162255 | ||||||
chr9:122162264 | A | G | 67 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0016 others(64): Show |
77 | HG00639.hp2 HG00735.hp1 HG00735.hp2 others(74): Show |
intron_variant | MODIFIER | c.47+2245A>G | MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 1/4 | chr9 | 122162264 | |||||||
chr9:122162403 | C | T | 1 | a0001c0001t0001g0239 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.47+2384C>T | MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 1/4 | chr9 | 122162403 | |||||||
chr9:122162412 | C | T | 40 | a0001c0001t0001g0033 a0001c0001t0001g0034 a0001c0001t0001g0238 others(37): Show |
43 | HG00639.hp1 HG01261.hp2 HG01496.hp2 others(40): Show |
intron_variant | MODIFIER | c.47+2393C>T | MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 1/4 | chr9 | 122162412 | |||||||
chr9:122162632 | C | T | 2 | a0001c0001t0001g0080 a0001c0001t0001g0081 |
2 | NA18983.hp2 NA19065.hp1 |
intron_variant | MODIFIER | c.47+2613C>T | MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 1/4 | chr9 | 122162632 | |||||||
chr9:122162663 | C | A | 1 | a0001c0001t0001g0239 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.47+2644C>A | MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 1/4 | chr9 | 122162663 | |||||||
chr9:122162796 | C | T | 1 | a0001c0001t0001g0286 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.47+2777C>T | MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 1/4 | chr9 | 122162796 | |||||||
chr9:122162985 | G | A | 117 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0016 others(114): Show |
130 | HG00639.hp1 HG00639.hp2 HG00735.hp1 others(127): Show |
intron_variant | MODIFIER | c.47+2966G>A | MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 1/4 | chr9 | 122162985 | |||||||
chr9:122163046 | TA | T | 201 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(198): Show |
234 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(231): Show |
intron_variant | MODIFIER | c.47+3038delA | MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr9 | 122163046 | ||||||
chr9:122163326 | C | T | 117 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0016 others(114): Show |
130 | HG00639.hp1 HG00639.hp2 HG00735.hp1 others(127): Show |
intron_variant | MODIFIER | c.47+3307C>T | MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 1/4 | chr9 | 122163326 | |||||||
chr9:122163630 | T | C | 41 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0018 others(38): Show |
52 | HG00438.hp1 HG00544.hp1 HG00558.hp1 others(49): Show |
intron_variant | MODIFIER | c.48-3138T>C | MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 1/4 | chr9 | 122163630 | |||||||
chr9:122163692 | G | A | 1 | a0001c0001t0001g0242 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.48-3076G>A | MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 1/4 | chr9 | 122163692 | |||||||
chr9:122163752 | C | T | 2 | a0001c0001t0001g0157 a0001c0001t0001g0158 |
2 | HG02451.hp2 HG02615.hp1 |
intron_variant | MODIFIER | c.48-3016C>T | MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 1/4 | chr9 | 122163752 | |||||||
chr9:122164098 | A | C | 2 | a0001c0001t0001g0188 a0001c0001t0001g0189 |
2 | NA18964.hp1 NA18972.hp2 |
intron_variant | MODIFIER | c.48-2670A>C | MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 1/4 | chr9 | 122164098 | |||||||
chr9:122164132 | T | C | 2 | a0001c0001t0001g0290 a0001c0001t0003g0289 |
2 | HG02622.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.48-2636T>C | MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 1/4 | chr9 | 122164132 | |||||||
chr9:122164138 | T | C | 4 | a0001c0002t0001g0327 a0001c0002t0001g0328 a0001c0002t0001g0329 others(1): Show |
4 | HG01243.hp1 HG02965.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.48-2630T>C | MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 1/4 | chr9 | 122164138 | |||||||
chr9:122164210 | G | T | 2 | a0001c0001t0001g0302 a0001c0001t0001g0303 |
2 | HG02809.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.48-2558G>T | MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 1/4 | chr9 | 122164210 | |||||||
chr9:122164217 | AAG | A | 325 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(322): Show |
382 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(379): Show |
intron_variant | MODIFIER | c.48-2538_48-2537del others(2): Show |
MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr9 | 122164217 | ||||||
chr9:122164230 | A | C | 20 | a0001c0001t0002g0317 a0001c0001t0002g0322 a0001c0001t0002g0323 others(17): Show |
21 | HG01496.hp2 HG01891.hp1 HG02055.hp1 others(18): Show |
intron_variant | MODIFIER | c.48-2538A>C | MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 1/4 | chr9 | 122164230 | |||||||
chr9:122164279 | A | G | 4 | a0001c0001t0001g0076 a0001c0001t0001g0077 a0001c0001t0001g0078 others(1): Show |
4 | NA18941.hp1 NA19060.hp1 NA19063.hp2 others(1): Show |
intron_variant | MODIFIER | c.48-2489A>G | MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 1/4 | chr9 | 122164279 | |||||||
chr9:122164334 | G | A | 19 | a0001c0001t0001g0033 a0001c0001t0001g0034 a0001c0001t0001g0290 others(16): Show |
21 | HG00639.hp1 HG01261.hp2 HG01891.hp2 others(18): Show |
intron_variant | MODIFIER | c.48-2434G>A | MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 1/4 | chr9 | 122164334 | |||||||
chr9:122164426 | T | C | 1 | a0001c0001t0001g0190 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.48-2342T>C | MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 1/4 | chr9 | 122164426 | |||||||
chr9:122164698 | A | T | 1 | a0001c0001t0001g0187 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.48-2070A>T | MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 1/4 | chr9 | 122164698 | |||||||
chr9:122164700 | G | A | 2 | a0001c0001t0001g0243 a0001c0001t0001g0244 |
2 | HG01081.hp1 HG01255.hp2 |
intron_variant | MODIFIER | c.48-2068G>A | MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 1/4 | chr9 | 122164700 | |||||||
chr9:122164761 | A | G | 1 | a0001c0001t0001g0187 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.48-2007A>G | MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 1/4 | chr9 | 122164761 | |||||||
chr9:122164762 | G | A | 1 | a0001c0001t0001g0187 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.48-2006G>A | MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 1/4 | chr9 | 122164762 | |||||||
chr9:122165112 | C | G | 1 | a0001c0001t0001g0156 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.48-1656C>G | MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 1/4 | chr9 | 122165112 | |||||||
chr9:122165201 | T | A | 1 | a0001c0001t0001g0159 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.48-1567T>A | MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 1/4 | chr9 | 122165201 | |||||||
chr9:122165395 | C | CA | 41 | a0001c0001t0001g0013 a0001c0001t0001g0018 a0001c0001t0001g0019 others(38): Show |
45 | HG00438.hp1 HG00438.hp2 HG00621.hp2 others(42): Show |
intron_variant | MODIFIER | c.48-1348dupA | MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr9 | 122165395 | ||||||
chr9:122165395 | C | CAA | 15 | a0001c0001t0001g0089 a0001c0001t0001g0090 a0001c0001t0001g0091 others(12): Show |
15 | HG01109.hp1 HG02055.hp1 HG02055.hp2 others(12): Show |
intron_variant | MODIFIER | c.48-1349_48-1348dup others(2): Show |
MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr9 | 122165395 | ||||||
chr9:122165395 | C | CAAA | 13 | a0001c0001t0006g0288 a0001c0002t0001g0028 a0001c0002t0001g0102 others(10): Show |
14 | HG01243.hp1 HG01258.hp1 HG01934.hp1 others(11): Show |
intron_variant | MODIFIER | c.48-1350_48-1348dup others(3): Show |
MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr9 | 122165395 | ||||||
chr9:122165395 | CA | C | 51 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0027 others(48): Show |
58 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(55): Show |
intron_variant | MODIFIER | c.48-1348delA | MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr9 | 122165395 | ||||||
chr9:122165395 | CAA | C | 7 | a0001c0001t0001g0233 a0001c0001t0001g0234 a0001c0001t0001g0235 others(4): Show |
7 | HG00738.hp2 HG01433.hp1 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.48-1349_48-1348del others(2): Show |
MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr9 | 122165395 | ||||||
chr9:122165395 | CAAA | C | 17 | a0001c0001t0001g0033 a0001c0001t0001g0034 a0001c0001t0001g0290 others(14): Show |
19 | HG00639.hp1 HG01261.hp2 HG01891.hp2 others(16): Show |
intron_variant | MODIFIER | c.48-1350_48-1348del others(3): Show |
MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr9 | 122165395 | ||||||
chr9:122165395 | CAAAAAA | C | 38 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0029 others(35): Show |
46 | HG00639.hp2 HG00735.hp2 HG00738.hp1 others(43): Show |
intron_variant | MODIFIER | c.48-1353_48-1348del others(6): Show |
MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr9 | 122165395 | ||||||
chr9:122165395 | CAAAAAAA others(3): Show |
C | 1 | a0001c0001t0003g0075 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.48-1357_48-1348del others(10): Show |
MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr9 | 122165395 | ||||||
chr9:122165477 | A | C | 2 | a0001c0001t0001g0251 a0001c0001t0001g0252 |
2 | HG02109.hp2 HG02258.hp1 |
intron_variant | MODIFIER | c.48-1291A>C | MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 1/4 | chr9 | 122165477 | |||||||
chr9:122165487 | A | C | 3 | a0001c0001t0001g0089 a0001c0001t0001g0090 a0001c0001t0001g0091 |
3 | HG01109.hp1 HG02280.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.48-1281A>C | MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 1/4 | chr9 | 122165487 | |||||||
chr9:122165489 | C | T | 19 | a0001c0001t0001g0033 a0001c0001t0001g0034 a0001c0001t0001g0290 others(16): Show |
21 | HG00639.hp1 HG01261.hp2 HG01891.hp2 others(18): Show |
intron_variant | MODIFIER | c.48-1279C>T | MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 1/4 | chr9 | 122165489 | |||||||
chr9:122165612 | A | G | 1 | a0001c0002t0002g0101 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.48-1156A>G | MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 1/4 | chr9 | 122165612 | |||||||
chr9:122165633 | G | C | 8 | a0001c0002t0001g0028 a0001c0002t0001g0102 a0001c0002t0001g0103 others(5): Show |
9 | HG01258.hp1 HG01934.hp1 HG03017.hp2 others(6): Show |
intron_variant | MODIFIER | c.48-1135G>C | MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 1/4 | chr9 | 122165633 | |||||||
chr9:122165727 | C | T | 1 | a0001c0001t0001g0232 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.48-1041C>T | MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 1/4 | chr9 | 122165727 | |||||||
chr9:122165899 | A | T | 2 | a0001c0001t0001g0249 a0001c0001t0001g0250 |
2 | HG02922.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.48-869A>T | MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 1/4 | chr9 | 122165899 | |||||||
chr9:122166016 | C | T | 4 | a0001c0001t0001g0299 a0001c0001t0001g0300 a0001c0001t0001g0301 others(1): Show |
4 | HG02258.hp2 HG02970.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.48-752C>T | MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 1/4 | chr9 | 122166016 | |||||||
chr9:122166184 | C | T | 4 | a0001c0001t0001g0299 a0001c0001t0001g0300 a0001c0001t0001g0301 others(1): Show |
4 | HG02258.hp2 HG02970.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.48-584C>T | MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 1/4 | chr9 | 122166184 | |||||||
chr9:122166233 | G | A | 2 | a0001c0001t0001g0202 a0001c0002t0002g0101 |
2 | HG00423.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.48-535G>A | MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 1/4 | chr9 | 122166233 | |||||||
chr9:122166278 | G | A | 44 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0027 others(41): Show |
51 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(48): Show |
intron_variant | MODIFIER | c.48-490G>A | MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 1/4 | chr9 | 122166278 | |||||||
chr9:122166280 | T | TTATA | 14 | a0001c0002t0001g0028 a0001c0002t0001g0092 a0001c0002t0001g0093 others(11): Show |
15 | HG01258.hp1 HG01934.hp1 HG02109.hp1 others(12): Show |
intron_variant | MODIFIER | c.48-477_48-474dupTA others(2): Show |
MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr9 | 122166280 | ||||||
chr9:122166280 | T | TTATATAT others(5): Show |
19 | a0001c0001t0002g0317 a0001c0001t0002g0322 a0001c0001t0002g0323 others(16): Show |
20 | HG01496.hp2 HG01891.hp1 HG02055.hp1 others(17): Show |
intron_variant | MODIFIER | c.48-485_48-474dupTA others(10): Show |
MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr9 | 122166280 | ||||||
chr9:122166280 | T | TTATATAT others(7): Show |
1 | a0001c0003t0001g0318 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.48-487_48-474dupTA others(12): Show |
MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr9 | 122166280 | ||||||
chr9:122166280 | T | TTATATAT others(27): Show |
4 | a0001c0002t0001g0327 a0001c0002t0001g0328 a0001c0002t0001g0329 others(1): Show |
4 | HG01243.hp1 HG02965.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.48-474_48-473insTA others(32): Show |
MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr9 | 122166280 | ||||||
chr9:122166483 | G | A | 96 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0029 others(93): Show |
106 | HG00639.hp1 HG00639.hp2 HG00735.hp2 others(103): Show |
intron_variant | MODIFIER | c.48-285G>A | MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 1/4 | chr9 | 122166483 | |||||||
chr9:122166574 | A | T | 1 | a0001c0001t0001g0155 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.48-194A>T | MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 1/4 | chr9 | 122166574 | |||||||
chr9:122166684 | G | A | 1 | a0001c0001t0001g0113 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.48-84G>A | MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 1/4 | chr9 | 122166684 | |||||||
chr9:122166727 | G | C | 42 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0029 others(39): Show |
50 | HG00639.hp2 HG00735.hp2 HG00738.hp1 others(47): Show |
intron_variant | MODIFIER | c.48-41G>C | MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 1/4 | chr9 | 122166727 | |||||||
chr9:122166932 | A | G | 97 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0029 others(94): Show |
107 | HG00639.hp1 HG00639.hp2 HG00735.hp2 others(104): Show |
intron_variant | MODIFIER | c.195+17A>G | MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 2/4 | chr9 | 122166932 | |||||||
chr9:122166960 | G | A | 3 | a0001c0001t0001g0007 a0001c0001t0001g0164 a0001c0001t0001g0165 |
5 | HG00558.hp2 NA18943.hp1 NA18944.hp2 others(2): Show |
intron_variant | MODIFIER | c.195+45G>A | MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 2/4 | chr9 | 122166960 | |||||||
chr9:122166984 | A | G | 41 | a0001c0001t0001g0292 a0001c0001t0001g0299 a0001c0001t0001g0300 others(38): Show |
43 | HG00639.hp1 HG01243.hp1 HG01258.hp1 others(40): Show |
intron_variant | MODIFIER | c.195+69A>G | MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 2/4 | chr9 | 122166984 | |||||||
chr9:122167054 | C | A | 1 | a0001c0001t0001g0047 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.195+139C>A | MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 2/4 | chr9 | 122167054 | |||||||
chr9:122167055 | A | C | 1 | a0001c0001t0001g0047 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.195+140A>C | MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 2/4 | chr9 | 122167055 | |||||||
chr9:122167056 | C | CT | 80 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0027 others(77): Show |
88 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(85): Show |
intron_variant | MODIFIER | c.195+158dupT | MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr9 | 122167056 | ||||||
chr9:122167056 | C | CTT | 11 | a0001c0001t0001g0194 a0001c0001t0001g0195 a0001c0001t0001g0228 others(8): Show |
12 | HG00621.hp1 HG01258.hp1 HG01934.hp1 others(9): Show |
intron_variant | MODIFIER | c.195+157_195+158dup others(2): Show |
MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr9 | 122167056 | ||||||
chr9:122167056 | C | T | 1 | a0001c0001t0001g0047 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.195+141C>T | MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 2/4 | chr9 | 122167056 | |||||||
chr9:122167151 | G | A | 58 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0025 others(55): Show |
69 | HG00280.hp1 HG00639.hp2 HG00735.hp2 others(66): Show |
intron_variant | MODIFIER | c.195+236G>A | MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 2/4 | chr9 | 122167151 | |||||||
chr9:122167188 | CG | C | 3 | a0001c0001t0001g0191 a0001c0001t0001g0203 a0001c0001t0001g0204 |
3 | HG01074.hp2 HG01346.hp2 HG01993.hp2 |
intron_variant | MODIFIER | c.195+276delG | MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr9 | 122167188 | ||||||
chr9:122167190 | G | A | 3 | a0001c0001t0001g0191 a0001c0001t0001g0203 a0001c0001t0001g0204 |
3 | HG01074.hp2 HG01346.hp2 HG01993.hp2 |
intron_variant | MODIFIER | c.195+275G>A | MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 2/4 | chr9 | 122167190 | |||||||
chr9:122167193 | G | A | 1 | a0001c0001t0001g0256 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.195+278G>A | MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 2/4 | chr9 | 122167193 | |||||||
chr9:122167284 | G | C | 3 | a0001c0001t0001g0238 a0001c0001t0001g0302 a0001c0001t0001g0303 |
3 | HG02809.hp1 HG03098.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.195+369G>C | MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 2/4 | chr9 | 122167284 | |||||||
chr9:122167331 | G | A | 13 | a0001c0003t0001g0035 a0001c0003t0001g0308 a0001c0003t0001g0309 others(10): Show |
14 | HG02055.hp2 HG02280.hp1 HG02559.hp1 others(11): Show |
intron_variant | MODIFIER | c.195+416G>A | MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 2/4 | chr9 | 122167331 | |||||||
chr9:122167353 | C | CT | 15 | a0001c0001t0001g0010 a0001c0001t0001g0046 a0001c0001t0001g0066 others(12): Show |
17 | HG01346.hp2 HG01978.hp2 HG02145.hp1 others(14): Show |
intron_variant | MODIFIER | c.195+459dupT | MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr9 | 122167353 | ||||||
chr9:122167353 | C | CTTT | 55 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0025 others(52): Show |
66 | HG00280.hp1 HG00639.hp2 HG00735.hp2 others(63): Show |
intron_variant | MODIFIER | c.195+457_195+459dup others(3): Show |
MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr9 | 122167353 | ||||||
chr9:122167353 | CTT | C | 9 | a0001c0001t0001g0292 a0001c0001t0001g0299 a0001c0001t0001g0300 others(6): Show |
9 | HG00639.hp1 HG01496.hp2 HG02258.hp2 others(6): Show |
intron_variant | MODIFIER | c.195+458_195+459del others(2): Show |
MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr9 | 122167353 | ||||||
chr9:122167353 | CTTT | C | 32 | a0001c0001t0006g0288 a0001c0002t0001g0028 a0001c0002t0001g0092 others(29): Show |
34 | HG01243.hp1 HG01258.hp1 HG01934.hp1 others(31): Show |
intron_variant | MODIFIER | c.195+457_195+459del others(3): Show |
MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr9 | 122167353 | ||||||
chr9:122167389 | G | A | 2 | a0001c0001t0001g0205 a0001c0001t0001g0227 |
2 | NA18966.hp1 NA18975.hp2 |
intron_variant | MODIFIER | c.195+474G>A | MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 2/4 | chr9 | 122167389 | |||||||
chr9:122167391 | C | T | 1 | a0001c0001t0001g0283 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.195+476C>T | MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 2/4 | chr9 | 122167391 | |||||||
chr9:122167398 | G | A | 1 | a0001c0001t0001g0293 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.195+483G>A | MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 2/4 | chr9 | 122167398 | |||||||
chr9:122167433 | A | G | 1 | a0001c0001t0001g0255 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.195+518A>G | MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 2/4 | chr9 | 122167433 | |||||||
chr9:122167645 | G | A | 1 | a0001c0001t0001g0260 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.195+730G>A | MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 2/4 | chr9 | 122167645 | |||||||
chr9:122167696 | C | T | 2 | a0001c0001t0001g0027 a0001c0001t0001g0226 |
3 | HG00280.hp2 HG00642.hp2 HG00741.hp2 |
intron_variant | MODIFIER | c.195+781C>T | MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 2/4 | chr9 | 122167696 | |||||||
chr9:122167758 | G | T | 1 | a0001c0001t0001g0116 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.195+843G>T | MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 2/4 | chr9 | 122167758 | |||||||
chr9:122167824 | G | A | 17 | a0001c0002t0001g0028 a0001c0002t0001g0092 a0001c0002t0001g0093 others(14): Show |
18 | HG01243.hp1 HG01258.hp1 HG01934.hp1 others(15): Show |
intron_variant | MODIFIER | c.195+909G>A | MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 2/4 | chr9 | 122167824 | |||||||
chr9:122167825 | GCT | G | 17 | a0001c0002t0001g0028 a0001c0002t0001g0092 a0001c0002t0001g0093 others(14): Show |
18 | HG01243.hp1 HG01258.hp1 HG01934.hp1 others(15): Show |
intron_variant | MODIFIER | c.195+913_195+914del others(2): Show |
MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr9 | 122167825 | ||||||
chr9:122167831 | C | T | 3 | a0001c0002t0002g0088 a0001c0002t0002g0094 a0001c0002t0005g0087 |
3 | HG02615.hp2 HG02630.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.195+916C>T | MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 2/4 | chr9 | 122167831 | |||||||
chr9:122167899 | G | A | 1 | a0001c0001t0001g0196 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.195+984G>A | MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 2/4 | chr9 | 122167899 | |||||||
chr9:122167929 | C | T | 1 | a0001c0001t0001g0180 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.195+1014C>T | MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 2/4 | chr9 | 122167929 | |||||||
chr9:122168002 | A | G | 14 | a0001c0001t0001g0292 a0001c0001t0001g0304 a0001c0001t0001g0305 others(11): Show |
15 | HG00639.hp1 HG01258.hp1 HG01496.hp2 others(12): Show |
intron_variant | MODIFIER | c.195+1087A>G | MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 2/4 | chr9 | 122168002 | |||||||
chr9:122168062 | A | T | 1 | a0001c0001t0001g0182 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.195+1147A>T | MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 2/4 | chr9 | 122168062 | |||||||
chr9:122168082 | T | C | 2 | a0001c0001t0001g0037 a0001c0001t0003g0075 |
2 | HG03098.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.195+1167T>C | MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 2/4 | chr9 | 122168082 | |||||||
chr9:122168122 | G | C | 2 | a0001c0001t0001g0038 a0001c0001t0001g0048 |
2 | HG00438.hp2 NA18747.hp1 |
intron_variant | MODIFIER | c.195+1207G>C | MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 2/4 | chr9 | 122168122 | |||||||
chr9:122168196 | A | T | 1 | a0001c0001t0001g0285 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.195+1281A>T | MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 2/4 | chr9 | 122168196 | |||||||
chr9:122168403 | T | G | 1 | a0001c0001t0001g0010 | 3 | HG02559.hp2 HG03139.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.196-1242T>G | MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 2/4 | chr9 | 122168403 | |||||||
chr9:122168492 | G | T | 62 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0025 others(59): Show |
71 | HG00639.hp1 HG00639.hp2 HG00735.hp2 others(68): Show |
intron_variant | MODIFIER | c.196-1153G>T | MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 2/4 | chr9 | 122168492 | |||||||
chr9:122168537 | A | T | 1 | a0001c0001t0001g0237 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.196-1108A>T | MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 2/4 | chr9 | 122168537 | |||||||
chr9:122168606 | C | T | 5 | a0001c0001t0001g0115 a0001c0001t0001g0150 a0001c0001t0001g0151 others(2): Show |
5 | HG02451.hp2 HG02615.hp1 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.196-1039C>T | MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 2/4 | chr9 | 122168606 | |||||||
chr9:122168611 | G | A | 1 | a0001c0001t0002g0322 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.196-1034G>A | MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 2/4 | chr9 | 122168611 | |||||||
chr9:122168821 | G | C | 1 | a0001c0001t0001g0294 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.196-824G>C | MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 2/4 | chr9 | 122168821 | |||||||
chr9:122169076 | G | A | 3 | a0001c0001t0001g0295 a0001c0001t0001g0296 a0001c0001t0001g0297 |
3 | HG02257.hp1 HG02886.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.196-569G>A | MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 2/4 | chr9 | 122169076 | |||||||
chr9:122169098 | A | C | 1 | a0001c0001t0001g0282 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.196-547A>C | MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 2/4 | chr9 | 122169098 | |||||||
chr9:122169458 | T | G | 2 | a0001c0001t0001g0198 a0001c0001t0001g0201 |
2 | HG02145.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.196-187T>G | MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 2/4 | chr9 | 122169458 | |||||||
chr9:122169462 | C | T | 1 | a0001c0001t0001g0149 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.196-183C>T | MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 2/4 | chr9 | 122169462 | |||||||
chr9:122169538 | T | A | 4 | a0001c0002t0001g0327 a0001c0002t0001g0328 a0001c0002t0001g0329 others(1): Show |
4 | HG01243.hp1 HG02965.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.196-107T>A | MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 2/4 | chr9 | 122169538 | |||||||
chr9:122169888 | A | C | 1 | a0001c0001t0001g0065 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.307+132A>C | MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 3/4 | chr9 | 122169888 | |||||||
chr9:122170016 | C | T | 1 | a0001c0001t0001g0242 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.307+260C>T | MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 3/4 | chr9 | 122170016 | |||||||
chr9:122170018 | G | A | 1 | a0001c0001t0001g0089 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.307+262G>A | MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 3/4 | chr9 | 122170018 | |||||||
chr9:122170079 | C | A | 5 | a0001c0002t0001g0092 a0001c0002t0001g0093 a0001c0002t0002g0088 others(2): Show |
5 | HG02109.hp1 HG02615.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.307+323C>A | MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 3/4 | chr9 | 122170079 | |||||||
chr9:122170274 | C | T | 1 | a0001c0001t0001g0281 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.307+518C>T | MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 3/4 | chr9 | 122170274 | |||||||
chr9:122170298 | G | GA | 74 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0025 others(71): Show |
85 | HG00280.hp1 HG00639.hp1 HG00639.hp2 others(82): Show |
intron_variant | MODIFIER | c.307+559dupA | MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr9 | 122170298 | ||||||
chr9:122170298 | GA | G | 25 | a0001c0001t0001g0299 a0001c0001t0001g0300 a0001c0001t0001g0301 others(22): Show |
27 | HG01258.hp1 HG01934.hp1 HG02055.hp2 others(24): Show |
intron_variant | MODIFIER | c.307+559delA | MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr9 | 122170298 | ||||||
chr9:122170300 | A | G | 8 | a0001c0002t0001g0028 a0001c0002t0001g0102 a0001c0002t0001g0103 others(5): Show |
9 | HG01258.hp1 HG01934.hp1 HG03017.hp2 others(6): Show |
intron_variant | MODIFIER | c.307+544A>G | MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 3/4 | chr9 | 122170300 | |||||||
chr9:122170343 | C | T | 2 | a0001c0001t0001g0032 a0001c0001t0001g0254 |
3 | HG01255.hp1 HG03831.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.307+587C>T | MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 3/4 | chr9 | 122170343 | |||||||
chr9:122170464 | A | T | 1 | a0001c0001t0001g0078 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.307+708A>T | MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 3/4 | chr9 | 122170464 | |||||||
chr9:122170465 | A | C | 1 | a0001c0001t0001g0078 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.307+709A>C | MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 3/4 | chr9 | 122170465 | |||||||
chr9:122170707 | T | G | 103 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0025 others(100): Show |
116 | HG00280.hp1 HG00639.hp1 HG00639.hp2 others(113): Show |
intron_variant | MODIFIER | c.307+951T>G | MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 3/4 | chr9 | 122170707 | |||||||
chr9:122170734 | G | A | 1 | a0001c0001t0001g0068 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.307+978G>A | MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 3/4 | chr9 | 122170734 | |||||||
chr9:122170737 | T | A | 17 | a0001c0002t0001g0028 a0001c0002t0001g0092 a0001c0002t0001g0093 others(14): Show |
18 | HG01243.hp1 HG01258.hp1 HG01934.hp1 others(15): Show |
intron_variant | MODIFIER | c.307+981T>A | MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 3/4 | chr9 | 122170737 | |||||||
chr9:122170738 | C | T | 62 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0025 others(59): Show |
73 | HG00280.hp1 HG00639.hp1 HG00639.hp2 others(70): Show |
intron_variant | MODIFIER | c.307+982C>T | MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 3/4 | chr9 | 122170738 | |||||||
chr9:122170807 | G | A | 4 | a0001c0001t0001g0089 a0001c0001t0001g0090 a0001c0001t0001g0091 others(1): Show |
4 | HG01109.hp1 HG02280.hp2 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.307+1051G>A | MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 3/4 | chr9 | 122170807 | |||||||
chr9:122170852 | A | G | 37 | a0001c0001t0001g0285 a0001c0001t0001g0299 a0001c0001t0001g0300 others(34): Show |
39 | HG01243.hp1 HG01258.hp1 HG01934.hp1 others(36): Show |
intron_variant | MODIFIER | c.307+1096A>G | MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 3/4 | chr9 | 122170852 | |||||||
chr9:122170894 | T | C | 1 | a0001c0001t0001g0278 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.307+1138T>C | MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 3/4 | chr9 | 122170894 | |||||||
chr9:122170903 | C | T | 1 | a0001c0001t0001g0067 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.307+1147C>T | MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 3/4 | chr9 | 122170903 | |||||||
chr9:122171326 | G | A | 2 | a0001c0002t0001g0092 a0001c0002t0001g0093 |
2 | HG02109.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.307+1570G>A | MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 3/4 | chr9 | 122171326 | |||||||
chr9:122171327 | G | A | 1 | a0001c0001t0004g0326 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.307+1571G>A | MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 3/4 | chr9 | 122171327 | |||||||
chr9:122171332 | G | A | 2 | a0001c0002t0001g0103 a0001c0002t0001g0104 |
2 | NA18906.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.307+1576G>A | MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 3/4 | chr9 | 122171332 | |||||||
chr9:122171790 | T | C | 34 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0018 others(31): Show |
44 | HG00438.hp1 HG00544.hp1 HG00558.hp1 others(41): Show |
intron_variant | MODIFIER | c.307+2034T>C | MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 3/4 | chr9 | 122171790 | |||||||
chr9:122171946 | C | CT | 33 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0017 others(30): Show |
34 | HG00438.hp1 HG00438.hp2 HG01106.hp1 others(31): Show |
intron_variant | MODIFIER | c.307+2216dupT | MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr9 | 122171946 | ||||||
chr9:122171946 | C | CTT | 6 | a0001c0001t0001g0017 a0001c0001t0001g0049 a0001c0001t0001g0096 others(3): Show |
6 | HG01361.hp1 HG01978.hp2 HG01981.hp2 others(3): Show |
intron_variant | MODIFIER | c.307+2215_307+2216d others(4): Show |
MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr9 | 122171946 | ||||||
chr9:122171946 | CT | C | 140 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(137): Show |
162 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(159): Show |
intron_variant | MODIFIER | c.307+2216delT | MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr9 | 122171946 | ||||||
chr9:122171947 | T | A | 1 | a0001c0001t0001g0199 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.307+2191T>A | MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 3/4 | chr9 | 122171947 | |||||||
chr9:122171998 | A | G | 1 | a0001c0001t0004g0326 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.307+2242A>G | MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 3/4 | chr9 | 122171998 | |||||||
chr9:122172128 | AT | A | 15 | a0001c0001t0001g0049 a0001c0001t0001g0050 a0001c0001t0001g0097 others(12): Show |
16 | HG01069.hp2 HG01934.hp1 HG01981.hp2 others(13): Show |
intron_variant | MODIFIER | c.308-2352delT | MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr9 | 122172128 | ||||||
chr9:122172166 | G | C | 100 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0025 others(97): Show |
111 | HG00639.hp1 HG00639.hp2 HG00735.hp2 others(108): Show |
intron_variant | MODIFIER | c.308-2330G>C | MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 3/4 | chr9 | 122172166 | |||||||
chr9:122172172 | A | G | 5 | a0001c0001t0004g0326 a0001c0002t0001g0327 a0001c0002t0001g0328 others(2): Show |
5 | HG01243.hp1 HG02723.hp2 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.308-2324A>G | MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 3/4 | chr9 | 122172172 | |||||||
chr9:122172254 | C | A | 71 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0025 others(68): Show |
81 | HG00639.hp2 HG00735.hp2 HG00738.hp1 others(78): Show |
intron_variant | MODIFIER | c.308-2242C>A | MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 3/4 | chr9 | 122172254 | |||||||
chr9:122172442 | C | T | 13 | a0001c0003t0001g0035 a0001c0003t0001g0308 a0001c0003t0001g0309 others(10): Show |
14 | HG02055.hp2 HG02280.hp1 HG02559.hp1 others(11): Show |
intron_variant | MODIFIER | c.308-2054C>T | MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 3/4 | chr9 | 122172442 | |||||||
chr9:122172445 | T | C | 5 | a0001c0001t0001g0292 a0001c0001t0001g0304 a0001c0001t0001g0305 others(2): Show |
5 | HG00639.hp1 HG01496.hp2 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.308-2051T>C | MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 3/4 | chr9 | 122172445 | |||||||
chr9:122172653 | C | T | 1 | a0001c0001t0001g0176 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.308-1843C>T | MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 3/4 | chr9 | 122172653 | |||||||
chr9:122172683 | G | A | 2 | a0001c0001t0001g0198 a0001c0001t0001g0201 |
2 | HG02145.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.308-1813G>A | MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 3/4 | chr9 | 122172683 | |||||||
chr9:122172765 | G | A | 55 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0025 others(52): Show |
64 | HG00639.hp2 HG00735.hp2 HG00738.hp1 others(61): Show |
intron_variant | MODIFIER | c.308-1731G>A | MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 3/4 | chr9 | 122172765 | |||||||
chr9:122172877 | G | A | 100 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0025 others(97): Show |
111 | HG00639.hp1 HG00639.hp2 HG00735.hp2 others(108): Show |
intron_variant | MODIFIER | c.308-1619G>A | MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 3/4 | chr9 | 122172877 | |||||||
chr9:122172939 | A | G | 1 | a0001c0005t0001g0009 | 3 | HG00280.hp1 HG01168.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.308-1557A>G | MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 3/4 | chr9 | 122172939 | |||||||
chr9:122172979 | C | T | 15 | a0001c0002t0001g0092 a0001c0002t0001g0093 a0001c0003t0001g0035 others(12): Show |
16 | HG02055.hp2 HG02109.hp1 HG02280.hp1 others(13): Show |
intron_variant | MODIFIER | c.308-1517C>T | MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 3/4 | chr9 | 122172979 | |||||||
chr9:122172980 | G | A | 5 | a0001c0001t0001g0114 a0001c0001t0001g0121 a0001c0001t0001g0124 others(2): Show |
5 | HG00099.hp2 HG01069.hp2 HG01175.hp2 others(2): Show |
intron_variant | MODIFIER | c.308-1516G>A | MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 3/4 | chr9 | 122172980 | |||||||
chr9:122172990 | T | A | 1 | a0001c0001t0001g0127 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.308-1506T>A | MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 3/4 | chr9 | 122172990 | |||||||
chr9:122173083 | G | A | 2 | a0001c0002t0001g0092 a0001c0002t0001g0093 |
2 | HG02109.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.308-1413G>A | MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 3/4 | chr9 | 122173083 | |||||||
chr9:122173199 | G | T | 11 | a0001c0002t0001g0028 a0001c0002t0001g0102 a0001c0002t0001g0103 others(8): Show |
12 | HG01258.hp1 HG01934.hp1 HG02615.hp2 others(9): Show |
intron_variant | MODIFIER | c.308-1297G>T | MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 3/4 | chr9 | 122173199 | |||||||
chr9:122173400 | T | G | 2 | a0001c0002t0001g0103 a0001c0002t0001g0104 |
2 | NA18906.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.308-1096T>G | MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 3/4 | chr9 | 122173400 | |||||||
chr9:122173431 | T | C | 25 | a0001c0001t0001g0292 a0001c0001t0001g0304 a0001c0001t0001g0305 others(22): Show |
26 | HG00639.hp1 HG01243.hp1 HG01496.hp2 others(23): Show |
intron_variant | MODIFIER | c.308-1065T>C | MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 3/4 | chr9 | 122173431 | |||||||
chr9:122173453 | G | T | 1 | a0001c0001t0001g0225 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.308-1043G>T | MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 3/4 | chr9 | 122173453 | |||||||
chr9:122173470 | G | A | 3 | a0001c0001t0001g0089 a0001c0001t0001g0090 a0001c0001t0001g0091 |
3 | HG01109.hp1 HG02280.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.308-1026G>A | MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 3/4 | chr9 | 122173470 | |||||||
chr9:122173480 | G | A | 2 | a0001c0003t0001g0311 a0001c0003t0001g0316 |
2 | HG02970.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.308-1016G>A | MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 3/4 | chr9 | 122173480 | |||||||
chr9:122173629 | C | T | 1 | a0001c0001t0001g0184 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.308-867C>T | MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 3/4 | chr9 | 122173629 | |||||||
chr9:122173657 | G | A | 1 | a0001c0001t0001g0118 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.308-839G>A | MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 3/4 | chr9 | 122173657 | |||||||
chr9:122173718 | C | T | 1 | a0001c0001t0004g0326 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.308-778C>T | MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 3/4 | chr9 | 122173718 | |||||||
chr9:122173796 | G | T | 1 | a0001c0001t0004g0326 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.308-700G>T | MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 3/4 | chr9 | 122173796 | |||||||
chr9:122173885 | G | C | 2 | a0001c0001t0001g0206 a0001c0001t0001g0207 |
2 | HG02602.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.308-611G>C | MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 3/4 | chr9 | 122173885 | |||||||
chr9:122173896 | C | T | 14 | a0001c0001t0001g0292 a0001c0001t0001g0299 a0001c0001t0001g0300 others(11): Show |
14 | HG00639.hp1 HG01243.hp1 HG01496.hp2 others(11): Show |
intron_variant | MODIFIER | c.308-600C>T | MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 3/4 | chr9 | 122173896 | |||||||
chr9:122173906 | G | A | 10 | a0001c0001t0001g0292 a0001c0001t0001g0304 a0001c0001t0001g0305 others(7): Show |
10 | HG00639.hp1 HG01243.hp1 HG01496.hp2 others(7): Show |
intron_variant | MODIFIER | c.308-590G>A | MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 3/4 | chr9 | 122173906 | |||||||
chr9:122173918 | G | A | 1 | a0001c0001t0001g0128 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.308-578G>A | MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 3/4 | chr9 | 122173918 | |||||||
chr9:122173927 | A | C | 1 | a0001c0001t0001g0236 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.308-569A>C | MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 3/4 | chr9 | 122173927 | |||||||
chr9:122173991 | A | C | 2 | a0001c0001t0001g0123 a0001c0001t0001g0241 |
2 | NA19056.hp2 NA19086.hp2 |
intron_variant | MODIFIER | c.308-505A>C | MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 3/4 | chr9 | 122173991 | |||||||
chr9:122174085 | G | T | 54 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0025 others(51): Show |
64 | HG00280.hp1 HG00738.hp1 HG01069.hp1 others(61): Show |
intron_variant | MODIFIER | c.308-411G>T | MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 3/4 | chr9 | 122174085 | |||||||
chr9:122174118 | C | T | 7 | a0001c0001t0001g0005 a0001c0001t0001g0047 a0001c0001t0001g0050 others(4): Show |
9 | NA18971.hp2 NA18973.hp2 NA18974.hp1 others(6): Show |
intron_variant | MODIFIER | c.308-378C>T | MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 3/4 | chr9 | 122174118 | |||||||
chr9:122174119 | G | A | 8 | a0001c0002t0001g0028 a0001c0002t0001g0102 a0001c0002t0001g0103 others(5): Show |
9 | HG01258.hp1 HG01934.hp1 HG03017.hp2 others(6): Show |
intron_variant | MODIFIER | c.308-377G>A | MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 3/4 | chr9 | 122174119 | |||||||
chr9:122174119 | G | T | 3 | a0001c0001t0001g0089 a0001c0001t0001g0090 a0001c0001t0001g0091 |
3 | HG01109.hp1 HG02280.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.308-377G>T | MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 3/4 | chr9 | 122174119 | |||||||
chr9:122174305 | A | G | 2 | a0001c0002t0001g0103 a0001c0002t0001g0104 |
2 | NA18906.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.308-191A>G | MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 3/4 | chr9 | 122174305 | |||||||
chr9:122174336 | G | A | 15 | a0001c0002t0001g0092 a0001c0002t0001g0093 a0001c0003t0001g0035 others(12): Show |
16 | HG02055.hp2 HG02109.hp1 HG02280.hp1 others(13): Show |
intron_variant | MODIFIER | c.308-160G>A | MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 3/4 | chr9 | 122174336 | |||||||
chr9:122174347 | G | A | 1 | a0001c0001t0001g0264 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.308-149G>A | MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 3/4 | chr9 | 122174347 | |||||||
chr9:122174796 | A | T | 3 | a0001c0001t0001g0089 a0001c0001t0001g0090 a0001c0001t0001g0091 |
3 | HG01109.hp1 HG02280.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.439+169A>T | MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 4/4 | chr9 | 122174796 | |||||||
chr9:122174828 | C | G | 10 | a0001c0001t0001g0292 a0001c0001t0001g0304 a0001c0001t0001g0305 others(7): Show |
10 | HG00639.hp1 HG01243.hp1 HG01496.hp2 others(7): Show |
intron_variant | MODIFIER | c.439+201C>G | MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 4/4 | chr9 | 122174828 | |||||||
chr9:122174833 | T | C | 15 | a0001c0002t0001g0092 a0001c0002t0001g0093 a0001c0003t0001g0035 others(12): Show |
16 | HG02055.hp2 HG02109.hp1 HG02280.hp1 others(13): Show |
intron_variant | MODIFIER | c.439+206T>C | MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 4/4 | chr9 | 122174833 | |||||||
chr9:122174866 | CACTGAAA others(10): Show |
C | 3 | a0001c0001t0001g0089 a0001c0001t0001g0090 a0001c0001t0001g0091 |
3 | HG01109.hp1 HG02280.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.439+243_439+259del others(17): Show |
MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr9 | 122174866 | ||||||
chr9:122174905 | T | A | 1 | a0001c0001t0001g0285 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.439+278T>A | MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 4/4 | chr9 | 122174905 | |||||||
chr9:122174941 | T | C | 4 | a0001c0002t0001g0327 a0001c0002t0001g0328 a0001c0002t0001g0329 others(1): Show |
4 | HG01243.hp1 HG02965.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.439+314T>C | MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 4/4 | chr9 | 122174941 | |||||||
chr9:122175277 | G | A | 1 | a0001c0001t0004g0326 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.439+650G>A | MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 4/4 | chr9 | 122175277 | |||||||
chr9:122175289 | G | A | 5 | a0001c0001t0001g0245 a0001c0001t0001g0246 a0001c0001t0001g0247 others(2): Show |
5 | HG02109.hp2 HG02145.hp2 HG02258.hp1 others(2): Show |
intron_variant | MODIFIER | c.439+662G>A | MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 4/4 | chr9 | 122175289 | |||||||
chr9:122175357 | C | A | 5 | a0001c0001t0001g0292 a0001c0001t0001g0304 a0001c0001t0001g0305 others(2): Show |
5 | HG00639.hp1 HG01496.hp2 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.439+730C>A | MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 4/4 | chr9 | 122175357 | |||||||
chr9:122175444 | G | A | 1 | a0001c0001t0004g0326 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.439+817G>A | MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 4/4 | chr9 | 122175444 | |||||||
chr9:122175457 | C | A | 3 | a0001c0001t0001g0089 a0001c0001t0001g0090 a0001c0001t0001g0091 |
3 | HG01109.hp1 HG02280.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.439+830C>A | MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 4/4 | chr9 | 122175457 | |||||||
chr9:122175545 | C | T | 2 | a0001c0002t0002g0088 a0001c0002t0002g0094 |
2 | HG02615.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.439+918C>T | MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 4/4 | chr9 | 122175545 | |||||||
chr9:122175581 | C | A | 1 | a0001c0001t0004g0326 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.439+954C>A | MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 4/4 | chr9 | 122175581 | |||||||
chr9:122175617 | T | TACAC | 95 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0016 others(92): Show |
107 | HG00280.hp1 HG00639.hp1 HG00735.hp1 others(104): Show |
intron_variant | MODIFIER | c.439+998_439+1001du others(5): Show |
MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr9 | 122175617 | ||||||
chr9:122175714 | G | T | 62 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0016 others(59): Show |
73 | HG00280.hp1 HG00735.hp1 HG00738.hp1 others(70): Show |
intron_variant | MODIFIER | c.439+1087G>T | MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 4/4 | chr9 | 122175714 | |||||||
chr9:122175732 | T | C | 4 | a0001c0001t0001g0299 a0001c0001t0001g0300 a0001c0001t0001g0301 others(1): Show |
4 | HG02258.hp2 HG02970.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.439+1105T>C | MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 4/4 | chr9 | 122175732 | |||||||
chr9:122175852 | T | C | 5 | a0001c0001t0004g0326 a0001c0002t0001g0327 a0001c0002t0001g0328 others(2): Show |
5 | HG01243.hp1 HG02723.hp2 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.439+1225T>C | MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 4/4 | chr9 | 122175852 | |||||||
chr9:122175885 | A | C | 107 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0016 others(104): Show |
120 | HG00280.hp1 HG00639.hp1 HG00735.hp1 others(117): Show |
intron_variant | MODIFIER | c.439+1258A>C | MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 4/4 | chr9 | 122175885 | |||||||
chr9:122175904 | G | T | 4 | a0001c0001t0001g0089 a0001c0001t0001g0090 a0001c0001t0001g0091 others(1): Show |
4 | HG01109.hp1 HG02280.hp2 HG02486.hp2 others(1): Show |
intron_variant | MODIFIER | c.439+1277G>T | MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 4/4 | chr9 | 122175904 | |||||||
chr9:122175924 | T | C | 5 | a0001c0001t0004g0326 a0001c0002t0001g0327 a0001c0002t0001g0328 others(2): Show |
5 | HG01243.hp1 HG02723.hp2 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.439+1297T>C | MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 4/4 | chr9 | 122175924 | |||||||
chr9:122175951 | A | G | 72 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0016 others(69): Show |
83 | HG00280.hp1 HG00639.hp1 HG00735.hp1 others(80): Show |
intron_variant | MODIFIER | c.439+1324A>G | MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 4/4 | chr9 | 122175951 | |||||||
chr9:122175983 | G | A | 2 | a0001c0001t0001g0208 a0001c0001t0001g0209 |
2 | HG01109.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.439+1356G>A | MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 4/4 | chr9 | 122175983 | |||||||
chr9:122175989 | C | T | 1 | a0001c0001t0004g0326 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.439+1362C>T | MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 4/4 | chr9 | 122175989 | |||||||
chr9:122175996 | C | G | 7 | a0001c0001t0001g0017 a0001c0001t0001g0096 a0001c0001t0001g0097 others(4): Show |
8 | HG01106.hp1 HG01361.hp1 HG01928.hp1 others(5): Show |
intron_variant | MODIFIER | c.439+1369C>G | MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 4/4 | chr9 | 122175996 | |||||||
chr9:122176007 | A | G | 96 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0016 others(93): Show |
108 | HG00280.hp1 HG00639.hp1 HG00735.hp1 others(105): Show |
intron_variant | MODIFIER | c.439+1380A>G | MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 4/4 | chr9 | 122176007 | |||||||
chr9:122176035 | G | A | 1 | a0001c0001t0001g0089 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.439+1408G>A | MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 4/4 | chr9 | 122176035 | |||||||
chr9:122176066 | C | T | 13 | a0001c0001t0001g0034 a0001c0001t0001g0298 a0001c0002t0001g0028 others(10): Show |
15 | HG01258.hp1 HG01261.hp2 HG01891.hp2 others(12): Show |
intron_variant | MODIFIER | c.439+1439C>T | MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 4/4 | chr9 | 122176066 | |||||||
chr9:122176098 | A | C | 4 | a0001c0001t0001g0299 a0001c0001t0001g0300 a0001c0001t0001g0301 others(1): Show |
4 | HG02258.hp2 HG02970.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.439+1471A>C | MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 4/4 | chr9 | 122176098 | |||||||
chr9:122176113 | G | A | 1 | a0001c0001t0001g0018 | 2 | NA19001.hp1 NA19065.hp2 |
intron_variant | MODIFIER | c.439+1486G>A | MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 4/4 | chr9 | 122176113 | |||||||
chr9:122176117 | C | CA | 33 | a0001c0001t0001g0049 a0001c0001t0001g0051 a0001c0001t0001g0052 others(30): Show |
33 | HG00639.hp1 HG01123.hp2 HG01243.hp1 others(30): Show |
intron_variant | MODIFIER | c.439+1510dupA | MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr9 | 122176117 | ||||||
chr9:122176117 | CA | C | 10 | a0001c0001t0001g0062 a0001c0001t0001g0125 a0001c0001t0001g0126 others(7): Show |
10 | HG00099.hp2 HG01169.hp2 HG01256.hp2 others(7): Show |
intron_variant | MODIFIER | c.439+1510delA | MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr9 | 122176117 | ||||||
chr9:122176310 | C | T | 5 | a0001c0001t0001g0292 a0001c0001t0001g0304 a0001c0001t0001g0305 others(2): Show |
5 | HG00639.hp1 HG01496.hp2 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.439+1683C>T | MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 4/4 | chr9 | 122176310 | |||||||
chr9:122176361 | T | A | 1 | a0001c0001t0004g0326 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.439+1734T>A | MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 4/4 | chr9 | 122176361 | |||||||
chr9:122176555 | G | A | 1 | a0001c0001t0001g0014 | 2 | HG03490.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.439+1928G>A | MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 4/4 | chr9 | 122176555 | |||||||
chr9:122176594 | A | C | 1 | a0001c0001t0001g0117 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.439+1967A>C | MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 4/4 | chr9 | 122176594 | |||||||
chr9:122176658 | T | C | 7 | a0001c0001t0001g0005 a0001c0001t0001g0047 a0001c0001t0001g0050 others(4): Show |
9 | NA18971.hp2 NA18973.hp2 NA18974.hp1 others(6): Show |
intron_variant | MODIFIER | c.439+2031T>C | MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 4/4 | chr9 | 122176658 | |||||||
chr9:122176739 | G | A | 1 | a0001c0001t0003g0075 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.439+2112G>A | MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 4/4 | chr9 | 122176739 | |||||||
chr9:122176853 | G | A | 5 | a0001c0001t0001g0292 a0001c0001t0001g0304 a0001c0001t0001g0305 others(2): Show |
5 | HG00639.hp1 HG01496.hp2 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.439+2226G>A | MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 4/4 | chr9 | 122176853 | |||||||
chr9:122176874 | T | C | 3 | a0001c0001t0001g0295 a0001c0001t0001g0296 a0001c0001t0001g0297 |
3 | HG02257.hp1 HG02886.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.439+2247T>C | MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 4/4 | chr9 | 122176874 | |||||||
chr9:122176920 | T | C | 1 | a0001c0001t0004g0326 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.439+2293T>C | MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 4/4 | chr9 | 122176920 | |||||||
chr9:122176921 | T | C | 4 | a0001c0001t0001g0299 a0001c0001t0001g0300 a0001c0001t0001g0301 others(1): Show |
4 | HG02258.hp2 HG02970.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.439+2294T>C | MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 4/4 | chr9 | 122176921 | |||||||
chr9:122177044 | TAGA | T | 1 | a0001c0005t0001g0009 | 3 | HG00280.hp1 HG01168.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.439+2420_439+2422d others(5): Show |
MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr9 | 122177044 | ||||||
chr9:122177057 | G | A | 1 | a0001c0001t0001g0014 | 2 | HG03490.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.439+2430G>A | MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 4/4 | chr9 | 122177057 | |||||||
chr9:122177143 | A | C | 1 | a0001c0001t0004g0326 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.439+2516A>C | MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 4/4 | chr9 | 122177143 | |||||||
chr9:122177303 | C | T | 1 | a0001c0001t0001g0205 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.439+2676C>T | MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 4/4 | chr9 | 122177303 | |||||||
chr9:122177307 | T | A | 1 | a0001c0001t0004g0326 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.439+2680T>A | MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 4/4 | chr9 | 122177307 | |||||||
chr9:122177340 | C | T | 1 | a0001c0001t0003g0291 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.439+2713C>T | MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 4/4 | chr9 | 122177340 | |||||||
chr9:122177400 | G | A | 1 | a0001c0001t0004g0326 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.439+2773G>A | MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 4/4 | chr9 | 122177400 | |||||||
chr9:122177445 | A | G | 1 | a0001c0001t0001g0068 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.439+2818A>G | MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 4/4 | chr9 | 122177445 | |||||||
chr9:122177486 | A | G | 1 | a0001c0001t0001g0294 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.439+2859A>G | MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 4/4 | chr9 | 122177486 | |||||||
chr9:122177493 | C | T | 2 | a0001c0001t0001g0251 a0001c0001t0001g0252 |
2 | HG02109.hp2 HG02258.hp1 |
intron_variant | MODIFIER | c.439+2866C>T | MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 4/4 | chr9 | 122177493 | |||||||
chr9:122177496 | G | A | 2 | a0001c0001t0001g0090 a0001c0001t0001g0091 |
2 | HG01109.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.439+2869G>A | MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 4/4 | chr9 | 122177496 | |||||||
chr9:122177546 | C | T | 1 | a0001c0001t0001g0086 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.439+2919C>T | MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 4/4 | chr9 | 122177546 | |||||||
chr9:122177581 | T | C | 6 | a0001c0001t0001g0292 a0001c0001t0001g0304 a0001c0001t0001g0305 others(3): Show |
6 | HG00639.hp1 HG01496.hp2 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.439+2954T>C | MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 4/4 | chr9 | 122177581 | |||||||
chr9:122177589 | T | G | 15 | a0001c0002t0001g0028 a0001c0002t0001g0102 a0001c0002t0001g0103 others(12): Show |
16 | HG01243.hp1 HG01258.hp1 HG01934.hp1 others(13): Show |
intron_variant | MODIFIER | c.439+2962T>G | MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 4/4 | chr9 | 122177589 | |||||||
chr9:122177642 | G | A | 100 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0025 others(97): Show |
110 | HG00639.hp1 HG00738.hp1 HG01069.hp1 others(107): Show |
intron_variant | MODIFIER | c.439+3015G>A | MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 4/4 | chr9 | 122177642 | |||||||
chr9:122177917 | C | A | 2 | a0001c0001t0001g0304 a0001c0001t0001g0305 |
2 | HG00639.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.439+3290C>A | MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 4/4 | chr9 | 122177917 | |||||||
chr9:122177959 | T | G | 18 | a0001c0001t0001g0299 a0001c0001t0001g0300 a0001c0001t0001g0301 others(15): Show |
19 | HG01243.hp1 HG01258.hp1 HG02258.hp2 others(16): Show |
intron_variant | MODIFIER | c.439+3332T>G | MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 4/4 | chr9 | 122177959 | |||||||
chr9:122177998 | C | T | 1 | a0001c0001t0001g0089 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.439+3371C>T | MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 4/4 | chr9 | 122177998 | |||||||
chr9:122178003 | A | C | 1 | a0001c0001t0001g0085 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.439+3376A>C | MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 4/4 | chr9 | 122178003 | |||||||
chr9:122178047 | G | T | 3 | a0001c0001t0001g0145 a0001c0001t0001g0146 a0001c0001t0001g0147 |
3 | HG01346.hp1 HG01934.hp2 HG01975.hp1 |
intron_variant | MODIFIER | c.439+3420G>T | MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 4/4 | chr9 | 122178047 | |||||||
chr9:122178263 | C | T | 2 | a0001c0001t0001g0182 a0001c0001t0001g0186 |
2 | HG02451.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.439+3636C>T | MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 4/4 | chr9 | 122178263 | |||||||
chr9:122178404 | G | A | 1 | a0001c0001t0004g0326 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.439+3777G>A | MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 4/4 | chr9 | 122178404 | |||||||
chr9:122178481 | C | G | 1 | a0001c0001t0001g0175 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.439+3854C>G | MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 4/4 | chr9 | 122178481 | |||||||
chr9:122178546 | G | C | 2 | a0001c0001t0001g0020 a0001c0001t0001g0183 |
3 | HG00544.hp1 HG02071.hp2 HG02165.hp2 |
intron_variant | MODIFIER | c.439+3919G>C | MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 4/4 | chr9 | 122178546 | |||||||
chr9:122178562 | C | A | 1 | a0001c0001t0001g0211 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.439+3935C>A | MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 4/4 | chr9 | 122178562 | |||||||
chr9:122178628 | C | T | 7 | a0001c0002t0001g0028 a0001c0002t0001g0102 a0001c0002t0001g0103 others(4): Show |
8 | HG01258.hp1 HG03017.hp2 HG03491.hp2 others(5): Show |
intron_variant | MODIFIER | c.439+4001C>T | MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 4/4 | chr9 | 122178628 | |||||||
chr9:122178699 | C | G | 4 | a0001c0002t0001g0327 a0001c0002t0001g0328 a0001c0002t0001g0329 others(1): Show |
4 | HG01243.hp1 HG02965.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.439+4072C>G | MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 4/4 | chr9 | 122178699 | |||||||
chr9:122178800 | G | A | 1 | a0001c0001t0001g0176 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.439+4173G>A | MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 4/4 | chr9 | 122178800 | |||||||
chr9:122179018 | G | T | 1 | a0001c0001t0004g0326 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.439+4391G>T | MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 4/4 | chr9 | 122179018 | |||||||
chr9:122179137 | C | T | 1 | a0001c0001t0001g0045 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.439+4510C>T | MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 4/4 | chr9 | 122179137 | |||||||
chr9:122179215 | A | C | 21 | a0001c0001t0001g0299 a0001c0001t0001g0300 a0001c0001t0001g0301 others(18): Show |
22 | HG02055.hp2 HG02109.hp1 HG02258.hp2 others(19): Show |
intron_variant | MODIFIER | c.439+4588A>C | MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 4/4 | chr9 | 122179215 | |||||||
chr9:122179575 | T | G | 105 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0016 others(102): Show |
118 | HG00280.hp1 HG00639.hp1 HG00735.hp1 others(115): Show |
intron_variant | MODIFIER | c.439+4948T>G | MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 4/4 | chr9 | 122179575 | |||||||
chr9:122179636 | A | G | 1 | a0001c0001t0001g0293 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.439+5009A>G | MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 4/4 | chr9 | 122179636 | |||||||
chr9:122179926 | G | A | 5 | a0001c0002t0001g0028 a0001c0002t0001g0102 a0001c0002t0001g0106 others(2): Show |
6 | HG01258.hp1 HG03017.hp2 HG03491.hp2 others(3): Show |
intron_variant | MODIFIER | c.439+5299G>A | MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 4/4 | chr9 | 122179926 | |||||||
chr9:122180003 | G | A | 1 | a0001c0001t0004g0326 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.439+5376G>A | MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 4/4 | chr9 | 122180003 | |||||||
chr9:122180043 | C | G | 1 | a0001c0001t0001g0062 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.439+5416C>G | MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 4/4 | chr9 | 122180043 | |||||||
chr9:122180099 | C | A | 1 | a0001c0003t0001g0318 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.439+5472C>A | MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 4/4 | chr9 | 122180099 | |||||||
chr9:122180108 | T | A | 4 | a0001c0002t0001g0327 a0001c0002t0001g0328 a0001c0002t0001g0329 others(1): Show |
4 | HG01243.hp1 HG02965.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.439+5481T>A | MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 4/4 | chr9 | 122180108 | |||||||
chr9:122180188 | T | TC | 5 | a0001c0002t0001g0028 a0001c0002t0001g0102 a0001c0002t0001g0106 others(2): Show |
6 | HG01258.hp1 HG03017.hp2 HG03491.hp2 others(3): Show |
intron_variant | MODIFIER | c.439+5561_439+5562i others(3): Show |
MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 4/4 | chr9 | 122180188 | |||||||
chr9:122180190 | A | G | 5 | a0001c0002t0001g0028 a0001c0002t0001g0102 a0001c0002t0001g0106 others(2): Show |
6 | HG01258.hp1 HG03017.hp2 HG03491.hp2 others(3): Show |
intron_variant | MODIFIER | c.439+5563A>G | MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 4/4 | chr9 | 122180190 | |||||||
chr9:122180238 | G | A | 1 | a0001c0001t0001g0279 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.439+5611G>A | MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 4/4 | chr9 | 122180238 | |||||||
chr9:122180265 | A | T | 97 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0025 others(94): Show |
107 | HG00639.hp1 HG00738.hp1 HG01069.hp1 others(104): Show |
intron_variant | MODIFIER | c.439+5638A>T | MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 4/4 | chr9 | 122180265 | |||||||
chr9:122180282 | C | CT | 78 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0025 others(75): Show |
90 | HG00280.hp1 HG00738.hp1 HG01069.hp1 others(87): Show |
intron_variant | MODIFIER | c.439+5676dupT | MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr9 | 122180282 | ||||||
chr9:122180282 | C | CTTT | 6 | a0001c0001t0001g0246 a0001c0001t0001g0247 a0001c0001t0001g0249 others(3): Show |
6 | HG02109.hp2 HG02145.hp2 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.439+5674_439+5676d others(5): Show |
MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr9 | 122180282 | ||||||
chr9:122180282 | CT | C | 11 | a0001c0001t0001g0039 a0001c0001t0001g0050 a0001c0001t0001g0053 others(8): Show |
11 | HG00099.hp2 HG01167.hp1 HG02080.hp1 others(8): Show |
intron_variant | MODIFIER | c.439+5676delT | MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr9 | 122180282 | ||||||
chr9:122180309 | G | A | 1 | a0001c0001t0001g0149 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.439+5682G>A | MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 4/4 | chr9 | 122180309 | |||||||
chr9:122180446 | G | A | 1 | a0001c0001t0001g0202 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.439+5819G>A | MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 4/4 | chr9 | 122180446 | |||||||
chr9:122180446 | G | C | 97 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0025 others(94): Show |
107 | HG00639.hp1 HG00738.hp1 HG01069.hp1 others(104): Show |
intron_variant | MODIFIER | c.439+5819G>C | MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 4/4 | chr9 | 122180446 | |||||||
chr9:122180491 | A | G | 97 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0025 others(94): Show |
107 | HG00639.hp1 HG00738.hp1 HG01069.hp1 others(104): Show |
intron_variant | MODIFIER | c.439+5864A>G | MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 4/4 | chr9 | 122180491 | |||||||
chr9:122180528 | C | T | 2 | a0001c0001t0001g0033 a0001c0001t0001g0294 |
3 | HG02922.hp1 HG02965.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.439+5901C>T | MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 4/4 | chr9 | 122180528 | |||||||
chr9:122180529 | G | A | 96 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0025 others(93): Show |
106 | HG00639.hp1 HG00738.hp1 HG01069.hp1 others(103): Show |
intron_variant | MODIFIER | c.439+5902G>A | MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 4/4 | chr9 | 122180529 | |||||||
chr9:122180641 | A | G | 2 | a0001c0001t0001g0290 a0001c0001t0003g0289 |
2 | HG02622.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.439+6014A>G | MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 4/4 | chr9 | 122180641 | |||||||
chr9:122180751 | C | T | 55 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0025 others(52): Show |
63 | HG00738.hp1 HG01069.hp1 HG01071.hp2 others(60): Show |
intron_variant | MODIFIER | c.439+6124C>T | MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 4/4 | chr9 | 122180751 | |||||||
chr9:122180833 | C | A | 1 | a0001c0001t0006g0288 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.439+6206C>A | MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 4/4 | chr9 | 122180833 | |||||||
chr9:122180875 | C | T | 95 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0025 others(92): Show |
105 | HG00639.hp1 HG00738.hp1 HG01069.hp1 others(102): Show |
intron_variant | MODIFIER | c.439+6248C>T | MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 4/4 | chr9 | 122180875 | |||||||
chr9:122180911 | G | T | 1 | a0001c0001t0001g0026 | 2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.439+6284G>T | MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 4/4 | chr9 | 122180911 | |||||||
chr9:122181063 | A | G | 1 | a0001c0001t0001g0045 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.439+6436A>G | MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 4/4 | chr9 | 122181063 | |||||||
chr9:122181263 | C | T | 14 | a0001c0001t0001g0299 a0001c0001t0001g0300 a0001c0001t0001g0301 others(11): Show |
15 | HG01258.hp1 HG02258.hp2 HG02615.hp2 others(12): Show |
intron_variant | MODIFIER | c.439+6636C>T | MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 4/4 | chr9 | 122181263 | |||||||
chr9:122181277 | T | C | 1 | a0001c0001t0001g0278 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.439+6650T>C | MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 4/4 | chr9 | 122181277 | |||||||
chr9:122181290 | C | A | 3 | a0001c0001t0001g0089 a0001c0001t0001g0090 a0001c0001t0001g0091 |
3 | HG01109.hp1 HG02280.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.439+6663C>A | MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 4/4 | chr9 | 122181290 | |||||||
chr9:122181435 | A | G | 43 | a0001c0001t0001g0089 a0001c0001t0001g0090 a0001c0001t0001g0091 others(40): Show |
45 | HG00639.hp1 HG01109.hp1 HG01243.hp1 others(42): Show |
intron_variant | MODIFIER | c.439+6808A>G | MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 4/4 | chr9 | 122181435 | |||||||
chr9:122181472 | G | A | 6 | a0001c0001t0001g0292 a0001c0001t0001g0304 a0001c0001t0001g0305 others(3): Show |
6 | HG00639.hp1 HG01496.hp2 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.439+6845G>A | MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 4/4 | chr9 | 122181472 | |||||||
chr9:122181528 | TA | T | 3 | a0001c0001t0001g0089 a0001c0001t0001g0090 a0001c0001t0001g0091 |
3 | HG01109.hp1 HG02280.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.439+6902delA | MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 4/4 | chr9 | 122181528 | |||||||
chr9:122181616 | G | A | 1 | a0001c0001t0001g0199 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.439+6989G>A | MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 4/4 | chr9 | 122181616 | |||||||
chr9:122181616 | G | T | 1 | a0001c0001t0001g0179 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.439+6989G>T | MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 4/4 | chr9 | 122181616 | |||||||
chr9:122181617 | A | T | 1 | a0001c0001t0001g0179 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.439+6990A>T | MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 4/4 | chr9 | 122181617 | |||||||
chr9:122181633 | A | C | 7 | a0001c0001t0001g0031 a0001c0001t0001g0260 a0001c0001t0001g0266 others(4): Show |
9 | HG01192.hp1 HG01243.hp2 HG01261.hp1 others(6): Show |
intron_variant | MODIFIER | c.439+7006A>C | MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 4/4 | chr9 | 122181633 | |||||||
chr9:122181642 | G | A | 1 | a0001c0001t0004g0326 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.439+7015G>A | MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 4/4 | chr9 | 122181642 | |||||||
chr9:122181878 | C | G | 4 | a0001c0001t0001g0031 a0001c0001t0001g0260 a0001c0001t0001g0275 others(1): Show |
5 | HG01192.hp1 HG01243.hp2 HG01358.hp1 others(2): Show |
intron_variant | MODIFIER | c.439+7251C>G | MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 4/4 | chr9 | 122181878 | |||||||
chr9:122181913 | G | T | 1 | a0001c0001t0001g0195 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.439+7286G>T | MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 4/4 | chr9 | 122181913 | |||||||
chr9:122182270 | C | T | 2 | a0001c0001t0001g0182 a0001c0001t0001g0186 |
2 | HG02451.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.439+7643C>T | MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 4/4 | chr9 | 122182270 | |||||||
chr9:122182300 | T | C | 4 | a0001c0002t0001g0327 a0001c0002t0001g0328 a0001c0002t0001g0329 others(1): Show |
4 | HG01243.hp1 HG02965.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.439+7673T>C | MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 4/4 | chr9 | 122182300 | |||||||
chr9:122182324 | A | G | 33 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0018 others(30): Show |
43 | HG00438.hp1 HG00544.hp1 HG00558.hp1 others(40): Show |
intron_variant | MODIFIER | c.439+7697A>G | MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 4/4 | chr9 | 122182324 | |||||||
chr9:122182377 | T | G | 2 | a0001c0001t0001g0163 a0001c0001t0001g0169 |
2 | NA18942.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.439+7750T>G | MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 4/4 | chr9 | 122182377 | |||||||
chr9:122182577 | C | A | 1 | a0001c0001t0001g0251 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.439+7950C>A | MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 4/4 | chr9 | 122182577 | |||||||
chr9:122182610 | G | A | 1 | a0001c0001t0004g0326 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.439+7983G>A | MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 4/4 | chr9 | 122182610 | |||||||
chr9:122182756 | C | T | 1 | a0001c0001t0001g0027 | 2 | HG00280.hp2 HG00642.hp2 |
intron_variant | MODIFIER | c.439+8129C>T | MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 4/4 | chr9 | 122182756 | |||||||
chr9:122182935 | T | G | 8 | a0001c0001t0001g0299 a0001c0001t0001g0300 a0001c0001t0001g0301 others(5): Show |
8 | HG01243.hp1 HG02258.hp2 HG02965.hp1 others(5): Show |
intron_variant | MODIFIER | c.439+8308T>G | MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 4/4 | chr9 | 122182935 | |||||||
chr9:122183217 | C | T | 1 | a0001c0001t0001g0060 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.439+8590C>T | MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 4/4 | chr9 | 122183217 | |||||||
chr9:122183325 | T | C | 138 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0011 others(135): Show |
161 | HG00280.hp1 HG00438.hp1 HG00544.hp1 others(158): Show |
intron_variant | MODIFIER | c.439+8698T>C | MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 4/4 | chr9 | 122183325 | |||||||
chr9:122183420 | C | T | 1 | a0001c0001t0001g0263 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.439+8793C>T | MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 4/4 | chr9 | 122183420 | |||||||
chr9:122183707 | C | T | 1 | a0001c0001t0001g0073 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.439+9080C>T | MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 4/4 | chr9 | 122183707 | |||||||
chr9:122183742 | A | G | 196 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0007 others(193): Show |
230 | HG00280.hp1 HG00280.hp2 HG00423.hp2 others(227): Show |
intron_variant | MODIFIER | c.439+9115A>G | MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 4/4 | chr9 | 122183742 | |||||||
chr9:122183992 | T | C | 52 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0018 others(49): Show |
65 | HG00438.hp1 HG00544.hp1 HG00558.hp1 others(62): Show |
intron_variant | MODIFIER | c.439+9365T>C | MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 4/4 | chr9 | 122183992 | |||||||
chr9:122184113 | C | A | 1 | a0001c0003t0001g0321 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.439+9486C>A | MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 4/4 | chr9 | 122184113 | |||||||
chr9:122184213 | G | A | 1 | a0001c0001t0001g0233 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.439+9586G>A | MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 4/4 | chr9 | 122184213 | |||||||
chr9:122184217 | G | A | 1 | a0001c0001t0006g0288 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.439+9590G>A | MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 4/4 | chr9 | 122184217 | |||||||
chr9:122184301 | A | G | 21 | a0001c0001t0001g0061 a0001c0001t0001g0089 a0001c0001t0001g0238 others(18): Show |
21 | HG00639.hp1 HG01891.hp1 HG02055.hp1 others(18): Show |
intron_variant | MODIFIER | c.439+9674A>G | MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 4/4 | chr9 | 122184301 | |||||||
chr9:122184466 | T | A | 1 | a0001c0001t0001g0285 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.439+9839T>A | MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 4/4 | chr9 | 122184466 | |||||||
chr9:122184546 | C | T | 2 | a0001c0002t0001g0102 a0001c0002t0001g0108 |
2 | HG03491.hp2 HG03688.hp1 |
intron_variant | MODIFIER | c.439+9919C>T | MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 4/4 | chr9 | 122184546 | |||||||
chr9:122184547 | G | A | 2 | a0001c0001t0001g0170 a0001c0001t0003g0075 |
2 | HG03225.hp2 NA19087.hp1 |
intron_variant | MODIFIER | c.439+9920G>A | MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 4/4 | chr9 | 122184547 | |||||||
chr9:122184682 | TATTTTAT others(3): Show |
T | 1 | a0001c0001t0001g0175 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.439+10065_439+1007 others(14): Show |
MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr9 | 122184682 | ||||||
chr9:122184892 | A | T | 1 | a0001c0001t0001g0297 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.439+10265A>T | MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 4/4 | chr9 | 122184892 | |||||||
chr9:122184904 | C | A | 21 | a0001c0001t0001g0033 a0001c0001t0001g0089 a0001c0001t0001g0238 others(18): Show |
23 | HG00639.hp1 HG01258.hp1 HG02109.hp2 others(20): Show |
intron_variant | MODIFIER | c.439+10277C>A | MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 4/4 | chr9 | 122184904 | |||||||
chr9:122184904 | C | CAAGA | 5 | a0001c0001t0001g0192 a0001c0001t0001g0210 a0001c0001t0001g0213 others(2): Show |
5 | HG00408.hp2 HG02056.hp2 NA18953.hp1 others(2): Show |
intron_variant | MODIFIER | c.439+10287_439+1029 others(8): Show |
MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr9 | 122184904 | ||||||
chr9:122185059 | CT | C | 5 | a0001c0002t0001g0028 a0001c0002t0001g0102 a0001c0002t0001g0106 others(2): Show |
6 | HG01258.hp1 HG03017.hp2 HG03491.hp2 others(3): Show |
intron_variant | MODIFIER | c.439+10442delT | MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr9 | 122185059 | ||||||
chr9:122185126 | G | C | 2 | a0001c0001t0001g0238 a0001c0001t0003g0075 |
2 | HG03098.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.439+10499G>C | MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 4/4 | chr9 | 122185126 | |||||||
chr9:122185181 | AAGTAGCT others(160): Show |
A | 1 | a0001c0001t0001g0161 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.439+10587_439+1075 others(4): Show |
MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr9 | 122185181 | ||||||
chr9:122185233 | T | A | 2 | a0001c0001t0001g0234 a0001c0001t0001g0235 |
2 | HG00738.hp2 HG01433.hp1 |
intron_variant | MODIFIER | c.439+10606T>A | MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 4/4 | chr9 | 122185233 | |||||||
chr9:122185238 | T | C | 1 | a0001c0002t0002g0101 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.439+10611T>C | MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 4/4 | chr9 | 122185238 | |||||||
chr9:122185283 | T | C | 2 | a0001c0002t0001g0106 a0001c0002t0001g0107 |
2 | HG01258.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.439+10656T>C | MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 4/4 | chr9 | 122185283 | |||||||
chr9:122185284 | G | A | 2 | a0001c0002t0001g0106 a0001c0002t0001g0107 |
2 | HG01258.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.439+10657G>A | MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 4/4 | chr9 | 122185284 | |||||||
chr9:122185286 | G | A | 2 | a0001c0002t0001g0106 a0001c0002t0001g0107 |
2 | HG01258.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.439+10659G>A | MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 4/4 | chr9 | 122185286 | |||||||
chr9:122185308 | C | T | 2 | a0001c0002t0001g0106 a0001c0002t0001g0107 |
2 | HG01258.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.439+10681C>T | MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 4/4 | chr9 | 122185308 | |||||||
chr9:122185315 | C | T | 2 | a0001c0002t0001g0106 a0001c0002t0001g0107 |
2 | HG01258.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.439+10688C>T | MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 4/4 | chr9 | 122185315 | |||||||
chr9:122185347 | C | T | 1 | a0001c0003t0001g0321 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.439+10720C>T | MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 4/4 | chr9 | 122185347 | |||||||
chr9:122185348 | G | A | 2 | a0001c0002t0001g0106 a0001c0002t0001g0107 |
2 | HG01258.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.439+10721G>A | MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 4/4 | chr9 | 122185348 | |||||||
chr9:122185379 | T | C | 1 | a0001c0001t0001g0215 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.439+10752T>C | MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 4/4 | chr9 | 122185379 | |||||||
chr9:122185381 | C | T | 2 | a0001c0002t0001g0106 a0001c0002t0001g0107 |
2 | HG01258.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.439+10754C>T | MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 4/4 | chr9 | 122185381 | |||||||
chr9:122185382 | C | T | 2 | a0001c0002t0001g0106 a0001c0002t0001g0107 |
2 | HG01258.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.439+10755C>T | MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 4/4 | chr9 | 122185382 | |||||||
chr9:122185383 | T | C | 2 | a0001c0002t0001g0106 a0001c0002t0001g0107 |
2 | HG01258.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.439+10756T>C | MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 4/4 | chr9 | 122185383 | |||||||
chr9:122185384 | G | A | 2 | a0001c0002t0001g0106 a0001c0002t0001g0107 |
2 | HG01258.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.439+10757G>A | MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 4/4 | chr9 | 122185384 | |||||||
chr9:122185386 | C | A | 2 | a0001c0002t0001g0106 a0001c0002t0001g0107 |
2 | HG01258.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.439+10759C>A | MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 4/4 | chr9 | 122185386 | |||||||
chr9:122185389 | AT | A | 219 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(216): Show |
260 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(257): Show |
intron_variant | MODIFIER | c.439+10773delT | MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr9 | 122185389 | ||||||
chr9:122185395 | TTTTTTGT others(125): Show |
T | 14 | a0001c0001t0001g0089 a0001c0001t0001g0238 a0001c0001t0001g0245 others(11): Show |
14 | HG00639.hp1 HG02109.hp2 HG02145.hp2 others(11): Show |
intron_variant | MODIFIER | c.439+10774_439+1090 others(4): Show |
MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr9 | 122185395 | ||||||
chr9:122185409 | A | T | 2 | a0001c0002t0001g0106 a0001c0002t0001g0107 |
2 | HG01258.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.439+10782A>T | MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 4/4 | chr9 | 122185409 | |||||||
chr9:122185410 | G | T | 2 | a0001c0002t0001g0106 a0001c0002t0001g0107 |
2 | HG01258.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.439+10783G>T | MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 4/4 | chr9 | 122185410 | |||||||
chr9:122185412 | A | T | 2 | a0001c0002t0001g0106 a0001c0002t0001g0107 |
2 | HG01258.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.439+10785A>T | MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 4/4 | chr9 | 122185412 | |||||||
chr9:122185416 | T | A | 2 | a0001c0002t0001g0106 a0001c0002t0001g0107 |
2 | HG01258.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.439+10789T>A | MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 4/4 | chr9 | 122185416 | |||||||
chr9:122185417 | C | CGGGGTTT others(126): Show |
1 | a0001c0001t0001g0176 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.439+10802_439+1093 others(137): Show |
MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr9 | 122185417 | ||||||
chr9:122185417 | CGGGGTTT others(126): Show |
C | 3 | a0001c0002t0001g0028 a0001c0002t0001g0102 a0001c0002t0001g0108 |
4 | HG03017.hp2 HG03491.hp2 HG03688.hp1 others(1): Show |
intron_variant | MODIFIER | c.439+10802_439+1093 others(4): Show |
MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr9 | 122185417 | ||||||
chr9:122185418 | G | A | 2 | a0001c0002t0001g0106 a0001c0002t0001g0107 |
2 | HG01258.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.439+10791G>A | MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 4/4 | chr9 | 122185418 | |||||||
chr9:122185420 | G | A | 2 | a0001c0002t0001g0106 a0001c0002t0001g0107 |
2 | HG01258.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.439+10793G>A | MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 4/4 | chr9 | 122185420 | |||||||
chr9:122185423 | T | C | 2 | a0001c0002t0001g0106 a0001c0002t0001g0107 |
2 | HG01258.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.439+10796T>C | MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 4/4 | chr9 | 122185423 | |||||||
chr9:122185425 | C | T | 2 | a0001c0002t0001g0106 a0001c0002t0001g0107 |
2 | HG01258.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.439+10798C>T | MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 4/4 | chr9 | 122185425 | |||||||
chr9:122185426 | A | G | 2 | a0001c0002t0001g0106 a0001c0002t0001g0107 |
2 | HG01258.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.439+10799A>G | MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 4/4 | chr9 | 122185426 | |||||||
chr9:122185428 | C | T | 2 | a0001c0002t0001g0106 a0001c0002t0001g0107 |
2 | HG01258.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.439+10801C>T | MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 4/4 | chr9 | 122185428 | |||||||
chr9:122185429 | A | C | 2 | a0001c0002t0001g0106 a0001c0002t0001g0107 |
2 | HG01258.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.439+10802A>C | MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 4/4 | chr9 | 122185429 | |||||||
chr9:122185434 | G | C | 2 | a0001c0002t0001g0106 a0001c0002t0001g0107 |
2 | HG01258.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.439+10807G>C | MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 4/4 | chr9 | 122185434 | |||||||
chr9:122185440 | A | C | 2 | a0001c0002t0001g0106 a0001c0002t0001g0107 |
2 | HG01258.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.439+10813A>C | MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 4/4 | chr9 | 122185440 | |||||||
chr9:122185444 | T | A | 2 | a0001c0002t0001g0106 a0001c0002t0001g0107 |
2 | HG01258.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.439+10817T>A | MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 4/4 | chr9 | 122185444 | |||||||
chr9:122185445 | C | G | 2 | a0001c0002t0001g0106 a0001c0002t0001g0107 |
2 | HG01258.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.439+10818C>G | MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 4/4 | chr9 | 122185445 | |||||||
chr9:122185456 | G | C | 2 | a0001c0002t0001g0106 a0001c0002t0001g0107 |
2 | HG01258.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.439+10829G>C | MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 4/4 | chr9 | 122185456 | |||||||
chr9:122185459 | C | T | 2 | a0001c0002t0001g0106 a0001c0002t0001g0107 |
2 | HG01258.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.439+10832C>T | MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 4/4 | chr9 | 122185459 | |||||||
chr9:122185460 | T | G | 2 | a0001c0002t0001g0106 a0001c0002t0001g0107 |
2 | HG01258.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.439+10833T>G | MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 4/4 | chr9 | 122185460 | |||||||
chr9:122185462 | G | A | 2 | a0001c0002t0001g0106 a0001c0002t0001g0107 |
2 | HG01258.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.439+10835G>A | MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 4/4 | chr9 | 122185462 | |||||||
chr9:122185463 | T | A | 2 | a0001c0002t0001g0106 a0001c0002t0001g0107 |
2 | HG01258.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.439+10836T>A | MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 4/4 | chr9 | 122185463 | |||||||
chr9:122185465 | A | C | 2 | a0001c0002t0001g0106 a0001c0002t0001g0107 |
2 | HG01258.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.439+10838A>C | MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 4/4 | chr9 | 122185465 | |||||||
chr9:122185468 | T | C | 4 | a0001c0001t0001g0003 a0001c0001t0001g0186 a0001c0002t0001g0106 others(1): Show |
4 | HG01258.hp1 HG02895.hp1 NA20129.hp1 others(1): Show |
intron_variant | MODIFIER | c.439+10841T>C | MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 4/4 | chr9 | 122185468 | |||||||
chr9:122185470 | C | CCTCCCGG others(14): Show |
2 | a0001c0002t0001g0106 a0001c0002t0001g0107 |
2 | HG01258.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.439+10844_439+1084 others(25): Show |
MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr9 | 122185470 | ||||||
chr9:122185477 | T | C | 2 | a0001c0002t0001g0106 a0001c0002t0001g0107 |
2 | HG01258.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.439+10850T>C | MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 4/4 | chr9 | 122185477 | |||||||
chr9:122185478 | G | A | 2 | a0001c0002t0001g0106 a0001c0002t0001g0107 |
2 | HG01258.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.439+10851G>A | MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 4/4 | chr9 | 122185478 | |||||||
chr9:122185486 | A | G | 2 | a0001c0002t0001g0106 a0001c0002t0001g0107 |
2 | HG01258.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.439+10859A>G | MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 4/4 | chr9 | 122185486 | |||||||
chr9:122185488 | A | G | 2 | a0001c0002t0001g0106 a0001c0002t0001g0107 |
2 | HG01258.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.439+10861A>G | MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 4/4 | chr9 | 122185488 | |||||||
chr9:122185489 | G | T | 2 | a0001c0002t0001g0106 a0001c0002t0001g0107 |
2 | HG01258.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.439+10862G>T | MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 4/4 | chr9 | 122185489 | |||||||
chr9:122185490 | T | A | 2 | a0001c0002t0001g0106 a0001c0002t0001g0107 |
2 | HG01258.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.439+10863T>A | MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 4/4 | chr9 | 122185490 | |||||||
chr9:122185498 | T | C | 2 | a0001c0002t0001g0106 a0001c0002t0001g0107 |
2 | HG01258.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.439+10871T>C | MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 4/4 | chr9 | 122185498 | |||||||
chr9:122185506 | G | A | 2 | a0001c0001t0001g0234 a0001c0001t0001g0235 |
2 | HG00738.hp2 HG01433.hp1 |
intron_variant | MODIFIER | c.439+10879G>A | MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 4/4 | chr9 | 122185506 | |||||||
chr9:122185507 | T | C | 2 | a0001c0002t0001g0106 a0001c0002t0001g0107 |
2 | HG01258.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.439+10880T>C | MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 4/4 | chr9 | 122185507 | |||||||
chr9:122185508 | G | C | 2 | a0001c0002t0001g0106 a0001c0002t0001g0107 |
2 | HG01258.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.439+10881G>C | MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 4/4 | chr9 | 122185508 | |||||||
chr9:122185509 | A | C | 2 | a0001c0002t0001g0106 a0001c0002t0001g0107 |
2 | HG01258.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.439+10882A>C | MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 4/4 | chr9 | 122185509 | |||||||
chr9:122185510 | G | A | 2 | a0001c0002t0001g0106 a0001c0002t0001g0107 |
2 | HG01258.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.439+10883G>A | MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 4/4 | chr9 | 122185510 | |||||||
chr9:122185525 | C | T | 2 | a0001c0002t0001g0106 a0001c0002t0001g0107 |
2 | HG01258.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.439+10898C>T | MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 4/4 | chr9 | 122185525 | |||||||
chr9:122185549 | A | T | 16 | a0001c0001t0001g0089 a0001c0001t0001g0238 a0001c0001t0001g0245 others(13): Show |
16 | HG00639.hp1 HG01258.hp1 HG02109.hp2 others(13): Show |
intron_variant | MODIFIER | c.439+10922A>T | MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 4/4 | chr9 | 122185549 | |||||||
chr9:122185550 | T | C | 16 | a0001c0001t0001g0089 a0001c0001t0001g0238 a0001c0001t0001g0245 others(13): Show |
16 | HG00639.hp1 HG01258.hp1 HG02109.hp2 others(13): Show |
intron_variant | MODIFIER | c.439+10923T>C | MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 4/4 | chr9 | 122185550 | |||||||
chr9:122185562 | G | A | 210 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(207): Show |
247 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(244): Show |
intron_variant | MODIFIER | c.439+10935G>A | MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 4/4 | chr9 | 122185562 | |||||||
chr9:122185603 | G | A | 1 | a0001c0001t0001g0080 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.439+10976G>A | MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 4/4 | chr9 | 122185603 | |||||||
chr9:122185606 | C | T | 57 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0016 others(54): Show |
68 | HG00639.hp2 HG00735.hp1 HG00735.hp2 others(65): Show |
intron_variant | MODIFIER | c.439+10979C>T | MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 4/4 | chr9 | 122185606 | |||||||
chr9:122185728 | T | C | 1 | a0001c0001t0001g0285 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.439+11101T>C | MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 4/4 | chr9 | 122185728 | |||||||
chr9:122185750 | C | A | 9 | a0001c0001t0001g0006 a0001c0001t0001g0054 a0001c0001t0001g0113 others(6): Show |
11 | HG02027.hp1 HG02071.hp1 NA18955.hp1 others(8): Show |
intron_variant | MODIFIER | c.439+11123C>A | MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 4/4 | chr9 | 122185750 | |||||||
chr9:122185833 | G | C | 3 | a0001c0002t0001g0103 a0001c0002t0001g0104 a0001c0003t0001g0321 |
3 | HG02723.hp1 NA18906.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.439+11206G>C | MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 4/4 | chr9 | 122185833 | |||||||
chr9:122185936 | C | T | 1 | a0001c0001t0001g0305 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.439+11309C>T | MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 4/4 | chr9 | 122185936 | |||||||
chr9:122186023 | G | A | 1 | a0001c0001t0001g0062 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.439+11396G>A | MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 4/4 | chr9 | 122186023 | |||||||
chr9:122186041 | G | A | 18 | a0001c0001t0001g0238 a0001c0001t0001g0245 a0001c0001t0001g0246 others(15): Show |
19 | HG00639.hp1 HG01258.hp1 HG02109.hp2 others(16): Show |
intron_variant | MODIFIER | c.439+11414G>A | MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 4/4 | chr9 | 122186041 | |||||||
chr9:122186250 | A | G | 19 | a0001c0001t0001g0089 a0001c0001t0001g0238 a0001c0001t0001g0245 others(16): Show |
20 | HG00639.hp1 HG01258.hp1 HG02109.hp2 others(17): Show |
intron_variant | MODIFIER | c.439+11623A>G | MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 4/4 | chr9 | 122186250 | |||||||
chr9:122186345 | A | C | 1 | a0001c0001t0001g0052 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.439+11718A>C | MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 4/4 | chr9 | 122186345 | |||||||
chr9:122186402 | C | A | 1 | a0001c0001t0001g0244 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.439+11775C>A | MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 4/4 | chr9 | 122186402 | |||||||
chr9:122186423 | C | T | 1 | a0001c0001t0001g0273 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.439+11796C>T | MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 4/4 | chr9 | 122186423 | |||||||
chr9:122186476 | A | G | 1 | a0001c0001t0001g0186 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.439+11849A>G | MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 4/4 | chr9 | 122186476 | |||||||
chr9:122186515 | C | T | 1 | a0001c0001t0001g0254 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.439+11888C>T | MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 4/4 | chr9 | 122186515 | |||||||
chr9:122186598 | C | T | 1 | a0001c0001t0001g0018 | 2 | NA19001.hp1 NA19065.hp2 |
intron_variant | MODIFIER | c.439+11971C>T | MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 4/4 | chr9 | 122186598 | |||||||
chr9:122186704 | C | T | 207 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(204): Show |
244 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(241): Show |
intron_variant | MODIFIER | c.439+12077C>T | MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 4/4 | chr9 | 122186704 | |||||||
chr9:122186751 | G | C | 1 | a0001c0001t0001g0145 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.439+12124G>C | MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 4/4 | chr9 | 122186751 | |||||||
chr9:122186767 | A | G | 211 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(208): Show |
248 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(245): Show |
intron_variant | MODIFIER | c.439+12140A>G | MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 4/4 | chr9 | 122186767 | |||||||
chr9:122186768 | C | G | 1 | a0001c0003t0001g0321 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.439+12141C>G | MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 4/4 | chr9 | 122186768 | |||||||
chr9:122186884 | A | G | 3 | a0001c0002t0001g0103 a0001c0002t0001g0104 a0001c0003t0001g0321 |
3 | HG02723.hp1 NA18906.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.439+12257A>G | MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 4/4 | chr9 | 122186884 | |||||||
chr9:122186911 | C | T | 2 | a0001c0001t0001g0091 a0001c0001t0001g0299 |
2 | HG02280.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.439+12284C>T | MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 4/4 | chr9 | 122186911 | |||||||
chr9:122187046 | G | A | 3 | a0001c0001t0004g0326 a0001c0002t0002g0088 a0001c0002t0002g0094 |
3 | HG02615.hp2 HG02723.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.439+12419G>A | MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 4/4 | chr9 | 122187046 | |||||||
chr9:122187077 | G | T | 193 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(190): Show |
231 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(228): Show |
intron_variant | MODIFIER | c.439+12450G>T | MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 4/4 | chr9 | 122187077 | |||||||
chr9:122187099 | C | T | 2 | a0001c0001t0001g0302 a0001c0001t0001g0303 |
2 | HG02809.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.439+12472C>T | MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 4/4 | chr9 | 122187099 | |||||||
chr9:122187259 | T | C | 135 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0011 others(132): Show |
156 | HG00438.hp1 HG00544.hp1 HG00558.hp1 others(153): Show |
intron_variant | MODIFIER | c.440-12626T>C | MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 4/4 | chr9 | 122187259 | |||||||
chr9:122187322 | G | A | 127 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(124): Show |
153 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(150): Show |
intron_variant | MODIFIER | c.440-12563G>A | MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 4/4 | chr9 | 122187322 | |||||||
chr9:122187377 | C | T | 1 | a0001c0001t0001g0225 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.440-12508C>T | MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 4/4 | chr9 | 122187377 | |||||||
chr9:122187442 | C | G | 1 | a0001c0001t0001g0026 | 2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.440-12443C>G | MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 4/4 | chr9 | 122187442 | |||||||
chr9:122187465 | T | C | 112 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(109): Show |
128 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(125): Show |
intron_variant | MODIFIER | c.440-12420T>C | MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 4/4 | chr9 | 122187465 | |||||||
chr9:122187506 | G | C | 1 | a0001c0001t0001g0196 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.440-12379G>C | MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 4/4 | chr9 | 122187506 | |||||||
chr9:122187683 | A | G | 1 | a0001c0002t0001g0105 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.440-12202A>G | MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 4/4 | chr9 | 122187683 | |||||||
chr9:122187727 | G | A | 1 | a0001c0001t0001g0301 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.440-12158G>A | MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 4/4 | chr9 | 122187727 | |||||||
chr9:122187736 | A | G | 1 | a0001c0001t0001g0284 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.440-12149A>G | MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 4/4 | chr9 | 122187736 | |||||||
chr9:122187842 | G | C | 1 | a0001c0001t0001g0248 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.440-12043G>C | MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 4/4 | chr9 | 122187842 | |||||||
chr9:122187890 | A | G | 1 | a0001c0001t0001g0072 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.440-11995A>G | MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 4/4 | chr9 | 122187890 | |||||||
chr9:122188021 | T | G | 2 | a0001c0001t0001g0302 a0001c0001t0001g0303 |
2 | HG02809.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.440-11864T>G | MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 4/4 | chr9 | 122188021 | |||||||
chr9:122188109 | G | T | 1 | a0001c0001t0001g0170 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.440-11776G>T | MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 4/4 | chr9 | 122188109 | |||||||
chr9:122188154 | T | A | 1 | a0001c0001t0001g0135 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.440-11731T>A | MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 4/4 | chr9 | 122188154 | |||||||
chr9:122188198 | C | T | 5 | a0001c0001t0001g0025 a0001c0001t0001g0196 a0001c0001t0001g0197 others(2): Show |
6 | HG02738.hp2 HG03239.hp2 NA18939.hp1 others(3): Show |
intron_variant | MODIFIER | c.440-11687C>T | MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 4/4 | chr9 | 122188198 | |||||||
chr9:122188477 | A | G | 4 | a0001c0001t0001g0033 a0001c0001t0001g0089 a0001c0001t0001g0294 others(1): Show |
5 | HG02258.hp2 HG02922.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.440-11408A>G | MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 4/4 | chr9 | 122188477 | |||||||
chr9:122188494 | A | C | 5 | a0001c0001t0001g0245 a0001c0001t0001g0246 a0001c0001t0001g0247 others(2): Show |
5 | HG02109.hp2 HG02145.hp2 HG02258.hp1 others(2): Show |
intron_variant | MODIFIER | c.440-11391A>C | MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 4/4 | chr9 | 122188494 | |||||||
chr9:122188531 | G | A | 6 | a0001c0001t0002g0317 a0001c0001t0002g0322 a0001c0001t0002g0323 others(3): Show |
7 | HG01891.hp1 HG02055.hp1 HG02055.hp2 others(4): Show |
intron_variant | MODIFIER | c.440-11354G>A | MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 4/4 | chr9 | 122188531 | |||||||
chr9:122188564 | G | A | 1 | a0001c0002t0001g0092 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.440-11321G>A | MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 4/4 | chr9 | 122188564 | |||||||
chr9:122188630 | G | A | 14 | a0001c0001t0001g0090 a0001c0001t0001g0198 a0001c0001t0001g0201 others(11): Show |
14 | HG01109.hp1 HG01496.hp2 HG02145.hp1 others(11): Show |
intron_variant | MODIFIER | c.440-11255G>A | MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 4/4 | chr9 | 122188630 | |||||||
chr9:122188669 | G | A | 3 | a0001c0001t0001g0068 a0001c0001t0001g0069 a0001c0001t0001g0073 |
3 | NA18966.hp2 NA18983.hp1 NA19088.hp2 |
intron_variant | MODIFIER | c.440-11216G>A | MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 4/4 | chr9 | 122188669 | |||||||
chr9:122188695 | G | A | 1 | a0001c0001t0001g0301 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.440-11190G>A | MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 4/4 | chr9 | 122188695 | |||||||
chr9:122188805 | G | A | 5 | a0001c0001t0001g0208 a0001c0001t0001g0209 a0001c0001t0003g0075 others(2): Show |
5 | HG01109.hp2 HG02630.hp1 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.440-11080G>A | MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 4/4 | chr9 | 122188805 | |||||||
chr9:122189023 | C | T | 1 | a0001c0001t0001g0143 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.440-10862C>T | MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 4/4 | chr9 | 122189023 | |||||||
chr9:122189053 | G | A | 2 | a0001c0001t0001g0024 a0001c0001t0001g0185 |
3 | HG01070.hp2 HG01071.hp1 HG01192.hp2 |
intron_variant | MODIFIER | c.440-10832G>A | MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 4/4 | chr9 | 122189053 | |||||||
chr9:122189345 | G | A | 1 | a0001c0002t0001g0092 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.440-10540G>A | MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 4/4 | chr9 | 122189345 | |||||||
chr9:122189447 | T | A | 206 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(203): Show |
239 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(236): Show |
intron_variant | MODIFIER | c.440-10438T>A | MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 4/4 | chr9 | 122189447 | |||||||
chr9:122189470 | C | A | 7 | a0001c0001t0001g0083 a0001c0001t0001g0114 a0001c0001t0001g0121 others(4): Show |
9 | HG00099.hp2 HG00280.hp1 HG01069.hp2 others(6): Show |
intron_variant | MODIFIER | c.440-10415C>A | MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 4/4 | chr9 | 122189470 | |||||||
chr9:122189556 | T | C | 210 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(207): Show |
243 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(240): Show |
intron_variant | MODIFIER | c.440-10329T>C | MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 4/4 | chr9 | 122189556 | |||||||
chr9:122189742 | G | A | 1 | a0001c0001t0001g0218 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.440-10143G>A | MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 4/4 | chr9 | 122189742 | |||||||
chr9:122189984 | A | T | 1 | a0001c0002t0002g0101 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.440-9901A>T | MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 4/4 | chr9 | 122189984 | |||||||
chr9:122190152 | G | A | 8 | a0001c0001t0001g0208 a0001c0001t0001g0209 a0001c0001t0001g0302 others(5): Show |
8 | HG01109.hp2 HG02622.hp2 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.440-9733G>A | MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 4/4 | chr9 | 122190152 | |||||||
chr9:122190359 | A | C | 1 | a0001c0003t0001g0312 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.440-9526A>C | MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 4/4 | chr9 | 122190359 | |||||||
chr9:122190362 | CTT | C | 33 | a0001c0001t0001g0006 a0001c0001t0001g0010 a0001c0001t0001g0027 others(30): Show |
39 | HG00280.hp2 HG00408.hp2 HG00544.hp2 others(36): Show |
intron_variant | MODIFIER | c.440-9521_440-9520d others(4): Show |
MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr9 | 122190362 | ||||||
chr9:122190421 | G | T | 1 | a0001c0001t0001g0301 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.440-9464G>T | MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 4/4 | chr9 | 122190421 | |||||||
chr9:122190740 | A | G | 67 | a0001c0001t0001g0005 a0001c0001t0001g0011 a0001c0001t0001g0012 others(64): Show |
79 | HG00140.hp2 HG00621.hp1 HG00639.hp2 others(76): Show |
intron_variant | MODIFIER | c.440-9145A>G | MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 4/4 | chr9 | 122190740 | |||||||
chr9:122190782 | A | G | 1 | a0001c0002t0005g0087 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.440-9103A>G | MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 4/4 | chr9 | 122190782 | |||||||
chr9:122190918 | G | A | 1 | a0001c0001t0001g0013 | 2 | NA18971.hp1 NA18979.hp2 |
intron_variant | MODIFIER | c.440-8967G>A | MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 4/4 | chr9 | 122190918 | |||||||
chr9:122191036 | A | G | 1 | a0001c0001t0001g0118 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.440-8849A>G | MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 4/4 | chr9 | 122191036 | |||||||
chr9:122191047 | T | G | 209 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(206): Show |
242 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(239): Show |
intron_variant | MODIFIER | c.440-8838T>G | MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 4/4 | chr9 | 122191047 | |||||||
chr9:122191092 | T | C | 1 | a0001c0002t0001g0093 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.440-8793T>C | MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 4/4 | chr9 | 122191092 | |||||||
chr9:122191143 | C | T | 2 | a0001c0001t0001g0015 a0001c0001t0001g0171 |
3 | HG01123.hp1 HG01256.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.440-8742C>T | MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 4/4 | chr9 | 122191143 | |||||||
chr9:122191146 | T | C | 3 | a0001c0001t0001g0118 a0001c0001t0001g0128 a0001c0001t0001g0136 |
3 | HG02080.hp1 HG02155.hp1 NA18982.hp1 |
intron_variant | MODIFIER | c.440-8739T>C | MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 4/4 | chr9 | 122191146 | |||||||
chr9:122191232 | G | A | 8 | a0001c0001t0001g0208 a0001c0001t0001g0209 a0001c0001t0001g0302 others(5): Show |
8 | HG01109.hp2 HG02622.hp2 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.440-8653G>A | MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 4/4 | chr9 | 122191232 | |||||||
chr9:122191281 | C | T | 79 | a0001c0001t0001g0005 a0001c0001t0001g0011 a0001c0001t0001g0012 others(76): Show |
93 | HG00140.hp2 HG00621.hp1 HG00639.hp2 others(90): Show |
intron_variant | MODIFIER | c.440-8604C>T | MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 4/4 | chr9 | 122191281 | |||||||
chr9:122191292 | G | T | 1 | a0001c0001t0001g0237 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.440-8593G>T | MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 4/4 | chr9 | 122191292 | |||||||
chr9:122191328 | G | A | 1 | a0001c0003t0001g0313 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.440-8557G>A | MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 4/4 | chr9 | 122191328 | |||||||
chr9:122191574 | C | T | 2 | a0001c0001t0001g0198 a0001c0001t0001g0201 |
2 | HG02145.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.440-8311C>T | MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 4/4 | chr9 | 122191574 | |||||||
chr9:122191575 | G | A | 2 | a0001c0001t0001g0068 a0001c0001t0001g0305 |
2 | HG03486.hp2 NA18983.hp1 |
intron_variant | MODIFIER | c.440-8310G>A | MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 4/4 | chr9 | 122191575 | |||||||
chr9:122191665 | G | A | 2 | a0001c0001t0001g0033 a0001c0001t0001g0294 |
3 | HG02922.hp1 HG02965.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.440-8220G>A | MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 4/4 | chr9 | 122191665 | |||||||
chr9:122191789 | T | C | 2 | a0001c0001t0001g0302 a0001c0001t0001g0303 |
2 | HG02809.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.440-8096T>C | MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 4/4 | chr9 | 122191789 | |||||||
chr9:122191842 | C | T | 8 | a0001c0001t0001g0006 a0001c0001t0001g0054 a0001c0001t0001g0116 others(5): Show |
10 | HG02027.hp1 HG02027.hp2 NA18940.hp2 others(7): Show |
intron_variant | MODIFIER | c.440-8043C>T | MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 4/4 | chr9 | 122191842 | |||||||
chr9:122191866 | A | G | 71 | a0001c0001t0001g0006 a0001c0001t0001g0010 a0001c0001t0001g0024 others(68): Show |
78 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(75): Show |
intron_variant | MODIFIER | c.440-8019A>G | MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 4/4 | chr9 | 122191866 | |||||||
chr9:122191873 | C | T | 1 | a0001c0001t0001g0221 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.440-8012C>T | MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 4/4 | chr9 | 122191873 | |||||||
chr9:122191947 | C | T | 35 | a0001c0001t0001g0024 a0001c0001t0001g0090 a0001c0001t0001g0091 others(32): Show |
36 | HG00642.hp1 HG01070.hp2 HG01071.hp1 others(33): Show |
intron_variant | MODIFIER | c.440-7938C>T | MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 4/4 | chr9 | 122191947 | |||||||
chr9:122192019 | C | T | 4 | a0001c0001t0001g0208 a0001c0001t0001g0209 a0001c0001t0003g0075 others(1): Show |
4 | HG01109.hp2 HG02717.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.440-7866C>T | MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 4/4 | chr9 | 122192019 | |||||||
chr9:122192112 | C | T | 17 | a0001c0001t0001g0008 a0001c0001t0001g0018 a0001c0001t0001g0020 others(14): Show |
23 | HG00544.hp1 HG00558.hp1 HG00558.hp2 others(20): Show |
intron_variant | MODIFIER | c.440-7773C>T | MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 4/4 | chr9 | 122192112 | |||||||
chr9:122192209 | G | T | 35 | a0001c0001t0001g0024 a0001c0001t0001g0090 a0001c0001t0001g0091 others(32): Show |
36 | HG00642.hp1 HG01070.hp2 HG01071.hp1 others(33): Show |
intron_variant | MODIFIER | c.440-7676G>T | MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 4/4 | chr9 | 122192209 | |||||||
chr9:122192211 | C | T | 35 | a0001c0001t0001g0024 a0001c0001t0001g0090 a0001c0001t0001g0091 others(32): Show |
36 | HG00642.hp1 HG01070.hp2 HG01071.hp1 others(33): Show |
intron_variant | MODIFIER | c.440-7674C>T | MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 4/4 | chr9 | 122192211 | |||||||
chr9:122192253 | T | C | 1 | a0001c0001t0001g0040 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.440-7632T>C | MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 4/4 | chr9 | 122192253 | |||||||
chr9:122192275 | C | A | 34 | a0001c0001t0001g0024 a0001c0001t0001g0090 a0001c0001t0001g0091 others(31): Show |
35 | HG00642.hp1 HG01070.hp2 HG01071.hp1 others(32): Show |
intron_variant | MODIFIER | c.440-7610C>A | MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 4/4 | chr9 | 122192275 | |||||||
chr9:122192292 | C | T | 1 | a0001c0001t0001g0263 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.440-7593C>T | MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 4/4 | chr9 | 122192292 | |||||||
chr9:122192306 | G | A | 2 | a0001c0001t0001g0248 a0001c0001t0001g0301 |
2 | HG02258.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.440-7579G>A | MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 4/4 | chr9 | 122192306 | |||||||
chr9:122192405 | G | A | 34 | a0001c0001t0001g0024 a0001c0001t0001g0090 a0001c0001t0001g0091 others(31): Show |
35 | HG00642.hp1 HG01070.hp2 HG01071.hp1 others(32): Show |
intron_variant | MODIFIER | c.440-7480G>A | MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 4/4 | chr9 | 122192405 | |||||||
chr9:122192418 | A | G | 208 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(205): Show |
241 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(238): Show |
intron_variant | MODIFIER | c.440-7467A>G | MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 4/4 | chr9 | 122192418 | |||||||
chr9:122192423 | A | T | 1 | a0001c0001t0001g0293 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.440-7462A>T | MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 4/4 | chr9 | 122192423 | |||||||
chr9:122192440 | C | G | 34 | a0001c0001t0001g0024 a0001c0001t0001g0090 a0001c0001t0001g0091 others(31): Show |
35 | HG00642.hp1 HG01070.hp2 HG01071.hp1 others(32): Show |
intron_variant | MODIFIER | c.440-7445C>G | MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 4/4 | chr9 | 122192440 | |||||||
chr9:122192527 | T | C | 5 | a0001c0001t0001g0208 a0001c0001t0001g0209 a0001c0001t0003g0075 others(2): Show |
5 | HG01109.hp2 HG02630.hp1 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.440-7358T>C | MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 4/4 | chr9 | 122192527 | |||||||
chr9:122192540 | GC | G | 34 | a0001c0001t0001g0024 a0001c0001t0001g0090 a0001c0001t0001g0091 others(31): Show |
35 | HG00642.hp1 HG01070.hp2 HG01071.hp1 others(32): Show |
intron_variant | MODIFIER | c.440-7344delC | MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 4/4 | chr9 | 122192540 | |||||||
chr9:122192694 | A | G | 1 | a0001c0001t0001g0243 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.440-7191A>G | MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 4/4 | chr9 | 122192694 | |||||||
chr9:122192749 | A | G | 72 | a0001c0001t0001g0006 a0001c0001t0001g0010 a0001c0001t0001g0024 others(69): Show |
79 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(76): Show |
intron_variant | MODIFIER | c.440-7136A>G | MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 4/4 | chr9 | 122192749 | |||||||
chr9:122192763 | A | G | 35 | a0001c0001t0001g0024 a0001c0001t0001g0090 a0001c0001t0001g0091 others(32): Show |
36 | HG00642.hp1 HG01070.hp2 HG01071.hp1 others(33): Show |
intron_variant | MODIFIER | c.440-7122A>G | MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 4/4 | chr9 | 122192763 | |||||||
chr9:122192836 | T | C | 209 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(206): Show |
242 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(239): Show |
intron_variant | MODIFIER | c.440-7049T>C | MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 4/4 | chr9 | 122192836 | |||||||
chr9:122192848 | G | A | 1 | a0001c0001t0001g0065 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.440-7037G>A | MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 4/4 | chr9 | 122192848 | |||||||
chr9:122192945 | C | G | 206 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(203): Show |
239 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(236): Show |
intron_variant | MODIFIER | c.440-6940C>G | MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 4/4 | chr9 | 122192945 | |||||||
chr9:122192963 | T | A | 5 | a0001c0001t0001g0208 a0001c0001t0001g0209 a0001c0001t0003g0075 others(2): Show |
5 | HG01109.hp2 HG02630.hp1 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.440-6922T>A | MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 4/4 | chr9 | 122192963 | |||||||
chr9:122193011 | A | AGG | 38 | a0001c0001t0001g0006 a0001c0001t0001g0010 a0001c0001t0001g0027 others(35): Show |
44 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(41): Show |
intron_variant | MODIFIER | c.440-6873_440-6872d others(4): Show |
MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr9 | 122193011 | ||||||
chr9:122193016 | G | A | 2 | a0001c0001t0001g0131 a0001c0001t0001g0149 |
2 | HG02015.hp1 HG02523.hp1 |
intron_variant | MODIFIER | c.440-6869G>A | MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 4/4 | chr9 | 122193016 | |||||||
chr9:122193034 | G | A | 2 | a0001c0003t0001g0310 a0001c0003t0001g0315 |
2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.440-6851G>A | MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 4/4 | chr9 | 122193034 | |||||||
chr9:122193067 | A | C | 1 | a0001c0001t0001g0296 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.440-6818A>C | MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 4/4 | chr9 | 122193067 | |||||||
chr9:122193249 | T | G | 1 | a0001c0001t0001g0162 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.440-6636T>G | MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 4/4 | chr9 | 122193249 | |||||||
chr9:122193305 | C | T | 1 | a0001c0001t0001g0262 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.440-6580C>T | MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 4/4 | chr9 | 122193305 | |||||||
chr9:122193367 | G | A | 2 | a0001c0001t0001g0302 a0001c0001t0001g0303 |
2 | HG02809.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.440-6518G>A | MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 4/4 | chr9 | 122193367 | |||||||
chr9:122193542 | G | A | 132 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(129): Show |
158 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(155): Show |
intron_variant | MODIFIER | c.440-6343G>A | MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 4/4 | chr9 | 122193542 | |||||||
chr9:122193570 | C | T | 1 | a0001c0001t0001g0265 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.440-6315C>T | MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 4/4 | chr9 | 122193570 | |||||||
chr9:122193579 | G | A | 1 | a0001c0001t0001g0091 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.440-6306G>A | MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 4/4 | chr9 | 122193579 | |||||||
chr9:122193631 | C | T | 34 | a0001c0001t0001g0024 a0001c0001t0001g0090 a0001c0001t0001g0091 others(31): Show |
35 | HG00642.hp1 HG01070.hp2 HG01071.hp1 others(32): Show |
intron_variant | MODIFIER | c.440-6254C>T | MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 4/4 | chr9 | 122193631 | |||||||
chr9:122193643 | G | T | 203 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(200): Show |
236 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(233): Show |
intron_variant | MODIFIER | c.440-6242G>T | MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 4/4 | chr9 | 122193643 | |||||||
chr9:122193818 | C | T | 2 | a0001c0001t0001g0026 a0001c0001t0001g0199 |
3 | HG01106.hp2 HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.440-6067C>T | MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 4/4 | chr9 | 122193818 | |||||||
chr9:122193860 | C | G | 1 | a0001c0001t0001g0167 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.440-6025C>G | MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 4/4 | chr9 | 122193860 | |||||||
chr9:122193865 | G | A | 1 | a0001c0002t0001g0092 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.440-6020G>A | MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 4/4 | chr9 | 122193865 | |||||||
chr9:122194178 | G | A | 1 | a0001c0001t0001g0269 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.440-5707G>A | MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 4/4 | chr9 | 122194178 | |||||||
chr9:122194320 | A | T | 35 | a0001c0001t0001g0024 a0001c0001t0001g0090 a0001c0001t0001g0091 others(32): Show |
36 | HG00642.hp1 HG01070.hp2 HG01071.hp1 others(33): Show |
intron_variant | MODIFIER | c.440-5565A>T | MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 4/4 | chr9 | 122194320 | |||||||
chr9:122194746 | A | G | 208 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(205): Show |
241 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(238): Show |
intron_variant | MODIFIER | c.440-5139A>G | MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 4/4 | chr9 | 122194746 | |||||||
chr9:122194808 | T | C | 206 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(203): Show |
239 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(236): Show |
intron_variant | MODIFIER | c.440-5077T>C | MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 4/4 | chr9 | 122194808 | |||||||
chr9:122194860 | A | C | 206 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(203): Show |
239 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(236): Show |
intron_variant | MODIFIER | c.440-5025A>C | MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 4/4 | chr9 | 122194860 | |||||||
chr9:122194884 | G | A | 1 | a0001c0001t0001g0167 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.440-5001G>A | MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 4/4 | chr9 | 122194884 | |||||||
chr9:122194968 | T | C | 208 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(205): Show |
241 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(238): Show |
intron_variant | MODIFIER | c.440-4917T>C | MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 4/4 | chr9 | 122194968 | |||||||
chr9:122194998 | T | C | 207 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(204): Show |
240 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(237): Show |
intron_variant | MODIFIER | c.440-4887T>C | MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 4/4 | chr9 | 122194998 | |||||||
chr9:122195047 | T | A | 1 | a0001c0001t0001g0137 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.440-4838T>A | MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 4/4 | chr9 | 122195047 | |||||||
chr9:122195107 | C | G | 15 | a0001c0001t0001g0090 a0001c0001t0001g0198 a0001c0001t0001g0201 others(12): Show |
15 | HG01109.hp1 HG01496.hp2 HG02145.hp1 others(12): Show |
intron_variant | MODIFIER | c.440-4778C>G | MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 4/4 | chr9 | 122195107 | |||||||
chr9:122195111 | A | G | 1 | a0001c0001t0001g0301 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.440-4774A>G | MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 4/4 | chr9 | 122195111 | |||||||
chr9:122195153 | A | C | 1 | a0001c0001t0001g0235 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.440-4732A>C | MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 4/4 | chr9 | 122195153 | |||||||
chr9:122195246 | A | G | 206 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(203): Show |
239 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(236): Show |
intron_variant | MODIFIER | c.440-4639A>G | MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 4/4 | chr9 | 122195246 | |||||||
chr9:122195262 | T | A | 206 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(203): Show |
239 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(236): Show |
intron_variant | MODIFIER | c.440-4623T>A | MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 4/4 | chr9 | 122195262 | |||||||
chr9:122195497 | T | C | 206 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(203): Show |
239 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(236): Show |
intron_variant | MODIFIER | c.440-4388T>C | MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 4/4 | chr9 | 122195497 | |||||||
chr9:122195968 | A | ATATTTAT others(1): Show |
11 | a0001c0001t0001g0055 a0001c0001t0001g0182 a0001c0001t0001g0208 others(8): Show |
11 | HG01109.hp2 HG02109.hp1 HG02135.hp1 others(8): Show |
intron_variant | MODIFIER | c.440-3902_440-3895d others(10): Show |
MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr9 | 122195968 | ||||||
chr9:122195968 | A | ATATTTAT others(5): Show |
11 | a0001c0001t0001g0037 a0001c0001t0001g0054 a0001c0001t0001g0091 others(8): Show |
11 | HG02280.hp2 HG02451.hp2 HG02615.hp1 others(8): Show |
intron_variant | MODIFIER | c.440-3906_440-3895d others(14): Show |
MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr9 | 122195968 | ||||||
chr9:122195968 | A | ATATTTAT others(9): Show |
122 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(119): Show |
151 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(148): Show |
intron_variant | MODIFIER | c.440-3910_440-3895d others(18): Show |
MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr9 | 122195968 | ||||||
chr9:122195968 | A | ATATTTAT others(13): Show |
51 | a0001c0001t0001g0010 a0001c0001t0001g0033 a0001c0001t0001g0034 others(48): Show |
55 | HG00408.hp2 HG00423.hp2 HG00544.hp2 others(52): Show |
intron_variant | MODIFIER | c.440-3914_440-3895d others(22): Show |
MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr9 | 122195968 | ||||||
chr9:122195968 | A | ATATTTAT others(17): Show |
11 | a0001c0001t0001g0027 a0001c0001t0001g0130 a0001c0001t0001g0132 others(8): Show |
12 | HG00280.hp2 HG00642.hp1 HG00642.hp2 others(9): Show |
intron_variant | MODIFIER | c.440-3895_440-3894i others(26): Show |
MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr9 | 122195968 | ||||||
chr9:122195968 | A | ATATTTAT others(21): Show |
2 | a0001c0001t0001g0024 a0001c0001t0001g0185 |
3 | HG01070.hp2 HG01071.hp1 HG01192.hp2 |
intron_variant | MODIFIER | c.440-3895_440-3894i others(30): Show |
MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr9 | 122195968 | ||||||
chr9:122195985 | T | TATTTATT others(10): Show |
1 | a0001c0001t0001g0301 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.440-3895_440-3894i others(19): Show |
MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr9 | 122195985 | ||||||
chr9:122196066 | G | C | 179 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(176): Show |
210 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(207): Show |
intron_variant | MODIFIER | c.440-3819G>C | MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 4/4 | chr9 | 122196066 | |||||||
chr9:122196293 | A | G | 213 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(210): Show |
248 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(245): Show |
intron_variant | MODIFIER | c.440-3592A>G | MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 4/4 | chr9 | 122196293 | |||||||
chr9:122196335 | A | AT | 37 | a0001c0001t0001g0010 a0001c0001t0001g0027 a0001c0001t0001g0033 others(34): Show |
41 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(38): Show |
intron_variant | MODIFIER | c.440-3533dupT | MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr9 | 122196335 | ||||||
chr9:122196335 | AT | A | 172 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(169): Show |
203 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(200): Show |
intron_variant | MODIFIER | c.440-3533delT | MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr9 | 122196335 | ||||||
chr9:122196335 | ATT | A | 6 | a0001c0001t0001g0041 a0001c0001t0001g0130 a0001c0001t0001g0140 others(3): Show |
6 | HG02809.hp1 HG06807.hp1 NA18961.hp1 others(3): Show |
intron_variant | MODIFIER | c.440-3534_440-3533d others(4): Show |
MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr9 | 122196335 | ||||||
chr9:122196453 | T | C | 291 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(288): Show |
338 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(335): Show |
intron_variant | MODIFIER | c.440-3432T>C | MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 4/4 | chr9 | 122196453 | |||||||
chr9:122196527 | T | A | 2 | a0001c0001t0001g0037 a0001c0002t0001g0103 |
2 | HG03098.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.440-3358T>A | MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 4/4 | chr9 | 122196527 | |||||||
chr9:122196611 | G | A | 1 | a0001c0002t0001g0092 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.440-3274G>A | MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 4/4 | chr9 | 122196611 | |||||||
chr9:122196718 | C | T | 1 | a0001c0001t0001g0281 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.440-3167C>T | MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 4/4 | chr9 | 122196718 | |||||||
chr9:122196727 | C | T | 2 | a0001c0001t0001g0024 a0001c0001t0001g0185 |
3 | HG01070.hp2 HG01071.hp1 HG01192.hp2 |
intron_variant | MODIFIER | c.440-3158C>T | MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 4/4 | chr9 | 122196727 | |||||||
chr9:122196731 | G | A | 5 | a0001c0001t0001g0208 a0001c0001t0001g0209 a0001c0001t0003g0075 others(2): Show |
5 | HG01109.hp2 HG02630.hp1 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.440-3154G>A | MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 4/4 | chr9 | 122196731 | |||||||
chr9:122196778 | G | C | 1 | a0001c0001t0001g0157 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.440-3107G>C | MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 4/4 | chr9 | 122196778 | |||||||
chr9:122196972 | A | T | 1 | a0001c0001t0001g0305 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.440-2913A>T | MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 4/4 | chr9 | 122196972 | |||||||
chr9:122197007 | T | C | 1 | a0001c0002t0001g0092 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.440-2878T>C | MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 4/4 | chr9 | 122197007 | |||||||
chr9:122197147 | A | C | 1 | a0001c0001t0004g0326 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.440-2738A>C | MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 4/4 | chr9 | 122197147 | |||||||
chr9:122197252 | G | GT | 19 | a0001c0001t0001g0037 a0001c0001t0001g0089 a0001c0001t0001g0090 others(16): Show |
19 | HG00741.hp2 HG01109.hp1 HG01109.hp2 others(16): Show |
intron_variant | MODIFIER | c.440-2628dupT | MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr9 | 122197252 | ||||||
chr9:122197257 | T | TTC | 11 | a0001c0001t0001g0061 a0001c0001t0001g0091 a0001c0001t0001g0157 others(8): Show |
11 | HG01496.hp2 HG02055.hp1 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.440-2628_440-2627i others(4): Show |
MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 4/4 | chr9 | 122197257 | |||||||
chr9:122197257 | TC | T | 8 | a0001c0001t0001g0016 a0001c0001t0001g0085 a0001c0001t0001g0121 others(5): Show |
11 | HG00280.hp1 HG01069.hp2 HG01168.hp2 others(8): Show |
intron_variant | MODIFIER | c.440-2623delC | MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr9 | 122197257 | ||||||
chr9:122197258 | C | T | 46 | a0001c0001t0001g0004 a0001c0001t0001g0012 a0001c0001t0001g0037 others(43): Show |
48 | HG00408.hp1 HG01109.hp1 HG01109.hp2 others(45): Show |
intron_variant | MODIFIER | c.440-2627C>T | MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 4/4 | chr9 | 122197258 | |||||||
chr9:122197808 | G | A | 1 | a0001c0001t0001g0010 | 3 | HG02559.hp2 HG03139.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.440-2077G>A | MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 4/4 | chr9 | 122197808 | |||||||
chr9:122197829 | G | A | 1 | a0001c0001t0001g0248 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.440-2056G>A | MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 4/4 | chr9 | 122197829 | |||||||
chr9:122197890 | G | A | 1 | a0001c0001t0001g0264 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.440-1995G>A | MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 4/4 | chr9 | 122197890 | |||||||
chr9:122197895 | A | T | 1 | a0001c0001t0001g0196 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.440-1990A>T | MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 4/4 | chr9 | 122197895 | |||||||
chr9:122197937 | T | C | 6 | a0001c0001t0001g0302 a0001c0001t0001g0303 a0001c0001t0003g0075 others(3): Show |
6 | HG02559.hp1 HG02809.hp1 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.440-1948T>C | MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 4/4 | chr9 | 122197937 | |||||||
chr9:122197971 | G | A | 1 | a0001c0001t0001g0153 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.440-1914G>A | MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 4/4 | chr9 | 122197971 | |||||||
chr9:122198203 | A | G | 1 | a0001c0001t0001g0181 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.440-1682A>G | MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 4/4 | chr9 | 122198203 | |||||||
chr9:122198213 | T | C | 3 | a0001c0001t0001g0302 a0001c0001t0001g0303 a0001c0003t0001g0313 |
3 | HG02559.hp1 HG02809.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.440-1672T>C | MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 4/4 | chr9 | 122198213 | |||||||
chr9:122198336 | T | C | 94 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(91): Show |
114 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(111): Show |
intron_variant | MODIFIER | c.440-1549T>C | MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 4/4 | chr9 | 122198336 | |||||||
chr9:122198497 | G | T | 178 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0008 others(175): Show |
209 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(206): Show |
intron_variant | MODIFIER | c.440-1388G>T | MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 4/4 | chr9 | 122198497 | |||||||
chr9:122198513 | A | G | 1 | a0001c0001t0001g0049 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.440-1372A>G | MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 4/4 | chr9 | 122198513 | |||||||
chr9:122198647 | G | A | 26 | a0001c0001t0001g0003 a0001c0001t0001g0061 a0001c0001t0001g0208 others(23): Show |
30 | HG01109.hp2 HG01243.hp1 HG01891.hp1 others(27): Show |
intron_variant | MODIFIER | c.440-1238G>A | MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 4/4 | chr9 | 122198647 | |||||||
chr9:122198670 | G | A | 1 | a0001c0001t0002g0323 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.440-1215G>A | MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 4/4 | chr9 | 122198670 | |||||||
chr9:122198676 | G | A | 11 | a0001c0001t0001g0037 a0001c0001t0001g0115 a0001c0001t0001g0150 others(8): Show |
11 | HG02145.hp1 HG02559.hp1 HG02622.hp2 others(8): Show |
intron_variant | MODIFIER | c.440-1209G>A | MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 4/4 | chr9 | 122198676 | |||||||
chr9:122198697 | C | T | 3 | a0001c0001t0003g0075 a0001c0001t0003g0289 a0001c0001t0003g0291 |
3 | HG02886.hp1 HG03041.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.440-1188C>T | MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 4/4 | chr9 | 122198697 | |||||||
chr9:122198700 | T | G | 16 | a0001c0001t0001g0003 a0001c0001t0001g0061 a0001c0001t0001g0208 others(13): Show |
20 | HG01109.hp2 HG01243.hp1 HG01891.hp1 others(17): Show |
intron_variant | MODIFIER | c.440-1185T>G | MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 4/4 | chr9 | 122198700 | |||||||
chr9:122198855 | T | C | 2 | a0001c0001t0001g0007 a0001c0001t0001g0164 |
4 | NA18943.hp1 NA18944.hp2 NA19012.hp1 others(1): Show |
intron_variant | MODIFIER | c.440-1030T>C | MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 4/4 | chr9 | 122198855 | |||||||
chr9:122198909 | A | G | 1 | a0001c0001t0001g0228 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.440-976A>G | MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 4/4 | chr9 | 122198909 | |||||||
chr9:122199021 | G | T | 2 | a0001c0001t0001g0250 a0001c0003t0001g0321 |
2 | HG02723.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.440-864G>T | MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 4/4 | chr9 | 122199021 | |||||||
chr9:122199025 | G | A | 289 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(286): Show |
341 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(338): Show |
intron_variant | MODIFIER | c.440-860G>A | MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 4/4 | chr9 | 122199025 | |||||||
chr9:122199123 | T | C | 2 | a0001c0002t0001g0092 a0001c0002t0005g0087 |
2 | HG02622.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.440-762T>C | MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 4/4 | chr9 | 122199123 | |||||||
chr9:122199279 | A | G | 1 | a0001c0001t0001g0236 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.440-606A>G | MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 4/4 | chr9 | 122199279 | |||||||
chr9:122199598 | T | C | 4 | a0001c0001t0001g0025 a0001c0001t0001g0156 a0001c0001t0001g0172 others(1): Show |
5 | HG00558.hp1 NA18939.hp1 NA18949.hp2 others(2): Show |
intron_variant | MODIFIER | c.440-287T>C | MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 4/4 | chr9 | 122199598 | |||||||
chr9:122199681 | A | G | 7 | a0001c0001t0001g0037 a0001c0001t0001g0115 a0001c0001t0001g0150 others(4): Show |
7 | HG02145.hp1 HG03098.hp1 HG03209.hp1 others(4): Show |
intron_variant | MODIFIER | c.440-204A>G | MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 4/4 | chr9 | 122199681 | |||||||
chr9:122199770 | C | G | 1 | a0001c0003t0001g0313 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.440-115C>G | MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 4/4 | chr9 | 122199770 | |||||||
chr9:122199786 | G | A | 5 | a0001c0001t0001g0018 a0001c0001t0001g0129 a0001c0001t0001g0162 others(2): Show |
6 | HG02056.hp1 HG02071.hp1 NA18964.hp2 others(3): Show |
intron_variant | MODIFIER | c.440-99G>A | MORN5 | ENSG00000185681.13 | transcript | ENST00000373764.8 | protein_coding | 4/4 | chr9 | 122199786 |