Item | Value |
---|---|
geneid | 29880 |
ensemblid | ENSG00000120697.10 |
hgncid | 20266 |
symbol | ALG5 |
name | ALG5 dolichyl-phosphate beta-glucosyltransferase |
refseq_nuc | NM_013338.5 |
refseq_prot | NP_037470.1 |
ensembl_nuc | ENST00000239891.4 |
ensembl_prot | ENSP00000239891.3 |
mane_status | MANE Select |
chr | chr13 |
start | 36949738 |
end | 36999340 |
strand | - |
ver | v1.2 |
region | chr13:36949738-36999340 |
region5000 | chr13:36944738-37004340 |
regionname0 | ALG5_chr13_36949738_36999340 |
regionname5000 | ALG5_chr13_36944738_37004340 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 324 | 269 | 86 | 65 | 78 | 12 | 26 | 60 | ALG5_chr13_36944738_37004340 | ALG5 | MAPLL others(319): Show |
chr13 | 36944738 | 37004340 |
a0002 | 0/0 | 324 | 3 | 2 | 0 | 1 | 0 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | MAPLL others(319): Show |
chr13 | 36944738 | 37004340 |
a0003 | 0/0 | 324 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | MAPLL others(319): Show |
chr13 | 36944738 | 37004340 |
a0004 | 0/0 | 324 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | MAPLL others(319): Show |
chr13 | 36944738 | 37004340 |
a0005 | 0/0 | 324 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | MAPLL others(319): Show |
chr13 | 36944738 | 37004340 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 972 | 266 | 85 | 65 | 78 | 12 | 24 | ALG5_chr13_36944738_37004340 | ALG5 | ATGGC others(967): Show |
chr13 | 36944738 | 37004340 | ||
a0001c0004 | 0/0 | 972 | 2 | 0 | 0 | 0 | 0 | 2 | ALG5_chr13_36944738_37004340 | ALG5 | ATGGC others(967): Show |
chr13 | 36944738 | 37004340 | ||
a0001c0007 | 0/0 | 972 | 1 | 1 | 0 | 0 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | ATGGC others(967): Show |
chr13 | 36944738 | 37004340 | ||
a0002c0002 | 0/0 | 972 | 3 | 2 | 0 | 1 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | ATGGC others(967): Show |
chr13 | 36944738 | 37004340 | ||
a0003c0003 | 0/0 | 972 | 2 | 2 | 0 | 0 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | ATGGC others(967): Show |
chr13 | 36944738 | 37004340 | ||
a0004c0005 | 0/0 | 972 | 1 | 0 | 1 | 0 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | ATGGC others(967): Show |
chr13 | 36944738 | 37004340 | ||
a0005c0006 | 0/0 | 972 | 1 | 0 | 0 | 1 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | ATGGC others(967): Show |
chr13 | 36944738 | 37004340 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 1/1 | 1219 | 265 | 84 | 65 | 78 | 12 | 24 | ALG5_chr13_36944738_37004340 | ALG5 | GTGGA others(1214): Show |
chr13 | 36944738 | 37004340 |
a0001c0001t0002 | 0/0 | 1219 | 1 | 1 | 0 | 0 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | GTGGA others(1214): Show |
chr13 | 36944738 | 37004340 |
a0001c0004t0001 | 0/0 | 1219 | 2 | 0 | 0 | 0 | 0 | 2 | ALG5_chr13_36944738_37004340 | ALG5 | GTGGA others(1214): Show |
chr13 | 36944738 | 37004340 |
a0001c0007t0001 | 0/0 | 1219 | 1 | 1 | 0 | 0 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | GTGGA others(1214): Show |
chr13 | 36944738 | 37004340 |
a0002c0002t0001 | 0/0 | 1219 | 3 | 2 | 0 | 1 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | GTGGA others(1214): Show |
chr13 | 36944738 | 37004340 |
a0003c0003t0001 | 0/0 | 1219 | 2 | 2 | 0 | 0 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | GTGGA others(1214): Show |
chr13 | 36944738 | 37004340 |
a0004c0005t0001 | 0/0 | 1219 | 1 | 0 | 1 | 0 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | GTGGA others(1214): Show |
chr13 | 36944738 | 37004340 |
a0005c0006t0001 | 0/0 | 1219 | 1 | 0 | 0 | 1 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | GTGGA others(1214): Show |
chr13 | 36944738 | 37004340 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 7 | 0 | 3 | 1 | 1 | 2 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
a0001c0001t0001g0002 | 0/0 | 7 | 0 | 5 | 0 | 1 | 1 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
a0001c0001t0001g0003 | 0/0 | 6 | 1 | 1 | 2 | 2 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
a0001c0001t0001g0004 | 0/0 | 4 | 0 | 1 | 2 | 1 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
a0001c0001t0001g0005 | 0/0 | 3 | 0 | 2 | 1 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
a0001c0001t0001g0006 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
a0001c0001t0001g0007 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
a0001c0001t0001g0008 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
a0001c0001t0001g0009 | 0/0 | 3 | 1 | 2 | 0 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
a0001c0001t0001g0010 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
a0001c0001t0001g0011 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
a0001c0001t0001g0012 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
a0001c0001t0001g0013 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
a0001c0001t0001g0014 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
a0001c0001t0001g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
a0001c0001t0001g0016 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
a0001c0001t0001g0017 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
a0001c0001t0001g0018 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
a0001c0001t0001g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
a0001c0001t0001g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
a0001c0001t0001g0021 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
a0001c0001t0001g0022 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
a0001c0001t0001g0023 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
a0001c0001t0001g0024 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
a0001c0001t0001g0025 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
a0001c0001t0001g0026 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
a0001c0001t0001g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
a0001c0001t0001g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
a0001c0001t0001g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
a0001c0001t0001g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
a0001c0001t0001g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
a0001c0001t0001g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
a0001c0001t0001g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
a0001c0001t0001g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
a0001c0001t0001g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
a0001c0001t0001g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
a0001c0001t0001g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
a0001c0001t0001g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
a0001c0001t0001g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
a0001c0001t0001g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
a0001c0001t0001g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
a0001c0001t0001g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
a0001c0001t0001g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
a0001c0001t0001g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
a0001c0001t0001g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
a0001c0001t0001g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
a0001c0001t0001g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
a0001c0001t0001g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
a0001c0001t0001g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
a0001c0001t0001g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
a0001c0001t0001g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
a0001c0001t0001g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
a0001c0001t0001g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
a0001c0001t0001g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
a0001c0001t0001g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
a0001c0001t0001g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
a0001c0001t0001g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
a0001c0001t0001g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
a0001c0001t0001g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
a0001c0001t0001g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
a0001c0001t0001g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
a0001c0001t0001g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
a0001c0001t0001g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
a0001c0001t0001g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
a0001c0001t0001g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
a0001c0001t0001g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
a0001c0001t0001g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
a0001c0001t0001g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
a0001c0001t0001g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
a0001c0001t0001g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
a0001c0001t0001g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
a0001c0001t0001g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
a0001c0001t0001g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
a0001c0001t0001g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
a0001c0001t0001g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
a0001c0001t0001g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
a0001c0001t0001g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
a0001c0001t0001g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
a0001c0001t0001g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
a0001c0001t0001g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
a0001c0001t0001g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
a0001c0001t0001g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
a0001c0001t0001g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
a0001c0001t0001g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
a0001c0001t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
a0001c0001t0001g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
a0001c0001t0001g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
a0001c0001t0001g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
a0001c0001t0001g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
a0001c0001t0001g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
a0001c0001t0001g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
a0001c0001t0001g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
a0001c0001t0001g0159 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
a0001c0001t0001g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
a0001c0001t0001g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
a0001c0001t0001g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
a0001c0001t0001g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
a0001c0001t0001g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
a0001c0001t0001g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
a0001c0001t0001g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
a0001c0001t0001g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
a0001c0001t0001g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
a0001c0001t0001g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
a0001c0001t0001g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
a0001c0001t0001g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
a0001c0001t0001g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
a0001c0001t0001g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
a0001c0001t0001g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
a0001c0001t0001g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
a0001c0001t0001g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
a0001c0001t0001g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
a0001c0001t0001g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
a0001c0001t0001g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
a0001c0001t0001g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
a0001c0001t0001g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
a0001c0001t0001g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
a0001c0001t0001g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
a0001c0001t0001g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
a0001c0001t0001g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
a0001c0001t0001g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
a0001c0001t0001g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
a0001c0001t0001g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
a0001c0001t0001g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
a0001c0001t0001g0213 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
a0001c0001t0001g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
a0001c0001t0001g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
a0001c0001t0001g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
a0001c0001t0001g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
a0001c0001t0001g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
a0001c0001t0001g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
a0001c0001t0001g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
a0001c0001t0001g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
a0001c0001t0001g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
a0001c0001t0001g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
a0001c0001t0002g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
a0001c0004t0001g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
a0001c0004t0001g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
a0001c0007t0001g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
a0002c0002t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
a0002c0002t0001g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
a0002c0002t0001g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
a0003c0003t0001g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
a0003c0003t0001g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
a0004c0005t0001g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
a0005c0006t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0001 | g0070 | EUR | GBR | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
HG00099 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | GBR | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
HG00140 | hp1 | a0001 | c0001 | t0001 | g0145 | EUR | GBR | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
HG00140 | hp2 | a0001 | c0001 | t0001 | g0002 | EUR | GBR | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
HG00323 | hp1 | a0001 | c0001 | t0001 | g0148 | EUR | FIN | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
HG00323 | hp2 | a0001 | c0001 | t0001 | g0217 | EUR | FIN | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
HG00438 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | CHS | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
HG00438 | hp2 | a0001 | c0001 | t0001 | g0137 | EAS | CHS | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
HG00609 | hp1 | a0002 | c0002 | t0001 | g0165 | EAS | CHS | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
HG00609 | hp2 | a0001 | c0001 | t0001 | g0058 | EAS | CHS | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
HG00621 | hp1 | a0001 | c0001 | t0001 | g0135 | EAS | CHS | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
HG00621 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | CHS | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
HG00639 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
HG00639 | hp2 | a0001 | c0001 | t0001 | g0205 | AMR | PUR | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
HG00673 | hp1 | a0001 | c0001 | t0001 | g0072 | EAS | CHS | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
HG00673 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | CHS | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
HG00733 | hp1 | a0001 | c0001 | t0001 | g0086 | AMR | PUR | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
HG00733 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | PUR | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
HG00741 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | PUR | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
HG00741 | hp2 | a0001 | c0001 | t0001 | g0054 | AMR | PUR | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
HG01069 | hp1 | a0001 | c0001 | t0001 | g0022 | AMR | PUR | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
HG01069 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
HG01071 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
HG01071 | hp2 | a0001 | c0001 | t0001 | g0022 | AMR | PUR | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
HG01074 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
HG01074 | hp2 | a0001 | c0001 | t0001 | g0216 | AMR | PUR | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
HG01081 | hp1 | a0001 | c0001 | t0001 | g0116 | AMR | PUR | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
HG01081 | hp2 | a0001 | c0001 | t0001 | g0059 | AMR | PUR | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
HG01109 | hp1 | a0001 | c0001 | t0001 | g0074 | AMR | PUR | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
HG01109 | hp2 | a0001 | c0001 | t0001 | g0038 | AMR | PUR | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
HG01167 | hp1 | a0001 | c0001 | t0001 | g0065 | AMR | PUR | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
HG01167 | hp2 | a0001 | c0001 | t0001 | g0158 | AMR | PUR | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
HG01169 | hp1 | a0001 | c0001 | t0001 | g0028 | AMR | PUR | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
HG01169 | hp2 | a0001 | c0001 | t0001 | g0221 | AMR | PUR | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
HG01175 | hp1 | a0001 | c0001 | t0001 | g0152 | AMR | PUR | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
HG01175 | hp2 | a0001 | c0001 | t0001 | g0104 | AMR | PUR | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
HG01192 | hp1 | a0001 | c0001 | t0001 | g0125 | AMR | PUR | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
HG01192 | hp2 | a0001 | c0001 | t0001 | g0040 | AMR | PUR | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
HG01243 | hp1 | a0001 | c0001 | t0001 | g0016 | AMR | PUR | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
HG01243 | hp2 | a0001 | c0001 | t0001 | g0069 | AMR | PUR | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
HG01255 | hp1 | a0001 | c0001 | t0001 | g0009 | AMR | CLM | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
HG01255 | hp2 | a0001 | c0001 | t0001 | g0220 | AMR | CLM | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
HG01257 | hp1 | a0001 | c0001 | t0001 | g0121 | AMR | CLM | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
HG01257 | hp2 | a0001 | c0001 | t0001 | g0201 | AMR | CLM | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
HG01258 | hp1 | a0001 | c0001 | t0001 | g0120 | AMR | CLM | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
HG01258 | hp2 | a0001 | c0001 | t0001 | g0144 | AMR | CLM | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
HG01261 | hp1 | a0001 | c0001 | t0001 | g0055 | AMR | CLM | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
HG01261 | hp2 | a0001 | c0001 | t0001 | g0136 | AMR | CLM | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
HG01346 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
HG01346 | hp2 | a0001 | c0001 | t0001 | g0088 | AMR | CLM | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
HG01358 | hp1 | a0001 | c0001 | t0001 | g0090 | AMR | CLM | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
HG01358 | hp2 | a0001 | c0001 | t0001 | g0026 | AMR | CLM | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
HG01361 | hp1 | a0001 | c0001 | t0001 | g0117 | AMR | CLM | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
HG01361 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | CLM | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
HG01496 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
HG01496 | hp2 | a0001 | c0001 | t0001 | g0130 | AMR | CLM | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
HG01515 | hp1 | a0001 | c0001 | t0001 | g0149 | EUR | IBS | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
HG01515 | hp2 | a0001 | c0001 | t0001 | g0203 | EUR | IBS | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
HG01516 | hp1 | a0001 | c0001 | t0001 | g0199 | EUR | IBS | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
HG01516 | hp2 | a0001 | c0001 | t0001 | g0003 | EUR | IBS | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
HG01517 | hp1 | a0001 | c0001 | t0001 | g0004 | EUR | IBS | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
HG01517 | hp2 | a0001 | c0001 | t0001 | g0003 | EUR | IBS | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
HG01891 | hp1 | a0001 | c0001 | t0001 | g0215 | AFR | ACB | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
HG01891 | hp2 | a0001 | c0001 | t0001 | g0006 | AFR | ACB | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
HG01928 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
HG01928 | hp2 | a0001 | c0001 | t0001 | g0105 | AMR | PEL | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
HG01934 | hp1 | a0001 | c0001 | t0001 | g0062 | AMR | PEL | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
HG01934 | hp2 | a0004 | c0005 | t0001 | g0167 | AMR | PEL | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
HG01943 | hp1 | a0001 | c0001 | t0001 | g0073 | AMR | PEL | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
HG01943 | hp2 | a0001 | c0001 | t0001 | g0021 | AMR | PEL | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
HG01952 | hp1 | a0001 | c0001 | t0001 | g0014 | AMR | PEL | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
HG01952 | hp2 | a0001 | c0001 | t0001 | g0009 | AMR | PEL | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
HG01978 | hp1 | a0001 | c0001 | t0001 | g0021 | AMR | PEL | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
HG01978 | hp2 | a0001 | c0001 | t0001 | g0157 | AMR | PEL | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
HG01981 | hp1 | a0001 | c0001 | t0001 | g0154 | AMR | PEL | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
HG01981 | hp2 | a0001 | c0001 | t0001 | g0033 | AMR | PEL | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
HG01993 | hp1 | a0001 | c0001 | t0001 | g0218 | AMR | PEL | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
HG01993 | hp2 | a0001 | c0001 | t0001 | g0092 | AMR | PEL | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
HG02027 | hp1 | a0001 | c0001 | t0001 | g0124 | EAS | KHV | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
HG02027 | hp2 | a0001 | c0001 | t0001 | g0096 | EAS | KHV | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
HG02040 | hp1 | a0001 | c0001 | t0001 | g0051 | EAS | KHV | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
HG02040 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | KHV | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
HG02055 | hp1 | a0001 | c0001 | t0001 | g0012 | AFR | ACB | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
HG02055 | hp2 | a0001 | c0001 | t0001 | g0113 | AFR | ACB | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
HG02071 | hp1 | a0005 | c0006 | t0001 | g0226 | EAS | KHV | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
HG02071 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | KHV | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
HG02074 | hp1 | a0001 | c0001 | t0001 | g0164 | EAS | KHV | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
HG02074 | hp2 | a0001 | c0001 | t0001 | g0057 | EAS | KHV | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
HG02080 | hp1 | a0001 | c0001 | t0001 | g0067 | EAS | KHV | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
HG02080 | hp2 | a0001 | c0001 | t0001 | g0150 | EAS | KHV | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
HG02145 | hp1 | a0001 | c0001 | t0001 | g0099 | AFR | ACB | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
HG02145 | hp2 | a0001 | c0001 | t0001 | g0182 | AFR | ACB | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
HG02148 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PEL | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
HG02148 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
HG02257 | hp1 | a0001 | c0001 | t0001 | g0025 | AFR | ACB | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
HG02257 | hp2 | a0001 | c0001 | t0001 | g0208 | AFR | ACB | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
HG02273 | hp1 | a0001 | c0001 | t0001 | g0153 | AMR | PEL | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
HG02273 | hp2 | a0001 | c0001 | t0001 | g0093 | AMR | PEL | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
HG02280 | hp1 | a0001 | c0001 | t0001 | g0194 | AFR | ACB | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
HG02280 | hp2 | a0001 | c0001 | t0001 | g0174 | AFR | ACB | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
HG02293 | hp1 | a0001 | c0001 | t0001 | g0026 | AMR | PEL | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
HG02293 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
HG02300 | hp1 | a0001 | c0001 | t0001 | g0147 | AMR | PEL | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
HG02300 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
HG02451 | hp1 | a0001 | c0001 | t0001 | g0128 | AFR | ACB | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
HG02451 | hp2 | a0001 | c0001 | t0001 | g0046 | AFR | ACB | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
HG02523 | hp1 | a0001 | c0001 | t0001 | g0141 | EAS | KHV | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
HG02523 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | KHV | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
HG02572 | hp1 | a0001 | c0001 | t0001 | g0044 | AFR | GWD | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
HG02572 | hp2 | a0001 | c0001 | t0001 | g0024 | AFR | GWD | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
HG02615 | hp1 | a0001 | c0001 | t0001 | g0180 | AFR | GWD | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
HG02615 | hp2 | a0001 | c0001 | t0001 | g0176 | AFR | GWD | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
HG02630 | hp1 | a0001 | c0007 | t0001 | g0227 | AFR | GWD | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
HG02630 | hp2 | a0001 | c0001 | t0001 | g0012 | AFR | GWD | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
HG02647 | hp1 | a0001 | c0001 | t0001 | g0179 | AFR | GWD | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
HG02647 | hp2 | a0001 | c0001 | t0001 | g0196 | AFR | GWD | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
HG02683 | hp1 | a0001 | c0001 | t0001 | g0081 | SAS | PJL | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
HG02683 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
HG02717 | hp1 | a0001 | c0001 | t0001 | g0129 | AFR | GWD | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
HG02717 | hp2 | a0001 | c0001 | t0001 | g0023 | AFR | GWD | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
HG02723 | hp1 | a0001 | c0001 | t0001 | g0183 | AFR | GWD | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
HG02723 | hp2 | a0001 | c0001 | t0001 | g0031 | AFR | GWD | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
HG02735 | hp1 | a0001 | c0001 | t0001 | g0018 | SAS | PJL | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
HG02735 | hp2 | a0001 | c0001 | t0001 | g0122 | SAS | PJL | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
HG02738 | hp1 | a0001 | c0001 | t0001 | g0133 | SAS | PJL | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
HG02738 | hp2 | a0001 | c0001 | t0001 | g0053 | SAS | PJL | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
HG02809 | hp1 | a0001 | c0001 | t0001 | g0032 | AFR | GWD | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
HG02809 | hp2 | a0001 | c0001 | t0001 | g0060 | AFR | GWD | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
HG02818 | hp1 | a0001 | c0001 | t0001 | g0214 | AFR | GWD | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
HG02818 | hp2 | a0001 | c0001 | t0001 | g0225 | AFR | GWD | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
HG02886 | hp1 | a0003 | c0003 | t0001 | g0189 | AFR | GWD | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
HG02886 | hp2 | a0001 | c0001 | t0001 | g0011 | AFR | GWD | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
HG02895 | hp1 | a0001 | c0001 | t0001 | g0023 | AFR | GWD | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
HG02895 | hp2 | a0003 | c0003 | t0001 | g0188 | AFR | GWD | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
HG02896 | hp1 | a0001 | c0001 | t0001 | g0030 | AFR | GWD | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
HG02896 | hp2 | a0001 | c0001 | t0001 | g0110 | AFR | GWD | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
HG02897 | hp1 | a0001 | c0001 | t0001 | g0109 | AFR | GWD | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
HG02897 | hp2 | a0001 | c0001 | t0001 | g0029 | AFR | GWD | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
HG02922 | hp1 | a0001 | c0001 | t0001 | g0006 | AFR | ESN | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
HG02922 | hp2 | a0001 | c0001 | t0001 | g0181 | AFR | ESN | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
HG02965 | hp1 | a0001 | c0001 | t0001 | g0037 | AFR | ESN | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
HG02965 | hp2 | a0001 | c0001 | t0001 | g0039 | AFR | ESN | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
HG02970 | hp1 | a0001 | c0001 | t0001 | g0017 | AFR | ESN | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
HG02970 | hp2 | a0001 | c0001 | t0001 | g0192 | AFR | ESN | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
HG02976 | hp1 | a0001 | c0001 | t0001 | g0024 | AFR | ESN | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
HG02976 | hp2 | a0001 | c0001 | t0001 | g0111 | AFR | ESN | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
HG03017 | hp1 | a0001 | c0001 | t0001 | g0138 | SAS | PJL | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
HG03017 | hp2 | a0001 | c0001 | t0001 | g0076 | SAS | PJL | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
HG03041 | hp1 | a0001 | c0001 | t0001 | g0172 | AFR | GWD | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
HG03041 | hp2 | a0001 | c0001 | t0001 | g0050 | AFR | GWD | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
HG03098 | hp1 | a0001 | c0001 | t0001 | g0139 | AFR | MSL | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
HG03098 | hp2 | a0001 | c0001 | t0001 | g0185 | AFR | MSL | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
HG03130 | hp1 | a0001 | c0001 | t0001 | g0006 | AFR | ESN | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
HG03130 | hp2 | a0002 | c0002 | t0001 | g0191 | AFR | ESN | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
HG03139 | hp1 | a0001 | c0001 | t0001 | g0101 | AFR | ESN | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
HG03139 | hp2 | a0001 | c0001 | t0001 | g0035 | AFR | ESN | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
HG03195 | hp1 | a0001 | c0001 | t0001 | g0112 | AFR | ESN | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
HG03195 | hp2 | a0001 | c0001 | t0001 | g0184 | AFR | ESN | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
HG03209 | hp1 | a0001 | c0001 | t0001 | g0178 | AFR | MSL | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
HG03209 | hp2 | a0001 | c0001 | t0001 | g0210 | AFR | MSL | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
HG03225 | hp1 | a0002 | c0002 | t0001 | g0190 | AFR | MSL | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
HG03225 | hp2 | a0001 | c0001 | t0001 | g0224 | AFR | MSL | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
HG03453 | hp1 | a0001 | c0001 | t0001 | g0016 | AFR | MSL | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
HG03453 | hp2 | a0001 | c0001 | t0001 | g0041 | AFR | MSL | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
HG03486 | hp1 | a0001 | c0001 | t0001 | g0175 | AFR | MSL | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
HG03486 | hp2 | a0001 | c0001 | t0001 | g0212 | AFR | MSL | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
HG03492 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
HG03492 | hp2 | a0001 | c0004 | t0001 | g0064 | SAS | PJL | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
HG03516 | hp1 | a0001 | c0001 | t0001 | g0025 | AFR | ESN | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
HG03516 | hp2 | a0001 | c0001 | t0001 | g0132 | AFR | ESN | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
HG03540 | hp1 | a0001 | c0001 | t0001 | g0211 | AFR | GWD | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
HG03540 | hp2 | a0001 | c0001 | t0001 | g0193 | AFR | GWD | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
HG03579 | hp1 | a0001 | c0001 | t0001 | g0131 | AFR | MSL | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
HG03579 | hp2 | a0001 | c0001 | t0001 | g0011 | AFR | MSL | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
HG03654 | hp1 | a0001 | c0001 | t0001 | g0097 | SAS | PJL | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
HG03654 | hp2 | a0001 | c0001 | t0001 | g0123 | SAS | PJL | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
HG03688 | hp1 | a0001 | c0001 | t0001 | g0094 | SAS | STU | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
HG03688 | hp2 | a0001 | c0001 | t0001 | g0168 | SAS | STU | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
HG03834 | hp1 | a0001 | c0001 | t0001 | g0187 | SAS | BEB | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
HG03834 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | BEB | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
HG03927 | hp1 | a0001 | c0001 | t0001 | g0134 | SAS | BEB | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
HG03927 | hp2 | a0001 | c0001 | t0001 | g0013 | SAS | BEB | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
HG03942 | hp1 | a0001 | c0001 | t0001 | g0102 | SAS | BEB | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
HG03942 | hp2 | a0001 | c0001 | t0001 | g0084 | SAS | BEB | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
HG04199 | hp1 | a0001 | c0001 | t0001 | g0219 | SAS | STU | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
HG04199 | hp2 | a0001 | c0001 | t0001 | g0155 | SAS | STU | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
HG04228 | hp1 | a0001 | c0001 | t0001 | g0103 | SAS | STU | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
HG04228 | hp2 | a0001 | c0001 | t0001 | g0151 | SAS | STU | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
NA18522 | hp1 | a0001 | c0001 | t0001 | g0017 | AFR | YRI | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
NA18522 | hp2 | a0001 | c0001 | t0001 | g0204 | AFR | YRI | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
NA18939 | hp1 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
NA18939 | hp2 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
NA18943 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
NA18943 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
NA18945 | hp1 | a0001 | c0001 | t0001 | g0091 | EAS | JPT | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
NA18945 | hp2 | a0001 | c0001 | t0001 | g0198 | EAS | JPT | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
NA18946 | hp1 | a0001 | c0001 | t0001 | g0197 | EAS | JPT | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
NA18946 | hp2 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
NA18947 | hp1 | a0001 | c0001 | t0001 | g0169 | EAS | JPT | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
NA18947 | hp2 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
NA18950 | hp1 | a0001 | c0001 | t0001 | g0100 | EAS | JPT | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
NA18950 | hp2 | a0001 | c0001 | t0001 | g0163 | EAS | JPT | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
NA18952 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
NA18952 | hp2 | a0001 | c0001 | t0001 | g0056 | EAS | JPT | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
NA18959 | hp1 | a0001 | c0001 | t0001 | g0170 | EAS | JPT | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
NA18959 | hp2 | a0001 | c0001 | t0001 | g0066 | EAS | JPT | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
NA18961 | hp1 | a0001 | c0001 | t0001 | g0075 | EAS | JPT | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
NA18961 | hp2 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
NA18965 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
NA18965 | hp2 | a0001 | c0001 | t0001 | g0077 | EAS | JPT | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
NA18973 | hp1 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
NA18973 | hp2 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
NA18980 | hp1 | a0001 | c0001 | t0001 | g0047 | EAS | JPT | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
NA18980 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
NA18983 | hp1 | a0001 | c0001 | t0001 | g0068 | EAS | JPT | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
NA18983 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
NA18986 | hp1 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
NA18986 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
NA18991 | hp1 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
NA18991 | hp2 | a0001 | c0001 | t0001 | g0200 | EAS | JPT | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
NA19000 | hp1 | a0001 | c0001 | t0001 | g0202 | EAS | JPT | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
NA19000 | hp2 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
NA19002 | hp1 | a0001 | c0001 | t0001 | g0079 | EAS | JPT | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
NA19002 | hp2 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
NA19003 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
NA19003 | hp2 | a0001 | c0001 | t0001 | g0049 | EAS | JPT | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
NA19006 | hp1 | a0001 | c0001 | t0001 | g0186 | EAS | JPT | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
NA19006 | hp2 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
NA19010 | hp1 | a0001 | c0001 | t0001 | g0078 | EAS | JPT | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
NA19010 | hp2 | a0001 | c0001 | t0001 | g0052 | EAS | JPT | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
NA19011 | hp1 | a0001 | c0001 | t0001 | g0061 | EAS | JPT | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
NA19011 | hp2 | a0001 | c0001 | t0001 | g0119 | EAS | JPT | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
NA19030 | hp1 | a0001 | c0001 | t0001 | g0036 | AFR | LWK | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
NA19030 | hp2 | a0001 | c0001 | t0001 | g0209 | AFR | LWK | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
NA19043 | hp1 | a0001 | c0001 | t0001 | g0042 | AFR | LWK | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
NA19043 | hp2 | a0001 | c0001 | t0001 | g0195 | AFR | LWK | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
NA19058 | hp1 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
NA19058 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
NA19063 | hp1 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
NA19063 | hp2 | a0001 | c0001 | t0001 | g0087 | EAS | JPT | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
NA19067 | hp1 | a0001 | c0001 | t0001 | g0161 | EAS | JPT | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
NA19067 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
NA19068 | hp1 | a0001 | c0001 | t0001 | g0083 | EAS | JPT | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
NA19068 | hp2 | a0001 | c0001 | t0001 | g0160 | EAS | JPT | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
NA19077 | hp1 | a0001 | c0001 | t0001 | g0162 | EAS | JPT | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
NA19077 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
NA19080 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
NA19080 | hp2 | a0001 | c0001 | t0001 | g0071 | EAS | JPT | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
NA19087 | hp1 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
NA19087 | hp2 | a0001 | c0001 | t0001 | g0082 | EAS | JPT | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
NA19088 | hp1 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
NA19088 | hp2 | a0001 | c0001 | t0001 | g0048 | EAS | JPT | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
NA19090 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
NA19090 | hp2 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
NA19240 | hp1 | a0001 | c0001 | t0001 | g0171 | AFR | YRI | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
NA19240 | hp2 | a0001 | c0001 | t0001 | g0011 | AFR | YRI | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
NA20129 | hp1 | a0001 | c0001 | t0001 | g0173 | AFR | ASW | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
NA20129 | hp2 | a0001 | c0001 | t0001 | g0009 | AFR | ASW | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
NA20905 | hp1 | a0001 | c0001 | t0001 | g0146 | SAS | GIH | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
NA20905 | hp2 | a0001 | c0004 | t0001 | g0063 | SAS | GIH | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
HG01123 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
HG01123 | hp2 | a0001 | c0001 | t0001 | g0115 | AMR | CLM | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
HG02109 | hp1 | a0001 | c0001 | t0001 | g0108 | AFR | ACB | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
HG02109 | hp2 | a0001 | c0001 | t0001 | g0207 | AFR | ACB | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
HG02486 | hp1 | a0001 | c0001 | t0001 | g0206 | AFR | ACB | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
HG02486 | hp2 | a0001 | c0001 | t0001 | g0177 | AFR | ACB | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
HG02559 | hp1 | a0001 | c0001 | t0001 | g0223 | AFR | ACB | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
HG02559 | hp2 | a0001 | c0001 | t0002 | g0034 | AFR | ACB | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
HG06807 | hp1 | a0001 | c0001 | t0001 | g0114 | AFR | USA | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
HG06807 | hp2 | a0001 | c0001 | t0001 | g0222 | AFR | USA | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
NA20300 | hp1 | a0001 | c0001 | t0001 | g0043 | AFR | USA | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
NA20300 | hp2 | a0001 | c0001 | t0001 | g0142 | AFR | USA | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
NA21309 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | LWK | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
NA21309 | hp2 | a0001 | c0001 | t0001 | g0045 | AFR | LWK | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0159 | REF | REF | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0213 | REF | REF | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr13:36949948 | C | T | 1 | a0002 | 3 | HG00609.hp1 HG03130.hp2 HG03225.hp1 |
missense_variant | MODERATE | c.969G>A | p.Met323Ile | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 10/10 | 1009/1219 | 969/975 | 323/324 | chr13 | 36949948 | |||
chr13:36985714 | C | A | 1 | a0004 | 1 | HG01934.hp2 | missense_variant | MODERATE | c.474G>T | p.Lys158Asn | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 6/10 | 514/1219 | 474/975 | 158/324 | chr13 | 36985714 | |||
chr13:36995485 | A | G | 1 | a0003 | 2 | HG02886.hp1 HG02895.hp2 |
missense_variant | MODERATE | c.178T>C | p.Trp60Arg | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 2/10 | 218/1219 | 178/975 | 60/324 | chr13 | 36995485 | |||
chr13:36999245 | G | C | 1 | a0005 | 1 | HG02071.hp1 | missense_variant | MODERATE | c.56C>G | p.Ala19Gly | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 1/10 | 96/1219 | 56/975 | 19/324 | chr13 | 36999245 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr13:36952539 | A | T | 1 | a0001c0004 | 2 | HG03492.hp2 NA20905.hp2 |
synonymous_variant | LOW | c.834T>A | p.Ile278Ile | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 9/10 | 874/1219 | 834/975 | 278/324 | chr13 | 36952539 | |||
chr13:36999247 | T | G | 1 | a0001c0007 | 1 | HG02630.hp1 | synonymous_variant | LOW | c.54A>C | p.Ala18Ala | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 1/10 | 94/1219 | 54/975 | 18/324 | chr13 | 36999247 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr13:36949910 | G | C | 1 | a0001c0001t0002 | 1 | HG02559.hp2 | 3_prime_UTR_variant | MODIFIER | c.*32C>G | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 10/10 | 32 | chr13 | 36949910 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr13:36950118 | A | C | 69 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(66): Show |
94 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(91): Show |
intron_variant | MODIFIER | c.860-61T>G | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 9/9 | chr13 | 36950118 | |||||||
chr13:36950588 | GT | G | 208 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(205): Show |
249 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(246): Show |
intron_variant | MODIFIER | c.860-532delA | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 9/9 | chr13 | 36950588 | |||||||
chr13:36950642 | C | T | 1 | a0001c0001t0001g0180 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.860-585G>A | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 9/9 | chr13 | 36950642 | |||||||
chr13:36950863 | GGCATGAG others(5): Show |
G | 2 | a0001c0001t0001g0080 a0001c0001t0001g0082 |
2 | NA19087.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.860-818_860-807del others(12): Show |
ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 9/9 | chr13 | 36950863 | |||||||
chr13:36951037 | A | G | 25 | a0001c0001t0001g0012 a0001c0001t0001g0031 a0001c0001t0001g0032 others(22): Show |
26 | HG01109.hp2 HG01192.hp2 HG01515.hp2 others(23): Show |
intron_variant | MODIFIER | c.860-980T>C | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 9/9 | chr13 | 36951037 | |||||||
chr13:36951125 | C | T | 2 | a0002c0002t0001g0190 a0002c0002t0001g0191 |
2 | HG03130.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.860-1068G>A | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 9/9 | chr13 | 36951125 | |||||||
chr13:36951430 | T | C | 215 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(212): Show |
256 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(253): Show |
intron_variant | MODIFIER | c.859+1084A>G | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 9/9 | chr13 | 36951430 | |||||||
chr13:36951832 | G | A | 1 | a0001c0001t0001g0222 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.859+682C>T | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 9/9 | chr13 | 36951832 | |||||||
chr13:36951878 | G | A | 1 | a0001c0001t0001g0055 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.859+636C>T | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 9/9 | chr13 | 36951878 | |||||||
chr13:36952082 | G | A | 1 | a0001c0001t0001g0186 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.859+432C>T | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 9/9 | chr13 | 36952082 | |||||||
chr13:36952230 | T | C | 213 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(210): Show |
254 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(251): Show |
intron_variant | MODIFIER | c.859+284A>G | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 9/9 | chr13 | 36952230 | |||||||
chr13:36952239 | A | T | 1 | a0001c0001t0001g0147 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.859+275T>A | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 9/9 | chr13 | 36952239 | |||||||
chr13:36952423 | G | A | 182 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(179): Show |
222 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(219): Show |
intron_variant | MODIFIER | c.859+91C>T | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 9/9 | chr13 | 36952423 | |||||||
chr13:36952680 | A | C | 2 | a0002c0002t0001g0190 a0002c0002t0001g0191 |
2 | HG03130.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.774-81T>G | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 8/9 | chr13 | 36952680 | |||||||
chr13:36953018 | C | T | 1 | a0001c0007t0001g0227 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.774-419G>A | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 8/9 | chr13 | 36953018 | |||||||
chr13:36953160 | G | C | 1 | a0001c0001t0001g0208 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.774-561C>G | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 8/9 | chr13 | 36953160 | |||||||
chr13:36953217 | T | C | 2 | a0003c0003t0001g0188 a0003c0003t0001g0189 |
2 | HG02886.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.774-618A>G | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 8/9 | chr13 | 36953217 | |||||||
chr13:36953401 | A | C | 1 | a0001c0001t0001g0077 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.774-802T>G | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 8/9 | chr13 | 36953401 | |||||||
chr13:36953530 | T | C | 86 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0013 others(83): Show |
97 | HG00099.hp1 HG00438.hp1 HG00609.hp2 others(94): Show |
intron_variant | MODIFIER | c.774-931A>G | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 8/9 | chr13 | 36953530 | |||||||
chr13:36953603 | G | A | 2 | a0002c0002t0001g0190 a0002c0002t0001g0191 |
2 | HG03130.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.774-1004C>T | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 8/9 | chr13 | 36953603 | |||||||
chr13:36953705 | G | T | 1 | a0001c0001t0001g0084 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.774-1106C>A | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 8/9 | chr13 | 36953705 | |||||||
chr13:36953805 | T | C | 3 | a0001c0001t0001g0210 a0001c0001t0001g0211 a0001c0001t0001g0212 |
3 | HG03209.hp2 HG03486.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.774-1206A>G | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 8/9 | chr13 | 36953805 | |||||||
chr13:36953934 | T | C | 1 | a0001c0001t0001g0115 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.774-1335A>G | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 8/9 | chr13 | 36953934 | |||||||
chr13:36954023 | G | A | 9 | a0001c0001t0001g0020 a0001c0001t0001g0161 a0001c0001t0001g0162 others(6): Show |
10 | HG00609.hp1 HG02074.hp1 NA18947.hp1 others(7): Show |
intron_variant | MODIFIER | c.774-1424C>T | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 8/9 | chr13 | 36954023 | |||||||
chr13:36954063 | T | TA | 215 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(212): Show |
256 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(253): Show |
intron_variant | MODIFIER | c.774-1465dupT | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 8/9 | chr13 | 36954063 | |||||||
chr13:36954148 | G | A | 1 | a0001c0001t0001g0052 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.774-1549C>T | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 8/9 | chr13 | 36954148 | |||||||
chr13:36954263 | ATCT | A | 188 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(185): Show |
228 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(225): Show |
intron_variant | MODIFIER | c.774-1667_774-1665d others(5): Show |
ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 8/9 | chr13 | 36954263 | |||||||
chr13:36954392 | A | G | 1 | a0001c0001t0001g0053 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.774-1793T>C | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 8/9 | chr13 | 36954392 | |||||||
chr13:36954416 | C | A | 1 | a0001c0001t0001g0222 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.774-1817G>T | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 8/9 | chr13 | 36954416 | |||||||
chr13:36954694 | C | G | 1 | a0001c0001t0001g0097 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.774-2095G>C | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 8/9 | chr13 | 36954694 | |||||||
chr13:36955206 | A | G | 1 | a0001c0007t0001g0227 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.774-2607T>C | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 8/9 | chr13 | 36955206 | |||||||
chr13:36955284 | C | T | 1 | a0001c0001t0001g0129 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.774-2685G>A | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 8/9 | chr13 | 36955284 | |||||||
chr13:36955347 | G | C | 1 | a0001c0001t0001g0210 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.774-2748C>G | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 8/9 | chr13 | 36955347 | |||||||
chr13:36955686 | G | GA | 25 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0045 others(22): Show |
27 | HG00438.hp2 HG00621.hp1 HG01175.hp1 others(24): Show |
intron_variant | MODIFIER | c.774-3088dupT | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 8/9 | chr13 | 36955686 | |||||||
chr13:36955686 | GA | G | 34 | a0001c0001t0001g0011 a0001c0001t0001g0017 a0001c0001t0001g0024 others(31): Show |
39 | HG00323.hp1 HG00639.hp2 HG01081.hp2 others(36): Show |
intron_variant | MODIFIER | c.774-3088delT | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 8/9 | chr13 | 36955686 | |||||||
chr13:36955686 | GAAAAAAA | G | 26 | a0001c0001t0001g0012 a0001c0001t0001g0020 a0001c0001t0001g0031 others(23): Show |
28 | HG00609.hp1 HG01109.hp2 HG01192.hp2 others(25): Show |
intron_variant | MODIFIER | c.774-3094_774-3088d others(9): Show |
ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 8/9 | chr13 | 36955686 | |||||||
chr13:36955911 | A | G | 5 | a0001c0001t0001g0113 a0001c0001t0001g0114 a0001c0001t0001g0115 others(2): Show |
5 | HG01081.hp1 HG01123.hp2 HG01361.hp1 others(2): Show |
intron_variant | MODIFIER | c.774-3312T>C | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 8/9 | chr13 | 36955911 | |||||||
chr13:36956078 | G | A | 5 | a0001c0001t0001g0011 a0001c0001t0001g0205 a0001c0001t0001g0206 others(2): Show |
7 | HG00639.hp2 HG02109.hp2 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.774-3479C>T | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 8/9 | chr13 | 36956078 | |||||||
chr13:36956376 | G | A | 1 | a0001c0001t0001g0208 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.774-3777C>T | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 8/9 | chr13 | 36956376 | |||||||
chr13:36956416 | T | C | 2 | a0003c0003t0001g0188 a0003c0003t0001g0189 |
2 | HG02886.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.774-3817A>G | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 8/9 | chr13 | 36956416 | |||||||
chr13:36956686 | A | G | 215 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(212): Show |
256 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(253): Show |
intron_variant | MODIFIER | c.774-4087T>C | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 8/9 | chr13 | 36956686 | |||||||
chr13:36956703 | A | T | 215 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(212): Show |
256 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(253): Show |
intron_variant | MODIFIER | c.774-4104T>A | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 8/9 | chr13 | 36956703 | |||||||
chr13:36956957 | G | C | 1 | a0001c0001t0001g0198 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.774-4358C>G | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 8/9 | chr13 | 36956957 | |||||||
chr13:36957130 | A | G | 2 | a0002c0002t0001g0190 a0002c0002t0001g0191 |
2 | HG03130.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.774-4531T>C | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 8/9 | chr13 | 36957130 | |||||||
chr13:36957367 | A | G | 1 | a0001c0001t0001g0187 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.774-4768T>C | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 8/9 | chr13 | 36957367 | |||||||
chr13:36957474 | G | C | 1 | a0001c0001t0001g0148 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.774-4875C>G | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 8/9 | chr13 | 36957474 | |||||||
chr13:36957526 | G | A | 18 | a0001c0001t0001g0012 a0001c0001t0001g0031 a0001c0001t0001g0032 others(15): Show |
19 | HG01109.hp2 HG01192.hp2 HG01515.hp2 others(16): Show |
intron_variant | MODIFIER | c.774-4927C>T | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 8/9 | chr13 | 36957526 | |||||||
chr13:36957586 | CT | C | 23 | a0001c0001t0001g0012 a0001c0001t0001g0031 a0001c0001t0001g0032 others(20): Show |
24 | HG01109.hp2 HG01192.hp2 HG01515.hp2 others(21): Show |
intron_variant | MODIFIER | c.774-4988delA | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 8/9 | chr13 | 36957586 | |||||||
chr13:36957604 | G | A | 1 | a0001c0001t0001g0047 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.774-5005C>T | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 8/9 | chr13 | 36957604 | |||||||
chr13:36957697 | C | T | 25 | a0001c0001t0001g0012 a0001c0001t0001g0031 a0001c0001t0001g0032 others(22): Show |
26 | HG01109.hp2 HG01192.hp2 HG01515.hp2 others(23): Show |
intron_variant | MODIFIER | c.774-5098G>A | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 8/9 | chr13 | 36957697 | |||||||
chr13:36957720 | C | G | 1 | a0001c0001t0001g0091 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.774-5121G>C | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 8/9 | chr13 | 36957720 | |||||||
chr13:36958098 | G | A | 1 | a0001c0001t0001g0059 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.774-5499C>T | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 8/9 | chr13 | 36958098 | |||||||
chr13:36958193 | A | G | 18 | a0001c0001t0001g0012 a0001c0001t0001g0031 a0001c0001t0001g0032 others(15): Show |
19 | HG01109.hp2 HG01192.hp2 HG01515.hp2 others(16): Show |
intron_variant | MODIFIER | c.774-5594T>C | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 8/9 | chr13 | 36958193 | |||||||
chr13:36958196 | G | A | 2 | a0001c0001t0001g0184 a0001c0001t0001g0185 |
2 | HG03098.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.774-5597C>T | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 8/9 | chr13 | 36958196 | |||||||
chr13:36958212 | G | A | 1 | a0001c0001t0001g0118 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.774-5613C>T | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 8/9 | chr13 | 36958212 | |||||||
chr13:36958373 | G | A | 1 | a0001c0001t0001g0076 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.774-5774C>T | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 8/9 | chr13 | 36958373 | |||||||
chr13:36958561 | G | A | 11 | a0001c0001t0001g0023 a0001c0001t0001g0029 a0001c0001t0001g0171 others(8): Show |
12 | HG02145.hp2 HG02280.hp2 HG02486.hp2 others(9): Show |
intron_variant | MODIFIER | c.774-5962C>T | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 8/9 | chr13 | 36958561 | |||||||
chr13:36958798 | T | C | 1 | a0001c0001t0001g0225 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.774-6199A>G | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 8/9 | chr13 | 36958798 | |||||||
chr13:36958903 | C | G | 1 | a0001c0001t0001g0168 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.774-6304G>C | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 8/9 | chr13 | 36958903 | |||||||
chr13:36959148 | A | C | 11 | a0001c0001t0001g0023 a0001c0001t0001g0029 a0001c0001t0001g0171 others(8): Show |
12 | HG02145.hp2 HG02280.hp2 HG02486.hp2 others(9): Show |
intron_variant | MODIFIER | c.773+6427T>G | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 8/9 | chr13 | 36959148 | |||||||
chr13:36959163 | A | G | 2 | a0001c0001t0001g0008 a0001c0001t0001g0126 |
4 | HG00673.hp2 NA18947.hp2 NA18986.hp2 others(1): Show |
intron_variant | MODIFIER | c.773+6412T>C | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 8/9 | chr13 | 36959163 | |||||||
chr13:36959219 | G | T | 183 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(180): Show |
223 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(220): Show |
intron_variant | MODIFIER | c.773+6356C>A | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 8/9 | chr13 | 36959219 | |||||||
chr13:36959410 | T | C | 215 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(212): Show |
256 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(253): Show |
intron_variant | MODIFIER | c.773+6165A>G | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 8/9 | chr13 | 36959410 | |||||||
chr13:36959411 | A | G | 182 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(179): Show |
222 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(219): Show |
intron_variant | MODIFIER | c.773+6164T>C | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 8/9 | chr13 | 36959411 | |||||||
chr13:36959529 | A | G | 2 | a0001c0001t0001g0025 a0001c0001t0001g0045 |
3 | HG02257.hp1 HG03516.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.773+6046T>C | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 8/9 | chr13 | 36959529 | |||||||
chr13:36959533 | C | A | 2 | a0001c0001t0001g0024 a0001c0001t0001g0030 |
3 | HG02572.hp2 HG02896.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.773+6042G>T | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 8/9 | chr13 | 36959533 | |||||||
chr13:36959551 | T | A | 1 | a0001c0001t0001g0118 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.773+6024A>T | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 8/9 | chr13 | 36959551 | |||||||
chr13:36959836 | T | A | 1 | a0001c0001t0001g0208 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.773+5739A>T | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 8/9 | chr13 | 36959836 | |||||||
chr13:36959917 | G | C | 3 | a0001c0001t0001g0184 a0001c0001t0001g0185 a0001c0007t0001g0227 |
3 | HG02630.hp1 HG03098.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.773+5658C>G | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 8/9 | chr13 | 36959917 | |||||||
chr13:36960085 | C | A | 1 | a0001c0001t0001g0077 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.773+5490G>T | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 8/9 | chr13 | 36960085 | |||||||
chr13:36960199 | G | C | 3 | a0001c0001t0001g0184 a0001c0001t0001g0185 a0001c0007t0001g0227 |
3 | HG02630.hp1 HG03098.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.773+5376C>G | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 8/9 | chr13 | 36960199 | |||||||
chr13:36960517 | T | C | 1 | a0001c0001t0001g0093 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.773+5058A>G | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 8/9 | chr13 | 36960517 | |||||||
chr13:36960602 | C | G | 4 | a0001c0001t0001g0065 a0001c0001t0001g0074 a0001c0001t0001g0090 others(1): Show |
4 | HG01109.hp1 HG01167.hp1 HG01175.hp2 others(1): Show |
intron_variant | MODIFIER | c.773+4973G>C | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 8/9 | chr13 | 36960602 | |||||||
chr13:36960644 | G | C | 215 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(212): Show |
256 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(253): Show |
intron_variant | MODIFIER | c.773+4931C>G | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 8/9 | chr13 | 36960644 | |||||||
chr13:36960651 | T | C | 1 | a0001c0001t0001g0078 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.773+4924A>G | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 8/9 | chr13 | 36960651 | |||||||
chr13:36960687 | CT | C | 81 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0013 others(78): Show |
92 | HG00099.hp1 HG00438.hp1 HG00609.hp2 others(89): Show |
intron_variant | MODIFIER | c.773+4887delA | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 8/9 | chr13 | 36960687 | |||||||
chr13:36960983 | G | C | 182 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(179): Show |
222 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(219): Show |
intron_variant | MODIFIER | c.773+4592C>G | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 8/9 | chr13 | 36960983 | |||||||
chr13:36960989 | C | T | 3 | a0001c0001t0001g0006 a0001c0001t0001g0128 a0001c0001t0001g0129 |
5 | HG01891.hp2 HG02451.hp1 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.773+4586G>A | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 8/9 | chr13 | 36960989 | |||||||
chr13:36961051 | A | C | 2 | a0001c0001t0001g0025 a0001c0001t0001g0045 |
3 | HG02257.hp1 HG03516.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.773+4524T>G | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 8/9 | chr13 | 36961051 | |||||||
chr13:36961141 | T | A | 2 | a0002c0002t0001g0190 a0002c0002t0001g0191 |
2 | HG03130.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.773+4434A>T | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 8/9 | chr13 | 36961141 | |||||||
chr13:36961673 | T | C | 213 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(210): Show |
254 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(251): Show |
intron_variant | MODIFIER | c.773+3902A>G | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 8/9 | chr13 | 36961673 | |||||||
chr13:36961842 | C | T | 2 | a0003c0003t0001g0188 a0003c0003t0001g0189 |
2 | HG02886.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.773+3733G>A | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 8/9 | chr13 | 36961842 | |||||||
chr13:36961848 | C | A | 2 | a0001c0001t0001g0210 a0001c0001t0001g0212 |
2 | HG03209.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.773+3727G>T | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 8/9 | chr13 | 36961848 | |||||||
chr13:36961877 | G | T | 1 | a0001c0001t0001g0193 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.773+3698C>A | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 8/9 | chr13 | 36961877 | |||||||
chr13:36961935 | C | T | 2 | a0001c0001t0001g0184 a0001c0001t0001g0185 |
2 | HG03098.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.773+3640G>A | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 8/9 | chr13 | 36961935 | |||||||
chr13:36961953 | T | G | 2 | a0001c0001t0001g0184 a0001c0001t0001g0185 |
2 | HG03098.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.773+3622A>C | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 8/9 | chr13 | 36961953 | |||||||
chr13:36962071 | A | T | 4 | a0001c0001t0001g0193 a0001c0001t0001g0194 a0001c0001t0001g0195 others(1): Show |
4 | HG02280.hp1 HG02647.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.773+3504T>A | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 8/9 | chr13 | 36962071 | |||||||
chr13:36962332 | T | C | 1 | a0001c0001t0001g0079 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.773+3243A>G | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 8/9 | chr13 | 36962332 | |||||||
chr13:36962373 | G | A | 2 | a0001c0001t0001g0184 a0001c0001t0001g0185 |
2 | HG03098.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.773+3202C>T | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 8/9 | chr13 | 36962373 | |||||||
chr13:36962945 | G | A | 23 | a0001c0001t0001g0012 a0001c0001t0001g0031 a0001c0001t0001g0032 others(20): Show |
24 | HG01109.hp2 HG01192.hp2 HG01515.hp2 others(21): Show |
intron_variant | MODIFIER | c.773+2630C>T | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 8/9 | chr13 | 36962945 | |||||||
chr13:36963010 | G | A | 2 | a0001c0001t0001g0184 a0001c0001t0001g0185 |
2 | HG03098.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.773+2565C>T | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 8/9 | chr13 | 36963010 | |||||||
chr13:36963090 | G | A | 14 | a0001c0001t0001g0023 a0001c0001t0001g0029 a0001c0001t0001g0171 others(11): Show |
15 | HG02145.hp2 HG02280.hp2 HG02486.hp2 others(12): Show |
intron_variant | MODIFIER | c.773+2485C>T | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 8/9 | chr13 | 36963090 | |||||||
chr13:36963178 | C | T | 25 | a0001c0001t0001g0012 a0001c0001t0001g0031 a0001c0001t0001g0032 others(22): Show |
26 | HG01109.hp2 HG01192.hp2 HG01515.hp2 others(23): Show |
intron_variant | MODIFIER | c.773+2397G>A | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 8/9 | chr13 | 36963178 | |||||||
chr13:36963498 | G | GC | 215 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(212): Show |
256 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(253): Show |
intron_variant | MODIFIER | c.773+2076dupG | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 8/9 | chr13 | 36963498 | |||||||
chr13:36963505 | C | T | 1 | a0001c0001t0001g0151 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.773+2070G>A | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 8/9 | chr13 | 36963505 | |||||||
chr13:36963517 | T | C | 1 | a0001c0001t0001g0171 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.773+2058A>G | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 8/9 | chr13 | 36963517 | |||||||
chr13:36963526 | C | A | 3 | a0001c0001t0001g0179 a0001c0001t0001g0180 a0001c0001t0001g0181 |
3 | HG02615.hp1 HG02647.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.773+2049G>T | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 8/9 | chr13 | 36963526 | |||||||
chr13:36963830 | T | C | 215 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(212): Show |
256 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(253): Show |
intron_variant | MODIFIER | c.773+1745A>G | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 8/9 | chr13 | 36963830 | |||||||
chr13:36963885 | T | G | 1 | a0001c0001t0001g0134 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.773+1690A>C | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 8/9 | chr13 | 36963885 | |||||||
chr13:36964131 | C | T | 1 | a0001c0001t0001g0217 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.773+1444G>A | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 8/9 | chr13 | 36964131 | |||||||
chr13:36964360 | A | G | 2 | a0002c0002t0001g0190 a0002c0002t0001g0191 |
2 | HG03130.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.773+1215T>C | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 8/9 | chr13 | 36964360 | |||||||
chr13:36964450 | T | C | 18 | a0001c0001t0001g0012 a0001c0001t0001g0031 a0001c0001t0001g0032 others(15): Show |
19 | HG01109.hp2 HG01192.hp2 HG01515.hp2 others(16): Show |
intron_variant | MODIFIER | c.773+1125A>G | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 8/9 | chr13 | 36964450 | |||||||
chr13:36964507 | A | G | 223 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(220): Show |
272 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(269): Show |
intron_variant | MODIFIER | c.773+1068T>C | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 8/9 | chr13 | 36964507 | |||||||
chr13:36964850 | G | A | 3 | a0001c0001t0001g0015 a0001c0001t0001g0083 a0001c0001t0001g0119 |
4 | HG02523.hp2 NA19011.hp2 NA19058.hp2 others(1): Show |
intron_variant | MODIFIER | c.773+725C>T | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 8/9 | chr13 | 36964850 | |||||||
chr13:36964897 | C | A | 5 | a0001c0001t0001g0011 a0001c0001t0001g0205 a0001c0001t0001g0206 others(2): Show |
7 | HG00639.hp2 HG02109.hp2 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.773+678G>T | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 8/9 | chr13 | 36964897 | |||||||
chr13:36964919 | C | CA | 181 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(178): Show |
221 | HG00099.hp2 HG00323.hp1 HG00438.hp1 others(218): Show |
intron_variant | MODIFIER | c.773+655dupT | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 8/9 | chr13 | 36964919 | |||||||
chr13:36965015 | A | G | 2 | a0001c0001t0001g0184 a0001c0001t0001g0185 |
2 | HG03098.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.773+560T>C | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 8/9 | chr13 | 36965015 | |||||||
chr13:36965070 | A | T | 1 | a0001c0001t0001g0072 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.773+505T>A | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 8/9 | chr13 | 36965070 | |||||||
chr13:36965207 | G | T | 1 | a0001c0001t0001g0103 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.773+368C>A | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 8/9 | chr13 | 36965207 | |||||||
chr13:36965305 | A | AAAGGAAA others(13): Show |
213 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(210): Show |
254 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(251): Show |
intron_variant | MODIFIER | c.773+269_773+270ins others(20): Show |
ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 8/9 | chr13 | 36965305 | |||||||
chr13:36965305 | A | AAAGGAGA others(13): Show |
2 | a0002c0002t0001g0190 a0002c0002t0001g0191 |
2 | HG03130.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.773+269_773+270ins others(20): Show |
ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 8/9 | chr13 | 36965305 | |||||||
chr13:36966077 | G | A | 215 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(212): Show |
256 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(253): Show |
intron_variant | MODIFIER | c.622-351C>T | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 7/9 | chr13 | 36966077 | |||||||
chr13:36966437 | A | C | 2 | a0002c0002t0001g0190 a0002c0002t0001g0191 |
2 | HG03130.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.622-711T>G | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 7/9 | chr13 | 36966437 | |||||||
chr13:36966603 | G | A | 1 | a0001c0001t0001g0126 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.622-877C>T | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 7/9 | chr13 | 36966603 | |||||||
chr13:36966655 | G | A | 2 | a0001c0001t0001g0184 a0001c0001t0001g0185 |
2 | HG03098.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.622-929C>T | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 7/9 | chr13 | 36966655 | |||||||
chr13:36966850 | T | C | 1 | a0001c0001t0001g0084 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.622-1124A>G | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 7/9 | chr13 | 36966850 | |||||||
chr13:36967017 | G | T | 1 | a0001c0001t0001g0049 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.622-1291C>A | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 7/9 | chr13 | 36967017 | |||||||
chr13:36967053 | T | C | 2 | a0001c0001t0001g0184 a0001c0001t0001g0185 |
2 | HG03098.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.622-1327A>G | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 7/9 | chr13 | 36967053 | |||||||
chr13:36967238 | G | A | 1 | a0001c0001t0001g0049 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.622-1512C>T | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 7/9 | chr13 | 36967238 | |||||||
chr13:36967239 | A | G | 1 | a0001c0001t0001g0049 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.622-1513T>C | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 7/9 | chr13 | 36967239 | |||||||
chr13:36967286 | G | T | 214 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(211): Show |
255 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(252): Show |
intron_variant | MODIFIER | c.622-1560C>A | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 7/9 | chr13 | 36967286 | |||||||
chr13:36967425 | A | C | 1 | a0001c0001t0001g0208 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.622-1699T>G | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 7/9 | chr13 | 36967425 | |||||||
chr13:36967530 | T | C | 1 | a0001c0001t0001g0097 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.622-1804A>G | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 7/9 | chr13 | 36967530 | |||||||
chr13:36967743 | C | T | 4 | a0001c0001t0001g0193 a0001c0001t0001g0194 a0001c0001t0001g0195 others(1): Show |
4 | HG02280.hp1 HG02647.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.622-2017G>A | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 7/9 | chr13 | 36967743 | |||||||
chr13:36967883 | A | T | 1 | a0001c0001t0001g0205 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.622-2157T>A | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 7/9 | chr13 | 36967883 | |||||||
chr13:36967894 | G | A | 18 | a0001c0001t0001g0012 a0001c0001t0001g0031 a0001c0001t0001g0032 others(15): Show |
19 | HG01109.hp2 HG01192.hp2 HG01515.hp2 others(16): Show |
intron_variant | MODIFIER | c.622-2168C>T | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 7/9 | chr13 | 36967894 | |||||||
chr13:36968055 | A | C | 2 | a0002c0002t0001g0190 a0002c0002t0001g0191 |
2 | HG03130.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.622-2329T>G | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 7/9 | chr13 | 36968055 | |||||||
chr13:36968095 | C | A | 5 | a0001c0001t0001g0011 a0001c0001t0001g0205 a0001c0001t0001g0206 others(2): Show |
7 | HG00639.hp2 HG02109.hp2 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.622-2369G>T | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 7/9 | chr13 | 36968095 | |||||||
chr13:36968234 | T | C | 6 | a0001c0001t0001g0178 a0001c0001t0001g0204 a0001c0001t0001g0222 others(3): Show |
6 | HG02559.hp1 HG02818.hp2 HG03209.hp1 others(3): Show |
intron_variant | MODIFIER | c.622-2508A>G | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 7/9 | chr13 | 36968234 | |||||||
chr13:36968283 | C | T | 18 | a0001c0001t0001g0012 a0001c0001t0001g0031 a0001c0001t0001g0032 others(15): Show |
19 | HG01109.hp2 HG01192.hp2 HG01515.hp2 others(16): Show |
intron_variant | MODIFIER | c.622-2557G>A | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 7/9 | chr13 | 36968283 | |||||||
chr13:36968366 | T | C | 1 | a0001c0001t0001g0199 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.622-2640A>G | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 7/9 | chr13 | 36968366 | |||||||
chr13:36968383 | A | C | 1 | a0001c0001t0001g0056 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.622-2657T>G | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 7/9 | chr13 | 36968383 | |||||||
chr13:36968506 | A | T | 17 | a0001c0001t0001g0061 a0001c0001t0001g0070 a0001c0001t0001g0071 others(14): Show |
17 | HG00099.hp1 HG01081.hp1 HG01123.hp2 others(14): Show |
intron_variant | MODIFIER | c.622-2780T>A | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 7/9 | chr13 | 36968506 | |||||||
chr13:36968520 | T | A | 2 | a0001c0001t0001g0179 a0001c0001t0001g0180 |
2 | HG02615.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.622-2794A>T | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 7/9 | chr13 | 36968520 | |||||||
chr13:36968667 | C | CATTAGGC others(27): Show |
1 | a0001c0001t0001g0062 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.622-2975_622-2942d others(36): Show |
ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 7/9 | chr13 | 36968667 | |||||||
chr13:36968779 | C | T | 83 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0013 others(80): Show |
93 | HG00099.hp1 HG00438.hp1 HG00609.hp2 others(90): Show |
intron_variant | MODIFIER | c.622-3053G>A | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 7/9 | chr13 | 36968779 | |||||||
chr13:36969021 | A | G | 215 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(212): Show |
256 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(253): Show |
intron_variant | MODIFIER | c.621+2956T>C | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 7/9 | chr13 | 36969021 | |||||||
chr13:36969053 | A | G | 18 | a0001c0001t0001g0012 a0001c0001t0001g0031 a0001c0001t0001g0032 others(15): Show |
19 | HG01109.hp2 HG01192.hp2 HG01515.hp2 others(16): Show |
intron_variant | MODIFIER | c.621+2924T>C | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 7/9 | chr13 | 36969053 | |||||||
chr13:36969061 | A | G | 4 | a0001c0001t0001g0011 a0001c0001t0001g0206 a0001c0001t0001g0207 others(1): Show |
6 | HG02109.hp2 HG02486.hp1 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.621+2916T>C | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 7/9 | chr13 | 36969061 | |||||||
chr13:36969101 | C | T | 2 | a0001c0001t0001g0025 a0001c0001t0001g0045 |
3 | HG02257.hp1 HG03516.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.621+2876G>A | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 7/9 | chr13 | 36969101 | |||||||
chr13:36969342 | G | GTC | 215 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(212): Show |
256 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(253): Show |
intron_variant | MODIFIER | c.621+2634_621+2635i others(4): Show |
ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 7/9 | chr13 | 36969342 | |||||||
chr13:36969346 | A | G | 1 | a0001c0001t0001g0225 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.621+2631T>C | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 7/9 | chr13 | 36969346 | |||||||
chr13:36969416 | AT | A | 211 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(208): Show |
252 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(249): Show |
intron_variant | MODIFIER | c.621+2560delA | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 7/9 | chr13 | 36969416 | |||||||
chr13:36969551 | G | A | 2 | a0001c0001t0001g0060 a0001c0001t0001g0099 |
2 | HG02145.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.621+2426C>T | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 7/9 | chr13 | 36969551 | |||||||
chr13:36969585 | G | A | 6 | a0001c0001t0001g0097 a0001c0001t0001g0113 a0001c0001t0001g0114 others(3): Show |
6 | HG01081.hp1 HG01123.hp2 HG01361.hp1 others(3): Show |
intron_variant | MODIFIER | c.621+2392C>T | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 7/9 | chr13 | 36969585 | |||||||
chr13:36969636 | G | A | 1 | a0001c0001t0001g0102 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.621+2341C>T | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 7/9 | chr13 | 36969636 | |||||||
chr13:36969731 | C | A | 18 | a0001c0001t0001g0012 a0001c0001t0001g0031 a0001c0001t0001g0032 others(15): Show |
19 | HG01109.hp2 HG01192.hp2 HG01515.hp2 others(16): Show |
intron_variant | MODIFIER | c.621+2246G>T | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 7/9 | chr13 | 36969731 | |||||||
chr13:36969789 | C | T | 1 | a0001c0007t0001g0227 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.621+2188G>A | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 7/9 | chr13 | 36969789 | |||||||
chr13:36969870 | A | G | 2 | a0002c0002t0001g0190 a0002c0002t0001g0191 |
2 | HG03130.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.621+2107T>C | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 7/9 | chr13 | 36969870 | |||||||
chr13:36970027 | C | A | 1 | a0001c0001t0001g0025 | 2 | HG02257.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.621+1950G>T | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 7/9 | chr13 | 36970027 | |||||||
chr13:36970038 | A | C | 1 | a0001c0001t0001g0170 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.621+1939T>G | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 7/9 | chr13 | 36970038 | |||||||
chr13:36970089 | C | T | 215 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(212): Show |
256 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(253): Show |
intron_variant | MODIFIER | c.621+1888G>A | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 7/9 | chr13 | 36970089 | |||||||
chr13:36970091 | T | C | 1 | a0001c0001t0001g0208 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.621+1886A>G | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 7/9 | chr13 | 36970091 | |||||||
chr13:36970145 | C | T | 2 | a0003c0003t0001g0188 a0003c0003t0001g0189 |
2 | HG02886.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.621+1832G>A | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 7/9 | chr13 | 36970145 | |||||||
chr13:36970492 | C | T | 3 | a0001c0001t0001g0007 a0001c0001t0001g0144 a0001c0001t0001g0154 |
5 | HG00733.hp2 HG00741.hp1 HG01258.hp2 others(2): Show |
intron_variant | MODIFIER | c.621+1485G>A | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 7/9 | chr13 | 36970492 | |||||||
chr13:36970672 | G | A | 17 | a0001c0001t0001g0012 a0001c0001t0001g0031 a0001c0001t0001g0032 others(14): Show |
18 | HG01109.hp2 HG01192.hp2 HG01981.hp2 others(15): Show |
intron_variant | MODIFIER | c.621+1305C>T | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 7/9 | chr13 | 36970672 | |||||||
chr13:36970728 | C | T | 1 | a0001c0001t0001g0217 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.621+1249G>A | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 7/9 | chr13 | 36970728 | |||||||
chr13:36971042 | G | A | 1 | a0001c0001t0001g0171 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.621+935C>T | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 7/9 | chr13 | 36971042 | |||||||
chr13:36971258 | G | T | 1 | a0001c0001t0001g0143 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.621+719C>A | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 7/9 | chr13 | 36971258 | |||||||
chr13:36971269 | A | T | 3 | a0001c0001t0001g0193 a0003c0003t0001g0188 a0003c0003t0001g0189 |
3 | HG02886.hp1 HG02895.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.621+708T>A | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 7/9 | chr13 | 36971269 | |||||||
chr13:36971310 | G | A | 2 | a0001c0001t0001g0184 a0001c0001t0001g0185 |
2 | HG03098.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.621+667C>T | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 7/9 | chr13 | 36971310 | |||||||
chr13:36971373 | G | A | 3 | a0001c0001t0001g0010 a0001c0001t0001g0198 a0001c0001t0001g0202 |
5 | HG02040.hp2 NA18945.hp2 NA18965.hp1 others(2): Show |
intron_variant | MODIFIER | c.621+604C>T | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 7/9 | chr13 | 36971373 | |||||||
chr13:36971378 | A | G | 215 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(212): Show |
256 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(253): Show |
intron_variant | MODIFIER | c.621+599T>C | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 7/9 | chr13 | 36971378 | |||||||
chr13:36971506 | G | A | 1 | a0001c0001t0001g0211 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.621+471C>T | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 7/9 | chr13 | 36971506 | |||||||
chr13:36971613 | C | T | 3 | a0001c0001t0001g0141 a0001c0001t0001g0143 a0001c0001t0001g0156 |
3 | HG02523.hp1 NA18939.hp1 NA19058.hp1 |
intron_variant | MODIFIER | c.621+364G>A | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 7/9 | chr13 | 36971613 | |||||||
chr13:36971649 | C | CA | 6 | a0001c0001t0001g0184 a0001c0001t0001g0185 a0001c0001t0001g0215 others(3): Show |
6 | HG01891.hp1 HG01993.hp1 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.621+327dupT | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 7/9 | chr13 | 36971649 | |||||||
chr13:36971649 | C | CAA | 20 | a0001c0001t0001g0012 a0001c0001t0001g0025 a0001c0001t0001g0032 others(17): Show |
22 | HG01109.hp2 HG01981.hp2 HG02055.hp1 others(19): Show |
intron_variant | MODIFIER | c.621+326_621+327dup others(2): Show |
ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 7/9 | chr13 | 36971649 | |||||||
chr13:36971649 | C | CAAA | 130 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(127): Show |
156 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(153): Show |
intron_variant | MODIFIER | c.621+325_621+327dup others(3): Show |
ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 7/9 | chr13 | 36971649 | |||||||
chr13:36971649 | C | CAAAA | 57 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0011 others(54): Show |
70 | HG00438.hp1 HG00609.hp1 HG00609.hp2 others(67): Show |
intron_variant | MODIFIER | c.621+324_621+327dup others(4): Show |
ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 7/9 | chr13 | 36971649 | |||||||
chr13:36971715 | C | T | 1 | a0001c0001t0001g0194 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.621+262G>A | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 7/9 | chr13 | 36971715 | |||||||
chr13:36971780 | T | C | 2 | a0001c0001t0001g0039 a0001c0001t0001g0040 |
2 | HG01192.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.621+197A>G | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 7/9 | chr13 | 36971780 | |||||||
chr13:36971786 | TA | T | 22 | a0001c0001t0001g0012 a0001c0001t0001g0031 a0001c0001t0001g0032 others(19): Show |
23 | HG01109.hp2 HG01192.hp2 HG01981.hp2 others(20): Show |
intron_variant | MODIFIER | c.621+190delT | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 7/9 | chr13 | 36971786 | |||||||
chr13:36971828 | T | G | 4 | a0001c0001t0001g0193 a0001c0001t0001g0194 a0001c0001t0001g0195 others(1): Show |
4 | HG02280.hp1 HG02647.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.621+149A>C | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 7/9 | chr13 | 36971828 | |||||||
chr13:36972143 | G | C | 86 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0013 others(83): Show |
97 | HG00099.hp1 HG00438.hp1 HG00609.hp2 others(94): Show |
intron_variant | MODIFIER | c.562-107C>G | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 6/9 | chr13 | 36972143 | |||||||
chr13:36972310 | T | C | 71 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(68): Show |
97 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(94): Show |
intron_variant | MODIFIER | c.562-274A>G | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 6/9 | chr13 | 36972310 | |||||||
chr13:36972312 | C | T | 17 | a0001c0001t0001g0012 a0001c0001t0001g0031 a0001c0001t0001g0032 others(14): Show |
18 | HG01109.hp2 HG01192.hp2 HG01981.hp2 others(15): Show |
intron_variant | MODIFIER | c.562-276G>A | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 6/9 | chr13 | 36972312 | |||||||
chr13:36972431 | A | G | 3 | a0001c0001t0001g0210 a0001c0001t0001g0211 a0001c0001t0001g0212 |
3 | HG03209.hp2 HG03486.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.562-395T>C | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 6/9 | chr13 | 36972431 | |||||||
chr13:36972519 | A | AAGAC | 198 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(195): Show |
238 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(235): Show |
intron_variant | MODIFIER | c.562-484_562-483ins others(4): Show |
ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 6/9 | chr13 | 36972519 | |||||||
chr13:36972719 | G | A | 2 | a0001c0001t0001g0097 a0001c0001t0001g0205 |
2 | HG00639.hp2 HG03654.hp1 |
intron_variant | MODIFIER | c.562-683C>T | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 6/9 | chr13 | 36972719 | |||||||
chr13:36972720 | T | C | 1 | a0001c0001t0001g0198 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.562-684A>G | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 6/9 | chr13 | 36972720 | |||||||
chr13:36972723 | T | C | 2 | a0002c0002t0001g0190 a0002c0002t0001g0191 |
2 | HG03130.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.562-687A>G | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 6/9 | chr13 | 36972723 | |||||||
chr13:36972763 | A | C | 1 | a0001c0001t0001g0068 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.562-727T>G | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 6/9 | chr13 | 36972763 | |||||||
chr13:36972768 | A | G | 1 | a0001c0001t0001g0142 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.562-732T>C | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 6/9 | chr13 | 36972768 | |||||||
chr13:36972782 | G | C | 1 | a0001c0001t0001g0203 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.562-746C>G | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 6/9 | chr13 | 36972782 | |||||||
chr13:36972793 | T | C | 1 | a0001c0001t0001g0113 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.562-757A>G | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 6/9 | chr13 | 36972793 | |||||||
chr13:36972800 | G | A | 3 | a0001c0001t0001g0194 a0001c0001t0001g0195 a0001c0001t0001g0196 |
3 | HG02280.hp1 HG02647.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.562-764C>T | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 6/9 | chr13 | 36972800 | |||||||
chr13:36972848 | T | C | 1 | a0001c0001t0001g0084 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.562-812A>G | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 6/9 | chr13 | 36972848 | |||||||
chr13:36972872 | A | G | 215 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(212): Show |
256 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(253): Show |
intron_variant | MODIFIER | c.562-836T>C | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 6/9 | chr13 | 36972872 | |||||||
chr13:36972884 | C | T | 1 | a0001c0007t0001g0227 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.562-848G>A | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 6/9 | chr13 | 36972884 | |||||||
chr13:36972900 | G | A | 9 | a0001c0001t0001g0020 a0001c0001t0001g0161 a0001c0001t0001g0162 others(6): Show |
10 | HG00609.hp1 HG02074.hp1 NA18947.hp1 others(7): Show |
intron_variant | MODIFIER | c.562-864C>T | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 6/9 | chr13 | 36972900 | |||||||
chr13:36972908 | C | T | 1 | a0001c0001t0001g0193 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.562-872G>A | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 6/9 | chr13 | 36972908 | |||||||
chr13:36972917 | A | G | 1 | a0001c0001t0001g0152 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.562-881T>C | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 6/9 | chr13 | 36972917 | |||||||
chr13:36972950 | C | T | 1 | a0001c0001t0001g0069 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.562-914G>A | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 6/9 | chr13 | 36972950 | |||||||
chr13:36972986 | C | T | 2 | a0002c0002t0001g0190 a0002c0002t0001g0191 |
2 | HG03130.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.562-950G>A | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 6/9 | chr13 | 36972986 | |||||||
chr13:36972987 | G | A | 2 | a0002c0002t0001g0190 a0002c0002t0001g0191 |
2 | HG03130.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.562-951C>T | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 6/9 | chr13 | 36972987 | |||||||
chr13:36972991 | C | CA | 85 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0013 others(82): Show |
96 | HG00099.hp1 HG00438.hp1 HG00621.hp2 others(93): Show |
intron_variant | MODIFIER | c.562-956dupT | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 6/9 | chr13 | 36972991 | |||||||
chr13:36972991 | C | CAA | 104 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(101): Show |
133 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(130): Show |
intron_variant | MODIFIER | c.562-957_562-956dup others(2): Show |
ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 6/9 | chr13 | 36972991 | |||||||
chr13:36973123 | A | T | 85 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0013 others(82): Show |
95 | HG00099.hp1 HG00438.hp1 HG00609.hp2 others(92): Show |
intron_variant | MODIFIER | c.562-1087T>A | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 6/9 | chr13 | 36973123 | |||||||
chr13:36973177 | A | G | 1 | a0001c0001t0001g0141 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.562-1141T>C | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 6/9 | chr13 | 36973177 | |||||||
chr13:36973362 | A | G | 17 | a0001c0001t0001g0012 a0001c0001t0001g0031 a0001c0001t0001g0032 others(14): Show |
18 | HG01109.hp2 HG01192.hp2 HG01981.hp2 others(15): Show |
intron_variant | MODIFIER | c.562-1326T>C | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 6/9 | chr13 | 36973362 | |||||||
chr13:36973383 | T | C | 16 | a0001c0001t0001g0012 a0001c0001t0001g0031 a0001c0001t0001g0032 others(13): Show |
17 | HG01109.hp2 HG01192.hp2 HG01981.hp2 others(14): Show |
intron_variant | MODIFIER | c.562-1347A>G | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 6/9 | chr13 | 36973383 | |||||||
chr13:36973694 | C | T | 1 | a0001c0001t0001g0221 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.562-1658G>A | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 6/9 | chr13 | 36973694 | |||||||
chr13:36973699 | G | A | 17 | a0001c0001t0001g0012 a0001c0001t0001g0031 a0001c0001t0001g0032 others(14): Show |
18 | HG01109.hp2 HG01192.hp2 HG01981.hp2 others(15): Show |
intron_variant | MODIFIER | c.562-1663C>T | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 6/9 | chr13 | 36973699 | |||||||
chr13:36973726 | A | T | 1 | a0001c0001t0001g0068 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.562-1690T>A | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 6/9 | chr13 | 36973726 | |||||||
chr13:36973863 | G | A | 1 | a0001c0001t0001g0184 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.562-1827C>T | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 6/9 | chr13 | 36973863 | |||||||
chr13:36973876 | A | G | 2 | a0003c0003t0001g0188 a0003c0003t0001g0189 |
2 | HG02886.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.562-1840T>C | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 6/9 | chr13 | 36973876 | |||||||
chr13:36974049 | T | C | 4 | a0001c0001t0001g0017 a0001c0001t0001g0130 a0001c0001t0001g0131 others(1): Show |
5 | HG01496.hp2 HG02970.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.562-2013A>G | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 6/9 | chr13 | 36974049 | |||||||
chr13:36974125 | A | G | 1 | a0001c0001t0001g0108 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.562-2089T>C | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 6/9 | chr13 | 36974125 | |||||||
chr13:36974141 | G | A | 1 | a0001c0001t0001g0151 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.562-2105C>T | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 6/9 | chr13 | 36974141 | |||||||
chr13:36974174 | T | C | 1 | a0001c0001t0001g0138 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.562-2138A>G | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 6/9 | chr13 | 36974174 | |||||||
chr13:36974200 | AAAG | A | 17 | a0001c0001t0001g0012 a0001c0001t0001g0031 a0001c0001t0001g0032 others(14): Show |
18 | HG01109.hp2 HG01192.hp2 HG01981.hp2 others(15): Show |
intron_variant | MODIFIER | c.562-2167_562-2165d others(5): Show |
ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 6/9 | chr13 | 36974200 | |||||||
chr13:36974259 | T | G | 85 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0013 others(82): Show |
95 | HG00099.hp1 HG00438.hp1 HG00609.hp2 others(92): Show |
intron_variant | MODIFIER | c.562-2223A>C | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 6/9 | chr13 | 36974259 | |||||||
chr13:36974315 | T | C | 5 | a0001c0001t0001g0009 a0001c0001t0001g0123 a0001c0001t0001g0152 others(2): Show |
7 | HG01175.hp1 HG01255.hp1 HG01952.hp2 others(4): Show |
intron_variant | MODIFIER | c.562-2279A>G | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 6/9 | chr13 | 36974315 | |||||||
chr13:36974329 | T | C | 1 | a0001c0001t0001g0037 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.562-2293A>G | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 6/9 | chr13 | 36974329 | |||||||
chr13:36974338 | A | C | 1 | a0002c0002t0001g0190 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.562-2302T>G | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 6/9 | chr13 | 36974338 | |||||||
chr13:36974340 | C | T | 1 | a0002c0002t0001g0190 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.562-2304G>A | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 6/9 | chr13 | 36974340 | |||||||
chr13:36974341 | A | T | 1 | a0002c0002t0001g0190 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.562-2305T>A | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 6/9 | chr13 | 36974341 | |||||||
chr13:36974343 | A | T | 1 | a0002c0002t0001g0190 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.562-2307T>A | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 6/9 | chr13 | 36974343 | |||||||
chr13:36974344 | A | AAATGCTC others(3): Show |
1 | a0002c0002t0001g0190 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.562-2309_562-2308i others(12): Show |
ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 6/9 | chr13 | 36974344 | |||||||
chr13:36974349 | A | T | 1 | a0002c0002t0001g0190 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.562-2313T>A | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 6/9 | chr13 | 36974349 | |||||||
chr13:36974355 | A | T | 1 | a0002c0002t0001g0190 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.562-2319T>A | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 6/9 | chr13 | 36974355 | |||||||
chr13:36974357 | G | A | 1 | a0002c0002t0001g0190 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.562-2321C>T | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 6/9 | chr13 | 36974357 | |||||||
chr13:36974579 | T | C | 68 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(65): Show |
93 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(90): Show |
intron_variant | MODIFIER | c.562-2543A>G | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 6/9 | chr13 | 36974579 | |||||||
chr13:36974618 | C | T | 2 | a0001c0001t0001g0184 a0001c0001t0001g0185 |
2 | HG03098.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.562-2582G>A | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 6/9 | chr13 | 36974618 | |||||||
chr13:36974671 | T | G | 1 | a0001c0001t0001g0090 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.562-2635A>C | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 6/9 | chr13 | 36974671 | |||||||
chr13:36974712 | G | GC | 11 | a0001c0001t0001g0032 a0001c0001t0001g0091 a0001c0001t0001g0099 others(8): Show |
11 | HG01981.hp1 HG02071.hp1 HG02145.hp1 others(8): Show |
intron_variant | MODIFIER | c.562-2677dupG | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 6/9 | chr13 | 36974712 | |||||||
chr13:36974716 | C | A | 1 | a0001c0001t0001g0221 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.562-2680G>T | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 6/9 | chr13 | 36974716 | |||||||
chr13:36974720 | A | C | 185 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(182): Show |
225 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(222): Show |
intron_variant | MODIFIER | c.562-2684T>G | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 6/9 | chr13 | 36974720 | |||||||
chr13:36974722 | C | G | 1 | a0001c0007t0001g0227 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.562-2686G>C | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 6/9 | chr13 | 36974722 | |||||||
chr13:36974939 | G | A | 1 | a0001c0001t0001g0067 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.562-2903C>T | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 6/9 | chr13 | 36974939 | |||||||
chr13:36975075 | G | A | 2 | a0003c0003t0001g0188 a0003c0003t0001g0189 |
2 | HG02886.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.562-3039C>T | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 6/9 | chr13 | 36975075 | |||||||
chr13:36975083 | C | T | 1 | a0001c0001t0001g0045 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.562-3047G>A | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 6/9 | chr13 | 36975083 | |||||||
chr13:36975113 | C | T | 2 | a0003c0003t0001g0188 a0003c0003t0001g0189 |
2 | HG02886.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.562-3077G>A | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 6/9 | chr13 | 36975113 | |||||||
chr13:36975216 | A | G | 2 | a0003c0003t0001g0188 a0003c0003t0001g0189 |
2 | HG02886.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.562-3180T>C | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 6/9 | chr13 | 36975216 | |||||||
chr13:36975791 | T | G | 22 | a0001c0001t0001g0012 a0001c0001t0001g0031 a0001c0001t0001g0032 others(19): Show |
23 | HG01109.hp2 HG01192.hp2 HG01981.hp2 others(20): Show |
intron_variant | MODIFIER | c.562-3755A>C | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 6/9 | chr13 | 36975791 | |||||||
chr13:36975841 | C | T | 68 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(65): Show |
93 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(90): Show |
intron_variant | MODIFIER | c.562-3805G>A | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 6/9 | chr13 | 36975841 | |||||||
chr13:36975973 | C | CA | 10 | a0001c0001t0001g0092 a0001c0001t0001g0093 a0001c0001t0001g0132 others(7): Show |
10 | HG01993.hp2 HG02273.hp2 HG02818.hp2 others(7): Show |
intron_variant | MODIFIER | c.562-3938dupT | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 6/9 | chr13 | 36975973 | |||||||
chr13:36975982 | A | C | 2 | a0001c0001t0001g0120 a0001c0001t0001g0121 |
2 | HG01257.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.562-3946T>G | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 6/9 | chr13 | 36975982 | |||||||
chr13:36976080 | A | G | 6 | a0001c0001t0001g0178 a0001c0001t0001g0204 a0001c0001t0001g0222 others(3): Show |
6 | HG02559.hp1 HG02818.hp2 HG03209.hp1 others(3): Show |
intron_variant | MODIFIER | c.562-4044T>C | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 6/9 | chr13 | 36976080 | |||||||
chr13:36976310 | C | T | 2 | a0001c0001t0001g0135 a0001c0001t0001g0140 |
2 | HG00621.hp1 NA18946.hp2 |
intron_variant | MODIFIER | c.562-4274G>A | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 6/9 | chr13 | 36976310 | |||||||
chr13:36976355 | G | A | 1 | a0001c0001t0001g0208 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.562-4319C>T | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 6/9 | chr13 | 36976355 | |||||||
chr13:36976425 | C | CA | 33 | a0001c0001t0001g0023 a0001c0001t0001g0029 a0001c0001t0001g0053 others(30): Show |
34 | HG01175.hp2 HG01361.hp1 HG01515.hp2 others(31): Show |
intron_variant | MODIFIER | c.562-4390dupT | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 6/9 | chr13 | 36976425 | |||||||
chr13:36976425 | CA | C | 21 | a0001c0001t0001g0058 a0001c0001t0001g0060 a0001c0001t0001g0062 others(18): Show |
21 | HG00609.hp2 HG01074.hp2 HG01167.hp1 others(18): Show |
intron_variant | MODIFIER | c.562-4390delT | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 6/9 | chr13 | 36976425 | |||||||
chr13:36976425 | CAAA | C | 18 | a0001c0001t0001g0012 a0001c0001t0001g0031 a0001c0001t0001g0032 others(15): Show |
19 | HG01109.hp2 HG01192.hp2 HG01981.hp2 others(16): Show |
intron_variant | MODIFIER | c.562-4392_562-4390d others(5): Show |
ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 6/9 | chr13 | 36976425 | |||||||
chr13:36976446 | A | G | 17 | a0001c0001t0001g0012 a0001c0001t0001g0031 a0001c0001t0001g0032 others(14): Show |
18 | HG01109.hp2 HG01192.hp2 HG01981.hp2 others(15): Show |
intron_variant | MODIFIER | c.562-4410T>C | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 6/9 | chr13 | 36976446 | |||||||
chr13:36976648 | T | C | 1 | a0001c0001t0001g0055 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.562-4612A>G | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 6/9 | chr13 | 36976648 | |||||||
chr13:36976734 | C | T | 1 | a0001c0001t0001g0025 | 2 | HG02257.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.562-4698G>A | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 6/9 | chr13 | 36976734 | |||||||
chr13:36976750 | G | GA | 214 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(211): Show |
255 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(252): Show |
intron_variant | MODIFIER | c.562-4715dupT | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 6/9 | chr13 | 36976750 | |||||||
chr13:36976947 | G | C | 2 | a0001c0001t0001g0028 a0001c0001t0001g0158 |
2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.562-4911C>G | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 6/9 | chr13 | 36976947 | |||||||
chr13:36977050 | C | A | 2 | a0001c0001t0001g0024 a0001c0001t0001g0030 |
3 | HG02572.hp2 HG02896.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.562-5014G>T | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 6/9 | chr13 | 36977050 | |||||||
chr13:36977064 | G | A | 6 | a0001c0001t0001g0023 a0001c0001t0001g0029 a0001c0001t0001g0171 others(3): Show |
7 | HG02615.hp2 HG02717.hp2 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.562-5028C>T | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 6/9 | chr13 | 36977064 | |||||||
chr13:36977096 | T | C | 68 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(65): Show |
93 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(90): Show |
intron_variant | MODIFIER | c.562-5060A>G | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 6/9 | chr13 | 36977096 | |||||||
chr13:36977245 | T | A | 1 | a0001c0001t0001g0219 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.562-5209A>T | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 6/9 | chr13 | 36977245 | |||||||
chr13:36977363 | A | G | 4 | a0001c0001t0001g0193 a0001c0001t0001g0194 a0001c0001t0001g0195 others(1): Show |
4 | HG02280.hp1 HG02647.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.562-5327T>C | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 6/9 | chr13 | 36977363 | |||||||
chr13:36977539 | C | T | 1 | a0001c0001t0001g0045 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.562-5503G>A | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 6/9 | chr13 | 36977539 | |||||||
chr13:36977630 | A | G | 3 | a0001c0001t0001g0184 a0001c0001t0001g0185 a0001c0007t0001g0227 |
3 | HG02630.hp1 HG03098.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.562-5594T>C | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 6/9 | chr13 | 36977630 | |||||||
chr13:36977725 | T | C | 1 | a0001c0007t0001g0227 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.562-5689A>G | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 6/9 | chr13 | 36977725 | |||||||
chr13:36977760 | C | G | 2 | a0003c0003t0001g0188 a0003c0003t0001g0189 |
2 | HG02886.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.562-5724G>C | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 6/9 | chr13 | 36977760 | |||||||
chr13:36977770 | C | T | 2 | a0003c0003t0001g0188 a0003c0003t0001g0189 |
2 | HG02886.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.562-5734G>A | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 6/9 | chr13 | 36977770 | |||||||
chr13:36977779 | G | A | 1 | a0001c0001t0001g0041 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.562-5743C>T | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 6/9 | chr13 | 36977779 | |||||||
chr13:36977790 | C | CA | 5 | a0001c0001t0001g0026 a0001c0001t0001g0215 a0001c0001t0001g0219 others(2): Show |
6 | HG01358.hp2 HG01891.hp1 HG02293.hp1 others(3): Show |
intron_variant | MODIFIER | c.562-5755dupT | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 6/9 | chr13 | 36977790 | |||||||
chr13:36977790 | C | CAAA | 11 | a0001c0001t0001g0012 a0001c0001t0001g0035 a0001c0001t0001g0036 others(8): Show |
12 | HG01109.hp2 HG01192.hp2 HG02055.hp1 others(9): Show |
intron_variant | MODIFIER | c.562-5757_562-5755d others(5): Show |
ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 6/9 | chr13 | 36977790 | |||||||
chr13:36977790 | C | CAAAAAAA others(4): Show |
1 | a0003c0003t0001g0189 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.562-5765_562-5755d others(13): Show |
ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 6/9 | chr13 | 36977790 | |||||||
chr13:36977790 | C | CAAAAAAA others(23): Show |
1 | a0001c0001t0001g0037 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.562-5755_562-5754i others(32): Show |
ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 6/9 | chr13 | 36977790 | |||||||
chr13:36977799 | AAAAAAAA others(9): Show |
A | 1 | a0001c0001t0001g0177 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.562-5779_562-5764d others(18): Show |
ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 6/9 | chr13 | 36977799 | |||||||
chr13:36977812 | AAAC | A | 65 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(62): Show |
75 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(72): Show |
intron_variant | MODIFIER | c.562-5779_562-5777d others(5): Show |
ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 6/9 | chr13 | 36977812 | |||||||
chr13:36977813 | AAC | A | 118 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(115): Show |
135 | HG00099.hp1 HG00438.hp1 HG00438.hp2 others(132): Show |
intron_variant | MODIFIER | c.562-5779_562-5778d others(4): Show |
ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 6/9 | chr13 | 36977813 | |||||||
chr13:36977814 | AC | A | 15 | a0001c0001t0001g0024 a0001c0001t0001g0050 a0001c0001t0001g0054 others(12): Show |
15 | HG00741.hp2 HG01175.hp2 HG01261.hp2 others(12): Show |
intron_variant | MODIFIER | c.562-5779delG | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 6/9 | chr13 | 36977814 | |||||||
chr13:36977815 | C | A | 20 | a0001c0001t0001g0010 a0001c0001t0001g0012 a0001c0001t0001g0032 others(17): Show |
21 | HG01109.hp2 HG01192.hp2 HG02055.hp1 others(18): Show |
intron_variant | MODIFIER | c.562-5779G>T | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 6/9 | chr13 | 36977815 | |||||||
chr13:36977891 | A | AT | 103 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0012 others(100): Show |
115 | HG00099.hp1 HG00438.hp1 HG00609.hp2 others(112): Show |
intron_variant | MODIFIER | c.562-5856dupA | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 6/9 | chr13 | 36977891 | |||||||
chr13:36977954 | T | C | 1 | a0001c0001t0001g0134 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.562-5918A>G | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 6/9 | chr13 | 36977954 | |||||||
chr13:36977955 | C | T | 1 | a0001c0001t0001g0134 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.562-5919G>A | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 6/9 | chr13 | 36977955 | |||||||
chr13:36977990 | G | A | 2 | a0001c0001t0001g0184 a0001c0001t0001g0185 |
2 | HG03098.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.562-5954C>T | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 6/9 | chr13 | 36977990 | |||||||
chr13:36978021 | C | T | 1 | a0001c0001t0001g0061 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.562-5985G>A | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 6/9 | chr13 | 36978021 | |||||||
chr13:36978045 | C | T | 4 | a0001c0001t0001g0193 a0001c0001t0001g0194 a0001c0001t0001g0195 others(1): Show |
4 | HG02280.hp1 HG02647.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.562-6009G>A | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 6/9 | chr13 | 36978045 | |||||||
chr13:36978077 | G | A | 1 | a0001c0001t0001g0203 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.562-6041C>T | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 6/9 | chr13 | 36978077 | |||||||
chr13:36978122 | A | C | 2 | a0001c0001t0001g0184 a0001c0001t0001g0185 |
2 | HG03098.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.562-6086T>G | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 6/9 | chr13 | 36978122 | |||||||
chr13:36978189 | G | GT | 62 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(59): Show |
87 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(84): Show |
intron_variant | MODIFIER | c.562-6154dupA | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 6/9 | chr13 | 36978189 | |||||||
chr13:36978189 | G | GTT | 11 | a0001c0001t0001g0132 a0001c0001t0001g0134 a0001c0001t0001g0135 others(8): Show |
11 | HG00438.hp2 HG00621.hp1 HG01261.hp2 others(8): Show |
intron_variant | MODIFIER | c.562-6155_562-6154d others(4): Show |
ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 6/9 | chr13 | 36978189 | |||||||
chr13:36978206 | G | A | 1 | a0001c0001t0001g0059 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.562-6170C>T | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 6/9 | chr13 | 36978206 | |||||||
chr13:36978249 | A | G | 214 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(211): Show |
255 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(252): Show |
intron_variant | MODIFIER | c.562-6213T>C | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 6/9 | chr13 | 36978249 | |||||||
chr13:36978280 | T | C | 1 | a0001c0001t0001g0166 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.562-6244A>G | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 6/9 | chr13 | 36978280 | |||||||
chr13:36978344 | A | G | 3 | a0001c0001t0001g0184 a0001c0001t0001g0185 a0001c0007t0001g0227 |
3 | HG02630.hp1 HG03098.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.562-6308T>C | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 6/9 | chr13 | 36978344 | |||||||
chr13:36978467 | G | A | 1 | a0001c0001t0001g0212 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.562-6431C>T | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 6/9 | chr13 | 36978467 | |||||||
chr13:36978476 | T | G | 1 | a0001c0001t0001g0204 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.562-6440A>C | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 6/9 | chr13 | 36978476 | |||||||
chr13:36978477 | G | A | 1 | a0003c0003t0001g0189 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.562-6441C>T | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 6/9 | chr13 | 36978477 | |||||||
chr13:36978638 | G | A | 188 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(185): Show |
228 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(225): Show |
intron_variant | MODIFIER | c.562-6602C>T | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 6/9 | chr13 | 36978638 | |||||||
chr13:36978649 | C | T | 1 | a0001c0001t0001g0059 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.562-6613G>A | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 6/9 | chr13 | 36978649 | |||||||
chr13:36978727 | C | A | 5 | a0001c0001t0001g0010 a0001c0001t0001g0127 a0001c0001t0001g0160 others(2): Show |
7 | HG02040.hp2 NA18945.hp2 NA18965.hp1 others(4): Show |
intron_variant | MODIFIER | c.562-6691G>T | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 6/9 | chr13 | 36978727 | |||||||
chr13:36978798 | C | T | 1 | a0001c0001t0001g0058 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.562-6762G>A | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 6/9 | chr13 | 36978798 | |||||||
chr13:36978805 | G | C | 214 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(211): Show |
255 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(252): Show |
intron_variant | MODIFIER | c.562-6769C>G | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 6/9 | chr13 | 36978805 | |||||||
chr13:36978814 | G | T | 1 | a0001c0001t0001g0205 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.562-6778C>A | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 6/9 | chr13 | 36978814 | |||||||
chr13:36978877 | C | T | 1 | a0001c0007t0001g0227 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.561+6750G>A | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 6/9 | chr13 | 36978877 | |||||||
chr13:36978890 | TG | T | 17 | a0001c0001t0001g0012 a0001c0001t0001g0031 a0001c0001t0001g0032 others(14): Show |
18 | HG01109.hp2 HG01192.hp2 HG01981.hp2 others(15): Show |
intron_variant | MODIFIER | c.561+6736delC | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 6/9 | chr13 | 36978890 | |||||||
chr13:36978919 | T | TA | 207 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(204): Show |
248 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(245): Show |
intron_variant | MODIFIER | c.561+6707dupT | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 6/9 | chr13 | 36978919 | |||||||
chr13:36978934 | G | A | 1 | a0001c0001t0001g0100 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.561+6693C>T | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 6/9 | chr13 | 36978934 | |||||||
chr13:36978996 | T | C | 1 | a0001c0001t0001g0038 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.561+6631A>G | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 6/9 | chr13 | 36978996 | |||||||
chr13:36979134 | G | C | 1 | a0001c0001t0001g0100 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.561+6493C>G | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 6/9 | chr13 | 36979134 | |||||||
chr13:36979175 | C | T | 2 | a0001c0001t0001g0042 a0001c0001t0001g0192 |
2 | HG02970.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.561+6452G>A | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 6/9 | chr13 | 36979175 | |||||||
chr13:36979360 | G | A | 1 | a0001c0001t0001g0204 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.561+6267C>T | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 6/9 | chr13 | 36979360 | |||||||
chr13:36979445 | A | G | 2 | a0001c0001t0001g0184 a0001c0001t0001g0185 |
2 | HG03098.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.561+6182T>C | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 6/9 | chr13 | 36979445 | |||||||
chr13:36979599 | C | G | 1 | a0004c0005t0001g0167 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.561+6028G>C | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 6/9 | chr13 | 36979599 | |||||||
chr13:36979772 | G | C | 2 | a0003c0003t0001g0188 a0003c0003t0001g0189 |
2 | HG02886.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.561+5855C>G | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 6/9 | chr13 | 36979772 | |||||||
chr13:36979805 | T | C | 1 | a0001c0001t0001g0205 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.561+5822A>G | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 6/9 | chr13 | 36979805 | |||||||
chr13:36979815 | G | C | 12 | a0001c0001t0001g0023 a0001c0001t0001g0029 a0001c0001t0001g0171 others(9): Show |
13 | HG01515.hp2 HG02145.hp2 HG02280.hp2 others(10): Show |
intron_variant | MODIFIER | c.561+5812C>G | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 6/9 | chr13 | 36979815 | |||||||
chr13:36980020 | C | T | 68 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(65): Show |
93 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(90): Show |
intron_variant | MODIFIER | c.561+5607G>A | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 6/9 | chr13 | 36980020 | |||||||
chr13:36980062 | A | T | 5 | a0001c0001t0001g0193 a0001c0001t0001g0194 a0001c0001t0001g0195 others(2): Show |
5 | HG02257.hp2 HG02280.hp1 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.561+5565T>A | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 6/9 | chr13 | 36980062 | |||||||
chr13:36980107 | G | T | 1 | a0001c0001t0001g0208 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.561+5520C>A | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 6/9 | chr13 | 36980107 | |||||||
chr13:36980208 | A | G | 22 | a0001c0001t0001g0012 a0001c0001t0001g0031 a0001c0001t0001g0032 others(19): Show |
23 | HG01109.hp2 HG01192.hp2 HG01981.hp2 others(20): Show |
intron_variant | MODIFIER | c.561+5419T>C | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 6/9 | chr13 | 36980208 | |||||||
chr13:36980239 | T | G | 183 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(180): Show |
223 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(220): Show |
intron_variant | MODIFIER | c.561+5388A>C | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 6/9 | chr13 | 36980239 | |||||||
chr13:36980388 | C | T | 4 | a0002c0002t0001g0190 a0002c0002t0001g0191 a0003c0003t0001g0188 others(1): Show |
4 | HG02886.hp1 HG02895.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.561+5239G>A | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 6/9 | chr13 | 36980388 | |||||||
chr13:36980415 | C | T | 1 | a0001c0001t0001g0056 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.561+5212G>A | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 6/9 | chr13 | 36980415 | |||||||
chr13:36980739 | G | A | 4 | a0001c0001t0001g0193 a0001c0001t0001g0194 a0001c0001t0001g0195 others(1): Show |
4 | HG02280.hp1 HG02647.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.561+4888C>T | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 6/9 | chr13 | 36980739 | |||||||
chr13:36980828 | G | A | 1 | a0001c0001t0001g0186 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.561+4799C>T | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 6/9 | chr13 | 36980828 | |||||||
chr13:36980834 | C | A | 1 | a0001c0001t0001g0107 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.561+4793G>T | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 6/9 | chr13 | 36980834 | |||||||
chr13:36980902 | A | T | 3 | a0001c0001t0001g0184 a0001c0001t0001g0185 a0001c0007t0001g0227 |
3 | HG02630.hp1 HG03098.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.561+4725T>A | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 6/9 | chr13 | 36980902 | |||||||
chr13:36981089 | C | A | 1 | a0001c0001t0001g0025 | 2 | HG02257.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.561+4538G>T | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 6/9 | chr13 | 36981089 | |||||||
chr13:36981281 | G | C | 7 | a0001c0001t0001g0178 a0001c0001t0001g0204 a0001c0001t0001g0220 others(4): Show |
7 | HG01255.hp2 HG02559.hp1 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.561+4346C>G | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 6/9 | chr13 | 36981281 | |||||||
chr13:36981296 | C | G | 1 | a0001c0001t0001g0172 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.561+4331G>C | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 6/9 | chr13 | 36981296 | |||||||
chr13:36981368 | T | C | 3 | a0001c0001t0001g0210 a0001c0001t0001g0211 a0001c0001t0001g0212 |
3 | HG03209.hp2 HG03486.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.561+4259A>G | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 6/9 | chr13 | 36981368 | |||||||
chr13:36981393 | C | T | 1 | a0001c0001t0001g0025 | 2 | HG02257.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.561+4234G>A | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 6/9 | chr13 | 36981393 | |||||||
chr13:36981633 | C | T | 82 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0013 others(79): Show |
92 | HG00099.hp1 HG00438.hp1 HG00609.hp2 others(89): Show |
intron_variant | MODIFIER | c.561+3994G>A | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 6/9 | chr13 | 36981633 | |||||||
chr13:36981745 | C | A | 86 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0013 others(83): Show |
97 | HG00099.hp1 HG00438.hp1 HG00609.hp2 others(94): Show |
intron_variant | MODIFIER | c.561+3882G>T | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 6/9 | chr13 | 36981745 | |||||||
chr13:36981828 | C | T | 1 | a0001c0001t0001g0055 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.561+3799G>A | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 6/9 | chr13 | 36981828 | |||||||
chr13:36981852 | G | A | 2 | a0001c0001t0001g0102 a0001c0001t0001g0103 |
2 | HG03942.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.561+3775C>T | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 6/9 | chr13 | 36981852 | |||||||
chr13:36982109 | AAAC | A | 13 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0020 others(10): Show |
16 | HG00609.hp1 HG01243.hp1 HG01496.hp2 others(13): Show |
intron_variant | MODIFIER | c.561+3515_561+3517d others(5): Show |
ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 6/9 | chr13 | 36982109 | |||||||
chr13:36982247 | G | A | 1 | a0001c0001t0001g0132 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.561+3380C>T | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 6/9 | chr13 | 36982247 | |||||||
chr13:36982271 | A | G | 214 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(211): Show |
255 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(252): Show |
intron_variant | MODIFIER | c.561+3356T>C | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 6/9 | chr13 | 36982271 | |||||||
chr13:36982306 | T | A | 1 | a0001c0001t0001g0017 | 2 | HG02970.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.561+3321A>T | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 6/9 | chr13 | 36982306 | |||||||
chr13:36982360 | T | G | 1 | a0001c0007t0001g0227 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.561+3267A>C | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 6/9 | chr13 | 36982360 | |||||||
chr13:36982508 | T | G | 1 | a0001c0001t0001g0104 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.561+3119A>C | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 6/9 | chr13 | 36982508 | |||||||
chr13:36982744 | A | C | 2 | a0001c0001t0001g0024 a0001c0001t0001g0030 |
3 | HG02572.hp2 HG02896.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.561+2883T>G | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 6/9 | chr13 | 36982744 | |||||||
chr13:36982862 | A | G | 8 | a0001c0001t0001g0006 a0001c0001t0001g0016 a0001c0001t0001g0017 others(5): Show |
12 | HG01243.hp1 HG01496.hp2 HG01891.hp2 others(9): Show |
intron_variant | MODIFIER | c.561+2765T>C | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 6/9 | chr13 | 36982862 | |||||||
chr13:36982922 | C | T | 1 | a0001c0001t0001g0203 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.561+2705G>A | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 6/9 | chr13 | 36982922 | |||||||
chr13:36983149 | C | T | 1 | a0001c0001t0001g0031 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.561+2478G>A | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 6/9 | chr13 | 36983149 | |||||||
chr13:36983164 | C | G | 2 | a0003c0003t0001g0188 a0003c0003t0001g0189 |
2 | HG02886.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.561+2463G>C | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 6/9 | chr13 | 36983164 | |||||||
chr13:36983512 | G | A | 1 | a0001c0001t0001g0105 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.561+2115C>T | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 6/9 | chr13 | 36983512 | |||||||
chr13:36983526 | G | C | 17 | a0001c0001t0001g0012 a0001c0001t0001g0031 a0001c0001t0001g0032 others(14): Show |
18 | HG01109.hp2 HG01192.hp2 HG01981.hp2 others(15): Show |
intron_variant | MODIFIER | c.561+2101C>G | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 6/9 | chr13 | 36983526 | |||||||
chr13:36983571 | T | TA | 222 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(219): Show |
271 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(268): Show |
intron_variant | MODIFIER | c.561+2055dupT | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 6/9 | chr13 | 36983571 | |||||||
chr13:36983735 | A | G | 5 | a0001c0001t0001g0011 a0001c0001t0001g0205 a0001c0001t0001g0206 others(2): Show |
7 | HG00639.hp2 HG02109.hp2 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.561+1892T>C | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 6/9 | chr13 | 36983735 | |||||||
chr13:36983760 | T | G | 189 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(186): Show |
230 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(227): Show |
intron_variant | MODIFIER | c.561+1867A>C | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 6/9 | chr13 | 36983760 | |||||||
chr13:36983792 | C | CA | 6 | a0001c0001t0001g0011 a0001c0001t0001g0206 a0001c0001t0001g0207 others(3): Show |
8 | HG02109.hp2 HG02486.hp1 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.561+1834dupT | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 6/9 | chr13 | 36983792 | |||||||
chr13:36983877 | T | C | 1 | a0001c0007t0001g0227 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.561+1750A>G | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 6/9 | chr13 | 36983877 | |||||||
chr13:36984100 | A | AT | 7 | a0001c0001t0001g0113 a0001c0001t0001g0127 a0001c0001t0001g0179 others(4): Show |
7 | HG02055.hp2 HG02647.hp1 HG03209.hp2 others(4): Show |
intron_variant | MODIFIER | c.561+1526dupA | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 6/9 | chr13 | 36984100 | |||||||
chr13:36984148 | G | C | 1 | a0001c0001t0001g0208 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.561+1479C>G | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 6/9 | chr13 | 36984148 | |||||||
chr13:36984533 | ACT | A | 184 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(181): Show |
225 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(222): Show |
intron_variant | MODIFIER | c.561+1092_561+1093d others(4): Show |
ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 6/9 | chr13 | 36984533 | |||||||
chr13:36984550 | G | A | 6 | a0001c0001t0001g0178 a0001c0001t0001g0204 a0001c0001t0001g0222 others(3): Show |
6 | HG02559.hp1 HG02818.hp2 HG03209.hp1 others(3): Show |
intron_variant | MODIFIER | c.561+1077C>T | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 6/9 | chr13 | 36984550 | |||||||
chr13:36984831 | G | A | 216 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(213): Show |
258 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(255): Show |
intron_variant | MODIFIER | c.561+796C>T | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 6/9 | chr13 | 36984831 | |||||||
chr13:36984961 | C | T | 1 | a0001c0001t0001g0171 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.561+666G>A | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 6/9 | chr13 | 36984961 | |||||||
chr13:36985030 | C | T | 4 | a0002c0002t0001g0190 a0002c0002t0001g0191 a0003c0003t0001g0188 others(1): Show |
4 | HG02886.hp1 HG02895.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.561+597G>A | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 6/9 | chr13 | 36985030 | |||||||
chr13:36985101 | G | A | 1 | a0001c0001t0001g0215 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.561+526C>T | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 6/9 | chr13 | 36985101 | |||||||
chr13:36985169 | A | C | 84 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0013 others(81): Show |
94 | HG00099.hp1 HG00438.hp1 HG00609.hp2 others(91): Show |
intron_variant | MODIFIER | c.561+458T>G | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 6/9 | chr13 | 36985169 | |||||||
chr13:36985286 | A | G | 1 | a0001c0007t0001g0227 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.561+341T>C | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 6/9 | chr13 | 36985286 | |||||||
chr13:36985540 | A | G | 1 | a0001c0001t0001g0126 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.561+87T>C | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 6/9 | chr13 | 36985540 | |||||||
chr13:36985595 | G | A | 1 | a0001c0007t0001g0227 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.561+32C>T | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 6/9 | chr13 | 36985595 | |||||||
chr13:36985824 | T | C | 1 | a0001c0001t0001g0168 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.448-84A>G | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 5/9 | chr13 | 36985824 | |||||||
chr13:36986071 | T | C | 1 | a0001c0001t0001g0022 | 2 | HG01069.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.448-331A>G | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 5/9 | chr13 | 36986071 | |||||||
chr13:36986350 | G | C | 2 | a0001c0001t0001g0039 a0001c0001t0001g0040 |
2 | HG01192.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.448-610C>G | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 5/9 | chr13 | 36986350 | |||||||
chr13:36986376 | T | C | 15 | a0001c0001t0001g0023 a0001c0001t0001g0029 a0001c0001t0001g0171 others(12): Show |
16 | HG01515.hp2 HG02145.hp2 HG02280.hp2 others(13): Show |
intron_variant | MODIFIER | c.448-636A>G | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 5/9 | chr13 | 36986376 | |||||||
chr13:36986468 | T | A | 1 | a0001c0001t0001g0106 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.448-728A>T | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 5/9 | chr13 | 36986468 | |||||||
chr13:36986526 | T | C | 1 | a0001c0001t0001g0046 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.448-786A>G | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 5/9 | chr13 | 36986526 | |||||||
chr13:36986665 | C | G | 5 | a0001c0001t0001g0193 a0001c0001t0001g0194 a0001c0001t0001g0195 others(2): Show |
5 | HG02257.hp2 HG02280.hp1 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.448-925G>C | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 5/9 | chr13 | 36986665 | |||||||
chr13:36986771 | T | A | 86 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0013 others(83): Show |
97 | HG00099.hp1 HG00438.hp1 HG00609.hp2 others(94): Show |
intron_variant | MODIFIER | c.448-1031A>T | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 5/9 | chr13 | 36986771 | |||||||
chr13:36986810 | C | A | 1 | a0001c0001t0001g0107 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.448-1070G>T | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 5/9 | chr13 | 36986810 | |||||||
chr13:36986988 | T | C | 1 | a0001c0001t0001g0025 | 2 | HG02257.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.448-1248A>G | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 5/9 | chr13 | 36986988 | |||||||
chr13:36987041 | T | C | 1 | a0001c0001t0001g0208 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.448-1301A>G | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 5/9 | chr13 | 36987041 | |||||||
chr13:36987050 | C | A | 12 | a0001c0001t0001g0023 a0001c0001t0001g0029 a0001c0001t0001g0171 others(9): Show |
13 | HG01515.hp2 HG02145.hp2 HG02280.hp2 others(10): Show |
intron_variant | MODIFIER | c.448-1310G>T | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 5/9 | chr13 | 36987050 | |||||||
chr13:36987282 | C | T | 3 | a0001c0001t0001g0210 a0001c0001t0001g0211 a0001c0001t0001g0212 |
3 | HG03209.hp2 HG03486.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.448-1542G>A | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 5/9 | chr13 | 36987282 | |||||||
chr13:36987508 | C | T | 1 | a0001c0001t0001g0204 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.448-1768G>A | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 5/9 | chr13 | 36987508 | |||||||
chr13:36987509 | G | A | 1 | a0001c0001t0001g0198 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.448-1769C>T | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 5/9 | chr13 | 36987509 | |||||||
chr13:36987542 | G | A | 2 | a0003c0003t0001g0188 a0003c0003t0001g0189 |
2 | HG02886.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.448-1802C>T | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 5/9 | chr13 | 36987542 | |||||||
chr13:36988074 | T | C | 70 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(67): Show |
96 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(93): Show |
intron_variant | MODIFIER | c.447+1410A>G | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 5/9 | chr13 | 36988074 | |||||||
chr13:36988077 | G | T | 216 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(213): Show |
258 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(255): Show |
intron_variant | MODIFIER | c.447+1407C>A | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 5/9 | chr13 | 36988077 | |||||||
chr13:36988124 | C | T | 3 | a0001c0001t0001g0210 a0001c0001t0001g0211 a0001c0001t0001g0212 |
3 | HG03209.hp2 HG03486.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.447+1360G>A | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 5/9 | chr13 | 36988124 | |||||||
chr13:36988300 | A | C | 2 | a0003c0003t0001g0188 a0003c0003t0001g0189 |
2 | HG02886.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.447+1184T>G | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 5/9 | chr13 | 36988300 | |||||||
chr13:36988472 | C | A | 3 | a0001c0001t0001g0010 a0001c0001t0001g0198 a0001c0001t0001g0202 |
5 | HG02040.hp2 NA18945.hp2 NA18965.hp1 others(2): Show |
intron_variant | MODIFIER | c.447+1012G>T | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 5/9 | chr13 | 36988472 | |||||||
chr13:36988484 | T | C | 15 | a0001c0001t0001g0023 a0001c0001t0001g0029 a0001c0001t0001g0171 others(12): Show |
16 | HG01515.hp2 HG02145.hp2 HG02280.hp2 others(13): Show |
intron_variant | MODIFIER | c.447+1000A>G | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 5/9 | chr13 | 36988484 | |||||||
chr13:36988717 | T | C | 3 | a0001c0001t0001g0210 a0001c0001t0001g0211 a0001c0001t0001g0212 |
3 | HG03209.hp2 HG03486.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.447+767A>G | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 5/9 | chr13 | 36988717 | |||||||
chr13:36988719 | T | TGAGA | 26 | a0001c0001t0001g0012 a0001c0001t0001g0031 a0001c0001t0001g0032 others(23): Show |
27 | HG01109.hp2 HG01192.hp2 HG01981.hp2 others(24): Show |
intron_variant | MODIFIER | c.447+764_447+765ins others(4): Show |
ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 5/9 | chr13 | 36988719 | |||||||
chr13:36988720 | C | A | 26 | a0001c0001t0001g0012 a0001c0001t0001g0031 a0001c0001t0001g0032 others(23): Show |
27 | HG01109.hp2 HG01192.hp2 HG01981.hp2 others(24): Show |
intron_variant | MODIFIER | c.447+764G>T | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 5/9 | chr13 | 36988720 | |||||||
chr13:36988851 | C | G | 1 | a0001c0001t0001g0125 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.447+633G>C | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 5/9 | chr13 | 36988851 | |||||||
chr13:36989065 | C | T | 1 | a0001c0001t0001g0054 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.447+419G>A | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 5/9 | chr13 | 36989065 | |||||||
chr13:36989119 | T | C | 5 | a0001c0001t0001g0011 a0001c0001t0001g0205 a0001c0001t0001g0206 others(2): Show |
7 | HG00639.hp2 HG02109.hp2 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.447+365A>G | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 5/9 | chr13 | 36989119 | |||||||
chr13:36989639 | T | C | 1 | a0001c0001t0001g0169 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.355-63A>G | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 4/9 | chr13 | 36989639 | |||||||
chr13:36989654 | C | T | 72 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(69): Show |
99 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(96): Show |
intron_variant | MODIFIER | c.355-78G>A | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 4/9 | chr13 | 36989654 | |||||||
chr13:36989788 | C | T | 1 | a0001c0001t0001g0198 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.355-212G>A | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 4/9 | chr13 | 36989788 | |||||||
chr13:36989831 | C | T | 22 | a0001c0001t0001g0012 a0001c0001t0001g0031 a0001c0001t0001g0032 others(19): Show |
23 | HG01109.hp2 HG01192.hp2 HG01981.hp2 others(20): Show |
intron_variant | MODIFIER | c.355-255G>A | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 4/9 | chr13 | 36989831 | |||||||
chr13:36989878 | C | A | 5 | a0001c0001t0001g0108 a0001c0001t0001g0109 a0001c0001t0001g0110 others(2): Show |
5 | HG02109.hp1 HG02896.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.355-302G>T | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 4/9 | chr13 | 36989878 | |||||||
chr13:36989896 | C | A | 4 | a0001c0001t0001g0193 a0001c0001t0001g0194 a0001c0001t0001g0195 others(1): Show |
4 | HG02280.hp1 HG02647.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.355-320G>T | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 4/9 | chr13 | 36989896 | |||||||
chr13:36990131 | C | T | 1 | a0001c0001t0001g0053 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.355-555G>A | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 4/9 | chr13 | 36990131 | |||||||
chr13:36990258 | C | T | 1 | a0001c0001t0001g0052 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.355-682G>A | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 4/9 | chr13 | 36990258 | |||||||
chr13:36990345 | C | T | 16 | a0001c0001t0001g0012 a0001c0001t0001g0031 a0001c0001t0001g0032 others(13): Show |
17 | HG01109.hp2 HG01192.hp2 HG01981.hp2 others(14): Show |
intron_variant | MODIFIER | c.355-769G>A | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 4/9 | chr13 | 36990345 | |||||||
chr13:36990556 | T | C | 5 | a0001c0001t0001g0113 a0001c0001t0001g0114 a0001c0001t0001g0115 others(2): Show |
5 | HG01081.hp1 HG01123.hp2 HG01361.hp1 others(2): Show |
intron_variant | MODIFIER | c.355-980A>G | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 4/9 | chr13 | 36990556 | |||||||
chr13:36990604 | C | CAT | 216 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(213): Show |
258 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(255): Show |
intron_variant | MODIFIER | c.355-1029_355-1028i others(4): Show |
ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 4/9 | chr13 | 36990604 | |||||||
chr13:36990754 | TG | T | 184 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(181): Show |
225 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(222): Show |
intron_variant | MODIFIER | c.355-1179delC | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 4/9 | chr13 | 36990754 | |||||||
chr13:36990923 | C | T | 1 | a0001c0007t0001g0227 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.355-1347G>A | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 4/9 | chr13 | 36990923 | |||||||
chr13:36991140 | G | C | 1 | a0001c0001t0001g0204 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.355-1564C>G | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 4/9 | chr13 | 36991140 | |||||||
chr13:36991164 | C | G | 11 | a0001c0001t0001g0023 a0001c0001t0001g0029 a0001c0001t0001g0171 others(8): Show |
12 | HG02145.hp2 HG02280.hp2 HG02486.hp2 others(9): Show |
intron_variant | MODIFIER | c.355-1588G>C | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 4/9 | chr13 | 36991164 | |||||||
chr13:36991174 | C | T | 4 | a0001c0001t0001g0193 a0001c0001t0001g0194 a0001c0001t0001g0195 others(1): Show |
4 | HG02280.hp1 HG02647.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.355-1598G>A | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 4/9 | chr13 | 36991174 | |||||||
chr13:36991330 | A | ACTACTGA others(309): Show |
3 | a0001c0001t0001g0184 a0001c0001t0001g0185 a0001c0007t0001g0227 |
3 | HG02630.hp1 HG03098.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.355-1755_355-1754i others(318): Show |
ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 4/9 | chr13 | 36991330 | |||||||
chr13:36991330 | A | ACTACTGA others(317): Show |
1 | a0001c0001t0001g0046 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.355-1755_355-1754i others(326): Show |
ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 4/9 | chr13 | 36991330 | |||||||
chr13:36991428 | T | C | 1 | a0001c0001t0001g0170 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.355-1852A>G | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 4/9 | chr13 | 36991428 | |||||||
chr13:36991557 | T | G | 21 | a0001c0001t0001g0012 a0001c0001t0001g0031 a0001c0001t0001g0032 others(18): Show |
22 | HG01109.hp2 HG01192.hp2 HG01981.hp2 others(19): Show |
intron_variant | MODIFIER | c.355-1981A>C | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 4/9 | chr13 | 36991557 | |||||||
chr13:36991644 | TG | T | 70 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(67): Show |
96 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(93): Show |
intron_variant | MODIFIER | c.354+1959delC | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 4/9 | chr13 | 36991644 | |||||||
chr13:36991702 | G | A | 1 | a0001c0001t0001g0118 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.354+1902C>T | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 4/9 | chr13 | 36991702 | |||||||
chr13:36991814 | C | T | 84 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0013 others(81): Show |
94 | HG00099.hp1 HG00438.hp1 HG00609.hp2 others(91): Show |
intron_variant | MODIFIER | c.354+1790G>A | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 4/9 | chr13 | 36991814 | |||||||
chr13:36992210 | A | C | 1 | a0001c0001t0001g0193 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.354+1394T>G | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 4/9 | chr13 | 36992210 | |||||||
chr13:36992210 | ATATTTCC others(2): Show |
A | 2 | a0001c0001t0001g0025 a0001c0001t0001g0045 |
3 | HG02257.hp1 HG03516.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.354+1385_354+1393d others(11): Show |
ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 4/9 | chr13 | 36992210 | |||||||
chr13:36992261 | C | T | 1 | a0001c0001t0001g0208 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.354+1343G>A | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 4/9 | chr13 | 36992261 | |||||||
chr13:36992395 | C | T | 4 | a0001c0001t0001g0046 a0001c0001t0001g0184 a0001c0001t0001g0185 others(1): Show |
4 | HG02451.hp2 HG02630.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.354+1209G>A | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 4/9 | chr13 | 36992395 | |||||||
chr13:36992453 | T | C | 1 | a0001c0007t0001g0227 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.354+1151A>G | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 4/9 | chr13 | 36992453 | |||||||
chr13:36992557 | T | C | 3 | a0001c0001t0001g0210 a0001c0001t0001g0211 a0001c0001t0001g0212 |
3 | HG03209.hp2 HG03486.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.354+1047A>G | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 4/9 | chr13 | 36992557 | |||||||
chr13:36992631 | C | T | 1 | a0001c0001t0001g0041 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.354+973G>A | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 4/9 | chr13 | 36992631 | |||||||
chr13:36992725 | C | T | 1 | a0001c0001t0001g0124 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.354+879G>A | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 4/9 | chr13 | 36992725 | |||||||
chr13:36992850 | A | G | 1 | a0001c0001t0001g0123 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.354+754T>C | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 4/9 | chr13 | 36992850 | |||||||
chr13:36993259 | T | C | 1 | a0001c0001t0001g0212 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.354+345A>G | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 4/9 | chr13 | 36993259 | |||||||
chr13:36993347 | C | T | 3 | a0001c0001t0001g0210 a0001c0001t0001g0211 a0001c0001t0001g0212 |
3 | HG03209.hp2 HG03486.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.354+257G>A | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 4/9 | chr13 | 36993347 | |||||||
chr13:36993762 | T | G | 2 | a0001c0001t0001g0182 a0001c0001t0001g0183 |
2 | HG02145.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.286-90A>C | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 3/9 | chr13 | 36993762 | |||||||
chr13:36993798 | T | C | 1 | a0001c0001t0001g0119 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.286-126A>G | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 3/9 | chr13 | 36993798 | |||||||
chr13:36993836 | AAG | A | 25 | a0001c0001t0001g0012 a0001c0001t0001g0031 a0001c0001t0001g0032 others(22): Show |
26 | HG01109.hp2 HG01192.hp2 HG01981.hp2 others(23): Show |
intron_variant | MODIFIER | c.286-166_286-165del others(2): Show |
ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 3/9 | chr13 | 36993836 | |||||||
chr13:36993838 | G | C | 1 | a0001c0001t0001g0004 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.286-166C>G | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 3/9 | chr13 | 36993838 | |||||||
chr13:36993976 | G | C | 2 | a0001c0001t0001g0120 a0001c0001t0001g0121 |
2 | HG01257.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.286-304C>G | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 3/9 | chr13 | 36993976 | |||||||
chr13:36994603 | T | TAAAAGTT others(287): Show |
4 | a0001c0001t0001g0193 a0001c0001t0001g0194 a0001c0001t0001g0195 others(1): Show |
4 | HG02280.hp1 HG02647.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.285+385_285+386ins others(294): Show |
ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 3/9 | chr13 | 36994603 | |||||||
chr13:36994603 | T | TAAAAGTT others(301): Show |
12 | a0001c0001t0001g0012 a0001c0001t0001g0031 a0001c0001t0001g0032 others(9): Show |
13 | HG01109.hp2 HG01192.hp2 HG01981.hp2 others(10): Show |
intron_variant | MODIFIER | c.285+385_285+386ins others(308): Show |
ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 3/9 | chr13 | 36994603 | |||||||
chr13:36994603 | T | TAAAAGTT others(302): Show |
4 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0043 others(1): Show |
4 | HG02572.hp1 HG03453.hp2 NA19043.hp1 others(1): Show |
intron_variant | MODIFIER | c.285+385_285+386ins others(309): Show |
ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 3/9 | chr13 | 36994603 | |||||||
chr13:36994603 | T | TAAAAGTT others(320): Show |
1 | a0001c0001t0001g0208 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.285+385_285+386ins others(327): Show |
ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 3/9 | chr13 | 36994603 | |||||||
chr13:36994805 | C | T | 1 | a0001c0001t0001g0051 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.285+184G>A | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 3/9 | chr13 | 36994805 | |||||||
chr13:36995063 | A | G | 216 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(213): Show |
258 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(255): Show |
intron_variant | MODIFIER | c.239-28T>C | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 2/9 | chr13 | 36995063 | |||||||
chr13:36995946 | G | A | 1 | a0001c0001t0001g0030 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.67-350C>T | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 1/9 | chr13 | 36995946 | |||||||
chr13:36996014 | C | T | 1 | a0001c0001t0001g0050 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.67-418G>A | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 1/9 | chr13 | 36996014 | |||||||
chr13:36996027 | T | TTTTGCAG others(4): Show |
5 | a0001c0001t0001g0011 a0001c0001t0001g0205 a0001c0001t0001g0206 others(2): Show |
7 | HG00639.hp2 HG02109.hp2 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.67-432_67-431insTG others(9): Show |
ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 1/9 | chr13 | 36996027 | |||||||
chr13:36996045 | C | T | 184 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(181): Show |
225 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(222): Show |
intron_variant | MODIFIER | c.67-449G>A | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 1/9 | chr13 | 36996045 | |||||||
chr13:36996141 | A | G | 1 | a0001c0001t0001g0186 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.67-545T>C | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 1/9 | chr13 | 36996141 | |||||||
chr13:36996219 | C | A | 1 | a0001c0001t0001g0186 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.67-623G>T | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 1/9 | chr13 | 36996219 | |||||||
chr13:36996280 | T | C | 1 | a0001c0001t0001g0122 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.67-684A>G | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 1/9 | chr13 | 36996280 | |||||||
chr13:36996347 | A | G | 84 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0013 others(81): Show |
94 | HG00099.hp1 HG00438.hp1 HG00609.hp2 others(91): Show |
intron_variant | MODIFIER | c.67-751T>C | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 1/9 | chr13 | 36996347 | |||||||
chr13:36996483 | A | G | 1 | a0001c0001t0001g0193 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.67-887T>C | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 1/9 | chr13 | 36996483 | |||||||
chr13:36996509 | T | G | 4 | a0002c0002t0001g0190 a0002c0002t0001g0191 a0003c0003t0001g0188 others(1): Show |
4 | HG02886.hp1 HG02895.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.67-913A>C | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 1/9 | chr13 | 36996509 | |||||||
chr13:36996525 | C | T | 4 | a0001c0001t0001g0193 a0001c0001t0001g0194 a0001c0001t0001g0195 others(1): Show |
4 | HG02280.hp1 HG02647.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.67-929G>A | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 1/9 | chr13 | 36996525 | |||||||
chr13:36996594 | T | C | 21 | a0001c0001t0001g0012 a0001c0001t0001g0031 a0001c0001t0001g0032 others(18): Show |
22 | HG01109.hp2 HG01192.hp2 HG01981.hp2 others(19): Show |
intron_variant | MODIFIER | c.67-998A>G | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 1/9 | chr13 | 36996594 | |||||||
chr13:36996689 | T | C | 1 | a0001c0001t0001g0187 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.67-1093A>G | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 1/9 | chr13 | 36996689 | |||||||
chr13:36996693 | C | T | 4 | a0001c0001t0001g0013 a0001c0001t0001g0047 a0001c0001t0001g0048 others(1): Show |
5 | HG03927.hp2 NA18943.hp2 NA18980.hp1 others(2): Show |
intron_variant | MODIFIER | c.67-1097G>A | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 1/9 | chr13 | 36996693 | |||||||
chr13:36996819 | C | T | 1 | a0001c0001t0001g0046 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.67-1223G>A | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 1/9 | chr13 | 36996819 | |||||||
chr13:36997046 | G | C | 223 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(220): Show |
272 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(269): Show |
intron_variant | MODIFIER | c.67-1450C>G | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 1/9 | chr13 | 36997046 | |||||||
chr13:36997381 | G | A | 5 | a0001c0001t0001g0193 a0001c0001t0001g0194 a0001c0001t0001g0195 others(2): Show |
5 | HG02257.hp2 HG02280.hp1 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.67-1785C>T | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 1/9 | chr13 | 36997381 | |||||||
chr13:36997397 | C | T | 1 | a0001c0001t0001g0045 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.67-1801G>A | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 1/9 | chr13 | 36997397 | |||||||
chr13:36997461 | C | T | 191 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(188): Show |
232 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(229): Show |
intron_variant | MODIFIER | c.66+1774G>A | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 1/9 | chr13 | 36997461 | |||||||
chr13:36997466 | CA | C | 16 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0197 others(13): Show |
20 | HG00639.hp2 HG01257.hp2 HG01515.hp2 others(17): Show |
intron_variant | MODIFIER | c.66+1768delT | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 1/9 | chr13 | 36997466 | |||||||
chr13:36997466 | CAA | C | 175 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(172): Show |
212 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(209): Show |
intron_variant | MODIFIER | c.66+1767_66+1768del others(2): Show |
ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 1/9 | chr13 | 36997466 | |||||||
chr13:36997466 | CAAA | C | 19 | a0001c0001t0001g0012 a0001c0001t0001g0027 a0001c0001t0001g0028 others(16): Show |
20 | HG01109.hp2 HG01169.hp1 HG01192.hp2 others(17): Show |
intron_variant | MODIFIER | c.66+1766_66+1768del others(3): Show |
ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 1/9 | chr13 | 36997466 | |||||||
chr13:36998811 | A | G | 216 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(213): Show |
258 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(255): Show |
intron_variant | MODIFIER | c.66+424T>C | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 1/9 | chr13 | 36998811 | |||||||
chr13:36998880 | G | C | 1 | a0001c0001t0001g0221 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.66+355C>G | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 1/9 | chr13 | 36998880 | |||||||
chr13:36999082 | C | A | 4 | a0001c0001t0001g0222 a0001c0001t0001g0223 a0001c0001t0001g0224 others(1): Show |
4 | HG02559.hp1 HG02818.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.66+153G>T | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 1/9 | chr13 | 36999082 |