Item | Value |
---|---|
geneid | 149951 |
ensemblid | ENSG00000149600.12 |
hgncid | 16223 |
symbol | COMMD7 |
name | COMM domain containing 7 |
refseq_nuc | NM_053041.3 |
refseq_prot | NP_444269.2 |
ensembl_nuc | ENST00000278980.11 |
ensembl_prot | ENSP00000278980.6 |
mane_status | MANE Select |
chr | chr20 |
start | 32702699 |
end | 32743467 |
strand | - |
ver | v1.2 |
region | chr20:32702699-32743467 |
region5000 | chr20:32697699-32748467 |
regionname0 | COMMD7_chr20_32702699_32743467 |
regionname5000 | COMMD7_chr20_32697699_32748467 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 200 | 399 | 90 | 76 | 171 | 16 | 44 | 132 | COMMD7_chr20_32697699_32748467 | COMMD7 | MGRLH others(195): Show |
chr20 | 32697699 | 32748467 |
a0002 | 0/0 | 190 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | MGRLH others(185): Show |
chr20 | 32697699 | 32748467 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 600 | 399 | 90 | 76 | 171 | 16 | 44 | COMMD7_chr20_32697699_32748467 | COMMD7 | ATGGG others(595): Show |
chr20 | 32697699 | 32748467 | ||
a0002c0002 | 0/0 | 600 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | ATGGG others(595): Show |
chr20 | 32697699 | 32748467 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/1 | 1362 | 217 | 48 | 37 | 90 | 13 | 28 | COMMD7_chr20_32697699_32748467 | COMMD7 | GGTGG others(1357): Show |
chr20 | 32697699 | 32748467 |
a0001c0001t0002 | 1/0 | 1362 | 168 | 31 | 38 | 80 | 3 | 15 | COMMD7_chr20_32697699_32748467 | COMMD7 | GGTGG others(1357): Show |
chr20 | 32697699 | 32748467 |
a0001c0001t0003 | 0/0 | 1361 | 5 | 5 | 0 | 0 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | GGTGG others(1356): Show |
chr20 | 32697699 | 32748467 |
a0001c0001t0004 | 0/0 | 1361 | 4 | 4 | 0 | 0 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | GGTGG others(1356): Show |
chr20 | 32697699 | 32748467 |
a0001c0001t0005 | 0/0 | 1362 | 1 | 1 | 0 | 0 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | GGTGG others(1357): Show |
chr20 | 32697699 | 32748467 |
a0001c0001t0006 | 0/0 | 1362 | 1 | 1 | 0 | 0 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | GGTGG others(1357): Show |
chr20 | 32697699 | 32748467 |
a0001c0001t0007 | 0/0 | 1362 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | GGTGG others(1357): Show |
chr20 | 32697699 | 32748467 |
a0001c0001t0008 | 0/0 | 1362 | 1 | 0 | 0 | 0 | 0 | 1 | COMMD7_chr20_32697699_32748467 | COMMD7 | GGTGG others(1357): Show |
chr20 | 32697699 | 32748467 |
a0001c0001t0009 | 0/0 | 1362 | 1 | 0 | 1 | 0 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | GGTGG others(1357): Show |
chr20 | 32697699 | 32748467 |
a0002c0002t0001 | 0/0 | 1362 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | GGTGG others(1357): Show |
chr20 | 32697699 | 32748467 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 7 | 0 | 7 | 0 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0001g0002 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0001g0004 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0001g0005 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0001g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0001g0011 | 0/0 | 2 | 1 | 0 | 0 | 0 | 1 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0001g0012 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0001g0013 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0001g0014 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0001g0015 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0001g0025 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0001g0026 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0001g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0001g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0001g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0001g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0001g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0001g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0001g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0001g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0001g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0001g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0001g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0001g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0001g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0001g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0001g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0001g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0001g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0001g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0001g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0001g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0001g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0001g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0001g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0001g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0001g0242 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0001g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0001g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0001g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0001g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0001g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0001g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0001g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0001g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0001g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0001g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0001g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0001g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0001g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0001g0292 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0001g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0001g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0001g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0001g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0001g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0001g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0001g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0001g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0001g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0001g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0001g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0001g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0001g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0001g0306 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0001g0307 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0001g0308 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0001g0309 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0001g0310 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0001g0311 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0001g0312 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0001g0313 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0001g0314 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0001g0317 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0001g0318 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0001g0319 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0001g0320 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0001g0321 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0001g0322 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0001g0325 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0001g0326 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0001g0327 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0001g0328 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0001g0329 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0001g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0001g0331 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0001g0332 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0001g0333 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0001g0334 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0001g0335 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0001g0336 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0001g0337 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0001g0338 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0001g0339 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0001g0340 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0001g0341 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0001g0342 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0001g0343 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0001g0344 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0001g0345 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0001g0349 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0001g0351 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0001g0352 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0001g0353 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0001g0354 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0001g0357 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0001g0359 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0001g0360 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0001g0361 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0002g0003 | 0/0 | 4 | 0 | 4 | 0 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0002g0006 | 0/0 | 3 | 0 | 2 | 1 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0002g0007 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0002g0010 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0002g0016 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0002g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0002g0018 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0002g0019 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0002g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0002g0021 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0002g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0002g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0002g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0002g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0002g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0002g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0002g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0002g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0002g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0002g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0002g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0002g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0002g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0002g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0002g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0002g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0002g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0002g0117 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0002g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0002g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0002g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0002g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0002g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0002g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0002g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0002g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0002g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0002g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0002g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0002g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0002g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0002g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0002g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0002g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0002g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0002g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0002g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0002g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0002g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0002g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0002g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0002g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0002g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0002g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0002g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0002g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0002g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0002g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0002g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0002g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0002g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0002g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0002g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0002g0180 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0002g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0002g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0002g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0002g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0002g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0002g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0002g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0002g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0002g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0002g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0002g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0002g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0002g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0002g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0002g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0002g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0002g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0002g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0002g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0002g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0002g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0002g0203 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0002g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0002g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0002g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0002g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0002g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0002g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0002g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0002g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0002g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0002g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0002g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0002g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0002g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0002g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0002g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0002g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0002g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0002g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0002g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0002g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0002g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0002g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0002g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0002g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0002g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0002g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0002g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0002g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0002g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0002g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0002g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0002g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0002g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0002g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0002g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0002g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0002g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0002g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0002g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0002g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0002g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0002g0250 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0002g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0002g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0002g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0002g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0002g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0002g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0002g0258 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0002g0259 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0002g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0002g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0002g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0002g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0002g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0002g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0002g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0002g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0002g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0002g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0002g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0002g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0002g0346 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0002g0347 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0002g0350 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0002g0355 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0002g0356 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0003g0008 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0003g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0003g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0003g0358 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0004g0024 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0004g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0004g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0005g0348 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0006g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0007g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0008g0239 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0009g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0002c0002t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0002 | g0117 | EUR | GBR | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
HG00099 | hp2 | a0001 | c0001 | t0001 | g0240 | EUR | GBR | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
HG00140 | hp1 | a0001 | c0001 | t0002 | g0203 | EUR | GBR | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
HG00140 | hp2 | a0001 | c0001 | t0001 | g0311 | EUR | GBR | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
HG00280 | hp1 | a0001 | c0001 | t0001 | g0313 | EUR | FIN | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
HG00280 | hp2 | a0001 | c0001 | t0001 | g0325 | EUR | FIN | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
HG00323 | hp1 | a0001 | c0001 | t0002 | g0180 | EUR | FIN | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
HG00323 | hp2 | a0001 | c0001 | t0001 | g0087 | EUR | FIN | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
HG00408 | hp1 | a0001 | c0001 | t0001 | g0267 | EAS | CHS | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
HG00408 | hp2 | a0001 | c0001 | t0002 | g0173 | EAS | CHS | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
HG00423 | hp1 | a0001 | c0001 | t0002 | g0247 | EAS | CHS | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
HG00423 | hp2 | a0001 | c0001 | t0001 | g0144 | EAS | CHS | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
HG00438 | hp1 | a0001 | c0001 | t0001 | g0141 | EAS | CHS | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
HG00438 | hp2 | a0001 | c0001 | t0002 | g0178 | EAS | CHS | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
HG00544 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
HG00544 | hp2 | a0001 | c0001 | t0002 | g0181 | EAS | CHS | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
HG00558 | hp1 | a0001 | c0001 | t0002 | g0184 | EAS | CHS | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
HG00558 | hp2 | a0002 | c0002 | t0001 | g0082 | EAS | CHS | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
HG00621 | hp1 | a0001 | c0001 | t0002 | g0130 | EAS | CHS | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
HG00621 | hp2 | a0001 | c0001 | t0002 | g0131 | EAS | CHS | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
HG00639 | hp1 | a0001 | c0001 | t0002 | g0156 | AMR | PUR | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
HG00639 | hp2 | a0001 | c0001 | t0001 | g0309 | AMR | PUR | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
HG00673 | hp1 | a0001 | c0001 | t0002 | g0161 | EAS | CHS | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
HG00673 | hp2 | a0001 | c0001 | t0001 | g0143 | EAS | CHS | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
HG00733 | hp1 | a0001 | c0001 | t0001 | g0075 | AMR | PUR | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
HG00733 | hp2 | a0001 | c0001 | t0001 | g0341 | AMR | PUR | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
HG00735 | hp1 | a0001 | c0001 | t0002 | g0116 | AMR | PUR | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
HG00735 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
HG00738 | hp1 | a0001 | c0001 | t0002 | g0236 | AMR | PUR | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
HG00738 | hp2 | a0001 | c0001 | t0002 | g0189 | AMR | PUR | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
HG00741 | hp1 | a0001 | c0001 | t0009 | g0281 | AMR | PUR | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
HG00741 | hp2 | a0001 | c0001 | t0001 | g0360 | AMR | PUR | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
HG01069 | hp1 | a0001 | c0001 | t0002 | g0010 | AMR | PUR | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
HG01069 | hp2 | a0001 | c0001 | t0001 | g0345 | AMR | PUR | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
HG01070 | hp1 | a0001 | c0001 | t0001 | g0310 | AMR | PUR | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
HG01070 | hp2 | a0001 | c0001 | t0002 | g0164 | AMR | PUR | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
HG01071 | hp1 | a0001 | c0001 | t0002 | g0010 | AMR | PUR | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
HG01071 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
HG01074 | hp1 | a0001 | c0001 | t0001 | g0333 | AMR | PUR | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
HG01074 | hp2 | a0001 | c0001 | t0001 | g0327 | AMR | PUR | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
HG01081 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
HG01081 | hp2 | a0001 | c0001 | t0001 | g0328 | AMR | PUR | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
HG01106 | hp1 | a0001 | c0001 | t0002 | g0223 | AMR | PUR | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
HG01106 | hp2 | a0001 | c0001 | t0002 | g0200 | AMR | PUR | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
HG01109 | hp1 | a0001 | c0001 | t0002 | g0243 | AMR | PUR | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
HG01109 | hp2 | a0001 | c0001 | t0001 | g0114 | AMR | PUR | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
HG01167 | hp1 | a0001 | c0001 | t0002 | g0160 | AMR | PUR | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
HG01167 | hp2 | a0001 | c0001 | t0001 | g0028 | AMR | PUR | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
HG01169 | hp1 | a0001 | c0001 | t0001 | g0241 | AMR | PUR | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
HG01169 | hp2 | a0001 | c0001 | t0002 | g0159 | AMR | PUR | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
HG01175 | hp1 | a0001 | c0001 | t0002 | g0019 | AMR | PUR | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
HG01175 | hp2 | a0001 | c0001 | t0001 | g0314 | AMR | PUR | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
HG01192 | hp1 | a0001 | c0001 | t0001 | g0340 | AMR | PUR | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
HG01192 | hp2 | a0001 | c0001 | t0001 | g0337 | AMR | PUR | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
HG01243 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
HG01243 | hp2 | a0001 | c0001 | t0001 | g0029 | AMR | PUR | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
HG01255 | hp1 | a0001 | c0001 | t0002 | g0219 | AMR | CLM | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
HG01255 | hp2 | a0001 | c0001 | t0001 | g0331 | AMR | CLM | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
HG01256 | hp1 | a0001 | c0001 | t0002 | g0018 | AMR | CLM | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
HG01256 | hp2 | a0001 | c0001 | t0001 | g0307 | AMR | CLM | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
HG01258 | hp1 | a0001 | c0001 | t0002 | g0018 | AMR | CLM | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
HG01258 | hp2 | a0001 | c0001 | t0001 | g0359 | AMR | CLM | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
HG01261 | hp1 | a0001 | c0001 | t0002 | g0230 | AMR | CLM | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
HG01261 | hp2 | a0001 | c0001 | t0002 | g0003 | AMR | CLM | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
HG01346 | hp1 | a0001 | c0001 | t0001 | g0320 | AMR | CLM | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
HG01346 | hp2 | a0001 | c0001 | t0002 | g0222 | AMR | CLM | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
HG01358 | hp1 | a0001 | c0001 | t0002 | g0006 | AMR | CLM | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
HG01358 | hp2 | a0001 | c0001 | t0001 | g0112 | AMR | CLM | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
HG01361 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
HG01361 | hp2 | a0001 | c0001 | t0002 | g0035 | AMR | CLM | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
HG01433 | hp1 | a0001 | c0001 | t0001 | g0025 | AMR | CLM | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
HG01433 | hp2 | a0001 | c0001 | t0002 | g0221 | AMR | CLM | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
HG01496 | hp1 | a0001 | c0001 | t0002 | g0021 | AMR | CLM | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
HG01496 | hp2 | a0001 | c0001 | t0001 | g0319 | AMR | CLM | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
HG01515 | hp1 | a0001 | c0001 | t0001 | g0074 | EUR | IBS | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
HG01515 | hp2 | a0001 | c0001 | t0001 | g0072 | EUR | IBS | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
HG01516 | hp1 | a0001 | c0001 | t0001 | g0329 | EUR | IBS | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
HG01516 | hp2 | a0001 | c0001 | t0001 | g0334 | EUR | IBS | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
HG01517 | hp1 | a0001 | c0001 | t0001 | g0026 | EUR | IBS | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
HG01517 | hp2 | a0001 | c0001 | t0001 | g0076 | EUR | IBS | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
HG01884 | hp1 | a0001 | c0001 | t0002 | g0030 | AFR | ACB | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
HG01884 | hp2 | a0001 | c0001 | t0002 | g0350 | AFR | ACB | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
HG01891 | hp1 | a0001 | c0001 | t0001 | g0136 | AFR | ACB | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
HG01891 | hp2 | a0001 | c0001 | t0001 | g0272 | AFR | ACB | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
HG01928 | hp1 | a0001 | c0001 | t0002 | g0256 | AMR | PEL | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
HG01928 | hp2 | a0001 | c0001 | t0002 | g0234 | AMR | PEL | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
HG01934 | hp1 | a0001 | c0001 | t0002 | g0277 | AMR | PEL | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
HG01934 | hp2 | a0001 | c0001 | t0001 | g0293 | AMR | PEL | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
HG01943 | hp1 | a0001 | c0001 | t0002 | g0021 | AMR | PEL | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
HG01943 | hp2 | a0001 | c0001 | t0002 | g0003 | AMR | PEL | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
HG01952 | hp1 | a0001 | c0001 | t0002 | g0006 | AMR | PEL | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
HG01952 | hp2 | a0001 | c0001 | t0002 | g0003 | AMR | PEL | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
HG01975 | hp1 | a0001 | c0001 | t0001 | g0026 | AMR | PEL | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
HG01975 | hp2 | a0001 | c0001 | t0002 | g0232 | AMR | PEL | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
HG01981 | hp1 | a0001 | c0001 | t0001 | g0321 | AMR | PEL | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
HG01981 | hp2 | a0001 | c0001 | t0002 | g0233 | AMR | PEL | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
HG01993 | hp1 | a0001 | c0001 | t0002 | g0003 | AMR | PEL | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
HG01993 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
HG02027 | hp1 | a0001 | c0001 | t0001 | g0101 | EAS | KHV | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
HG02027 | hp2 | a0001 | c0001 | t0001 | g0042 | EAS | KHV | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
HG02040 | hp1 | a0001 | c0001 | t0002 | g0027 | EAS | KHV | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
HG02040 | hp2 | a0001 | c0001 | t0001 | g0298 | EAS | KHV | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
HG02055 | hp1 | a0001 | c0001 | t0002 | g0245 | AFR | ACB | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
HG02055 | hp2 | a0001 | c0001 | t0002 | g0283 | AFR | ACB | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
HG02056 | hp1 | a0001 | c0001 | t0001 | g0129 | EAS | KHV | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
HG02056 | hp2 | a0001 | c0001 | t0001 | g0304 | EAS | KHV | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
HG02071 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
HG02071 | hp2 | a0001 | c0001 | t0002 | g0176 | EAS | KHV | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
HG02074 | hp1 | a0001 | c0001 | t0002 | g0177 | EAS | KHV | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
HG02074 | hp2 | a0001 | c0001 | t0002 | g0207 | EAS | KHV | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
HG02080 | hp1 | a0001 | c0001 | t0002 | g0263 | EAS | KHV | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
HG02080 | hp2 | a0001 | c0001 | t0002 | g0206 | EAS | KHV | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
HG02083 | hp1 | a0001 | c0001 | t0002 | g0172 | EAS | KHV | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
HG02083 | hp2 | a0001 | c0001 | t0002 | g0070 | EAS | KHV | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
HG02129 | hp1 | a0001 | c0001 | t0002 | g0022 | EAS | KHV | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
HG02129 | hp2 | a0001 | c0001 | t0002 | g0044 | EAS | KHV | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
HG02132 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
HG02132 | hp2 | a0001 | c0001 | t0002 | g0253 | EAS | KHV | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
HG02135 | hp1 | a0001 | c0001 | t0001 | g0361 | EAS | KHV | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
HG02135 | hp2 | a0001 | c0001 | t0001 | g0059 | EAS | KHV | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
HG02145 | hp1 | a0001 | c0001 | t0001 | g0262 | AFR | ACB | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
HG02145 | hp2 | a0001 | c0001 | t0001 | g0273 | AFR | ACB | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
HG02148 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
HG02148 | hp2 | a0001 | c0001 | t0001 | g0322 | AMR | PEL | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
HG02155 | hp1 | a0001 | c0001 | t0001 | g0269 | EAS | CDX | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
HG02155 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | CDX | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
HG02165 | hp1 | a0001 | c0001 | t0001 | g0092 | EAS | CDX | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
HG02165 | hp2 | a0001 | c0001 | t0002 | g0217 | EAS | CDX | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
HG02257 | hp1 | a0001 | c0001 | t0002 | g0323 | AFR | ACB | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
HG02257 | hp2 | a0001 | c0001 | t0001 | g0043 | AFR | ACB | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
HG02258 | hp1 | a0001 | c0001 | t0002 | g0188 | AFR | ACB | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
HG02258 | hp2 | a0001 | c0001 | t0001 | g0137 | AFR | ACB | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
HG02273 | hp1 | a0001 | c0001 | t0002 | g0231 | AMR | PEL | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
HG02273 | hp2 | a0001 | c0001 | t0002 | g0198 | AMR | PEL | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
HG02280 | hp1 | a0001 | c0001 | t0003 | g0008 | AFR | ACB | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
HG02280 | hp2 | a0001 | c0001 | t0001 | g0115 | AFR | ACB | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
HG02293 | hp1 | a0001 | c0001 | t0002 | g0153 | AMR | PEL | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
HG02293 | hp2 | a0001 | c0001 | t0002 | g0190 | AMR | PEL | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
HG02300 | hp1 | a0001 | c0001 | t0001 | g0308 | AMR | PEL | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
HG02300 | hp2 | a0001 | c0001 | t0002 | g0220 | AMR | PEL | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
HG02451 | hp1 | a0001 | c0001 | t0001 | g0015 | AFR | ACB | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
HG02451 | hp2 | a0001 | c0001 | t0001 | g0290 | AFR | ACB | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
HG02572 | hp1 | a0001 | c0001 | t0001 | g0354 | AFR | GWD | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
HG02572 | hp2 | a0001 | c0001 | t0002 | g0278 | AFR | GWD | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
HG02602 | hp1 | a0001 | c0001 | t0001 | g0339 | SAS | PJL | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
HG02602 | hp2 | a0001 | c0001 | t0002 | g0212 | SAS | PJL | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
HG02615 | hp1 | a0001 | c0001 | t0002 | g0007 | AFR | GWD | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
HG02615 | hp2 | a0001 | c0001 | t0001 | g0349 | AFR | GWD | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
HG02622 | hp1 | a0001 | c0001 | t0002 | g0037 | AFR | GWD | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
HG02622 | hp2 | a0001 | c0001 | t0001 | g0142 | AFR | GWD | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
HG02630 | hp1 | a0001 | c0001 | t0004 | g0024 | AFR | GWD | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
HG02630 | hp2 | a0001 | c0001 | t0001 | g0352 | AFR | GWD | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
HG02647 | hp1 | a0001 | c0001 | t0002 | g0118 | AFR | GWD | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
HG02647 | hp2 | a0001 | c0001 | t0001 | g0038 | AFR | GWD | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
HG02683 | hp1 | a0001 | c0001 | t0001 | g0097 | SAS | PJL | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
HG02683 | hp2 | a0001 | c0001 | t0001 | g0344 | SAS | PJL | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
HG02698 | hp1 | a0001 | c0001 | t0002 | g0174 | SAS | PJL | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
HG02698 | hp2 | a0001 | c0001 | t0001 | g0096 | SAS | PJL | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
HG02717 | hp1 | a0001 | c0001 | t0001 | g0351 | AFR | GWD | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
HG02717 | hp2 | a0001 | c0001 | t0001 | g0032 | AFR | GWD | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
HG02723 | hp1 | a0001 | c0001 | t0001 | g0146 | AFR | GWD | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
HG02723 | hp2 | a0001 | c0001 | t0001 | g0014 | AFR | GWD | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
HG02735 | hp1 | a0001 | c0001 | t0001 | g0326 | SAS | PJL | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
HG02735 | hp2 | a0001 | c0001 | t0002 | g0258 | SAS | PJL | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
HG02738 | hp1 | a0001 | c0001 | t0001 | g0089 | SAS | PJL | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
HG02738 | hp2 | a0001 | c0001 | t0001 | g0292 | SAS | PJL | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
HG02809 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | GWD | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
HG02809 | hp2 | a0001 | c0001 | t0001 | g0152 | AFR | GWD | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
HG02818 | hp1 | a0001 | c0001 | t0002 | g0039 | AFR | GWD | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
HG02818 | hp2 | a0001 | c0001 | t0001 | g0014 | AFR | GWD | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
HG02886 | hp1 | a0001 | c0001 | t0004 | g0024 | AFR | GWD | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
HG02886 | hp2 | a0001 | c0001 | t0002 | g0324 | AFR | GWD | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
HG02922 | hp1 | a0001 | c0001 | t0002 | g0182 | AFR | ESN | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
HG02922 | hp2 | a0001 | c0001 | t0001 | g0132 | AFR | ESN | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
HG02965 | hp1 | a0001 | c0001 | t0002 | g0034 | AFR | ESN | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
HG02965 | hp2 | a0001 | c0001 | t0001 | g0134 | AFR | ESN | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
HG02970 | hp1 | a0001 | c0001 | t0004 | g0287 | AFR | ESN | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
HG02970 | hp2 | a0001 | c0001 | t0002 | g0126 | AFR | ESN | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
HG02976 | hp1 | a0001 | c0001 | t0002 | g0183 | AFR | ESN | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
HG02976 | hp2 | a0001 | c0001 | t0002 | g0123 | AFR | ESN | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
HG03017 | hp1 | a0001 | c0001 | t0001 | g0128 | SAS | PJL | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
HG03017 | hp2 | a0001 | c0001 | t0001 | g0113 | SAS | PJL | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
HG03041 | hp1 | a0001 | c0001 | t0001 | g0013 | AFR | GWD | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
HG03041 | hp2 | a0001 | c0001 | t0004 | g0285 | AFR | GWD | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
HG03098 | hp1 | a0001 | c0001 | t0002 | g0119 | AFR | MSL | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
HG03098 | hp2 | a0001 | c0001 | t0002 | g0279 | AFR | MSL | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
HG03130 | hp1 | a0001 | c0001 | t0001 | g0149 | AFR | ESN | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
HG03130 | hp2 | a0001 | c0001 | t0002 | g0162 | AFR | ESN | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
HG03139 | hp1 | a0001 | c0001 | t0001 | g0270 | AFR | ESN | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
HG03139 | hp2 | a0001 | c0001 | t0001 | g0291 | AFR | ESN | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
HG03195 | hp1 | a0001 | c0001 | t0003 | g0008 | AFR | ESN | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
HG03195 | hp2 | a0001 | c0001 | t0001 | g0015 | AFR | ESN | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
HG03209 | hp1 | a0001 | c0001 | t0002 | g0033 | AFR | MSL | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
HG03209 | hp2 | a0001 | c0001 | t0001 | g0280 | AFR | MSL | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
HG03225 | hp1 | a0001 | c0001 | t0001 | g0013 | AFR | MSL | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
HG03225 | hp2 | a0001 | c0001 | t0001 | g0289 | AFR | MSL | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
HG03239 | hp1 | a0001 | c0001 | t0001 | g0312 | SAS | PJL | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
HG03239 | hp2 | a0001 | c0001 | t0002 | g0201 | SAS | PJL | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
HG03453 | hp1 | a0001 | c0001 | t0001 | g0260 | AFR | MSL | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
HG03453 | hp2 | a0001 | c0001 | t0001 | g0271 | AFR | MSL | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
HG03486 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | MSL | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
HG03486 | hp2 | a0001 | c0001 | t0001 | g0122 | AFR | MSL | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
HG03491 | hp1 | a0001 | c0001 | t0002 | g0179 | SAS | PJL | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
HG03491 | hp2 | a0001 | c0001 | t0001 | g0317 | SAS | PJL | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
HG03492 | hp1 | a0001 | c0001 | t0002 | g0199 | SAS | PJL | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
HG03492 | hp2 | a0001 | c0001 | t0001 | g0335 | SAS | PJL | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
HG03516 | hp1 | a0001 | c0001 | t0001 | g0353 | AFR | ESN | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
HG03516 | hp2 | a0001 | c0001 | t0006 | g0125 | AFR | ESN | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
HG03540 | hp1 | a0001 | c0001 | t0002 | g0246 | AFR | GWD | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
HG03540 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | GWD | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
HG03579 | hp1 | a0001 | c0001 | t0001 | g0012 | AFR | MSL | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
HG03579 | hp2 | a0001 | c0001 | t0001 | g0121 | AFR | MSL | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
HG03654 | hp1 | a0001 | c0001 | t0001 | g0077 | SAS | PJL | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
HG03654 | hp2 | a0001 | c0001 | t0002 | g0109 | SAS | PJL | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
HG03669 | hp1 | a0001 | c0001 | t0001 | g0343 | SAS | PJL | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
HG03669 | hp2 | a0001 | c0001 | t0001 | g0086 | SAS | PJL | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
HG03688 | hp1 | a0001 | c0001 | t0002 | g0208 | SAS | STU | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
HG03688 | hp2 | a0001 | c0001 | t0001 | g0105 | SAS | STU | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
HG03704 | hp1 | a0001 | c0001 | t0002 | g0016 | SAS | PJL | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
HG03704 | hp2 | a0001 | c0001 | t0001 | g0108 | SAS | PJL | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
HG03710 | hp1 | a0001 | c0001 | t0001 | g0342 | SAS | PJL | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
HG03710 | hp2 | a0001 | c0001 | t0001 | g0336 | SAS | PJL | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
HG03831 | hp1 | a0001 | c0001 | t0001 | g0338 | SAS | BEB | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
HG03831 | hp2 | a0001 | c0001 | t0001 | g0106 | SAS | BEB | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
HG03927 | hp1 | a0001 | c0001 | t0001 | g0111 | SAS | BEB | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
HG03927 | hp2 | a0001 | c0001 | t0002 | g0259 | SAS | BEB | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
HG03942 | hp1 | a0001 | c0001 | t0002 | g0250 | SAS | BEB | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
HG03942 | hp2 | a0001 | c0001 | t0002 | g0191 | SAS | BEB | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
HG04115 | hp1 | a0001 | c0001 | t0001 | g0093 | SAS | STU | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
HG04115 | hp2 | a0001 | c0001 | t0001 | g0318 | SAS | STU | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
HG04199 | hp1 | a0001 | c0001 | t0002 | g0225 | SAS | STU | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
HG04199 | hp2 | a0001 | c0001 | t0001 | g0107 | SAS | STU | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
HG04204 | hp1 | a0001 | c0001 | t0001 | g0011 | SAS | STU | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
HG04204 | hp2 | a0001 | c0001 | t0002 | g0347 | SAS | STU | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
HG04228 | hp1 | a0001 | c0001 | t0001 | g0306 | SAS | STU | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
HG04228 | hp2 | a0001 | c0001 | t0008 | g0239 | SAS | STU | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
NA18522 | hp1 | a0001 | c0001 | t0005 | g0348 | AFR | YRI | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
NA18522 | hp2 | a0001 | c0001 | t0003 | g0358 | AFR | YRI | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
NA18612 | hp1 | a0001 | c0001 | t0002 | g0249 | EAS | CHB | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
NA18612 | hp2 | a0001 | c0001 | t0001 | g0148 | EAS | CHB | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
NA18906 | hp1 | a0001 | c0001 | t0002 | g0036 | AFR | YRI | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
NA18906 | hp2 | a0001 | c0001 | t0001 | g0124 | AFR | YRI | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
NA18940 | hp1 | a0001 | c0001 | t0002 | g0196 | EAS | JPT | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
NA18940 | hp2 | a0001 | c0001 | t0001 | g0102 | EAS | JPT | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
NA18942 | hp1 | a0001 | c0001 | t0002 | g0154 | EAS | JPT | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
NA18942 | hp2 | a0001 | c0001 | t0001 | g0300 | EAS | JPT | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
NA18943 | hp1 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
NA18943 | hp2 | a0001 | c0001 | t0002 | g0248 | EAS | JPT | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
NA18944 | hp1 | a0001 | c0001 | t0002 | g0068 | EAS | JPT | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
NA18944 | hp2 | a0001 | c0001 | t0002 | g0187 | EAS | JPT | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
NA18945 | hp1 | a0001 | c0001 | t0002 | g0171 | EAS | JPT | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
NA18945 | hp2 | a0001 | c0001 | t0001 | g0297 | EAS | JPT | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
NA18946 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
NA18946 | hp2 | a0001 | c0001 | t0001 | g0276 | EAS | JPT | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
NA18947 | hp1 | a0001 | c0001 | t0001 | g0264 | EAS | JPT | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
NA18947 | hp2 | a0001 | c0001 | t0001 | g0296 | EAS | JPT | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
NA18948 | hp1 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
NA18948 | hp2 | a0001 | c0001 | t0002 | g0218 | EAS | JPT | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
NA18949 | hp1 | a0001 | c0001 | t0001 | g0302 | EAS | JPT | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
NA18949 | hp2 | a0001 | c0001 | t0002 | g0315 | EAS | JPT | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
NA18950 | hp1 | a0001 | c0001 | t0001 | g0099 | EAS | JPT | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
NA18950 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
NA18951 | hp1 | a0001 | c0001 | t0002 | g0346 | EAS | JPT | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
NA18951 | hp2 | a0001 | c0001 | t0002 | g0167 | EAS | JPT | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
NA18953 | hp1 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
NA18953 | hp2 | a0001 | c0001 | t0001 | g0067 | EAS | JPT | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
NA18956 | hp1 | a0001 | c0001 | t0002 | g0166 | EAS | JPT | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
NA18956 | hp2 | a0001 | c0001 | t0001 | g0054 | EAS | JPT | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
NA18959 | hp1 | a0001 | c0001 | t0001 | g0060 | EAS | JPT | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
NA18959 | hp2 | a0001 | c0001 | t0002 | g0244 | EAS | JPT | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
NA18960 | hp1 | a0001 | c0001 | t0001 | g0073 | EAS | JPT | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
NA18960 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
NA18961 | hp1 | a0001 | c0001 | t0002 | g0227 | EAS | JPT | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
NA18961 | hp2 | a0001 | c0001 | t0001 | g0055 | EAS | JPT | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
NA18962 | hp1 | a0001 | c0001 | t0001 | g0053 | EAS | JPT | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
NA18962 | hp2 | a0001 | c0001 | t0002 | g0237 | EAS | JPT | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
NA18964 | hp1 | a0001 | c0001 | t0002 | g0022 | EAS | JPT | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
NA18964 | hp2 | a0001 | c0001 | t0001 | g0045 | EAS | JPT | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
NA18965 | hp1 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
NA18965 | hp2 | a0001 | c0001 | t0001 | g0047 | EAS | JPT | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
NA18966 | hp1 | a0001 | c0001 | t0002 | g0316 | EAS | JPT | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
NA18966 | hp2 | a0001 | c0001 | t0002 | g0169 | EAS | JPT | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
NA18967 | hp1 | a0001 | c0001 | t0001 | g0275 | EAS | JPT | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
NA18967 | hp2 | a0001 | c0001 | t0002 | g0175 | EAS | JPT | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
NA18970 | hp1 | a0001 | c0001 | t0001 | g0303 | EAS | JPT | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
NA18970 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
NA18971 | hp1 | a0001 | c0001 | t0002 | g0205 | EAS | JPT | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
NA18971 | hp2 | a0001 | c0001 | t0002 | g0185 | EAS | JPT | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
NA18975 | hp1 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
NA18975 | hp2 | a0001 | c0001 | t0002 | g0204 | EAS | JPT | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
NA18977 | hp1 | a0001 | c0001 | t0001 | g0295 | EAS | JPT | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
NA18977 | hp2 | a0001 | c0001 | t0001 | g0268 | EAS | JPT | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
NA18979 | hp1 | a0001 | c0001 | t0001 | g0100 | EAS | JPT | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
NA18979 | hp2 | a0001 | c0001 | t0001 | g0046 | EAS | JPT | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
NA18980 | hp1 | a0001 | c0001 | t0001 | g0050 | EAS | JPT | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
NA18980 | hp2 | a0001 | c0001 | t0001 | g0065 | EAS | JPT | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
NA18981 | hp1 | a0001 | c0001 | t0001 | g0228 | EAS | JPT | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
NA18981 | hp2 | a0001 | c0001 | t0001 | g0057 | EAS | JPT | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
NA18982 | hp1 | a0001 | c0001 | t0001 | g0061 | EAS | JPT | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
NA18982 | hp2 | a0001 | c0001 | t0002 | g0215 | EAS | JPT | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
NA18983 | hp1 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
NA18983 | hp2 | a0001 | c0001 | t0002 | g0023 | EAS | JPT | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
NA18985 | hp1 | a0001 | c0001 | t0002 | g0170 | EAS | JPT | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
NA18985 | hp2 | a0001 | c0001 | t0001 | g0063 | EAS | JPT | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
NA18986 | hp1 | a0001 | c0001 | t0001 | g0048 | EAS | JPT | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
NA18986 | hp2 | a0001 | c0001 | t0002 | g0019 | EAS | JPT | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
NA18987 | hp1 | a0001 | c0001 | t0001 | g0069 | EAS | JPT | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
NA18987 | hp2 | a0001 | c0001 | t0002 | g0235 | EAS | JPT | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
NA18988 | hp1 | a0001 | c0001 | t0001 | g0257 | EAS | JPT | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
NA18988 | hp2 | a0001 | c0001 | t0002 | g0017 | EAS | JPT | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
NA18989 | hp1 | a0001 | c0001 | t0002 | g0224 | EAS | JPT | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
NA18989 | hp2 | a0001 | c0001 | t0001 | g0058 | EAS | JPT | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
NA18991 | hp1 | a0001 | c0001 | t0002 | g0213 | EAS | JPT | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
NA18991 | hp2 | a0001 | c0001 | t0001 | g0056 | EAS | JPT | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
NA18992 | hp1 | a0001 | c0001 | t0002 | g0197 | EAS | JPT | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
NA18992 | hp2 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
NA18993 | hp1 | a0001 | c0001 | t0002 | g0155 | EAS | JPT | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
NA18993 | hp2 | a0001 | c0001 | t0002 | g0238 | EAS | JPT | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
NA18995 | hp1 | a0001 | c0001 | t0002 | g0168 | EAS | JPT | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
NA18995 | hp2 | a0001 | c0001 | t0002 | g0020 | EAS | JPT | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
NA18998 | hp1 | a0001 | c0001 | t0002 | g0023 | EAS | JPT | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
NA18998 | hp2 | a0001 | c0001 | t0001 | g0261 | EAS | JPT | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
NA18999 | hp1 | a0001 | c0001 | t0001 | g0062 | EAS | JPT | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
NA18999 | hp2 | a0001 | c0001 | t0002 | g0251 | EAS | JPT | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
NA19000 | hp1 | a0001 | c0001 | t0002 | g0255 | EAS | JPT | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
NA19000 | hp2 | a0001 | c0001 | t0002 | g0165 | EAS | JPT | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
NA19002 | hp1 | a0001 | c0001 | t0002 | g0163 | EAS | JPT | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
NA19002 | hp2 | a0001 | c0001 | t0001 | g0145 | EAS | JPT | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
NA19003 | hp1 | a0001 | c0001 | t0002 | g0252 | EAS | JPT | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
NA19003 | hp2 | a0001 | c0001 | t0001 | g0071 | EAS | JPT | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
NA19004 | hp1 | a0001 | c0001 | t0002 | g0158 | EAS | JPT | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
NA19004 | hp2 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
NA19005 | hp1 | a0001 | c0001 | t0001 | g0051 | EAS | JPT | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
NA19005 | hp2 | a0001 | c0001 | t0001 | g0079 | EAS | JPT | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
NA19009 | hp1 | a0001 | c0001 | t0002 | g0229 | EAS | JPT | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
NA19009 | hp2 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
NA19010 | hp1 | a0001 | c0001 | t0002 | g0083 | EAS | JPT | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
NA19010 | hp2 | a0001 | c0001 | t0002 | g0211 | EAS | JPT | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
NA19011 | hp1 | a0001 | c0001 | t0002 | g0192 | EAS | JPT | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
NA19011 | hp2 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
NA19030 | hp1 | a0001 | c0001 | t0003 | g0288 | AFR | LWK | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
NA19030 | hp2 | a0001 | c0001 | t0002 | g0226 | AFR | LWK | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
NA19043 | hp1 | a0001 | c0001 | t0001 | g0012 | AFR | LWK | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
NA19043 | hp2 | a0001 | c0001 | t0002 | g0157 | AFR | LWK | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
NA19054 | hp1 | a0001 | c0001 | t0002 | g0151 | EAS | JPT | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
NA19054 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
NA19056 | hp1 | a0001 | c0001 | t0001 | g0301 | EAS | JPT | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
NA19056 | hp2 | a0001 | c0001 | t0001 | g0066 | EAS | JPT | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
NA19057 | hp1 | a0001 | c0001 | t0001 | g0064 | EAS | JPT | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
NA19057 | hp2 | a0001 | c0001 | t0002 | g0020 | EAS | JPT | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
NA19058 | hp1 | a0001 | c0001 | t0002 | g0193 | EAS | JPT | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
NA19058 | hp2 | a0001 | c0001 | t0001 | g0305 | EAS | JPT | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
NA19062 | hp1 | a0001 | c0001 | t0001 | g0049 | EAS | JPT | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
NA19062 | hp2 | a0001 | c0001 | t0002 | g0209 | EAS | JPT | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
NA19064 | hp1 | a0001 | c0001 | t0001 | g0052 | EAS | JPT | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
NA19064 | hp2 | a0001 | c0001 | t0002 | g0017 | EAS | JPT | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
NA19066 | hp1 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
NA19066 | hp2 | a0001 | c0001 | t0002 | g0195 | EAS | JPT | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
NA19070 | hp1 | a0001 | c0001 | t0001 | g0091 | EAS | JPT | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
NA19070 | hp2 | a0001 | c0001 | t0002 | g0194 | EAS | JPT | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
NA19072 | hp1 | a0001 | c0001 | t0002 | g0186 | EAS | JPT | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
NA19072 | hp2 | a0001 | c0001 | t0001 | g0081 | EAS | JPT | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
NA19074 | hp1 | a0001 | c0001 | t0002 | g0274 | EAS | JPT | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
NA19074 | hp2 | a0001 | c0001 | t0001 | g0084 | EAS | JPT | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
NA19077 | hp1 | a0001 | c0001 | t0001 | g0265 | EAS | JPT | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
NA19077 | hp2 | a0001 | c0001 | t0002 | g0216 | EAS | JPT | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
NA19079 | hp1 | a0001 | c0001 | t0001 | g0299 | EAS | JPT | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
NA19079 | hp2 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
NA19081 | hp1 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
NA19081 | hp2 | a0001 | c0001 | t0002 | g0016 | EAS | JPT | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
NA19082 | hp1 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
NA19082 | hp2 | a0001 | c0001 | t0002 | g0254 | EAS | JPT | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
NA19085 | hp1 | a0001 | c0001 | t0001 | g0294 | EAS | JPT | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
NA19085 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
NA19088 | hp1 | a0001 | c0001 | t0001 | g0266 | EAS | JPT | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
NA19088 | hp2 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
NA19091 | hp1 | a0001 | c0001 | t0002 | g0214 | EAS | JPT | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
NA19091 | hp2 | a0001 | c0001 | t0007 | g0202 | EAS | JPT | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
NA19240 | hp1 | a0001 | c0001 | t0003 | g0286 | AFR | YRI | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
NA19240 | hp2 | a0001 | c0001 | t0001 | g0031 | AFR | YRI | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
NA20129 | hp1 | a0001 | c0001 | t0001 | g0133 | AFR | ASW | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
NA20129 | hp2 | a0001 | c0001 | t0001 | g0011 | AFR | ASW | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
NA20805 | hp1 | a0001 | c0001 | t0001 | g0104 | EUR | TSI | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
NA20805 | hp2 | a0001 | c0001 | t0001 | g0025 | EUR | TSI | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
NA20905 | hp1 | a0001 | c0001 | t0001 | g0103 | SAS | GIH | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
NA20905 | hp2 | a0001 | c0001 | t0002 | g0110 | SAS | GIH | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
HG01123 | hp1 | a0001 | c0001 | t0001 | g0332 | AMR | CLM | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
HG01123 | hp2 | a0001 | c0001 | t0001 | g0078 | AMR | CLM | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
HG02109 | hp1 | a0001 | c0001 | t0002 | g0355 | AFR | ACB | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
HG02109 | hp2 | a0001 | c0001 | t0001 | g0330 | AFR | ACB | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
HG02486 | hp1 | a0001 | c0001 | t0002 | g0284 | AFR | ACB | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
HG02486 | hp2 | a0001 | c0001 | t0001 | g0135 | AFR | ACB | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
HG03471 | hp1 | a0001 | c0001 | t0002 | g0282 | AFR | MSL | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
HG03471 | hp2 | a0001 | c0001 | t0002 | g0120 | AFR | MSL | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
HG06807 | hp1 | a0001 | c0001 | t0002 | g0210 | AFR | USA | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
HG06807 | hp2 | a0001 | c0001 | t0002 | g0007 | AFR | USA | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
NA21309 | hp1 | a0001 | c0001 | t0001 | g0357 | AFR | LWK | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
NA21309 | hp2 | a0001 | c0001 | t0001 | g0150 | AFR | LWK | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0242 | REF | REF | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
homoSapiens | grch38p0 | a0001 | c0001 | t0002 | g0356 | REF | REF | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr20:32703414 | G | A | 1 | a0002 | 1 | HG00558.hp2 | stop_gained | HIGH | c.571C>T | p.Arg191* | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 9/9 | 647/1362 | 571/603 | 191/200 | chr20 | 32703414 |
view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|
view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr20:32702754 | C | G | 1 | a0001c0001t0006 | 1 | HG03516.hp2 | 3_prime_UTR_variant | MODIFIER | c.*628G>C | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 9/9 | 628 | chr20 | 32702754 | ||||||
chr20:32703003 | G | T | 1 | a0001c0001t0008 | 1 | HG04228.hp2 | 3_prime_UTR_variant | MODIFIER | c.*379C>A | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 9/9 | 379 | chr20 | 32703003 | ||||||
chr20:32703060 | C | G | 1 | a0001c0001t0005 | 1 | NA18522.hp1 | 3_prime_UTR_variant | MODIFIER | c.*322G>C | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 9/9 | 322 | chr20 | 32703060 | ||||||
chr20:32703114 | G | A | 1 | a0001c0001t0004 | 4 | HG02630.hp1 HG02886.hp1 HG02970.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*268C>T | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 9/9 | 268 | chr20 | 32703114 | ||||||
chr20:32703135 | TA | T | 2 | a0001c0001t0003 a0001c0001t0004 |
9 | HG02280.hp1 HG02630.hp1 HG02886.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*246delT | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 9/9 | 246 | chr20 | 32703135 | ||||||
chr20:32703178 | A | G | 1 | a0001c0001t0007 | 1 | NA19091.hp2 | 3_prime_UTR_variant | MODIFIER | c.*204T>C | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 9/9 | 204 | chr20 | 32703178 | ||||||
chr20:32703354 | G | A | 1 | a0001c0001t0009 | 1 | HG00741.hp1 | 3_prime_UTR_variant | MODIFIER | c.*28C>T | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 9/9 | 28 | chr20 | 32703354 | ||||||
chr20:32703359 | C | T | 4 | a0001c0001t0001 a0001c0001t0005 a0001c0001t0006 others(1): Show |
219 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(216): Show |
3_prime_UTR_variant | MODIFIER | c.*23G>A | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 9/9 | 23 | chr20 | 32703359 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr20:32703625 | A | T | 1 | a0001c0001t0002g0083 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.527-167T>A | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 8/8 | chr20 | 32703625 | |||||||
chr20:32703681 | C | A | 173 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(170): Show |
193 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(190): Show |
intron_variant | MODIFIER | c.527-223G>T | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 8/8 | chr20 | 32703681 | |||||||
chr20:32703738 | G | C | 1 | a0001c0001t0002g0157 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.527-280C>G | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 8/8 | chr20 | 32703738 | |||||||
chr20:32703796 | C | T | 1 | a0001c0001t0001g0352 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.526+227G>A | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 8/8 | chr20 | 32703796 | |||||||
chr20:32703823 | A | G | 72 | a0001c0001t0001g0009 a0001c0001t0001g0012 a0001c0001t0001g0025 others(69): Show |
78 | HG00280.hp2 HG00733.hp2 HG00741.hp2 others(75): Show |
intron_variant | MODIFIER | c.526+200T>C | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 8/8 | chr20 | 32703823 | |||||||
chr20:32703939 | C | T | 2 | a0001c0001t0001g0094 a0001c0001t0001g0095 |
2 | NA18953.hp1 NA19066.hp1 |
intron_variant | MODIFIER | c.526+84G>A | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 8/8 | chr20 | 32703939 | |||||||
chr20:32704020 | C | T | 9 | a0001c0001t0001g0114 a0001c0001t0003g0008 a0001c0001t0003g0286 others(6): Show |
11 | HG01109.hp2 HG02280.hp1 HG02630.hp1 others(8): Show |
splice_region_variant&intron_variant | LOW | c.526+3G>A | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 8/8 | chr20 | 32704020 | |||||||
chr20:32704117 | GGGCA | G | 69 | a0001c0001t0001g0009 a0001c0001t0001g0012 a0001c0001t0001g0014 others(66): Show |
74 | HG00280.hp2 HG00733.hp2 HG00741.hp2 others(71): Show |
intron_variant | MODIFIER | c.478-50_478-47delTG others(2): Show |
COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 7/8 | chr20 | 32704117 | |||||||
chr20:32704178 | G | A | 1 | a0001c0001t0005g0348 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.478-107C>T | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 7/8 | chr20 | 32704178 | |||||||
chr20:32704240 | C | T | 8 | a0001c0001t0002g0068 a0001c0001t0002g0163 a0001c0001t0002g0164 others(5): Show |
8 | HG01070.hp2 NA18944.hp1 NA18951.hp2 others(5): Show |
intron_variant | MODIFIER | c.478-169G>A | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 7/8 | chr20 | 32704240 | |||||||
chr20:32704241 | G | A | 1 | a0001c0001t0001g0322 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.478-170C>T | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 7/8 | chr20 | 32704241 | |||||||
chr20:32704286 | G | A | 2 | a0001c0001t0002g0022 a0001c0001t0002g0238 |
3 | HG02129.hp1 NA18964.hp1 NA18993.hp2 |
intron_variant | MODIFIER | c.477+154C>T | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 7/8 | chr20 | 32704286 | |||||||
chr20:32704342 | G | T | 1 | a0001c0001t0005g0348 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.477+98C>A | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 7/8 | chr20 | 32704342 | |||||||
chr20:32704382 | T | TATG | 207 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(204): Show |
231 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(228): Show |
intron_variant | MODIFIER | c.477+57_477+58insCA others(1): Show |
COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 7/8 | chr20 | 32704382 | |||||||
chr20:32704496 | CA | C | 169 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(166): Show |
189 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(186): Show |
splice_region_variant&intron_variant | LOW | c.428-8delT | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 6/8 | chr20 | 32704496 | |||||||
chr20:32704496 | CAA | C | 29 | a0001c0001t0001g0004 a0001c0001t0001g0046 a0001c0001t0001g0047 others(26): Show |
32 | HG02040.hp2 HG02056.hp2 HG02280.hp1 others(29): Show |
splice_region_variant&intron_variant | LOW | c.428-9_428-8delTT | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 6/8 | chr20 | 32704496 | |||||||
chr20:32704496 | CAAA | C | 8 | a0001c0001t0001g0114 a0001c0001t0003g0286 a0001c0001t0003g0288 others(5): Show |
9 | HG01109.hp2 HG02630.hp1 HG02886.hp1 others(6): Show |
splice_region_variant&intron_variant | LOW | c.428-10_428-8delTTT | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 6/8 | chr20 | 32704496 | |||||||
chr20:32704510 | A | G | 1 | a0001c0001t0003g0008 | 2 | HG02280.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.428-21T>C | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 6/8 | chr20 | 32704510 | |||||||
chr20:32704701 | G | T | 9 | a0001c0001t0001g0114 a0001c0001t0003g0008 a0001c0001t0003g0286 others(6): Show |
11 | HG01109.hp2 HG02280.hp1 HG02630.hp1 others(8): Show |
intron_variant | MODIFIER | c.427+113C>A | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 6/8 | chr20 | 32704701 | |||||||
chr20:32704992 | G | A | 6 | a0001c0001t0003g0286 a0001c0001t0003g0288 a0001c0001t0003g0358 others(3): Show |
7 | HG02630.hp1 HG02886.hp1 HG02970.hp1 others(4): Show |
intron_variant | MODIFIER | c.337-88C>T | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 5/8 | chr20 | 32704992 | |||||||
chr20:32704996 | CAGATAGT others(14): Show |
C | 1 | a0001c0001t0002g0123 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.337-113_337-93delT others(20): Show |
COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 5/8 | chr20 | 32704996 | |||||||
chr20:32705031 | G | A | 9 | a0001c0001t0001g0114 a0001c0001t0003g0008 a0001c0001t0003g0286 others(6): Show |
11 | HG01109.hp2 HG02280.hp1 HG02630.hp1 others(8): Show |
intron_variant | MODIFIER | c.337-127C>T | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 5/8 | chr20 | 32705031 | |||||||
chr20:32705075 | G | T | 1 | a0001c0001t0001g0122 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.337-171C>A | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 5/8 | chr20 | 32705075 | |||||||
chr20:32705312 | G | GTATATAT others(15): Show |
9 | a0001c0001t0001g0114 a0001c0001t0003g0008 a0001c0001t0003g0286 others(6): Show |
11 | HG01109.hp2 HG02280.hp1 HG02630.hp1 others(8): Show |
intron_variant | MODIFIER | c.337-409_337-408ins others(22): Show |
COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 5/8 | chr20 | 32705312 | |||||||
chr20:32705316 | A | G | 9 | a0001c0001t0001g0114 a0001c0001t0003g0008 a0001c0001t0003g0286 others(6): Show |
11 | HG01109.hp2 HG02280.hp1 HG02630.hp1 others(8): Show |
intron_variant | MODIFIER | c.337-412T>C | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 5/8 | chr20 | 32705316 | |||||||
chr20:32705338 | G | GTA | 13 | a0001c0001t0002g0130 a0001c0001t0002g0131 a0001c0001t0002g0173 others(10): Show |
13 | HG00408.hp2 HG00544.hp2 HG00621.hp1 others(10): Show |
intron_variant | MODIFIER | c.337-436_337-435dup others(2): Show |
COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 5/8 | chr20 | 32705338 | |||||||
chr20:32705348 | A | G | 3 | a0001c0001t0001g0002 a0001c0001t0001g0098 a0001c0001t0001g0267 |
7 | HG00408.hp1 HG00544.hp1 HG02071.hp1 others(4): Show |
intron_variant | MODIFIER | c.337-444T>C | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 5/8 | chr20 | 32705348 | |||||||
chr20:32705350 | G | A | 7 | a0001c0001t0001g0069 a0001c0001t0001g0081 a0001c0001t0001g0085 others(4): Show |
7 | NA18947.hp1 NA18983.hp1 NA18987.hp1 others(4): Show |
intron_variant | MODIFIER | c.337-446C>T | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 5/8 | chr20 | 32705350 | |||||||
chr20:32705358 | G | A | 7 | a0001c0001t0003g0008 a0001c0001t0003g0286 a0001c0001t0003g0288 others(4): Show |
9 | HG02280.hp1 HG02630.hp1 HG02886.hp1 others(6): Show |
intron_variant | MODIFIER | c.337-454C>T | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 5/8 | chr20 | 32705358 | |||||||
chr20:32705358 | G | GTATATAT others(15): Show |
1 | a0001c0001t0001g0114 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.337-455_337-454ins others(22): Show |
COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 5/8 | chr20 | 32705358 | |||||||
chr20:32705358 | GTA | G | 37 | a0001c0001t0001g0009 a0001c0001t0001g0012 a0001c0001t0001g0014 others(34): Show |
40 | HG01346.hp1 HG01358.hp2 HG01884.hp2 others(37): Show |
intron_variant | MODIFIER | c.337-456_337-455del others(2): Show |
COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 5/8 | chr20 | 32705358 | |||||||
chr20:32705360 | A | G | 28 | a0001c0001t0001g0001 a0001c0001t0001g0069 a0001c0001t0001g0081 others(25): Show |
33 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(30): Show |
intron_variant | MODIFIER | c.337-456T>C | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 5/8 | chr20 | 32705360 | |||||||
chr20:32705369 | TATATATA | T | 6 | a0001c0001t0003g0286 a0001c0001t0003g0288 a0001c0001t0003g0358 others(3): Show |
7 | HG02630.hp1 HG02886.hp1 HG02970.hp1 others(4): Show |
intron_variant | MODIFIER | c.337-472_337-466del others(7): Show |
COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 5/8 | chr20 | 32705369 | |||||||
chr20:32705371 | TA | T | 4 | a0001c0001t0001g0025 a0001c0001t0001g0115 a0001c0001t0001g0322 others(1): Show |
4 | HG01258.hp2 HG02148.hp2 HG02280.hp2 others(1): Show |
intron_variant | MODIFIER | c.337-468delT | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 5/8 | chr20 | 32705371 | |||||||
chr20:32705372 | A | T | 1 | a0001c0001t0002g0243 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.337-468T>A | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 5/8 | chr20 | 32705372 | |||||||
chr20:32705373 | TA | T | 26 | a0001c0001t0001g0025 a0001c0001t0001g0026 a0001c0001t0001g0038 others(23): Show |
27 | HG00280.hp2 HG00733.hp2 HG00741.hp2 others(24): Show |
intron_variant | MODIFIER | c.337-470delT | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 5/8 | chr20 | 32705373 | |||||||
chr20:32705374 | A | T | 10 | a0001c0001t0001g0025 a0001c0001t0001g0115 a0001c0001t0001g0320 others(7): Show |
10 | HG01109.hp1 HG01258.hp2 HG01346.hp1 others(7): Show |
intron_variant | MODIFIER | c.337-470T>A | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 5/8 | chr20 | 32705374 | |||||||
chr20:32705374 | ATAT | A | 5 | a0001c0001t0001g0005 a0001c0001t0001g0013 a0001c0001t0001g0015 others(2): Show |
9 | HG02451.hp1 HG02809.hp1 HG03041.hp1 others(6): Show |
intron_variant | MODIFIER | c.337-473_337-471del others(3): Show |
COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 5/8 | chr20 | 32705374 | |||||||
chr20:32705375 | TA | T | 6 | a0001c0001t0001g0095 a0001c0001t0001g0293 a0001c0001t0001g0297 others(3): Show |
6 | HG01496.hp2 HG01934.hp2 HG02683.hp2 others(3): Show |
intron_variant | MODIFIER | c.337-472delT | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 5/8 | chr20 | 32705375 | |||||||
chr20:32705376 | A | AT | 6 | a0001c0001t0002g0039 a0001c0001t0002g0183 a0001c0001t0002g0231 others(3): Show |
6 | HG02055.hp2 HG02109.hp1 HG02273.hp1 others(3): Show |
intron_variant | MODIFIER | c.337-473dupA | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 5/8 | chr20 | 32705376 | |||||||
chr20:32705376 | A | ATATATAT others(11): Show |
1 | a0001c0001t0006g0125 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.337-473_337-472ins others(18): Show |
COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 5/8 | chr20 | 32705376 | |||||||
chr20:32705376 | A | ATATATAT others(7): Show |
1 | a0001c0001t0003g0008 | 2 | HG02280.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.337-473_337-472ins others(14): Show |
COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 5/8 | chr20 | 32705376 | |||||||
chr20:32705376 | A | T | 83 | a0001c0001t0001g0009 a0001c0001t0001g0012 a0001c0001t0001g0025 others(80): Show |
91 | HG00140.hp1 HG00280.hp2 HG00733.hp2 others(88): Show |
intron_variant | MODIFIER | c.337-472T>A | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 5/8 | chr20 | 32705376 | |||||||
chr20:32705376 | AT | A | 107 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(104): Show |
120 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(117): Show |
intron_variant | MODIFIER | c.337-473delA | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 5/8 | chr20 | 32705376 | |||||||
chr20:32705377 | T | TA | 9 | a0001c0001t0001g0069 a0001c0001t0001g0081 a0001c0001t0001g0085 others(6): Show |
9 | HG02572.hp2 NA18947.hp1 NA18967.hp2 others(6): Show |
intron_variant | MODIFIER | c.337-474_337-473ins others(1): Show |
COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 5/8 | chr20 | 32705377 | |||||||
chr20:32705378 | T | A | 5 | a0001c0001t0002g0018 a0001c0001t0002g0196 a0001c0001t0002g0201 others(2): Show |
6 | HG01256.hp1 HG01258.hp1 HG01346.hp2 others(3): Show |
intron_variant | MODIFIER | c.337-474A>T | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 5/8 | chr20 | 32705378 | |||||||
chr20:32705379 | T | A | 4 | a0001c0001t0001g0260 a0001c0001t0001g0262 a0001c0001t0001g0270 others(1): Show |
4 | HG02056.hp2 HG02145.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.337-475A>T | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 5/8 | chr20 | 32705379 | |||||||
chr20:32705448 | G | A | 1 | a0001c0001t0002g0200 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.337-544C>T | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 5/8 | chr20 | 32705448 | |||||||
chr20:32705518 | C | T | 1 | a0001c0001t0001g0152 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.337-614G>A | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 5/8 | chr20 | 32705518 | |||||||
chr20:32705531 | G | A | 9 | a0001c0001t0001g0114 a0001c0001t0003g0008 a0001c0001t0003g0286 others(6): Show |
11 | HG01109.hp2 HG02280.hp1 HG02630.hp1 others(8): Show |
intron_variant | MODIFIER | c.337-627C>T | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 5/8 | chr20 | 32705531 | |||||||
chr20:32705563 | T | C | 1 | a0001c0001t0001g0145 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.337-659A>G | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 5/8 | chr20 | 32705563 | |||||||
chr20:32705591 | T | C | 26 | a0001c0001t0001g0004 a0001c0001t0001g0046 a0001c0001t0001g0047 others(23): Show |
28 | HG02040.hp2 HG02056.hp2 NA18942.hp2 others(25): Show |
intron_variant | MODIFIER | c.337-687A>G | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 5/8 | chr20 | 32705591 | |||||||
chr20:32705594 | C | T | 60 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0040 others(57): Show |
65 | HG00323.hp2 HG00408.hp1 HG00423.hp2 others(62): Show |
intron_variant | MODIFIER | c.337-690G>A | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 5/8 | chr20 | 32705594 | |||||||
chr20:32705703 | T | C | 9 | a0001c0001t0001g0114 a0001c0001t0003g0008 a0001c0001t0003g0286 others(6): Show |
11 | HG01109.hp2 HG02280.hp1 HG02630.hp1 others(8): Show |
intron_variant | MODIFIER | c.337-799A>G | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 5/8 | chr20 | 32705703 | |||||||
chr20:32705714 | A | G | 9 | a0001c0001t0001g0114 a0001c0001t0003g0008 a0001c0001t0003g0286 others(6): Show |
11 | HG01109.hp2 HG02280.hp1 HG02630.hp1 others(8): Show |
intron_variant | MODIFIER | c.337-810T>C | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 5/8 | chr20 | 32705714 | |||||||
chr20:32705833 | C | T | 2 | a0001c0001t0001g0289 a0001c0001t0001g0290 |
2 | HG02451.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.336+750G>A | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 5/8 | chr20 | 32705833 | |||||||
chr20:32706027 | C | T | 9 | a0001c0001t0001g0114 a0001c0001t0003g0008 a0001c0001t0003g0286 others(6): Show |
11 | HG01109.hp2 HG02280.hp1 HG02630.hp1 others(8): Show |
intron_variant | MODIFIER | c.336+556G>A | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 5/8 | chr20 | 32706027 | |||||||
chr20:32706135 | T | C | 4 | a0001c0001t0001g0032 a0001c0001t0001g0271 a0001c0001t0001g0272 others(1): Show |
4 | HG01891.hp2 HG02145.hp2 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.336+448A>G | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 5/8 | chr20 | 32706135 | |||||||
chr20:32706138 | C | T | 2 | a0001c0001t0001g0134 a0001c0001t0001g0135 |
2 | HG02486.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.336+445G>A | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 5/8 | chr20 | 32706138 | |||||||
chr20:32706161 | G | A | 9 | a0001c0001t0001g0114 a0001c0001t0003g0008 a0001c0001t0003g0286 others(6): Show |
11 | HG01109.hp2 HG02280.hp1 HG02630.hp1 others(8): Show |
intron_variant | MODIFIER | c.336+422C>T | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 5/8 | chr20 | 32706161 | |||||||
chr20:32706198 | CA | C | 18 | a0001c0001t0001g0004 a0001c0001t0001g0046 a0001c0001t0001g0047 others(15): Show |
20 | HG02080.hp2 HG02273.hp2 HG03491.hp1 others(17): Show |
intron_variant | MODIFIER | c.336+384delT | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 5/8 | chr20 | 32706198 | |||||||
chr20:32706253 | C | T | 1 | a0001c0001t0001g0086 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.336+330G>A | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 5/8 | chr20 | 32706253 | |||||||
chr20:32706294 | A | G | 4 | a0001c0001t0001g0032 a0001c0001t0001g0271 a0001c0001t0001g0272 others(1): Show |
4 | HG01891.hp2 HG02145.hp2 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.336+289T>C | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 5/8 | chr20 | 32706294 | |||||||
chr20:32706414 | G | A | 1 | a0001c0001t0005g0348 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.336+169C>T | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 5/8 | chr20 | 32706414 | |||||||
chr20:32706512 | C | CA | 12 | a0001c0001t0001g0014 a0001c0001t0001g0114 a0001c0001t0002g0151 others(9): Show |
15 | HG01109.hp2 HG02280.hp1 HG02630.hp1 others(12): Show |
intron_variant | MODIFIER | c.336+70dupT | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 5/8 | chr20 | 32706512 | |||||||
chr20:32706688 | C | T | 13 | a0001c0001t0001g0114 a0001c0001t0001g0121 a0001c0001t0001g0134 others(10): Show |
15 | HG01109.hp2 HG02280.hp1 HG02486.hp2 others(12): Show |
intron_variant | MODIFIER | c.298+16G>A | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 4/8 | chr20 | 32706688 | |||||||
chr20:32706853 | A | G | 195 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(192): Show |
217 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(214): Show |
intron_variant | MODIFIER | c.242-93T>C | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32706853 | |||||||
chr20:32706888 | A | C | 13 | a0001c0001t0001g0114 a0001c0001t0001g0121 a0001c0001t0001g0134 others(10): Show |
15 | HG01109.hp2 HG02280.hp1 HG02486.hp2 others(12): Show |
intron_variant | MODIFIER | c.242-128T>G | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32706888 | |||||||
chr20:32706978 | A | G | 103 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0011 others(100): Show |
110 | HG00323.hp2 HG00408.hp1 HG00423.hp2 others(107): Show |
intron_variant | MODIFIER | c.242-218T>C | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32706978 | |||||||
chr20:32707045 | A | G | 2 | a0001c0001t0002g0201 a0001c0001t0002g0222 |
2 | HG01346.hp2 HG03239.hp2 |
intron_variant | MODIFIER | c.242-285T>C | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32707045 | |||||||
chr20:32707069 | C | T | 5 | a0001c0001t0001g0005 a0001c0001t0001g0013 a0001c0001t0001g0015 others(2): Show |
9 | HG02451.hp1 HG02809.hp1 HG03041.hp1 others(6): Show |
intron_variant | MODIFIER | c.242-309G>A | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32707069 | |||||||
chr20:32707070 | G | A | 61 | a0001c0001t0001g0009 a0001c0001t0001g0012 a0001c0001t0001g0025 others(58): Show |
65 | HG00280.hp2 HG00733.hp2 HG00741.hp2 others(62): Show |
intron_variant | MODIFIER | c.242-310C>T | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32707070 | |||||||
chr20:32707117 | C | CA | 8 | a0001c0001t0001g0114 a0001c0001t0002g0178 a0001c0001t0002g0182 others(5): Show |
8 | HG00438.hp2 HG01109.hp2 HG01928.hp1 others(5): Show |
intron_variant | MODIFIER | c.242-358dupT | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32707117 | |||||||
chr20:32707117 | CA | C | 140 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(137): Show |
157 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(154): Show |
intron_variant | MODIFIER | c.242-358delT | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32707117 | |||||||
chr20:32707117 | CAA | C | 61 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0040 others(58): Show |
66 | HG00323.hp2 HG00408.hp1 HG00423.hp2 others(63): Show |
intron_variant | MODIFIER | c.242-359_242-358del others(2): Show |
COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32707117 | |||||||
chr20:32707210 | G | A | 17 | a0001c0001t0001g0001 a0001c0001t0001g0128 a0001c0001t0001g0142 others(14): Show |
23 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(20): Show |
intron_variant | MODIFIER | c.242-450C>T | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32707210 | |||||||
chr20:32707263 | A | G | 9 | a0001c0001t0001g0114 a0001c0001t0003g0008 a0001c0001t0003g0286 others(6): Show |
11 | HG01109.hp2 HG02280.hp1 HG02630.hp1 others(8): Show |
intron_variant | MODIFIER | c.242-503T>C | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32707263 | |||||||
chr20:32707288 | A | AATAT | 16 | a0001c0001t0001g0001 a0001c0001t0001g0128 a0001c0001t0001g0142 others(13): Show |
22 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(19): Show |
intron_variant | MODIFIER | c.242-529_242-528ins others(4): Show |
COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32707288 | |||||||
chr20:32707290 | A | T | 17 | a0001c0001t0001g0001 a0001c0001t0001g0128 a0001c0001t0001g0142 others(14): Show |
23 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(20): Show |
intron_variant | MODIFIER | c.242-530T>A | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32707290 | |||||||
chr20:32707292 | A | AAT | 49 | a0001c0001t0001g0009 a0001c0001t0001g0025 a0001c0001t0001g0026 others(46): Show |
52 | HG00280.hp2 HG00733.hp2 HG00741.hp2 others(49): Show |
intron_variant | MODIFIER | c.242-533_242-532ins others(2): Show |
COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32707292 | |||||||
chr20:32707292 | A | T | 17 | a0001c0001t0001g0001 a0001c0001t0001g0128 a0001c0001t0001g0142 others(14): Show |
23 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(20): Show |
intron_variant | MODIFIER | c.242-532T>A | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32707292 | |||||||
chr20:32707294 | A | T | 160 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(157): Show |
181 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(178): Show |
intron_variant | MODIFIER | c.242-534T>A | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32707294 | |||||||
chr20:32707296 | T | A | 5 | a0001c0001t0001g0050 a0001c0001t0001g0055 a0001c0001t0003g0286 others(2): Show |
5 | NA18522.hp2 NA18961.hp2 NA18980.hp1 others(2): Show |
intron_variant | MODIFIER | c.242-536A>T | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32707296 | |||||||
chr20:32707322 | T | A | 8 | a0001c0001t0001g0014 a0001c0001t0001g0124 a0001c0001t0001g0136 others(5): Show |
9 | HG01891.hp1 HG02572.hp1 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.242-562A>T | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32707322 | |||||||
chr20:32707324 | T | C | 2 | a0001c0001t0001g0111 a0001c0001t0001g0113 |
2 | HG03017.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.242-564A>G | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32707324 | |||||||
chr20:32707380 | C | T | 1 | a0001c0001t0002g0214 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.242-620G>A | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32707380 | |||||||
chr20:32707502 | TAG | T | 5 | a0001c0001t0001g0005 a0001c0001t0001g0013 a0001c0001t0001g0015 others(2): Show |
9 | HG02451.hp1 HG02809.hp1 HG03041.hp1 others(6): Show |
intron_variant | MODIFIER | c.242-744_242-743del others(2): Show |
COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32707502 | |||||||
chr20:32707531 | G | C | 2 | a0001c0001t0001g0114 a0001c0001t0006g0125 |
2 | HG01109.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.242-771C>G | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32707531 | |||||||
chr20:32707564 | C | T | 1 | a0001c0001t0001g0291 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.242-804G>A | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32707564 | |||||||
chr20:32707639 | T | C | 1 | a0001c0001t0005g0348 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.242-879A>G | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32707639 | |||||||
chr20:32707824 | A | G | 1 | a0001c0001t0001g0320 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.242-1064T>C | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32707824 | |||||||
chr20:32707832 | A | G | 1 | a0001c0001t0002g0221 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.242-1072T>C | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32707832 | |||||||
chr20:32708042 | A | G | 208 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(205): Show |
232 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(229): Show |
intron_variant | MODIFIER | c.242-1282T>C | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32708042 | |||||||
chr20:32708498 | C | T | 4 | a0001c0001t0001g0127 a0001c0001t0001g0300 a0001c0001t0001g0301 others(1): Show |
4 | NA18942.hp2 NA18949.hp1 NA19056.hp1 others(1): Show |
intron_variant | MODIFIER | c.242-1738G>A | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32708498 | |||||||
chr20:32708577 | T | C | 1 | a0001c0001t0001g0308 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.242-1817A>G | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32708577 | |||||||
chr20:32708656 | C | CTT | 15 | a0001c0001t0001g0071 a0001c0001t0001g0087 a0001c0001t0001g0114 others(12): Show |
17 | HG00323.hp2 HG01070.hp1 HG01109.hp2 others(14): Show |
intron_variant | MODIFIER | c.242-1898_242-1897d others(4): Show |
COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32708656 | |||||||
chr20:32708656 | C | CTTT | 174 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(171): Show |
196 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(193): Show |
intron_variant | MODIFIER | c.242-1899_242-1897d others(5): Show |
COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32708656 | |||||||
chr20:32708656 | C | CTTTT | 12 | a0001c0001t0001g0041 a0001c0001t0001g0094 a0001c0001t0001g0124 others(9): Show |
12 | HG02056.hp1 HG02148.hp2 HG02572.hp1 others(9): Show |
intron_variant | MODIFIER | c.242-1900_242-1897d others(6): Show |
COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32708656 | |||||||
chr20:32708735 | C | T | 1 | a0001c0001t0002g0212 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.242-1975G>A | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32708735 | |||||||
chr20:32709164 | G | A | 1 | a0001c0001t0002g0116 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.242-2404C>T | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32709164 | |||||||
chr20:32709196 | G | A | 23 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0013 others(20): Show |
33 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(30): Show |
intron_variant | MODIFIER | c.242-2436C>T | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32709196 | |||||||
chr20:32709285 | A | C | 5 | a0001c0001t0001g0005 a0001c0001t0001g0013 a0001c0001t0001g0015 others(2): Show |
9 | HG02451.hp1 HG02809.hp1 HG03041.hp1 others(6): Show |
intron_variant | MODIFIER | c.242-2525T>G | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32709285 | |||||||
chr20:32709291 | C | T | 1 | a0001c0001t0001g0014 | 2 | HG02723.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.242-2531G>A | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32709291 | |||||||
chr20:32709307 | C | T | 13 | a0001c0001t0002g0109 a0001c0001t0002g0179 a0001c0001t0002g0180 others(10): Show |
13 | HG00323.hp1 HG01106.hp2 HG01433.hp2 others(10): Show |
intron_variant | MODIFIER | c.242-2547G>A | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32709307 | |||||||
chr20:32709399 | C | CA | 20 | a0001c0001t0002g0006 a0001c0001t0002g0019 a0001c0001t0002g0036 others(17): Show |
23 | HG00673.hp1 HG01175.hp1 HG01358.hp1 others(20): Show |
intron_variant | MODIFIER | c.242-2640dupT | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32709399 | |||||||
chr20:32709399 | CA | C | 17 | a0001c0001t0001g0076 a0001c0001t0001g0102 a0001c0001t0001g0106 others(14): Show |
18 | HG00438.hp1 HG01109.hp2 HG01255.hp2 others(15): Show |
intron_variant | MODIFIER | c.242-2640delT | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32709399 | |||||||
chr20:32709399 | CAA | C | 189 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(186): Show |
211 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(208): Show |
intron_variant | MODIFIER | c.242-2641_242-2640d others(4): Show |
COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32709399 | |||||||
chr20:32709455 | G | C | 2 | a0001c0001t0001g0114 a0001c0001t0006g0125 |
2 | HG01109.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.242-2695C>G | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32709455 | |||||||
chr20:32709478 | C | G | 208 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(205): Show |
232 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(229): Show |
intron_variant | MODIFIER | c.242-2718G>C | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32709478 | |||||||
chr20:32709634 | C | T | 69 | a0001c0001t0001g0009 a0001c0001t0001g0012 a0001c0001t0001g0014 others(66): Show |
74 | HG00280.hp2 HG00733.hp2 HG00741.hp2 others(71): Show |
intron_variant | MODIFIER | c.242-2874G>A | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32709634 | |||||||
chr20:32709766 | G | A | 207 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(204): Show |
231 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(228): Show |
intron_variant | MODIFIER | c.242-3006C>T | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32709766 | |||||||
chr20:32709807 | C | T | 1 | a0001c0001t0001g0113 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.242-3047G>A | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32709807 | |||||||
chr20:32709947 | C | T | 1 | a0001c0001t0002g0172 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.242-3187G>A | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32709947 | |||||||
chr20:32709986 | C | T | 98 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0011 others(95): Show |
105 | HG00323.hp2 HG00408.hp1 HG00423.hp2 others(102): Show |
intron_variant | MODIFIER | c.242-3226G>A | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32709986 | |||||||
chr20:32710057 | T | C | 1 | a0001c0001t0001g0136 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.242-3297A>G | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32710057 | |||||||
chr20:32710070 | A | G | 7 | a0001c0001t0003g0008 a0001c0001t0003g0286 a0001c0001t0003g0288 others(4): Show |
9 | HG02280.hp1 HG02630.hp1 HG02886.hp1 others(6): Show |
intron_variant | MODIFIER | c.242-3310T>C | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32710070 | |||||||
chr20:32710102 | G | A | 1 | a0001c0001t0002g0185 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.242-3342C>T | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32710102 | |||||||
chr20:32710213 | G | A | 2 | a0001c0001t0001g0073 a0001c0001t0001g0080 |
2 | NA18960.hp1 NA18975.hp1 |
intron_variant | MODIFIER | c.242-3453C>T | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32710213 | |||||||
chr20:32710474 | G | A | 1 | a0001c0001t0002g0209 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.242-3714C>T | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32710474 | |||||||
chr20:32710515 | G | C | 194 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(191): Show |
216 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(213): Show |
intron_variant | MODIFIER | c.242-3755C>G | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32710515 | |||||||
chr20:32710632 | G | T | 207 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(204): Show |
231 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(228): Show |
intron_variant | MODIFIER | c.242-3872C>A | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32710632 | |||||||
chr20:32710695 | C | T | 2 | a0001c0001t0001g0303 a0001c0001t0001g0305 |
2 | NA18970.hp1 NA19058.hp2 |
intron_variant | MODIFIER | c.242-3935G>A | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32710695 | |||||||
chr20:32710728 | CA | C | 6 | a0001c0001t0001g0134 a0001c0001t0002g0160 a0001c0001t0002g0184 others(3): Show |
6 | HG00558.hp1 HG01167.hp1 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.242-3969delT | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32710728 | |||||||
chr20:32710728 | CAA | C | 132 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(129): Show |
151 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(148): Show |
intron_variant | MODIFIER | c.242-3970_242-3969d others(4): Show |
COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32710728 | |||||||
chr20:32710733 | A | AC | 69 | a0001c0001t0001g0009 a0001c0001t0001g0012 a0001c0001t0001g0014 others(66): Show |
74 | HG00280.hp2 HG00733.hp2 HG00741.hp2 others(71): Show |
intron_variant | MODIFIER | c.242-3974_242-3973i others(3): Show |
COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32710733 | |||||||
chr20:32711057 | G | A | 134 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(131): Show |
153 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(150): Show |
intron_variant | MODIFIER | c.242-4297C>T | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32711057 | |||||||
chr20:32711132 | C | T | 4 | a0001c0001t0001g0121 a0001c0001t0001g0134 a0001c0001t0001g0135 others(1): Show |
4 | HG02486.hp2 HG02965.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.242-4372G>A | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32711132 | |||||||
chr20:32711139 | A | G | 207 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(204): Show |
231 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(228): Show |
intron_variant | MODIFIER | c.242-4379T>C | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32711139 | |||||||
chr20:32711167 | C | T | 3 | a0001c0001t0001g0260 a0001c0001t0001g0262 a0001c0001t0001g0270 |
3 | HG02145.hp1 HG03139.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.242-4407G>A | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32711167 | |||||||
chr20:32711184 | G | A | 1 | a0001c0001t0002g0117 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.242-4424C>T | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32711184 | |||||||
chr20:32711258 | G | A | 1 | a0001c0001t0005g0348 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.242-4498C>T | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32711258 | |||||||
chr20:32711259 | T | C | 1 | a0001c0001t0002g0251 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.242-4499A>G | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32711259 | |||||||
chr20:32711376 | G | A | 2 | a0001c0001t0001g0267 a0001c0001t0002g0277 |
2 | HG00408.hp1 HG01934.hp1 |
intron_variant | MODIFIER | c.242-4616C>T | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32711376 | |||||||
chr20:32711378 | C | T | 1 | a0001c0001t0001g0304 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.242-4618G>A | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32711378 | |||||||
chr20:32711380 | G | C | 5 | a0001c0001t0001g0032 a0001c0001t0001g0271 a0001c0001t0001g0272 others(2): Show |
5 | HG01884.hp2 HG01891.hp2 HG02145.hp2 others(2): Show |
intron_variant | MODIFIER | c.242-4620C>G | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32711380 | |||||||
chr20:32711407 | A | AT | 206 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(203): Show |
230 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(227): Show |
intron_variant | MODIFIER | c.242-4648dupA | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32711407 | |||||||
chr20:32711415 | T | TA | 7 | a0001c0001t0001g0056 a0001c0001t0001g0065 a0001c0001t0001g0141 others(4): Show |
7 | HG00438.hp1 HG02602.hp1 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.242-4656dupT | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32711415 | |||||||
chr20:32711716 | T | A | 1 | a0001c0001t0005g0348 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.242-4956A>T | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32711716 | |||||||
chr20:32711795 | T | C | 207 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(204): Show |
231 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(228): Show |
intron_variant | MODIFIER | c.242-5035A>G | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32711795 | |||||||
chr20:32711921 | G | A | 207 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(204): Show |
231 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(228): Show |
intron_variant | MODIFIER | c.242-5161C>T | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32711921 | |||||||
chr20:32711950 | C | T | 207 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(204): Show |
231 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(228): Show |
intron_variant | MODIFIER | c.242-5190G>A | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32711950 | |||||||
chr20:32711951 | G | A | 1 | a0001c0001t0002g0277 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.242-5191C>T | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32711951 | |||||||
chr20:32711962 | A | T | 97 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0011 others(94): Show |
104 | HG00323.hp2 HG00408.hp1 HG00423.hp2 others(101): Show |
intron_variant | MODIFIER | c.242-5202T>A | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32711962 | |||||||
chr20:32712014 | GT | G | 207 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(204): Show |
231 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(228): Show |
intron_variant | MODIFIER | c.242-5255delA | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32712014 | |||||||
chr20:32712037 | C | T | 17 | a0001c0001t0001g0001 a0001c0001t0001g0128 a0001c0001t0001g0142 others(14): Show |
23 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(20): Show |
intron_variant | MODIFIER | c.242-5277G>A | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32712037 | |||||||
chr20:32712120 | A | C | 2 | a0001c0001t0001g0114 a0001c0001t0006g0125 |
2 | HG01109.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.242-5360T>G | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32712120 | |||||||
chr20:32712218 | C | T | 1 | a0001c0001t0002g0226 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.242-5458G>A | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32712218 | |||||||
chr20:32712251 | C | A | 61 | a0001c0001t0001g0009 a0001c0001t0001g0012 a0001c0001t0001g0025 others(58): Show |
65 | HG00280.hp2 HG00733.hp2 HG00741.hp2 others(62): Show |
intron_variant | MODIFIER | c.242-5491G>T | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32712251 | |||||||
chr20:32712267 | C | T | 207 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(204): Show |
231 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(228): Show |
intron_variant | MODIFIER | c.242-5507G>A | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32712267 | |||||||
chr20:32712269 | C | CA | 116 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(113): Show |
129 | HG00323.hp2 HG00408.hp1 HG00423.hp2 others(126): Show |
intron_variant | MODIFIER | c.242-5510dupT | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32712269 | |||||||
chr20:32712269 | C | CAA | 29 | a0001c0001t0001g0001 a0001c0001t0001g0088 a0001c0001t0001g0089 others(26): Show |
35 | HG00099.hp2 HG00280.hp1 HG00639.hp2 others(32): Show |
intron_variant | MODIFIER | c.242-5511_242-5510d others(4): Show |
COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32712269 | |||||||
chr20:32712269 | C | CAAA | 6 | a0001c0001t0001g0032 a0001c0001t0001g0135 a0001c0001t0001g0271 others(3): Show |
6 | HG00140.hp2 HG01891.hp2 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.242-5512_242-5510d others(5): Show |
COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32712269 | |||||||
chr20:32712269 | CA | C | 6 | a0001c0001t0002g0020 a0001c0001t0002g0154 a0001c0001t0002g0166 others(3): Show |
7 | HG00741.hp1 HG02300.hp2 NA18942.hp1 others(4): Show |
intron_variant | MODIFIER | c.242-5510delT | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32712269 | |||||||
chr20:32712269 | CAAAAAAA | C | 70 | a0001c0001t0001g0009 a0001c0001t0001g0012 a0001c0001t0001g0014 others(67): Show |
75 | HG00280.hp2 HG00733.hp2 HG00741.hp2 others(72): Show |
intron_variant | MODIFIER | c.242-5516_242-5510d others(9): Show |
COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32712269 | |||||||
chr20:32712293 | A | AAAAAAAA others(8): Show |
1 | a0001c0001t0001g0114 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.242-5534_242-5533i others(17): Show |
COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32712293 | |||||||
chr20:32712340 | C | A | 1 | a0001c0001t0002g0123 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.242-5580G>T | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32712340 | |||||||
chr20:32712437 | G | A | 1 | a0001c0001t0001g0122 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.242-5677C>T | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32712437 | |||||||
chr20:32712465 | G | A | 3 | a0001c0001t0002g0163 a0001c0001t0002g0165 a0001c0001t0002g0168 |
3 | NA18995.hp1 NA19000.hp2 NA19002.hp1 |
intron_variant | MODIFIER | c.242-5705C>T | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32712465 | |||||||
chr20:32712507 | A | C | 3 | a0001c0001t0001g0121 a0001c0001t0001g0134 a0001c0001t0001g0135 |
3 | HG02486.hp2 HG02965.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.242-5747T>G | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32712507 | |||||||
chr20:32712612 | T | TA | 76 | a0001c0001t0001g0009 a0001c0001t0001g0012 a0001c0001t0001g0014 others(73): Show |
84 | HG00280.hp2 HG00423.hp1 HG00673.hp1 others(81): Show |
intron_variant | MODIFIER | c.242-5853dupT | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32712612 | |||||||
chr20:32712612 | T | TAA | 10 | a0001c0001t0001g0047 a0001c0001t0001g0071 a0001c0001t0001g0084 others(7): Show |
10 | HG01109.hp2 HG01891.hp2 HG02165.hp1 others(7): Show |
intron_variant | MODIFIER | c.242-5854_242-5853d others(4): Show |
COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32712612 | |||||||
chr20:32712612 | T | TAAA | 128 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(125): Show |
147 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(144): Show |
intron_variant | MODIFIER | c.242-5855_242-5853d others(5): Show |
COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32712612 | |||||||
chr20:32712677 | G | A | 69 | a0001c0001t0001g0009 a0001c0001t0001g0012 a0001c0001t0001g0014 others(66): Show |
74 | HG00280.hp2 HG00733.hp2 HG00741.hp2 others(71): Show |
intron_variant | MODIFIER | c.242-5917C>T | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32712677 | |||||||
chr20:32712727 | C | CT | 203 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(200): Show |
227 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(224): Show |
intron_variant | MODIFIER | c.242-5968dupA | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32712727 | |||||||
chr20:32712727 | C | T | 2 | a0001c0001t0001g0114 a0001c0001t0006g0125 |
2 | HG01109.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.242-5967G>A | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32712727 | |||||||
chr20:32712745 | G | A | 1 | a0001c0001t0002g0207 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.242-5985C>T | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32712745 | |||||||
chr20:32712750 | CT | C | 14 | a0001c0001t0001g0026 a0001c0001t0001g0038 a0001c0001t0001g0132 others(11): Show |
15 | HG00280.hp2 HG00733.hp2 HG01123.hp1 others(12): Show |
intron_variant | MODIFIER | c.242-5991delA | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32712750 | |||||||
chr20:32712750 | CTT | C | 52 | a0001c0001t0001g0009 a0001c0001t0001g0012 a0001c0001t0001g0014 others(49): Show |
55 | HG00140.hp2 HG00741.hp2 HG01074.hp1 others(52): Show |
intron_variant | MODIFIER | c.242-5992_242-5991d others(4): Show |
COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32712750 | |||||||
chr20:32712750 | CTTT | C | 138 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(135): Show |
158 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(155): Show |
intron_variant | MODIFIER | c.242-5993_242-5991d others(5): Show |
COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32712750 | |||||||
chr20:32712770 | G | A | 207 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(204): Show |
231 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(228): Show |
intron_variant | MODIFIER | c.242-6010C>T | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32712770 | |||||||
chr20:32712875 | C | T | 207 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(204): Show |
231 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(228): Show |
intron_variant | MODIFIER | c.242-6115G>A | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32712875 | |||||||
chr20:32713049 | CT | C | 6 | a0001c0001t0001g0071 a0001c0001t0001g0114 a0001c0001t0001g0115 others(3): Show |
6 | HG01109.hp2 HG01167.hp1 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.242-6290delA | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32713049 | |||||||
chr20:32713125 | T | C | 8 | a0001c0001t0002g0027 a0001c0001t0002g0131 a0001c0001t0002g0195 others(5): Show |
8 | HG00621.hp2 HG02040.hp1 HG02165.hp2 others(5): Show |
intron_variant | MODIFIER | c.242-6365A>G | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32713125 | |||||||
chr20:32713297 | G | A | 96 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0011 others(93): Show |
103 | HG00323.hp2 HG00408.hp1 HG00423.hp2 others(100): Show |
intron_variant | MODIFIER | c.242-6537C>T | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32713297 | |||||||
chr20:32713335 | C | T | 2 | a0001c0001t0001g0114 a0001c0001t0006g0125 |
2 | HG01109.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.242-6575G>A | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32713335 | |||||||
chr20:32713342 | G | A | 1 | a0001c0001t0001g0240 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.242-6582C>T | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32713342 | |||||||
chr20:32713444 | G | A | 1 | a0001c0001t0002g0183 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.242-6684C>T | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32713444 | |||||||
chr20:32713446 | C | T | 207 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(204): Show |
231 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(228): Show |
intron_variant | MODIFIER | c.242-6686G>A | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32713446 | |||||||
chr20:32713600 | T | C | 207 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(204): Show |
231 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(228): Show |
intron_variant | MODIFIER | c.242-6840A>G | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32713600 | |||||||
chr20:32713653 | G | A | 1 | a0001c0001t0003g0008 | 2 | HG02280.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.242-6893C>T | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32713653 | |||||||
chr20:32713693 | T | C | 207 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(204): Show |
231 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(228): Show |
intron_variant | MODIFIER | c.242-6933A>G | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32713693 | |||||||
chr20:32713865 | T | C | 207 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(204): Show |
231 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(228): Show |
intron_variant | MODIFIER | c.242-7105A>G | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32713865 | |||||||
chr20:32713973 | C | T | 1 | a0001c0001t0001g0336 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.242-7213G>A | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32713973 | |||||||
chr20:32713993 | A | G | 2 | a0001c0001t0001g0114 a0001c0001t0006g0125 |
2 | HG01109.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.242-7233T>C | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32713993 | |||||||
chr20:32714017 | G | A | 69 | a0001c0001t0001g0009 a0001c0001t0001g0012 a0001c0001t0001g0014 others(66): Show |
74 | HG00280.hp2 HG00733.hp2 HG00741.hp2 others(71): Show |
intron_variant | MODIFIER | c.242-7257C>T | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32714017 | |||||||
chr20:32714040 | G | A | 1 | a0001c0001t0001g0342 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.242-7280C>T | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32714040 | |||||||
chr20:32714062 | G | A | 1 | a0001c0001t0001g0352 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.242-7302C>T | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32714062 | |||||||
chr20:32714136 | C | A | 205 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(202): Show |
229 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(226): Show |
intron_variant | MODIFIER | c.242-7376G>T | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32714136 | |||||||
chr20:32714152 | A | C | 207 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(204): Show |
231 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(228): Show |
intron_variant | MODIFIER | c.242-7392T>G | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32714152 | |||||||
chr20:32714195 | G | A | 1 | a0001c0001t0001g0107 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.242-7435C>T | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32714195 | |||||||
chr20:32714376 | G | A | 135 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(132): Show |
154 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(151): Show |
intron_variant | MODIFIER | c.242-7616C>T | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32714376 | |||||||
chr20:32714516 | C | T | 1 | a0001c0001t0002g0211 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.242-7756G>A | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32714516 | |||||||
chr20:32714645 | G | A | 1 | a0001c0001t0002g0161 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.242-7885C>T | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32714645 | |||||||
chr20:32714646 | A | C | 1 | a0001c0001t0002g0161 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.242-7886T>G | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32714646 | |||||||
chr20:32714786 | T | C | 5 | a0001c0001t0001g0077 a0001c0001t0001g0105 a0001c0001t0001g0106 others(2): Show |
5 | HG03654.hp1 HG03688.hp2 HG03704.hp2 others(2): Show |
intron_variant | MODIFIER | c.242-8026A>G | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32714786 | |||||||
chr20:32714824 | A | AAAC | 7 | a0001c0001t0002g0118 a0001c0001t0002g0119 a0001c0001t0002g0120 others(4): Show |
7 | HG01261.hp1 HG02647.hp1 HG03098.hp1 others(4): Show |
intron_variant | MODIFIER | c.242-8067_242-8065d others(5): Show |
COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32714824 | |||||||
chr20:32714824 | A | AAACAAC | 3 | a0001c0001t0001g0040 a0001c0001t0001g0079 a0001c0001t0001g0091 |
3 | NA18948.hp1 NA19005.hp2 NA19070.hp1 |
intron_variant | MODIFIER | c.242-8070_242-8065d others(8): Show |
COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32714824 | |||||||
chr20:32714824 | A | AAACAACA others(2): Show |
115 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0011 others(112): Show |
126 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(123): Show |
intron_variant | MODIFIER | c.242-8073_242-8065d others(11): Show |
COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32714824 | |||||||
chr20:32714824 | A | AAACAACA others(5): Show |
23 | a0001c0001t0001g0002 a0001c0001t0001g0041 a0001c0001t0001g0042 others(20): Show |
28 | HG00544.hp1 HG01258.hp2 HG02027.hp1 others(25): Show |
intron_variant | MODIFIER | c.242-8076_242-8065d others(14): Show |
COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32714824 | |||||||
chr20:32714824 | A | AAACAACA others(8): Show |
38 | a0001c0001t0001g0009 a0001c0001t0001g0026 a0001c0001t0001g0056 others(35): Show |
40 | HG01074.hp1 HG01074.hp2 HG01081.hp2 others(37): Show |
intron_variant | MODIFIER | c.242-8079_242-8065d others(17): Show |
COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32714824 | |||||||
chr20:32714824 | A | AAACAACA others(11): Show |
18 | a0001c0001t0001g0025 a0001c0001t0001g0038 a0001c0001t0001g0111 others(15): Show |
20 | HG00280.hp2 HG01255.hp2 HG01433.hp1 others(17): Show |
intron_variant | MODIFIER | c.242-8082_242-8065d others(20): Show |
COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32714824 | |||||||
chr20:32714824 | A | AAACAACA others(14): Show |
1 | a0001c0001t0001g0112 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.242-8085_242-8065d others(23): Show |
COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32714824 | |||||||
chr20:32714824 | AAAC | A | 3 | a0001c0001t0001g0318 a0001c0001t0001g0360 a0001c0001t0002g0223 |
3 | HG00741.hp2 HG01106.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.242-8067_242-8065d others(5): Show |
COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32714824 | |||||||
chr20:32714991 | C | T | 4 | a0001c0001t0001g0031 a0001c0001t0001g0260 a0001c0001t0001g0262 others(1): Show |
4 | HG02145.hp1 HG03139.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.242-8231G>A | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32714991 | |||||||
chr20:32715017 | T | C | 69 | a0001c0001t0001g0009 a0001c0001t0001g0012 a0001c0001t0001g0014 others(66): Show |
74 | HG00280.hp2 HG00733.hp2 HG00741.hp2 others(71): Show |
intron_variant | MODIFIER | c.242-8257A>G | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32715017 | |||||||
chr20:32715022 | A | T | 1 | a0001c0001t0002g0235 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.242-8262T>A | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32715022 | |||||||
chr20:32715023 | T | A | 1 | a0001c0001t0002g0235 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.242-8263A>T | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32715023 | |||||||
chr20:32715025 | A | AAAATAAA others(3): Show |
8 | a0001c0001t0001g0127 a0001c0001t0001g0295 a0001c0001t0001g0297 others(5): Show |
8 | HG02040.hp2 NA18942.hp2 NA18945.hp2 others(5): Show |
intron_variant | MODIFIER | c.242-8266_242-8265i others(12): Show |
COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32715025 | |||||||
chr20:32715027 | A | AATAAAT | 21 | a0001c0001t0001g0004 a0001c0001t0001g0028 a0001c0001t0001g0029 others(18): Show |
23 | HG01167.hp2 HG01243.hp2 HG02056.hp2 others(20): Show |
intron_variant | MODIFIER | c.242-8273_242-8268d others(8): Show |
COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32715027 | |||||||
chr20:32715100 | C | A | 14 | a0001c0001t0001g0040 a0001c0001t0001g0071 a0001c0001t0001g0073 others(11): Show |
14 | HG00558.hp2 HG00673.hp2 NA18940.hp2 others(11): Show |
intron_variant | MODIFIER | c.242-8340G>T | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32715100 | |||||||
chr20:32715221 | T | C | 3 | a0001c0001t0001g0260 a0001c0001t0001g0262 a0001c0001t0001g0270 |
3 | HG02145.hp1 HG03139.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.242-8461A>G | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32715221 | |||||||
chr20:32715486 | A | AAAAC | 205 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(202): Show |
229 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(226): Show |
intron_variant | MODIFIER | c.242-8730_242-8727d others(6): Show |
COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32715486 | |||||||
chr20:32715589 | T | C | 102 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0011 others(99): Show |
109 | HG00323.hp2 HG00408.hp1 HG00423.hp2 others(106): Show |
intron_variant | MODIFIER | c.242-8829A>G | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32715589 | |||||||
chr20:32715628 | G | A | 51 | a0001c0001t0001g0009 a0001c0001t0001g0025 a0001c0001t0001g0026 others(48): Show |
54 | HG00280.hp2 HG00733.hp2 HG00741.hp2 others(51): Show |
intron_variant | MODIFIER | c.242-8868C>T | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32715628 | |||||||
chr20:32715700 | G | A | 30 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0013 others(27): Show |
42 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(39): Show |
intron_variant | MODIFIER | c.242-8940C>T | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32715700 | |||||||
chr20:32715839 | T | A | 1 | a0001c0001t0005g0348 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.242-9079A>T | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32715839 | |||||||
chr20:32716140 | T | C | 205 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(202): Show |
229 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(226): Show |
intron_variant | MODIFIER | c.242-9380A>G | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32716140 | |||||||
chr20:32716337 | C | T | 1 | a0001c0001t0003g0008 | 2 | HG02280.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.242-9577G>A | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32716337 | |||||||
chr20:32716411 | C | T | 1 | a0001c0001t0001g0046 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.242-9651G>A | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32716411 | |||||||
chr20:32716442 | T | C | 1 | a0001c0001t0001g0150 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.242-9682A>G | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32716442 | |||||||
chr20:32716507 | T | C | 3 | a0001c0001t0002g0243 a0001c0001t0002g0245 a0001c0001t0002g0246 |
3 | HG01109.hp1 HG02055.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.242-9747A>G | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32716507 | |||||||
chr20:32716601 | T | C | 205 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(202): Show |
229 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(226): Show |
intron_variant | MODIFIER | c.242-9841A>G | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32716601 | |||||||
chr20:32716690 | A | C | 1 | a0001c0001t0001g0085 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.242-9930T>G | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32716690 | |||||||
chr20:32716854 | A | G | 1 | a0001c0001t0001g0104 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.242-10094T>C | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32716854 | |||||||
chr20:32716859 | C | CT | 6 | a0001c0001t0001g0121 a0001c0001t0001g0134 a0001c0001t0001g0135 others(3): Show |
6 | HG02486.hp2 HG02965.hp2 HG03579.hp2 others(3): Show |
intron_variant | MODIFIER | c.242-10100dupA | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32716859 | |||||||
chr20:32716859 | CT | C | 73 | a0001c0001t0001g0009 a0001c0001t0001g0012 a0001c0001t0001g0014 others(70): Show |
78 | HG00280.hp2 HG00639.hp2 HG00733.hp2 others(75): Show |
intron_variant | MODIFIER | c.242-10100delA | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32716859 | |||||||
chr20:32716911 | C | T | 205 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(202): Show |
229 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(226): Show |
intron_variant | MODIFIER | c.242-10151G>A | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32716911 | |||||||
chr20:32716935 | C | T | 1 | a0001c0001t0002g0196 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.242-10175G>A | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32716935 | |||||||
chr20:32716940 | C | T | 16 | a0001c0001t0001g0001 a0001c0001t0001g0128 a0001c0001t0001g0142 others(13): Show |
22 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(19): Show |
intron_variant | MODIFIER | c.242-10180G>A | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32716940 | |||||||
chr20:32717011 | G | T | 205 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(202): Show |
229 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(226): Show |
intron_variant | MODIFIER | c.242-10251C>A | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32717011 | |||||||
chr20:32717192 | G | A | 202 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(199): Show |
226 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(223): Show |
intron_variant | MODIFIER | c.242-10432C>T | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32717192 | |||||||
chr20:32717321 | A | AT | 11 | a0001c0001t0002g0035 a0001c0001t0002g0161 a0001c0001t0002g0165 others(8): Show |
11 | HG00673.hp1 HG00741.hp1 HG01361.hp2 others(8): Show |
intron_variant | MODIFIER | c.242-10562dupA | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32717321 | |||||||
chr20:32717321 | AT | A | 8 | a0001c0001t0002g0027 a0001c0001t0002g0160 a0001c0001t0002g0162 others(5): Show |
8 | HG01167.hp1 HG01975.hp2 HG02040.hp1 others(5): Show |
intron_variant | MODIFIER | c.242-10562delA | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32717321 | |||||||
chr20:32717321 | ATTTTT | A | 101 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0009 others(98): Show |
118 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(115): Show |
intron_variant | MODIFIER | c.242-10566_242-1056 others(9): Show |
COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32717321 | |||||||
chr20:32717321 | ATTTTTT | A | 96 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0011 others(93): Show |
103 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(100): Show |
intron_variant | MODIFIER | c.241+10566_242-1056 others(10): Show |
COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32717321 | |||||||
chr20:32717382 | G | A | 42 | a0001c0001t0002g0003 a0001c0001t0002g0006 a0001c0001t0002g0017 others(39): Show |
50 | HG00099.hp1 HG00423.hp1 HG00558.hp1 others(47): Show |
intron_variant | MODIFIER | c.241+10511C>T | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32717382 | |||||||
chr20:32717413 | C | T | 1 | a0001c0001t0002g0156 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.241+10480G>A | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32717413 | |||||||
chr20:32717532 | G | A | 7 | a0001c0001t0001g0002 a0001c0001t0001g0092 a0001c0001t0001g0094 others(4): Show |
11 | HG00544.hp1 HG02027.hp1 HG02071.hp1 others(8): Show |
intron_variant | MODIFIER | c.241+10361C>T | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32717532 | |||||||
chr20:32717627 | A | G | 1 | a0001c0001t0001g0114 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.241+10266T>C | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32717627 | |||||||
chr20:32717839 | T | C | 202 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(199): Show |
226 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(223): Show |
intron_variant | MODIFIER | c.241+10054A>G | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32717839 | |||||||
chr20:32717896 | C | G | 1 | a0001c0001t0001g0260 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.241+9997G>C | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32717896 | |||||||
chr20:32718065 | G | A | 201 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(198): Show |
225 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(222): Show |
intron_variant | MODIFIER | c.241+9828C>T | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32718065 | |||||||
chr20:32718068 | G | A | 1 | a0001c0001t0001g0298 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.241+9825C>T | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32718068 | |||||||
chr20:32718088 | C | CA | 14 | a0001c0001t0001g0292 a0001c0001t0002g0006 a0001c0001t0002g0019 others(11): Show |
17 | HG00423.hp1 HG00673.hp1 HG01175.hp1 others(14): Show |
intron_variant | MODIFIER | c.241+9804dupT | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32718088 | |||||||
chr20:32718088 | CA | C | 196 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(193): Show |
215 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(212): Show |
intron_variant | MODIFIER | c.241+9804delT | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32718088 | |||||||
chr20:32718122 | G | A | 1 | a0001c0001t0001g0352 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.241+9771C>T | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32718122 | |||||||
chr20:32718200 | C | T | 1 | a0001c0001t0003g0008 | 2 | HG02280.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.241+9693G>A | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32718200 | |||||||
chr20:32718231 | C | T | 1 | a0001c0001t0002g0010 | 2 | HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.241+9662G>A | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32718231 | |||||||
chr20:32718272 | C | T | 3 | a0001c0001t0002g0007 a0001c0001t0002g0035 a0001c0001t0002g0036 |
4 | HG01361.hp2 HG02615.hp1 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.241+9621G>A | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32718272 | |||||||
chr20:32718353 | G | C | 62 | a0001c0001t0001g0009 a0001c0001t0001g0012 a0001c0001t0001g0025 others(59): Show |
66 | HG00280.hp2 HG00733.hp2 HG00741.hp2 others(63): Show |
intron_variant | MODIFIER | c.241+9540C>G | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32718353 | |||||||
chr20:32718412 | A | G | 1 | a0001c0001t0002g0236 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.241+9481T>C | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32718412 | |||||||
chr20:32718413 | G | A | 201 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(198): Show |
225 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(222): Show |
intron_variant | MODIFIER | c.241+9480C>T | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32718413 | |||||||
chr20:32718424 | C | T | 2 | a0001c0001t0002g0283 a0001c0001t0002g0284 |
2 | HG02055.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.241+9469G>A | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32718424 | |||||||
chr20:32718497 | G | A | 1 | a0001c0001t0002g0234 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.241+9396C>T | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32718497 | |||||||
chr20:32718507 | T | C | 1 | a0001c0001t0001g0031 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.241+9386A>G | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32718507 | |||||||
chr20:32718515 | A | G | 1 | a0001c0001t0001g0352 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.241+9378T>C | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32718515 | |||||||
chr20:32718549 | A | C | 1 | a0001c0001t0002g0251 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.241+9344T>G | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32718549 | |||||||
chr20:32718607 | G | A | 2 | a0001c0001t0002g0020 a0001c0001t0002g0151 |
3 | NA18995.hp2 NA19054.hp1 NA19057.hp2 |
intron_variant | MODIFIER | c.241+9286C>T | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32718607 | |||||||
chr20:32718631 | G | A | 1 | a0001c0001t0001g0096 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.241+9262C>T | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32718631 | |||||||
chr20:32718710 | T | C | 3 | a0001c0001t0001g0121 a0001c0001t0001g0134 a0001c0001t0001g0135 |
3 | HG02486.hp2 HG02965.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.241+9183A>G | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32718710 | |||||||
chr20:32718729 | T | C | 97 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0011 others(94): Show |
104 | HG00323.hp2 HG00408.hp1 HG00423.hp2 others(101): Show |
intron_variant | MODIFIER | c.241+9164A>G | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32718729 | |||||||
chr20:32718780 | C | CA | 9 | a0001c0001t0001g0005 a0001c0001t0001g0013 a0001c0001t0001g0015 others(6): Show |
13 | HG01123.hp2 HG02451.hp1 HG02647.hp1 others(10): Show |
intron_variant | MODIFIER | c.241+9112dupT | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32718780 | |||||||
chr20:32718814 | T | C | 1 | a0001c0001t0001g0093 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.241+9079A>G | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32718814 | |||||||
chr20:32718830 | G | A | 2 | a0001c0001t0002g0116 a0001c0001t0002g0117 |
2 | HG00099.hp1 HG00735.hp1 |
intron_variant | MODIFIER | c.241+9063C>T | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32718830 | |||||||
chr20:32718912 | C | T | 1 | a0001c0001t0001g0352 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.241+8981G>A | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32718912 | |||||||
chr20:32718923 | T | C | 62 | a0001c0001t0001g0009 a0001c0001t0001g0012 a0001c0001t0001g0025 others(59): Show |
66 | HG00280.hp2 HG00733.hp2 HG00741.hp2 others(63): Show |
intron_variant | MODIFIER | c.241+8970A>G | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32718923 | |||||||
chr20:32718926 | C | G | 205 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(202): Show |
229 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(226): Show |
intron_variant | MODIFIER | c.241+8967G>C | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32718926 | |||||||
chr20:32719059 | G | A | 29 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0013 others(26): Show |
41 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(38): Show |
intron_variant | MODIFIER | c.241+8834C>T | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32719059 | |||||||
chr20:32719099 | C | A | 1 | a0001c0001t0001g0142 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.241+8794G>T | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32719099 | |||||||
chr20:32719271 | T | C | 1 | a0001c0001t0001g0012 | 2 | HG03579.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.241+8622A>G | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32719271 | |||||||
chr20:32719275 | C | T | 1 | a0001c0001t0002g0231 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.241+8618G>A | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32719275 | |||||||
chr20:32719409 | A | G | 1 | a0001c0001t0002g0282 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.241+8484T>C | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32719409 | |||||||
chr20:32719477 | C | T | 1 | a0001c0001t0001g0152 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.241+8416G>A | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32719477 | |||||||
chr20:32719822 | C | T | 2 | a0001c0001t0001g0134 a0001c0001t0001g0135 |
2 | HG02486.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.241+8071G>A | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32719822 | |||||||
chr20:32719905 | G | A | 1 | a0001c0001t0002g0250 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.241+7988C>T | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32719905 | |||||||
chr20:32719950 | A | G | 5 | a0001c0001t0001g0005 a0001c0001t0001g0013 a0001c0001t0001g0015 others(2): Show |
9 | HG02451.hp1 HG02809.hp1 HG03041.hp1 others(6): Show |
intron_variant | MODIFIER | c.241+7943T>C | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32719950 | |||||||
chr20:32720232 | C | T | 1 | a0001c0001t0002g0010 | 2 | HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.241+7661G>A | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32720232 | |||||||
chr20:32720233 | G | A | 1 | a0001c0001t0009g0281 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.241+7660C>T | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32720233 | |||||||
chr20:32720237 | A | G | 205 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(202): Show |
229 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(226): Show |
intron_variant | MODIFIER | c.241+7656T>C | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32720237 | |||||||
chr20:32720377 | C | A | 1 | a0001c0001t0001g0048 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.241+7516G>T | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32720377 | |||||||
chr20:32720387 | C | T | 1 | a0001c0001t0005g0348 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.241+7506G>A | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32720387 | |||||||
chr20:32720594 | A | G | 348 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(345): Show |
384 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(381): Show |
intron_variant | MODIFIER | c.241+7299T>C | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32720594 | |||||||
chr20:32720637 | C | T | 1 | a0001c0001t0001g0112 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.241+7256G>A | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32720637 | |||||||
chr20:32720638 | G | A | 3 | a0001c0001t0002g0154 a0001c0001t0002g0187 a0001c0001t0002g0227 |
3 | NA18942.hp1 NA18944.hp2 NA18961.hp1 |
intron_variant | MODIFIER | c.241+7255C>T | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32720638 | |||||||
chr20:32720701 | G | A | 2 | a0001c0001t0002g0027 a0001c0001t0002g0131 |
2 | HG00621.hp2 HG02040.hp1 |
intron_variant | MODIFIER | c.241+7192C>T | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32720701 | |||||||
chr20:32720856 | T | C | 1 | a0001c0001t0002g0209 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.241+7037A>G | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32720856 | |||||||
chr20:32720857 | A | T | 1 | a0001c0001t0002g0209 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.241+7036T>A | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32720857 | |||||||
chr20:32720881 | C | T | 205 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(202): Show |
229 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(226): Show |
intron_variant | MODIFIER | c.241+7012G>A | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32720881 | |||||||
chr20:32721091 | G | A | 3 | a0001c0001t0001g0121 a0001c0001t0001g0134 a0001c0001t0001g0135 |
3 | HG02486.hp2 HG02965.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.241+6802C>T | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32721091 | |||||||
chr20:32721199 | C | T | 3 | a0001c0001t0001g0121 a0001c0001t0001g0134 a0001c0001t0001g0135 |
3 | HG02486.hp2 HG02965.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.241+6694G>A | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32721199 | |||||||
chr20:32721251 | T | C | 202 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(199): Show |
226 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(223): Show |
intron_variant | MODIFIER | c.241+6642A>G | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32721251 | |||||||
chr20:32721289 | C | T | 1 | a0001c0001t0005g0348 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.241+6604G>A | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32721289 | |||||||
chr20:32721522 | A | G | 1 | a0001c0001t0002g0245 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.241+6371T>C | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32721522 | |||||||
chr20:32721809 | T | C | 2 | a0001c0001t0001g0114 a0001c0001t0006g0125 |
2 | HG01109.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.241+6084A>G | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32721809 | |||||||
chr20:32721896 | CA | C | 201 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(198): Show |
225 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(222): Show |
intron_variant | MODIFIER | c.241+5996delT | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32721896 | |||||||
chr20:32721986 | G | A | 8 | a0001c0001t0001g0004 a0001c0001t0001g0046 a0001c0001t0001g0047 others(5): Show |
10 | NA18946.hp2 NA18960.hp2 NA18962.hp1 others(7): Show |
intron_variant | MODIFIER | c.241+5907C>T | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32721986 | |||||||
chr20:32721993 | G | A | 18 | a0001c0001t0002g0006 a0001c0001t0002g0017 a0001c0001t0002g0018 others(15): Show |
23 | HG00423.hp1 HG00558.hp1 HG00639.hp1 others(20): Show |
intron_variant | MODIFIER | c.241+5900C>T | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32721993 | |||||||
chr20:32722103 | G | A | 202 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(199): Show |
226 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(223): Show |
intron_variant | MODIFIER | c.241+5790C>T | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32722103 | |||||||
chr20:32722138 | G | A | 1 | a0001c0001t0002g0123 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.241+5755C>T | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32722138 | |||||||
chr20:32722173 | C | T | 1 | a0001c0001t0001g0291 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.241+5720G>A | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32722173 | |||||||
chr20:32722246 | G | GA | 202 | a0001c0001t0001g0009 a0001c0001t0001g0012 a0001c0001t0001g0014 others(199): Show |
223 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(220): Show |
intron_variant | MODIFIER | c.241+5646dupT | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32722246 | |||||||
chr20:32722246 | G | GAA | 47 | a0001c0001t0001g0004 a0001c0001t0001g0028 a0001c0001t0001g0029 others(44): Show |
49 | HG01109.hp2 HG01167.hp2 HG01243.hp2 others(46): Show |
intron_variant | MODIFIER | c.241+5645_241+5646d others(4): Show |
COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32722246 | |||||||
chr20:32722246 | G | GAAA | 63 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0032 others(60): Show |
68 | HG00323.hp2 HG00408.hp1 HG00423.hp2 others(65): Show |
intron_variant | MODIFIER | c.241+5644_241+5646d others(5): Show |
COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32722246 | |||||||
chr20:32722246 | GA | G | 5 | a0001c0001t0001g0013 a0001c0001t0001g0015 a0001c0001t0001g0308 others(2): Show |
7 | HG00140.hp2 HG02300.hp1 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.241+5646delT | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32722246 | |||||||
chr20:32722276 | G | C | 10 | a0001c0001t0002g0118 a0001c0001t0002g0119 a0001c0001t0002g0120 others(7): Show |
10 | HG00738.hp2 HG01167.hp1 HG01169.hp2 others(7): Show |
intron_variant | MODIFIER | c.241+5617C>G | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32722276 | |||||||
chr20:32722347 | G | A | 1 | a0001c0001t0002g0034 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.241+5546C>T | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32722347 | |||||||
chr20:32722411 | G | A | 1 | a0001c0001t0001g0304 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.241+5482C>T | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32722411 | |||||||
chr20:32722478 | G | A | 1 | a0001c0001t0003g0008 | 2 | HG02280.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.241+5415C>T | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32722478 | |||||||
chr20:32722648 | C | T | 3 | a0001c0001t0001g0121 a0001c0001t0001g0134 a0001c0001t0001g0135 |
3 | HG02486.hp2 HG02965.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.241+5245G>A | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32722648 | |||||||
chr20:32722649 | G | A | 3 | a0001c0001t0001g0266 a0001c0001t0001g0267 a0001c0001t0001g0269 |
3 | HG00408.hp1 HG02155.hp1 NA19088.hp1 |
intron_variant | MODIFIER | c.241+5244C>T | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32722649 | |||||||
chr20:32722720 | GA | G | 13 | a0001c0001t0001g0009 a0001c0001t0001g0032 a0001c0001t0001g0056 others(10): Show |
14 | HG01884.hp2 HG01891.hp2 HG02145.hp2 others(11): Show |
intron_variant | MODIFIER | c.241+5172delT | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32722720 | |||||||
chr20:32722902 | G | T | 1 | a0001c0001t0001g0104 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.241+4991C>A | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32722902 | |||||||
chr20:32722936 | G | A | 2 | a0001c0001t0001g0026 a0001c0001t0001g0334 |
3 | HG01516.hp2 HG01517.hp1 HG01975.hp1 |
intron_variant | MODIFIER | c.241+4957C>T | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32722936 | |||||||
chr20:32722940 | A | C | 1 | a0001c0001t0002g0192 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.241+4953T>G | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32722940 | |||||||
chr20:32722976 | G | A | 97 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0011 others(94): Show |
104 | HG00323.hp2 HG00408.hp1 HG00423.hp2 others(101): Show |
intron_variant | MODIFIER | c.241+4917C>T | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32722976 | |||||||
chr20:32723045 | A | AAAT | 150 | a0001c0001t0001g0114 a0001c0001t0001g0228 a0001c0001t0002g0003 others(147): Show |
165 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(162): Show |
intron_variant | MODIFIER | c.241+4845_241+4847d others(5): Show |
COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32723045 | |||||||
chr20:32723048 | T | TA | 123 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(120): Show |
142 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(139): Show |
intron_variant | MODIFIER | c.241+4844dupT | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32723048 | |||||||
chr20:32723050 | A | AAT | 7 | a0001c0001t0001g0073 a0001c0001t0001g0080 a0001c0001t0001g0137 others(4): Show |
7 | HG00558.hp2 HG02258.hp2 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.241+4842_241+4843i others(4): Show |
COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32723050 | |||||||
chr20:32723051 | T | A | 7 | a0001c0001t0001g0073 a0001c0001t0001g0080 a0001c0001t0001g0137 others(4): Show |
7 | HG00558.hp2 HG02258.hp2 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.241+4842A>T | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32723051 | |||||||
chr20:32723057 | T | A | 5 | a0001c0001t0001g0005 a0001c0001t0001g0013 a0001c0001t0001g0015 others(2): Show |
9 | HG02451.hp1 HG02809.hp1 HG03041.hp1 others(6): Show |
intron_variant | MODIFIER | c.241+4836A>T | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32723057 | |||||||
chr20:32723063 | TAAAGACT others(1886): Show |
T | 1 | a0001c0001t0001g0353 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.241+2937_241+4829d others(2): Show |
COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32723063 | |||||||
chr20:32723063 | TAAAGACT others(1889): Show |
T | 10 | a0001c0001t0001g0014 a0001c0001t0001g0124 a0001c0001t0001g0136 others(7): Show |
11 | HG01891.hp1 HG01934.hp2 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.241+2934_241+4829d others(2): Show |
COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32723063 | |||||||
chr20:32723063 | TAAAGACT others(1892): Show |
T | 58 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(55): Show |
71 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(68): Show |
intron_variant | MODIFIER | c.241+2931_241+4829d others(2): Show |
COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32723063 | |||||||
chr20:32723063 | TAAAGACT others(1895): Show |
T | 131 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0011 others(128): Show |
141 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(138): Show |
intron_variant | MODIFIER | c.241+2928_241+4829d others(2): Show |
COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32723063 | |||||||
chr20:32723063 | TAAAGACT others(1898): Show |
T | 5 | a0001c0001t0001g0121 a0001c0001t0001g0134 a0001c0001t0001g0135 others(2): Show |
5 | HG00733.hp2 HG02486.hp2 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.241+2925_241+4829d others(2): Show |
COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32723063 | |||||||
chr20:32723076 | T | TCCTCTC | 9 | a0001c0001t0002g0182 a0001c0001t0002g0226 a0001c0001t0002g0243 others(6): Show |
9 | HG01109.hp1 HG02055.hp1 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.241+4811_241+4816d others(8): Show |
COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32723076 | |||||||
chr20:32723076 | T | TCCTCTCC others(5): Show |
1 | a0001c0001t0001g0114 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.241+4805_241+4816d others(14): Show |
COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32723076 | |||||||
chr20:32723090 | CTCTCCCT others(5): Show |
C | 3 | a0001c0001t0002g0159 a0001c0001t0002g0160 a0001c0001t0002g0189 |
3 | HG00738.hp2 HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.241+4791_241+4802d others(14): Show |
COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32723090 | |||||||
chr20:32723102 | G | C | 1 | a0001c0001t0009g0281 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.241+4791C>G | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32723102 | |||||||
chr20:32723108 | C | G | 1 | a0001c0001t0009g0281 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.241+4785G>C | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32723108 | |||||||
chr20:32723125 | C | CCTCTCCC others(23): Show |
1 | a0001c0001t0009g0281 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.241+4767_241+4768i others(32): Show |
COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32723125 | |||||||
chr20:32723129 | C | T | 2 | a0001c0001t0001g0114 a0001c0001t0006g0125 |
2 | HG01109.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.241+4764G>A | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32723129 | |||||||
chr20:32723130 | C | G | 1 | a0001c0001t0009g0281 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.241+4763G>C | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32723130 | |||||||
chr20:32723131 | T | C | 2 | a0001c0001t0001g0114 a0001c0001t0006g0125 |
2 | HG01109.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.241+4762A>G | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32723131 | |||||||
chr20:32723135 | C | G | 1 | a0001c0001t0002g0212 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.241+4758G>C | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32723135 | |||||||
chr20:32723136 | G | C | 2 | a0001c0001t0001g0114 a0001c0001t0006g0125 |
2 | HG01109.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.241+4757C>G | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32723136 | |||||||
chr20:32723176 | G | A | 1 | a0001c0001t0001g0114 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.241+4717C>T | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32723176 | |||||||
chr20:32723197 | C | T | 2 | a0001c0001t0002g0278 a0001c0001t0002g0355 |
2 | HG02109.hp1 HG02572.hp2 |
intron_variant | MODIFIER | c.241+4696G>A | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32723197 | |||||||
chr20:32723227 | C | G | 2 | a0001c0001t0002g0022 a0001c0001t0002g0238 |
3 | HG02129.hp1 NA18964.hp1 NA18993.hp2 |
intron_variant | MODIFIER | c.241+4666G>C | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32723227 | |||||||
chr20:32723270 | GAGTGCCT others(8): Show |
G | 4 | a0001c0001t0002g0226 a0001c0001t0002g0243 a0001c0001t0002g0245 others(1): Show |
4 | HG01109.hp1 HG02055.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.241+4608_241+4622d others(17): Show |
COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32723270 | |||||||
chr20:32723292 | G | A | 7 | a0001c0001t0002g0027 a0001c0001t0002g0131 a0001c0001t0002g0195 others(4): Show |
7 | HG00621.hp2 HG02040.hp1 NA18949.hp2 others(4): Show |
intron_variant | MODIFIER | c.241+4601C>T | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32723292 | |||||||
chr20:32723324 | C | T | 3 | a0001c0001t0002g0243 a0001c0001t0002g0245 a0001c0001t0002g0246 |
3 | HG01109.hp1 HG02055.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.241+4569G>A | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32723324 | |||||||
chr20:32723406 | G | A | 1 | a0001c0001t0002g0221 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.241+4487C>T | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32723406 | |||||||
chr20:32723554 | A | AC | 19 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0023 others(16): Show |
19 | HG00741.hp1 HG01358.hp1 HG02615.hp1 others(16): Show |
intron_variant | MODIFIER | c.241+4338dupG | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32723554 | |||||||
chr20:32723660 | C | A | 8 | a0001c0001t0002g0068 a0001c0001t0002g0163 a0001c0001t0002g0164 others(5): Show |
8 | HG01070.hp2 NA18944.hp1 NA18951.hp2 others(5): Show |
intron_variant | MODIFIER | c.241+4233G>T | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32723660 | |||||||
chr20:32723742 | C | T | 5 | a0001c0001t0002g0118 a0001c0001t0002g0119 a0001c0001t0002g0120 others(2): Show |
5 | HG01261.hp1 HG02647.hp1 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.241+4151G>A | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32723742 | |||||||
chr20:32723822 | C | A | 1 | a0001c0001t0002g0225 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.241+4071G>T | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32723822 | |||||||
chr20:32723891 | T | C | 2 | a0001c0001t0002g0182 a0001c0001t0002g0279 |
2 | HG02922.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.241+4002A>G | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32723891 | |||||||
chr20:32724012 | G | A | 9 | a0001c0001t0002g0006 a0001c0001t0002g0019 a0001c0001t0002g0154 others(6): Show |
11 | HG00423.hp1 HG00673.hp1 HG01175.hp1 others(8): Show |
intron_variant | MODIFIER | c.241+3881C>T | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32724012 | |||||||
chr20:32724046 | G | T | 1 | a0001c0001t0002g0355 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.241+3847C>A | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32724046 | |||||||
chr20:32724131 | A | G | 154 | a0001c0001t0001g0114 a0001c0001t0001g0228 a0001c0001t0002g0003 others(151): Show |
169 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(166): Show |
intron_variant | MODIFIER | c.241+3762T>C | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32724131 | |||||||
chr20:32724158 | C | G | 1 | a0001c0001t0002g0186 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.241+3735G>C | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32724158 | |||||||
chr20:32724174 | C | T | 1 | a0001c0001t0002g0282 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.241+3719G>A | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32724174 | |||||||
chr20:32724180 | GGGAGGTG others(168): Show |
G | 1 | a0001c0001t0002g0116 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.241+3538_241+3712d others(2): Show |
COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32724180 | |||||||
chr20:32724302 | G | A | 1 | a0001c0001t0002g0323 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.241+3591C>T | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32724302 | |||||||
chr20:32724323 | G | A | 1 | a0001c0001t0002g0019 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.241+3570C>T | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32724323 | |||||||
chr20:32724951 | T | A | 4 | a0001c0001t0001g0114 a0001c0001t0002g0030 a0001c0001t0006g0125 others(1): Show |
4 | HG00741.hp1 HG01109.hp2 HG01884.hp1 others(1): Show |
intron_variant | MODIFIER | c.241+2942A>T | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32724951 | |||||||
chr20:32724951 | T | TA | 6 | a0001c0001t0001g0228 a0001c0001t0002g0018 a0001c0001t0002g0178 others(3): Show |
6 | HG00438.hp2 HG00544.hp2 HG01258.hp1 others(3): Show |
intron_variant | MODIFIER | c.241+2941dupT | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32724951 | |||||||
chr20:32724951 | TA | T | 9 | a0001c0001t0002g0007 a0001c0001t0002g0022 a0001c0001t0002g0039 others(6): Show |
9 | HG00140.hp1 HG01167.hp1 HG02818.hp1 others(6): Show |
intron_variant | MODIFIER | c.241+2941delT | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32724951 | |||||||
chr20:32724959 | A | T | 1 | a0001c0001t0001g0353 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.241+2934T>A | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32724959 | |||||||
chr20:32724962 | A | T | 11 | a0001c0001t0001g0014 a0001c0001t0001g0124 a0001c0001t0001g0136 others(8): Show |
12 | HG01891.hp1 HG01934.hp2 HG02258.hp2 others(9): Show |
intron_variant | MODIFIER | c.241+2931T>A | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32724962 | |||||||
chr20:32724965 | A | T | 69 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(66): Show |
83 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(80): Show |
intron_variant | MODIFIER | c.241+2928T>A | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32724965 | |||||||
chr20:32724968 | A | T | 200 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(197): Show |
224 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(221): Show |
intron_variant | MODIFIER | c.241+2925T>A | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32724968 | |||||||
chr20:32724971 | A | T | 205 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(202): Show |
229 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(226): Show |
intron_variant | MODIFIER | c.241+2922T>A | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32724971 | |||||||
chr20:32725030 | C | A | 6 | a0001c0001t0003g0286 a0001c0001t0003g0288 a0001c0001t0003g0358 others(3): Show |
7 | HG02630.hp1 HG02886.hp1 HG02970.hp1 others(4): Show |
intron_variant | MODIFIER | c.241+2863G>T | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32725030 | |||||||
chr20:32725076 | T | C | 1 | a0001c0001t0002g0191 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.241+2817A>G | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32725076 | |||||||
chr20:32725109 | A | G | 202 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(199): Show |
226 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(223): Show |
intron_variant | MODIFIER | c.241+2784T>C | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32725109 | |||||||
chr20:32725120 | C | G | 1 | a0001c0001t0001g0014 | 2 | HG02723.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.241+2773G>C | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32725120 | |||||||
chr20:32725258 | G | A | 61 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0040 others(58): Show |
66 | HG00323.hp2 HG00408.hp1 HG00423.hp2 others(63): Show |
intron_variant | MODIFIER | c.241+2635C>T | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32725258 | |||||||
chr20:32725356 | C | G | 1 | a0001c0001t0001g0129 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.241+2537G>C | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32725356 | |||||||
chr20:32725384 | A | C | 2 | a0001c0001t0002g0007 a0001c0001t0002g0035 |
3 | HG01361.hp2 HG02615.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.241+2509T>G | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32725384 | |||||||
chr20:32725431 | G | GT | 11 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0001g0138 others(8): Show |
11 | HG00438.hp2 HG01167.hp2 HG01243.hp2 others(8): Show |
intron_variant | MODIFIER | c.241+2461dupA | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32725431 | |||||||
chr20:32725431 | G | GTT | 162 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(159): Show |
179 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(176): Show |
intron_variant | MODIFIER | c.241+2460_241+2461d others(4): Show |
COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32725431 | |||||||
chr20:32725431 | G | GTTT | 33 | a0001c0001t0001g0001 a0001c0001t0001g0041 a0001c0001t0001g0043 others(30): Show |
40 | HG00099.hp2 HG00280.hp1 HG00639.hp2 others(37): Show |
intron_variant | MODIFIER | c.241+2459_241+2461d others(5): Show |
COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32725431 | |||||||
chr20:32725435 | T | TG | 3 | a0001c0001t0001g0121 a0001c0001t0001g0134 a0001c0001t0001g0135 |
3 | HG02486.hp2 HG02965.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.241+2457_241+2458i others(3): Show |
COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32725435 | |||||||
chr20:32725491 | C | T | 70 | a0001c0001t0001g0009 a0001c0001t0001g0012 a0001c0001t0001g0014 others(67): Show |
75 | HG00280.hp2 HG00741.hp2 HG01074.hp1 others(72): Show |
intron_variant | MODIFIER | c.241+2402G>A | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32725491 | |||||||
chr20:32725503 | A | C | 5 | a0001c0001t0001g0032 a0001c0001t0001g0271 a0001c0001t0001g0272 others(2): Show |
5 | HG01884.hp2 HG01891.hp2 HG02145.hp2 others(2): Show |
intron_variant | MODIFIER | c.241+2390T>G | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32725503 | |||||||
chr20:32725529 | C | T | 1 | a0002c0002t0001g0082 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.241+2364G>A | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32725529 | |||||||
chr20:32725636 | G | A | 31 | a0001c0001t0001g0004 a0001c0001t0001g0028 a0001c0001t0001g0029 others(28): Show |
33 | HG01167.hp2 HG01243.hp2 HG02040.hp2 others(30): Show |
intron_variant | MODIFIER | c.241+2257C>T | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32725636 | |||||||
chr20:32725689 | A | C | 5 | a0001c0001t0001g0005 a0001c0001t0001g0013 a0001c0001t0001g0015 others(2): Show |
9 | HG02451.hp1 HG02809.hp1 HG03041.hp1 others(6): Show |
intron_variant | MODIFIER | c.241+2204T>G | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32725689 | |||||||
chr20:32725840 | C | G | 3 | a0001c0001t0001g0121 a0001c0001t0001g0134 a0001c0001t0001g0135 |
3 | HG02486.hp2 HG02965.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.241+2053G>C | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32725840 | |||||||
chr20:32725843 | G | A | 1 | a0001c0001t0001g0352 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.241+2050C>T | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32725843 | |||||||
chr20:32725930 | G | A | 90 | a0001c0001t0001g0228 a0001c0001t0002g0010 a0001c0001t0002g0016 others(87): Show |
96 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(93): Show |
intron_variant | MODIFIER | c.241+1963C>T | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32725930 | |||||||
chr20:32725969 | G | A | 2 | a0001c0001t0001g0114 a0001c0001t0006g0125 |
2 | HG01109.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.241+1924C>T | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32725969 | |||||||
chr20:32725974 | G | A | 2 | a0001c0001t0002g0068 a0001c0001t0002g0169 |
2 | NA18944.hp1 NA18966.hp2 |
intron_variant | MODIFIER | c.241+1919C>T | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32725974 | |||||||
chr20:32726000 | T | G | 1 | a0001c0001t0003g0288 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.241+1893A>C | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32726000 | |||||||
chr20:32726062 | C | CA | 12 | a0001c0001t0001g0228 a0001c0001t0002g0123 a0001c0001t0002g0161 others(9): Show |
12 | HG00438.hp2 HG00673.hp1 HG02486.hp1 others(9): Show |
intron_variant | MODIFIER | c.241+1830dupT | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32726062 | |||||||
chr20:32726062 | CA | C | 166 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0009 others(163): Show |
179 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(176): Show |
intron_variant | MODIFIER | c.241+1830delT | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32726062 | |||||||
chr20:32726121 | T | G | 9 | a0001c0001t0001g0326 a0001c0001t0001g0327 a0001c0001t0001g0329 others(6): Show |
9 | HG01074.hp2 HG01192.hp2 HG01255.hp2 others(6): Show |
intron_variant | MODIFIER | c.241+1772A>C | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32726121 | |||||||
chr20:32726172 | G | A | 2 | a0001c0001t0002g0118 a0001c0001t0002g0120 |
2 | HG02647.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.241+1721C>T | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32726172 | |||||||
chr20:32726190 | C | G | 1 | a0001c0001t0005g0348 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.241+1703G>C | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32726190 | |||||||
chr20:32726259 | C | T | 5 | a0001c0001t0001g0012 a0001c0001t0001g0111 a0001c0001t0001g0112 others(2): Show |
6 | HG01358.hp2 HG02615.hp2 HG03017.hp2 others(3): Show |
intron_variant | MODIFIER | c.241+1634G>A | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32726259 | |||||||
chr20:32726465 | A | G | 202 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(199): Show |
226 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(223): Show |
intron_variant | MODIFIER | c.241+1428T>C | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32726465 | |||||||
chr20:32726466 | C | G | 202 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(199): Show |
226 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(223): Show |
intron_variant | MODIFIER | c.241+1427G>C | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32726466 | |||||||
chr20:32726477 | G | T | 3 | a0001c0001t0001g0121 a0001c0001t0001g0134 a0001c0001t0001g0135 |
3 | HG02486.hp2 HG02965.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.241+1416C>A | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32726477 | |||||||
chr20:32726622 | G | C | 1 | a0001c0001t0005g0348 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.241+1271C>G | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32726622 | |||||||
chr20:32726640 | T | C | 2 | a0001c0001t0001g0114 a0001c0001t0006g0125 |
2 | HG01109.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.241+1253A>G | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32726640 | |||||||
chr20:32726781 | C | T | 4 | a0001c0001t0001g0152 a0001c0001t0002g0243 a0001c0001t0002g0245 others(1): Show |
4 | HG01109.hp1 HG02055.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.241+1112G>A | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32726781 | |||||||
chr20:32726818 | A | G | 207 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(204): Show |
231 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(228): Show |
intron_variant | MODIFIER | c.241+1075T>C | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32726818 | |||||||
chr20:32726950 | C | G | 205 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(202): Show |
229 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(226): Show |
intron_variant | MODIFIER | c.241+943G>C | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32726950 | |||||||
chr20:32727120 | T | TG | 202 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(199): Show |
226 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(223): Show |
intron_variant | MODIFIER | c.241+772dupC | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32727120 | |||||||
chr20:32727133 | G | A | 205 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(202): Show |
229 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(226): Show |
intron_variant | MODIFIER | c.241+760C>T | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32727133 | |||||||
chr20:32727286 | C | T | 1 | a0001c0001t0001g0122 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.241+607G>A | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32727286 | |||||||
chr20:32727346 | T | C | 202 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(199): Show |
226 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(223): Show |
intron_variant | MODIFIER | c.241+547A>G | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32727346 | |||||||
chr20:32727351 | A | G | 202 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(199): Show |
226 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(223): Show |
intron_variant | MODIFIER | c.241+542T>C | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32727351 | |||||||
chr20:32727458 | C | A | 1 | a0001c0001t0001g0122 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.241+435G>T | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32727458 | |||||||
chr20:32727534 | C | CA | 114 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(111): Show |
126 | HG00323.hp2 HG00408.hp1 HG00423.hp2 others(123): Show |
intron_variant | MODIFIER | c.241+358dupT | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32727534 | |||||||
chr20:32727534 | CA | C | 15 | a0001c0001t0001g0012 a0001c0001t0001g0111 a0001c0001t0001g0112 others(12): Show |
16 | HG01069.hp2 HG01169.hp2 HG01358.hp2 others(13): Show |
intron_variant | MODIFIER | c.241+358delT | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32727534 | |||||||
chr20:32727543 | A | G | 3 | a0001c0001t0001g0121 a0001c0001t0001g0134 a0001c0001t0001g0135 |
3 | HG02486.hp2 HG02965.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.241+350T>C | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32727543 | |||||||
chr20:32727563 | T | A | 3 | a0001c0001t0001g0121 a0001c0001t0001g0134 a0001c0001t0001g0135 |
3 | HG02486.hp2 HG02965.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.241+330A>T | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32727563 | |||||||
chr20:32727684 | C | T | 1 | a0001c0001t0002g0123 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.241+209G>A | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32727684 | |||||||
chr20:32727687 | GCTGTGCT others(4): Show |
G | 202 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(199): Show |
226 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(223): Show |
intron_variant | MODIFIER | c.241+195_241+205del others(11): Show |
COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32727687 | |||||||
chr20:32727773 | C | T | 2 | a0001c0001t0002g0177 a0001c0001t0002g0178 |
2 | HG00438.hp2 HG02074.hp1 |
intron_variant | MODIFIER | c.241+120G>A | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32727773 | |||||||
chr20:32728018 | A | G | 3 | a0001c0001t0001g0121 a0001c0001t0001g0134 a0001c0001t0001g0135 |
3 | HG02486.hp2 HG02965.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.139-23T>C | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 2/8 | chr20 | 32728018 | |||||||
chr20:32728054 | C | T | 1 | a0001c0001t0001g0331 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.138+35G>A | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 2/8 | chr20 | 32728054 | |||||||
chr20:32728055 | G | A | 97 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0011 others(94): Show |
104 | HG00323.hp2 HG00408.hp1 HG00423.hp2 others(101): Show |
intron_variant | MODIFIER | c.138+34C>T | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 2/8 | chr20 | 32728055 | |||||||
chr20:32728060 | C | T | 102 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0011 others(99): Show |
109 | HG00323.hp2 HG00408.hp1 HG00423.hp2 others(106): Show |
intron_variant | MODIFIER | c.138+29G>A | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 2/8 | chr20 | 32728060 | |||||||
chr20:32728208 | G | GGCTAT | 9 | a0001c0001t0001g0009 a0001c0001t0001g0056 a0001c0001t0001g0057 others(6): Show |
10 | NA18946.hp1 NA18950.hp2 NA18959.hp1 others(7): Show |
intron_variant | MODIFIER | c.85-67_85-66insATAG others(1): Show |
COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 1/8 | chr20 | 32728208 | |||||||
chr20:32728212 | A | G | 9 | a0001c0001t0001g0009 a0001c0001t0001g0056 a0001c0001t0001g0057 others(6): Show |
10 | NA18946.hp1 NA18950.hp2 NA18959.hp1 others(7): Show |
intron_variant | MODIFIER | c.85-70T>C | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 1/8 | chr20 | 32728212 | |||||||
chr20:32728213 | C | T | 9 | a0001c0001t0001g0009 a0001c0001t0001g0056 a0001c0001t0001g0057 others(6): Show |
10 | NA18946.hp1 NA18950.hp2 NA18959.hp1 others(7): Show |
intron_variant | MODIFIER | c.85-71G>A | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 1/8 | chr20 | 32728213 | |||||||
chr20:32728447 | T | G | 1 | a0001c0001t0006g0125 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.85-305A>C | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 1/8 | chr20 | 32728447 | |||||||
chr20:32728447 | TACAC | T | 56 | a0001c0001t0001g0009 a0001c0001t0001g0012 a0001c0001t0001g0025 others(53): Show |
60 | HG00280.hp2 HG00741.hp2 HG01074.hp1 others(57): Show |
intron_variant | MODIFIER | c.85-309_85-306delGT others(2): Show |
COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 1/8 | chr20 | 32728447 | |||||||
chr20:32728447 | TACACAC | T | 149 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(146): Show |
169 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(166): Show |
intron_variant | MODIFIER | c.85-311_85-306delGT others(4): Show |
COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 1/8 | chr20 | 32728447 | |||||||
chr20:32728480 | G | A | 205 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(202): Show |
229 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(226): Show |
intron_variant | MODIFIER | c.85-338C>T | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 1/8 | chr20 | 32728480 | |||||||
chr20:32728679 | ACCTCAGC | A | 102 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0011 others(99): Show |
109 | HG00323.hp2 HG00408.hp1 HG00423.hp2 others(106): Show |
intron_variant | MODIFIER | c.85-544_85-538delGC others(5): Show |
COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 1/8 | chr20 | 32728679 | |||||||
chr20:32728930 | G | C | 7 | a0001c0001t0003g0008 a0001c0001t0003g0286 a0001c0001t0003g0288 others(4): Show |
9 | HG02280.hp1 HG02630.hp1 HG02886.hp1 others(6): Show |
intron_variant | MODIFIER | c.85-788C>G | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 1/8 | chr20 | 32728930 | |||||||
chr20:32728960 | T | G | 207 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(204): Show |
231 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(228): Show |
intron_variant | MODIFIER | c.85-818A>C | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 1/8 | chr20 | 32728960 | |||||||
chr20:32729055 | C | T | 202 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(199): Show |
226 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(223): Show |
intron_variant | MODIFIER | c.85-913G>A | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 1/8 | chr20 | 32729055 | |||||||
chr20:32729099 | A | C | 1 | a0001c0001t0001g0128 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.85-957T>G | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 1/8 | chr20 | 32729099 | |||||||
chr20:32729167 | A | AT | 75 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0040 others(72): Show |
80 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(77): Show |
intron_variant | MODIFIER | c.85-1026dupA | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 1/8 | chr20 | 32729167 | |||||||
chr20:32729167 | A | ATT | 9 | a0001c0001t0001g0043 a0001c0001t0001g0075 a0001c0001t0001g0079 others(6): Show |
9 | HG00673.hp2 HG00733.hp1 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.85-1027_85-1026dup others(2): Show |
COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 1/8 | chr20 | 32729167 | |||||||
chr20:32729167 | AT | A | 16 | a0001c0001t0001g0032 a0001c0001t0001g0128 a0001c0001t0001g0271 others(13): Show |
17 | HG01070.hp1 HG01884.hp2 HG01891.hp2 others(14): Show |
intron_variant | MODIFIER | c.85-1026delA | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 1/8 | chr20 | 32729167 | |||||||
chr20:32729229 | T | A | 3 | a0001c0001t0002g0037 a0001c0001t0002g0157 a0001c0001t0002g0282 |
3 | HG02622.hp1 HG03471.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.85-1087A>T | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 1/8 | chr20 | 32729229 | |||||||
chr20:32729293 | C | A | 59 | a0001c0001t0001g0009 a0001c0001t0001g0012 a0001c0001t0001g0025 others(56): Show |
63 | HG00280.hp2 HG00741.hp2 HG01074.hp1 others(60): Show |
intron_variant | MODIFIER | c.85-1151G>T | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 1/8 | chr20 | 32729293 | |||||||
chr20:32729463 | C | T | 1 | a0001c0001t0002g0162 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.85-1321G>A | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 1/8 | chr20 | 32729463 | |||||||
chr20:32729518 | C | T | 1 | a0001c0001t0002g0172 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.85-1376G>A | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 1/8 | chr20 | 32729518 | |||||||
chr20:32729616 | T | TA | 196 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(193): Show |
215 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(212): Show |
intron_variant | MODIFIER | c.85-1475dupT | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 1/8 | chr20 | 32729616 | |||||||
chr20:32729854 | CAA | C | 124 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(121): Show |
141 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(138): Show |
intron_variant | MODIFIER | c.85-1714_85-1713del others(2): Show |
COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 1/8 | chr20 | 32729854 | |||||||
chr20:32729873 | C | T | 1 | a0001c0001t0002g0350 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.85-1731G>A | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 1/8 | chr20 | 32729873 | |||||||
chr20:32729921 | G | A | 1 | a0001c0001t0001g0141 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.85-1779C>T | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 1/8 | chr20 | 32729921 | |||||||
chr20:32730095 | G | A | 1 | a0001c0001t0001g0241 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.85-1953C>T | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 1/8 | chr20 | 32730095 | |||||||
chr20:32730110 | A | G | 2 | a0001c0001t0001g0114 a0001c0001t0006g0125 |
2 | HG01109.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.85-1968T>C | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 1/8 | chr20 | 32730110 | |||||||
chr20:32730110 | AGCCTGAG others(42): Show |
A | 6 | a0001c0001t0001g0094 a0001c0001t0001g0095 a0001c0001t0001g0133 others(3): Show |
6 | HG00733.hp2 HG01192.hp1 HG03710.hp1 others(3): Show |
intron_variant | MODIFIER | c.85-2017_85-1969del others(49): Show |
COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 1/8 | chr20 | 32730110 | |||||||
chr20:32730123 | T | C | 1 | a0001c0001t0002g0172 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.85-1981A>G | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 1/8 | chr20 | 32730123 | |||||||
chr20:32730144 | ATCATGTC others(42): Show |
A | 16 | a0001c0001t0001g0001 a0001c0001t0001g0128 a0001c0001t0001g0142 others(13): Show |
22 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(19): Show |
intron_variant | MODIFIER | c.85-2051_85-2003del others(49): Show |
COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 1/8 | chr20 | 32730144 | |||||||
chr20:32730265 | T | A | 102 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0011 others(99): Show |
109 | HG00323.hp2 HG00408.hp1 HG00423.hp2 others(106): Show |
intron_variant | MODIFIER | c.85-2123A>T | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 1/8 | chr20 | 32730265 | |||||||
chr20:32730280 | C | T | 1 | a0001c0001t0001g0329 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.85-2138G>A | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 1/8 | chr20 | 32730280 | |||||||
chr20:32730282 | C | T | 1 | a0001c0001t0001g0352 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.85-2140G>A | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 1/8 | chr20 | 32730282 | |||||||
chr20:32730297 | G | A | 3 | a0001c0001t0001g0121 a0001c0001t0001g0134 a0001c0001t0001g0135 |
3 | HG02486.hp2 HG02965.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.85-2155C>T | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 1/8 | chr20 | 32730297 | |||||||
chr20:32730329 | C | T | 1 | a0001c0001t0005g0348 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.85-2187G>A | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 1/8 | chr20 | 32730329 | |||||||
chr20:32730424 | G | A | 1 | a0001c0001t0002g0217 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.85-2282C>T | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 1/8 | chr20 | 32730424 | |||||||
chr20:32730442 | C | T | 6 | a0001c0001t0003g0286 a0001c0001t0003g0288 a0001c0001t0003g0358 others(3): Show |
7 | HG02630.hp1 HG02886.hp1 HG02970.hp1 others(4): Show |
intron_variant | MODIFIER | c.85-2300G>A | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 1/8 | chr20 | 32730442 | |||||||
chr20:32730489 | A | G | 1 | a0001c0001t0001g0148 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.85-2347T>C | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 1/8 | chr20 | 32730489 | |||||||
chr20:32730527 | C | G | 3 | a0001c0001t0001g0121 a0001c0001t0001g0134 a0001c0001t0001g0135 |
3 | HG02486.hp2 HG02965.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.85-2385G>C | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 1/8 | chr20 | 32730527 | |||||||
chr20:32730558 | A | AAAC | 195 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(192): Show |
217 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(214): Show |
intron_variant | MODIFIER | c.85-2419_85-2417dup others(3): Show |
COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 1/8 | chr20 | 32730558 | |||||||
chr20:32730592 | A | T | 1 | a0001c0001t0005g0348 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.85-2450T>A | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 1/8 | chr20 | 32730592 | |||||||
chr20:32730596 | T | C | 68 | a0001c0001t0001g0009 a0001c0001t0001g0012 a0001c0001t0001g0014 others(65): Show |
73 | HG00280.hp2 HG00741.hp2 HG01074.hp1 others(70): Show |
intron_variant | MODIFIER | c.85-2454A>G | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 1/8 | chr20 | 32730596 | |||||||
chr20:32730597 | G | A | 68 | a0001c0001t0001g0009 a0001c0001t0001g0012 a0001c0001t0001g0014 others(65): Show |
73 | HG00280.hp2 HG00741.hp2 HG01074.hp1 others(70): Show |
intron_variant | MODIFIER | c.85-2455C>T | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 1/8 | chr20 | 32730597 | |||||||
chr20:32730632 | T | G | 1 | a0001c0001t0005g0348 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.85-2490A>C | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 1/8 | chr20 | 32730632 | |||||||
chr20:32730921 | C | T | 17 | a0001c0001t0002g0022 a0001c0001t0002g0068 a0001c0001t0002g0158 others(14): Show |
18 | HG01070.hp2 HG02129.hp1 HG04199.hp1 others(15): Show |
intron_variant | MODIFIER | c.85-2779G>A | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 1/8 | chr20 | 32730921 | |||||||
chr20:32730930 | T | C | 202 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(199): Show |
226 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(223): Show |
intron_variant | MODIFIER | c.85-2788A>G | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 1/8 | chr20 | 32730930 | |||||||
chr20:32731147 | T | C | 1 | a0001c0001t0002g0218 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.85-3005A>G | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 1/8 | chr20 | 32731147 | |||||||
chr20:32731309 | T | A | 202 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(199): Show |
226 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(223): Show |
intron_variant | MODIFIER | c.85-3167A>T | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 1/8 | chr20 | 32731309 | |||||||
chr20:32731313 | A | G | 1 | a0001c0001t0002g0039 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.85-3171T>C | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 1/8 | chr20 | 32731313 | |||||||
chr20:32731342 | A | C | 1 | a0001c0001t0001g0352 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.85-3200T>G | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 1/8 | chr20 | 32731342 | |||||||
chr20:32731342 | A | G | 200 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(197): Show |
224 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(221): Show |
intron_variant | MODIFIER | c.85-3200T>C | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 1/8 | chr20 | 32731342 | |||||||
chr20:32731400 | G | A | 2 | a0001c0001t0001g0014 a0001c0001t0001g0136 |
3 | HG01891.hp1 HG02723.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.85-3258C>T | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 1/8 | chr20 | 32731400 | |||||||
chr20:32731428 | T | C | 4 | a0001c0001t0001g0041 a0001c0001t0001g0064 a0001c0001t0001g0065 others(1): Show |
4 | NA18953.hp2 NA18980.hp2 NA19057.hp1 others(1): Show |
intron_variant | MODIFIER | c.85-3286A>G | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 1/8 | chr20 | 32731428 | |||||||
chr20:32731571 | C | A | 31 | a0001c0001t0001g0004 a0001c0001t0001g0028 a0001c0001t0001g0029 others(28): Show |
33 | HG01167.hp2 HG01243.hp2 HG02040.hp2 others(30): Show |
intron_variant | MODIFIER | c.85-3429G>T | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 1/8 | chr20 | 32731571 | |||||||
chr20:32731792 | G | C | 1 | a0001c0001t0002g0253 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.85-3650C>G | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 1/8 | chr20 | 32731792 | |||||||
chr20:32732034 | A | G | 202 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(199): Show |
226 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(223): Show |
intron_variant | MODIFIER | c.85-3892T>C | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 1/8 | chr20 | 32732034 | |||||||
chr20:32732121 | C | T | 6 | a0001c0001t0003g0286 a0001c0001t0003g0288 a0001c0001t0003g0358 others(3): Show |
7 | HG02630.hp1 HG02886.hp1 HG02970.hp1 others(4): Show |
intron_variant | MODIFIER | c.85-3979G>A | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 1/8 | chr20 | 32732121 | |||||||
chr20:32732153 | G | A | 131 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(128): Show |
150 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(147): Show |
intron_variant | MODIFIER | c.85-4011C>T | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 1/8 | chr20 | 32732153 | |||||||
chr20:32732156 | C | T | 8 | a0001c0001t0001g0014 a0001c0001t0001g0124 a0001c0001t0001g0136 others(5): Show |
9 | HG01891.hp1 HG02572.hp1 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.85-4014G>A | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 1/8 | chr20 | 32732156 | |||||||
chr20:32732157 | G | A | 1 | a0001c0001t0002g0251 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.85-4015C>T | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 1/8 | chr20 | 32732157 | |||||||
chr20:32732198 | C | T | 1 | a0001c0001t0009g0281 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.85-4056G>A | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 1/8 | chr20 | 32732198 | |||||||
chr20:32732291 | A | G | 1 | a0001c0001t0002g0323 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.85-4149T>C | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 1/8 | chr20 | 32732291 | |||||||
chr20:32732296 | G | T | 1 | a0001c0001t0001g0097 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.85-4154C>A | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 1/8 | chr20 | 32732296 | |||||||
chr20:32732354 | G | T | 5 | a0001c0001t0001g0005 a0001c0001t0001g0013 a0001c0001t0001g0015 others(2): Show |
9 | HG02451.hp1 HG02809.hp1 HG03041.hp1 others(6): Show |
intron_variant | MODIFIER | c.85-4212C>A | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 1/8 | chr20 | 32732354 | |||||||
chr20:32732390 | C | A | 1 | a0001c0001t0002g0161 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.85-4248G>T | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 1/8 | chr20 | 32732390 | |||||||
chr20:32732390 | C | T | 1 | a0001c0001t0002g0162 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.85-4248G>A | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 1/8 | chr20 | 32732390 | |||||||
chr20:32732475 | T | C | 3 | a0001c0001t0002g0021 a0001c0001t0002g0219 a0001c0001t0002g0220 |
4 | HG01255.hp1 HG01496.hp1 HG01943.hp1 others(1): Show |
intron_variant | MODIFIER | c.85-4333A>G | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 1/8 | chr20 | 32732475 | |||||||
chr20:32732793 | G | T | 1 | a0001c0001t0001g0111 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.85-4651C>A | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 1/8 | chr20 | 32732793 | |||||||
chr20:32732807 | G | A | 1 | a0001c0001t0002g0230 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.85-4665C>T | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 1/8 | chr20 | 32732807 | |||||||
chr20:32732829 | G | A | 1 | a0001c0001t0002g0123 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.85-4687C>T | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 1/8 | chr20 | 32732829 | |||||||
chr20:32732885 | G | A | 3 | a0001c0001t0001g0114 a0001c0001t0001g0280 a0001c0001t0006g0125 |
3 | HG01109.hp2 HG03209.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.85-4743C>T | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 1/8 | chr20 | 32732885 | |||||||
chr20:32732963 | G | A | 1 | a0001c0001t0003g0288 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.85-4821C>T | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 1/8 | chr20 | 32732963 | |||||||
chr20:32733293 | A | G | 1 | a0001c0001t0001g0013 | 2 | HG03041.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.85-5151T>C | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 1/8 | chr20 | 32733293 | |||||||
chr20:32733305 | G | C | 1 | a0001c0001t0001g0327 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.85-5163C>G | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 1/8 | chr20 | 32733305 | |||||||
chr20:32733351 | C | T | 67 | a0001c0001t0001g0009 a0001c0001t0001g0012 a0001c0001t0001g0014 others(64): Show |
72 | HG00280.hp2 HG00741.hp2 HG01074.hp1 others(69): Show |
intron_variant | MODIFIER | c.85-5209G>A | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 1/8 | chr20 | 32733351 | |||||||
chr20:32733417 | T | C | 59 | a0001c0001t0001g0009 a0001c0001t0001g0012 a0001c0001t0001g0025 others(56): Show |
63 | HG00280.hp2 HG00741.hp2 HG01074.hp1 others(60): Show |
intron_variant | MODIFIER | c.85-5275A>G | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 1/8 | chr20 | 32733417 | |||||||
chr20:32733678 | T | C | 1 | a0001c0001t0001g0311 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.85-5536A>G | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 1/8 | chr20 | 32733678 | |||||||
chr20:32733711 | C | T | 67 | a0001c0001t0001g0009 a0001c0001t0001g0012 a0001c0001t0001g0014 others(64): Show |
72 | HG00280.hp2 HG00741.hp2 HG01074.hp1 others(69): Show |
intron_variant | MODIFIER | c.85-5569G>A | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 1/8 | chr20 | 32733711 | |||||||
chr20:32733716 | C | CA | 9 | a0001c0001t0001g0032 a0001c0001t0001g0150 a0001c0001t0001g0271 others(6): Show |
9 | HG01346.hp2 HG01433.hp2 HG01891.hp2 others(6): Show |
intron_variant | MODIFIER | c.85-5575dupT | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 1/8 | chr20 | 32733716 | |||||||
chr20:32733716 | CA | C | 182 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(179): Show |
201 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(198): Show |
intron_variant | MODIFIER | c.85-5575delT | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 1/8 | chr20 | 32733716 | |||||||
chr20:32733716 | CAA | C | 7 | a0001c0001t0001g0012 a0001c0001t0001g0111 a0001c0001t0001g0112 others(4): Show |
8 | HG01256.hp2 HG01358.hp2 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.85-5576_85-5575del others(2): Show |
COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 1/8 | chr20 | 32733716 | |||||||
chr20:32733867 | G | C | 1 | a0001c0001t0002g0223 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.85-5725C>G | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 1/8 | chr20 | 32733867 | |||||||
chr20:32733934 | T | G | 5 | a0001c0001t0001g0124 a0001c0001t0001g0351 a0001c0001t0001g0353 others(2): Show |
5 | HG02572.hp1 HG02717.hp1 HG03516.hp1 others(2): Show |
intron_variant | MODIFIER | c.85-5792A>C | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 1/8 | chr20 | 32733934 | |||||||
chr20:32733944 | C | T | 1 | a0001c0001t0001g0325 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.85-5802G>A | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 1/8 | chr20 | 32733944 | |||||||
chr20:32733951 | C | T | 8 | a0001c0001t0001g0012 a0001c0001t0001g0043 a0001c0001t0001g0077 others(5): Show |
9 | HG01123.hp2 HG02257.hp2 HG03579.hp1 others(6): Show |
intron_variant | MODIFIER | c.85-5809G>A | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 1/8 | chr20 | 32733951 | |||||||
chr20:32733991 | C | T | 98 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0011 others(95): Show |
105 | HG00323.hp2 HG00408.hp1 HG00423.hp2 others(102): Show |
intron_variant | MODIFIER | c.85-5849G>A | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 1/8 | chr20 | 32733991 | |||||||
chr20:32734029 | A | C | 1 | a0001c0001t0009g0281 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.85-5887T>G | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 1/8 | chr20 | 32734029 | |||||||
chr20:32734107 | G | A | 4 | a0001c0001t0001g0005 a0001c0001t0001g0015 a0001c0001t0001g0149 others(1): Show |
7 | HG02451.hp1 HG02809.hp1 HG03130.hp1 others(4): Show |
intron_variant | MODIFIER | c.85-5965C>T | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 1/8 | chr20 | 32734107 | |||||||
chr20:32734113 | A | G | 202 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(199): Show |
226 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(223): Show |
intron_variant | MODIFIER | c.85-5971T>C | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 1/8 | chr20 | 32734113 | |||||||
chr20:32734131 | A | C | 2 | a0001c0001t0002g0033 a0001c0001t0002g0034 |
2 | HG02965.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.85-5989T>G | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 1/8 | chr20 | 32734131 | |||||||
chr20:32734161 | A | T | 202 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(199): Show |
226 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(223): Show |
intron_variant | MODIFIER | c.85-6019T>A | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 1/8 | chr20 | 32734161 | |||||||
chr20:32734180 | C | CA | 23 | a0001c0001t0001g0097 a0001c0001t0001g0102 a0001c0001t0001g0115 others(20): Show |
24 | HG01261.hp1 HG01346.hp1 HG01928.hp2 others(21): Show |
intron_variant | MODIFIER | c.85-6039dupT | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 1/8 | chr20 | 32734180 | |||||||
chr20:32734180 | CA | C | 25 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0013 others(22): Show |
35 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(32): Show |
intron_variant | MODIFIER | c.85-6039delT | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 1/8 | chr20 | 32734180 | |||||||
chr20:32734245 | C | T | 2 | a0001c0001t0001g0303 a0001c0001t0001g0305 |
2 | NA18970.hp1 NA19058.hp2 |
intron_variant | MODIFIER | c.85-6103G>A | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 1/8 | chr20 | 32734245 | |||||||
chr20:32734466 | C | T | 57 | a0001c0001t0001g0009 a0001c0001t0001g0012 a0001c0001t0001g0025 others(54): Show |
61 | HG00280.hp2 HG00741.hp2 HG01074.hp1 others(58): Show |
intron_variant | MODIFIER | c.85-6324G>A | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 1/8 | chr20 | 32734466 | |||||||
chr20:32734467 | G | A | 1 | a0001c0001t0001g0312 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.85-6325C>T | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 1/8 | chr20 | 32734467 | |||||||
chr20:32734536 | T | C | 1 | a0001c0001t0001g0313 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.85-6394A>G | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 1/8 | chr20 | 32734536 | |||||||
chr20:32734548 | A | T | 1 | a0001c0001t0001g0104 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.85-6406T>A | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 1/8 | chr20 | 32734548 | |||||||
chr20:32734748 | T | C | 1 | a0001c0001t0005g0348 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.85-6606A>G | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 1/8 | chr20 | 32734748 | |||||||
chr20:32734789 | G | T | 3 | a0001c0001t0001g0121 a0001c0001t0001g0134 a0001c0001t0001g0135 |
3 | HG02486.hp2 HG02965.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.85-6647C>A | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 1/8 | chr20 | 32734789 | |||||||
chr20:32734816 | C | T | 1 | a0001c0001t0001g0280 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.85-6674G>A | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 1/8 | chr20 | 32734816 | |||||||
chr20:32734905 | C | T | 3 | a0001c0001t0001g0072 a0001c0001t0001g0075 a0001c0001t0001g0076 |
3 | HG00733.hp1 HG01515.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.85-6763G>A | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 1/8 | chr20 | 32734905 | |||||||
chr20:32734924 | AAAAAT | A | 4 | a0001c0001t0001g0032 a0001c0001t0001g0271 a0001c0001t0001g0272 others(1): Show |
4 | HG01891.hp2 HG02145.hp2 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.85-6787_85-6783del others(5): Show |
COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 1/8 | chr20 | 32734924 | |||||||
chr20:32735195 | G | A | 1 | a0001c0001t0002g0256 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.85-7053C>T | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 1/8 | chr20 | 32735195 | |||||||
chr20:32735231 | CA | C | 8 | a0001c0001t0001g0045 a0001c0001t0001g0138 a0001c0001t0001g0139 others(5): Show |
8 | HG00438.hp1 HG02135.hp1 NA18612.hp2 others(5): Show |
intron_variant | MODIFIER | c.85-7090delT | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 1/8 | chr20 | 32735231 | |||||||
chr20:32735243 | AT | A | 194 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(191): Show |
218 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(215): Show |
intron_variant | MODIFIER | c.85-7102delA | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 1/8 | chr20 | 32735243 | |||||||
chr20:32735244 | T | A | 153 | a0001c0001t0001g0058 a0001c0001t0001g0121 a0001c0001t0001g0134 others(150): Show |
168 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(165): Show |
intron_variant | MODIFIER | c.85-7102A>T | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 1/8 | chr20 | 32735244 | |||||||
chr20:32735253 | A | G | 1 | a0001c0001t0001g0329 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.85-7111T>C | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 1/8 | chr20 | 32735253 | |||||||
chr20:32735380 | C | T | 1 | a0001c0001t0001g0074 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.85-7238G>A | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 1/8 | chr20 | 32735380 | |||||||
chr20:32735506 | A | G | 1 | a0001c0001t0001g0260 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.85-7364T>C | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 1/8 | chr20 | 32735506 | |||||||
chr20:32735566 | C | T | 3 | a0001c0001t0001g0042 a0001c0001t0001g0059 a0001c0001t0001g0129 |
3 | HG02027.hp2 HG02056.hp1 HG02135.hp2 |
intron_variant | MODIFIER | c.85-7424G>A | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 1/8 | chr20 | 32735566 | |||||||
chr20:32735598 | T | C | 1 | a0001c0001t0001g0291 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.85-7456A>G | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 1/8 | chr20 | 32735598 | |||||||
chr20:32735810 | T | C | 1 | a0001c0001t0001g0147 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.84+7498A>G | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 1/8 | chr20 | 32735810 | |||||||
chr20:32735843 | A | G | 6 | a0001c0001t0001g0293 a0001c0001t0001g0306 a0001c0001t0001g0318 others(3): Show |
6 | HG00741.hp2 HG01081.hp2 HG01496.hp2 others(3): Show |
intron_variant | MODIFIER | c.84+7465T>C | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 1/8 | chr20 | 32735843 | |||||||
chr20:32736112 | A | C | 205 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(202): Show |
229 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(226): Show |
intron_variant | MODIFIER | c.84+7196T>G | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 1/8 | chr20 | 32736112 | |||||||
chr20:32736180 | C | T | 348 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(345): Show |
384 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(381): Show |
intron_variant | MODIFIER | c.84+7128G>A | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 1/8 | chr20 | 32736180 | |||||||
chr20:32736228 | A | C | 205 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(202): Show |
229 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(226): Show |
intron_variant | MODIFIER | c.84+7080T>G | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 1/8 | chr20 | 32736228 | |||||||
chr20:32736328 | C | T | 200 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(197): Show |
224 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(221): Show |
intron_variant | MODIFIER | c.84+6980G>A | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 1/8 | chr20 | 32736328 | |||||||
chr20:32736339 | A | T | 1 | a0001c0001t0002g0161 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.84+6969T>A | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 1/8 | chr20 | 32736339 | |||||||
chr20:32736354 | G | A | 1 | a0001c0001t0001g0150 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.84+6954C>T | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 1/8 | chr20 | 32736354 | |||||||
chr20:32736480 | C | T | 8 | a0001c0001t0001g0014 a0001c0001t0001g0124 a0001c0001t0001g0136 others(5): Show |
9 | HG01891.hp1 HG02572.hp1 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.84+6828G>A | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 1/8 | chr20 | 32736480 | |||||||
chr20:32736487 | G | A | 1 | a0001c0001t0002g0235 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.84+6821C>T | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 1/8 | chr20 | 32736487 | |||||||
chr20:32736492 | A | G | 1 | a0001c0001t0002g0110 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.84+6816T>C | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 1/8 | chr20 | 32736492 | |||||||
chr20:32736626 | T | C | 202 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(199): Show |
226 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(223): Show |
intron_variant | MODIFIER | c.84+6682A>G | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 1/8 | chr20 | 32736626 | |||||||
chr20:32737368 | T | A | 2 | a0001c0001t0001g0014 a0001c0001t0001g0136 |
3 | HG01891.hp1 HG02723.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.84+5940A>T | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 1/8 | chr20 | 32737368 | |||||||
chr20:32737379 | A | AAAAAAAA others(12): Show |
1 | a0001c0001t0001g0314 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.84+5928_84+5929ins others(19): Show |
COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 1/8 | chr20 | 32737379 | |||||||
chr20:32737379 | A | AAAAAAAA others(11): Show |
19 | a0001c0001t0001g0001 a0001c0001t0001g0128 a0001c0001t0001g0133 others(16): Show |
26 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(23): Show |
intron_variant | MODIFIER | c.84+5928_84+5929ins others(18): Show |
COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 1/8 | chr20 | 32737379 | |||||||
chr20:32737379 | A | AAAAAAAA others(10): Show |
31 | a0001c0001t0001g0005 a0001c0001t0001g0012 a0001c0001t0001g0013 others(28): Show |
37 | HG00741.hp2 HG01358.hp2 HG02027.hp1 others(34): Show |
intron_variant | MODIFIER | c.84+5928_84+5929ins others(17): Show |
COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 1/8 | chr20 | 32737379 | |||||||
chr20:32737379 | A | AAAAAAAA others(9): Show |
135 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0009 others(132): Show |
146 | HG00323.hp2 HG00408.hp1 HG00423.hp2 others(143): Show |
intron_variant | MODIFIER | c.84+5928_84+5929ins others(16): Show |
COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 1/8 | chr20 | 32737379 | |||||||
chr20:32737379 | A | AAAAAAAA others(8): Show |
15 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0001g0032 others(12): Show |
15 | HG00280.hp2 HG01074.hp2 HG01167.hp2 others(12): Show |
intron_variant | MODIFIER | c.84+5928_84+5929ins others(15): Show |
COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 1/8 | chr20 | 32737379 | |||||||
chr20:32737379 | A | AAAAAAAA others(6): Show |
1 | a0001c0001t0002g0350 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.84+5928_84+5929ins others(13): Show |
COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 1/8 | chr20 | 32737379 | |||||||
chr20:32737393 | C | T | 1 | a0001c0001t0001g0152 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.84+5915G>A | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 1/8 | chr20 | 32737393 | |||||||
chr20:32737558 | A | G | 207 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(204): Show |
231 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(228): Show |
intron_variant | MODIFIER | c.84+5750T>C | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 1/8 | chr20 | 32737558 | |||||||
chr20:32737572 | T | C | 202 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(199): Show |
226 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(223): Show |
intron_variant | MODIFIER | c.84+5736A>G | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 1/8 | chr20 | 32737572 | |||||||
chr20:32737612 | T | TA | 134 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(131): Show |
153 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(150): Show |
intron_variant | MODIFIER | c.84+5695dupT | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 1/8 | chr20 | 32737612 | |||||||
chr20:32737665 | TA | T | 207 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(204): Show |
231 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(228): Show |
intron_variant | MODIFIER | c.84+5642delT | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 1/8 | chr20 | 32737665 | |||||||
chr20:32737832 | T | C | 1 | a0001c0001t0002g0236 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.84+5476A>G | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 1/8 | chr20 | 32737832 | |||||||
chr20:32737837 | T | TA | 6 | a0001c0001t0001g0072 a0001c0001t0001g0073 a0001c0001t0001g0137 others(3): Show |
6 | HG01515.hp2 HG02258.hp2 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.84+5470dupT | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 1/8 | chr20 | 32737837 | |||||||
chr20:32737837 | T | TAA | 177 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(174): Show |
195 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(192): Show |
intron_variant | MODIFIER | c.84+5469_84+5470dup others(2): Show |
COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 1/8 | chr20 | 32737837 | |||||||
chr20:32737837 | T | TAAA | 20 | a0001c0001t0001g0001 a0001c0001t0001g0054 a0001c0001t0001g0102 others(17): Show |
26 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(23): Show |
intron_variant | MODIFIER | c.84+5468_84+5470dup others(3): Show |
COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 1/8 | chr20 | 32737837 | |||||||
chr20:32737837 | TA | T | 6 | a0001c0001t0002g0016 a0001c0001t0002g0039 a0001c0001t0002g0154 others(3): Show |
7 | HG01167.hp1 HG01169.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.84+5470delT | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 1/8 | chr20 | 32737837 | |||||||
chr20:32737947 | TA | T | 205 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(202): Show |
230 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(227): Show |
intron_variant | MODIFIER | c.84+5360delT | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 1/8 | chr20 | 32737947 | |||||||
chr20:32738025 | A | G | 1 | a0001c0001t0002g0153 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.84+5283T>C | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 1/8 | chr20 | 32738025 | |||||||
chr20:32738036 | A | G | 3 | a0001c0001t0001g0121 a0001c0001t0001g0134 a0001c0001t0001g0135 |
3 | HG02486.hp2 HG02965.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.84+5272T>C | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 1/8 | chr20 | 32738036 | |||||||
chr20:32738081 | C | T | 202 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(199): Show |
226 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(223): Show |
intron_variant | MODIFIER | c.84+5227G>A | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 1/8 | chr20 | 32738081 | |||||||
chr20:32738304 | T | G | 202 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(199): Show |
226 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(223): Show |
intron_variant | MODIFIER | c.84+5004A>C | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 1/8 | chr20 | 32738304 | |||||||
chr20:32738364 | A | G | 202 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(199): Show |
226 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(223): Show |
intron_variant | MODIFIER | c.84+4944T>C | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 1/8 | chr20 | 32738364 | |||||||
chr20:32738423 | T | A | 1 | a0001c0001t0001g0067 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.84+4885A>T | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 1/8 | chr20 | 32738423 | |||||||
chr20:32738478 | T | C | 14 | a0001c0001t0001g0004 a0001c0001t0001g0046 a0001c0001t0001g0047 others(11): Show |
16 | NA18946.hp2 NA18956.hp2 NA18960.hp2 others(13): Show |
intron_variant | MODIFIER | c.84+4830A>G | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 1/8 | chr20 | 32738478 | |||||||
chr20:32738560 | C | T | 1 | a0001c0001t0001g0071 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.84+4748G>A | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 1/8 | chr20 | 32738560 | |||||||
chr20:32738969 | C | G | 200 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(197): Show |
224 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(221): Show |
intron_variant | MODIFIER | c.84+4339G>C | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 1/8 | chr20 | 32738969 | |||||||
chr20:32739184 | T | C | 5 | a0001c0001t0001g0032 a0001c0001t0001g0271 a0001c0001t0001g0272 others(2): Show |
5 | HG01884.hp2 HG01891.hp2 HG02145.hp2 others(2): Show |
intron_variant | MODIFIER | c.84+4124A>G | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 1/8 | chr20 | 32739184 | |||||||
chr20:32739337 | C | G | 202 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(199): Show |
226 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(223): Show |
intron_variant | MODIFIER | c.84+3971G>C | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 1/8 | chr20 | 32739337 | |||||||
chr20:32739369 | G | C | 3 | a0001c0001t0001g0121 a0001c0001t0001g0134 a0001c0001t0001g0135 |
3 | HG02486.hp2 HG02965.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.84+3939C>G | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 1/8 | chr20 | 32739369 | |||||||
chr20:32739451 | C | A | 15 | a0001c0001t0001g0001 a0001c0001t0001g0128 a0001c0001t0001g0240 others(12): Show |
21 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(18): Show |
intron_variant | MODIFIER | c.84+3857G>T | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 1/8 | chr20 | 32739451 | |||||||
chr20:32739525 | C | G | 202 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(199): Show |
225 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(222): Show |
intron_variant | MODIFIER | c.84+3783G>C | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 1/8 | chr20 | 32739525 | |||||||
chr20:32739527 | C | A | 2 | a0001c0001t0002g0022 a0001c0001t0002g0238 |
3 | HG02129.hp1 NA18964.hp1 NA18993.hp2 |
intron_variant | MODIFIER | c.84+3781G>T | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 1/8 | chr20 | 32739527 | |||||||
chr20:32739538 | G | A | 1 | a0001c0001t0002g0277 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.84+3770C>T | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 1/8 | chr20 | 32739538 | |||||||
chr20:32739555 | GAATGGCG others(665): Show |
G | 103 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0011 others(100): Show |
110 | HG00323.hp2 HG00408.hp1 HG00423.hp2 others(107): Show |
intron_variant | MODIFIER | c.84+3081_84+3752del | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 1/8 | chr20 | 32739555 | |||||||
chr20:32739628 | G | C | 1 | a0001c0001t0002g0243 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.84+3680C>G | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 1/8 | chr20 | 32739628 | |||||||
chr20:32739644 | C | CA | 20 | a0001c0001t0001g0114 a0001c0001t0002g0039 a0001c0001t0002g0044 others(17): Show |
20 | HG00408.hp2 HG00741.hp1 HG01109.hp1 others(17): Show |
intron_variant | MODIFIER | c.84+3663dupT | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 1/8 | chr20 | 32739644 | |||||||
chr20:32739644 | C | CAAAAAA | 54 | a0001c0001t0001g0009 a0001c0001t0001g0012 a0001c0001t0001g0014 others(51): Show |
58 | HG00280.hp2 HG00733.hp2 HG01074.hp1 others(55): Show |
intron_variant | MODIFIER | c.84+3658_84+3663dup others(6): Show |
COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 1/8 | chr20 | 32739644 | |||||||
chr20:32739644 | C | CAAAAAAA | 28 | a0001c0001t0001g0005 a0001c0001t0001g0013 a0001c0001t0001g0014 others(25): Show |
31 | HG01081.hp2 HG01255.hp2 HG01358.hp2 others(28): Show |
intron_variant | MODIFIER | c.84+3657_84+3663dup others(7): Show |
COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 1/8 | chr20 | 32739644 | |||||||
chr20:32739644 | C | CAAAAAAA others(2): Show |
12 | a0001c0001t0001g0001 a0001c0001t0001g0128 a0001c0001t0001g0240 others(9): Show |
14 | HG00099.hp2 HG00280.hp1 HG00639.hp2 others(11): Show |
intron_variant | MODIFIER | c.84+3655_84+3663dup others(9): Show |
COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 1/8 | chr20 | 32739644 | |||||||
chr20:32739644 | C | CAAAAAAA others(3): Show |
4 | a0001c0001t0001g0001 a0001c0001t0001g0308 a0001c0001t0001g0311 others(1): Show |
7 | HG00140.hp2 HG00735.hp2 HG01175.hp2 others(4): Show |
intron_variant | MODIFIER | c.84+3654_84+3663dup others(10): Show |
COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 1/8 | chr20 | 32739644 | |||||||
chr20:32739717 | G | T | 1 | a0001c0001t0005g0348 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.84+3591C>A | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 1/8 | chr20 | 32739717 | |||||||
chr20:32739748 | T | G | 1 | a0001c0001t0003g0288 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.84+3560A>C | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 1/8 | chr20 | 32739748 | |||||||
chr20:32739843 | G | T | 101 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0009 others(98): Show |
118 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(115): Show |
intron_variant | MODIFIER | c.84+3465C>A | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 1/8 | chr20 | 32739843 | |||||||
chr20:32739878 | T | C | 102 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0009 others(99): Show |
119 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(116): Show |
intron_variant | MODIFIER | c.84+3430A>G | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 1/8 | chr20 | 32739878 | |||||||
chr20:32739879 | G | A | 99 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0009 others(96): Show |
116 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(113): Show |
intron_variant | MODIFIER | c.84+3429C>T | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 1/8 | chr20 | 32739879 | |||||||
chr20:32739926 | G | A | 6 | a0001c0001t0001g0025 a0001c0001t0001g0115 a0001c0001t0001g0320 others(3): Show |
7 | HG01258.hp2 HG01346.hp1 HG01433.hp1 others(4): Show |
intron_variant | MODIFIER | c.84+3382C>T | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 1/8 | chr20 | 32739926 | |||||||
chr20:32739949 | T | C | 1 | a0001c0001t0003g0286 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.84+3359A>G | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 1/8 | chr20 | 32739949 | |||||||
chr20:32739969 | C | T | 15 | a0001c0001t0001g0001 a0001c0001t0001g0128 a0001c0001t0001g0240 others(12): Show |
21 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(18): Show |
intron_variant | MODIFIER | c.84+3339G>A | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 1/8 | chr20 | 32739969 | |||||||
chr20:32739971 | G | A | 2 | a0001c0001t0002g0182 a0001c0001t0002g0279 |
2 | HG02922.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.84+3337C>T | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 1/8 | chr20 | 32739971 | |||||||
chr20:32739985 | G | A | 17 | a0001c0001t0001g0001 a0001c0001t0001g0128 a0001c0001t0001g0240 others(14): Show |
24 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(21): Show |
intron_variant | MODIFIER | c.84+3323C>T | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 1/8 | chr20 | 32739985 | |||||||
chr20:32740067 | C | G | 1 | a0001c0001t0002g0070 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.84+3241G>C | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 1/8 | chr20 | 32740067 | |||||||
chr20:32740114 | G | A | 98 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0009 others(95): Show |
115 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(112): Show |
intron_variant | MODIFIER | c.84+3194C>T | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 1/8 | chr20 | 32740114 | |||||||
chr20:32740184 | G | A | 2 | a0001c0001t0001g0289 a0001c0001t0001g0290 |
2 | HG02451.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.84+3124C>T | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 1/8 | chr20 | 32740184 | |||||||
chr20:32740191 | G | C | 100 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0009 others(97): Show |
117 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(114): Show |
intron_variant | MODIFIER | c.84+3117C>G | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 1/8 | chr20 | 32740191 | |||||||
chr20:32740233 | C | T | 1 | a0001c0001t0002g0151 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.84+3075G>A | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 1/8 | chr20 | 32740233 | |||||||
chr20:32740242 | G | A | 2 | a0001c0001t0001g0014 a0001c0001t0001g0136 |
3 | HG01891.hp1 HG02723.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.84+3066C>T | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 1/8 | chr20 | 32740242 | |||||||
chr20:32740272 | A | G | 103 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0011 others(100): Show |
110 | HG00323.hp2 HG00408.hp1 HG00423.hp2 others(107): Show |
intron_variant | MODIFIER | c.84+3036T>C | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 1/8 | chr20 | 32740272 | |||||||
chr20:32740316 | CA | C | 201 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(198): Show |
225 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(222): Show |
intron_variant | MODIFIER | c.84+2991delT | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 1/8 | chr20 | 32740316 | |||||||
chr20:32740364 | G | A | 201 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(198): Show |
225 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(222): Show |
intron_variant | MODIFIER | c.84+2944C>T | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 1/8 | chr20 | 32740364 | |||||||
chr20:32740494 | A | G | 3 | a0001c0001t0001g0121 a0001c0001t0001g0134 a0001c0001t0001g0135 |
3 | HG02486.hp2 HG02965.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.84+2814T>C | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 1/8 | chr20 | 32740494 | |||||||
chr20:32740542 | TC | T | 202 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(199): Show |
227 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(224): Show |
intron_variant | MODIFIER | c.84+2765delG | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 1/8 | chr20 | 32740542 | |||||||
chr20:32740556 | G | A | 1 | a0001c0001t0001g0343 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.84+2752C>T | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 1/8 | chr20 | 32740556 | |||||||
chr20:32740562 | G | A | 1 | a0001c0001t0001g0343 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.84+2746C>T | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 1/8 | chr20 | 32740562 | |||||||
chr20:32740575 | G | A | 1 | a0001c0001t0008g0239 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.84+2733C>T | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 1/8 | chr20 | 32740575 | |||||||
chr20:32740620 | T | A | 206 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(203): Show |
230 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(227): Show |
intron_variant | MODIFIER | c.84+2688A>T | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 1/8 | chr20 | 32740620 | |||||||
chr20:32740640 | C | G | 1 | a0001c0001t0005g0348 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.84+2668G>C | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 1/8 | chr20 | 32740640 | |||||||
chr20:32740813 | C | CA | 208 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(205): Show |
233 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(230): Show |
intron_variant | MODIFIER | c.84+2494dupT | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 1/8 | chr20 | 32740813 | |||||||
chr20:32740813 | C | CAA | 10 | a0001c0001t0001g0032 a0001c0001t0001g0121 a0001c0001t0001g0124 others(7): Show |
11 | HG01884.hp2 HG02280.hp1 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.84+2493_84+2494dup others(2): Show |
COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 1/8 | chr20 | 32740813 | |||||||
chr20:32740873 | T | A | 1 | a0001c0001t0001g0121 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.84+2435A>T | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 1/8 | chr20 | 32740873 | |||||||
chr20:32740929 | G | A | 1 | a0001c0001t0001g0042 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.84+2379C>T | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 1/8 | chr20 | 32740929 | |||||||
chr20:32740969 | G | C | 1 | a0001c0001t0001g0280 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.84+2339C>G | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 1/8 | chr20 | 32740969 | |||||||
chr20:32740977 | T | C | 5 | a0001c0001t0002g0023 a0001c0001t0002g0253 a0001c0001t0002g0254 others(2): Show |
6 | HG01928.hp1 HG02132.hp2 NA18983.hp2 others(3): Show |
intron_variant | MODIFIER | c.84+2331A>G | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 1/8 | chr20 | 32740977 | |||||||
chr20:32740986 | T | C | 62 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0040 others(59): Show |
71 | HG00140.hp2 HG00280.hp1 HG00639.hp2 others(68): Show |
intron_variant | MODIFIER | c.84+2322A>G | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 1/8 | chr20 | 32740986 | |||||||
chr20:32741105 | T | C | 2 | a0001c0001t0001g0114 a0001c0001t0001g0136 |
2 | HG01109.hp2 HG01891.hp1 |
intron_variant | MODIFIER | c.84+2203A>G | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 1/8 | chr20 | 32741105 | |||||||
chr20:32741150 | C | CA | 3 | a0001c0001t0001g0042 a0001c0001t0001g0292 a0001c0001t0001g0360 |
3 | HG00741.hp2 HG02027.hp2 HG02738.hp2 |
intron_variant | MODIFIER | c.84+2157dupT | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 1/8 | chr20 | 32741150 | |||||||
chr20:32741154 | C | A | 38 | a0001c0001t0001g0026 a0001c0001t0001g0041 a0001c0001t0001g0042 others(35): Show |
39 | HG00280.hp2 HG00733.hp2 HG00741.hp2 others(36): Show |
intron_variant | MODIFIER | c.84+2154G>T | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 1/8 | chr20 | 32741154 | |||||||
chr20:32741158 | C | A | 67 | a0001c0001t0001g0009 a0001c0001t0001g0025 a0001c0001t0001g0026 others(64): Show |
71 | HG00280.hp2 HG00733.hp2 HG00741.hp2 others(68): Show |
intron_variant | MODIFIER | c.84+2150G>T | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 1/8 | chr20 | 32741158 | |||||||
chr20:32741158 | CA | C | 145 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(142): Show |
166 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(163): Show |
intron_variant | MODIFIER | c.84+2149delT | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 1/8 | chr20 | 32741158 | |||||||
chr20:32741209 | A | T | 12 | a0001c0001t0001g0134 a0001c0001t0001g0135 a0001c0001t0001g0136 others(9): Show |
12 | HG01884.hp2 HG01891.hp1 HG02486.hp2 others(9): Show |
intron_variant | MODIFIER | c.84+2099T>A | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 1/8 | chr20 | 32741209 | |||||||
chr20:32741259 | T | C | 1 | a0001c0001t0001g0357 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.84+2049A>G | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 1/8 | chr20 | 32741259 | |||||||
chr20:32741377 | G | A | 2 | a0001c0001t0001g0134 a0001c0001t0001g0135 |
2 | HG02486.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.84+1931C>T | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 1/8 | chr20 | 32741377 | |||||||
chr20:32741388 | G | A | 1 | a0001c0001t0001g0136 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.84+1920C>T | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 1/8 | chr20 | 32741388 | |||||||
chr20:32741395 | G | GT | 190 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(187): Show |
213 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(210): Show |
intron_variant | MODIFIER | c.84+1912dupA | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 1/8 | chr20 | 32741395 | |||||||
chr20:32741395 | G | GTT | 14 | a0001c0001t0001g0040 a0001c0001t0001g0041 a0001c0001t0001g0042 others(11): Show |
14 | HG01884.hp2 HG02027.hp2 HG02615.hp2 others(11): Show |
intron_variant | MODIFIER | c.84+1911_84+1912dup others(2): Show |
COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 1/8 | chr20 | 32741395 | |||||||
chr20:32741450 | G | A | 70 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0031 others(67): Show |
77 | HG00323.hp2 HG00408.hp1 HG00544.hp1 others(74): Show |
intron_variant | MODIFIER | c.84+1858C>T | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 1/8 | chr20 | 32741450 | |||||||
chr20:32741596 | G | A | 1 | a0001c0001t0002g0117 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.84+1712C>T | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 1/8 | chr20 | 32741596 | |||||||
chr20:32741597 | G | C | 1 | a0001c0001t0009g0281 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.84+1711C>G | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 1/8 | chr20 | 32741597 | |||||||
chr20:32741630 | C | G | 3 | a0001c0001t0002g0118 a0001c0001t0002g0119 a0001c0001t0002g0120 |
3 | HG02647.hp1 HG03098.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.84+1678G>C | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 1/8 | chr20 | 32741630 | |||||||
chr20:32741657 | A | G | 2 | a0001c0001t0002g0116 a0001c0001t0002g0117 |
2 | HG00099.hp1 HG00735.hp1 |
intron_variant | MODIFIER | c.84+1651T>C | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 1/8 | chr20 | 32741657 | |||||||
chr20:32741898 | A | G | 68 | a0001c0001t0001g0001 a0001c0001t0001g0025 a0001c0001t0001g0026 others(65): Show |
76 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(73): Show |
intron_variant | MODIFIER | c.84+1410T>C | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 1/8 | chr20 | 32741898 | |||||||
chr20:32741964 | G | A | 1 | a0001c0001t0001g0359 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.84+1344C>T | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 1/8 | chr20 | 32741964 | |||||||
chr20:32742060 | T | C | 1 | a0001c0001t0001g0360 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.84+1248A>G | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 1/8 | chr20 | 32742060 | |||||||
chr20:32742136 | G | A | 1 | a0001c0001t0002g0274 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.84+1172C>T | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 1/8 | chr20 | 32742136 | |||||||
chr20:32742143 | C | T | 77 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0009 others(74): Show |
86 | HG00323.hp2 HG00544.hp1 HG00558.hp2 others(83): Show |
intron_variant | MODIFIER | c.84+1165G>A | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 1/8 | chr20 | 32742143 | |||||||
chr20:32742309 | C | T | 285 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(282): Show |
316 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(313): Show |
intron_variant | MODIFIER | c.84+999G>A | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 1/8 | chr20 | 32742309 | |||||||
chr20:32742369 | G | C | 1 | a0001c0001t0002g0277 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.84+939C>G | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 1/8 | chr20 | 32742369 | |||||||
chr20:32742462 | A | G | 1 | a0001c0001t0001g0032 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.84+846T>C | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 1/8 | chr20 | 32742462 | |||||||
chr20:32742529 | G | A | 4 | a0001c0001t0001g0280 a0001c0001t0002g0278 a0001c0001t0002g0279 others(1): Show |
4 | HG00741.hp1 HG02572.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.84+779C>T | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 1/8 | chr20 | 32742529 | |||||||
chr20:32742546 | C | A | 1 | a0001c0001t0002g0282 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.84+762G>T | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 1/8 | chr20 | 32742546 | |||||||
chr20:32742551 | G | C | 9 | a0001c0001t0001g0289 a0001c0001t0001g0290 a0001c0001t0002g0283 others(6): Show |
10 | HG02055.hp2 HG02451.hp2 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.84+757C>G | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 1/8 | chr20 | 32742551 | |||||||
chr20:32742554 | G | A | 4 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0001g0031 others(1): Show |
4 | HG01167.hp2 HG01243.hp2 HG01884.hp1 others(1): Show |
intron_variant | MODIFIER | c.84+754C>T | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 1/8 | chr20 | 32742554 | |||||||
chr20:32742555 | G | A | 4 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0001g0031 others(1): Show |
4 | HG01167.hp2 HG01243.hp2 HG01884.hp1 others(1): Show |
intron_variant | MODIFIER | c.84+753C>T | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 1/8 | chr20 | 32742555 | |||||||
chr20:32742607 | G | A | 286 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(283): Show |
317 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(314): Show |
intron_variant | MODIFIER | c.84+701C>T | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 1/8 | chr20 | 32742607 | |||||||
chr20:32742806 | A | G | 287 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(284): Show |
318 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(315): Show |
intron_variant | MODIFIER | c.84+502T>C | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 1/8 | chr20 | 32742806 | |||||||
chr20:32742940 | C | T | 9 | a0001c0001t0001g0032 a0001c0001t0001g0038 a0001c0001t0002g0007 others(6): Show |
11 | HG01361.hp2 HG02280.hp1 HG02615.hp1 others(8): Show |
intron_variant | MODIFIER | c.84+368G>A | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 1/8 | chr20 | 32742940 | |||||||
chr20:32743085 | G | T | 4 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0001g0031 others(1): Show |
4 | HG01167.hp2 HG01243.hp2 HG01884.hp1 others(1): Show |
intron_variant | MODIFIER | c.84+223C>A | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 1/8 | chr20 | 32743085 | |||||||
chr20:32743224 | G | T | 1 | a0001c0001t0002g0027 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.84+84C>A | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 1/8 | chr20 | 32743224 | |||||||
chr20:32743280 | G | A | 1 | a0001c0001t0001g0361 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.84+28C>T | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 1/8 | chr20 | 32743280 |